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%% This BibTeX bibliography file was created using BibDesk.
%% http://bibdesk.sourceforge.net/
%% Created for Walton Jones at 2015-10-15 20:15:09 +0900
%% Saved with string encoding Unicode (UTF-8)
@article{shaw:2002aa,
Author author = {Shaw, Paul J. and Tononi, Giulio and Greenspan, Ralph J. and Robinson, Donald F.},
Date-Added date-added = {2015-10-15 08:50:10 +0000},
Date-Modified date-modified = {2015-10-15 08:50:10 +0000},
Journal journal = {Nature},
Month month = {may},
Number number = {6886},
Pages pages = {287--291},
Publisher publisher = {Nature Publishing Group},
Title title =
{Stress {{Stress response genes protect against lethal effects of sleep deprivation in
Drosophila},
Volume Drosophila}},
volume = {417},
Year year =
2002,
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Bdsk-Url-1 bdsk-url-1 =
{http://dx.doi.org/10.1038/417287a}} {http://dx.doi.org/10.1038/417287a},
}
@article{shang:2011aa,
Author author = {Shang, Yuhua and Haynes, Paula and P{\'{\i}}rez, Nicol{\'{a}}s and Harrington, Kyle I and Guo, Fang and Pollack, Jordan and Hong, Pengyu and Griffith, Leslie C and Rosbash, Michael},
Date-Added date-added = {2015-10-14 07:05:38 +0000},
Date-Modified date-modified = {2015-10-14 07:05:38 +0000},
Journal journal = {Nature Neuroscience},
Month month = {jun},
Number number = {7},
Pages pages = {889--895},
Publisher publisher = {Nature Publishing Group},
Title title =
{Imaging {{Imaging analysis of clock neurons reveals light buffers the wake-promoting effect of
dopamine},
Volume dopamine}},
volume = {14},
Year year =
2011,
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Bdsk-Url-1 bdsk-url-1 =
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}
@article{ueno:2012aa,
Author author = {Ueno, Taro and Tomita, Jun and Tanimoto, Hiromu and Endo, Keita and Ito, Kei and Kume, Shoen and Kume, Kazuhiko},
Date-Added date-added = {2015-10-14 07:05:30 +0000},
Date-Modified date-modified = {2015-10-14 07:05:30 +0000},
Journal journal = {Nature Neuroscience},
Month month = {oct},
Number number = {11},
Pages pages = {1516--1523},
Publisher publisher = {Nature Publishing Group},
Title title =
{Identification {{Identification of a dopamine pathway that regulates sleep and arousal in
Drosophila},
Volume Drosophila}},
volume = {15},
Year year =
2012,
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Bdsk-Url-1 bdsk-url-1 =
{http://dx.doi.org/10.1038/nn.3238}} {http://dx.doi.org/10.1038/nn.3238},
}
@article{chung:2009aa,
Author author = {Chung, Brian Y. and Kilman, Valerie L. and Keath, J. Russel and Pitman, Jena L. and Allada, Ravi},
Date-Added date-added = {2015-10-14 07:05:20 +0000},
Date-Modified date-modified = {2015-10-14 07:05:20 +0000},
Journal journal = {Current Biology},
Month month = {mar},
Number number = {5},
Pages pages = {386--390},
Publisher publisher = {Elsevier {BV}},
Title title =
{The {{The {GABAA} Receptor {RDL} Acts in Peptidergic {PDF} Neurons to Promote Sleep in
Drosophila},
Volume Drosophila}},
volume = {19},
Year year =
2009,
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Bdsk-Url-1 bdsk-url-1 =
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@article{astori:2011aa,
Author author = {Astori, S. and Wimmer, R. D. and Prosser, H. M. and Corti, C. and Corsi, M. and Liaudet, N. and Volterra, A. and Franken, P. and Adelman, J. P. and Luthi, A.},
Date-Added date-added = {2015-10-09 06:36:44 +0000},
Date-Modified date-modified = {2015-10-09 06:36:44 +0000},
Journal journal = {Proceedings of the National Academy of Sciences},
Month month = {aug},
Number number = {33},
Pages pages = {13823--13828},
Publisher publisher = {Proceedings of the National Academy of Sciences},
Title title =
{The {{The {CaV}3.3 calcium channel is the major sleep spindle pacemaker in
thalamus},
Volume thalamus}},
volume = {108},
Year year =
2011,
Bdsk-File-1 {2011},
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Bdsk-Url-1 bdsk-url-1 =
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@article{cheong:2013aa,
Author author = {Cheong, E. and Shin, H.-S.},
Date-Added date-added = {2015-07-27 14:27:09 +0000},
Date-Modified date-modified = {2015-07-27 14:27:46 +0000},
Doi doi = {10.1152/physrev.00010.2012},
Journal journal = {Physiological Reviews},
Month month = {jul},
Number number = {3},
Pages pages = {961--992},
Publisher publisher = {American Physiological Society},
Title title =
{T-Type {{T-Type Ca2+ Channels in Normal and Abnormal Brain
Functions},
Volume Functions}},
volume = {93},
Year year =
2013,
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@article{weyand:2001aa,
Author author = {Weyand, Theodore G and Boudreaux, Michael and Guido, William},
Date-Added date-added = {2015-07-27 08:17:50 +0000},
Date-Modified date-modified = {2015-07-27 08:17:58 +0000},
Journal journal = {Journal of neurophysiology},
Number number = {3},
Pages pages = {1107--1118},
Publisher publisher = {Am Physiological Soc},
Title title =
{Burst {{Burst and tonic response modes in thalamic neurons during sleep and
wakefulness},
Volume wakefulness}},
volume = {85},
Year year = {2001},
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@article{crunelli:2006aa,
Author author = {Crunelli, V and Cope, D and Hughes, S},
Date-Added date-added = {2015-07-27 08:15:39 +0000},
Date-Modified date-modified = {2015-07-27 08:16:12 +0000},
Doi doi = {10.1016/j.ceca.2006.04.022},
Journal journal = {Cell Calcium},
Month month = {aug},
Number number = {2},
Pages pages = {175--190},
Publisher publisher = {Elsevier {BV}},
Title title =
{Thalamic {{Thalamic T-type Ca2+ channels and {NREM}
sleep},
Volume sleep}},
volume = {40},
Year year =
2006,
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@article{anderson:2005aa,
Author author = {Anderson, M. P. and Mochizuki, T. and Xie, J. and Fischler, W. and Manger, J. P. and Talley, E. M. and Scammell, T. E. and Tonegawa, S.},
Date-Added date-added = {2015-07-27 07:09:04 +0000},
Date-Modified date-modified = {2015-07-27 07:11:45 +0000},
Doi doi = {10.1073/pnas.0409644102},
Journal journal = {Proceedings of the National Academy of Sciences},
Month month = {jan},
Number number = {5},
Pages pages = {1743--1748},
Publisher publisher = {Proceedings of the National Academy of Sciences},
Title title =
{Thalamic {{Thalamic Cav3.1 T-type Ca2+ channel plays a crucial role in stabilizing
sleep},
Volume sleep}},
volume = {102},
Year year =
2005,
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}
@article{lambert:2013aa,
Author author = {Lambert, R{\'{e}}gis C. and Bessa\"{\i}h, Thomas and Crunelli, Vincenzo and Leresche, Nathalie},
Date-Added date-added = {2015-07-27 01:17:27 +0000},
Date-Modified date-modified = {2015-07-27 01:17:27 +0000},
Journal journal = {Pfl\"{u}gers Archiv - European Journal of Physiology},
Month month = {sep},
Number number = {3},
Pages pages = {415--423},
Publisher publisher = {Springer Science \$\mathplus\$ Business Media},
Title title =
{The {{The many faces of T-type calcium
channels},
Volume channels}},
volume = {466},
Year year =
2013,
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Bdsk-Url-1 bdsk-url-1 =
{http://dx.doi.org/10.1007/s00424-013-1353-6}} {http://dx.doi.org/10.1007/s00424-013-1353-6},
}
@article{steriade:1991aa,
Author author = {Steriade, M and Dossi, R Curro and Nu{\~{n}}ez, A},
Date-Added date-added = {2015-07-24 07:20:43 +0000},
Date-Modified date-modified = {2015-07-24 07:21:43 +0000},
Journal journal = {J Neurosci},
Number number = {10},
Pages pages = {3200--3217},
Publisher publisher = {Soc Neuroscience},
Title title =
{Network {{Network modulation of a slow intrinsic oscillation of cat thalamocortical neurons implicated in sleep delta waves: cortically induced synchronization and brainstem cholinergic
suppression},
Volume suppression}},
volume = {11},
Year year = {1991},
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@article{dossi:1992aa,
Author author = {Dossi, R C and Nu{\~{n}}ez, A and Steriade, M},
Date-Added date-added = {2015-07-24 07:17:26 +0000},
Date-Modified date-modified = {2015-07-24 07:18:06 +0000},
Doi doi = {10.1113/jphysiol.1992.sp018999},
Journal journal = {The Journal of Physiology},
Month month = {Feb},
Number number = {1},
Pages pages = {215--234},
Publisher publisher = {Wiley-Blackwell},
Title title =
{Electrophysiology {{Electrophysiology of a slow (0.5-4 Hz) intrinsic oscillation of cat thalamocortical neurones in
vivo.},
Volume vivo.}},
volume = {447},
Year year =
1992,
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@article{Osterwalder:2001cl,
Affiliation affiliation = {Department of Molecular, Cellular, and Developmental Biology, and Pharmacology Department, Yale University, P. O. Box 208103, New Haven, CT 06511, USA.
[email protected]},
Author author = {Osterwalder, T and Yoon, K S and White, B H and Keshishian, H},
Date-Added date-added = {2015-07-23 03:52:13 +0000},
Date-Modified date-modified = {2015-07-23 03:52:13 +0000},
Doi doi = {10.1073/pnas.221303298},
File file = {{Osterwalder2001cl.pdf:/Users/walton/Google Drive/Papers/2001/O/Osterwalder2001cl.pdf:application/pdf}},
Journal journal = {PNAS},
Language language = {eng},
Month month = {oct},
Number number = {22},
Pages pages = {12596--12601},
Pmid pmid = {11675495},
Rating rating = {0},
Title title = {{A conditional tissue-specific transgene expression system using inducible GAL4}},
Volume volume = {98},
Year year = {2001},
Abstract abstract = {In Drosophila, the most widely used system for generating spatially restricted transgene expression is based on the yeast GAL4 protein and its target upstream activating sequence (UAS). To permit temporal as well as spatial control over UAS-transgene expression, we have explored the use of a conditional RU486-dependent GAL4 protein (GeneSwitch) in Drosophila. By using cloned promoter fragments of the embryonic lethal abnormal vision gene or the myosin heavy chain gene, we have expressed GeneSwitch specifically in neurons or muscles and show that its transcriptional activity within the target tissues depends on the presence of the activator RU486 (mifepristone). We used available UAS-reporter lines to demonstrate RU486-dependent tissue-specific transgene expression in larvae. Reporter protein expression could be detected 5 h after systemic application of RU486 by either feeding or {larval bathing.} Transgene expression levels were dose-dependent on RU486 concentration in larval food, with low background expression in the absence of RU486. By using genetically altered ion channels as reporters, we were able to change the physiological properties of larval bodywall muscles in an RU486-dependent fashion. We demonstrate here the applicability of GeneSwitch for conditional tissue-specific expression in Drosophila, and we provide tools to control pre- and postsynaptic expression of transgenes at the larval neuromuscular junction during postembryonic life.},
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Bdsk-Url-2 bdsk-url-2 =
{http://dx.doi.org/10.1073/pnas.221303298}} {http://dx.doi.org/10.1073/pnas.221303298},
}
@article{perez-reyes:2003aa,
Author author = {Perez-Reyes, E.},
Date-Added date-added = {2015-07-22 05:44:30 +0000},
Date-Modified date-modified = {2015-07-22 05:45:23 +0000},
Doi doi = {10.1152/physrev.00018.2002},
Journal journal = {Physiological Reviews},
Month month = {jan},
Number number = {1},
Pages pages = {117--161},
Publisher publisher = {American Physiological Society},
Title title = {{Molecular Physiology of Low-Voltage-Activated T-type Calcium Channels}},
Volume volume = {83},
Year year = {2003},
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Bdsk-Url-1 bdsk-url-1 =
{http://dx.doi.org/10.1152/physrev.00018.2002}} {http://dx.doi.org/10.1152/physrev.00018.2002},
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@article{senatore:2012aa,
Author author = {Senatore, Adriano and Zhorov, Boris S. and Spafford, J. David},
Date-Added date-added = {2015-07-22 05:43:27 +0000},
Date-Modified date-modified = {2015-07-22 05:45:40 +0000},
Doi doi = {10.1002/wmts.41},
Journal journal = {{WIREs} Membr Transp Signal},
Month month = {feb},
Number number = {4},
Pages pages = {467--491},
Publisher publisher = {Wiley-Blackwell},
Title title = {{Cav3 T-type calcium channels}},
Volume volume = {1},
Year year = {2012},
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Bdsk-Url-1 bdsk-url-1 =
{http://dx.doi.org/10.1002/wmts.41}} {http://dx.doi.org/10.1002/wmts.41},
}
@article{Young:2010jq,
Affiliation affiliation = {Institute for Adaptive and Neural Computation, University of Edinburgh, Edinburgh, UK.
[email protected]},
Author author = {Young, J M and Armstrong, J D},
Date-Added date-added = {2015-07-18 12:19:25 +0000},
Date-Modified date-modified = {2015-07-18 12:19:25 +0000},
Doi doi = {10.1002/cne.22284},
File file = {{Young2010jq.pdf:/Users/walton/Google Drive/Papers/2010/Y/Young2010jq.pdf:application/pdf}},
Journal journal = {J Comp Neurol},
Keywords keywords = {fly, behavior},
Language language = {English},
Month month = {may},
Number number = {9},
Pages pages = {1500--1524},
Pmid pmid = {20187142},
Rating rating = {0},
Title title = {{Structure of the adult central complex in Drosophila: organization of distinct neuronal subsets.}},
Volume volume = {518},
Year year = {2010},
Abstract abstract = {The central complex (CX) is a defined set of neuropils located on the midline of the protocerebrum in several arthropods and has been implicated in a number of behaviors. To investigate the function of the CX further it is imperative to know the neuroarchitecture of this structure and to ensure all known neuron types conform to a common nomenclature system. Several types of CX neuron have been identified but it is not known if these exist singly or as components of isomorphic sets. We used an enhancer trap approach to study the adult structure, connectivity, and polarity of CX neurons in Drosophila. We observed several isomorphic sets of small-field neurons including pontine and fb-eb neurons, and also isomorphic sets of large-field neurons including R neurons and F neurons. We found that several types of large-field F neurons existed in isomorphic sets of approximately eight (four per hemisphere) and found evidence for small-field neuron types existing as isomorphic sets of 16. Small-field neurons were observed in clearly organized layers. This study provides a novel insight into CX structure and connectivity and provides a set of characterized enhancer trap lines that will be valuable for future study.},
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{http://dx.doi.org/10.1002/cne.22284}} {http://dx.doi.org/10.1002/cne.22284},
}
@article{Kitamoto:2001ue,
Affiliation affiliation = {Division of Neurosciences, Beckman Research Institute of the City of Hope, 1450 East Duarte Road, Duarte, California 91010, USA.
[email protected]},
Author author = {Kitamoto, T},
Date-Added date-added = {2015-07-18 12:17:04 +0000},
Date-Modified date-modified = {2015-07-18 12:17:21 +0000},
Doi doi = {10.1002/neu.1018},
File file = {{Kitamoto2001ue.pdf:/Users/walton/Google Drive/Papers/2001/K/Kitamoto2001ue.pdf:application/pdf}},
Journal journal = {J Neurobiol},
Language language = {eng},
Month month = {may},
Number number = {2},
Pages pages = {81--92},
Pmid pmid = {11291099},
Rating rating = {0},
Title title = {{Conditional modification of behavior in Drosophila by targeted expression of a temperature-sensitive shibire allele in defined neurons}},
Volume volume = {47},
Year year = {2001},
Abstract abstract = {Behavior is a manifestation of temporally and spatially defined neuronal activities. To understand how behavior is controlled by the nervous system, it is important to identify the neuronal substrates responsible for these activities, and to elucidate how they are integrated into a functional circuit. I introduce a novel and general method to conditionally perturb anatomically defined neurons in intact Drosophila. In this method, a temperature-sensitive allele of shibire (shi(ts1)) is overexpressed in neuronal subsets using the GAL4/UAS system. Because the shi gene product is essential for synaptic vesicle recycling, and shi(ts1) is semidominant, a simple temperature shift should lead to fast and reversible effects on synaptic transmission of shi(ts1) expressing neurons. When shi(ts1) expression was directed to cholinergic neurons, adult flies showed a dramatic response to the restrictive temperature, becoming motionless within 2 min at 30 degrees C. This temperature-induced paralysis was reversible. After being shifted back to the permissive temperature, they readily regained their activity and started to walk in 1 min. When shi(ts1) was expressed in photoreceptor cells, adults and larvae exhibited temperature-dependent blindness. These observations show that the GAL4/UAS system can be used to express shi(ts1) in a specific subset of neurons to cause temperature-dependent changes in behavior. Because this method allows perturbation of the neuronal activities rapidly and reversibly in a spatially and temporally restricted manner, it will be useful to study the functional significance of particular neuronal subsets in the behavior of intact animals.},
Annote annote = {Temperature-sensitive shibire},
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Bdsk-Url-1 bdsk-url-1 =
{http://www3.interscience.wiley.com/journal/78504228/abstract?CRETRY=1&SRETRY=0}} {http://www3.interscience.wiley.com/journal/78504228/abstract?CRETRY=1&SRETRY=0},
}
@article{Shaw:2000ui,
Affiliation affiliation = {The Neurosciences Institute, 10640 John Jay Hopkins Drive, San Diego, CA 92121, USA.},
Author author = {Shaw, P J and Cirelli, C and Greenspan, Ralph J and Tononi, G},
Date-Added date-added = {2015-07-18 12:16:05 +0000},
Date-Modified date-modified = {2015-07-18 12:16:05 +0000},
File file = {{Shaw2000ui.pdf:/Users/walton/Google Drive/Papers/2000/S/Shaw2000ui.pdf:application/pdf}},
Journal journal = {Science},
Language language = {eng},
Month month = {mar},
Number number = {5459},
Pages pages = {1834--1837},
Pmid pmid = {10710313},
Rating rating = {0},
Title title = {{Correlates of sleep and waking in Drosophila melanogaster}},
Volume volume = {287},
Year year = {2000},
Abstract abstract = {Drosophila exhibits a circadian rest-activity cycle, but it is not known whether fly rest constitutes sleep or is mere inactivity. It is shown here that, like mammalian sleep, rest in Drosophila is characterized by an increased arousal threshold and is homeostatically regulated independently of the circadian clock. As in mammals, rest is abundant in young flies, is reduced in older flies, and is modulated by stimulants and hypnotics. Several molecular markers modulated by sleep and waking in mammals are modulated by rest and activity in Drosophila, including cytochrome oxidase C, the endoplasmic reticulum chaperone protein BiP, and enzymes implicated in the catabolism of monoamines. Flies lacking one such enzyme, arylalkylamine N-acetyltransferase, show increased rest after rest deprivation. These results implicate the catabolism of monoamines in the regulation of sleep and waking in the fly and suggest that Drosophila may serve as a model system for the genetic dissection of sleep.},
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}
@article{Iniguez:2013ib,
Affiliation affiliation = {Department of Developmental and Cell Biology and Department of Anatomy and Neurobiology, University of California, Irvine, California.},
Author author = {Iniguez, Jorge and Schutte, Soleil S and O'Dowd, Diane K},
Date-Added date-added = {2015-07-18 12:14:51 +0000},
Date-Modified date-modified = {2015-07-18 12:14:51 +0000},
Doi doi = {10.1152/jn.00368.2013},
File file = {{Iniguez2013ib.pdf:/Users/walton/Google Drive/Papers/2013/I/Iniguez2013ib.pdf:application/pdf}},
Journal journal = {J Neurophysiol},
Language language = {English},
Month month = {oct},
Number number = {7},
Pages pages = {1490--1496},
Pmid pmid = {23864373},
Rating rating = {0},
Title title = {{Cav3-type $\alpha$1T calcium channels mediate transient calcium currents that regulate repetitive firing in Drosophila antennal lobe PNs.}},
Volume volume = {110},
Year year = {2013},
Abstract abstract = {Projection neurons (PNs), located in the antennal lobe region of the insect brain, play a key role in processing olfactory information. To explore how activity is regulated at the level of single PNs within this central circuit we have recorded from these neurons in adult Drosophila melanogaster brains. Our previous study demonstrated that PNs express voltage-gated calcium currents with a transient and sustained component. We found that the sustained component is mediated by cac gene-encoded Cav2-type channels involved in regulating action potential-independent release of neurotransmitter at excitatory cholinergic synapses. The function of the transient calcium current and the gene encoding the underlying channels, however, were unknown. Here we report that the transient current blocked by prepulse inactivation is sensitive to amiloride, a vertebrate Cav3-type channel blocker. In addition PN-specific RNAi knockdown of $\alpha$1T, the Drosophila Cav3-type gene, caused a dramatic reduction in the transient current without altering the sustained component. These data demonstrate that the $\alpha$1T gene encodes voltage-gated calcium channels underlying the amiloride-sensitive transient current. Alterations in evoked firing and spontaneous burst firing in the $\alpha$1T knockdowns demonstrate that the Cav3-type calcium channels are important in regulating excitability in adult PNs.},
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Bdsk-Url-2 bdsk-url-2 =
{http://dx.doi.org/10.1152/jn.00368.2013}} {http://dx.doi.org/10.1152/jn.00368.2013},
}
@article{alphen:2013aa,
Author author = {van Alphen, B. and Yap, M. H. W. and Kirszenblat, L. and Kottler, B. and van Swinderen, B.},
Date-Added date-added = {2015-07-17 22:46:47 +0000},
Date-Modified date-modified = {2015-07-17 22:47:15 +0000},
Doi doi = {10.1523/jneurosci.0061-13.2013},
Journal journal = {Journal of Neuroscience},
Month month = {apr},
Number number = {16},
Pages pages = {6917--6927},
Publisher publisher = {Society for Neuroscience},
Title title = {{A Dynamic Deep Sleep Stage in Drosophila}},
Volume volume = {33},
Year year = {2013},
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Bdsk-Url-1 bdsk-url-1 =
{http://dx.doi.org/10.1523/jneurosci.0061-13.2013}} {http://dx.doi.org/10.1523/jneurosci.0061-13.2013},
}
@article{nitz:2002aa,
Author author = {Nitz, Douglas A and van Swinderen, Bruno and Tononi, Giulio and Greenspan, Ralph J},
Date-Added date-added = {2015-07-17 22:45:49 +0000},
Date-Modified date-modified = {2015-07-17 22:46:47 +0000},
Doi doi = {10.1016/S0960-9822(02)01300-3},
Journal journal = {Current Biology},
Number number = {22},
Pages pages = {1934--1940},
Publisher publisher = {Elsevier},
Title title = {{Electrophysiological correlates of rest and activity in Drosophila melanogaster}},
Volume volume = {12},
Year year = {2002},
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@manual{R,
Address address = {Vienna, Austria},
Author author = {{R Core Team}},
Date-Modified date-modified = {2015-07-16 07:13:43 +0000},
Organization organization = {R Foundation for Statistical Computing},
Title title = {{R: A Language and Environment for Statistical Computing}},
Year year = {2015},
Bdsk-Url-1 bdsk-url-1 =
{http://www.r-project.org/}} {http://www.r-project.org/},
}
@manual{user,
Author author = {Peters, Gjalt-JOrn},
Date-Modified date-modified = {2015-07-16 07:13:43 +0000},
Note note = {R package version 0.3-0},
Title title = {{{userfriendlyscience}: Quantitative analysis made accessible}},
Year year = {2015},
Bdsk-Url-1 bdsk-url-1 =
{http://CRAN.R-project.org/package=userfriendlyscience}} {http://CRAN.R-project.org/package=userfriendlyscience},
}
@book{car,
Address address = {Thousand Oaks {CA}},
Author author = {Fox, John and Weisberg, Sanford},
Date-Modified date-modified = {2015-07-16 07:13:43 +0000},
Edition edition = {Second},
Publisher publisher = {Sage},
Title title = {{An {R} Companion to Applied Regression}},
Year year = {2011},
Bdsk-Url-1 bdsk-url-1 =
{http://socserv.socsci.mcmaster.ca/jfox/Books/Companion}} {http://socserv.socsci.mcmaster.ca/jfox/Books/Companion},
}
@article{Huang:2009ei,
Affiliation affiliation = {Department of Cell Biology and Physiology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.},
Author author = {Huang, Juan and Zhou, Wenke and Dong, Wei and Watson, Annie M and Hong, Yang},
Date-Added date-added = {2015-06-20 11:36:49 +0000},
Date-Modified date-modified = {2015-06-20 11:36:49 +0000},
Doi doi = {10.1073/pnas.0900641106},
File file = {{Huang2009ei.pdf:/Users/walton/Google Drive/Papers/2009/H/Huang2009ei.pdf:application/pdf;Huang2009ei.pdf:/Users/walton/Google Drive/Papers/2009/H/Huang2009ei.pdf:application/pdf}},
Journal journal = {PNAS},
Language language = {English},
Month month = {may},
Number number = {20},
Pages pages = {8284--8289},
Pmid pmid = {19429710},
Rating rating = {0},
Title title = {{Directed, efficient, and versatile modifications of the Drosophila genome by genomic engineering.}},
Volume volume = {106},
Year year = {2009},
Abstract abstract = {With the completion of genome sequences of major model organisms, increasingly sophisticated genetic tools are necessary for investigating the complex and coordinated functions of genes. Here we describe a genetic manipulation system termed {genomic engineering} in Drosophila. Genomic engineering is a 2-step process that combines the ends-out (replacement) gene targeting with phage integrase phiC31-mediated DNA integration. First, through an improved and modified gene targeting method, a founder knock-out line is generated by deleting the target gene and replacing it with an integration site of phiC31. Second, DNA integration by phiC31 is used to reintroduce modified target-gene DNA into the native locus in the founder knock-out line. Genomic engineering permits directed and highly efficient modifications of a chosen genomic locus into virtually any desired mutant allele. We have successfully applied the genomic engineering scheme on 6 different genes and have generated at their loci more than 70 unique alleles.},
Annote annote = {2012-07-18},
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Bdsk-Url-2 bdsk-url-2 =
{http://dx.doi.org/10.1073/pnas.0900641106}} {http://dx.doi.org/10.1073/pnas.0900641106},
}
@article{park:2006aa,
Author author = {Park, Jin-Yong and Kang, Ho-Won and Moon, Hyung-Jo and Huh, Sung-Un and Jeong, Seong-Woo and Soldatov, Nikolai M. and Lee, Jung-Ha},
Date-Added date-added = {2015-06-12 09:32:22 +0000},
Date-Modified date-modified = {2015-06-12 09:33:38 +0000},
Doi doi = {10.1113/jphysiol.2006.117440},
Journal journal = {J Physiol},
Month month = {nov},
Number number = {2},
Pages pages = {513--523},
Publisher publisher = {Wiley-Blackwell},
Title title = {{Activation of protein kinase {{C}} augments {{T-type}} {{Ca2+}} channel activity without changing channel surface density}},
Volume volume = {577},
Year year = {2006},
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@article{zars:2000aa,
Author author = {Zars, T and Fischer, M and Schulz, R and Heisenberg, M},
Date-Added date-added = {2015-06-11 14:36:47 +0000},
Date-Modified date-modified = {2015-06-11 14:37:34 +0000},
Doi doi = {10.1126/science.288.5466.672},
Journal journal = {Science},
Month month = {Apr},
Number number = {5466},
Pages pages = {672--675},
Publisher publisher = {American Association for the Advancement of Science ({AAAS})},
Title title = {{Localization of a Short-Term Memory in \emph{Drosophila}}},
Volume volume = {288},
Year year = {2000},
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Bdsk-Url-1 bdsk-url-1 =
{http://dx.doi.org/10.1126/science.288.5466.672}} {http://dx.doi.org/10.1126/science.288.5466.672},
}
@article{swadlow:2001aa,
Author author = {Swadlow, Harvey A. and Gusev, Alexander G.},
Date-Added date-added = {2015-06-11 14:36:11 +0000},
Date-Modified date-modified = {2015-06-11 14:40:56 +0000},
Doi doi = {10.1038/86054},
Journal journal = {Nat Neurosci},
Month month = {Apr},
Number number = {4},
Pages pages = {402--408},
Publisher publisher = {Nature Publishing Group},
Title title = {{The impact of 'bursting' thalamic impulses at a neocortical synapse}},
Volume volume = {4},
Year year = {2001},
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Bdsk-Url-1 bdsk-url-1 =
{http://dx.doi.org/10.1038/86054}} {http://dx.doi.org/10.1038/86054},
}
@article{steriade:2001aa,
Author author = {Steriade, Mircea},
Date-Added date-added = {2015-06-11 14:33:46 +0000},
Date-Modified date-modified = {2015-06-11 14:40:51 +0000},
Doi doi = {10.1038/89434},
Journal journal = {Nat Neurosci},
Number number = {7},
Pages pages = {671--671},
Publisher publisher = {Nature Publishing Group},
Title title = {{To burst, or rather, not to burst}},
Volume volume = {4},
Year year = {2001},
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}
@article{Rulifson:2002cg,
Author author = {Rulifson, Eric J and Kim, Seung K and Nusse, Roel},
Date-Added date-added = {2015-06-11 14:16:05 +0000},
Date-Modified date-modified = {2015-06-11 14:16:05 +0000},
Doi doi = {10.1126/science.1070058},
File file = {{Rulifson2002cg.pdf:/Users/walton/Google Drive/Papers/2002/R/Rulifson2002cg.pdf:application/pdf}},
Journal journal = {Science},
Language language = {English},
Month month = {may},
Number number = {5570},
Pages pages = {1118--1120},
Pmid pmid = {12004130},
Rating rating = {0},
Title title = {{Ablation of insulin-producing neurons in flies: growth and diabetic phenotypes.}},
Volume volume = {296},
Year year = {2002},
Abstract abstract = {In the fruit fly Drosophila, four insulin genes are coexpressed in small clusters of cells [insulin-producing cells (IPCs)] in the brain. Here, we show that ablation of these IPCs causes developmental delay, growth retardation, and elevated carbohydrate levels in larval hemolymph. All of the defects were reversed by ectopic expression of a Drosophila insulin transgene. On the basis of these functional data and the observation that IPCs release insulin into the circulatory system, we conclude that brain IPCs are the main systemic supply of insulin during larval growth. We propose that IPCs and pancreatic islet beta cells are functionally analogous and may have evolved from a common ancestral insulin-producing neuron. Interestingly, the phenotype of flies lacking IPCs includes certain features of diabetes mellitus.},
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Bdsk-Url-1 bdsk-url-1 = {http://www.sciencemag.org/content/296/5570/1118.short},
Bdsk-Url-2 bdsk-url-2 =
{http://dx.doi.org/10.1126/science.1070058}} {http://dx.doi.org/10.1126/science.1070058},
}
@article{glossop:2003aa,
Author author = {Glossop, Nicholas RJ and Houl, Jerry H and Zheng, Hao and Ng, Fanny S and Dudek, Scott M and Hardin, Paul E},
Date-Added date-added = {2015-06-11 14:14:47 +0000},
Date-Modified date-modified = {2015-06-11 14:15:28 +0000},
Doi doi = {10.1016/S0896-6273(03)00002-3},
Journal journal = {Neuron},
Number number = {2},
Pages pages = {249--261},
Publisher publisher = {Elsevier},
Title title = {{{{VRILLE}} feeds back to control circadian transcription of Clock in the \emph{Drosophila} circadian oscillator}},
Volume volume = {37},
Year year = {2003},
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@article{taghert:2001aa,
Author author = {Taghert, Paul H and Hewes, Randall S and Park, Jae H and O'Brien, Martha A and Han, Mei and Peck, Molly E},
Date-Added date-added = {2015-06-11 14:13:46 +0000},
Date-Modified date-modified = {2015-06-11 14:13:46 +0000},
Journal journal = {J Neurosci},
Number number = {17},
Pages pages = {6673--6686},
Publisher publisher = {Soc Neuroscience},
Title title = {{Multiple amidated neuropeptides are required for normal circadian locomotor rhythms in Drosophila}},
Volume volume = {21},
Year year = {2001},
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}
@article{freeman:1996aa,
Author author = {Freeman, Matthew},
Date-Added date-added = {2015-06-11 14:09:09 +0000},
Date-Modified date-modified = {2015-06-11 14:09:44 +0000},
Doi doi = {10.1016/S0092-8674(00)81385-9},
Journal journal = {Cell},
Number number = {4},
Pages pages = {651--660},
Publisher publisher = {Elsevier},
Title title = {{Reiterative use of the EGF receptor triggers differentiation of all cell types in the Drosophila eye}},
Volume volume = {87},
Year year = {1996},
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}
@article{alekseyenko:2010aa,
Author author = {Alekseyenko, Olga V. and Lee, Carol and Kravitz, Edward A.},
Date-Added date-added = {2015-06-11 14:08:05 +0000},
Date-Modified date-modified = {2015-06-11 14:42:43 +0000},
Doi doi = {10.1371/journal.pone.0010806},
Editor editor = {McCabe, Brian D.},
Journal journal = {{{PLoS ONE}}},
Month month = {may},
Number number = {5},
Pages pages = {e10806},
Publisher publisher = {Public Library of Science ({PLoS})},
Title title = {{Targeted Manipulation of Serotonergic Neurotransmission Affects the Escalation of Aggression in Adult Male \emph{Drosophila melanogaster}}},
Volume volume = {5},
Year year = {2010},
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}
@article{cole:2005aa,
Author author = {Cole, S. H. and Carney, G. E. and McClung, C. A. and Willard, S. S. and Taylor, B. J. and Hirsh, J.},
Date-Added date-added = {2015-06-11 14:04:57 +0000},
Date-Modified date-modified = {2015-06-11 14:40:40 +0000},
Doi doi = {10.1074/jbc.M414197200},
Journal journal = {J Biol Chem},
Month month = {Feb},
Number number = {15},
Pages pages = {14948--14955},
Publisher publisher = {American Society for Biochemistry {\\&} Molecular Biology ({ASBMB})},
Title title = {{Two Functional but Noncomplementing Drosophila Tyrosine Decarboxylase Genes: Distinct Roles For Neural Tyramine And Octopamine In Female Fertility}},
Volume volume = {280},
Year year = {2005},
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}
@article{friggi-grelin:2003aa,
Author author = {Friggi-Grelin, Florence and Coulom, H{\'e}l{\`e}ne and Meller, Margaret and Gomez, Delphine and Hirsh, Jay and Birman, Serge},
Date-Added date-added = {2015-06-11 14:02:37 +0000},
Date-Modified date-modified = {2015-06-11 14:40:17 +0000},
Doi doi = {10.1002/neu.10185},
Journal journal = {J Neurobiol},
Number number = {4},
Pages pages = {618--627},
Publisher publisher = {Wiley Online Library},
Title title = {{Targeted gene expression in \emph{Drosophila} dopaminergic cells using regulatory sequences from tyrosine hydroxylase}},
Volume volume = {54},
Year year = {2003},
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@article{renn:1999ab,
Author author = {Renn, Susan CP and Park, Jae H and Rosbash, Michael and Hall, Jeffrey C and Taghert, Paul H},
Date-Added date-added = {2015-06-11 13:58:40 +0000},
Date-Modified date-modified = {2015-06-11 13:58:40 +0000},
Doi doi = {10.1016/S0092-8674(00)81676-1},
Journal journal = {Cell},
Number number = {7},
Pages pages = {791--802},
Publisher publisher = {Elsevier},
Title title = {{A pdf neuropeptide gene mutation and ablation of PDF neurons each cause severe abnormalities of behavioral circadian rhythms in \emph{Drosophila}}},
Volume volume = {99},
Year year = {1999},
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@article{connolly:1996aa,
Author author = {Connolly, J. B. and Roberts, I. J. H. and Armstrong, J. D. and Kaiser, K. and Forte, M. and Tully, T. and O'Kane, C. J.},
Date-Added date-added = {2015-06-11 13:52:12 +0000},
Date-Modified date-modified = {2015-06-11 13:53:27 +0000},
Doi doi = {10.1126/science.274.5295.2104},
Journal journal = {Science},
Month month = {Dec},
Number number = {5295},
Pages pages = {2104--2107},
Publisher publisher = {American Association for the Advancement of Science ({AAAS})},
Title title = {{Associative Learning Disrupted by Impaired Gs Signaling in \emph{Drosophila} Mushroom Bodies}},
Volume volume = {274},
Year year = {1996},
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@article{sakai:2006aa,
Author author = {Sakai, Takaomi and Kitamoto, Toshihiro},
Date-Added date-added = {2015-06-11 13:49:29 +0000},
Date-Modified date-modified = {2015-06-11 14:40:02 +0000},
Doi doi = {10.1002/neu.20262},
Journal journal = {J Neurobiol},
Month month = {Jul},
Number number = {8},
Pages pages = {821--834},
Publisher publisher = {Wiley-Blackwell},
Title title = {{Differential roles of two major brain structures, mushroom bodies and central complex, for Drosophila male courtship behavior}},
Volume volume = {66},
Year year = {2006},
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@article{renn:1999aa,
Author author = {Renn, Susan CP and Armstrong, J Douglas and Yang, Mingyao and Wang, Zongsheng and An, Xin and Kaiser, Kim and Taghert, Paul H},
Date-Added date-added = {2015-06-11 13:48:26 +0000},
Date-Modified date-modified = {2015-06-11 14:39:49 +0000},
Doi doi = {10.1002/(SICI)1097-4695(19991105)41:2<189::AID-NEU3>3.0.CO;2-Q},
Journal journal = {J Neurobiol},
Number number = {2},
Pages pages = {189--207},
Title title = {{Genetic analysis of the \emph{Drosophila} ellipsoid body neuropil: organization and development of the central complex}},
Volume volume = {41},
Year year = {1999},
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@article{kraus:2010aa,
Author author = {Kraus, R. L. and Li, Y. and Gregan, Y. and Gotter, A. L. and Uebele, V. N. and Fox, S. V. and Doran, S. M. and Barrow, J. C. and Yang, Z.-Q. and Reger, T. S. and Koblan, K. S. and Renger, J. J.},
Date-Added date-added = {2015-06-11 13:43:49 +0000},
Date-Modified date-modified = {2015-06-11 14:41:26 +0000},
Doi doi = {10.1124/jpet.110.171058},
Journal journal = {J Pharmacology and Experimental Therapeutics},
Month month = {Aug},
Number number = {2},
Pages pages = {409--417},
Publisher publisher = {American Society for Pharmacology {\\&} Experimental Therapeutics ({ASPET})},
Title title = {{In Vitro Characterization of T-Type Calcium Channel Antagonist {TTA}-A2 and In Vivo Effects on Arousal in Mice}},
Volume volume = {335},
Year year = {2010},
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@article{talley:1999aa,
Author author = {Talley, Edmund M and Cribbs, Leanne L and Lee, Jung-Ha and Daud, Asif and Perez-Reyes, Edward and Bayliss, Douglas A},
Date-Added date-added = {2015-06-11 13:41:34 +0000},
Date-Modified date-modified = {2015-06-11 13:42:05 +0000},
Journal journal = {J Neurosci},
Number number = {6},
Pages pages = {1895--1911},
Publisher publisher = {Soc Neuroscience},
Title title = {{Differential distribution of three members of a gene family encoding low voltage-activated (T-type) calcium channels}},
Volume volume = {19},
Year year = {1999},
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@article{dreyfus:2010aa,
Author author = {Dreyfus, F. M. and Tscherter, A. and Errington, A. C. and Renger, J. J. and Shin, H.-S. and Uebele, V. N. and Crunelli, V. and Lambert, R. C. and Leresche, N.},
Date-Added date-added = {2015-06-11 13:37:56 +0000},
Date-Modified date-modified = {2015-06-11 13:38:42 +0000},
Doi doi = {10.1523/JNEUROSCI.4305-09.2010},
Journal journal = {J Neurosci},
Month month = {Jan},
Number number = {1},
Pages pages = {99--109},
Publisher publisher = {Society for Neuroscience},
Title title = {{Selective T-Type Calcium Channel Block in Thalamic Neurons Reveals Channel Redundancy and Physiological Impact of {ITwindow}}},
Volume volume = {30},
Year year = {2010},
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}
@article{crunelli:2004aa,
Author author = {Crunelli, Vincenzo and T{\'{o}}th, Tibor I. and Cope, David W. and Blethyn, Kate and Hughes, Stuart W.},
Date-Added date-added = {2015-06-11 13:36:15 +0000},
Date-Modified date-modified = {2015-07-16 07:23:39 +0000},
Doi doi = {10.1113/jphysiol.2004.076273},
Journal journal = {J Physiol},
Month month = {Dec},
Number number = {1},
Pages pages = {121--129},
Publisher publisher = {Wiley-Blackwell},
Title title = {{The 'window' T-type calcium current in brain dynamics of different behavioural states}},
Volume volume = {562},
Year year = {2004},
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Bdsk-Url-1 bdsk-url-1 =
{http://dx.doi.org/10.1113/jphysiol.2004.076273}} {http://dx.doi.org/10.1113/jphysiol.2004.076273},
}
@article{Lin:1994vn,
Affiliation affiliation = {Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley 94720.},
Author author = {Lin, D M and Goodman, C S},
Date-Added date-added = {2015-06-11 13:33:42 +0000},
Date-Modified date-modified = {2015-06-11 13:33:42 +0000},
File file = {{Lin1994vn.pdf:/Users/walton/Google Drive/Papers/1994/L/Lin1994vn.pdf:application/pdf}},
Journal journal = {Neuron},
Language language = {eng},
Month month = {sep},
Number number = {3},
Pages pages = {507--523},
Pmid pmid = {7917288},
Rating rating = {0},
Title title = {{Ectopic and increased expression of Fasciclin II alters motoneuron growth cone guidance}},
Volume volume = {13},
Year year = {1994},
Abstract abstract = {We used the enhancer detection/GAL4 system in Drosophila to direct increased levels of Fasciclin II (Fas II) expression on motoneuron growth cones and axons and to direct ectopic Fas II expression on other cells they encounter. Four classes of abnormal phenotypes are observed: {bypass} phenotypes, in which axons fail to defasciculate at the choice point where they would normally enter their muscle target region and instead extend past their target; {detour} phenotypes, in which these bypass growth cones enter their muscle target region at a different location; {stall} phenotypes, in which axons that enter their muscle target region fail to defasciculate from one another to probe their muscle targets; and {misroute} phenotypes, in which growth cones are diverted onto abnormal pathways by contact with Fas II-positive cells. These phenotypes show that changes in the pattern and level of Fas II expression can alter growth cone guidance, apparently in part by modulating the ability of these growth cones to respond to other guidance cues.},
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}
@article{carbone:1984aa,
Author author = {Carbone, E. and Lux, H.D.},
Date-Added date-added = {2015-06-11 08:43:08 +0000},
Date-Modified date-modified = {2015-06-11 08:43:08 +0000},
Journal journal = {Nature},
Month month = {Aug},
Number number = {5977},
Pages pages = {501--502},
Publisher publisher = {Nature Publishing Group},
Title title = {{A low voltage-activated, fully inactivating Ca channel in vertebrate sensory neurones}},
Volume volume = {310},
Year year = {1984},
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Bdsk-Url-1 bdsk-url-1 =
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@article{PerezReyes:2003bw,
Affiliation affiliation = {Department of Pharmacology, University of Virginia, Charlottesville, Virginia 22908-0735, USA.
[email protected]},
Author author = {Perez-Reyes, Edward},
Date-Added date-added = {2015-06-11 08:40:34 +0000},
Date-Modified date-modified = {2015-07-16 07:23:16 +0000},
Doi doi = {10.1152/physrev.00018.2002},
File file = {{PerezReyes2003bw.pdf:/Users/walton/Google Drive/Papers/2003/P/PerezReyes2003bw.pdf:application/pdf}},
Journal journal = {Physiol Rev},
Language language = {English},
Month month = {jan},
Number number = {1},
Pages pages = {117--161},
Pmid pmid = {12506128},
Rating rating = {0},
Title title = {{Molecular physiology of low-voltage-activated T-type calcium channels.}},
Volume volume = {83},
Year year = {2003},
Abstract abstract = {T-type Ca2+ channels were originally called low-voltage-activated (LVA) channels because they can be activated by small depolarizations of the plasma membrane. In many neurons Ca2+ influx through LVA channels triggers low-threshold spikes, which in turn triggers a burst of action potentials mediated by Na+ channels. Burst firing is thought to play an important role in the synchronized activity of the thalamus observed in absence epilepsy, but may also underlie a wider range of thalamocortical dysrhythmias. In addition to a pacemaker role, Ca2+ entry via T-type channels can directly regulate intracellular Ca2+ concentrations, which is an important second messenger for a variety of cellular processes. Molecular cloning revealed the existence of three T-type channel genes. The deduced amino acid sequence shows a similar four-repeat structure to that found in high-voltage-activated (HVA) Ca2+ channels, and Na+ channels, indicating that they are evolutionarily related. Hence, the alpha1-subunits of T-type channels are now designated Cav3. Although mRNAs for all three Cav3 subtypes are expressed in brain, they vary in terms of their peripheral expression, with Cav3.2 showing the widest expression. The electrophysiological activities of recombinant Cav3 channels are very similar to native T-type currents and can be differentiated from HVA channels by their activation at lower voltages, faster inactivation, slower deactivation, and smaller conductance of Ba2+. The Cav3 subtypes can be differentiated by their kinetics and sensitivity to block by Ni2+. The goal of this review is to provide a comprehensive description of T-type currents, their distribution, regulation, pharmacology, and cloning.},
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@article{senatore:2010aa,
Author author = {Senatore, A. and Spafford, J. D.},
Date-Added date-added = {2015-06-11 08:39:56 +0000},
Date-Modified date-modified = {2015-06-11 14:41:37 +0000},
Doi doi = {10.1074/jbc.M109.090753},
Journal journal = {J Biol Chem},
Month month = {Jan},
Number number = {10},
Pages pages = {7447--7458},
Publisher publisher = {American Society for Biochemistry {\\&} Molecular Biology ({ASBMB})},
Title title = {{Transient and Big Are Key Features of an Invertebrate T-type Channel ({LCav}3) from the Central Nervous System of Lymnaea stagnalis}},
Volume volume = {285},
Year year = {2010},
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@article{lee:1999ab,
Author author = {Lee, Jung-Ha and Gomora, Juan Carlos and Cribbs, Leanne L and Perez-Reyes, Edward},
Date-Added date-added = {2015-06-11 08:20:50 +0000},
Date-Modified date-modified = {2015-06-11 14:41:46 +0000},
Doi doi = {10.1016/S0006-3495(99)77134-1},
Journal journal = {Biophys J},
Number number = {6},
Pages pages = {3034--3042},
Publisher publisher = {Elsevier},
Title title = {{Nickel block of three cloned T-type calcium channels: low concentrations selectively block $\alpha$1H}},
Volume volume = {77},
Year year = {1999},
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Bdsk-Url-1 bdsk-url-1 =
{http://www.sciencedirect.com/science/article/pii/S0006349599771341#}} {http://www.sciencedirect.com/science/article/pii/S0006349599771341#},
}
@article{shcheglovitov:2007aa,
Author author = {Shcheglovitov, Aleksandr and Kostyuk, Platon and Shuba, Yaroslav},
Date-Added date-added = {2015-06-11 08:16:39 +0000},
Date-Modified date-modified = {2015-06-11 14:42:10 +0000},
Doi doi = {10.1016/j.bbamem.2007.02.017},
Journal journal = {Biochimica et Biophysica Acta - Biomembranes},
Month month = {Jun},
Number number = {6},
Pages pages = {1406--1419},
Publisher publisher = {Elsevier},
Title title = {{Selectivity signatures of three isoforms of recombinant T-type Ca2+ channels}},
Volume volume = {1768},
Year year = {2007},
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{http://dx.doi.org/10.1016/j.bbamem.2007.02.017}} {http://dx.doi.org/10.1016/j.bbamem.2007.02.017},
}
@article{mcrory:2000aa,
Author author = {McRory, John E and Santi, Celia M and Hamming, Kevin SC and Mezeyova, Janette and Sutton, Kathy G and Baillie, David L and Stea, Anthony and Snutch, Terrance P},
Date-Added date-added = {2015-06-11 08:13:28 +0000},
Date-Modified date-modified = {2015-06-11 14:39:12 +0000},
Doi doi = {10.1074/jbc.M008215200},
Journal journal = {J Biol Chem},
Month month = {Nov},
Number number = {6},
Pages pages = {3999--4011},
Title title = {{Molecular and Functional Characterization of a Family of Rat Brain T-type Calcium Channels}},
Volume volume = {276},
Year year = {2001},
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}
@article{klockner:1999aa,
Author author = {Kl{\"o}ckner, Udo and Lee, Jung-Ha and Cribbs, Leanne L and Daud, Asif and Hescheler, J{\"u}rgen and Pereverzev, Alexei and Perez-Reyes, Edward and Schneider, Toni},
Date-Added date-added = {2015-06-11 08:10:13 +0000},
Date-Modified date-modified = {2015-06-11 14:38:50 +0000},
Journal journal = {Euro J Neurosci},
Number number = {12},
Pages pages = {4171--4178},
Publisher publisher = {Wiley Online Library},
Title title = {{Comparison of the Ca2+ currents induced by expression of three cloned $\alpha$1 subunits, $\alpha$1G, $\alpha$1H and $\alpha$1I, of low-voltage-activated T-type Ca2+ channels}},
Volume volume = {11},
Year year = {1999},
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@article{lee:1999aa,
Author author = {Lee, Jung-Ha and Daud, Asif N and Cribbs, Leanne L and Lacerda, Antonio E and Pereverzev, Alexei and Kl{\"o}ckner, Udo and Schneider, Toni and Perez-Reyes, Edward},
Date-Added date-added = {2015-06-11 08:02:15 +0000},
Date-Modified date-modified = {2015-06-11 08:02:26 +0000},
Journal journal = {J Neurosci},
Number number = {6},
Pages pages = {1912--1921},
Publisher publisher = {Soc Neuroscience},
Title title = {{Cloning and expression of a novel member of the low voltage-activated T-type calcium channel family}},
Volume volume = {19},
Year year = {1999},
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@article{Cribbs:1998vc,
Affiliation affiliation = {Department of Physiology, Cardiovascular Institute, Loyola University Medical Center, Maywood, Ill 60153, USA.
[email protected]},
Author author = {Cribbs, L L and Lee, J H and Yang, J and Satin, J and Zhang, Y and Daud, A and Barclay, J and Williamson, M P and Fox, M and Rees, M and Perez-Reyes, E},
Date-Added date-added = {2015-06-11 07:52:04 +0000},
Date-Modified date-modified = {2015-06-11 07:52:45 +0000},
Doi doi = {10.1161/01.RES.83.1.103},
File file = {{Cribbs1998vc.pdf:/Users/walton/Google Drive/Papers/1998/C/Cribbs1998vc.pdf:application/pdf}},
Journal journal = {Circulation Research},
Language language = {English},
Month month = {jul},
Number number = {1},
Pages pages = {103--109},
Pmid pmid = {9670923},
Rating rating = {0},
Title title = {{Cloning and characterization of alpha1H from human heart, a member of the T-type Ca2+ channel gene family.}},
Volume volume = {83},
Year year = {1998},
Abstract abstract = {Voltage-activated Ca2+ channels exist as multigene families that share common structural features. Different Ca2+ channels are distinguished by their electrophysiology and pharmacology and can be classified as either low or high voltage-activated channels. Six alpha1 subunit genes cloned previously code for high voltage-activated Ca2+ channels; therefore, we have used a database search strategy to identify new Ca2+ channel genes, possibly including low voltage-activated (T-type) channels. A novel expressed sequence-tagged cDNA clone of alpha1G was used to screen a cDNA library, and in the present study, we report the cloning of alpha1H (or CavT.2), a low voltage-activated Ca2+ channel from human heart. Northern blots of human mRNA detected more alpha1H expression in peripheral tissues, such as kidney and heart, than in brain. We mapped the gene, CACNA1H, to human chromosome 16p13.3 and mouse chromosome 17. Expression of alpha1H in HEK-293 cells resulted in Ca2+ channel currents displaying voltage dependence, kinetics, and unitary conductance characteristic of native T-type Ca2+ channels. The alpha1H channel is sensitive to mibefradil, a nondihydropyridine Ca2+ channel blocker, with an IC50 of 1.4 micromol/L, consistent with the reported potency of mibefradil for T-type Ca2+ channels. Together with alpha1G, a rat brain T-type Ca2+ channel also cloned in our laboratory, these genes define a unique family of Ca2+ channels.},
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@article{PerezReyes:1998gn,
Affiliation affiliation = {Department of Physiology, and Cardiovascular Institute, Loyola University Medical Center, Maywood, Illinois 60153, USA.
[email protected]},
Author author = {Perez-Reyes, E and Cribbs, L L and Daud, A and Lacerda, A E and Barclay, J and Williamson, M P and Fox, M and Rees, M and Lee, J H},
Date-Added date-added = {2015-06-11 07:49:43 +0000},
Date-Modified date-modified = {2015-06-11 07:49:43 +0000},
Doi doi = {10.1038/36110},
File file = {{PerezReyes1998gn.pdf:/Users/walton/Google Drive/Papers/1998/P/PerezReyes1998gn.pdf:application/pdf}},
Journal journal = {Nature},
Language language = {English},
Month month = {feb},
Number number = {6670},
Pages pages = {896--900},
Pmid pmid = {9495342},
Rating rating = {0},
Title title = {{Molecular characterization of a neuronal low-voltage-activated T-type calcium channel.}},
Volume volume = {391},
Year year = {1998},
Abstract abstract = {The molecular diversity of voltage-activated calcium channels was established by studies showing that channels could be distinguished by their voltage-dependence, deactivation and single-channel conductance. Low-voltage-activated channels are called 'T' type because their currents are both transient (owing to fast inactivation) and tiny (owing to small conductance). T-type channels are thought to be involved in pacemaker activity, low-threshold calcium spikes, neuronal oscillations and resonance, and rebound burst firing. Here we report the identification of a neuronal T-type channel. Our cloning strategy began with an analysis of Genbank sequences defined as sharing homology with calcium channels. We sequenced an expressed sequence tag (EST), then used it to clone a full-length complementary DNA from rat brain. Northern blot analysis indicated that this gene is expressed predominantly in brain, in particular the amygdala, cerebellum and thalamus. We mapped the human gene to chromosome 17q22, and the mouse gene to chromosome 11. Functional expression of the channel was measured in Xenopus oocytes. Based on the channel's distinctive voltage dependence, slow deactivation kinetics, and 7.5-pS single-channel conductance, we conclude that this channel is a low-voltage-activated T-type calcium channel.},
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@article{Ryglewski:2012jk,
Affiliation affiliation = {School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
[email protected]},
Author author = {Ryglewski, Stefanie and Lance, Kimberly and Levine, Richard B and Duch, Carsten},
Date-Added date-added = {2015-06-11 07:47:52 +0000},
Date-Modified date-modified = {2015-06-11 07:48:18 +0000},
Doi doi = {10.1113/jphysiol.2011.222836},
File file = {{Ryglewski2012jk.pdf:/Users/walton/Google Drive/Papers/2012/R/Ryglewski2012jk.pdf:application/pdf}},
Journal journal = {J Physiol},
Language language = {English},
Month month = {feb},
Number number = {Pt 4},
Pages pages = {809--825},
Pmid pmid = {22183725},
Rating rating = {0},
Read read = {Yes},
Title title = {{Ca(v)2 channels mediate low and high voltage-activated calcium currents in Drosophila motoneurons.}},
Volume volume = {590},
Year year = {2012},
Abstract abstract = {Different blends of membrane currents underlie distinct functions of neurons in the brain. A major step towards understanding neuronal function, therefore, is to identify the genes that encode different ionic currents. This study combined in situ patch clamp recordings of somatodendritic calcium currents in an identified adult Drosophila motoneuron with targeted genetic manipulation. Voltage clamp recordings revealed transient low voltage-activated (LVA) currents with activation between --60 mV and --70 mV as well as high voltage-activated (HVA) current with an activation voltage around --30 mV. LVA could be fully inactivated by prepulses to --50 mV and was partially amiloride sensitive. Recordings from newly generated mutant flies demonstrated that Dm$\alpha$G (Ca(v)3 homolog) encoded the amiloride-sensitive portion of the transient LVA calcium current. We further demonstrated that the Ca(v)2 homolog, Dmca1A, mediated the amiloride-insensitive component of LVA current. This novel role of Ca(v)2 channels was substantiated by patch clamp recordings from conditional mutants, RNAi knock-downs, and following Dmca1A overexpression. In addition, we show that Dmca1A underlies the HVA somatodendritic calcium currents in vivo. Therefore, the Drosophila Ca(v)2 homolog, Dmca1A, underlies HVA and LVA somatodendritic calcium currents in the same neuron. Interestingly, Dm$\alpha$G is required for regulating LVA and HVA derived from Dmca1A in vivo. In summary, each vertebrate gene family for voltage-gated calcium channels is represented by a single gene in Drosophila, namely Dmca1D (Ca(v)1), Dmca1A (Ca(v)2) and Dm$\alpha$G (Ca(v)3), but the commonly held view that LVA calcium currents are usually mediated by Ca(v)3 rather than Ca(v)2 channels may require reconsideration.},
Annote annote = {2012-06-18 Kyunghwa (JC)},
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@article{Lee:2004ey,
Affiliation affiliation = {Center for Calcium and Learning, Division of Life Sciences, Korea Institute of Science and Technology, Seoul 136-791, Korea.},
Author author = {Lee, Jungryun and Kim, Daesoo and Shin, Hee-Sup},
Date-Added date-added = {2015-06-11 07:46:03 +0000},
Date-Modified date-modified = {2015-06-11 07:46:03 +0000},
Doi doi = {10.1073/pnas.0408089101},
File file = {{Lee2004ey.pdf:/Users/walton/Google Drive/Papers/2004/L/Lee2004ey.pdf:application/pdf}},
Journal journal = {PNAS},
Language language = {English},
Month month = {dec},
Number number = {52},
Pages pages = {18195--18199},
Pmid pmid = {15601764},
Rating rating = {0},
Title title = {{Lack of delta waves and sleep disturbances during non-rapid eye movement sleep in mice lacking alpha1G-subunit of T-type calcium channels.}},
Volume volume = {101},
Year year = {2004},
Abstract abstract = {T-type calcium channels have been implicated as a pacemaker for brain rhythms during sleep but their contribution to behavioral states of sleep has been relatively uncertain. Here, we found that mice lacking alpha1(G) T-type Ca(2+) channels showed a loss of the thalamic delta (1-4 Hz) waves and a reduction of sleep spindles (7-14 Hz), whereas slow (<1 Hz) rhythms were relatively intact, when compared with the wild-type during urethane anesthesia and non-rapid eye movement (NREM) sleep. Analysis of sleep disturbances, as defined by the occurrence of brief awakening (BA) episodes during NREM sleep, revealed that mutant mice exhibited a higher incidence of BAs of >16 sec compared with the wild-type, whereas no difference was seen in BAs of <16 sec between the two genotypes. These results are consistent with the previous idea of the distinct nature of delta oscillations and sleep spindles from cortically generated slow waves. These results also suggest that the alpha1(G)-subunit of T-type calcium channels plays a critical role in the genesis of thalamocortical oscillations and contributes to the modulation of sleep states and the transition between NREM sleep and wake states.},
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Bdsk-Url-2 bdsk-url-2 =
{http://dx.doi.org/10.1073/pnas.0408089101}} {http://dx.doi.org/10.1073/pnas.0408089101},
}
@article{matteson:1986aa,
Author author = {Matteson, DR and Armstrong, CM},
Authors authors = {Matteson, DR and Armstrong, CM},
Date date = {1986 Jan},
Date-Modified date-modified = {2015-07-20 01:29:07 +0000},
Doi doi = {10.1085/jgp.87.1.161},
Journal journal = {J Gen Physiol},
Month month = {Jan},
Pages pages = {161-82},
Pubmed_Id pubmed_id = {2419479},
Source source = {J Gen Physiol},
Title title = {{Properties of two types of calcium channels in clonal pituitary cells.}},
Volume volume = {87},
Year year = {1986},
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@article{park:2004aa,
Author author = {Park, JY and Kang, HW and Jeong, SW and Lee, JH},
Authors authors = {Park, JY and Kang, HW and Jeong, SW and Lee, JH},
Date date = {2004 May 21},
Date-Modified date-modified = {2015-07-20 01:45:27 +0000},
Doi doi = {10.1074/jbc.M400684200},
Journal journal = {J Biol Chem},
Month month = {May},
Pages pages = {21707-13},
Pubmed_Id pubmed_id = {15016809},
Source source = {J Biol Chem},
Title title = {{Multiple structural elements contribute to the slow kinetics of the Cav3.3 T-type channel.}},
Volume volume = {279},
Year year = {2004},
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@article{demers-giroux:2013aa,
Author author = {Demers-Giroux, PO and Bourdin, B and Sauv{\'e}, R and Parent, L},
Authors authors = {Demers-Giroux, PO and Bourdin, B and Sauv{\'e}, R and Parent, L},
Date date = {2013 Oct 11},
Date-Modified date-modified = {2015-07-20 01:30:34 +0000},
Doi doi = {10.1074/jbc.M113.500975},
Journal journal = {J Biol Chem},
Month month = {Oct},
Pages pages = {29281-93},
Pubmed_Id pubmed_id = {23970551},
Source source = {J Biol Chem},
Title title = {{Cooperative activation of the T-type CaV3.2 channel: interaction between Domains II and III.}},
Volume volume = {288},
Year year = {2013},
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@article{chemin:2002aa,
Author author = {Chemin, J and Monteil, A and Perez-Reyes, E and Bourinet, E and Nargeot, J and Lory, P},
Authors authors = {Chemin, J and Monteil, A and Perez-Reyes, E and Bourinet, E and Nargeot, J and Lory, P},
Date date = {2002 Apr 1},
Date-Modified date-modified = {2015-07-20 01:33:38 +0000},
Doi doi = {10.1113/jphysiol.2001.013269},
Journal journal = {J Physiol},
Month month = {Apr},
Pages pages = {3-14},
Pubmed_Id pubmed_id = {11927664},
Source source = {J Physiol},
Title title = {{Specific contribution of human T-type calcium channel isotypes (alpha(1G), alpha(1H) and alpha(1I)) to neuronal excitability.}},
Volume volume = {540},
Year year = {2002},
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@article{kang:2006aa,
Author author = {Kang, HW and Park, JY and Jeong, SW and Kim, JA and Moon, HJ and Perez-Reyes, E and Lee, JH},
Authors authors = {Kang, HW and Park, JY and Jeong, SW and Kim, JA and Moon, HJ and Perez-Reyes, E and Lee, JH},
Date date = {2006 Feb 24},
Date-Modified date-modified = {2015-07-20 01:46:57 +0000},
Doi doi = {10.1074/jbc.M510197200},
Journal journal = {J Biol Chem},
Month month = {Feb},
Pages pages = {4823-30},
Pubmed_Id pubmed_id = {16377633},
Source source = {J Biol Chem},
Title title = {{A molecular determinant of nickel inhibition in Cav3.2 T-type calcium channels.}},
Volume volume = {281},
Year year = {2006},
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@article{pfeiffenberger:2010ab,
Author author = {Pfeiffenberger, C and Lear, BC and Keegan, KP and Allada, R},
Authors authors = {Pfeiffenberger, C and Lear, BC and Keegan, KP and Allada, R},
Date date = {2010 Nov 1},
Date-Modified date-modified = {2015-07-20 01:39:55 +0000},
Doi doi = {10.1101/pdb.prot5520},
Journal journal = {Cold Spring Harb Protoc},
Month month = {Nov},
Pages pages = {pdb.prot5520},
Pubmed_Id pubmed_id = {21041393},
Source source = {Cold Spring Harb Protoc},
Title title = {{Processing sleep data created with the Drosophila Activity Monitoring (DAM) System.}},
Volume volume = {2010},
Year year = {2010},
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@article{pfeiffenberger:2010aa,
Author author = {Pfeiffenberger, C and Lear, BC and Keegan, KP and Allada, R},
Authors authors = {Pfeiffenberger, C and Lear, BC and Keegan, KP and Allada, R},
Date date = {2010 Nov 1},
Date-Modified date-modified = {2015-07-20 01:38:25 +0000},
Doi doi = {10.1101/pdb.prot5519},
Journal journal = {Cold Spring Harb Protoc},
Month month = {Nov},
Pages pages = {pdb.prot5519},
Pubmed_Id pubmed_id = {21041392},
Source source = {Cold Spring Harb Protoc},
Title title = {{Processing circadian data collected from the Drosophila Activity Monitoring (DAM) System.}},
Volume volume = {2010},
Year year = {2010},
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@article{hendricks:2003aa,
Author author = {Hendricks, JC and Lu, S and Kume, K and Yin, JC and Yang, Z and Sehgal, A},
Authors authors = {Hendricks, JC and Lu, S and Kume, K and Yin, JC and Yang, Z and Sehgal, A},
Date date = {2003 Feb},
Date-Modified date-modified = {2015-07-20 01:36:11 +0000},
Doi doi = {10.1177/0748730402239673},
Journal journal = {J Biol Rhythms},
Month month = {Feb},
Pages pages = {12-25},
Pubmed_Id pubmed_id = {12568241},
Source source = {J Biol Rhythms},
Title title = {{Gender dimorphism in the role of cycle (BMAL1) in rest, rest regulation, and longevity in Drosophila melanogaster.}},
Volume volume = {18},
Year year = {2003},
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@article{parisky:2008aa,
Author author = {Parisky, KM and Agosto, J and Pulver, SR and Shang, Y and Kuklin, E and Hodge, JJ and Kang, K and Liu, X and Garrity, PA and Rosbash, M and Griffith, LC},
Authors authors = {Parisky, KM and Agosto, J and Pulver, SR and Shang, Y and Kuklin, E and Hodge, JJ and Kang, K and Liu, X and Garrity, PA and Rosbash, M and Griffith, LC},
Date date = {2008 Nov 26},
Date-Modified date-modified = {2015-07-20 01:43:42 +0000},
Doi doi = {10.1016/j.neuron.2008.10.042},
Journal journal = {Neuron},
Month month = {Nov},
Pages pages = {672-82},
Pubmed_Id pubmed_id = {19038223},
Source source = {Neuron},
Title title = {{PDF cells are a GABA-responsive wake-promoting component of the Drosophila sleep circuit.}},
Volume volume = {60},
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@article{park:2013aa,
Author author = {Park, HJ and Park, SJ and Ahn, EJ and Lee, SY and Seo, H and Lee, JH},
Authors authors = {Park, HJ and Park, SJ and Ahn, EJ and Lee, SY and Seo, H and Lee, JH},
Date date = {2013 Sep},
Date-Modified date-modified = {2015-07-20 01:26:13 +0000},
Doi doi = {10.1016/j.ceca.2013.06.006},
Journal journal = {Cell Calcium},
Month month = {Sep},
Pages pages = {226-35},
Pubmed_Id pubmed_id = {23849427},
Source source = {Cell Calcium},
Title title = {{Asp residues of the Glu-Glu-Asp-Asp pore filter contribute to ion permeation and selectivity of the Ca(v)3.2 T-type channel.}},
Volume volume = {54},
Year year = {2013},
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@misc{Budnik_2002,
doi = {10.3410/f.1010905.170408},
url = {http://dx.doi.org/10.3410/f.1010905.170408},
year = {2002},
month = {dec},
publisher = {Faculty of 1000 Ltd.},
author = {Vivian Budnik},
title = {{Faculty of 1000 evaluation for Electrophysiological correlates of rest and activity in Drosophila melanogaster.}},
}
