Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels.
about
Ca2+-dependent modulation of voltage-gated Ca2+ channelsBiophysical properties, pharmacology, and modulation of human, neuronal L-type (alpha(1D), Ca(V)1.3) voltage-dependent calcium currentsLoss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessRequirement for the L-type Ca(2+) channel alpha(1D) subunit in postnatal pancreatic beta cell generationIon channel gene expression in the inner earBiophysical and pharmacological characterization of voltage-gated calcium currents in turtle auditory hair cellsMechanisms underlying the cardiac pacemaker: the role of SK4 calcium-activated potassium channelsThe Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic PotentialGenetic disruption of voltage-gated calcium channels in psychiatric and neurological disordersNimodipine in otolaryngology: from past evidence to clinical perspectivesPopeye domain-containing proteins and stress-mediated modulation of cardiac pacemakingNew therapeutic targets in cardiology: arrhythmias and Ca2+/calmodulin-dependent kinase II (CaMKII)Rab3-interacting molecules 2α and 2β promote the abundance of voltage-gated CaV1.3 Ca2+ channels at hair cell active zonesThe Ca2+ channel subunit beta2 regulates Ca2+ channel abundance and function in inner hair cells and is required for hearingSensorineural deafness and seizures in mice lacking vesicular glutamate transporter 3.Characterization of voltage-dependent sodium and calcium channels in mouse pancreatic A- and B-cells.New insights into cochlear sound encodingConverging roles of ion channels, calcium, metabolic stress, and activity pattern of Substantia nigra dopaminergic neurons in health and Parkinson's diseaseL-type calcium channels as drug targets in CNS disordersDecreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorderVoltage-Gated Cav1 Channels in Disorders of Vision and HearingVoltage-gated calcium channelsThe role of L-type voltage-gated calcium channels Cav1.2 and Cav1.3 in normal and pathological brain functionL-type calcium channels: the low downChick cochlear hair cell exocytosis mediated by dihydropyridine-sensitive calcium channelsContribution of L-type Ca(2+) channels to evoked transmitter release in cultured Xenopus nerve-muscle synapsesFast exocytosis with few Ca(2+) channels in insulin-secreting mouse pancreatic B cellsFunctional disorders of the sympathetic nervous system in mice lacking the alpha 1B subunit (Cav 2.2) of N-type calcium channelsSilencing of Cav1.2 gene in neonatal cardiomyocytes by lentiviral delivered shRNACalcium- and calmodulin-dependent inactivation of calcium channels in inner hair cells of the rat cochleaCa1.2 and CaV1.3 neuronal L-type calcium channels: differential targeting and signaling to pCREBSlowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a.Enhanced expression of L-type Cav1.3 calcium channels in murine embryonic hearts from Cav1.2-deficient miceFunctional role of L-type Cav1.3 Ca2+ channels in cardiac pacemaker activityA perforated patch-clamp study of calcium currents and exocytosis in chromaffin cells of wild-type and alpha(1A) knockout miceDisruption of growth hormone secretion alters Ca2+ current density and expression of Ca2+ channel and insulin-like growth factor genes in rat atria.Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like Cells.Hair cells use active zones with different voltage dependence of Ca2+ influx to decompose sounds into complementary neural codes.Excessive activation of ionotropic glutamate receptors induces apoptotic hair-cell death independent of afferent and efferent innervationCochlear hair cells: The sound-sensing machines.
P2860
Q21564049-457D8A1A-4FDC-408F-9C22-E6081E5A7453Q24290750-10D318BF-9441-4098-B1E3-0ECDE0185BEDQ24311948-4780E871-3409-4680-88B9-D9BEF1EA6D37Q24564910-2D81FB53-D4CD-4294-947C-749C23F964D4Q24650344-A15C5E3A-EE26-47B5-9635-E8408DE2047CQ24656926-B0A0285D-95A6-4CBD-BADF-355AF80A2517Q26771350-07F202F3-1E5D-4A8B-96B3-BE7635C0ABD3Q26781422-AC3D531B-CA5D-4726-9034-AAD7C14BCCDAQ26783154-884F80E0-E15B-409C-B299-57E67FDCFA3EQ26798286-6AE3C11D-85A0-4038-AE48-3A8EE126CE01Q26861426-1ACFE4C3-A41E-4C90-B432-D1295EA970DCQ27016402-68264FBA-AED6-433B-9798-D44446683156Q27326298-99367BD2-0A15-4CEF-85BC-0E7B38A4A08EQ27347987-540D3187-DCDF-45B5-975F-5404B8198315Q27863377-DCFDFBF2-5637-4EAA-8C75-F00607900DDBQ27863914-35648410-66AD-4D98-A78D-A0ED31379B34Q28068730-C3925735-A620-4D45-A6F0-C896760883F7Q28074143-B0CDE6B1-7DDD-4C57-B5B6-0E0E307A2F4BQ28081812-E7724B6A-00EB-405D-BE1D-4F260492A642Q28081905-4609EBE5-566D-47FB-8044-2543E65B93E4Q28084651-DD5A6935-072A-4DB9-8C3D-CD94B69274C3Q28242997-B809558F-4B2A-4006-B52B-E540756314FFQ28243321-D6682E29-5FB0-4F83-9488-E8C7E53B44A8Q28288051-1110F858-E178-48BA-B3ED-3F22FE2FF675Q28354051-F81EC847-266B-4248-B556-C6DA19ED2E70Q28360568-C78E7882-5DBD-4F09-ADF8-CA7A7FADCC37Q28365153-83BEC590-09E2-4B8B-AECE-7B23E51A7D64Q28508109-ECFCED95-E527-4EE2-9BC0-6FD352533F24Q28569159-F2436263-3C63-4B53-865B-BE36E42278F7Q28571486-89518ABF-2C60-449D-A742-6C27E78D6C63Q28579963-E6325AE1-66F5-495A-AE5B-9F1E07012EDDQ28587543-FAA35F30-299D-424A-98B7-DDAAB5B16133Q28590749-91FC2C38-8018-4806-93B6-BFE85C21FAF3Q28593156-467C9A92-29DD-4138-8B88-CDF24187EE35Q28594172-624BCE01-A525-4131-A528-1FD636077DFEQ30273593-03265B77-2FC8-4901-9981-60D227DB9F0EQ30357879-9527C71C-7207-4744-8262-5F8090A8BC78Q30363786-7EFFD9B0-8CF5-46F7-A586-FE28ABFDB748Q30365181-8443C25B-8C3D-458D-85D1-F4BA44727748Q30370018-DFF39030-4C46-45FC-998D-184F07ED3946
P2860
Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh-hant
name
Congenital deafness and sinoat ...... class D L-type Ca2+ channels.
@en
Congenital deafness and sinoat ...... class D L-type Ca2+ channels.
@nl
type
label
Congenital deafness and sinoat ...... class D L-type Ca2+ channels.
@en
Congenital deafness and sinoat ...... class D L-type Ca2+ channels.
@nl
prefLabel
Congenital deafness and sinoat ...... class D L-type Ca2+ channels.
@en
Congenital deafness and sinoat ...... class D L-type Ca2+ channels.
@nl
P2093
P1433
P1476
Congenital deafness and sinoat ...... class D L-type Ca2+ channels.
@en
P2093
Schrott-Fischer A
Striessnig J
P356
10.1016/S0092-8674(00)00013-1
P407
P577
2000-07-01T00:00:00Z