Functional embryonic cardiomyocytes after disruption of the L-type alpha1C (Cav1.2) calcium channel gene in the mouse. - Wikidata - wikimedia - TriplyDB

Functional embryonic cardiomyocytes after disruption of the L-type alpha1C (Cav1.2) calcium channel gene in the mouse.

Functional embryonic cardiomyocytes after disruption of the L-type alpha1C (Cav1.2) calcium channel gene in the mouse.

http://www.wikidata.org/entity/Q31438008

about

Ca2+-dependent modulation of voltage-gated Ca2+ channels Neuronal precursor cell-expressed developmentally down-regulated 4-1 (NEDD4-1) controls the sorting of newly synthesized Ca(V)1.2 calcium channels Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function Sox6 regulation of cardiac myocyte development The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential Characterization of voltage-dependent sodium and calcium channels in mouse pancreatic A- and B-cells.Functional characterization of CaVα2δ mutations associated with sudden cardiac death Pain perception in mice lacking the beta3 subunit of voltage-activated calcium channels The role of L-type voltage-gated calcium channels Cav1.2 and Cav1.3 in normal and pathological brain function Functional disorders of the sympathetic nervous system in mice lacking the alpha 1B subunit (Cav 2.2) of N-type calcium channels Silencing of Cav1.2 gene in neonatal cardiomyocytes by lentiviral delivered shRNA Ca1.2 and CaV1.3 neuronal L-type calcium channels: differential targeting and signaling to pCREB Dominant role of smooth muscle L-type calcium channel Cav1.2 for blood pressure regulation Impaired insulin secretion and glucose tolerance in beta cell-selective Ca(v)1.2 Ca2+ channel null mice Enhanced expression of L-type Cav1.3 calcium channels in murine embryonic hearts from Cav1.2-deficient mice Functional role of L-type Cav1.3 Ca2+ channels in cardiac pacemaker activity The calcium channel beta2 (CACNB2) subunit repertoire in teleosts.L-type Calcium Channel Cav1.2 Is Required for Maintenance of Auditory Brainstem Nuclei.L-type CaV1.2 deletion in the cochlea but not in the brainstem reduces noise vulnerability: implication for CaV1.2-mediated control of cochlear BDNF expression.Mood disorder susceptibility gene CACNA1C modifies mood-related behaviors in mice and interacts with sex to influence behavior in mice and diagnosis in humans.Excitation-contraction coupling of the mouse embryonic cardiomyocyte.Mathematical model of mouse embryonic cardiomyocyte excitation-contraction coupling.Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome Calcium influx through L-type CaV1.2 Ca2+ channels regulates mandibular development Characterization and regulation of T-type Ca2+ channels in embryonic stem cell-derived cardiomyocytes.L-type Ca2+ channel function in the avian embryonic heart after cardiac neural crest ablation.Developmental aspects of cardiac Ca(2+) signaling: interplay between RyR- and IP(3)R-gated Ca(2+) stores Role of calcium channels in congenital heart block Calcium buffering and excitation-contraction coupling in developing avian myocardium Amino acid substitutions in the FXYD motif enhance phospholemman-induced modulation of cardiac L-type calcium channels.Identical phenotypes of CatSper1 and CatSper2 null sperm.Cardiac T-Tubule Microanatomy and Function.Mathematical model of the neonatal mouse ventricular action potential.Deletion of the distal C terminus of CaV1.2 channels leads to loss of beta-adrenergic regulation and heart failure in vivo.Control of hyperactivation in sperm.Ion channels that control fertility in mammalian spermatozoa Circadian profiles in the embryonic chick heart: L-type voltage-gated calcium channels and signaling pathways Hyperinsulinism and diabetes: genetic dissection of beta cell metabolism-excitation coupling in mice Interaction of H2S with Calcium Permeable Channels and Transporters.Computer modeling of siRNA knockdown effects indicates an essential role of the Ca2+ channel alpha2delta-1 subunit in cardiac excitation-contraction coupling.

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P2860

Functional embryonic cardiomyocytes after disruption of the L-type alpha1C (Cav1.2) calcium channel gene in the mouse.

http://www.wikidata.org/entity/Q31438008

description

2000 nî lūn-bûn

@nan

2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2000年の論文

@ja

2000年論文

@yue

2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

@zh-tw

2000年论文

@wuu

name

Functional embryonic cardiomyo ...... ium channel gene in the mouse.

@ast

Functional embryonic cardiomyo ...... ium channel gene in the mouse.

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type

label

Functional embryonic cardiomyo ...... ium channel gene in the mouse.

@ast

Functional embryonic cardiomyo ...... ium channel gene in the mouse.

@en

prefLabel

Functional embryonic cardiomyo ...... ium channel gene in the mouse.

@ast

Functional embryonic cardiomyo ...... ium channel gene in the mouse.

@en

P1433

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P1476

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P1433

Journal of Biological Chemistry

P1476

Functional embryonic cardiomyo ...... cium channel gene in the mouse

@en

P2093

Hofmann F

http://www.w3.org/2001/XMLSchema#string

Klugbauer N

http://www.w3.org/2001/XMLSchema#string

Kühbandner S

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Pfeifer A

http://www.w3.org/2001/XMLSchema#string

Platzer J

http://www.w3.org/2001/XMLSchema#string

Seisenberger C

http://www.w3.org/2001/XMLSchema#string

Specht V

http://www.w3.org/2001/XMLSchema#string

Welling A

http://www.w3.org/2001/XMLSchema#string

P2860

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

Genomic structure of human L-type Ca2+ channel

Ca2+ channel sensitivity towards the blocker isradipine is affected by alternative splicing of the human alpha1C subunit gene

Different voltage-dependent inhibition by dihydropyridines of human Ca2+ channel splice variants

A lethal mutation in mice eliminates the slow calcium current in skeletal muscle cells

Altered pain responses in mice lacking alpha 1E subunit of the voltage-dependent Ca2+ channel.

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit

Pharmacological properties of Ca(V)3.2, a low voltage-activated Ca2+ channel cloned from human heart.

Pharmacology, structure and function of cardiac L-type Ca(2+) channels.

P304

39193-39199

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P31

scholarly article

P356

10.1074/JBC.M006467200

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P407

P433

50

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P478

275

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P50

Joerg Striessnig

P577

2000-12-01T00:00:00Z

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P698

10973973

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