Impaired motor coordination and persistent multiple climbing fiber innervation of cerebellar Purkinje cells in mice lacking Galphaq
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'Medusa-head ataxia': the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 1: Anti-mGluR1, anti-Homer-3, anti-Sj/ITPR1 and anti-CARP VIIIGeneration and characterization of Rgs4 mutant miceSynapse elimination in the developing cerebellumAblation of RIC8A function in mouse neurons leads to a severe neuromuscular phenotype and postnatal deathDevelopmental delay in motor skill acquisition in Niemann-Pick C1 mice reveals abnormal cerebellar morphogenesis.LTD-like molecular pathways in developmental synaptic pruningThe P2Y1 receptor plays an essential role in the platelet shape change induced by collagen when TxA2 formation is preventedHeterotrimeric G proteins of the Gq/11 family are crucial for the induction of maternal behavior in miceNormal hematopoiesis and inflammatory responses despite discrete signaling defects in Galpha15 knockout miceDisturbance of cerebellar synaptic maturation in mutant mice lacking BSRPs, a novel brain-specific receptor-like protein familyEmbryonic cardiomyocyte hypoplasia and craniofacial defects in G alpha q/G alpha 11-mutant mice.Forebrain-specific inactivation of Gq/G11 family G proteins results in age-dependent epilepsy and impaired endocannabinoid formationSignaling and cross-talk by C5a and UDP in macrophages selectively use PLCbeta3 to regulate intracellular free calcium.Formation of hippocampal synapses on patterned substrates of a laminin-derived synthetic peptide.Patterned neuroprotection in the Inpp4a(wbl) mutant mouse cerebellum correlates with the expression of Eaat4Phospholipase cbeta4 is specifically involved in climbing fiber synapse elimination in the developing cerebellum.A positive feedback loop linking enhanced mGluR function and basal calcium in spinocerebellar ataxia type 2Clostridium difficile toxin B differentially affects GPCR-stimulated Ca2+ responses in macrophages: independent roles for Rho and PLA2.Loss of Gq/11 family G proteins in the nervous system causes pituitary somatotroph hypoplasia and dwarfism in miceReal-time visualization of heterotrimeric G protein Gq activation in living cellsG alpha q-containing G proteins regulate B cell selection and survival and are required to prevent B cell-dependent autoimmunityThe vesicular monoamine content regulates VMAT2 activity through Galphaq in mouse platelets. Evidence for autoregulation of vesicular transmitter uptake.In vivo functions of heterotrimeric G-proteins: studies in Galpha-deficient mice.Modifier genes for mouse phosphatidylinositol transfer protein α (vibrator) that bypass juvenile lethality.Postsynaptic P/Q-type Ca2+ channel in Purkinje cell mediates synaptic competition and elimination in developing cerebellumDetection of chromosomal breakpoints in patients with developmental delay and speech disordersDifferential PKC-dependent and -independent PKD activation by G protein α subunits of the Gq family: selective stimulation of PKD Ser⁷⁴⁸ autophosphorylation by Gαq.Requirement of TrkB for synapse elimination in developing cerebellar Purkinje cellsRole of G(q) protein in behavioral effects of the hallucinogenic drug 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane.β-III spectrin is critical for development of purkinje cell dendritic tree and spine morphogenesis.Neurobehavioral phenotyping of G(αq) knockout mice reveals impairments in motor functions and spatial working memory without changes in anxiety or behavioral despairGnRH Neuron-Specific Ablation of Gαq/11 Results in Only Partial Inactivation of the Neuroendocrine-Reproductive Axis in Both Male and Female Mice: In Vivo Evidence for Kiss1r-Coupled Gαq/11-Independent GnRH SecretionCerebellar control of gait and interlimb coordination.Identification of an alternative G{alpha}q-dependent chemokine receptor signal transduction pathway in dendritic cells and granulocytes.G proteins in development.Epidermal loss of Gαq confers a migratory and differentiation defect in keratinocytesDevelopmental Activation of the AHR Increases Effector CD4+ T Cells and Exacerbates Symptoms in Autoimmune Disease-Prone Gnaq+/- Mice.G(q/11)α and G(s)α mediate distinct physiological responses to central melanocortinsArchitecture and development of olivocerebellar circuit topography.Future innovations in anti-platelet therapies.
P2860
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P2860
Impaired motor coordination and persistent multiple climbing fiber innervation of cerebellar Purkinje cells in mice lacking Galphaq
description
1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 1997
@ast
im Dezember 1997 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1997/12/09)
@sk
vědecký článek publikovaný v roce 1997
@cs
wetenschappelijk artikel (gepubliceerd op 1997/12/09)
@nl
наукова стаття, опублікована в грудні 1997
@uk
name
Impaired motor coordination an ...... cells in mice lacking Galphaq
@ast
Impaired motor coordination an ...... cells in mice lacking Galphaq
@en
Impaired motor coordination an ...... cells in mice lacking Galphaq
@nl
type
label
Impaired motor coordination an ...... cells in mice lacking Galphaq
@ast
Impaired motor coordination an ...... cells in mice lacking Galphaq
@en
Impaired motor coordination an ...... cells in mice lacking Galphaq
@nl
prefLabel
Impaired motor coordination an ...... cells in mice lacking Galphaq
@ast
Impaired motor coordination an ...... cells in mice lacking Galphaq
@en
Impaired motor coordination an ...... cells in mice lacking Galphaq
@nl
P2093
P2860
P921
P3181
P356
P1476
Impaired motor coordination an ...... cells in mice lacking Galphaq
@en
P2093
H. Kurihara
K. Hashimoto
M. I. Simon
M. Watanabe
R. F. Thompson
P2860
P304
14089–14094
P3181
P356
10.1073/PNAS.94.25.14089
P407
P577
1997-12-09T00:00:00Z