Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice
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Melanocytes in the skin--comparative whole transcriptome analysis of main skin cell types'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 VIIIIntegration of modeling with experimental and clinical findings synthesizes and refines the central role of inositol 1,4,5-trisphosphate receptor 1 in spinocerebellar ataxiaInactivation of ca10a and ca10b Genes Leads to Abnormal Embryonic Development and Alters Movement Pattern in ZebrafishCA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gaitmGluR1/TRPC3-mediated Synaptic Transmission and Calcium Signaling in Mammalian Central Neurons.A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ InfluxA single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab miceUner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stabilityCD3 and immunoglobulin G Fc receptor regulate cerebellar functions.Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice.Patterned neuroprotection in the Inpp4a(wbl) mutant mouse cerebellum correlates with the expression of Eaat4Phylogeny and expression of carbonic anhydrase-related proteins.Cerebellar zonal patterning relies on Purkinje cell neurotransmission.Loss of Purkinje cells in the PKCgamma H101Y transgenic mouseInositol trisphosphate receptor Ca2+ release channels in neurological diseases.Carbonic anhydrase-8 regulates inflammatory pain by inhibiting the ITPR1-cytosolic free calcium pathway.An insertion of intracisternal A-particle retrotransposon in a novel member of the phosphoglycerate mutase family in the lew allele of mutant miceAnimal models of dystonia: Lessons from a mutant rat.Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouse.Carbonic anhydrase-related protein VIII is expressed in rod bipolar cells and alters signaling at the rod bipolar to AII-amacrine cell synapse in the mammalian retina.Pathogenesis of severe ataxia and tremor without the typical signs of neurodegeneration.Abnormal motor function and dopamine neurotransmission in DYT1 DeltaGAG transgenic mice.A deletion mutation in Slc12a6 is associated with neuromuscular disease in gaxp mice.Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellumPTPRR protein tyrosine phosphatase isoforms and locomotion of vesicles and mice.A novel locus for episodic ataxia:UBR4 the likely candidate.Climbing fiber synapse elimination in cerebellar Purkinje cells.Structural annotation of human carbonic anhydrases.An update on carbonic anhydrase-related proteins VIII, X and XI.Oncogenic roles of carbonic anhydrase 8 in human osteosarcoma cells.Carbonic anhydrase-related protein CA10 is an evolutionarily conserved pan-neurexin ligand.IP3 receptor mutations and brain diseases in human and rodents.Altered expression of carbonic anhydrase-related protein XI in neuronal cells expressing mutant ataxin-3.Calcium signaling, PKC gamma, IP3R1 and CAR8 link spinocerebellar ataxias and Purkinje cell dendritic development.Motor phenotypes and molecular networks associated with germline deficiency of Ciz1.Expression of the CHOP-inducible carbonic anhydrase CAVI-b is required for BDNF-mediated protection from hypoxia.Identification of a nuclear carbonic anhydrase in Caenorhabditis elegans.Investigate the chronic neurotoxic effects of diquat.Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII.
P2860
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P2860
Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice
description
2005 nî lūn-bûn
@nan
2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@ast
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@en
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@nl
type
label
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@ast
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@en
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@nl
prefLabel
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@ast
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@en
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@nl
P2093
P2860
P1433
P1476
Carbonic anhydrase-related pro ...... gait disorder in waddles mice
@en
P2093
Bruce A Roe
Leah Rae Donahue
Mark S Ledoux
Weikuan Gu
Wesley G Beamer
P2860
P304
P356
10.1534/GENETICS.105.044487
P407
P577
2005-08-22T00:00:00Z