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ATP2B3 wt Allele

Known as: Plasma Membrane Ca(2+)-ATPase, Type 3 Gene, PMCA3a, SCAX1 
Human ATP2B3 wild-type allele is located within Xq28 and is approximately 65 kb in length. This allele, which encodes plasma membrane calcium… 
National Institutes of Health

Related topics

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7 relations
ATP HydrolysisHomo sapiensHydrolysisIonophore activity

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2012
Highly Cited
2012
Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis
Ca2+ in neurons is vital to processes such as neurotransmission, neurotoxicity, synaptic development, and gene expression… 
Highly Cited
2005
Highly Cited
2005
Grading of neuropathology in multiple system atrophy: Proposal for a novel scale
Multiple system atrophy (MSA), a sporadic progressive synucleinopathy of advanced age, is separated into two clinic opathological… 
Highly Cited
2004
Highly Cited
2004
The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations.
Multiple system atrophy (MSA) has varying clinical (MSA-P versus MSA-C) and pathological [striatonigral degeneration (SND) versus… 
Highly Cited
2003
Highly Cited
2003
PB1 domain-mediated heterodimerization in NADPH oxidase and signaling complexes of atypical protein kinase C with Par6 and p62.
Highly Cited
1995
Highly Cited
1995
Genetic evidence of a major role for glucose-6-phosphate dehydrogenase in nitrogen fixation and dark growth of the cyanobacterium Nostoc sp. strain ATCC 29133
Heterocysts, sites of nitrogen fixation in certain filamentous cyanobacteria, are limited to a heterotrophic metabolism, rather… 
Highly Cited
1994
Highly Cited
1994
Clinical features and natural history of multiple system atrophy. An analysis of 100 cases.
The clinical features and natural history of 100 patients diagnosed as probable multiple system atrophy (MSA) are described. In… 
Highly Cited
1994
Highly Cited
1994
Comparison of oculomotor findings in the progressive ataxia syndromes.
In this study we compare the results of quantitative oculomotor function testing in patients with Friedreich's ataxia (FA… 
Highly Cited
1992
Highly Cited
1992
Analysis of the tissue-specific distribution of mRNAs encoding the plasma membrane calcium-pumping ATPases and characterization of an alternately spliced form of PMCA4 at the cDNA and genomic levels.
Highly Cited
1989
Highly Cited
1989
Dominantly inherited olivopontocerebellar atrophy from eastern Cuba Clinical, neuropathological, and biochemical findings
Highly Cited
1988
Highly Cited
1988
Cognitive deficits in olivopontocerebellar atrophy: Implications for the cholinergic hypothesis of Alzheimer's dementia
A cerebral cortical cholinergic reduction in dominantly inherited olivopontocerebellar atrophy (OPCA) was recently described… 
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