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… (More)
National Institutes of Health

Papers overview

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2011
2011
This phase I clinical trial assessed the safety and immunogenicity of a native outer membrane vesicle (NOMV) vaccine prepared… (More)
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Review
2007
Review
2007
  • Mari Yoshida
  • Neuropathology : official journal of the Japanese…
  • 2007
Multiple system atrophy (MSA) is a sporadic neurodegenerative disorder that encompasses olivopontocerebellar atrophy (OPCA… (More)
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Highly Cited
2005
Highly Cited
2005
Multiple system atrophy (MSA), a sporadic progressive synucleinopathy of advanced age, is separated into two clinic opathological… (More)
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Highly Cited
2004
Highly Cited
2004
Multiple system atrophy (MSA) has varying clinical (MSA-P versus MSA-C) and pathological [striatonigral degeneration (SND) versus… (More)
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Highly Cited
2003
Highly Cited
2003
Maximal activation of NADPH oxidase requires formation of a complex between the p40(phox) and p67(phox) subunits via association… (More)
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Highly Cited
2003
Highly Cited
2003
An increasing number of ASes have been connecting to the Internet through the BGP inter-domain routing protocol. With increasing… (More)
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2003
2003
The PB1 (Phox and Bem 1) domain is a recently identified module that mediates formation of a heterodimeric complex with other PB1… (More)
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Highly Cited
1995
Highly Cited
1995
Heterocysts, sites of nitrogen fixation in certain filamentous cyanobacteria, are limited to a heterotrophic metabolism, rather… (More)
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1994
1994
The clinical features and natural history of 100 patients diagnosed as probable multiple system atrophy (MSA) are described. In… (More)
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Highly Cited
1989
Highly Cited
1989
A form of dominantly inherited olivopontocerebellar atrophy (OPCA) occurs commonly in persons of Spanish ancestry in northeastern… (More)
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