ATP10A gene

Known as: ATPase phospholipid transporting 10A (putative), ATPase, CLASS V, TYPE 10C, KIAA0566 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2001-2018
02420012018

Papers overview

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2015
2015
We showed previously that ATP11A and ATP11C have flippase activity toward aminophospholipids (phosphatidylserine (PS) and… (More)
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2011
2011
BACKGROUND Humans infected with Mycobacterium tuberculosis (MTB) can delete the pathogen or otherwise become latent infection or… (More)
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2009
2009
Mutations affecting a cluster of coordinately regulated imprinted genes located at 15q11-q13 underlie both Prader–Willi syndrome… (More)
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2003
2003
The mouse Atp10a gene is located at the border of an imprinted domain distal to the p-locus on mouse chromosome 7. The… (More)
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2003
2003
AbstractThe human chromosome 15q11-q13 region is one of the most intriguing imprinted domains, and the abnormalities inherited… (More)
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2003
2003
BACKGROUND Prader-Willi syndrome (PWS), the most common genetic cause of marked obesity, is caused by genomic imprinting and loss… (More)
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2003
2003
To the Editor: We read with interest a report by Kashiwagi et al. (2003) in the April issue of the journal, in which the authors… (More)
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2002
2002
Autism is a complex genetic disorder. Chromosome 15 is of particular interest in this disorder, because of previous reports of… (More)
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Highly Cited
2001
Highly Cited
2001
Lack of a maternal contribution to the genome at the imprinted domain on proximal chromosome 15 causes Angelman syndrome (AS… (More)
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2001
2001
Maternal duplications of the imprinted 15q11-13 domain result in an estimated 1%-2% of autism-spectrum disorders, and linkage to… (More)
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