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ATP10A gene

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

Papers overview

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2015
2015
Background: The enzymatic activities of the ATP10 family of mammalian P4-ATPases are unknown. Results: ATP10A catalyzes the… Expand
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Review
2012
Review
2012
  • S. Ribaric
  • Oxidative medicine and cellular longevity
  • 2012
  • Corpus ID: 15376725
Nutrition has important long-term consequences for health that are not only limited to the individual but can be passed on to the… Expand
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Highly Cited
2011
Highly Cited
2011
Epigenetics could help to explain individual differences in weight loss after an energy‐restriction intervention. Here, we… Expand
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2006
2006
Mice carrying two pink-eyed dilution (p) locus heterozygous deletions represent a novel polygenic mouse model of type 2 diabetes… Expand
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Highly Cited
2004
Highly Cited
2004
Atp10c is a novel type IV P-type ATPase and is a putative phospholipid transporter. The purpose of this study was to assess the… Expand
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Highly Cited
2003
Highly Cited
2003
Background: Prader-Willi syndrome (PWS), the most common genetic cause of marked obesity, is caused by genomic imprinting and… Expand
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2003
2003
AbstractThe human chromosome 15q11-q13 region is one of the most intriguing imprinted domains, and the abnormalities inherited… Expand
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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… Expand
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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… Expand
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Highly Cited
2001
Highly Cited
2001
Maternal duplications of the imprinted 15q11-13 domain result in an estimated 1%-2% of autism-spectrum disorders, and linkage to… Expand
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