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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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2019
2019
P4‐ATPases belonging to the P‐type ATPase superfamily mediate active transport of phospholipids across cellular membranes. Most… 
Review
2012
Review
2012
Nutrition has important long-term consequences for health that are not only limited to the individual but can be passed on to the… 
2012
2012
Atp10c is a strong candidate gene for diet-induced obesity and type 2 diabetes. To identify molecular and cellular targets of… 
2010
2010
Mutations affecting a cluster of coordinately regulated imprinted genes located at 15q11-q13 underlie both Prader–Willi syndrome… 
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… 
2003
2003
On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting? 
2002
2002
Autism is a complex genetic disorder. Chromosome 15 is of particular interest in this disorder, because of previous reports of… 
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… 
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…