SLC24A4 gene

Known as: SODIUM/POTASSIUM/CALCIUM EXCHANGER 4, SOLUTE CARRIER FAMILY 24 (SODIUM/POTASSIUM/CALCIUM EXCHANGER), MEMBER 4, SLC24A4 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2008-2016
02420082016

Papers overview

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2015
2015
IMPORTANCE Recent large-scale genome-wide association studies have discovered several genetic variants associated with Alzheimer… (More)
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2015
2015
Defects in WDR72 (WD repeat-containing protein 72) cause autosomal recessive hypomaturation amelogenesis imperfecta. We generated… (More)
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2015
2015
OBJECTIVE To investigate the top late-onset Alzheimer disease (LOAD) risk loci detected or confirmed by the International… (More)
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2015
2015
Ameloblasts express transmembrane proteins for transport of mineral ions and regulation of pH in the enamel space. Two major… (More)
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2014
2014
Amelogenesis imperfecta is a heterogeneous group of genetic conditions affecting enamel formation. Recently, mutations in solute… (More)
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2014
2014
Calcium ions in the uterine endometrium are essential for the establishment and maintenance of pregnancy, but the cellular and… (More)
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2013
2013
A combination of autozygosity mapping and exome sequencing identified a null mutation in SLC24A4 in a family with hypomineralized… (More)
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2012
2012
Sixteen nuclear magnetic resonance (NMR) spectroscopy lipoprotein measurements of more than 1,000 subjects of GOLDN study, at… (More)
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Highly Cited
2010
Highly Cited
2010
Despite the recent rapid growth in genome-wide data, much of human variation remains entirely unexplained. A significant… (More)
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Highly Cited
2009
Highly Cited
2009
The evidence for the existence of genetic susceptibility variants for the common form of hypertension ("essential hypertension… (More)
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