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FAM20C gene

Known as: IMAGE:4942737, FAMILY WITH SEQUENCE SIMILARITY 20, MEMBER C, DKFZp547D065 
 
National Institutes of Health

Papers overview

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2016
2016
Mutations in the Family with sequence similarity (FAM) 20 gene family are associated with mineralized tissue phenotypes in humans… Expand
2014
2014
BACKGROUND Hypophosphatemia and increased serum fibroblast growth factor 23 (FGF23) levels have been reported in young brothers… Expand
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2013
2013
FAM20C, also known as Golgi casein kinase (G‐CK), is proposed to be the archetype for a family of secreted kinases that… Expand
2013
2013
Previously, we showed that Sox2-Cre;Fam20Cfl/fl mice in which Fam20C was ubiquitously inactivated had severe defects in dentin… Expand
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Highly Cited
2012
Highly Cited
2012
Family with sequence similarity 20,-member C (FAM20C) is highly expressed in the mineralized tissues of mammals. Genetic studies… Expand
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Highly Cited
2012
Highly Cited
2012
Raine syndrome is caused by mutations in FAM20C, which had been reported to encode a secreted component of bone and teeth. We… Expand
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Highly Cited
2011
Highly Cited
2011
Fradin M, Stoetzel C, Muller J, Koob M, Christmann D, Debry C, Kohler M, Isnard M, Astruc D, Desprez P, Zorres C, Flori E… Expand
2010
2010
Mutations in FAM20C were recently identified as the cause of lethal osteosclerotic bone dysplasia, which highlighted the… Expand
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Highly Cited
2007
Highly Cited
2007
The generation and homeostasis of bone tissue throughout development and maturity is controlled by the carefully balanced… Expand
Highly Cited
2007
Highly Cited
2007
Formation of calcified tissues is a well regulated process. In dentin, the odontoblasts synthesize several biomolecules that… Expand
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