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FAM20C gene

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

Related topics

Related topics

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FAM20B gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
FAM20A binds to and regulates FAM20C localization
Mutations in the Family with sequence similarity (FAM) 20 gene family are associated with mineralized tissue phenotypes in humans… Expand
2014
2014
Hypophosphatemic osteomalacia and bone sclerosis caused by a novel homozygous mutation of the FAM20C gene in an elderly man with a mild variant of Raine syndrome.
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 Functions Intracellularly Within Both Ameloblasts and Odontoblasts In Vivo
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
The Specific Role of FAM20C in Amelogenesis
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
Inactivation of a Novel FGF23 Regulator, FAM20C, Leads to Hypophosphatemic Rickets in Mice
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
The Raine Syndrome Protein FAM20C Is a Golgi Kinase That Phosphorylates Bio-Mineralization Proteins
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
Osteosclerotic bone dysplasia in siblings with a Fam20C mutation
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
Expression of FAM20C in the Osteogenesis and Odontogenesis of Mouse
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
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development.
The generation and homeostasis of bone tissue throughout development and maturity is controlled by the carefully balanced… Expand
Highly Cited
2007
Highly Cited
2007
Dentin Matrix Protein 4, a Novel Secretory Calcium-binding Protein That Modulates Odontoblast Differentiation*
Formation of calcified tissues is a well regulated process. In dentin, the odontoblasts synthesize several biomolecules that… Expand
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