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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
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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
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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
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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2011
2011
Raine syndrome is an autosomal recessive disorder caused by mutations in the FAM20C gene. FAM20C codes for the human homolog of… Expand
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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
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2007
2007
Formation of calcified tissues is a well regulated process. In dentin, the odontoblasts synthesize several biomolecules that… Expand
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1985
1985
This work reports on the ages of gingival eruption of deciduous and permanent teeth observed from the time of birth until 30… Expand
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