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FAM20C gene
Known as:
IMAGE:4942737
, FAMILY WITH SEQUENCE SIMILARITY 20, MEMBER C
, DKFZp547D065
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National Institutes of Health
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Related topics
Related topics
1 relation
FAM20B gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Ser-Phosphorylation of PCSK9 (Proprotein Convertase Subtilisin-Kexin 9) by Fam20C (Family With Sequence Similarity 20, Member C) Kinase Enhances Its Ability to Degrade the LDLR (Low-Density…
Ali Ben Djoudi Ouadda
,
M. Gauthier
,
+15 authors
N. Seidah
Arteriosclerosis, Thrombosis and Vascular Biology
2019
Corpus ID: 202861190
OBJECTIVE PCSK9 (proprotein convertase subtilisin-kexin 9) enhances the degradation of the LDLR (low-density lipoprotein receptor…
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2016
2016
FAM20A binds to and regulates FAM20C localization
Y. Ohyama
,
Ju-hsien Lin
,
+8 authors
Y. Mochida
Scientific Reports
2016
Corpus ID: 4755064
Mutations in the Family with sequence similarity (FAM) 20 gene family are associated with mineralized tissue phenotypes in humans…
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2016
2016
Immunohistochemical analysis of dentin matrix protein 1 (Dmp1) phosphorylation by Fam20C in bone: implications for the induction of biomineralization
Kaori Oya
,
Ken Ishida
,
+9 authors
S. Toyosawa
Histochemistry and Cell Biology
2016
Corpus ID: 34678306
Dmp1 is an acidic phosphoprotein that is specifically expressed in osteocytes. During the secretory process, the full-length…
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2013
2013
The Specific Role of FAM20C in Amelogenesis
X. Wang
,
J. Jung
,
+4 authors
C. Qin
Journal of dentistry research
2013
Corpus ID: 206417818
Previously, we showed that Sox2-Cre;Fam20Cfl/fl mice in which Fam20C was ubiquitously inactivated had severe defects in dentin…
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Highly Cited
2012
Highly Cited
2012
Inactivation of a Novel FGF23 Regulator, FAM20C, Leads to Hypophosphatemic Rickets in Mice
Xiaofang Wang
,
Suzhen Wang
,
+11 authors
C. Qin
PLoS Genetics
2012
Corpus ID: 17596297
Family with sequence similarity 20,-member C (FAM20C) is highly expressed in the mineralized tissues of mammals. Genetic studies…
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Highly Cited
2012
Highly Cited
2012
The Raine Syndrome Protein FAM20C Is a Golgi Kinase That Phosphorylates Bio-Mineralization Proteins
Hiroyuki O. Ishikawa
,
A. Xu
,
Eri Ogura
,
G. Manning
,
K. Irvine
PLoS ONE
2012
Corpus ID: 730440
Raine syndrome is caused by mutations in FAM20C, which had been reported to encode a secreted component of bone and teeth. We…
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Highly Cited
2011
Highly Cited
2011
Osteosclerotic bone dysplasia in siblings with a Fam20C mutation
M. Fradin
,
C. Stoetzel
,
+11 authors
B. Doray
Clinical Genetics
2011
Corpus ID: 205408339
Fradin M, Stoetzel C, Muller J, Koob M, Christmann D, Debry C, Kohler M, Isnard M, Astruc D, Desprez P, Zorres C, Flori E…
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Highly Cited
2010
Highly Cited
2010
Expression of FAM20C in the Osteogenesis and Odontogenesis of Mouse
Xiaofang Wang
,
J. Hao
,
+7 authors
C. Qin
Journal of Histochemistry and Cytochemistry
2010
Corpus ID: 21554163
Mutations in FAM20C were recently identified as the cause of lethal osteosclerotic bone dysplasia, which highlighted the…
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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.
M. Simpson
,
R. Hsu
,
+13 authors
A. Crosby
American Journal of Human Genetics
2007
Corpus ID: 19467702
The generation and homeostasis of bone tissue throughout development and maturity is controlled by the carefully balanced…
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Highly Cited
2007
Highly Cited
2007
Dentin Matrix Protein 4, a Novel Secretory Calcium-binding Protein That Modulates Odontoblast Differentiation*
J. Hao
,
K. Narayanan
,
T. Muni
,
A. Ramachandran
,
A. George
Journal of Biological Chemistry
2007
Corpus ID: 25106679
Formation of calcified tissues is a well regulated process. In dentin, the odontoblasts synthesize several biomolecules that…
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