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FGD1 gene

Known as: FGD1, FYVE, RhoGEF and PH domain containing 1, ZFYVE3 
National Institutes of Health

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FGD1 protein, human

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Identification of novel mutations in Mexican patients with Aarskog–Scott syndrome
Aarskog–Scott syndrome (AAS), also known as faciogenital dysplasia (FGD, OMIM # 305400), is an X‐linked disorder of recessive… 
2014
2014
A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism
We present a male patient with sporadic Aarskog syndrome, cleft palate, mild intellectual disability, and autism spectrum… 
2013
2013
Mutational analysis of the GNA11, MMP27, FGD1, TRRAP and GRM3 genes in thyroid cancer
Frequent somatic mutations in the GNA11, matrix metalloproteinase (MMP)27, FGD1, TRRAP and GRM3 genes have been reported in… 
Highly Cited
1998
Highly Cited
1998
Frabin, a Novel FGD1-related Actin Filament-binding Protein Capable of Changing Cell Shape and Activating c-Jun N-terminal Kinase*
We purified from rat brain a novel F-actin-binding protein with a M r of about 105,000 (p105), which was estimated by SDS… 
1996
1996
Cloning of Genes with High Homology to the Faciogenital Dysplasia (FGD1) Gene; The Human FGD2, Mouse FGD2, and Zebra Fish FGD1 Genes
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