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CC2D1A gene

Known as: coiled-coil and C2 domain containing 1A, CC2D1A, mental retardation, nonsyndromic, autosomal recessive, 3 
 
National Institutes of Health

Papers overview

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2017
2017
Abstract Loss‐of‐function (LOF) mutations in CC2D1A cause a spectrum of neurodevelopmental disorders, including intellectual… Expand
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2014
2014
Autism spectrum disorder (ASD) and intellectual disability (ID) are often comorbid, but the extent to which they share common… Expand
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2012
2012
Endosomal sorting complexes required for transport (ESCRTs) regulate diverse processes ranging from receptor sorting at endosomes… Expand
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2012
2012
The detachment of human immunodeficiency type 1 (HIV-1) virions depends on CHPM4 family members, which are late-acting components… Expand
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2011
2011
The innate immune system elicits the first wave of immune responses against pathogen infection. Its operational modes are complex… Expand
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2011
2011
Cc2d1a is an evolutionarily conserved protein composed of NH(2)-terminal Drosophila melanogaster 14 domain (DM14) domains and a… Expand
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2010
2010
CC2D1A is an evolutionarily conserved protein that contains four DM14 domains at the N terminus and a C2 domain at the C terminus… Expand
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2008
2008
The phosphoinositide 3-kinase (PI3K)/3-phosphoinositide-dependent protein kinase 1 (PDK1)/Akt pathway regulates various cellular… Expand
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2007
2007
The CC2D1A/Freud-1 gene has recently been linked to non-syndromic mental retardation and a short isoform of mouse Five prime… Expand
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Highly Cited
2005
Highly Cited
2005
BACKGROUND The molecular basis of autosomal recessive non-syndromic mental retardation (NSMR) is poorly understood, mostly owing… Expand
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