CC2D1A gene

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

Topic mentions per year

Topic mentions per year

2006-2016
02420062016

Papers overview

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2017
2017
Loss-of-function (LOF) mutations in CC2D1A cause a spectrum of neurodevelopmental disorders, including intellectual disability… (More)
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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… (More)
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2013
2013
Cyclic adenosine 3′,5′-monophosphate (cAMP) is a key regulator of many cellular processes, including in the neuronal system, and… (More)
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2012
2012
Endosomal sorting complexes required for transport (ESCRTs) regulate diverse processes ranging from receptor sorting at endosomes… (More)
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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… (More)
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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… (More)
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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… (More)
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2008
2008
Autosomal-recessive inheritance is believed to be relatively common in mental retardation (MR), although only four genes for… (More)
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2008
2008
The phosphoinositide 3-kinase (PI3K)/3-phosphoinositide-dependent protein kinase 1 (PDK1)/Akt pathway regulates various cellular… (More)
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2006
2006
BACKGROUND The molecular basis of autosomal recessive non-syndromic mental retardation (NSMR) is poorly understood, mostly owing… (More)
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