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CLTCL1 wt Allele

Known as: Clathrin, Heavy Polypeptide D Gene, CHC17, FLJ36032 
Human CLTCL1 wild-type allele is located in the vicinity of 22q11.2 and is approximately 112 kb in length. This allele, which encodes clathrin heavy… Expand
National Institutes of Health

Papers overview

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2012
2012
Clathrin inactivation during S phase destabilizes the microtubule-binding protein ch-TOG, affecting its centrosomal localization… Expand
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Highly Cited
2010
Highly Cited
2010
CHC22 is needed for retrograde trafficking from endosomes to the trans-Golgi, unlike its clathrin sibling CHC17, and in a manner… Expand
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Highly Cited
2009
Highly Cited
2009
GLUT4, Clathrin, and Glucose In human muscle, the GLUT4 glucose transport pathway responds to insulin and is responsible for 70… Expand
Highly Cited
2005
Highly Cited
2005
In humans, there are two isoforms each of clathrin heavy chain (CHC17 and CHC22) and light chain (LCa and LCb) subunits, all… Expand
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2004
2004
The muscle isoform of clathrin heavy chain, CHC22, has 85% sequence identity to the ubiquitously expressed CHC17, yet its… Expand
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2001
2001
A persistent question concerning mechanisms underlying long-term, activity-dependent synaptic plasticity is whether the sites of… Expand
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Highly Cited
2001
Highly Cited
2001
A clathrin homolog encoded on human chromosome 22 (CHC22) displays distinct biochemistry, distribution and function compared with… Expand
Highly Cited
2000
Highly Cited
2000
Anaplastic lymphoma kinase (ALK)-positive lymphomas are characterized by expression of a hybrid protein, comprising the… Expand
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Highly Cited
1997
Highly Cited
1997
The smallest region of deletion overlap in the patients we have studied defines a DIGeorge syndrome/velocardiofacial syndrome… Expand
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Highly Cited
1996
Highly Cited
1996
Velo-cardio-facial syndrome (VCFS) and DiGeorge syndrome (DGS) are developmental disorders characterized by a spectrum of… Expand
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