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CLTCL1 wt Allele
Known as:
Clathrin, Heavy Polypeptide D Gene
, CHC17
, FLJ36032
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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…
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National Institutes of Health
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Related topics
Related topics
4 relations
CLTC gene
CLTC wt Allele
Receptor Mediated Endocytosis
Broader (1)
CLTCL1 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development
M. Nahorski
,
L. Al-Gazali
,
+10 authors
C. Woods
Brain : a journal of neurology
2015
Corpus ID: 8643543
Congenital inability to feel pain is rare, but the identification of causative genes is translating into the development of novel…
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Highly Cited
2012
Highly Cited
2012
Clathrin promotes centrosome integrity in early mitosis through stabilization of centrosomal ch-TOG
Amy B. Foraker
,
Stéphane M Camus
,
+6 authors
F. Brodsky
Journal of Cell Biology
2012
Corpus ID: 10828524
Clathrin inactivation during S phase destabilizes the microtubule-binding protein ch-TOG, affecting its centrosomal localization…
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Highly Cited
2010
Highly Cited
2010
The clathrin heavy chain isoform CHC22 functions in a novel endosomal sorting step
Christopher Esk
,
Chih‐Ying Chen
,
L. Johannes
,
F. Brodsky
Journal of Cell Biology
2010
Corpus ID: 6195840
CHC22 is needed for retrograde trafficking from endosomes to the trans-Golgi, unlike its clathrin sibling CHC17, and in a manner…
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Highly Cited
2009
Highly Cited
2009
A Role for the CHC22 Clathrin Heavy-Chain Isoform in Human Glucose Metabolism
S. Vassilopoulos
,
Christopher Esk
,
+6 authors
F. Brodsky
Science
2009
Corpus ID: 8089368
GLUT4, Clathrin, and Glucose In human muscle, the GLUT4 glucose transport pathway responds to insulin and is responsible for 70…
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Highly Cited
2005
Highly Cited
2005
Clathrin heavy and light chain isoforms originated by independent mechanisms of gene duplication during chordate evolution.
D. Wakeham
,
L. Abi-Rached
,
M. Towler
,
J. Wilbur
,
P. Parham
,
F. Brodsky
Proceedings of the National Academy of Sciences…
2005
Corpus ID: 12283404
In humans, there are two isoforms each of clathrin heavy chain (CHC17 and CHC22) and light chain (LCa and LCb) subunits, all…
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2004
2004
Clathrin isoform CHC22, a component of neuromuscular and myotendinous junctions, binds sorting nexin 5 and has increased expression during myogenesis and muscle regeneration.
M. Towler
,
P. Gleeson
,
+6 authors
F. Brodsky
Molecular Biology of the Cell
2004
Corpus ID: 9199557
The muscle isoform of clathrin heavy chain, CHC22, has 85% sequence identity to the ubiquitously expressed CHC17, yet its…
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Highly Cited
2001
Highly Cited
2001
A novel clathrin homolog that co‐distributes with cytoskeletal components functions in the trans‐Golgi network
Shu-Hui Liu
,
M. Towler
,
+4 authors
F. Brodsky
EMBO Journal
2001
Corpus ID: 31661267
A clathrin homolog encoded on human chromosome 22 (CHC22) displays distinct biochemistry, distribution and function compared with…
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2001
2001
FM1-43 Imaging Reveals cGMP-Dependent Long-Term Depression of Presynaptic Transmitter Release
P. Stanton
,
U. Heinemann
,
W. Müller
Journal of Neuroscience
2001
Corpus ID: 7794190
A persistent question concerning mechanisms underlying long-term, activity-dependent synaptic plasticity is whether the sites of…
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Highly Cited
2000
Highly Cited
2000
Further demonstration of the diversity of chromosomal changes involving 2p23 in ALK-positive lymphoma: 2 cases expressing ALK kinase fused to CLTCL (clathrin chain polypeptide-like).
Christian Touriol
,
C. Greenland
,
+5 authors
G. Delsol
Blood
2000
Corpus ID: 1490803
Anaplastic lymphoma kinase (ALK)-positive lymphomas are characterized by expression of a hybrid protein, comprising the…
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1997
1997
Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation.
Susan E. Holmes
,
M. Riazi
,
+15 authors
M. Budarf
Human Molecular Genetics
1997
Corpus ID: 24865760
The smallest region of deletion overlap in the patients we have studied defines a DIGeorge syndrome/velocardiofacial syndrome…
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