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COG4 gene
Known as:
DKFZP586E1519
, COMPONENT OF OLIGOMERIC GOLGI COMPLEX 4
, COD1
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National Institutes of Health
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Related topics
Related topics
1 relation
COG4 protein, S cerevisiae
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.
C. Ferreira
,
Zhi-Jie Xia
,
+51 authors
H. Freeze
American Journal of Human Genetics
2018
Corpus ID: 52923715
2015
2015
Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylation
H. Kodera
,
N. Ando
,
+7 authors
H. Saitsu
Clinical Genetics
2015
Corpus ID: 5370409
The conserved oligomeric Golgi (COG) complex is involved in intra‐Golgi retrograde trafficking, and mutations in six of its eight…
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2014
2014
Multipronged interaction of the COG complex with intracellular membranes
Rose A. Willett
,
I. Pokrovskaya
,
Tetyana Kudlyk
,
V. Lupashin
Cellular Logistics
2014
Corpus ID: 36826019
The conserved oligomeric Golgi complex is a peripheral membrane protein complex that orchestrates the tethering and fusion of…
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2011
2011
Identification of the first COG-CDG patient of Indian origin.
B. Ng
,
Vandana Sharma
,
+4 authors
H. Freeze
Molecular Genetics and Metabolism
2011
Corpus ID: 205828055
Highly Cited
2009
Highly Cited
2009
Golgi function and dysfunction in the first COG4-deficient CDG type II patient
E. Reynders
,
F. Foulquier
,
+5 authors
G. Matthijs
Human Molecular Genetics
2009
Corpus ID: 5895793
The conserved oligomeric Golgi (COG) complex is a hetero-octameric complex essential for normal glycosylation and intra-Golgi…
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Highly Cited
2009
Highly Cited
2009
Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene
B. Richardson
,
Richard D. Smith
,
+4 authors
F. Hughson
Proceedings of the National Academy of Sciences
2009
Corpus ID: 20688787
The proper glycosylation of proteins trafficking through the Golgi apparatus depends upon the conserved oligomeric Golgi (COG…
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Highly Cited
2009
Highly Cited
2009
Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation.
P. Paesold-Burda
,
C. Maag
,
+5 authors
T. Hennet
Human Molecular Genetics
2009
Corpus ID: 8632942
The conserved oligomeric Golgi (COG) complex is a tethering factor composed of eight subunits that is involved in the retrograde…
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Highly Cited
2002
Highly Cited
2002
Cod1p/Spf1p is a P-type ATPase involved in ER function and Ca2+ homeostasis
S. Cronin
,
R. Rao
,
R. Hampton
Journal of Cell Biology
2002
Corpus ID: 7944759
The internal environment of the ER is regulated to accommodate essential cellular processes, yet our understanding of this…
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1998
1998
Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3.
A. Seymour
,
A. Dash-Modi
,
+8 authors
M. Gorin
American Journal of Human Genetics
1998
Corpus ID: 31359861
Progressive X-linked cone-rod dystrophy (COD1) is a retinal disease affecting primarily the cone photoreceptors. The COD1 locus…
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1994
1994
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
H. Hong
,
R. Ferrell
,
M. Gorin
American Journal of Human Genetics
1994
Corpus ID: 26447353
X-linked progressive cone dystrophy (COD1) causes progressive deterioration of visual acuity, deepening of central scotomas…
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