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UNC45A gene
Known as:
SMAP1
, SMOOTH MUSCLE CELL-ASSOCIATED PROTEIN 1
, SMAP-1
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This gene plays a role in the modulation of protein folding.
National Institutes of Health
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Related topics
Related topics
6 relations
Cell Differentiation process
Myogenesis
Protein Unc-45 Homolog A
cellular response to unfolded protein
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Abstract 4493: The co-chaperone UNC45A controls cancer cell proliferation through Nek7 and centrosomal separation
Yasmeen Jilani
,
Nada H. Eisa
,
+7 authors
A. Chadli
2017
Corpus ID: 80068058
Recent findings have shown that the Heat Shock Protein 90 (Hsp90) co-chaperone UNC45A is overexpressed in ovarian and breast…
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2016
2016
Title : Molecular Genotyping of Transposable Elements Insertions in a Population of Uniform Mu Events
C. Campbell
,
J. Gottesman
,
Evelyn Juliussen
,
Anthony Acholonu
2016
Corpus ID: 39038560
There has been rising interest in cytochrome P450 (CYP) proteins due to their implication in tumor progression. CYP3A4 expression…
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2009
2009
UNC 45 A Confers Resistance to Histone Deacetylase Inhibitors and Retinoic Acid
M. Epping
,
L. Meijer
,
J. Bos
,
R. Bernards
2009
Corpus ID: 42433199
To identify potential biomarkers of therapy response, we have previously done a large-scale gain-of-function genetic screen to…
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2008
2008
Investigation of the role of Unc45a in aortic arch development
Matthew J. Anderson
2008
Corpus ID: 82782590
Thesis (Ph.D.)--Georgetown University, 2008.; Includes bibliographical references. Human congenital cardiovascular malformations…
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2007
2007
The role of Unc45a in the production of aortic arch malformations in the zebrafish kus mutant
Matthew J. Anderson
,
B. L. Roman
2007
Corpus ID: 81258228
2005
2005
Mutation screening of three candidate genes, ELOVL5, SMAP1 and GLULD1 in autosomal recessive retinitis pigmentosa.
I. Barragán
,
I. Marcos
,
S. Borrego
,
G. Antiñolo
International Journal of Molecular Medicine
2005
Corpus ID: 26112597
Retinitis pigmentosa (RP) is the most common form of retinal dystrophy. It is featured by a great clinical and genetic…
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