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MYH9 gene
Known as:
CELLULAR MYOSIN HEAVY CHAIN, TYPE A
, MHA
, EPSTS
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This gene is involved in both cytoskeleton modeling and cytokinesis.
National Institutes of Health
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Related topics
Related topics
11 relations
Angiogenic Process
Cell Movement
Cochleosaccular degeneration of the inner ear and progressive cataracts
Cytokinesis
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MYH9 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
In vivo Modeling Implicates APOL1 in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress
Blair R. Anderson
,
D. Howell
,
+5 authors
A. Ashley-Koch
PLoS Genetics
2015
Corpus ID: 54518885
African Americans have a disproportionate risk for developing nephropathy. This disparity has been attributed to coding variants…
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2007
2007
Generation and Characterization of Mice with Myh9 Deficiency
A. Mhatre
,
Yan Li
,
Nitin Bhatia
,
Kevin Wang
,
Graham Atkin
,
A. Lalwani
Neuromolecular medicine
2007
Corpus ID: 11526086
Mutant alleles of MYH9 encoding a class II non-muscle myosin heavy chain-A (NMMHC-IIA) have been linked to hereditary…
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2006
2006
Signaling via the Angiotensin-Converting Enzyme Results in the Phosphorylation of the Nonmuscle Myosin Heavy Chain IIA
K. Kohlstedt
,
R. Kellner
,
R. Busse
,
I. Fleming
Molecular Pharmacology
2006
Corpus ID: 18122529
The phosphorylation of the short C-terminal cytoplasmic domain of the somatic angiotensin-converting enzyme (ACE) is involved in…
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Highly Cited
2004
Highly Cited
2004
Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO…
T. Matsushita
,
Hideo Hayashi
,
+17 authors
H. Saito
Biochemical and Biophysical Research…
2004
Corpus ID: 21239336
Highly Cited
2003
Highly Cited
2003
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome.
S. Deutsch
,
A. Rideau
,
+7 authors
P. Beris
Blood
2003
Corpus ID: 14983469
May-Hegglin anomaly (MHA), Fechtner syndrome (FTNS), Sebastian syndrome (SBS), and Epstein syndrome (EPS) are a group of rare…
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Highly Cited
2002
Highly Cited
2002
Molecular Epidemiology of HIV Type 1 in Ecuador, Peru, Bolivia, Uruguay, and Argentina.
J. Hierholzer
,
S. Montano
,
+18 authors
J. Carr
AIDS Research and Human Retroviruses
2002
Corpus ID: 21356248
Surveillance for HIV infection among people at increased risk was conducted in five countries in South America. Seroprevalence…
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Highly Cited
2002
Highly Cited
2002
Evidence of a Role for Nonmuscle Myosin II in Herpes Simplex Virus Type 1 Egress
H. V. van Leeuwen
,
G. Elliott
,
P. O’Hare
Journal of Virology
2002
Corpus ID: 24337367
ABSTRACT After cell entry, herpes simplex virus (HSV) particles are transported through the host cell cytoplasm to nuclear pores…
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Highly Cited
2002
Highly Cited
2002
Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene
M. Seri
,
M. Savino
,
+13 authors
A. Savoia
Human Genetics
2002
Corpus ID: 2067546
Abstract. Epstein syndrome (EPTS) is an autosomal dominant disease characterized by nephritis, mild hearing loss, and…
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1994
1994
Construction of Syrian hamster lines congenic at the polymorphic acetyltransferase locus (NAT2): acetylator genotype-dependent N- and O-acetylation of arylamine carcinogens.
D. Hein
,
M. Doll
,
T. Rustan
,
K. Gray
,
R. J. Ferguson
,
Y. Feng
Toxicology and Applied Pharmacology
1994
Corpus ID: 22274775
Congenic Bio. 1.5/H-NAT2 Syrian hamster lines were constructed by introducing the NAT2r gene from MHA/SsLak inbred hamsters into…
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1964
1964
Studies on homografts of foetal and infant skin and further observations on the anomalous properties of pouch skin grafts in hamsters
R. Billingham
,
W. Silvers
Proceedings of the Royal Society of London…
1964
Corpus ID: 108952793
A systematic study has been made of the influence of donor age on the survival of skin homografts in Syrian hamsters. Estimates…
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