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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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Narrower (1)
MYH9 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
A novel approach for enhanced nanoparticle-sized bone substitute adhesion to chemically treated peri-implantitis-affected implant surfaces: an in vitro proof-of-principle study.
A. Gamal
,
Khaled Abdel-ghaffar
,
V. Iacono
The Journal of Periodontology
2013
Corpus ID: 25172971
BACKGROUND The objective of this study is to evaluate micro and nano-hydroxyapatite (NHA) blended clot adhesion to citric acid…
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2012
2012
Glomerular MYH9 expression is reduced by HIV-1
T. Hays
,
V. D’Agati
,
+5 authors
P. Klotman
AIDS (London)
2012
Corpus ID: 30057929
Background:The continuing disease burden of HIV-associated nephropathy (HIVAN) warrants better elucidation of its pathogenic…
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2011
2011
A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9
M. Klein
2011
Corpus ID: 75307186
2011
2011
Coincident idiopathic focal segmental glomerulosclerosis collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants.
Isai Gopalakrishnan
,
S. Iskandar
,
+6 authors
B. Freedman
Human Pathology
2011
Corpus ID: 22741718
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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2003
2003
MYH9 spectrum of autosomal‐dominant giant platelet syndromes: Unexpected association with fibulin‐1 variant‐D inactivation
A. Toren
,
G. Rozenfeld-Granot
,
+14 authors
G. Rechavi
American journal of hematology/oncology
2003
Corpus ID: 45735428
The autosomal‐dominant giant platelet syndromes (Fechtner, Epstein, and Sebastian platelet syndromes and May‐Hegglin anomaly…
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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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1990
1990
2-Hydroxy-4-(methylthio) butanoic acid is a naturally occurring methionine precursor in the chick.
J. Dibner
,
R. C. Durley
,
J. G. Kostelc
,
F. J. Ivey
Journal of NutriLife
1990
Corpus ID: 4442929
The objective of these experiments was to determine the origin of 2-hydroxy-4-(methylthio)-butanoic acid (HMB) detected in the…
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1980
1980
IMMUNOGENETIC RELATIONSHIPS AMONG GENETICALLY DEFINED, INBRED DOMESTIC SYRIAN HAMSTER STRAINS
J. Streilein
,
W. Duncan
,
F. Homburger
Transplantation
1980
Corpus ID: 31008479
A large number of genetically defined, isogenic strains of domestic Syrian hamsters (BIO) have been studied for their…
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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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