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MYH8 gene
Known as:
MyHC-pn
, MyHC-peri
, MYH8
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National Institutes of Health
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Related topics
Related topics
1 relation
MYH6 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMD
S. Guiraud
,
B. Edwards
,
+6 authors
K. Davies
Human Molecular Genetics
2018
Corpus ID: 52953958
Abstract Duchenne muscular dystrophy (DMD) is a lethal, X-linked muscle-wasting disease caused by lack of the cytoskeletal…
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2016
2016
Two novel MYH7 proline substitutions cause Laing Distal Myopathy-like phenotypes with variable expressivity and neck extensor contracture
Miora Feinstein-Linial
,
M. Buvoli
,
+7 authors
O. Birk
BMC Medical Genetics
2016
Corpus ID: 6638303
BackgroundHuman skeletal muscles express three major myosin heavy chain (MyHC) isoforms: MyHCIIx (MYH1) in fast type 2B muscle…
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2014
2014
β–Hydroxy β–Methylbutyrate Improves Dexamethasone-Induced Muscle Atrophy by Modulating the Muscle Degradation Pathway in SD Rat
Kyung Kyun Noh
,
K. Chung
,
+7 authors
H. Chung
PLoS ONE
2014
Corpus ID: 4544141
Skeletal muscle atrophy results from various conditions including high levels of glucocorticoids, and β–hydroxy β–methylbutyrate…
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2014
2014
Park7 Expression Influences Myotube Size and Myosin Expression in Muscle
Hui Yu
,
J. Waddell
,
S. Kuang
,
C. Bidwell
PLoS ONE
2014
Corpus ID: 12884549
Callipyge sheep exhibit postnatal muscle hypertrophy due to the up-regulation of DLK1 and/or RTL1. The up-regulation of PARK7 was…
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2013
2013
Genetic stretching factors in masseter muscle after orthognathic surgery.
W. Breuel
,
M. Krause
,
Matthias Schneider
,
W. Harzer
British Journal of Oral and Maxillofacial Surgery
2013
Corpus ID: 10348683
2011
2011
Developmental myosin heavy chain mRNA in masseter after orthognathic surgery: a preliminary study.
Khemais Oukhai
,
N. Maricic
,
Matthias Schneider
,
W. Harzer
,
E. Tausche
Journal of cranio-maxillo-facial surgery…
2011
Corpus ID: 21959229
Highly Cited
2008
Highly Cited
2008
Embryonic myosin heavy-chain mutations cause distal arthrogryposis and developmental myosin myopathy that persists postnatally.
H. Tajsharghi
,
E. Kimber
,
A. Kroksmark
,
R. Jerre
,
M. Tulinius
,
A. Oldfors
Archives of Neurology
2008
Corpus ID: 28746427
BACKGROUND Myosin is a molecular motor and the essential part of the thick filament of striated muscle. The expression of myosin…
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2007
2007
Shifts in the myosin heavy chain isozymes in the mouse heart result in increased energy efficiency.
Kirsten Hoyer
,
M. Krenz
,
J. Robbins
,
J. Ingwall
Journal of Molecular and Cellular Cardiology
2007
Corpus ID: 39098628
Highly Cited
2006
Highly Cited
2006
Trismus‐pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8
R. Toydemir
,
Harold Chen
,
+7 authors
M. Bamshad
American Journal of Medical Genetics. Part A
2006
Corpus ID: 1775227
Trismus‐pseudocamptodactyly syndrome (TPS) is a rare autosomal dominant distal arthrogryposis (DA) characterized by an inability…
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2006
2006
Human skeletal muscle myosin function at physiological and non‐physiological temperatures
A. Lionikas
,
M. Li
,
L. Larsson
Acta Physiologica
2006
Corpus ID: 32531710
Aim: The aim of the study was to assess the function of human skeletal muscle myosin across a wide range of temperatures…
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