Associated Papers
Genetic variants in myostatin and its receptors promote elite athlete status.
Leońska-Duniec A et al.
Bmc Genomics, 2023
Association of Myostatin Gene Polymorphisms with Strength and Muscle Mass in Athletes: A Systematic Review and Meta-Analysis of the MSTN rs1805086 Mutation.
Kruszewski M et al.
Genes, 2022
Association between polygenetic risk scores related to sarcopenia risk and their interactions with regular exercise in a large cohort of Korean adults.
Park S
Clinical Nutrition (edinburgh, Scotland), 2021
A novel mutation in the OAR domain of PITX3 associated with congenital posterior subcapsular cataract.
Fan Q et al.
Bmc Medical Genetics, 2019
30894134 (PubMed )
Supplement: 12881_2019_782_MOESM1_ESM.xlsx › Sheet2
Whole-exome sequencing identify a new mutation of MYH7 in a Chinese family with left ventricular noncompaction.
Yang J et al.
Gene, 2015
K153R polymorphism in myostatin gene increases the rate of promyostatin activation by furin.
Szláma G et al.
Febs Letters, 2015
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1405.506
Association of the K153R polymorphism in the myostatin gene and extreme longevity.
Garatachea N et al.
Age (dordrecht, Netherlands), 2013
Genes and the ageing muscle: a review on genetic association studies.
Garatachea N et al.
Age (dordrecht, Netherlands), 2013
Association of the Myostatin gene with obesity, abdominal obesity and low lean body mass and in non-diabetic Asian Indians in north India.
Bhatt SP et al.
Plos One, 2012
The K153R polymorphism in the myostatin gene and muscle power phenotypes in young, non-athletic men.
Santiago C et al.
Plos One, 2011
World-class performance in lightweight rowing: is it genetically influenced? A comparison with cyclists, runners and non-athletes.
Muniesa CA et al.
British Journal of Sports Medicine, 2010
The K153R variant in the myostatin gene and sarcopenia at the end of the human lifespan.
González-Freire M et al.
Age (dordrecht, Netherlands), 2010
Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease?
González-Freire M et al.
Neuromuscular Disorders : Nmd, 2009
Exploration of myostatin polymorphisms and the angiotensin-converting enzyme insertion/deletion genotype in responses of human muscle to strength training.
Thomis MA et al.
European Journal of Applied Physiology, 2004
Polymorphic variation in the human myostatin (GDF-8) gene and association with strength measures in the Women's Health and Aging Study II cohort.
Seibert MJ et al.
Journal of the American Geriatrics Society, 2001
Frequent sequence variation in the human myostatin (GDF8) gene as a marker for analysis of muscle-related phenotypes.
Ferrell RE et al.
Genomics, 1999
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