Showing results (171-180 of 11,950) with videos related to
Sort By:
Pageof 1,195
Human Molecular Genetics|August 13, 2015
Long-term engraftment of myogenic progenitors from adipose-derived stem cells and muscle regeneration in dystrophic miceYu Zhang, Yuling Zhu, Yaqin Li, et al.Human Molecular Genetics|August 13, 2015
Altered cytoskeletal organization characterized lethal but not surviving Brtl+/- mice: insight on phenotypic variability in osteogenesis imperfectaLaura Bianchi, Assunta Gagliardi, Silvia Maruelli, et al.Human Molecular Genetics|November 8, 2015
Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritisJavier Gutierrez-Achury, Maria Magdalena Zorro, Isis Ricaño-Ponce, et al.Human Molecular Genetics|November 8, 2015
Prenatal and early life influences on epigenetic age in children: a study of mother-offspring pairs from two cohort studiesAndrew J Simpkin, Gibran Hemani, Matthew Suderman, et al.Human Molecular Genetics|November 16, 2013
Graded Otx2 activities demonstrate dose-sensitive eye and retina phenotypesClémence Bernard, Hyoung-Tai Kim, Raoul Torero Ibad, et al.Human Molecular Genetics|July 27, 2013
A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasisStephan Weidinger, Saffron A G Willis-Owen, Yoichiro Kamatani, et al.Human Molecular Genetics|July 27, 2013
Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patientsSteven Marston, Massimiliano Memo, Andrew Messer, et al.Human Molecular Genetics|February 28, 2012
Tbx1 is a negative modulator of Mef2cLuna Simona Pane, Zhen Zhang, Rosa Ferrentino, et al.Human Molecular Genetics|March 3, 2012
Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genesQing Yin Zheng, John D Scarborough, Ye Zheng, et al.Human Molecular Genetics|March 2, 2012
Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expressionAlireza Baradaran-Heravi, Kyoung Sang Cho, Bas Tolhuis, et al.Pageof 1,195