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Human Molecular Genetics|June 7, 2013
Delayed myelination in a mouse model of fragile X syndromeLaura K K Pacey, Ingrid C Y Xuan, Sihui Guan, et al.Human Molecular Genetics|June 7, 2013
Method for widespread microRNA-155 inhibition prolongs survival in ALS-model miceErica D Koval, Carey Shaner, Peter Zhang, et al.Human Molecular Genetics|June 14, 2013
Transient systemic mtDNA damage leads to muscle wasting by reducing the satellite cell poolXiao Wang, Alicia M Pickrell, Susana G Rossi, et al.Human Molecular Genetics|March 26, 2013
Novel Drosophila model of myotonic dystrophy type 1: phenotypic characterization and genome-wide view of altered gene expressionLucie Picchio, Emilie Plantie, Yoan Renaud, et al.Human Molecular Genetics|March 27, 2013
DNA polymerase ε and δ exonuclease domain mutations in endometrial cancerDavid N Church, Sarah E W Briggs, Claire Palles, et al.Human Molecular Genetics|April 14, 2012
miRNA-34c regulates Notch signaling during bone developmentYangjin Bae, Tao Yang, Huan-Chang Zeng, et al.Human Molecular Genetics|March 3, 2012
Amelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the αMβ2 leukocyte integrin receptorBerta Vidal, Esther Ardite, Mònica Suelves, et al.Human Molecular Genetics|May 24, 2012
Microarray expression analysis and identification of serum biomarkers for Niemann-Pick disease, type C1Celine V M Cluzeau, Dawn E Watkins-Chow, Rao Fu, et al.Human Molecular Genetics|May 31, 2012
Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicityMarija Usenovic, Adam L Knight, Arpita Ray, et al.Human Molecular Genetics|May 31, 2012
ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreousLev Prasov, Tehmina Masud, Shagufta Khaliq, et al.Pageof 1,196