Robert B. Weiss Department of Human Genetics The University of Utah School of Medicine Biography Publications Institution JoVE Articles Robert B. Weiss has not added a biography. If you are Robert B. Weiss and would like to personalize this page please email our Author Liaison for assistance. Publications X-linked Muscular Dystrophy in a Labrador Retriever Strain: Phenotypic and Molecular Characterisation Skeletal Muscle. 08, 2020 | Pubmed ID: 32767978 Low-level Expression of EPG5 Leads to an Attenuated Vici Syndrome Phenotype American Journal of Medical Genetics. Part A. 05, 2018 | Pubmed ID: 29681093 Low-level Dystrophin Expression Attenuating the Dystrophinopathy Phenotype Neuromuscular Disorders : NMD. 02, 2018 | Pubmed ID: 29305136 Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 As a Modifier of Duchenne Muscular Dystrophy American Journal of Human Genetics. Nov, 2016 | Pubmed ID: 27745838 Clinical Phenotypes As Predictors of the Outcome of Skipping Around DMD Exon 45 Annals of Neurology. Apr, 2015 | Pubmed ID: 25612243 Translation from a DMD Exon 5 IRES Results in a Functional Dystrophin Isoform That Attenuates Dystrophinopathy in Humans and Mice Nature Medicine. 09, 2014 | Pubmed ID: 25108525 LTBP4 Genotype Predicts Age of Ambulatory Loss in Duchenne Muscular Dystrophy Annals of Neurology. Apr, 2013 | Pubmed ID: 23440719 Molecular Biology. Translation Goes Global Science (New York, N.Y.). Dec, 2011 | Pubmed ID: 22174241 A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region As a Risk Factor for Age-dependent Nicotine Addiction PLoS Genetics. Jul, 2008 | Pubmed ID: 18618000 From Genetics to Mechanism of Disease Liability Advances in Genetics. 2008 | Pubmed ID: 18358337 Nöromüsküler Bozukluklar için Tedavileri Araştırmak için İnsan Fibroblastlarının Myoblastlara Doğrudan Yeniden Programlanması Camila F. Almeida1, Emma C. Frair1, Nianyuan Huang1, Reid Neinast2, Kim L. McBride2,3,4,6, Robert B. Weiss5, Kevin M. Flanigan1,6, Nicolas Wein1,6 1Center for Gene Therapy, The Research Institute at Nationwide Children’s Hospital, 2Center for Cardiovascular Research, The Research Institute at Nationwide Children’s Hospital, 3The Heart Center, Nationwide Children’s Hospital, 4Division of Genetic and Genomic Medicine, Nationwide Children’s Hospital, 5Department of Human Genetics, The University of Utah School of Medicine, 6Department of Pediatrics, The Ohio State University JoVE 61991 Genetics
Nöromüsküler Bozukluklar için Tedavileri Araştırmak için İnsan Fibroblastlarının Myoblastlara Doğrudan Yeniden Programlanması Camila F. Almeida1, Emma C. Frair1, Nianyuan Huang1, Reid Neinast2, Kim L. McBride2,3,4,6, Robert B. Weiss5, Kevin M. Flanigan1,6, Nicolas Wein1,6 1Center for Gene Therapy, The Research Institute at Nationwide Children’s Hospital, 2Center for Cardiovascular Research, The Research Institute at Nationwide Children’s Hospital, 3The Heart Center, Nationwide Children’s Hospital, 4Division of Genetic and Genomic Medicine, Nationwide Children’s Hospital, 5Department of Human Genetics, The University of Utah School of Medicine, 6Department of Pediatrics, The Ohio State University JoVE 61991 Genetics