Eric P. Hoffman focuses on Muscular dystrophy, Duchenne muscular dystrophy, Dystrophin, Internal medicine and Genetics. He combines subjects such as Myocyte, Molecular biology, Lamin and Limb-girdle muscular dystrophy with his study of Muscular dystrophy. Eric P. Hoffman works on Duchenne muscular dystrophy which deals in particular with X-linked muscular dystrophy.
His Dystrophin research is multidisciplinary, incorporating elements of Exon, ITGA7 and Pathology. His Internal medicine research includes elements of Endocrinology and Cardiology. His Endocrinology study combines topics from a wide range of disciplines, such as Regulation of gene expression, Gene mutation and Regeneration.
Eric P. Hoffman mainly investigates Internal medicine, Endocrinology, Duchenne muscular dystrophy, Genetics and Dystrophin. Eric P. Hoffman has included themes like Genotype and Cardiology in his Internal medicine study. Eric P. Hoffman has researched Duchenne muscular dystrophy in several fields, including Exon skipping, Biopsy, Bioinformatics and Exon.
His Genetics and Gene, Locus, Genetic linkage, Mutation and X chromosome investigations all form part of his Genetics research activities. His study in Dystrophin is interdisciplinary in nature, drawing from both Molecular biology, ITGA7 and Pathology. He interconnects Limb-girdle muscular dystrophy and Gene mutation in the investigation of issues within Muscular dystrophy.
His main research concerns Duchenne muscular dystrophy, Internal medicine, Endocrinology, Dystrophin and Pathology. The various areas that he examines in his Duchenne muscular dystrophy study include Biomarker, Muscular dystrophy, Bioinformatics and Exon. His Internal medicine research is multidisciplinary, incorporating perspectives in Genotype and Cardiology.
His Dystrophin research incorporates elements of Muscle tissue, Exon skipping, Biopsy and Molecular biology. His work deals with themes such as Hypotonia and Missense mutation, which intersect with Pathology. He interconnects Myocyte and Cell biology in the investigation of issues within Skeletal muscle.
His scientific interests lie mostly in Duchenne muscular dystrophy, Internal medicine, Muscular dystrophy, Endocrinology and Dystrophin. His study of mdx mouse is a part of Duchenne muscular dystrophy. Eric P. Hoffman has researched Internal medicine in several fields, including Genotype and Pathology.
His Muscular dystrophy study integrates concerns from other disciplines, such as Limb-girdle muscular dystrophy, Cardiomyopathy, RNA interference and Pathogenesis. His Endocrinology study often links to related topics such as Case-control study. His Dystrophin study incorporates themes from Morpholino, Exon skipping, Molecular biology, Three prime untranslated region and ITGA7.
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Dystrophin: The protein product of the duchenne muscular dystrophy locus
Eric P. Hoffman;Robert H. Brown;Louis M. Kunkel;Louis M. Kunkel.
Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.
M. Koenig;E.P. Hoffman;C.J. Bertelson;A.P. Monaco.
Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts
T A Partridge;J E Morgan;G R Coulton;E P Hoffman.
Multiple-laboratory comparison of microarray platforms
Rafael A Irizarry;Daniel Warren;Forrest Spencer;Irene F Kim.
Nature Methods (2005)
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy
Hoffman Ep;Fischbeck Kh;Brown Rh;Johnson M.
The New England Journal of Medicine (1988)
Glucose Restriction Inhibits Skeletal Myoblast Differentiation by Activating SIRT1 through AMPK-Mediated Regulation of Nampt
Marcella Fulco;Yana Cen;Po Zhao;Eric P. Hoffman.
Developmental Cell (2008)
Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface
Eduardo Bonilla;Craig E. Samitt;Armand F. Miranda;Armand F. Miranda;Arthur P. Hays;Arthur P. Hays.
Sir2 Regulates Skeletal Muscle Differentiation as a Potential Sensor of the Redox State
Marcella Fulco;R.Louis Schiltz;Simona Iezzi;M.Todd King.
Molecular Cell (2003)
Expression Profiling in the Muscular Dystrophies Identification of Novel Aspects of Molecular Pathophysiology
Yi-Wen Chen;Po Zhao;Rehannah Borup;Eric P. Hoffman.
Journal of Cell Biology (2000)
Molecular cloning, structure, and chromosomal localization of the human inducible nitric oxide synthase gene.
N A Chartrain;D A Geller;P P Koty;N F Sitrin.
Journal of Biological Chemistry (1994)
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