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Times Cited: 178
Times Cited: 178
Times Cited
Times Co-cited
Similarity
Dystrophin: the protein product of the Duchenne muscular dystrophy locus.
E P Hoffman, R H Brown, L M Kunkel. Cell 1987
E P Hoffman, R H Brown, L M Kunkel. Cell 1987
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The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
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Evidence-based path to newborn screening for Duchenne muscular dystrophy.
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Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy.
David G Allen, Nicholas P Whitehead, Stanley C Froehner. Physiol Rev 2016
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Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management.
David J Birnkrant, Katharine Bushby, Carla M Bann, Susan D Apkon, Angela Blackwell, David Brumbaugh, Laura E Case, Paula R Clemens, Stasia Hadjiyannakis, Shree Pandya,[...]. Lancet Neurol 2018
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Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular Dystrophy.
Dongsheng Duan. Mol Ther 2018
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Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy.
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In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy.
Christopher E Nelson, Chady H Hakim, David G Ousterout, Pratiksha I Thakore, Eirik A Moreb, Ruth M Castellanos Rivera, Sarina Madhavan, Xiufang Pan, F Ann Ran, Winston X Yan,[...]. Science 2016
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Therapeutic developments for Duchenne muscular dystrophy.
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Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy.
Chengzu Long, Leonela Amoasii, Alex A Mireault, John R McAnally, Hui Li, Efrain Sanchez-Ortiz, Samadrita Bhattacharyya, John M Shelton, Rhonda Bassel-Duby, Eric N Olson. Science 2016
Chengzu Long, Leonela Amoasii, Alex A Mireault, John R McAnally, Hui Li, Efrain Sanchez-Ortiz, Samadrita Bhattacharyya, John M Shelton, Rhonda Bassel-Duby, Eric N Olson. Science 2016
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Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy.
Niclas E Bengtsson, John K Hall, Guy L Odom, Michael P Phelps, Colin R Andrus, R David Hawkins, Stephen D Hauschka, Joel R Chamberlain, Jeffrey S Chamberlain. Nat Commun 2017
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Pharmacological advances for treatment in Duchenne muscular dystrophy.
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Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle.
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Long-term evaluation of AAV-CRISPR genome editing for Duchenne muscular dystrophy.
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Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy.
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Dystrophin and mutations: one gene, several proteins, multiple phenotypes.
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X chromosome-linked muscular dystrophy (mdx) in the mouse.
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In vivo gene editing in dystrophic mouse muscle and muscle stem cells.
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CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells.
Yi-Li Min, Hui Li, Cristina Rodriguez-Caycedo, Alex A Mireault, Jian Huang, John M Shelton, John R McAnally, Leonela Amoasii, Pradeep P A Mammen, Rhonda Bassel-Duby,[...]. Sci Adv 2019
Yi-Li Min, Hui Li, Cristina Rodriguez-Caycedo, Alex A Mireault, Jian Huang, John M Shelton, John R McAnally, Leonela Amoasii, Pradeep P A Mammen, Rhonda Bassel-Duby,[...]. Sci Adv 2019
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Function and genetics of dystrophin and dystrophin-related proteins in muscle.
Derek J Blake, Andrew Weir, Sarah E Newey, Kay E Davies. Physiol Rev 2002
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The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscle.
Sandra Murphy, Kay Ohlendieck. Comput Struct Biotechnol J 2015
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Proteomic analysis of the sarcolemma-enriched fraction from dystrophic mdx-4cv skeletal muscle.
Sandra Murphy, Margit Zweyer, Michael Henry, Paula Meleady, Rustam R Mundegar, Dieter Swandulla, Kay Ohlendieck. J Proteomics 2019
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Discovery of serum protein biomarkers in the mdx mouse model and cross-species comparison to Duchenne muscular dystrophy patients.
Yetrib Hathout, Ramya L Marathi, Sree Rayavarapu, Aiping Zhang, Kristy J Brown, Haeri Seol, Heather Gordish-Dressman, Sebahattin Cirak, Luca Bello, Kanneboyina Nagaraju,[...]. Hum Mol Genet 2014
Yetrib Hathout, Ramya L Marathi, Sree Rayavarapu, Aiping Zhang, Kristy J Brown, Haeri Seol, Heather Gordish-Dressman, Sebahattin Cirak, Luca Bello, Kanneboyina Nagaraju,[...]. Hum Mol Genet 2014
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Large-scale serum protein biomarker discovery in Duchenne muscular dystrophy.
Yetrib Hathout, Edward Brody, Paula R Clemens, Linda Cripe, Robert Kirk DeLisle, Pat Furlong, Heather Gordish-Dressman, Lauren Hache, Erik Henricson, Eric P Hoffman,[...]. Proc Natl Acad Sci U S A 2015
Yetrib Hathout, Edward Brody, Paula R Clemens, Linda Cripe, Robert Kirk DeLisle, Pat Furlong, Heather Gordish-Dressman, Lauren Hache, Erik Henricson, Eric P Hoffman,[...]. Proc Natl Acad Sci U S A 2015
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Clinical utility of serum biomarkers in Duchenne muscular dystrophy.
Yetrib Hathout, Haeri Seol, Meng Hsuan J Han, Aiping Zhang, Kristy J Brown, Eric P Hoffman. Clin Proteomics 2016
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CRISPR Correction of Duchenne Muscular Dystrophy.
Yi-Li Min, Rhonda Bassel-Duby, Eric N Olson. Annu Rev Med 2019
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Proteomic profiling of the mouse diaphragm and refined mass spectrometric analysis of the dystrophic phenotype.
Sandra Murphy, Margit Zweyer, Maren Raucamp, Michael Henry, Paula Meleady, Dieter Swandulla, Kay Ohlendieck. J Muscle Res Cell Motil 2019
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Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy.
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Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations.
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Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management.
David J Birnkrant, Katharine Bushby, Carla M Bann, Benjamin A Alman, Susan D Apkon, Angela Blackwell, Laura E Case, Linda Cripe, Stasia Hadjiyannakis, Aaron K Olson,[...]. Lancet Neurol 2018
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Identification of disease specific pathways using in vivo SILAC proteomics in dystrophin deficient mdx mouse.
Sree Rayavarapu, William Coley, Erdinc Cakir, Vanessa Jahnke, Shin'ichi Takeda, Yoshitsugu Aoki, Heather Grodish-Dressman, Jyoti K Jaiswal, Eric P Hoffman, Kristy J Brown,[...]. Mol Cell Proteomics 2013
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Dystrophin protects the sarcolemma from stresses developed during muscle contraction.
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Proteomic profiling of mdx-4cv serum reveals highly elevated levels of the inflammation-induced plasma marker haptoglobin in muscular dystrophy.
Sandra Murphy, Paul Dowling, Margit Zweyer, Michael Henry, Paula Meleady, Rustam R Mundegar, Dieter Swandulla, Kay Ohlendieck. Int J Mol Med 2017
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Tracking disease progression non-invasively in Duchenne and Becker muscular dystrophies.
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Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.
Katharine Bushby, Richard Finkel, David J Birnkrant, Laura E Case, Paula R Clemens, Linda Cripe, Ajay Kaul, Kathi Kinnett, Craig McDonald, Shree Pandya,[...]. Lancet Neurol 2010
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The molecular basis of muscular dystrophy in the mdx mouse: a point mutation.
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The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein.
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A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy.
Jean K Mah, Lawrence Korngut, Jonathan Dykeman, Lundy Day, Tamara Pringsheim, Nathalie Jette. Neuromuscul Disord 2014
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Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy.
Jerry R Mendell, Nathalie Goemans, Linda P Lowes, Lindsay N Alfano, Katherine Berry, James Shao, Edward M Kaye, Eugenio Mercuri. Ann Neurol 2016
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Expression of full-length utrophin prevents muscular dystrophy in mdx mice.
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Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.