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1دورية أكاديميةDeletion of Dux ameliorates muscular dystrophy in mdx mice by attenuating oxidative stress via Nrf2.
المؤلفون: Sun S; Department of Children Health Care, Northwest Women's and Children's Hospital, Xi'an, Shaanxi, China., Zhai W; Department of Clinical Genetics, Northwest Women's and Children's Hospital, Xi'an, Shaanxi, China., Zhang R; Department of Clinical Genetics, Northwest Women's and Children's Hospital, Xi'an, Shaanxi, China., Cai N; Department of Clinical Genetics, Northwest Women's and Children's Hospital, Xi'an, Shaanxi, China.
المصدر: FASEB journal : official publication of the Federation of American Societies for Experimental Biology [FASEB J] 2024 Jul 31; Vol. 38 (14), pp. e23771.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Federation of American Societies for Experimental Biology Country of Publication: United States NLM ID: 8804484 Publication Model: Print Cited Medium: Internet ISSN: 1530-6860 (Electronic) Linking ISSN: 08926638 NLM ISO Abbreviation: FASEB J Subsets: MEDLINE
مواضيع طبية MeSH: NF-E2-Related Factor 2*/metabolism , NF-E2-Related Factor 2*/genetics , Oxidative Stress* , Mice, Inbred mdx* , Homeodomain Proteins*/genetics , Homeodomain Proteins*/metabolism , Muscular Dystrophy, Duchenne*/metabolism , Muscular Dystrophy, Duchenne*/genetics , Muscular Dystrophy, Duchenne*/pathology, Animals ; Mice ; Male ; Muscle, Skeletal/metabolism ; Muscle, Skeletal/pathology ; Satellite Cells, Skeletal Muscle/metabolism ; Mice, Inbred C57BL ; Mice, Knockout ; Gene Deletion
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2دورية أكاديمية
المؤلفون: Coles CA; Murdoch Childrens Research Institute, The Royal Children's Hospital, 50 Flemington Road, Parkville, Victoria 3052, Australia.; Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Flemington Road, Parkville, Victoria 3052, Australia., Woodman KG; Murdoch Childrens Research Institute, The Royal Children's Hospital, 50 Flemington Road, Parkville, Victoria 3052, Australia.; Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Flemington Road, Parkville, Victoria 3052, Australia.; Department of Genetics, Yale Medical School, Yale University, 333 Cedar Street, New Haven, Connecticut 06520, USA., Gibbs EM; Department of Integrative Biology and Physiology, University of California, 612 Charles E Young Dr S, Los Angeles 90095, California, USA.; Center for Duchenne Muscular Dystrophy, University of California, 615 Charles E Young Dr S, Los Angeles 90095, California, USA., Crosbie RH; Department of Integrative Biology and Physiology, University of California, 612 Charles E Young Dr S, Los Angeles 90095, California, USA.; Center for Duchenne Muscular Dystrophy, University of California, 615 Charles E Young Dr S, Los Angeles 90095, California, USA.; Department of Neurology, David Geffen School of Medicine, University of California, 610 Charles E Young Dr S, Los Angeles, California 90095, USA., White JD; Murdoch Childrens Research Institute, The Royal Children's Hospital, 50 Flemington Road, Parkville, Victoria 3052, Australia.; Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Flemington Road, Parkville, Victoria 3052, Australia.; Charles Sturt University, Office of the Deputy Vice Chancellor Research, Boorooma Street, Wagga Wagga, NSW 2678, Australia., Lamandé SR; Murdoch Childrens Research Institute, The Royal Children's Hospital, 50 Flemington Road, Parkville, Victoria 3052, Australia.; Department of Paediatrics, University of Melbourne, 50 Flemington Road, Parkville, Victoria 3052, Australia.
المصدر: Human molecular genetics [Hum Mol Genet] 2024 Jul 22; Vol. 33 (15), pp. 1339-1355.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
مواضيع طبية MeSH: Mice, Inbred mdx* , Fibrosis*/drug therapy , Muscular Dystrophy, Duchenne*/drug therapy , Muscular Dystrophy, Duchenne*/genetics , Muscular Dystrophy, Duchenne*/pathology , Muscular Dystrophy, Duchenne*/physiopathology , Muscular Dystrophy, Duchenne*/metabolism , Inflammation*/drug therapy , Inflammation*/genetics , Inflammation*/pathology , Muscle, Skeletal*/drug effects , Muscle, Skeletal*/metabolism , Thiamine*/analogs & derivatives , Thiamine*/pharmacology, Animals ; Mice ; Male ; Physical Conditioning, Animal ; Disease Models, Animal
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3دورية أكاديمية
المؤلفون: Zhou Y; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.; Department of Thoracic Surgery, Xiangya Hospital, Central South University, 410008, Changsha, Hunan, China., Zhang C; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, 46202, USA., Xiao W; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, 46202, USA., Herzog RW; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, 46202, USA., Han R; Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, 46202, USA. rh11@iu.edu.
المصدر: Nature communications [Nat Commun] 2024 Jul 21; Vol. 15 (1), pp. 6141. Date of Electronic Publication: 2024 Jul 21.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
مواضيع طبية MeSH: Dystrophin*/genetics , Dystrophin*/metabolism , Muscular Dystrophy, Duchenne*/genetics , Muscular Dystrophy, Duchenne*/metabolism , Muscular Dystrophy, Duchenne*/therapy , Muscular Dystrophy, Duchenne*/pathology , Genetic Therapy*/methods , Mice, Inbred mdx* , Dependovirus*/genetics , Muscle, Skeletal*/metabolism , Muscle, Skeletal*/pathology , Genetic Vectors*/genetics , Genetic Vectors*/administration & dosage, Animals ; Mice ; Male ; Disease Models, Animal ; Myocardium/metabolism ; Myocardium/pathology ; Sarcolemma/metabolism ; Humans ; Gene Transfer Techniques
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4دورية أكاديمية
المؤلفون: Chen J; Institutes for Systems Genetics, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China.; Department of Ecology and Evolution, The University of Chicago, Chicago, Illinois, USA., Jia Y; Institutes for Systems Genetics, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China.; Department of Chemistry, The University of Chicago, Chicago, Illinois, USA., Zhong J; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China., Zhang K; Department of Radiology, Key Laboratory of Birth Defects and Related Diseases of Women and Children of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China., Dai H; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, Texas, USA., He G; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China., Li F; Laboratory of Molecular Translational Medicine, Center for Translational Medicine, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Clinical Research Center for Birth Defects of Sichuan Province, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China., Zeng L; Department of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Fan C; Department of Biological Sciences, Wayne State University, Detroit, Michigan, USA., Xu H; Department of Radiology, Key Laboratory of Birth Defects and Related Diseases of Women and Children of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China xuhuayan89@sina.com.
المصدر: Journal of medical genetics [J Med Genet] 2024 Jul 19; Vol. 61 (8), pp. 741-749. Date of Electronic Publication: 2024 Jul 19.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
مواضيع طبية MeSH: Cryptorchidism*/genetics , Muscular Dystrophy, Duchenne*/genetics , Muscular Dystrophy, Duchenne*/pathology , Mutation*, Humans ; Male ; Animals ; Mice ; Genetic Predisposition to Disease ; Whole Genome Sequencing ; RNA Splice Sites/genetics ; Phenotype ; CRISPR-Cas Systems/genetics
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5دورية أكاديميةExploring lipin1 as a promising therapeutic target for the treatment of Duchenne muscular dystrophy.
المؤلفون: Jama A; Department of Biochemistry and Molecular Biology, Wright State University, 3640 Colonel Glenn Hwy., Dayton, OH, 45435-0001, USA., Alshudukhi AA; Department of Biochemistry and Molecular Biology, Wright State University, 3640 Colonel Glenn Hwy., Dayton, OH, 45435-0001, USA.; Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, Saudi Arabia., Burke S; Department of Biological Sciences, Wright State University, Dayton, OH, USA., Dong L; Mumetel LLC, University Technology Park at IIT, Chicago, IL, USA., Kamau JK; Department of Biochemistry and Molecular Biology, Wright State University, 3640 Colonel Glenn Hwy., Dayton, OH, 45435-0001, USA., Morris B; Department of Biochemistry and Molecular Biology, Wright State University, 3640 Colonel Glenn Hwy., Dayton, OH, 45435-0001, USA., Alkhomsi IA; Department of Biochemistry and Molecular Biology, Wright State University, 3640 Colonel Glenn Hwy., Dayton, OH, 45435-0001, USA., Finck BN; Division of Geriatrics & Nutritional Science, Washington University School of Medicine, St. Louis, USA., Voss AA; Department of Biological Sciences, Wright State University, Dayton, OH, USA., Ren H; Department of Biochemistry and Molecular Biology, Wright State University, 3640 Colonel Glenn Hwy., Dayton, OH, 45435-0001, USA. hongmei.ren@wright.edu.
المصدر: Journal of translational medicine [J Transl Med] 2024 Jul 16; Vol. 22 (1), pp. 664. Date of Electronic Publication: 2024 Jul 16.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876 (Electronic) Linking ISSN: 14795876 NLM ISO Abbreviation: J Transl Med Subsets: MEDLINE
مواضيع طبية MeSH: Mice, Inbred mdx* , Muscular Dystrophy, Duchenne*/pathology , Muscular Dystrophy, Duchenne*/metabolism , Phosphatidate Phosphatase*/metabolism , Muscle, Skeletal*/metabolism , Muscle, Skeletal*/pathology, Animals ; Mice, Transgenic ; Mice ; Muscle Contraction ; Molecular Targeted Therapy ; Mice, Inbred C57BL ; Genetic Therapy ; Male
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6دورية أكاديمية
المؤلفون: Lin J; Department of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China., Jin M; Department of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China., Yang D; HuidaGene Therapeutics Inc., Shanghai, China., Li Z; Lingang Laboratory, Shanghai, China., Zhang Y; HuidaGene Therapeutics Inc., Shanghai, China., Xiao Q; HuidaGene Therapeutics Inc., Shanghai, China., Wang Y; HuidaGene Therapeutics Inc., Shanghai, China., Yu Y; HuidaGene Therapeutics Inc., Shanghai, China., Zhang X; HuidaGene Therapeutics Inc., Shanghai, China., Shao Z; HuidaGene Therapeutics Inc., Shanghai, China., Shi L; HuidaGene Therapeutics Inc., Shanghai, China., Zhang S; Department of Neurology, First Medical Center of Chinese PLA General Hospital, Beijing, China., Chen WJ; Department of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China., Wang N; Department of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China. ningwang@fjmu.edu.cn., Wu S; Department of Neurology, First Medical Center of Chinese PLA General Hospital, Beijing, China. wu_shiwen@outlook.com., Yang H; HuidaGene Therapeutics Inc., Shanghai, China. huiyang@huidagene.com.; Shanghai Center for Brain Science and Brain-Inspired Technology, Shanghai, China. huiyang@huidagene.com., Xu C; Lingang Laboratory, Shanghai, China. xucl@lglab.ac.cn.; Shanghai Center for Brain Science and Brain-Inspired Technology, Shanghai, China. xucl@lglab.ac.cn., Li G; Department of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China. guolingli@huidagene.com.; HuidaGene Therapeutics Inc., Shanghai, China. guolingli@huidagene.com.
المصدر: Nature communications [Nat Commun] 2024 Jul 15; Vol. 15 (1), pp. 5927. Date of Electronic Publication: 2024 Jul 15.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
مواضيع طبية MeSH: Muscular Dystrophy, Duchenne*/genetics , Muscular Dystrophy, Duchenne*/therapy , Dystrophin*/genetics , Dystrophin*/metabolism , Exons*/genetics , Gene Editing*/methods , Disease Models, Animal* , Adenine*/metabolism , CRISPR-Cas Systems*, Animals ; Humans ; Male ; Mice ; Muscle, Skeletal/metabolism ; Dependovirus/genetics ; Genetic Therapy/methods
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7دورية أكاديمية
المؤلفون: Weintraub M; From the Department of Orthopaedic Surgery, Rutgers New Jersey Medical School, Newark, NJ., Gupta A, Khokhar A, Vives M, Kaushal N
المصدر: Journal of the American Academy of Orthopaedic Surgeons. Global research & reviews [J Am Acad Orthop Surg Glob Res Rev] 2024 Jul 10; Vol. 8 (7). Date of Electronic Publication: 2024 Jul 10 (Print Publication: 2024).
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: Wolters Kluwer Health, Inc Country of Publication: United States NLM ID: 101724868 Publication Model: eCollection Cited Medium: Internet ISSN: 2474-7661 (Electronic) Linking ISSN: 24747661 NLM ISO Abbreviation: J Am Acad Orthop Surg Glob Res Rev Subsets: MEDLINE
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8دورية أكاديمية
المؤلفون: Wernio E; Department of Clinical Nutrition and Dietetics, Medical University of Gdansk, 80-210 Gdansk, Poland., Wasilewska E; Department of Pulmonology & Allergology, Medical University of Gdansk, 80-210 Gdansk, Poland., Czaja-Stolc S; Department of Clinical Nutrition and Dietetics, Medical University of Gdansk, 80-210 Gdansk, Poland., Śledzińska K; Department of Paediatrics, Haemathology and Oncology, Medical University of Gdansk, 80-210 Gdansk, Poland., Wierzba J; Department of Internal and Paediatric Nursing, Medical University of Gdansk, 80-210 Gdansk, Poland., Szlagatys-Sidorkiewicz A; Department of Paediatrics, Gastroenterology, Allergology & Paediatric Nutrition, Medical University of Gdansk, 80-210 Gdansk, Poland., Małgorzewicz S; Department of Clinical Nutrition and Dietetics, Medical University of Gdansk, 80-210 Gdansk, Poland.
المصدر: Nutrients [Nutrients] 2024 Jul 04; Vol. 16 (13). Date of Electronic Publication: 2024 Jul 04.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: MDPI Publishing Country of Publication: Switzerland NLM ID: 101521595 Publication Model: Electronic Cited Medium: Internet ISSN: 2072-6643 (Electronic) Linking ISSN: 20726643 NLM ISO Abbreviation: Nutrients Subsets: MEDLINE
مواضيع طبية MeSH: Muscular Dystrophy, Duchenne*/complications , Muscular Dystrophy, Duchenne*/epidemiology , Nutritional Status* , Body Mass Index*, Humans ; Male ; Child ; Adolescent ; Child, Preschool ; Body Composition ; Nutrition Assessment ; Incidence ; Thinness/epidemiology ; Overweight/epidemiology ; Overweight/complications ; Basal Metabolism ; Absorptiometry, Photon ; Calorimetry, Indirect ; Malnutrition/epidemiology
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9دورية أكاديمية
المؤلفون: Shafrin J; Center for Healthcare Economics and Policy, FTI Consulting, 350 S Grande Ave, Los Angeles, CA 90071. Email: jason.shafrin@fticonsulting.com., Thahir S, Klimchak AC, Audhya I, Sedita LE, Romley JA
المصدر: The American journal of managed care [Am J Manag Care] 2024 Jul 01; Vol. 30 (7), pp. e217-e222. Date of Electronic Publication: 2024 Jul 01.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Clinical Care Targeted Communications Group, LLC Country of Publication: United States NLM ID: 9613960 Publication Model: Electronic Cited Medium: Internet ISSN: 1936-2692 (Electronic) Linking ISSN: 10880224 NLM ISO Abbreviation: Am J Manag Care Subsets: MEDLINE
مواضيع طبية MeSH: Muscular Dystrophy, Duchenne*/economics , Muscular Dystrophy, Duchenne*/therapy , Rare Diseases*/economics , Rare Diseases*/therapy, Humans ; Adult ; Prospective Studies ; United States ; Male ; Female ; Insurance, Health/economics ; Insurance, Health/statistics & numerical data ; Insurance Coverage/statistics & numerical data ; Insurance Coverage/economics ; Young Adult ; Quality-Adjusted Life Years ; Child ; Value-Based Health Insurance/economics
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10دورية أكاديمية
المؤلفون: De Wel B; Department of Neurology, University Hospitals Leuven, Leuven, Belgium.; Department of Neurosciences, Laboratory for Muscle Diseases and Neuropathies, KU Leuven, and Leuven Brain Institute (LBI), Leuven, Belgium., Iterbeke L; Department of Neurosciences, Laboratory for Muscle Diseases and Neuropathies, KU Leuven, and Leuven Brain Institute (LBI), Leuven, Belgium., Huysmans L; Medical Imaging Research Centre, University Hospitals Leuven, Leuven, Belgium.; Department ESAT - PSI, KU Leuven, Leuven, Belgium., Peeters R; Department of Radiology, University Hospitals Leuven, Leuven, Belgium., Goosens V; Department of Radiology, University Hospitals Leuven, Leuven, Belgium., Dubuisson N; Department of Neurology, Neuromuscular Reference Center, Cliniques Universitaires Saint-Luc, Brussels, Belgium., van den Bergh P; Department of Neurology, Neuromuscular Reference Center, Cliniques Universitaires Saint-Luc, Brussels, Belgium., Van Parijs V; Department of Neurology, Neuromuscular Reference Center, Cliniques Universitaires Saint-Luc, Brussels, Belgium., Remiche G; Department of Neurology, Centre de Référence Neuromusculaire, HUB-Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium., De Waele L; Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium.; Department of Development and Regeneration, KU Leuven, Leuven, Belgium., Maes F; Medical Imaging Research Centre, University Hospitals Leuven, Leuven, Belgium.; Department ESAT - PSI, KU Leuven, Leuven, Belgium., Dupont P; Department of Neurosciences, Laboratory for Cognitive Neurology, KU Leuven, and Leuven Brain Institute (LBI), Leuven, Belgium., Claeys KG; Department of Neurology, University Hospitals Leuven, Leuven, Belgium.; Department of Neurosciences, Laboratory for Muscle Diseases and Neuropathies, KU Leuven, and Leuven Brain Institute (LBI), Leuven, Belgium.
المصدر: European journal of neurology [Eur J Neurol] 2024 Jul; Vol. 31 (7), pp. e16282. Date of Electronic Publication: 2024 Mar 20.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Wiley Country of Publication: England NLM ID: 9506311 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-1331 (Electronic) Linking ISSN: 13515101 NLM ISO Abbreviation: Eur J Neurol Subsets: MEDLINE
مواضيع طبية MeSH: Patient Reported Outcome Measures* , Muscular Dystrophy, Duchenne*/diagnostic imaging , Muscular Dystrophy, Duchenne*/physiopathology , Magnetic Resonance Imaging* , Muscle, Skeletal*/diagnostic imaging , Muscle, Skeletal*/physiopathology , Disease Progression*, Humans ; Adult ; Male ; Female ; Middle Aged ; Clinical Trials as Topic ; Muscle Strength/physiology ; Young Adult