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Auteur Zhang Y |
Documents disponibles écrits par cet auteur



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The diagnostic value of GDF-15 for myocardial involvement in idiopathic inflammatory myopathy
Qiu M, Sun X, Qi X, et al.
Rheumatology (Oxford, England), 2020
Revue : Rheumatology (Oxford, England) Titre : The diagnostic value of GDF-15 for myocardial involvement in idiopathic inflammatory myopathy Type de document : Article Auteurs : Qiu M ; Sun X ; Qi X ; Liu X ; Zhang Y ; Zhang N ; Lu F ; Liu W ; Changjing F ; Wang Q ; Zhou L Editeur : England Année de publication : 25/11/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 33241419 / DOI : 10.1093/rheumatology/keaa721
N° Profil MNM : 2020121 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/33241419 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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A symptomatic female patient with duchenne muscular dystrophy gene mutation showing rimmed vacuoles in muscle biopsy
Ban R, Lu X, Pu C, et al.
Neurology India, 2020, 68, 2, p 518
Revue : Neurology India, 68, 2 Titre : A symptomatic female patient with duchenne muscular dystrophy gene mutation showing rimmed vacuoles in muscle biopsy Type de document : Article Auteurs : Ban R ; Lu X ; Pu C ; Shi Q ; Wang H ; Liu H ; Zhang Y ; Fang F Editeur : India Année de publication : 05/2020 Pages : p 518 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32415039 / DOI : 10.4103/0028-3886.284351
N° Profil MNM : 2020052 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32415039 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Analysis of myositis autoantibodies in Chinese patients with cancer-associated myositis
Li L, Liu C, Wang Q, et al.
Journal of clinical laboratory analysis, 2020
Revue : Journal of clinical laboratory analysis Titre : Analysis of myositis autoantibodies in Chinese patients with cancer-associated myositis Type de document : Article Auteurs : Li L, Auteur ; Liu C ; Wang Q ; Wu C ; Zhang Y ; Cheng L ; Wen X ; Zeng X ; Zhang F ; Li Y Editeur : United States Année de publication : 03/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32222002 / DOI : 10.1002/jcla.23307
N° Profil MNM : 2020032 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32222002 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy
Lek A, Zhang Y, Woodman KG, et al.
Science translational medicine, 2020, 12, 536
Revue : Science translational medicine, 12, 536 Titre : Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy Type de document : Article Auteurs : Lek A, Auteur ; Zhang Y ; Woodman KG ; Huang S ; DeSimone AM ; Cohen J ; Ho V ; Conner J ; Mead L ; Kodani A ; Pakula A ; Sanjana N ; King OD ; Jones PL ; Wagner KR ; Lek M ; Kunkel LM Editeur : United States Année de publication : 03/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32213627 / DOI : 10.1126/scitranslmed.aay0271
N° Profil MNM : 2020032 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32213627 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Mutations of MACF1, Encoding Microtubule-Actin Crosslinking-Factor 1, Cause Spectraplakinopathy
Kang L, Liu Y, Jin Y, et al.
Frontiers in neurology, 2020, 10
Revue : Frontiers in neurology, 10 Titre : Mutations of MACF1, Encoding Microtubule-Actin Crosslinking-Factor 1, Cause Spectraplakinopathy Type de document : Article Auteurs : Kang L ; Liu Y ; Jin Y ; Li M ; Song J ; Zhang Y ; Zhang Y ; Yang Y Editeur : Switzerland Année de publication : 01/2020 Langues : Anglais (eng) Mots-clés : Chine ; enfant ; étude de cas ; maladie neuromusculaire ; masculin ; myopathie congénitale ; spectraplakine (maladie neuromusculaire liée à) Pubmed / DOI : Pubmed : 32010038 / DOI : 10.3389/fneur.2019.01335
N° Profil MNM : 2020021 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32010038 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Clinical and Genetic Diversity of PMP22 Mutations in a Large Cohort of Chinese Patients With Charcot-Marie-Tooth Disease
Liu X, Duan X, Zhang Y, et al.
Frontiers in neurology, 2020, 11, p 630
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Cross-Sectional Study in a Large Cohort of Chinese Patients With GJB1 Gene Mutations
Liu X, Duan X, Zhang Y, et al.
Frontiers in neurology, 2020, 11, p 690
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The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study
Zhang Y, He J, Zhang Y, et al.
Medicine, 2020, 99, 3
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A novel application of tau PET in the diagnosis of sporadic inclusion body myositis: A case report
Zhang Y, Li K, Pu C, et al.
Medicine, 2020, 99, 31
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Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing
Min YL, Chemello F, Li H, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2020, 28, 9, p 2044
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Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations
Chen W, Zhang Y, Ni Y, et al.
BMC neurology, 2019, 19, 1, p 330
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Metformin attenuates autoimmune disease of the neuromotor system in animal models of myasthenia gravis
Cui Y, Chang L, Wang C, et al.
International immunopharmacology, 2019, 75
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In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse
Amoasii L, Li H, Zhang Y, et al.
Nature communications, 2019, 10, 1
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Clinical analysis of Chinese anti-low-density-lipoprotein-receptor-associated protein 4 antibodies in patients with myasthenia gravis
Li M, Han J, Zhang Y, et al.
European journal of neurology, 2019
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Diffuse pruritic erythema as a clinical manifestation in anti-SAE antibody-associated dermatomyositis: a case report and literature review
Jia E, Wei J, Geng H, et al.
Clinical rheumatology, 2019
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Overexpression of miR-29 Leads to Myopathy that Resemble Pathology of Ullrich Congenital Muscular Dystrophy
Liu C, Li L, Ge M, et al.
Cells, 2019, 8, 5, p 459
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Management strategies in facioscapulohumeral muscular dystrophy
Lu J, Yao Z, Yang Y, et al.
Intractable & rare diseases research, 2019, 8, 1, p 9
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Protein kinase A activation inhibits DUX4 gene expression in myotubes from patients with facioscapulohumeral muscular dystrophy
Cruz JM Jr, Hupper N, Wilson LS, et al.
The Journal of biological chemistry, 2018
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Chemical, biochemical, preclinical and clinical studies of Ganoderma lucidum polysaccharide as an approved drug for treating myopathy and other diseases in China
Zeng P, Guo Z, Zeng X, et al.
Journal of cellular and molecular medicine, 2018
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Clinical characteristics of AChRAb and MuSKAb double seropositive myasthenia gravis patients
Li M, Li M, Ren L, et al.
Clinical neurology and neurosurgery, 2018, 172, p 69
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Dual AAV gene therapy for Duchenne muscular dystrophy with a 7-kb mini-dystrophin gene in the canine model
Kodippili K, Hakim C, Pan X, et al.
Human gene therapy, 2018, 29, 3, p 299
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Myoediting: Toward Prevention of Muscular Dystrophy by Therapeutic Genome Editing
Zhang Y, Long C, Bassel-Duby R, et al.
Physiological reviews, 2018, 98, 3, p 1205
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A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like
Chen Z, Ren Z, Mei W, et al.
BMC Medical Genetics, 2017, 18, 1
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Anti-LRP4 Autoantibodies in Chinese Patients with Myasthenia Gravis
Li Y, Zhang Y, Cai G, et al.
Muscle & Nerve, 2017, 56, 5, p 938
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