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Auteur Zhang Y

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Alternative therapies in health and medicine Effects of Qishen Dihuang Granules on Intestinal Microbiota in Experimental Autoimmune Myasthenia Gravis Model Rats

Wu T ; Wang B ; Xu P ; Lv Z ; Zhang Y ; Zhang D ; Chang T ; Lu J ; Wu L ; Liu M ; Chen Z ; Lan T ; Wang J | 12/05/2023

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Cell Diverse CMT2 neuropathies are linked to aberrant G3BP interactions in stress granules

Cui Q ; Bi H ; Lv Z ; Wu Q ; Hua J ; Gu B ; Huo C ; Tang M ; Chen Y ; Chen C ; Chen S ; Zhang X ; Wu Z ; Lao Z ; Sheng N ; Shen C ; Zhang Y ; Wu ZY ; Jin Z ; Yang P ; Liu H ; Li J ; Bai G | United States | 31/01/2023

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Rheumatology (Oxford, England) Compound sulfamethoxazole improved the prognosis of dermatomyositis patients positive with anti-melanoma differentiation-associated gene 5

Liu L ; Zhang Y ; Liu S ; Wang C ; Zhang L ; Guan W ; Zhang X ; Li W ; Shu X ; Li T | England | 25/01/2023

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Annals of surgical oncology ASO Visual Abstract: Human Parvovirus B19 May Be a Risk Factor in Myasthenia Gravis with Thymoma

Gong L ; Tian J ; Zhang Y ; Feng Z ; Wang Q ; Wang Y ; Zhang F ; Zhang W ; Huang G | United States | 04/01/2023

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Annals of surgical oncology Human Parvovirus B19 May Be a Risk Factor in Myasthenia Gravis with Thymoma

Gong L ; Tian J ; Zhang Y ; Feng Z ; Wang Q ; Wang Y ; Zhang F ; Zhang W ; Huang G | United States | 12/12/2022

Erratum in Correction: Human Parvovirus B19 May Be a Risk Factor in Myasthenia Gravis with Thymoma. Gong L, Tian J, Zhang Y, Feng Z, Wang Q, Wang Y, Zhang F, Zhang W, Huang G. Ann Surg Oncol. 2022 Dec 22. doi: 10.1245/s10434-022-13017-7. Onlin[...]

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Methods in molecular biology (Clifton, N.J.) CRISPR-Cas9 Correction of Duchenne Muscular Dystrophy in Mice by a Self-Complementary AAV Delivery System

Zhang Y ; Bassel-Duby R ; Olson EN | United States | 17/11/2022

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Article

Clinical rheumatology A bibliometric analysis of idiopathic inflammatory myopathies from 1982 to 2021

Wu T ; Qi J ; Zhang Y ; Huang W ; Li Y ; Ying Z | Germany | 11/11/2022

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Molecular therapy. Nucleic acids, 29. A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing

Zhang Y ; Li H ; Nishiyama T ; McAnally JR ; Sanchez-Ortiz E ; Huang J ; Mammen PPA ; Bassel-Duby R ; Olson EN | 01/08/2022

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JCI insight Dynamin-2 reduction rescues the skeletal myopathy of SPEG-deficient mouse model

Li Q ; Lin J ; Widrick JJ ; Luo S ; Li G ; Zhang Y ; Laporte J ; Perrella MA ; Liu X ; Agrawal PB | United States | 28/06/2022

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JAMA Neurology Identification of Caveolae-Associated Protein 4 Autoantibodies as a Biomarker of Immune-Mediated Rippling Muscle Disease in Adults

Dubey D ; Beecher G ; Hammami MB ; Knight AM ; Liewluck T ; Triplett J ; Datta A ; Dasari S ; Zhang Y ; Roforth MM ; Jerde CR ; Murphy SJ ; Litchy WJ ; Amato A ; Lennon VA ; Mckeon A ; Mills JR ; Pittock SJ ; Milone M | United States | 13/06/2022

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Modern Rheumatology The Therapeutic Efficacy and Safety of Intravenous Immunoglobulin in Dermatomyositis and Polymyositis: A Systematic Review and Meta-Analysis

Xiong A ; Qiang Y ; Cao Y ; Shuai Y ; Chen H ; Xiang Q ; Hu Z ; Song Z ; Zhou S ; Zhang Y ; Cui H ; Wang Y ; Luo J ; Shuai S ; Yang Y | England | 04/06/2022

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Neurology(R) neuroimmunology & neuroinflammation, 9, 4. Clinicopathologic Profiles of Sporadic Late-Onset Nemaline Myopathy: Practical Importance of Anti-α-Actinin Immunostaining

Zhao B ; Dai T ; Zhao D ; Ma X ; Zhao C ; Li L ; Sun Y ; Zhang Y ; Yan Y ; Lu JQ ; Liu F ; Yan C | United States | 17/05/2022

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Journal of innate immunity Development, Characterization, and in vivo Validation of a Humanized C6 Monoclonal Antibody that Inhibits the Membrane Attack Complex

Gytz Olesen H ; Michailidou I ; Zelek WM ; Vreijling J ; Ruizendaal P ; de Klein F ; Marquart JA ; Kuipers TB ; Mei H ; Zhang Y ; Ahasan M ; Johnson KK ; Wang Y ; Morgan BP ; van Dijk M ; Fluiter K ; Andersen GR ; Baas F | Switzerland | 12/05/2022

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Article

Neuroepidemiology Global prevalence of myotonic dystrophy: an updated systematic review and meta-analysis

Liao Q ; Zhang Y ; He J ; Huang K | Switzerland | 28/04/2022

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Article

Nature, 604, 7905. AAV-delivered suppressor tRNA overcomes a nonsense mutation in mice

Wang J ; Zhang Y ; Mendonca CA ; Yukselen O ; Muneeruddin K ; Ren L ; Liang J ; Zhou C ; Xie J ; Li J ; Jiang Z ; Kucukural A ; Shaffer SA ; Gao G ; Wang D | England | 04/2022

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Molecular therapy. Nucleic acids, 28. Long-term maintenance of dystrophin expression and resistance to injury of skeletal muscle in gene edited DMD mice

Karri DR ; Zhang Y ; Chemello F ; Min YL ; Huang J ; Kim J ; Mammen PPA ; Xu L ; Liu N ; Bassel Duby R ; Olson EN | 08/03/2022

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Medicine, 101, 3. Treatment of myasthenia gravis with the method of tonifying spleen and replenishing qi in traditional Chinese medicine: A protocol for systematic review and meta-analysis

Jiang L ; Xu P ; Zhang D ; Lu J ; Chang T ; Zhang Y ; Wang J | 21/01/2022

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Article

Scientific Reports, 12, 1. Next generation sequencing is a highly reliable method to analyze exon 7 deletion of survival motor neuron 1 (SMN1) gene

Zhao S ; Wang Y ; Xin X ; Fang Z ; Fan L ; Peng Z ; Han R ; Shi C ; Zhang Y ; Fan C ; Sun J ; He X | 07/01/2022

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Rheumatology (Oxford, England) Comment on: Cardiovascular events in adult polymyositis and dermatomyositis: a meta-analysis of observational studies: Reply

Hu Z ; Cao Y ; Zhang Y ; Xiang Q ; Chen H ; Song Z ; Qiang Y ; Zhou S ; Cui H ; Luo J ; Wang Y ; Yang Y ; Xie X ; Zhou W ; Shuai S ; Xiong A | England | 28/12/2021

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Frontiers in immunology, 12. Antibodies to Full-Length Agrin Protein in Chinese Patients With Myasthenia Gravis

Wang S ; Yang H ; Guo R ; Wang L ; Zhang Y ; Lv J ; Zhao X ; Zhang J ; Fang H ; Zhang Q ; Zhang Y ; Yang J ; Cui X ; Gao P ; Chang T ; Gao F | 08/12/2021

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Article

Rheumatology (Oxford, England) Cardiovascular events in adult polymyositis and dermatomyositis: a meta-analysis of observational studies

Xiong A ; Hu Z ; Zhou S ; Qiang Y ; Song Z ; Chen H ; Xiang Q ; Zhang Y ; Cao Y ; Cui H ; Luo J ; Wang Y ; Yang Y ; Cui B ; Li M ; Shuai S | England | 16/11/2021

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Article

Circulation, 144,22. Therapeutic Exon Skipping via a CRISPR-guided Cytidine Deaminase Rescues Dystrophic Cardiomyopathy In Vivo

Li J ; Wang K ; Zhang Y ; Qi T ; Yuan J ; Zhang L ; Qiu H ; Wang J ; Yang HT ; Dai Y ; Song Y ; Chang X | United States | 26/10/2021

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Article

Frontiers in neurology, 12. The Genotype and Phenotype Features in a Large Chinese MFN2 Mutation Cohort

Ma Y ; Sun A ; Zhang Y ; Fan D ; Liu X | 13/10/2021

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Article

Frontiers in neurology, 12. Charcot-Marie-Tooth Disease With Episodic Rhabdomyolysis Due to Two Novel Mutations in the β Subunit of Mitochondrial Trifunctional Protein and Effective Response to Modified Diet Therapy

Guan Y ; Zhang Y ; Shen XM ; Zhou L ; Shang X ; Peng Y ; Hu Y ; Li W | 12/10/2021

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Article

Experimental cell research CRISPR/Cas Correction of Muscular Dystrophies

Zhang Y ; Nishiyama T ; Olson EN ; Bassel Duby R | United States | 24/09/2021

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Détail de l'auteur

Auteur Zhang Y

Documents disponibles écrits par cet auteur (95)

Alternative therapies in health and medicine Effects of Qishen Dihuang Granules on Intestinal Microbiota in Experimental Autoimmune Myasthenia Gravis Model Rats

Cell Diverse CMT2 neuropathies are linked to aberrant G3BP interactions in stress granules

Rheumatology (Oxford, England) Compound sulfamethoxazole improved the prognosis of dermatomyositis patients positive with anti-melanoma differentiation-associated gene 5

Annals of surgical oncology ASO Visual Abstract: Human Parvovirus B19 May Be a Risk Factor in Myasthenia Gravis with Thymoma

Annals of surgical oncology Human Parvovirus B19 May Be a Risk Factor in Myasthenia Gravis with Thymoma

Methods in molecular biology (Clifton, N.J.) CRISPR-Cas9 Correction of Duchenne Muscular Dystrophy in Mice by a Self-Complementary AAV Delivery System

Clinical rheumatology A bibliometric analysis of idiopathic inflammatory myopathies from 1982 to 2021

Molecular therapy. Nucleic acids, 29. A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing

JCI insight Dynamin-2 reduction rescues the skeletal myopathy of SPEG-deficient mouse model

JAMA Neurology Identification of Caveolae-Associated Protein 4 Autoantibodies as a Biomarker of Immune-Mediated Rippling Muscle Disease in Adults

Modern Rheumatology The Therapeutic Efficacy and Safety of Intravenous Immunoglobulin in Dermatomyositis and Polymyositis: A Systematic Review and Meta-Analysis

Neurology(R) neuroimmunology & neuroinflammation, 9, 4. Clinicopathologic Profiles of Sporadic Late-Onset Nemaline Myopathy: Practical Importance of Anti-α-Actinin Immunostaining

Journal of innate immunity Development, Characterization, and in vivo Validation of a Humanized C6 Monoclonal Antibody that Inhibits the Membrane Attack Complex

Neuroepidemiology Global prevalence of myotonic dystrophy: an updated systematic review and meta-analysis

Nature, 604, 7905. AAV-delivered suppressor tRNA overcomes a nonsense mutation in mice

Molecular therapy. Nucleic acids, 28. Long-term maintenance of dystrophin expression and resistance to injury of skeletal muscle in gene edited DMD mice

Medicine, 101, 3. Treatment of myasthenia gravis with the method of tonifying spleen and replenishing qi in traditional Chinese medicine: A protocol for systematic review and meta-analysis

Scientific Reports, 12, 1. Next generation sequencing is a highly reliable method to analyze exon 7 deletion of survival motor neuron 1 (SMN1) gene

Rheumatology (Oxford, England) Comment on: Cardiovascular events in adult polymyositis and dermatomyositis: a meta-analysis of observational studies: Reply

Frontiers in immunology, 12. Antibodies to Full-Length Agrin Protein in Chinese Patients With Myasthenia Gravis

Rheumatology (Oxford, England) Cardiovascular events in adult polymyositis and dermatomyositis: a meta-analysis of observational studies

Circulation, 144,22. Therapeutic Exon Skipping via a CRISPR-guided Cytidine Deaminase Rescues Dystrophic Cardiomyopathy In Vivo

Frontiers in neurology, 12. The Genotype and Phenotype Features in a Large Chinese MFN2 Mutation Cohort

Frontiers in neurology, 12. Charcot-Marie-Tooth Disease With Episodic Rhabdomyolysis Due to Two Novel Mutations in the β Subunit of Mitochondrial Trifunctional Protein and Effective Response to Modified Diet Therapy

Experimental cell research CRISPR/Cas Correction of Muscular Dystrophies