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Auteur Zhang Y

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Article

Circulation 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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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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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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Journal of neuroimmunology, 358. Sexual dysfunction in patients with myasthenia gravis

Wang J ; Yan C ; Zhao Z ; Chen H ; Shi Z ; Du Q ; Zhang Y ; Qiu Y ; Lang Y ; Kong L ; Cai L ; Zhou H | Netherlands | 15/09/2021

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Article

Orphanet journal of rare diseases, 16, 1. Anxiety and depression in school-age patients with spinal muscular atrophy: a cross-sectional study

Yao M ; Xia Y ; Feng Y ; Ma Y ; Hong Y ; Zhang Y ; Chen J ; Yuan C ; Mao S | 09/09/2021

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Article

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 50, 4. Screening of multiple acyl-CoA dehydrogenase deficiency in newborns and follow-up of patients

Zhou D ; Ye M ; Hu Z ; Zhang Y ; Zhu L ; Yang R ; Huang X | China | 25/08/2021

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Molecular therapy. Methods & clinical development, 22. A consolidated AAV system for single-cut CRISPR correction of a common Duchenne muscular dystrophy mutation

Zhang Y ; Nishiyama T ; Li H ; Huang J ; Atmanli A ; Sanchez-Ortiz E ; Wang Z ; Mireault AA ; Mammen PPA ; Bassel-Duby R ; Olson EN | 04/06/2021

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Brain and Behavior No correlation between acetylcholine receptor antibody concentration and individual clinical symptoms of myasthenia gravis: A systematic retrospective study involving 67 patients.

Wang L ; Wang S ; Yang H ; Han J ; Zhao X ; Han S ; Zhang Y ; Lv J ; Zhang J ; Li M ; Ji Y ; Zhou S ; He X ; Fang H ; Yang J ; Zhang Y ; Zhang Q ; Gao P ; Gao F | United States | 02/06/2021

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Biochemical and biophysical research communications, 545. Targeted addition of mini-dystrophin into rDNA locus of Duchenne muscular dystrophy patient-derived iPSCs

Zeng B ; Zhou M ; Liu B ; Shen F ; Xiao R ; Su J ; Hu Z ; Zhang Y ; Gu A ; Wu L ; Liu X ; Liang D | United States | 19/03/2021

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Clinical immunology (Orlando, Fla.), 224. Peripheral blood hsa-circRNA5333-4: A novel biomarker for myasthenia gravis

Lv J ; Ren L ; Han S ; Zhang J ; Zhao X ; Zhang Y ; Fang H ; Zhang L ; Yang H ; Wang S ; Yang J ; Cui X ; Zhang Q ; Zhang Y ; Gao F | United States | 03/2021

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Article

Nature communications, 12, 1. The nuclear envelope protein Net39 is essential for muscle nuclear integrity and chromatin organization

Ramirez-Martinez A ; Zhang Y ; Chen K ; Kim J ; Cenik BK ; McAnally JR ; Cai C ; Shelton JM ; Huang J ; Brennan A ; Evers BM ; Mammen PPA ; Xu L ; Bassel-Duby R ; Liu N ; Olson EN | 29/01/2021

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Article

Human molecular genetics SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins

Luo S ; Li Q ; Lin J ; Murphy Q ; Marty I ; Zhang Y ; Kazerounian S ; Agrawal PB | England | 23/12/2020

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Article

Rheumatology (Oxford, England) The diagnostic value of GDF-15 for myocardial involvement in idiopathic inflammatory myopathy

Qiu M ; Sun X ; Qi X ; Liu X ; Zhang Y ; Zhang N ; Lu F ; Liu W ; Changjing F ; Wang Q ; Zhou L | England | 25/11/2020

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Technology and health care : official journal of the European Society for Engineering and Medicine Implementation of an SSVEP-based intelligent home service robot system

Zhang Y ; Gao Q ; Song Y ; Wang Z | Netherlands | 22/09/2020

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Neurology India, 68, 2. A symptomatic female patient with duchenne muscular dystrophy gene mutation showing rimmed vacuoles in muscle biopsy

Ban R ; Lu X ; Pu C ; Shi Q ; Wang H ; Liu H ; Zhang Y ; Fang F | India | 05/2020

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Article

Journal of clinical laboratory analysis Analysis of myositis autoantibodies in Chinese patients with cancer-associated myositis

Li L ; Liu C ; Wang Q ; Wu C ; Zhang Y ; Cheng L ; Wen X ; Zeng X ; Zhang F ; Li Y | United States | 03/2020

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Article

Science translational medicine, 12, 536. Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy

Lek A ; 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 | United States | 03/2020

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Article

Frontiers in neurology, 10. Mutations of MACF1, Encoding Microtubule-Actin Crosslinking-Factor 1, Cause Spectraplakinopathy

Kang L ; Liu Y ; Jin Y ; Li M ; Song J ; Zhang Y ; Zhang Y ; Yang Y | Switzerland | 01/2020

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Article

Frontiers in neurology, 11. 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 ; Fan D | 2020

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Article

Frontiers in neurology, 11. Cross-Sectional Study in a Large Cohort of Chinese Patients With GJB1 Gene Mutations

Liu X ; Duan X ; Zhang Y ; Sun A ; Fan D | 2020

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Article

Medicine, 99, 3. 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 ; Li L ; Tang X ; Wang L ; Guo J ; Jin C ; Tighe S ; Zhang Y ; Zhu Y ; Zhu B | United States | 01/2020

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Article

Medicine, 99, 31. A novel application of tau PET in the diagnosis of sporadic inclusion body myositis: A case report

Zhang Y ; Li K ; Pu C ; Dang H ; Liu J ; Shi Q | 2020

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Article

Molecular therapy : the journal of the American Society of Gene Therapy, 28, 9. 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 ; Rodriguez-Caycedo C ; Sanchez-Ortiz E ; Mireault AA ; McAnally JR ; Shelton JM ; Zhang Y ; Bassel-Duby R ; Olson EN | 2020

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Article

BMC neurology, 19, 1. Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations

Chen W ; Zhang Y ; Ni Y ; Cai S ; Zheng X ; Mastaglia FL ; Wu J | England | 12/2019

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Détail de l'auteur

Auteur Zhang Y

Documents disponibles écrits par cet auteur (73)

Circulation 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

Journal of neuroimmunology, 358. Sexual dysfunction in patients with myasthenia gravis

Orphanet journal of rare diseases, 16, 1. Anxiety and depression in school-age patients with spinal muscular atrophy: a cross-sectional study

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 50, 4. Screening of multiple acyl-CoA dehydrogenase deficiency in newborns and follow-up of patients

Molecular therapy. Methods & clinical development, 22. A consolidated AAV system for single-cut CRISPR correction of a common Duchenne muscular dystrophy mutation

Brain and Behavior No correlation between acetylcholine receptor antibody concentration and individual clinical symptoms of myasthenia gravis: A systematic retrospective study involving 67 patients.

Biochemical and biophysical research communications, 545. Targeted addition of mini-dystrophin into rDNA locus of Duchenne muscular dystrophy patient-derived iPSCs

Clinical immunology (Orlando, Fla.), 224. Peripheral blood hsa-circRNA5333-4: A novel biomarker for myasthenia gravis

Nature communications, 12, 1. The nuclear envelope protein Net39 is essential for muscle nuclear integrity and chromatin organization

Human molecular genetics SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins

Rheumatology (Oxford, England) The diagnostic value of GDF-15 for myocardial involvement in idiopathic inflammatory myopathy

Technology and health care : official journal of the European Society for Engineering and Medicine Implementation of an SSVEP-based intelligent home service robot system

Neurology India, 68, 2. A symptomatic female patient with duchenne muscular dystrophy gene mutation showing rimmed vacuoles in muscle biopsy

Journal of clinical laboratory analysis Analysis of myositis autoantibodies in Chinese patients with cancer-associated myositis

Science translational medicine, 12, 536. Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy

Frontiers in neurology, 10. Mutations of MACF1, Encoding Microtubule-Actin Crosslinking-Factor 1, Cause Spectraplakinopathy

Frontiers in neurology, 11. Clinical and Genetic Diversity of PMP22 Mutations in a Large Cohort of Chinese Patients With Charcot-Marie-Tooth Disease

Frontiers in neurology, 11. Cross-Sectional Study in a Large Cohort of Chinese Patients With GJB1 Gene Mutations

Medicine, 99, 3. 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

Medicine, 99, 31. A novel application of tau PET in the diagnosis of sporadic inclusion body myositis: A case report

Molecular therapy : the journal of the American Society of Gene Therapy, 28, 9. Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing

BMC neurology, 19, 1. Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations