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Auteur Chen X

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Neuroscience, 544. Neurometabolic and Brain Functional Alterations Associated with Cognitive Impairment in Patients with Myasthenia Gravis: A Combined 1H-MRS and fMRI Study

Zhou X ; Yang Y ; Zhu F ; Chen X ; Zhu Y ; Gui T ; Li Y ; Xue Q | 28/02/2024

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EMBO Molecular Medicine Improved gene therapy for spinal muscular atrophy in mice using codon-optimized hSMN1 transgene and hSMN1 gene-derived promotor

Xie Q ; Chen X ; Ma H ; Zhu Y ; Ma Y ; Jalinous L ; Cox GF ; Weaver F ; Yang J ; Kennedy Z ; Gruntman A ; Du A ; Su Q ; He R ; Tai PW ; Gao G ; Xie J | 27/02/2024

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Seminars in arthritis and rheumatism, 65. Spontaneous pneumomediastinum in anti-MDA5-positive dermatomyositis: Prevalence, risk factors, and prognosis

Jin Q ; Lin S ; Chen X ; Xu Y ; Tian X ; He L ; Jiang W ; Chen F ; Shu X ; Lu X ; Peng Q ; Wang G | 03/01/2024

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Article

Journal of genetics and genomics = Yi chuan xue bao, Epub. CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy

Shi Y ; Cao C ; Zeng Y ; Ding Y ; Chen L ; Zheng F ; Chen X ; Zhou F ; Yang X ; Li J ; Xu L ; Xu G ; Lin M ; Ishiura H ; Tsuji S ; Wang N ; Wang Z ; Chen W ; Yang K | 28/12/2023

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Biochemical pharmacology, 214. Oxidative stress: Roles in skeletal muscle atrophy

Zhang H ; Qi G ; Wang K ; Yang J ; Shen Y ; Yang X ; Chen X ; Yao X ; Gu X ; Qi L ; Zhou C ; Sun H | 08/2023

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Article

Frontiers in neurology, 13. Editorial: Phenotypes of myasthenia gravis

Li HF ; Gilhus NE ; Yang H ; Chen X | 14/09/2022

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Nature reviews. Drug discovery, 21, 8. Evolution of innovative drug R&D in China

Li G ; Liu Y ; Hu H ; Yuan S ; Zhou L ; Chen X | England | 08/2022

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Article

Seizure, 101. Seizures and EEG characteristics in a cohort of pediatric patients with dystroglycanopathies

Yang H ; Yang HB ; Song D ; Liu Y ; Chen X ; Zhu Y ; Wei C ; Fu X ; Liu X ; Yang Z ; Xiong H | England | 13/07/2022

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Article

Neurology and therapy Therapeutic Effects of Batoclimab in Chinese Patients with Generalized Myasthenia Gravis: A Double-Blinded, Randomized, Placebo-Controlled Phase II Study

Yan C ; Duan RS ; Yang H ; Li HF ; Zou Z ; Zhang H ; Zhou H ; Li XL ; Zhou H ; Jiao L ; Chen J ; Yin J ; Du Q ; Lee M ; Chen Y ; Chen X ; Zhao C | New Zealand | 12/04/2022

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Article

Journal of neuroimmunology, 362. Berberine attenuates experimental autoimmune myasthenia gravis via rebalancing the T cell subsets

Song J ; Yang J ; Jing S ; Yan C ; Huan X ; Chen S ; Zhong H ; Lu J ; Xi J ; Luo L ; Chen X ; Wang Z ; Zhao C ; Chu M ; Luo S | Netherlands | 15/01/2022

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Article

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 50, 4. Screening and follow-up results of fatty acid oxidative metabolism disorders in 608 818 newborns in Jining, Shandong province

Yang C ; Shi C ; Zhou C ; Wan Q ; Zhou Y ; Chen X ; Jin X ; Huang C ; Xu P | China | 25/08/2021

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Article

BioMed research international, 2020. Identification of Candidate Genes Associated with Charcot-Marie-Tooth Disease by Network and Pathway Analysis

Zhong M ; Luo Q ; Ye T ; Zhu X ; Chen X ; Liu J | 23/09/2020

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Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 79. Central nervous system impairment detected by somatosensory evoked potentials in patients with Charcot-Marie-Tooth disease type 1A

Zhou X ; Zhang B ; Qiao K ; Lu J ; Chen X ; Wang Y ; Zhu D ; Wang Y | Scotland | 09/2020

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Article

The Journal of biological chemistry The intragenic microRNA miR199A1 in the dynamin 2 gene contributes to the pathology of X-linked centronuclear myopathy

Chen X ; Gao YQ ; Zheng YY ; Wang W ; Wang P ; Liang J ; Zhao W ; Tao T ; Sun J ; Wei L ; Li Y ; Zhou Y ; Gan Z ; Zhang X ; Chen HQ ; Zhu MS | United States | 04/2020

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Article

Genetics in medicine : official journal of the American College of Medical Genetics Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data

Chen X ; Sanchis-Juan A ; French CE ; Connell AJ ; Delon I ; Kingsbury Z ; Chawla A ; Halpern AL ; Taft RJ ; Bentley DR ; Butchbach MER ; Raymond FL ; Eberle MA | United States | 02/2020

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Human gene therapy Different serotypes of AAV vectors and lentivirus meditated tropism in choroid plexus by intracerebroventricular delivery

Chen X, Auteur ; He Y ; Tian Y ; Wang Y ; Wu Z ; Lan T ; Wang H ; Cheng K ; Xie P | United States | 02/2020

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Article

Frontiers in Genetics, 10. Newborn Screening for Spinal Muscular Atrophy in China Using DNA Mass Spectrometry

Lin Y ; Lin CH ; Yin X ; Zhu L ; Yang J ; Shen Y ; Yang C ; Chen X ; Hu H ; Ma Q ; Shi X ; Shen Y ; Hu Z ; Huang C ; Huang X | Switzerland | 12/2019

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Article

JACC. Basic to translational science, 4, 7. Gene Therapy Rescues Cardiac Dysfunction in Duchenne Muscular Dystrophy Mice by Elevating Cardiomyocyte Deoxy-Adenosine Triphosphate

Kolwicz SC Jr ; Hall JK ; Moussavi-Harami F ; Chen X ; Hauschka SD ; Chamberlain JS ; Regnier M ; Odom GL | United States | 10/2019

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Article

Nature communications, 10, 1. Structural insights of human mitofusin-2 into mitochondrial fusion and CMT2A onset

Li YJ, Auteur ; Cao YL ; Feng JX ; Qi Y ; Meng S ; Yang JF ; Zhong YT ; Kang S ; Chen X ; Lan L ; Luo L ; Yu B ; Chen S ; Chan DC ; Hu J ; Gao S | England | 10/2019

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Article

Journal of cachexia, sarcopenia and muscle, 10, 3. Hemojuvelin is a novel suppressor for Duchenne muscular dystrophy and age-related muscle wasting

Zhang P, Auteur ; He J ; Wang F ; Gong J ; Wang L ; Wu Q ; Li W ; Liu H ; Wang J ; Zhang K ; Li M ; Huang X ; Pu C ; Li Y ; Jiang F ; Wang F ; Min J ; Chen X | 06/2019

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Article

Journal of visualized experiments : JoVE, 132. An Objective and Child-friendly Assessment of Arm Function by Using a 3-D Sensor

Chen X, Auteur ; Wolf D ; Siebourg-Polster J ; Czech C ; Bonati U ; Fischer D ; Khwaja O ; Strahm M | 2018

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Article

PLoS ONE, 12, 1. Feasibility of Using Microsoft Kinect to Assess Upper Limb Movement in Type III Spinal Muscular Atrophy Patients

Chen X, Auteur ; Siebourg-Polster J ; Wolf D ; Czech C ; Bonati U ; Fischer D ; Khwaja O ; Strahm M | 2017

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Article

American journal of translational research, 8, 4. The mechanism of acetylcholine receptor in binding MuSK in myasthenia gravis and the role of HSP90 molecular chaperone

Chen R, Auteur ; Chen S ; Liao J ; Chen X ; Xu X | 2016

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Article

Genome medicine, 8, 1. The emerging role of viral vectors as vehicles for DMD gene editing

Maggio I, Auteur ; Chen X ; Goncalves MA | 2016

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Article

Nucleic acids research, 44, 3. Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations

Maggio I, Auteur ; Stefanucci L ; Janssen JM ; Liu J ; Chen X ; Mouly V ; Goncalves MA | 2016

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Détail de l'auteur

Auteur Chen X

Documents disponibles écrits par cet auteur (31)

Neuroscience, 544. Neurometabolic and Brain Functional Alterations Associated with Cognitive Impairment in Patients with Myasthenia Gravis: A Combined 1H-MRS and fMRI Study

EMBO Molecular Medicine Improved gene therapy for spinal muscular atrophy in mice using codon-optimized hSMN1 transgene and hSMN1 gene-derived promotor

Seminars in arthritis and rheumatism, 65. Spontaneous pneumomediastinum in anti-MDA5-positive dermatomyositis: Prevalence, risk factors, and prognosis

Journal of genetics and genomics = Yi chuan xue bao, Epub. CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy

Biochemical pharmacology, 214. Oxidative stress: Roles in skeletal muscle atrophy

Frontiers in neurology, 13. Editorial: Phenotypes of myasthenia gravis

Nature reviews. Drug discovery, 21, 8. Evolution of innovative drug R&D in China

Seizure, 101. Seizures and EEG characteristics in a cohort of pediatric patients with dystroglycanopathies

Neurology and therapy Therapeutic Effects of Batoclimab in Chinese Patients with Generalized Myasthenia Gravis: A Double-Blinded, Randomized, Placebo-Controlled Phase II Study

Journal of neuroimmunology, 362. Berberine attenuates experimental autoimmune myasthenia gravis via rebalancing the T cell subsets

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 50, 4. Screening and follow-up results of fatty acid oxidative metabolism disorders in 608 818 newborns in Jining, Shandong province

BioMed research international, 2020. Identification of Candidate Genes Associated with Charcot-Marie-Tooth Disease by Network and Pathway Analysis

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 79. Central nervous system impairment detected by somatosensory evoked potentials in patients with Charcot-Marie-Tooth disease type 1A

The Journal of biological chemistry The intragenic microRNA miR199A1 in the dynamin 2 gene contributes to the pathology of X-linked centronuclear myopathy

Genetics in medicine : official journal of the American College of Medical Genetics Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data

Human gene therapy Different serotypes of AAV vectors and lentivirus meditated tropism in choroid plexus by intracerebroventricular delivery

Frontiers in Genetics, 10. Newborn Screening for Spinal Muscular Atrophy in China Using DNA Mass Spectrometry

JACC. Basic to translational science, 4, 7. Gene Therapy Rescues Cardiac Dysfunction in Duchenne Muscular Dystrophy Mice by Elevating Cardiomyocyte Deoxy-Adenosine Triphosphate

Nature communications, 10, 1. Structural insights of human mitofusin-2 into mitochondrial fusion and CMT2A onset

Journal of cachexia, sarcopenia and muscle, 10, 3. Hemojuvelin is a novel suppressor for Duchenne muscular dystrophy and age-related muscle wasting

Journal of visualized experiments : JoVE, 132. An Objective and Child-friendly Assessment of Arm Function by Using a 3-D Sensor

PLoS ONE, 12, 1. Feasibility of Using Microsoft Kinect to Assess Upper Limb Movement in Type III Spinal Muscular Atrophy Patients

American journal of translational research, 8, 4. The mechanism of acetylcholine receptor in binding MuSK in myasthenia gravis and the role of HSP90 molecular chaperone

Genome medicine, 8, 1. The emerging role of viral vectors as vehicles for DMD gene editing

Nucleic acids research, 44, 3. Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations