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Auteur Li W

Documents disponibles écrits par cet auteur (36)

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Article

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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Nature communications, 13, 1. A small molecule antagonist of SMN disrupts the interaction between SMN and RNAP II

Liu Y ; Liu YD ; Iqbal A ; Li W ; Ni Z ; Wang Y ; Ramprasad J ; Abraham KJ ; Zhang M ; Zhao DY ; Qin S ; Loppnau P ; Jiang H ; Guo X ; Brown PJ ; Zhen X ; Xu G ; Mekhail K ; Ji X ; Bedford MT ; Greenblatt JF ; Min J | 16/09/2022

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Article

Clinical genetics A novel splice site variant in the POPDC3 causes autosomal recessive limb-girdle muscular dystrophy type 26

Zhang L ; Li W ; Weng Y ; Lin K ; Huang K ; Ma S ; Chu J ; Yang Z ; Zhang X ; Sun H | Denmark | 17/07/2022

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Article

Human molecular genetics Clinical, pathological and genetic features and follow-up of 110 patients with late-onset MADD: A single-center retrospective study

Wen B ; Tang S ; Lv X ; Li D ; Xu J ; Olsen RKJ ; Zhao Y ; Li W ; Wang T ; Shao K ; Zhao D ; Yan C | England | 27/10/2021

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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

HGG advances, 3, 1. RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing

Falzarano MS ; Grilli A ; Zia S ; Fang M ; Rossi R ; Gualandi F ; Rimessi P ; El Dani R ; Fabris M ; Lu Z ; Li W ; Mongini T ; Ricci F ; Pegoraro E ; Bello L ; Barp A ; Sansone VA ; Hegde M ; Roda B ; Reschiglian P ; Bicciato S ; Selvatici R ; Ferlini A | 24/08/2021

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International immunopharmacology, 98. Natural killer cells promote the differentiation of follicular helper T cells instead of inducing apoptosis in myasthenia gravis

Liu RT ; Li W ; Guo D ; Yang CL ; Ding J ; Xu JX ; Duan RS | Netherlands | 23/06/2021

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Article

Journal of neurology Anti-HMGCR myopathy overlaps with dermatomyositis-like rash: a distinct subtype of idiopathic inflammatory myopathy

Hou Y ; Shao K ; Yan Y ; Dai T ; Li W ; Zhao Y ; Li D ; Lu JQ ; Norman GL ; Yan C | Germany | 21/05/2021

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Article

CNS neuroscience & therapeutics Juvenile idiopathic inflammatory myopathies with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies in a Chinese cohort

Hou Y ; Shao K ; Zhao B ; Dai T ; Wang Q ; Zhao Y ; Yan C ; Yan Y ; Ma X ; Li W | England | 01/05/2021

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$The Efficacy of Tocilizumab in the Treatment of Patients with Refractory Immune-Mediated Necrotizing Myopathies: An Open-Label Pilot Study$

Article

Frontiers in pharmacology, 12. The Efficacy of Tocilizumab in the Treatment of Patients with Refractory Immune-Mediated Necrotizing Myopathies: An Open-Label Pilot Study

Li S ; Li W ; Jiang W ; He L ; Peng Q ; Wang G ; Lu X | 16/03/2021

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Article

Neuromuscular disorders : NMD A novel nonsense variant in MT-CO3 causes MELAS syndrome

Wang W ; Sun Y ; Lin Y ; Xu X ; Zhao D ; Ji K ; Li W ; Zhao Y ; Yan C | England | 03/03/2021

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Article

Arthritis research & therapy, 23, 1. Expansion of circulating peripheral TIGIT+CD226+ CD4 T cells with enhanced effector functions in dermatomyositis

Li W ; Deng C ; Yang H ; Lu X ; Li S ; Liu X ; Chen F ; Chen L ; Shu X ; Zhang L ; Liu Q ; Wang G ; Peng Q | 07/01/2021

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Article

Molecular therapy : the journal of the American Society of Gene Therapy Exosome-mediated improvement in membrane integrity and muscle function in dystrophic mice

Leng L ; Dong X ; Gao X ; Ran N ; Geng M ; Zuo B ; Wu Y ; Li W ; Yan H ; Han G ; Yin H | United States | 15/12/2020

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Article

Journal of neuropathology and experimental neurology, 79, 5. Gasdermine E-Dependent Mitochondrial Pyroptotic Pathway in Dermatomyositis: A Possible Mechanism of Perifascicular Atrophy

Liu M, Auteur ; Li L ; Dai T ; Hou Y ; Li W ; Zhao Y ; Fang Q ; Yan C | England | 05/2020

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Article

International Journal of molecular sciences, 21, 7. Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation Intermediates

Knottnerus SJG ; Mengarelli I ; Wust RCI ; Baartscheer A ; Bleeker JC ; Coronel R ; Ferdinandusse S ; Guan K ; Ijlst L ; Li W ; Luo X ; Portero VM ; Ulbricht Y ; Visser G ; Wanders RJA ; Wijburg FA ; Verkerk AO ; Houtkooper RH ; Bezzina CR | 04/2020

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Article

Scientific Reports, 10, 1. RNA Sequence Analyses throughout the Course of Mouse Cardiac Laminopathy Identify Differentially Expressed Genes for Cell Cycle Control and Mitochondrial Function

Shao Z, Auteur ; Koh W ; Ni Y ; Li W ; Agatisa Boyle B ; Merkurjev D ; Tang WHW | 04/2020

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Article

Developmental neurorehabilitation Cross-cultural Adaptation and Multi-centric Validation of the Motor Function Measure Chinese Version (MFM-32-CN) for Patients with Neuromuscular Diseases

Huang M, Auteur ; Cao J ; Sun J ; Li W ; Qin L ; Li H ; Zhai C ; Huang W ; Gui T ; Zhang K ; Wang J ; Vuillerot C ; Wang Y ; Dai M | 07/2019

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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

Prenatal diagnosis X-chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations

He WB, Auteur ; Du J ; Xie PY ; Zhou S ; Zhang YX ; Lu GX ; Lin G ; Li W ; Tan YQ | England | 08/05/2019

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Article

Arthritis research & therapy, 21, 1. The RIG-I pathway is involved in peripheral T cell lymphopenia in patients with dermatomyositis

Zhang L, Auteur ; Xia Q ; Li W ; Peng Q ; Yang H ; Lu X ; Wang G | England | 2019

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Article

Stem cell reports, 10, 1. Modeling the Pathogenesis of Charcot-Marie-Tooth Disease Type 1A Using Patient-Specific iPSCs

Shi L, Auteur ; Huang L ; He R ; Huang W ; Wang H ; Lai X ; Zou Z ; Sun J ; Ke Q ; Zheng M ; Lu X ; Pei Z ; Su H ; Xiang AP ; Li W ; Yao X | 2018

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Article

Journal of neurology, 264, 11. Efficacy and safety of tacrolimus for myasthenia gravis: a systematic review and meta-analysis

Wang L, Auteur ; Zhang S ; Xi J ; Li W ; Zhou L ; Lu J ; Zhang T ; Zhao C | 2017

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Article

Therapeutic advances in neurological disorders, 10, 9. Tacrolimus in the treatment of myasthenia gravis in patients with an inadequate response to glucocorticoid therapy: randomized, double-blind, placebo-controlled study conducted in China

Zhou L, Auteur ; Liu W ; Li W ; Li H ; Zhang X ; Shang H ; Bu B ; Deng H ; Fang Q ; Li J ; Zhang H ; Song Z ; Ou C ; Yan C ; Liu T ; Zhou H ; Bao J ; Lu J ; Shi H ; Zhao C | 2017

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Article

The Journal of clinical investigation, 126, 1. POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking

Schindler RF ; Scotton C ; Zhang J ; Passarelli C ; Ortiz-Bonnin B ; Simrick S ; Schwerte T ; Poon KL ; Fang M ; Rinne S ; Froese A ; Nikolaev VO ; Grunert C ; Müller T ; Tasca G ; Sarathchandra P ; Drago F ; Dallapiccola B ; Rapezzi C ; Arbustini E ; Di Raimo FR ; Neri M ; Selvatici R ; Gualandi F ; Fattori F ; Pietrangelo A ; Li W ; Jiang H ; Xu X ; Bertini E ; Decher N ; Wang J ; Brand T ; Ferlini A | 2016

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Article

European journal of radiology, 84, 10. The trefoil with single fruit sign in muscle magnetic resonance imaging is highly specific for dystrophinopathies

Zheng Y, Auteur ; Li W ; Du J ; Jin S ; Li S ; Zhao Y ; Xu C ; Wang Z ; Lv H ; Zhang W ; Xiao J ; Yuan Y | 2015

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Détail de l'auteur

Auteur Li W

Documents disponibles écrits par cet auteur (36)

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

Nature communications, 13, 1. A small molecule antagonist of SMN disrupts the interaction between SMN and RNAP II

Clinical genetics A novel splice site variant in the POPDC3 causes autosomal recessive limb-girdle muscular dystrophy type 26

Human molecular genetics Clinical, pathological and genetic features and follow-up of 110 patients with late-onset MADD: A single-center retrospective study

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

HGG advances, 3, 1. RNA-seq in DMD urinary stem cells recognized muscle-related transcription signatures and addressed the identification of atypical mutations by whole-genome sequencing

International immunopharmacology, 98. Natural killer cells promote the differentiation of follicular helper T cells instead of inducing apoptosis in myasthenia gravis

Journal of neurology Anti-HMGCR myopathy overlaps with dermatomyositis-like rash: a distinct subtype of idiopathic inflammatory myopathy

CNS neuroscience & therapeutics Juvenile idiopathic inflammatory myopathies with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies in a Chinese cohort

Frontiers in pharmacology, 12. The Efficacy of Tocilizumab in the Treatment of Patients with Refractory Immune-Mediated Necrotizing Myopathies: An Open-Label Pilot Study

Neuromuscular disorders : NMD A novel nonsense variant in MT-CO3 causes MELAS syndrome

Arthritis research & therapy, 23, 1. Expansion of circulating peripheral TIGIT+CD226+ CD4 T cells with enhanced effector functions in dermatomyositis

Molecular therapy : the journal of the American Society of Gene Therapy Exosome-mediated improvement in membrane integrity and muscle function in dystrophic mice

Journal of neuropathology and experimental neurology, 79, 5. Gasdermine E-Dependent Mitochondrial Pyroptotic Pathway in Dermatomyositis: A Possible Mechanism of Perifascicular Atrophy

International Journal of molecular sciences, 21, 7. Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation Intermediates

Scientific Reports, 10, 1. RNA Sequence Analyses throughout the Course of Mouse Cardiac Laminopathy Identify Differentially Expressed Genes for Cell Cycle Control and Mitochondrial Function

Developmental neurorehabilitation Cross-cultural Adaptation and Multi-centric Validation of the Motor Function Measure Chinese Version (MFM-32-CN) for Patients with Neuromuscular Diseases

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

Prenatal diagnosis X-chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations

Arthritis research & therapy, 21, 1. The RIG-I pathway is involved in peripheral T cell lymphopenia in patients with dermatomyositis

Stem cell reports, 10, 1. Modeling the Pathogenesis of Charcot-Marie-Tooth Disease Type 1A Using Patient-Specific iPSCs

Journal of neurology, 264, 11. Efficacy and safety of tacrolimus for myasthenia gravis: a systematic review and meta-analysis

Therapeutic advances in neurological disorders, 10, 9. Tacrolimus in the treatment of myasthenia gravis in patients with an inadequate response to glucocorticoid therapy: randomized, double-blind, placebo-controlled study conducted in China

The Journal of clinical investigation, 126, 1. POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking

European journal of radiology, 84, 10. The trefoil with single fruit sign in muscle magnetic resonance imaging is highly specific for dystrophinopathies