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Auteur Wang L

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Article

Human gene therapy Prevalence of Adeno-Associated Virus-9-Neutralizing Antibody in Chinese Patients with Duchenne Muscular Dystrophy

Wei C ; Li D ; Zhang M ; Zhao Y ; Liu Y ; Fan Y ; Wang L ; Liu J ; Chang X ; Jiang Y ; Xiong H | 27/12/2023

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Neurology, 101, 3. Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

Zheng F ; Qiu L ; Chen L ; Zheng Y ; Lin X ; He J ; Lin X ; He Q ; Lin Y ; Lin L ; Wang L ; Lin F ; Yang K ; Lin M ; Lin Y ; Fu Y ; Wang N ; Wang Z | 18/07/2023

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Article

Annals of clinical and translational neurology Provisional practice recommendation for the management of myopathy in VCP-associated multisystem proteinopathy

Roy B ; Peck A ; Evangelista T ; Pfeffer G ; Wang L ; Diaz-Manera J ; Korb M ; Wicklund MP ; Milone M ; Freimer M ; Kushlaf H ; Villar-Quiles RN ; Stojkovic T ; Needham M ; Palmio J ; Lloyd TE ; Keung B ; Mozaffar T ; Weihl CC ; Kimonis V | United States | 07/04/2023

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Clinical and experimental rheumatology, 41, 2. Current status of clinical outcome measures in inclusion body myositis: a systematised review

Roy B ; Lucchini M ; Lilleker JB ; Goyal NA ; Naddaf E ; Adler B ; Alfano LN ; Malandraki GA ; Focht Garand KL ; Mochel D ; Badrising U ; Machado PM ; Pagkatipunan R ; Ramdharry G ; Wang L ; Funaro MC ; Schmidt J ; Kushlaf H ; Schiopu E ; Stipancic K ; Goyal N ; D'Alessandro M ; Conticini E ; Cruz-Coble B ; Lloyd TE | Italy | 03/2023

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Article

Journal of controlled release : official journal of the Controlled Release Society, 355. AAV vectors applied to the treatment of CNS disorders: Clinical status and challenges

Kang L ; Jin S ; Wang J ; Lv Z ; Xin C ; Tan C ; Zhao M ; Wang L ; Liu J | Netherlands | 01/02/2023

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Article

Frontiers in Genetics, 13. Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review

Bi S ; Dai L ; Jiang L ; Wang L ; Teng M ; Liu G ; Teng RJ | Switzerland | 13/01/2023

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Article

Human molecular genetics A splicing silencer in SMN2 intron 6 is critical in spinal muscular atrophy

Wang L ; Ji Y ; Chen Y ; Bai J ; Gao P ; Feng P | England | 18/10/2022

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Article

Neurology Quantitative Muscle Analysis in FSHD Using Whole-Body Fat-Referenced MRI: Composite Scores for Longitudinal and Cross-Sectional Analysis

Mellion ML ; Widholm P ; Karlsson M ; Ahlgren A ; Tawil R ; Wagner KR ; Statland JM ; Wang L ; Shieh PB ; van Engelen BGM ; Kools J ; Ronco L ; Odueyungbo A ; Jiang J ; Han JJ ; Hatch M ; Towles J ; Leinhard OD ; Cadavid D | United States | 24/06/2022

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Article

Frontiers in Genetics, 13. Long-Read Sequencing Revealed Extragenic and Intragenic Duplications of Exons 56-61 in DMD in an Asymptomatic Male and a DMD Patient

Bai Y ; Liu J ; Xu J ; Sun Y ; Li J ; Gao Y ; Liu L ; Jia C ; Kong X ; Wang L | 09/05/2022

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Article

The Journal of clinical investigation ACVR1 antibodies exacerbate heterotopic ossification in fibrodysplasia ossificans progressiva (FOP) by activating FOP-mutant ACVR1

Aykul S ; Huang L ; Wang L ; Das NM ; Reisman S ; Ray Y ; Zhang Q ; Rothman NJ ; Nannuru KC ; Kamat V ; Brydges S ; Troncone L ; Johnsen L ; Yu PB ; Fazio S ; Lees-Shepard J ; Schutz K ; Murphy AJ ; Economides AN ; Idone V ; Hatsell SJ | United States | 05/05/2022

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Journal of animal science and biotechnology, 13, 1. Ryanodine receptor RyR1-mediated elevation of Ca(2+) concentration is required for the late stage of myogenic differentiation and fusion

Qiu K ; Wang Y ; Xu D ; He L ; Zhang X ; Yan E ; Wang L ; Yin J | 11/02/2022

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Article

Neurology Immunophenotyping of Inclusion Body Myositis Blood T and NK Cells

Goyal NA ; Coulis G ; Duarte J ; Farahat PK ; Mannaa AH ; Cauchii J ; Irani T ; Araujo N ; Wang L ; Wencel M ; Li V ; Zhang L ; Greenberg SA ; Mozaffar T ; Villalta SA | United States | 7/02/2022

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Article

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

The Lancet regional health. Western Pacific, 18. Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

Wang Z ; Qiu L ; Lin M ; Chen L ; Zheng F ; Lin L ; Lin F ; Ye Z ; Lin X ; He J ; Wang L ; Lin X ; He Q ; Chen W ; Lin Y ; Fu Y ; Wang N | 22/11/2021

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Article

Journal of translational medicine, 19, 1. Identification of the regulatory role of lncRNA HCG18 in myasthenia gravis by integrated bioinformatics and experimental analyses

Li S ; Wang X ; Wang T ; Zhang H ; Lu X ; Liu L ; Li L ; Bo C ; Kong X ; Xu S ; Ning S ; Wang J ; Wang L | 18/11/2021

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Article

Cell biology international Upregulation of circ-FBL promotes myogenic proliferation in myasthenia gravis by regulation of miR-133/PAX7

Lai X ; Bi Z ; Yang X ; Hu R ; Wang L ; Jin M ; Li L ; Bu B | England | 07/08/2021

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Article

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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Article

Annals of translational medicine, 9, 9. Genetic identification of pathogenic variations of the DMD gene: a retrospective study from 10,481 neonatal patients based on next-generation sequencing data

Xiao T ; Wu B ; Cao Y ; Liu R ; Cheng G ; Wang L ; Zhuang D ; Zhao Z ; Wang H ; Zhou W | 05/2021

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Article

13, 1. In vivo genome editing in mouse restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers

Chen M ; Shi H ; Gou S ; Wang X ; Li L ; Jin Q ; Wu H ; Zhang H ; Li Y ; Wang L ; Li H ; Lin J ; Guo W ; Jiang Z ; Yang X ; Xu A ; Zhu Y ; Zhang C ; Lai L ; Li X | 12/04/2021

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Scientific Reports, 11, 1. Construction of a TF-miRNA-gene feed-forward loop network predicts biomarkers and potential drugs for myasthenia gravis

Bo C ; Zhang H ; Cao Y ; Lu X ; Zhang C ; Li S ; Kong X ; Zhang X ; Bai M ; Tian K ; Saitgareeva A ; Lyaysan G ; Wang J ; Ning S ; Wang L | 28/01/2021

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Article

American journal of medical genetics. Part A CHRNB1-associated congenital myasthenia syndrome: Expanding the clinical spectrum

Freed AS ; Schwarz AC ; Brei BK ; Clowes Candadai SV ; Thies J ; Mah JK ; Chabra S ; Wang L ; Innes AM ; Bennett JT | United States | 09/12/2020

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Article

Journal of cachexia, sarcopenia and muscle TAK1 inhibition improves myoblast differentiation and alleviates fibrosis in a mouse model of Duchenne muscular dystrophy

Xu D ; Li S ; Wang L ; Jiang J ; Zhao L ; Huang X ; Sun Z ; Li C ; Sun L ; Li X ; Jiang Z ; Zhang L | Germany | 25/11/2020

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$Successful management with Janus kinase inhibitor tofacitinib in refractory juvenile dermatomyositis: a pilot study and literature review$

Article

Rheumatology (Oxford, England) Successful management with Janus kinase inhibitor tofacitinib in refractory juvenile dermatomyositis: a pilot study and literature review

Yu Z ; Wang L ; Quan M ; Zhang T ; Song H | England | 07/10/2020

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Article

Frontiers in neuroscience, 14. Emerging Roles of Dysregulated MicroRNAs in Myasthenia Gravis

Wang L ; Zhang L | 05/2020

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Article

Respiratory medicine, 165. Six-minute walk distance in healthy young adults

Halliday SJ, Auteur ; Wang L ; Yu C ; Vickers BP ; Newman JH ; Fremont RD ; Huerta LE ; Brittain EL ; Hemnes AR | 04/2020

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Détail de l'auteur

Auteur Wang L

Documents disponibles écrits par cet auteur (49)

Human gene therapy Prevalence of Adeno-Associated Virus-9-Neutralizing Antibody in Chinese Patients with Duchenne Muscular Dystrophy

Neurology, 101, 3. Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

Annals of clinical and translational neurology Provisional practice recommendation for the management of myopathy in VCP-associated multisystem proteinopathy

Clinical and experimental rheumatology, 41, 2. Current status of clinical outcome measures in inclusion body myositis: a systematised review

Journal of controlled release : official journal of the Controlled Release Society, 355. AAV vectors applied to the treatment of CNS disorders: Clinical status and challenges

Frontiers in Genetics, 13. Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review

Human molecular genetics A splicing silencer in SMN2 intron 6 is critical in spinal muscular atrophy

Neurology Quantitative Muscle Analysis in FSHD Using Whole-Body Fat-Referenced MRI: Composite Scores for Longitudinal and Cross-Sectional Analysis

Frontiers in Genetics, 13. Long-Read Sequencing Revealed Extragenic and Intragenic Duplications of Exons 56-61 in DMD in an Asymptomatic Male and a DMD Patient

The Journal of clinical investigation ACVR1 antibodies exacerbate heterotopic ossification in fibrodysplasia ossificans progressiva (FOP) by activating FOP-mutant ACVR1

Journal of animal science and biotechnology, 13, 1. Ryanodine receptor RyR1-mediated elevation of Ca(2+) concentration is required for the late stage of myogenic differentiation and fusion

Neurology Immunophenotyping of Inclusion Body Myositis Blood T and NK Cells

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

The Lancet regional health. Western Pacific, 18. Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

Journal of translational medicine, 19, 1. Identification of the regulatory role of lncRNA HCG18 in myasthenia gravis by integrated bioinformatics and experimental analyses

Cell biology international Upregulation of circ-FBL promotes myogenic proliferation in myasthenia gravis by regulation of miR-133/PAX7

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

Annals of translational medicine, 9, 9. Genetic identification of pathogenic variations of the DMD gene: a retrospective study from 10,481 neonatal patients based on next-generation sequencing data

13, 1. In vivo genome editing in mouse restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers

Scientific Reports, 11, 1. Construction of a TF-miRNA-gene feed-forward loop network predicts biomarkers and potential drugs for myasthenia gravis

American journal of medical genetics. Part A CHRNB1-associated congenital myasthenia syndrome: Expanding the clinical spectrum

Journal of cachexia, sarcopenia and muscle TAK1 inhibition improves myoblast differentiation and alleviates fibrosis in a mouse model of Duchenne muscular dystrophy

Rheumatology (Oxford, England) Successful management with Janus kinase inhibitor tofacitinib in refractory juvenile dermatomyositis: a pilot study and literature review

Frontiers in neuroscience, 14. Emerging Roles of Dysregulated MicroRNAs in Myasthenia Gravis

Respiratory medicine, 165. Six-minute walk distance in healthy young adults