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Auteur Chen L

Documents disponibles écrits par cet auteur (33)

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Article

The Canadian journal of cardiology Clinical and genetic profile of Chinese children with Danon disease: A single-center retrospective cohort study

Zhang Q ; Chan W ; Chen Y ; Wu J ; Chen H ; Yu T ; Yao R ; Chen L ; Zhang B ; Zhang H ; Zhang Z ; Fu L | 11/10/2024

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GeroScience What is normal age-related thigh muscle composition among 45- to 84-year-old adults from the UK Biobank study

Anderson DB ; Beach AJ ; Chen L ; Feng HJ ; McKay MJ ; Smith ZA ; Weber KA ; Wesselink EO ; Elliott JM | 12/08/2024

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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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Article

Orphanet journal of rare diseases, 18, 1. Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients

Lin F ; Yang K ; Lin X ; Jin M ; Chen L ; Zheng FZ ; Qiu LL ; Ye ZX ; Chen HZ ; Lin MT ; Wang N ; Wang ZQ | 16/11/2023

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Article

Neurotherapeutics, Epub. Intravenous Administration of an AAV9 Vector Ubiquitously Expressing C1orf194 Gene Improved CMT-Like Neuropathy in C1orf194-/- Mice

Shen Z ; Li M ; He F ; Huang C ; Zheng Y ; Wang Z ; Ma S ; Chen L ; Liu Z ; Zheng H ; Xiong F | 16/10/2023

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Article

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

Journal of translational medicine, 21, 1. The spatiotemporal matching pattern of Ezrin/Periaxin involved in myoblast differentiation and fusion and Charcot-Marie-Tooth disease-associated muscle atrophy

Zhang RN ; Bao X ; Liu Y ; Wang Y ; Li XY ; Tan G ; Mbadhi MN ; Xu W ; Yang Q ; Yao LY ; Chen L ; Zhao XY ; Hu CQ ; Zhang JX ; Zheng HT ; Wu Y ; Li S ; Chen SJ ; Chen SY ; Lv J ; Shi LL ; Tang JM | England | 03/2023

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Article

Research (Washington, D.C.), 6. Efficient Modulation of Exon Skipping via Antisense Circular RNAs

Ren S ; Huang M ; Bai R ; Chen L ; Yang J ; Zhang J ; Guo W ; Ji W ; Chen Y | United States | 2023

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Article

Journal of the American Academy of Dermatology Baricitinib for the treatment of cutaneous dermatomyositis: A prospective, open-label study

Zhao Q ; Zhao Q ; Zhu Z ; Fu Q ; Shih Y ; Wu D ; Chen L ; Zheng J ; Cao H | United States | 20/08/2022

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Article

Annals of neurology GGC repeat expansion of RILPL1 is associated with oculopharyngodistal myopathy

Zeng YH ; Yang K ; Du GQ ; Chen YK ; Cao CY ; Qiu YS ; He J ; Lv HD ; Qu QQ ; Chen JN ; Xu GR ; Chen L ; Zheng FZ ; Zhao M ; Lin MT ; Chen WJ ; Hu J ; Wang ZQ ; Wang N | United States | 14/06/2022

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Article

Frontiers in medicine, 8. Coronary Heart Disease and Cardiovascular Risk Factors in Patients With Idiopathic Inflammatory Myopathies: A Systemic Review and Meta-Analysis

Qin L ; Li F ; Luo Q ; Chen L ; Yang X ; Wang H | 14/01/2022

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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

International journal of molecular medicine, 48, 5. CAPN3: A muscle‑specific calpain with an important role in the pathogenesis of diseases (Review)

Chen L ; Tang F ; Gao H ; Zhang X ; Li X ; Xiao D | Greece | 11/2021

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Article

Brain communications, 3, 4. AAV1.NT-3 gene therapy in a CMT2D model: phenotypic improvements in Gars(P278KY/+) mice

Ozes B ; Moss K ; Myers M ; Ridgley A ; Chen L ; Murrey D ; Sahenk Z | 23/10/2021

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Article

CNS neuroscience & therapeutics, 27, 10. A novel frameshift ACTN2 variant causes a rare adult-onset distal myopathy with multi-minicores

Chen L ; Chen DF ; Dong HL ; Liu GL ; Wu ZY | 10/2021

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Article

Molecular therapy. Methods & clinical development, 22. Systemic delivery of AAVrh74.tMCK.hCAPN3 rescues the phenotype in a mouse model for LGMD2A/R1

Sahenk Z ; Ozes B ; Murrey D ; Myers M ; Moss K ; Yalvac ME ; Ridgley A ; Chen L ; Mendell JR | 24/06/2021

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Article

Cell reports, 35, 6. A high-throughput genome-wide RNAi screen identifies modifiers of survival motor neuron protein

McCormack NM ; Abera MB ; Arnold ES ; Gibbs RM ; Martin SE ; Buehler E ; Chen YC ; Chen L ; Fischbeck KH ; Burnett BG | United States | 11/05/2021

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Article

Neuromuscular disorders : NMD, 31, 5. Clinical and genetic characteristics of Chinese patients with reducing body myopathy

Chen L ; Lin HX ; Yang XX ; Chen DF ; Dong HL ; Yu H ; Liu GL ; Wu ZY | England | 05/2021

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Article

Gene therapy AAV1.NT-3 gene therapy for X-linked Charcot-Marie-Tooth neuropathy type 1

Ozes B ; Myers M ; Moss K ; Mckinney J ; Ridgley A ; Chen L ; Bai S ; Abrams CK ; Freidin MM ; Mendell JR ; Sahenk Z | England | 04/02/2021

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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

BMC musculoskeletal disorders, 22, 1. Polyglucosan body myopathy 1 may cause cognitive impairment: a case report from China

Chen L ; Wang N ; Hu W ; Yu X ; Yang R ; Han Y ; Yan Y ; Nian N ; Sha C | 07/01/2021

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Article

Journal of thoracic disease, 12, 4. Perioperative outcomes and mid-term effects in performing video-assisted thoracoscopic extended thymectomy for myasthenia gravis: subxiphoid versus right thoracic approaches

Qiu Z ; Chen L ; Lin Q ; Wu H ; Sun H ; Zhou X ; Hu Y ; Peng L ; Liu Y ; Xu Q | 04/2020

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Article

Medicine, 99, 17. Acupuncture for ocular myasthenia gravis: A protocol for systematic review and meta-analysis

Zhang D, Auteur ; Jin S ; Zhang L ; Chen L ; Liang F | United States | 04/2020

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Article

Acta neuropathologica communications, 8, 1. CMT2Q-causing mutation in the Dhtkd1 gene lead to sensory defects, mitochondrial accumulation and altered metabolism in a knock-in mouse model

Luan CJ ; Guo W ; Chen L ; Wei XW ; He Y ; Chen Y ; Dang SY ; Prior R ; Li X ; Kuang Y ; Wang ZG ; van den Bosch L ; Gu MM | 03/2020

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Article

Chinese medical journal A case of de novo dynamin 2-related centronuclear myopathy with electrical but not clinical myotonia

Huang X ; Liu XY ; Chen L ; Sun AP ; Zhang YS ; Zheng DF ; Zhong YF ; Fan DS | China | 2020

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Détail de l'auteur

Auteur Chen L

Documents disponibles écrits par cet auteur (33)

The Canadian journal of cardiology Clinical and genetic profile of Chinese children with Danon disease: A single-center retrospective cohort study

GeroScience What is normal age-related thigh muscle composition among 45- to 84-year-old adults from the UK Biobank study

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

Orphanet journal of rare diseases, 18, 1. Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients

Neurotherapeutics, Epub. Intravenous Administration of an AAV9 Vector Ubiquitously Expressing C1orf194 Gene Improved CMT-Like Neuropathy in C1orf194-/- Mice

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

Journal of translational medicine, 21, 1. The spatiotemporal matching pattern of Ezrin/Periaxin involved in myoblast differentiation and fusion and Charcot-Marie-Tooth disease-associated muscle atrophy

Research (Washington, D.C.), 6. Efficient Modulation of Exon Skipping via Antisense Circular RNAs

Journal of the American Academy of Dermatology Baricitinib for the treatment of cutaneous dermatomyositis: A prospective, open-label study

Annals of neurology GGC repeat expansion of RILPL1 is associated with oculopharyngodistal myopathy

Frontiers in medicine, 8. Coronary Heart Disease and Cardiovascular Risk Factors in Patients With Idiopathic Inflammatory Myopathies: A Systemic Review and Meta-Analysis

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

International journal of molecular medicine, 48, 5. CAPN3: A muscle‑specific calpain with an important role in the pathogenesis of diseases (Review)

Brain communications, 3, 4. AAV1.NT-3 gene therapy in a CMT2D model: phenotypic improvements in Gars(P278KY/+) mice

CNS neuroscience & therapeutics, 27, 10. A novel frameshift ACTN2 variant causes a rare adult-onset distal myopathy with multi-minicores

Molecular therapy. Methods & clinical development, 22. Systemic delivery of AAVrh74.tMCK.hCAPN3 rescues the phenotype in a mouse model for LGMD2A/R1

Cell reports, 35, 6. A high-throughput genome-wide RNAi screen identifies modifiers of survival motor neuron protein

Neuromuscular disorders : NMD, 31, 5. Clinical and genetic characteristics of Chinese patients with reducing body myopathy

Gene therapy AAV1.NT-3 gene therapy for X-linked Charcot-Marie-Tooth neuropathy type 1

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

BMC musculoskeletal disorders, 22, 1. Polyglucosan body myopathy 1 may cause cognitive impairment: a case report from China

Journal of thoracic disease, 12, 4. Perioperative outcomes and mid-term effects in performing video-assisted thoracoscopic extended thymectomy for myasthenia gravis: subxiphoid versus right thoracic approaches

Medicine, 99, 17. Acupuncture for ocular myasthenia gravis: A protocol for systematic review and meta-analysis

Acta neuropathologica communications, 8, 1. CMT2Q-causing mutation in the Dhtkd1 gene lead to sensory defects, mitochondrial accumulation and altered metabolism in a knock-in mouse model

Chinese medical journal A case of de novo dynamin 2-related centronuclear myopathy with electrical but not clinical myotonia