Yue-Bei Luo

发表

Primary over‐expression of AβPP in muscle does not lead to the development of inclusion body myositis in a new lineage of the MCK‐AβPP transgenic mouse

F. Mastaglia, S. Wilton, S. Fletcher, 2013, International journal of experimental pathology.

Findings of limb-girdle muscular dystrophy R7 telethonin-related patients from a Chinese neuromuscular center

Huan Yang, Yue-Bei Luo, Kun-yun Huang, 2022, neurogenetics.

Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center

Huan Yang, Yue-Bei Luo, Yuyao Peng, 2020, Frontiers in Neurology.

Investigation of splicing changes and post-translational processing of LMNA in sporadic inclusion body myositis.

F. Mastaglia, S. Wilton, S. Fletcher, 2013, International journal of clinical and experimental pathology.

An analysis of the sensitivity and specificity of MHC-I and MHC-II immunohistochemical staining in muscle biopsies for the diagnosis of inflammatory myopathies

F. Mastaglia, P. R. Cruz, Yue-Bei Luo, 2014, Neuromuscular Disorders.

Investigation of age-related changes in LMNA splicing and expression of progerin in human skeletal muscles.

F. Mastaglia, S. Wilton, S. Fletcher, 2013, International journal of clinical and experimental pathology.

Skeletal muscle increases FGF21 expression in mitochondrial disorders to compensate for energy metabolic insufficiency by activating the mTOR-YY1-PGC1α pathway.

Chuanzhu Yan, Jingwen Xu, Wei Li, 2015, Free radical biology & medicine.

Clinicopathological features of titinopathy from a Chinese neuromuscular center

Huan Yang, Yue-Bei Luo, Kun-yun Huang, 2021, Neuropathology : official journal of the Japanese Society of Neuropathology.

Integrating 16S RRNA gene sequencing and metabolomics to evaluate the association between gut microbiota and serum metabolites in patients with myositis

Zhaohui Luo, Huan Yang, Yue-Bei Luo, 2022, Journal of applied microbiology.

Revisiting Pathological Classification Criteria for Adult Idiopathic Inflammatory Myopathies: In-Depth Analysis of Muscle Biopsies and Correlation Between Pathological Diagnosis and Clinical Manifestations

Jian-Qiang Lu, T. Dai, Chuanzhu Yan, 2018, Journal of neuropathology and experimental neurology.

MiR-15a contributes abnormal immune response in myasthenia gravis by targeting CXCL10.

Hao Zhou, Zhaohui Luo, Q. Zeng, 2016, Clinical immunology.

Investigation of adult‐onset multiple acyl‐CoA dehydrogenase deficiency associated with peripheral neuropathy

Huan Yang, Yue-Bei Luo, Kun-yun Huang, 2020, Neuropathology : official journal of the Japanese Society of Neuropathology.

Betaine attenuates LPS-induced downregulation of Occludin and Claudin-1 and restores intestinal barrier function

Yulong Yin, Xiaoping Yang, Caimei He, 2019, BMC Veterinary Research.

The association between myositis-specific autoantibodies and muscle pathologies in idiopathic inflammatory myopathies

Huan Yang, Yue-Bei Luo, Qiuxiang Li, 2020, Clinical Rheumatology.

Normal and aberrant splicing of LMNA

F. Mastaglia, S. Wilton, Yue-Bei Luo, 2014, Journal of Medical Genetics.

Hepatitis B virus mutation may play a role in hepatocellular carcinoma recurrence: A systematic review and meta‐regression analysis

G. Gong, Yue-Bei Luo, Hua-ying Zhou, 2015, Journal of gastroenterology and hepatology.

Findings of limb-girdle muscular dystrophy R7 telethonin-related patients from a Chinese neuromuscular center

Han Yang, Yue-Bei Luo, Kun-yun Huang, 2022, neurogenetics.

Autoimmune Channelopathies at Neuromuscular Junction

Huan Yang, Yue-Bei Luo, Kun-yun Huang, 2019, Front. Neurol..

Dermatomyositis, polymyositis and immune-mediated necrotising myopathies.

F. Mastaglia, Yue-Bei Luo, 2015, Biochimica et biophysica acta.

IFNA-AS1 regulates CD4+ T cell activation in myasthenia gravis though HLA-DRB1.

Liqun Xu, Zhaohui Luo, Huan Yang, 2017, Clinical immunology.

Case Report: The Neuromusclar Triad of Immune Checkpoint Inhibitors: A Case Report of Myositis, Myocarditis, and Myasthenia Gravis Overlap Following Toripalimab Treatment

Q. Zeng, Weiting Tang, Yue-Bei Luo, 2021, Frontiers in Cardiovascular Medicine.

Antisense Oligonucleotide Induction of Progerin in Human Myogenic Cells

F. Mastaglia, S. Wilton, S. Fletcher, 2014, PloS one.

Clinicopathological‐genetic features of congenital myasthenic syndrome from a Chinese neuromuscular centre

Huan Yang, Yue-Bei Luo, Kun-yun Huang, 2022, Journal of cellular and molecular medicine.

Expanding the clinicopathological-genetic spectrum of glycogen storage disease type IXd by a Chinese neuromuscular center

Hua Yang, Yue-Bei Luo, Kun-yun Huang, 2022, Frontiers in Neurology.

Idiopathic inflammatory myopathies with anti-mitochondrial antibodies: Clinical features and treatment outcomes in a Chinese cohort

Yuan Sun, T. Dai, Chuanzhu Yan, 2019, Neuromuscular Disorders.

Novel Mitochondrial C15620A Variant may Modulate the Phenotype of Mitochondrial G11778A Mutation in a Chinese Family with Leigh Syndrome

Fuchen Liu, Chuanzhu Yan, Yuying Zhao, 2014, NeuroMolecular Medicine.

Pharmacological Strategy for Congenital Myasthenic Syndrome with CHRNE Mutations: A Meta-Analysis of Case Reports

Huan Yang, Yue-Bei Luo, Kun-yun Huang, 2020, Current neuropharmacology.

Expanding the clinicopathological‐genetic spectrum of GNE myopathy by a Chinese neuromuscular centre

Huan Yang, Yue-Bei Luo, Kun-yun Huang, 2021, Journal of cellular and molecular medicine.

Complement-mediated muscle cell lysis: A possible mechanism of myonecrosis in anti-SRP associated necrotizing myopathy (ASANM)

F. Mastaglia, S. Wilton, C. Mitrpant, 2013, Journal of Neuroimmunology.

Biomarker Studies in Multiple Sclerosis: From Proteins to Noncoding RNAs

Zhaohui Luo, Huan Yang, Yue-Bei Luo, 2014, Neurochemical Research.

Cylindrical Spirals in Skeletal Muscles Originate From the Longitudinal Sarcoplasmic Reticulum

Jian-Qiang Lu, Dandan Zhao, Wei Li, 2016, Journal of Neuropathology and Experimental Neurology.

A new multiparameter integrated MELD model for prognosis of HBV-related acute-on-chronic liver failure

G. Gong, Yue-Bei Luo, Ya Xie, 2016, Medicine.

Twinkle mutations in two Chinese families with autosomal dominant progressive external ophthalmoplegia

P. Lin, Chuanzhu Yan, Yuying Zhao, 2014, Neurological Sciences.

Biomarker Studies in Multiple Sclerosis: From Proteins to Noncoding RNAs

Han Yang, Y. Luo, Zhaohui Luo, 2014, Neurochemical Research.

Limb-girdle Muscular Dystrophy Type 2A with Muscular Eosinophilic Infiltration in a Chinese Patient

Huan Yang, Yue-Bei Luo, Qiuxiang Li, 2018, Chinese medical journal.

Circulating miRNA-199a and miRNA-122 Levels as Potential Diagnostic and Prognostic Biomarkers for Hepatocellular Carcinoma.

Yanfeng Lin, Yue-Bei Luo, Min Chen, 2020, Annals of clinical and laboratory science.

Novel Mitochondrial C15620A Variant may Modulate the Phenotype of Mitochondrial G11778A Mutation in a Chinese Family with Leigh Syndrome

Fuchen Liu, Chuanzhu Yan, Yuying Zhao, 2013, NeuroMolecular Medicine.