Zobrazeno 1 - 10 of 108 pro vyhledávání: '"Chuanqiang Pu"'
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Akademický článek
Hemojuvelin is a novel suppressor for Duchenne muscular dystrophy and age‐related muscle wasting
Autor: Peng Zhang, Jian He, Fei Wang, Jing Gong, Lu Wang, Qian Wu, Wenjiong Li, Hongju Liu, Jing Wang, Kunshan Zhang, Mao Li, Xusheng Huang, Chuanqiang Pu, Ying Li, Fengjie Jiang, Fudi Wang, Junxia Min, Xiaoping Chen
Publikováno v: Journal of Cachexia, Sarcopenia and Muscle, Vol 10, Iss 3, Pp 557-573 (2019)
Abstract Background Muscle wasting occurs in response to various physiological and pathological conditions, including ageing and Duchenne muscular dystrophy (DMD). Transforming growth factor‐β1 (TGF‐β1) contributes to muscle pathogenesis in eld
Externí odkaz: https://doaj.org/article/eb74dc2601d9463aac8b59fafc111de6
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2
Muscular pathological features in patients with myasthenia gravis
Autor: Yutong Zhang, Ying Lin, Lingya Qiao, Qiang Shi, Chuanqiang Pu, Rui Ban
Publikováno v: Clinical Neuropathology. 40:319-327
Objective To analyze muscle histopathology of myasthenia gravis (MG) patients and further explore the underlying mechanism comparing with previous literature. Materials and methods We analyzed the clinicopathological features of 8 MG patients who had
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c01c6d28ba04a574cb80abbc9606579e
https://doi.org/10.5414/np301382
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4
Data-independent acquisition-based quantitative proteomic analysis of m.3243AG MELAS reveals novel potential pathogenesis and therapeutic targets
Autor: Xueli Chang, Zhaoxu Yin, Wei Zhang, Jiaying Shi, Chuanqiang Pu, Qiang Shi, Juan Wang, Jing Zhang, Li Yan, Wenqu Yang, Junhong Guo
Publikováno v: Medicine. 101(41)
The pathogenesis of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke like episodes (MELAS) syndrome has not been fully elucidated. The m.3243A G mutation which is responsible for 80% MELAS patients affects proteins with undetermined
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d05c992b9b67678e8c8e2e74240b014
https://pubmed.ncbi.nlm.nih.gov/36254078
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6
Clinico-pathological features and mutational spectrum of 16 nemaline myopathy patients from a Chinese neuromuscular center
Autor: Huifang Wang, Chuanqiang Pu, Ke Li, Xi Yin, Zhenfu Wang
Publikováno v: Acta Neurologica Belgica. 122:631-639
Nemaline myopathy (NM) is a congenital myopathy of great heterogeneity, characterized by the presence of rods in the cytoplasm of muscle fibers. The samples of 16 nemaline myopathy patients diagnosed by characteristically pathological features went t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e930048a4261e46212a32f8b42b1068c
https://doi.org/10.1007/s13760-020-01542-9
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7
Muscular pathological features in patients with Lambert-Eaton myasthenic syndrome associated with small cell lung carcinoma
Autor: Yutong Zhang, Chuanqiang Pu, Qiang Shi, Rui Ban
Publikováno v: Clinical Neuropathology. 40:93-97
Aims Lambert-Eaton myasthenic syndrome (LEMS) is a kind of autoimmune disease of the neuromuscular junction that is often misdiagnosed as a peripheral nerve disease or myopathy. For some difficult cases, muscle biopsy examination is useful for differ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b0f799e9942d77d0e307c95dea07878
https://doi.org/10.5414/np301282
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10
A novel homozygous mutation in ATP13A2 gene causing pure hereditary spastic paraplegia
Autor: Qiang Shi, Fang Fang, Rui Ban, Chuanqiang Pu
Publikováno v: Parkinsonism & Related Disorders. 86:58-60
SPG78 is a subtype of hereditary spastic paraplegia(HSP) caused by ATP13A2 gene mutations. SPG78 was reported as complicated HSP in several cases, but was never associated with pure HSP. Here we report the first Chinese patient carrying a novel homoz
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::21d9f5b59817b195e8f5145626b0c424
https://doi.org/10.1016/j.parkreldis.2021.03.020
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