Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Ying-yin LIANG"'
Autor:
Ying-yin Liang, Lu-qi Yan, Ming-hui Tan, Gang-hui Li, Jian-hao Fang, Jie-ying Peng, Kun-tai Li
Publikováno v:
Frontiers in Microbiology, Vol 13 (2022)
Chitin deacetylase (CDA) is a chitin degradation enzyme that catalyzes the conversion of chitin to chitosan by the deacetylation of N-acetyl-D-glucosamine residues, playing an important role in the high-value utilization of waste chitin. The shells o
Externí odkaz:
https://doaj.org/article/735b93e1a52d446c964f1afd1d89a19d
Autor:
Yu-ling ZHU, Huan LI, Zhi-liang PAN, Ying-yin LIANG, Jing LI, Ruo-jie HE, Jin-fu LIN, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 18, Iss 8, Pp 582-588 (2018)
Objective To explore the clinical features and genetic characteristics of Charcot-Marie-Tooth disease type 4B2 (CMT4B2) patients. Methods MTMR13/SBF2 gene mutations were screened by target region capture sequencing among a CMT4B2 Chinese family which
Externí odkaz:
https://doaj.org/article/0573d19af11c4fcbbe0520dca4e819ec
Autor:
Ying-yin LIANG, Gui-dian LI, Rong-xing HE, Wei-wei QI, Xue XU, Xiang-xue ZHOU, Rong-lan1 ZHU, Lu YAO, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 18, Iss 7, Pp 501-505 (2018)
Objective To summarize the characteristics of fatty infiltration and edema of muscle MRI in Duchenne muscular dystrophy (DMD) patients. Methods A total of 70 DMD patients underwent Clinical Functional Scale and muscle MRI of the pelvic (gluteus maxim
Externí odkaz:
https://doaj.org/article/edc428847eab4ca8b871a09e63aa2a3b
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 17, Iss 8, Pp 609-615 (2017)
Objective To study the characteristics and diagnosis of limb-girdle muscular dystrophy type 2D (LGMD2D). Methods The clinical characteristics, EMG, muscle MRI and muscle pathological studies of 2 female patients in a family with LGMD2D were analyzed.
Externí odkaz:
https://doaj.org/article/c8c6ee7415a7435495fbfde6bac23495
Autor:
Ji-qing Cao, Ying-yin Liang, Ya-qin Li, Hui-li Zhang, Yu-ling Zhu, Jia Geng, Li-qing Yang, Shan-wei Feng, Juan Yang, Jie Kong, Cheng Zhang
Publikováno v:
Neural Regeneration Research, Vol 11, Iss 10, Pp 1638-1643 (2016)
Adipose-derived stem cells have been shown to promote peripheral nerve regeneration through the paracrine secretion of neurotrophic factors. However, it is unclear whether these cells can promote myogenic differentiation in muscular dystrophy. Adipos
Externí odkaz:
https://doaj.org/article/389b50d152e84bfa895a42550bca8a41
Autor:
Ji-qing CAO, Juan YANG, Ya-qin LI, Shan-wei FENG, Fei CHEN, Hui ZHENG, Ying-yin LIANG, Bao-jian ZHAO, Xu ZHANG, Hui-li ZHANG, Yu-ling ZHU, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 15, Iss 6, Pp 442-447 (2015)
Background DMD gene point mutation, mainly nonsense mutation, always cause the most severe Duchenne muscular dystrophy (DMD). However, we also observed some cases of Becker muscular dystrophy (BMD) carrying DMD point mutation. This paper aims to expl
Externí odkaz:
https://doaj.org/article/50a62ecc4b2d4cb3a357677a35a5ef25
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 15, Iss 6, Pp 437-441 (2015)
Objective Use T2 mapping to evaluate the fatty infiltration of thigh muscles in Duchenne muscular dystrophy (DMD) patients, so as to analyze the value of T2 mapping and T2 relaxation time in the diagnosis of DMD. Methods Sixteen DMD patients who were
Externí odkaz:
https://doaj.org/article/be7ee3b57b174b50a149b375eb4cf886
Autor:
Ji-qing CAO, Cheng ZHANG, Ya-qin LI, Juan YANG, Ying-yin LIANG, Shan-wei FENG, Xu ZHANG, Jing LI, Hui-li ZHANG, Yu-ling ZHU, Jia GENG, Li-qing YANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 14, Iss 6, Pp 479-484 (2014)
Objective The clinical manifestation and electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation of riboflavin-responsive lipid storage myopathy were analyzed for early diagnosis and treatment.mutation of riboflavin-responsive lipid storag
Externí odkaz:
https://doaj.org/article/fe0465402f494326bae6a2d1de7d572d
Autor:
Juan YANG, Ji-qing CAO, Zhen-hua LIU, Yi-xin ZHAN, Ying-yin LIANG, Gui-ling MO, Ya-qin LI, Yi-ming SUN, Min-zi LI, Jing LI, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 14, Iss 5, Pp 405-410 (2014)
Objective In order to make a well understanding on glycogen storage disease typeⅡ (GSDⅡ), this paper explored clinical features and genetic analysis of 7 patients with late-onset glycogen storage disease typeⅡ. Methods Clinical data of 7 patien
Externí odkaz:
https://doaj.org/article/e6308a0d0ff94917b03389c7e0c5554b
Autor:
Lin-ru Huang, Xiao-ning Ling, Shuai-ying Peng, Ming-hui Tan, Lu-qi Yan, Ying-yin Liang, Gang-hui Li, Kun-tai Li
Publikováno v:
World Journal of Microbiology and Biotechnology. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd4a4e3af02538001e1541698950b123
https://doi.org/10.1007/s11274-023-03643-y
https://doi.org/10.1007/s11274-023-03643-y