Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Shan-Wei Feng"'
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
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:
Jing LI, Cheng ZHANG, Yi⁃xin ZHANG, Shan⁃wei FENG, Juan YANG, Ji⁃qing CAO, Chang⁃shun YU, Ya⁃qin LI, Yan⁃yun WANG, Fei CHEN, Jie KONG, Min⁃ying ZHENG, Ling LIAO
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 12, Iss 3, Pp 282-287 (2012)
Objective To explore the clinical features, genetic characters and the importance of prenatal diagnosis in spinocerebellar ataxia 3 (SCA3) patients. Methods SCA3/ATXN3 gene was determined by using PCR and segmental analysis techniques in 2 patients a
Externí odkaz:
https://doaj.org/article/8976d63864d64f41bb273f938c0e28a5
Autor:
Ya⁃qin LI, Ji⁃qing CAO, Juan YANG, Bao⁃feng ZHANG, Shan⁃wei FENG, Yan⁃yun WANG, Yao ZHANG, Fei CHEN, Jie KONG, Min⁃ying ZHENG, Xu ZHANG, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 12, Iss 3, Pp 300-306 (2012)
Objective In order to understand tuberous sclerosis complex better, the clinical manifestation, imaging characteristics, and genetic characteristics of tuberous sclerosis complex from 3 pedigrees were investigated. Methods The clinical data of patien
Externí odkaz:
https://doaj.org/article/d8a74e925c86427eb16ca5d3e02e4501
Autor:
Jie Kong, Juan Yang, Yaqin Li, Shan-wei Feng, Hui-li Zhang, Liqing Yang, Cheng Zhang, Ji-qing Cao, Yuling Zhu, Yingyin Liang, Jia Geng
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e3d742461a3ac4cade6c5bc23be2b87
http://www.nrronline.org/article.asp?issn=1673-5374
http://www.nrronline.org/article.asp?issn=1673-5374
Publikováno v:
Biochemical and Biophysical Research Communications. 419:1-6
Duchenne muscular dystrophy is the most prevalent inheritable muscle disease. Transplantation of autologous stem cells with gene direction is an ideal therapeutic approach for the disease. The current study aimed to investigate the restoration of myo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413fb9611bc1819f8288a8cbec66b439
https://doi.org/10.1016/j.bbrc.2012.01.029
https://doi.org/10.1016/j.bbrc.2012.01.029
Publikováno v:
Cytotherapy. 9:44-52
BackgroundThe value of transplantation of BM stem cells in aged (12-month-old) mdx was evaluated because it is thought to be a more ideal model for studying the praxiology of Duchenne muscular dystrophy (DMD). The possible mechanisms of stem cell dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aeab9b9d5a0ac173cb9de037d823f72
https://doi.org/10.1080/14653240601114815
https://doi.org/10.1080/14653240601114815
Autor:
Meijuan Yu, Weihua Li, S.-N. Zhou, Chao Zhang, Huabing Huang, Chang Zhou, Shan-wei Feng, Y.-M. Xie, Cuiping Zhao, Yanchang Shang, Y.-H. Wang
Publikováno v:
Cytotherapy. 9:414-426
Amyotrophic lateral sclerosis (ALS) is a progressive, lethal, neurodegenerative disease, currently without any effective therapy. Multiple advantages make mesenchymal stromal cells (MSC) a good candidate for cellular therapy in many intractable disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f285d8256aa5c9bdedc6f94a62ddafbd
https://doi.org/10.1080/14653240701376413
https://doi.org/10.1080/14653240701376413
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 30(1)
To explore the characteristics of DNA mutations underlying Duchenne muscular dystrophy and provide prenatal diagnosis.Multiplex ligation-dependent probe amplification (MLPA) and denaturing high performance liquid chromatography (DHPLC) were applied f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed480c2c8308f395ba1f0cb83b6fdbc3
https://pubmed.ncbi.nlm.nih.gov/23450476
https://pubmed.ncbi.nlm.nih.gov/23450476