Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Gong-Lu Li"'
Autor:
Shi-Fei Li, Xiu-Yi Wang, Gong-Lu Li, Ying-Ying Jiao, Wen-Hao Wang, Xing-Kang Wu, Li-Wei Zhang
Publikováno v:
Phytochemistry. 203
Developing highly effective HIV latency-reversing agent is an inportmant approach for the treatment of AIDS via the "shock and kill" of latent HIV. In this study, two unreported modified daphnane-type diterpenes (chamaedaphnelide A and epi-chamaedaph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b8781e0d2bfb4b9d79ebbbf85c0a734
https://pubmed.ncbi.nlm.nih.gov/36027969
https://pubmed.ncbi.nlm.nih.gov/36027969
Autor:
Hong-Fu Li, Yu-Lan Chen, Ling Zhuang, Dian-Fu Chen, Hua-Zhen Ke, Wen-Jiao Luo, Gong-Lu Liu, Sheng-Nan Wu, Wen-Hao Zhou, Zhi-Qi Xiong, Zhi-Ying Wu
Publikováno v:
Cell Discovery, Vol 7, Iss 1, Pp 1-4 (2021)
Externí odkaz:
https://doaj.org/article/2ca3f68050574d9285259ab5681da437
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-5 (2021)
Abstract Sorbitol dehydrogenase gene (SORD) has been identified as a novel causative gene of recessive forms of hereditary neuropathy, including Charcot–Marie–Tooth disease type 2 and distal hereditary motor neuropathy (dHMN). Our findings reveal
Externí odkaz:
https://doaj.org/article/16f9d9bdfe284a10959058de45bf4c41
Autor:
Hong-Fu Li, Yu-Lan Chen, Ling Zhuang, Dian-Fu Chen, Hua-Zhen Ke, Wen-Jiao Luo, Gong-Lu Liu, Sheng-Nan Wu, Wen-Hao Zhou, Zhi-Qi Xiong, Zhi-Ying Wu
Publikováno v:
Cell Discovery, Vol 7, Iss 1, Pp 1-1 (2021)
Externí odkaz:
https://doaj.org/article/b370c4bb050f420094cfd2942ae7f1c5
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 19, Pp 2273-2278 (2017)
Background: Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive neuromuscular diseases resulting from dystrophin (DMD) gene mutations. It has been known that the carrier of DMD mutations may also have symptoms
Externí odkaz:
https://doaj.org/article/d7d6df49752e4c94a628bfe1b71bf1f7
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 9, Pp 1017-1021 (2016)
Background: Paroxysmal kinesigenic dyskinesia (PKD) is the most common subtype of paroxysmal dyskinesias and is caused by mutations in PRRT2 gene. The majority of familial PKD was identified to harbor PRRT2 mutations. However, over two-third of spora
Externí odkaz:
https://doaj.org/article/488822fc8dae4d869d710cc419199b48