Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Dan Na Chen"'
Autor:
Meichao Men, Dan‐Na Chen, Jia‐Da Li, Xinying Wang, Wang Zeng, Fang Jiang, Ruizhi Zheng, Wenting Dai
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background Isolated hypogonadotropic hypogonadism (IHH) is a clinical syndrome described by failure of gonadal function secondary to defects on the synthesis, secretion, or action of the gonadotropin‐releasing hormone (GnRH). The secreted
Externí odkaz:
https://doaj.org/article/7380da4e170b472ea1731bbcf0fa60da
Publikováno v:
Guoji Yanke Zazhi, Vol 19, Iss 3, Pp 434-437 (2019)
AIM: To compare the efficacy of intravitreal injection of ranibizumab plus low power 532 laser versus 532 laser alone for treating retinal vein occlusion(RVO)with macular edema complication.METHODS: Retrospective study of 48 patients diagnosed RVO co
Externí odkaz:
https://doaj.org/article/c10219d88d6d4044a0fd0b3d68e4e222
Autor:
Zhi-Ming Shao, Xin Hu, Ling Yao, Hong Ling, Feng Qiao, Shan Li, Li Chen, Dan-Na Chen, Chen Xia, Zhi-Gang Cao, Chuan-Gui Song, Fu-Gui Ye
Supplementary Tables S1-S5: Final concentrations of gemcitabine in the culture medium corresponding to each cycle (S1); Nucletide sequences of PCR primers used for amplification of ALDH1A3, CDA, DST, FMO3, MAOA, PTHLH, XDH, UGT1A1, hENT1, NT5C, DCK,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59717e2f8e366104601edd1dda674eb4
https://doi.org/10.1158/0008-5472.22406621.v1
https://doi.org/10.1158/0008-5472.22406621.v1
Autor:
Zhi-Ming Shao, Xin Hu, Ling Yao, Hong Ling, Feng Qiao, Shan Li, Li Chen, Dan-Na Chen, Chen Xia, Zhi-Gang Cao, Chuan-Gui Song, Fu-Gui Ye
There has been little study of how the evolution of chemoresistance in cancer affects other aspects of disease pathogenesis. Here, we show that an important chemoresistance axis driven by cytidine deaminase (CDA) also acts to suppress cell-cycle prog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2384c998a3c39fe71964aaab1ba45bb
https://doi.org/10.1158/0008-5472.c.6507131.v1
https://doi.org/10.1158/0008-5472.c.6507131.v1
Autor:
Zhi-Ming Shao, Xin Hu, Ling Yao, Hong Ling, Feng Qiao, Shan Li, Li Chen, Dan-Na Chen, Chen Xia, Zhi-Gang Cao, Chuan-Gui Song, Fu-Gui Ye
Supplementary Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac039331e21420c0a0e07e127390340
https://doi.org/10.1158/0008-5472.22406624
https://doi.org/10.1158/0008-5472.22406624
Autor:
Zhi-Ming Shao, Xin Hu, Ling Yao, Hong Ling, Feng Qiao, Shan Li, Li Chen, Dan-Na Chen, Chen Xia, Zhi-Gang Cao, Chuan-Gui Song, Fu-Gui Ye
Supplementary Figures S1-S6: qPCR analysis of selected genes was performed in MDA-231-Gem and parental MDA-231 cells (S1); qPCR analysis of 7 genes in the gemcitabine metabolism pathway was performed in MDA-231-Gem and parental MDA-231 cells (S2); Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31173f8ce17df9d209d9776533577485
https://doi.org/10.1158/0008-5472.22406627
https://doi.org/10.1158/0008-5472.22406627
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
RNF216, encoding an E3 ubiquitin ligase, has been identified as a causative gene for Gordon Holmes syndrome, characterized by ataxia, dementia, and hypogonadotropic hypogonadism. However, it is still elusive how deficiency in RNF216 leads to hypogona
Externí odkaz:
https://doaj.org/article/73fb1073af6d4388984d1542ed0bafc6
Autor:
Jiayu Wu, Zhenghuan Fang, Xinying Wang, Wang Zeng, Yaguang Zhao, Fang Jiang, Dan-Na Chen, Ruizhi Zheng, Jinchen Li, Meichao Men, Jia-Da Li
Publikováno v:
Hormone Research in Paediatrics. 95:384-392
Introduction: Idiopathic hypogonadotropic hypogonadism (IHH) is a rare reproductive disorder resulting from gonadotropin-releasing hormone (GnRH) deficiency. However, in only approximately half of patients with IHH is it possible to identify a likely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c784e1e33ee73c950650505b2ad82633
https://doi.org/10.1159/000525769
https://doi.org/10.1159/000525769
Autor:
Fang Jiang, Meichao Men, Jia-Da Li, Dan-Na Chen, Yaguang Zhao, Jiayu Wu, Wenting Dai, Ruizhi Zheng
Publikováno v:
Clinical Genetics. 97:696-703
Isolated hypogonadotropic hypogonadism (IHH) is a rare disorder characterized by impaired sexual development and infertility, caused by the deficiency of hypothalamic gonadotropin-releasing hormone neurons. IHH is named Kallmann's syndrome (KS) or no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e4264c530bdc5d919b152b4b91738af
https://doi.org/10.1111/cge.13723
https://doi.org/10.1111/cge.13723
Autor:
Jiayu, Wu, Zhenghuan, Fang, Xinying, Wang, Wang, Zeng, Yaguang, Zhao, Fang, Jiang, Dan-Na, Chen, Ruizhi, Zheng, Jinchen, Li, Meichao, Men, Jia-Da, Li
Publikováno v:
Hormone research in paediatrics. 95(4)
Idiopathic hypogonadotropic hypogonadism (IHH) is a rare reproductive disorder resulting from gonadotropin-releasing hormone (GnRH) deficiency. However, in only approximately half of patients with IHH is it possible to identify a likely molecular dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a4b978a7aa94031ea71abad6d6dfe31
https://pubmed.ncbi.nlm.nih.gov/35797970
https://pubmed.ncbi.nlm.nih.gov/35797970