Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ming-Fu Ma"'
Publikováno v:
International Journal of Ophthalmology, Vol 9, Iss 5, Pp 650-654 (2016)
AIM: To identify disease-causing mutation in a congenital cataract family using enrichment of targeted genes combined with next-generation sequencing. METHODS: A total of 371 known genes related to inherited eye diseases of the proband was selected
Externí odkaz:
https://doaj.org/article/fe3e5cd6aceb43d1ad804f82cfaf083a
Autor:
Dian Wang, Lian-Bing Li, Zhi-Wei Hou, Xiang-Jin Kang, Qing-Dong Xie, Xiao-jun Yu, Ming-Fu Ma, Bo-Lu Ma, Zheng-Song Wang, Yong Lei, Tian-Hua Huang
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e28586 (2011)
Complete understanding of the route of HIV-1 transmission is an important prerequisite for curbing the HIV/AIDS pandemic. So far, the known routes of HIV-1 transmission include sexual contact, needle sharing, puncture, transfusion and mother-to-child
Externí odkaz:
https://doaj.org/article/6e07d66a127d4209b293074b4a18e339
Autor:
Junlin He, Ming-fu Ma, Xi Lan, Hui-Jie Zhang, Yingxiong Wang, Xueqing Liu, Li-Juan Fu, Lian-bing Li, Yubin Ding, Jun Zhang, Xue Zhang, Xuemei Chen
Publikováno v:
Oncotarget
// Xi Lan 1 , Li-Juan Fu 1, 2 , Jun Zhang 3 , Xue-Qing Liu 1 , Hui-Jie Zhang 4 , Xue Zhang 1 , Ming-Fu Ma 5 , Xue-Mei Chen 1 , Jun-Lin He 1 , Lian-Bing Li 5 , Ying-Xiong Wang 1 and Yu-Bin Ding 1 1 Department of Reproductive Biology, School of Public
Publikováno v:
International Journal of Ophthalmology, Vol 9, Iss 5, Pp 650-654 (2016)
Aim To identify disease-causing mutation in a congenital cataract family using enrichment of targeted genes combined with next-generation sequencing. Methods A total of 371 known genes related to inherited eye diseases of the proband was selected and
Autor:
Ming Fu Ma, Yuan Fu Zhang
Publikováno v:
Advanced Materials Research. :3038-3041
Logging data, as representations of lithology and physical properties of stratum, hold abundant information related to sedimentary cycles with high vertical resolution. The use of various methods to extract and analyze corresponding information will
Autor:
Ming-fu Ma, Lian-bing Li, Shuqun Cheng, Yubing Ding, Yingxiong Wang, Yinyin Xia, Xuemei Chen, Junlin He, Xueqing Liu
Publikováno v:
Biochimica et biophysica acta. 1846(1)
The racial/ethnic disparities in DNA methylation patterns indicate that molecular markers may play a role in determining the individual susceptibility to diseases in different ethnic groups. Racial disparities in DNA methylation patterns have been id
Autor:
Shuqun Cheng, Yu‑Bing Ding, Yinyin Xia, Jun Lin He, Lian‑Bing Li, Ying Xiong Wang, Ming‑Fu Ma, Xue Qing Liu, Xue‑Mei Chen
Publikováno v:
Molecular medicine reports. 9(5)
Trisomy 21 is a chromosomal condition caused by the presence of all or part of an extra 21st chromosome. There has been limited research into the DNA methylation status of CpG islands (CGIs) in trisomy 21, therefore, exploring the DNA methylation sta
Autor:
Hua-Qiong, Bao, Xin-Hu, Li, Ni-Ya, Zhou, Ya-Fei, Li, Min, Cai, Lian-Bing, Li, Ming-Fu, Ma, Chuan-Hai, Li
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 17(4)
To investigate the quality and spatial distribution features of semen and to evaluate the reproductive health of the males in the Chongqing section of the Three-Gorge Reservoir area.We collected semen samples by masturbation after 2 -7 days of abstin
Autor:
Lian-Bing, Li, Yan-Kai, Xia, Xin-Sheng, Li, Jing, Lü, Ming-Fu, Ma, Ling, Song, Yuan, Ji, Ji-Gao, Yang, Tian-Feng, Zhang, Xiao-Xing, Chen, Ying, Rong, Le-Tian, Zhao
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 14(3)
To analyze the numerical aberration of chromosome X, Y and 18 in the spermatozoa of asthenospermia patients by triple-color fluorescence in situ hybridization.The experiment included 10 asthenospermia patients and 5 healthy men with normal semen qual
Autor:
YIN-YIN XIA, YU-BING DING, XUE-QING LIU, XUE-MEI CHEN, SHU-QUN CHENG, LIAN-BING LI, MING-FU MA, JUN-LIN HE, YING-XIONG WANG
Publikováno v:
Molecular Medicine Reports; 2014, Vol. 9 Issue 5, p1681-1688, 8p