Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yue-Qiang Song"'
Autor:
Yan-Kun Sha, Yan-Wei Sha, Lu Ding, Wei-Wu Liu, Yue-Qiang Song, Jin Lin, Xue-Mei He, Ping-Ping Qiu, Ling Zhang, Ping Li
Publikováno v:
International Journal of Fertility and Sterility, Vol 9, Iss 4, Pp 574-580 (2016)
21-hydroxylase deficiency (21-OHD) caused congenital adrenal hyperplasia (CAH) is a group of autosomal recessive genetic disorders resulting from mutations in genes involved with cortisol (CO) synthesis in the adrenal glands. Testicular adrenal rest
Externí odkaz:
https://doaj.org/article/4c3ad6474db449338e1ddbbe6e1e4560
Autor:
Xiao-Qin He, Yue-Qiang Song, Rui Liu, Yu Liu, Fei Zhang, Zhen Zhang, Yu-Ting Shen, Lin Xu, Ming-Huang Chen, Ya-Long Wang, Bai-Hui Xu, Xiang-Jun Yang, Hai-Long Wang
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0157197 (2016)
Axin-1, a negative regulator of Wnt signaling, is a versatile scaffold protein involved in centrosome separation and spindle assembly in mitosis, but its function in mammalian oogenesis remains unknown. Here we examined the localization and function
Externí odkaz:
https://doaj.org/article/f6c983375346413d84057c104e108560
Autor:
Yan-Wei Sha, Yan-Kun Sha, Lu Ding, Shao-Bin Lin, Zhi-Yong Ji, Xu Wang, Yue-Qiang Song, Ping Li
Publikováno v:
Asian Journal of Andrology, Vol 19, Iss 6, Pp 721-722 (2017)
Externí odkaz:
https://doaj.org/article/069f8d826df847c8b9534fb24a9716bc
Autor:
Hui Fu, Si-guang Li, Ke-ping Hu, Ying Zhao, Liang Le, Xue Bai, Yue-qiang Song, Xinsheng Nan, Li-xin Qi
Publikováno v:
Chinese Herbal Medicines. 11:39-44
Objective To investigate the effect of IMPX977 on MeCP2 targeted-genes and the feasibility of IMPX977 acting as a therapeutic candidate drug for Rett syndrome by genomewide transcription profiling. Methods Rats' cortex of control group, IMPX977-treat
Autor:
Yanwei Sha, Zhi-Yong Ji, Shaobin Lin, Xu Wang, Qing Zhang, Yan-Kun Sha, Ping Li, Yue-Qiang Song, Honggen Ouyang, Chong Shi, Lu Ding, Lin Shao
Publikováno v:
Annals of Human Genetics. 81:91-97
Robertsonian translocation (RT) is a common cause for male infertility, recurrent pregnancy loss, and birth defects. Studying meiotic recombination in RT-carrier patients helps decipher the mechanism and improve the clinical management of infertility
Autor:
Yu-Ting Shen, Yu Liu, Lin Xu, Yue-Qiang Song, Ming-Huang Chen, Rui Liu, Xiang-Jun Yang, Hai-Long Wang, Ya-Long Wang, Bai-Hui Xu, Fei Zhang, Xiao-Qin He, Zhen Zhang
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0157197 (2016)
PLoS ONE
PLoS ONE
Axin-1, a negative regulator of Wnt signaling, is a versatile scaffold protein involved in centrosome separation and spindle assembly in mitosis, but its function in mammalian oogenesis remains unknown. Here we examined the localization and function
Publikováno v:
Asian Journal of Andrology
Asian Journal of Andrology, Vol 19, Iss 6, Pp 721-722 (2017)
Asian Journal of Andrology, Vol 19, Iss 6, Pp 721-722 (2017)
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 18(12)
To investigate the clinical phenotype and genetic characteristics of an azoospermia patient with ring 22 chromosome syndrome.We analyzed the clinical data of an azoospermia patient with ring 22 chromosome syndrome and reviewed relevant literature.The
Publikováno v:
Journal of assisted reproduction and genetics. 30(4)
To report the cytogenetic and molecular genetic analysis of the first two cases of non-chimerism and chimerism karyotype in Chinese male patients who suffer from azoospermia, which may be caused by pseudo dicentric Y chromosomes.Case study.Academic r
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 18(8)
Sperm selection plays an important role in assisted reproductive technology. In recent years, sperm evaluation is not limited to the assessment of sperm motility and morphology, but involves more other sperm characteristics such as sperm ultrastructu