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Ying-Xia Cui

Showing results (41-50 of 63) with videos related to

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Molecular Medicine Reports|August 12, 2015
A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature reviewXin-Yi Xia, Cui Zhang, Tian-Fu Li, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|December 2, 2009
[Evaluation of sperm mitochondrial membrane potential in varicocele patients using JC-1 fluorescent staining]Yi Hu, Xin-yi Xia, Lian-jun Pan, et al.
Frontiers in Medicine|March 27, 2023
A mouse model for X-linked Alport syndrome induced by Del-ATGG in the <i>Col4a5</i> geneWei-Qing Wu, Jia-Xun Zhang, Ying-Xia Cui, et al.
Asian Journal of Andrology|March 29, 2011
Gonadotropin-releasing hormone positively regulates steroidogenesis via extracellular signal-regulated kinase in rat Leydig cellsBing Yao, Hai-Yan Liu, Yu-Chun Gu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 9, 2007
Molecular prenatal diagnosis in 2 pregnancies at risk for spondyloepiphyseal dysplasia congenitaXin-Yi Xia, Ying-Xia Cui, Yu-Feng Huang, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|January 23, 2009
[AZF microdeletions are not related with recurrent spontaneous abortion]Hong-Yong Lu, Ying-Xia Cui, Xin-Yi Xia, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|December 18, 2013
[Detection of DPY19L2 gene mutation in a globozoospermia patient]Qiu-Yue Wu, Na Li, Tian-Fu Li, et al.
BMC Medical Genetics|August 16, 2014
A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese familyXin-Yi Xia, Na Li, Xiang Cao, et al.
Molecular Cytogenetics|March 4, 2014
A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex developmentXin-Yi Xia, Wei-Ping Wang, Tian-Fu Li, et al.
BMC Ophthalmology|September 9, 2014
A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese familyXin-Yi Xia, Qiu-Yue Wu, Li-Mei An, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Molecular Medicine Reports|August 12, 2015
A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature reviewXin-Yi Xia, Cui Zhang, Tian-Fu Li, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|December 2, 2009
[Evaluation of sperm mitochondrial membrane potential in varicocele patients using JC-1 fluorescent staining]Yi Hu, Xin-yi Xia, Lian-jun Pan, et al.
Frontiers in Medicine|March 27, 2023
A mouse model for X-linked Alport syndrome induced by Del-ATGG in the <i>Col4a5</i> geneWei-Qing Wu, Jia-Xun Zhang, Ying-Xia Cui, et al.
Asian Journal of Andrology|March 29, 2011
Gonadotropin-releasing hormone positively regulates steroidogenesis via extracellular signal-regulated kinase in rat Leydig cellsBing Yao, Hai-Yan Liu, Yu-Chun Gu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 9, 2007
Molecular prenatal diagnosis in 2 pregnancies at risk for spondyloepiphyseal dysplasia congenitaXin-Yi Xia, Ying-Xia Cui, Yu-Feng Huang, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|January 23, 2009
[AZF microdeletions are not related with recurrent spontaneous abortion]Hong-Yong Lu, Ying-Xia Cui, Xin-Yi Xia, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|December 18, 2013
[Detection of DPY19L2 gene mutation in a globozoospermia patient]Qiu-Yue Wu, Na Li, Tian-Fu Li, et al.
BMC Medical Genetics|August 16, 2014
A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese familyXin-Yi Xia, Na Li, Xiang Cao, et al.
Molecular Cytogenetics|March 4, 2014
A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex developmentXin-Yi Xia, Wei-Ping Wang, Tian-Fu Li, et al.
BMC Ophthalmology|September 9, 2014
A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese familyXin-Yi Xia, Qiu-Yue Wu, Li-Mei An, et al.
Pageof 7