Wang XB - Search Results

1

A de novo frameshift mutation of the SRY gene leading to a patient with 46,XY complete gonadal dysgenesis.

Wang XB, Liang YL, Zhu ZJ, Zhu Y, Li P, Cao JP, Zhang QY, Liu Q, Li Z. Wang XB, et al. Asian J Androl. 2019 Sep-Oct;21(5):522-524. doi: 10.4103/aja.aja_123_18. Asian J Androl. 2019. PMID: 30785124 Free PMC article. No abstract available.

2

Real-time Raman microspectroscopy scanning of the single live sperm bound to human zona pellucida.

Liu F, Zhu Y, Liu Y, Wang X, Ping P, Zhu X, Hu H, Li Z, He L. Liu F, et al. Fertil Steril. 2013 Mar 1;99(3):684-689.e4. doi: 10.1016/j.fertnstert.2012.10.035. Epub 2012 Nov 10. Fertil Steril. 2013. PMID: 23148927 Free article.

3

Sertoli cells from non-obstructive azoospermia and obstructive azoospermia patients show distinct morphology, Raman spectrum and biochemical phenotype.

Ma M, Yang S, Zhang Z, Li P, Gong Y, Liu L, Zhu Y, Tian R, Liu Y, Wang X, Liu F, He L, Liu Y, Yang H, Li Z, He Z. Ma M, et al. Hum Reprod. 2013 Jul;28(7):1863-73. doi: 10.1093/humrep/det068. Epub 2013 Mar 15. Hum Reprod. 2013. PMID: 23503944

4

Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation.

Hou J, Niu M, Liu L, Zhu Z, Wang X, Sun M, Yuan Q, Yang S, Zeng W, Liu Y, Li Z, He Z. Hou J, et al. Sci Rep. 2015 Nov 20;5:16922. doi: 10.1038/srep16922. Sci Rep. 2015. PMID: 26585066 Free PMC article.

5

Generation and characteristics of human Sertoli cell line immortalized by overexpression of human telomerase.

Wen L, Yuan Q, Sun M, Niu M, Wang H, Fu H, Zhou F, Yao C, Wang X, Li Z, He Z. Wen L, et al. Oncotarget. 2017 Mar 7;8(10):16553-16570. doi: 10.18632/oncotarget.14985. Oncotarget. 2017. PMID: 28152522 Free PMC article.

6

Detection of heterozygous mutation in hook microtubule-tethering protein 1 in three patients with decapitated and decaudated spermatozoa syndrome.

Chen H, Zhu Y, Zhu Z, Zhi E, Lu K, Wang X, Liu F, Li Z, Xia W. Chen H, et al. J Med Genet. 2018 Mar;55(3):150-157. doi: 10.1136/jmedgenet-2016-104404. Epub 2018 Jan 12. J Med Genet. 2018. PMID: 29330334

7

[Spatio-temporal expression and function of KIFC1 in acrosomogenesis].

Zhi EL, Li P, Yao CC, Wang XB, Hong Y, Li Z. Zhi EL, et al. Among authors: wang xb. Zhonghua Nan Ke Xue. 2019 Dec;25(12):1059-1065. Zhonghua Nan Ke Xue. 2019. PMID: 32251555 Chinese.

8

Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome.

Huang C, Liu NC, Wang XB, Gu BH, Zhang JX, Li-Zhang, Li Z. Huang C, et al. Among authors: wang xb. Asian J Androl. 2021 May-Jun;23(3):330-332. doi: 10.4103/aja.aja_43_20. Asian J Androl. 2021. PMID: 33106461 Free PMC article. No abstract available.

9

Novel mutation in ODF2 causes multiple morphological abnormalities of the sperm flagella in an infertile male.

Zhu ZJ, Wang YZ, Wang XB, Yao CC, Zhao LY, Zhang ZB, Wu Y, Chen W, Li Z. Zhu ZJ, et al. Among authors: wang yz, wang xb. Asian J Androl. 2022 Sep-Oct;24(5):463-472. doi: 10.4103/aja202183. Asian J Androl. 2022. PMID: 35102900 Free PMC article.

10

Deleterious variants in TAF7L cause human oligoasthenoteratozoospermia and its impairing histone to protamine exchange inducing reduced in vitro fertilization.

Bai H, Sha Y, Tan Y, Li P, Zhang Y, Xu J, Xu S, Ji Z, Wang X, Chen W, Zhang J, Yao C, Li Z, Zhi E. Bai H, et al. Front Endocrinol (Lausanne). 2023 Jan 11;13:1099270. doi: 10.3389/fendo.2022.1099270. eCollection 2022. Front Endocrinol (Lausanne). 2023. PMID: 36714566 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,412 results

Search Page

Filters