Huang WJ - Search Results

1

Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study†.

Tan MQ, Huang WJ, Lan FH, Xu YJ, Zheng MY, Tang Y. Tan MQ, et al. Among authors: huang wj. Biol Reprod. 2022 Jan 13;106(1):108-117. doi: 10.1093/biolre/ioab194. Biol Reprod. 2022. PMID: 34673937

2

Pathogenesis of acephalic spermatozoa syndrome caused by SUN5 variant.

Zhang D, Huang WJ, Chen GY, Dong LH, Tang Y, Zhang H, Li QQ, Mei XY, Wang ZH, Lan FH. Zhang D, et al. Among authors: huang wj. Mol Hum Reprod. 2021 May 8;27(5):gaab028. doi: 10.1093/molehr/gaab028. Mol Hum Reprod. 2021. PMID: 33848337

3

Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study†.

Tan MQ, Huang WJ, Lan FH, Xu YJ, Zheng MY, Tang Y. Tan MQ, et al. Among authors: huang wj. Biol Reprod. 2022 Jan 13;106(1):227. doi: 10.1093/biolre/ioab230. Biol Reprod. 2022. PMID: 34904639 No abstract available.

4

[Detection of pathogenic variants in four patients with globozoospermia].

Tang Z, Li Q, Chen G, Huang W, Wang Y, Ye Y, Xie P, Lan F, Zhang D. Tang Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Mar 10;40(3):301-307. doi: 10.3760/cma.j.cn511374-20220328-00205. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36854405 Chinese.

5

Loss-of-function mutations in IQCN cause male infertility in humans and mice owing to total fertilization failure.

Wang Y, Chen G, Tang Z, Mei X, Lin C, Kang J, Lian J, Lu J, Liu Y, Lan F, Huang W, Zhang D. Wang Y, et al. Mol Hum Reprod. 2023 Jun 30;29(7):gaad018. doi: 10.1093/molehr/gaad018. Mol Hum Reprod. 2023. PMID: 37184908

6

Factors influencing mosaicism: a retrospective analysis.

Huang QX, Wang ZH, Huang WJ, Mao LH, Lin CL, Chen GY, Wang CX, Chen ZB, Lin YL, He LY, Liu Y. Huang QX, et al. Among authors: huang wj. Reprod Biomed Online. 2022 Sep;45(3):491-500. doi: 10.1016/j.rbmo.2022.04.020. Epub 2022 May 6. Reprod Biomed Online. 2022. PMID: 35843780

7

Abnormal expression of uncoupling protein-2 correlates with CYP11A1 expression in polycystic ovary syndrome.

Liu Y, Jiang H, He LY, Huang WJ, He XY, Xing FQ. Liu Y, et al. Among authors: huang wj. Reprod Fertil Dev. 2011;23(4):520-6. doi: 10.1071/RD10266. Reprod Fertil Dev. 2011. PMID: 21557918

8

The first report showing de novo partial 21q monosomy in an adult woman with occult primary ovarian insufficiency (POI).

Zeng J, Huang W, Huang M, Wang Z. Zeng J, et al. Clin Chem Lab Med. 2019 Aug 27;57(9):e230-e233. doi: 10.1515/cclm-2018-1271. Clin Chem Lab Med. 2019. PMID: 30710477 No abstract available.

9

[Application of mapping allele with resolved carrier status technique for preimplantation genetic testing in carriers with balanced chromosomal translocations].

Huang Q, Liu Y, Lin C, Chen Z, Liu Z, Huang W, Mao L, He L, Wang Z. Huang Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Sep 10;38(9):845-848. doi: 10.3760/cma.j.cn511374-20200629-00479. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34487527 Chinese.

10

Sequential interval micro-droplet loading in closed hemi-straw carrier system: A convenient and efficient method for ultra-rapid cryopreservation in extreme oligozoospermia.

Huang WJ, Zhang D, Hong ZW, Chen ZB, Dong LH, Zhang Y, Chen GY, Liu Y, Yao B. Huang WJ, et al. Cryobiology. 2020 Apr;93:75-83. doi: 10.1016/j.cryobiol.2020.02.005. Epub 2020 Feb 11. Cryobiology. 2020. PMID: 32057735 Free article.

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