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Quoted phrase not found in phrase index: "Spermatogenic failure 29"
Page 1
Genomic testing for copy number and single nucleotide variants in spermatogenic failure.
Hardy J, Pollock N, Gingrich T, Sweet P, Ramesh A, Kuong J, Basar A, Jiang H, Hwang K, Vukina J, Jaffe T, Olszewska M, Kurpisz M, Yatsenko AN. Hardy J, et al. J Assist Reprod Genet. 2022 Sep;39(9):2103-2114. doi: 10.1007/s10815-022-02538-5. Epub 2022 Jul 18. J Assist Reprod Genet. 2022. PMID: 35849255 Free PMC article.
PURPOSE: To identify clinically significant genomic copy number (CNV) and single nucleotide variants (SNV) in males with unexplained spermatogenic failure (SPGF). MATERIALS AND METHODS: Peripheral blood DNA from 97/102 study participants diagnosed with oligozoosperm …
PURPOSE: To identify clinically significant genomic copy number (CNV) and single nucleotide variants (SNV) in males with unexplained sper …
A Novel Locus Predicts Spermatogenic Recovery among Childhood Cancer Survivors Exposed to Alkylating Agents.
Sapkota Y, Wilson CL, Zaidi AK, Moon W, Fon Tacer K, Lu L, Liu Q, Baedke J, Dhaduk R, Wang Z, Chemaitilly W, Krasin MJ, Berry FB, Zhang J, Hudson MM, Robison LL, Green DM, Yasui Y. Sapkota Y, et al. Cancer Res. 2020 Sep 1;80(17):3755-3764. doi: 10.1158/0008-5472.CAN-20-0093. Epub 2020 Jun 17. Cancer Res. 2020. PMID: 32554749 Free PMC article.
No association was observed among survivors not exposed to alkylating agents included in the CED (P > 0.29). rs7784118 conferred 3.48- and 9.73-fold increases in risk for clinically defined oligospermia and azoospermia and improved prediction of normospermic, oligosperm …
No association was observed among survivors not exposed to alkylating agents included in the CED (P > 0.29). rs7784118 conferred 3 …
Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.
Chen S, Wang G, Zheng X, Ge S, Dai Y, Ping P, Chen X, Liu G, Zhang J, Yang Y, Zhang X, Zhong A, Zhu Y, Chu Q, Huang Y, Zhang Y, Shen C, Yuan Y, Yuan Q, Pei X, Cheng CY, Sun F. Chen S, et al. Hum Mol Genet. 2020 Aug 11;29(14):2451-2459. doi: 10.1093/hmg/ddaa101. Hum Mol Genet. 2020. PMID: 32469048
Rare coding variants have been proven to be one of the significant factors contributing to spermatogenic failure in patients with non-obstructive azoospermia (NOA) and severe oligospermia (SO). ...
Rare coding variants have been proven to be one of the significant factors contributing to spermatogenic failure in patients w …
Validation of flow cytometry analysis in the objective assessment of spermatogenesis: comparison to the quantitative testicular biopsy.
Hirsch IH, McCue P, Kulp-Hugues D, Sedor J, Flanigan M. Hirsch IH, et al. J Urol. 1993 Aug;150(2 Pt 1):342-6. doi: 10.1016/s0022-5347(17)35480-0. J Urol. 1993. PMID: 8326559
Nevertheless, this important modality has yet to be validated against quantitative micrometry of the testis. To determine this correlation we submitted 29 incisional testicular biopsies for simultaneous quantitative analysis and DNA flow cytometry. ...DNA flow cytometry an …
Nevertheless, this important modality has yet to be validated against quantitative micrometry of the testis. To determine this correlation w …