131 related articles for article (PubMed ID: 38258527)
21. A novel ADGRG2 truncating variant associated with X-linked obstructive azoospermia in a large Chinese pedigree.
Lu Y; Xie Y; Li M; Zuo N; Ning S; Luo B; Ning M; Song J; Liang Y; Qin Y
J Assist Reprod Genet; 2023 Jul; 40(7):1747-1754. PubMed ID: 37273165
[TBL] [Abstract][Full Text] [Related]
22. Single gene defects leading to sperm quantitative anomalies.
Mitchell MJ; Metzler-Guillemain C; Toure A; Coutton C; Arnoult C; Ray PF
Clin Genet; 2017 Feb; 91(2):208-216. PubMed ID: 27779755
[TBL] [Abstract][Full Text] [Related]
23. 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
Hum Mol Genet; 2020 Aug; 29(14):2451-2459. PubMed ID: 32469048
[TBL] [Abstract][Full Text] [Related]
24. The association of testis-specific hTAF7L gene variants with idiopathic azoospermic and severe oligozoospermic male infertility.
Ambulkar PS; Waghmare JE; Verma Shivkumar P; Chaudhari AR; Gangane NM; Narang P; Pal AK
Andrologia; 2022 Dec; 54(11):e14581. PubMed ID: 36068176
[TBL] [Abstract][Full Text] [Related]
25. Expression pattern of testicular claudin-11 in infertile men.
Chiba K; Yamaguchi K; Ando M; Miyake H; Fujisawa M
Urology; 2012 Nov; 80(5):1161.e13-7. PubMed ID: 22951003
[TBL] [Abstract][Full Text] [Related]
26. Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia.
Zhang Y; Li N; Ji Z; Bai H; Ou N; Tian R; Li P; Zhi E; Huang Y; Zhao J; Han Y; Zhang J; Zhou Y; Li Z; Yao C
J Hum Genet; 2023 Jun; 68(6):383-392. PubMed ID: 36759719
[TBL] [Abstract][Full Text] [Related]
27. [Analysis of Y chromosome microdeletion in non-obstructive male infertile patients with azoospermia and severe oligozoospermia].
Ting-Ting H; Xian-Ping D; Xia W; Jing R; Li-Yuan Z
Sichuan Da Xue Xue Bao Yi Xue Ban; 2013 Mar; 44(2):188-92. PubMed ID: 23745252
[TBL] [Abstract][Full Text] [Related]
28. Y chromosome microdeletions in Chinese men with infertility: prevalence, phenotypes, and intracytoplasmic sperm injection outcomes.
Chen D; Fan G; Zhu X; Chen Q; Chen X; Gao F; Guo Z; Luo P; Gao Y
Reprod Biol Endocrinol; 2023 Dec; 21(1):116. PubMed ID: 38053137
[TBL] [Abstract][Full Text] [Related]
29. Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.
Cerván-Martín M; Bossini-Castillo L; Guzmán-Jiménez A; Rivera-Egea R; Garrido N; Lujan S; Romeu G; Santos-Ribeiro S; ; ; Castilla JA; Gonzalvo MDC; Clavero A; Maldonado V; Vicente FJ; Burgos M; Jiménez R; González-Muñoz S; Sánchez-Curbelo J; López-Rodrigo O; Pereira-Caetano I; Marques PI; Carvalho F; Barros A; Bassas L; Seixas S; Gonçalves J; Larriba S; Lopes AM; Palomino-Morales RJ; Carmona FD
Andrology; 2022 Oct; 10(7):1339-1350. PubMed ID: 35752927
[TBL] [Abstract][Full Text] [Related]
30. An analysis of Y-chromosome microdeletion in infertile Korean men with severe oligozoospermia or azoospermia.
Lee TH; Song SH; Kim DK; Shim SH; Jeong D; Kim DS
Investig Clin Urol; 2024 Jan; 65(1):77-83. PubMed ID: 38197754
[TBL] [Abstract][Full Text] [Related]
31. SPATA16 promoter hypermethylation and downregulation in male infertility.
Sujit KM; Pallavi S; Singh V; Andrabi SW; Trivedi S; Sankhwar SN; Gupta G; Rajender S
Andrologia; 2022 Nov; 54(10):e14548. PubMed ID: 36177775
[TBL] [Abstract][Full Text] [Related]
32. A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens.
Wu H; Gao Y; Ma C; Shen Q; Wang J; Lv M; Liu C; Cheng H; Zhu F; Tian S; Elshewy N; Ni X; Tan Q; Xu X; Zhou P; Wei Z; Zhang F; He X; Cao Y
J Assist Reprod Genet; 2020 Jun; 37(6):1421-1429. PubMed ID: 32314195
[TBL] [Abstract][Full Text] [Related]
33. Genetic variants in meiotic program initiation pathway genes are associated with spermatogenic impairment in a Han Chinese population.
Lu C; Xu M; Wang Y; Qin Y; Du G; Wu W; Han X; Ji C; Yang Y; Gu A; Xia Y; Song L; Wang S; Wang X
PLoS One; 2013; 8(1):e53443. PubMed ID: 23320086
[TBL] [Abstract][Full Text] [Related]
34. High frequency of TTTY2-like gene-related deletions in patients with idiopathic oligozoospermia and azoospermia.
Yapijakis C; Serefoglou Z; Papadimitriou K; Makrinou E
Andrologia; 2015 Jun; 47(5):536-44. PubMed ID: 24919818
[TBL] [Abstract][Full Text] [Related]
35. Molecular analysis of testis biopsy and semen pellet as complementary methods with histopathological analysis of testis in non-obstructive azoospermia.
Eghbali M; Sadeghi MR; Lakpour N; Edalatkhah H; Zeraati H; Soltanghoraee H; Akhondi MM; Hashemi SB; Modarressi MH
J Assist Reprod Genet; 2014 Jun; 31(6):707-15. PubMed ID: 24728569
[TBL] [Abstract][Full Text] [Related]
36. Linking human Dead end 1 (DND1) variants to male infertility employing zebrafish embryos.
Westerich KJ; Reinecke S; Emich J; Wyrwoll MJ; Stallmeyer B; Meyer M; Oud MS; Fietz D; Pilatz A; Kliesch S; Reichman-Fried M; Tarbashevich K; Limon T; Stehling M; Friedrich C; Tüttelmann F; Raz E
Hum Reprod; 2023 Apr; 38(4):655-670. PubMed ID: 36807972
[TBL] [Abstract][Full Text] [Related]
37. X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
Yatsenko AN; Georgiadis AP; Röpke A; Berman AJ; Jaffe T; Olszewska M; Westernströer B; Sanfilippo J; Kurpisz M; Rajkovic A; Yatsenko SA; Kliesch S; Schlatt S; Tüttelmann F
N Engl J Med; 2015 May; 372(22):2097-107. PubMed ID: 25970010
[TBL] [Abstract][Full Text] [Related]
38. Identification and Functional Investigation of Novel Heterozygous
Murtaza G; Yang L; Khan I; Unar A; Khan M; Huan Z; Khan R; Shi Q
Genet Test Mol Biomarkers; 2021 Oct; 25(10):654-659. PubMed ID: 34672775
[No Abstract] [Full Text] [Related]
39. [Association of DAZL A260G and A386G polymorphisms with oligozoospermia- or azoospermia-induced male infertility: A meta-analysis].
Chen XY; Chen P; Xu C; Zhang XH
Zhonghua Nan Ke Xue; 2015 Apr; 21(4):345-56. PubMed ID: 26027104
[TBL] [Abstract][Full Text] [Related]
40. Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes.
Wyrwoll MJ; van Walree ES; Hamer G; Rotte N; Motazacker MM; Meijers-Heijboer H; Alders M; Meißner A; Kaminsky E; Wöste M; Krallmann C; Kliesch S; Hunt TJ; Clark AT; Silber S; Stallmeyer B; Friedrich C; van Pelt AMM; Mathijssen IB; Tüttelmann F
Hum Reprod; 2021 Dec; 37(1):178-189. PubMed ID: 34755185
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]