321 related articles for article (PubMed ID: 32741963)
21. Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle; 2023 May; 22(9):1021-1061. PubMed ID: 36740861
[TBL] [Abstract][Full Text] [Related]
22. A new
Yu XC; Li MJ; Cai FF; Yang SJ; Liu HB; Zhang HB
Asian J Androl; 2021; 23(5):510-515. PubMed ID: 33762476
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
Tang D; Li K; Geng H; Xu C; Lv M; Gao Y; Wang G; Yu H; Shao Z; Shen Q; Jiang H; Zhang X; He X; Cao Y
Reprod Biol Endocrinol; 2022 Apr; 20(1):63. PubMed ID: 35366911
[TBL] [Abstract][Full Text] [Related]
25. A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination.
Li Y; Wu Y; Zhou J; Zhang H; Zhang Y; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Apr; 36(5):1436-1445. PubMed ID: 33713115
[TBL] [Abstract][Full Text] [Related]
26. Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.
Malcher A; Stokowy T; Berman A; Olszewska M; Jedrzejczak P; Sielski D; Nowakowski A; Rozwadowska N; Yatsenko AN; Kurpisz MK
Andrology; 2022 Nov; 10(8):1605-1624. PubMed ID: 36017582
[TBL] [Abstract][Full Text] [Related]
27. Novel mutations of
Song J; Sha Y; Liu X; Zeng X; Zhao X
Front Endocrinol (Lausanne); 2023; 14():1159723. PubMed ID: 37124723
[TBL] [Abstract][Full Text] [Related]
28. Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.
Wang W; Meng L; He J; Su L; Li Y; Tan C; Xu X; Nie H; Zhang H; Du J; Lu G; Luo M; Lin G; Tu C; Tan YQ
Mol Hum Reprod; 2022 May; 28(6):. PubMed ID: 35485979
[TBL] [Abstract][Full Text] [Related]
29. Ultrasonographic caput epididymis diameter is reduced in non-obstructive azoospermia compared with normozoospermia but is not predictive for successful sperm retrieval after TESE.
Pezzella A; Barbonetti A; D'Andrea S; Necozione S; Micillo A; Di Gregorio A; Francavilla F; Francavilla S
Hum Reprod; 2014 Jul; 29(7):1368-74. PubMed ID: 24812316
[TBL] [Abstract][Full Text] [Related]
30. A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes.
Gershoni M; Hauser R; Yogev L; Lehavi O; Azem F; Yavetz H; Pietrokovski S; Kleiman SE
Genet Med; 2017 Sep; 19(9):998-1006. PubMed ID: 28206990
[TBL] [Abstract][Full Text] [Related]
31. Genetic Architecture of Azoospermia-Time to Advance the Standard of Care.
Wyrwoll MJ; Köckerling N; Vockel M; Dicke AK; Rotte N; Pohl E; Emich J; Wöste M; Ruckert C; Wabschke R; Seggewiss J; Ledig S; Tewes AC; Stratis Y; Cremers JF; Wistuba J; Krallmann C; Kliesch S; Röpke A; Stallmeyer B; Friedrich C; Tüttelmann F
Eur Urol; 2023 May; 83(5):452-462. PubMed ID: 35690514
[TBL] [Abstract][Full Text] [Related]
32. Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.
Colombo R; Pontoglio A; Bini M
Gynecol Obstet Invest; 2017; 82(3):283-286. PubMed ID: 28355598
[TBL] [Abstract][Full Text] [Related]
33. Rare missense variant in MSH4 associated with primary gonadal failure in both 46, XX and 46, XY individuals.
Akbari A; Padidar K; Salehi N; Mashayekhi M; Almadani N; Sadighi Gilani MA; Bashambou A; McElreavey K; Totonchi M
Hum Reprod; 2021 Mar; 36(4):1134-1145. PubMed ID: 33448284
[TBL] [Abstract][Full Text] [Related]
34. The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.
Pashaei M; Rahimi Bidgoli MM; Zare-Abdollahi D; Najmabadi H; Haji-Seyed-Javadi R; Fatehi F; Alavi A
J Assist Reprod Genet; 2020 Feb; 37(2):451-458. PubMed ID: 31916078
[TBL] [Abstract][Full Text] [Related]
35. Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia.
Zhu X; Hu K; Cheng H; Wu H; Li K; Gao Y; Lv M; Xu C; Geng H; Shen Q; Cao Y; He X; Tang D; Guo R
Clin Genet; 2024 Jan; 105(1):99-105. PubMed ID: 37715646
[TBL] [Abstract][Full Text] [Related]
36. Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure.
Cannarella R; Condorelli RA; Paolacci S; Barbagallo F; Guerri G; Bertelli M; La Vignera S; Calogero AE
Asian J Androl; 2021; 23(1):24-29. PubMed ID: 32655042
[TBL] [Abstract][Full Text] [Related]
37. Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees.
Xie X; Murtaza G; Li Y; Zhou J; Ye J; Khan R; Jiang L; Khan I; Zubair M; Yin H; Jiang H; Liu W; Shi B; Hou X; Gong C; Fan S; Wang Y; Jiang X; Zhang Y; Zhang H; Ma H; Shi Q
Hum Reprod; 2022 Jun; 37(7):1664-1677. PubMed ID: 35526155
[TBL] [Abstract][Full Text] [Related]
38. Expression analysis of genes encoding
Boroujeni PB; Sabbaghian M; Totonchi M; Sodeifi N; Sarkardeh H; Samadian A; Sadighi-Gilani MA; Gourabi H
JBRA Assist Reprod; 2018 Sep; 22(3):185-192. PubMed ID: 29932616
[TBL] [Abstract][Full Text] [Related]
39. Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.
Kasak L; Punab M; Nagirnaja L; Grigorova M; Minajeva A; Lopes AM; Punab AM; Aston KI; Carvalho F; Laasik E; Smith LB; ; Conrad DF; Laan M
Am J Hum Genet; 2018 Aug; 103(2):200-212. PubMed ID: 30075111
[TBL] [Abstract][Full Text] [Related]
40. A novel homozygote nonsense variant of MSH4 leads to primary ovarian insufficiency and non-obstructive azoospermia.
Hashemi Sheikhshabani S; Ghafouri-Fard S; Hosseini E; Omrani MD
Mol Biol Rep; 2024 Jan; 51(1):68. PubMed ID: 38175272
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]