263 related articles for article (PubMed ID: 29895858)
21. A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia.
Wu H; Zhang X; Shen Q; Liu Y; Gao Y; Wang G; Lv M; Hua R; Xu Y; Zhou P; Wei Z; Tao F; He X; Cao Y; Liu M
Clin Genet; 2022 Jan; 101(1):55-64. PubMed ID: 34595750
[TBL] [Abstract][Full Text] [Related]
22. Deletion and expression analysis of AZFa genes on the human Y chromosome revealed a major role for DBY in male infertility.
Foresta C; Ferlin A; Moro E
Hum Mol Genet; 2000 May; 9(8):1161-9. PubMed ID: 10767340
[TBL] [Abstract][Full Text] [Related]
23. Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility.
Tapanainen JS; Aittomäki K; Min J; Vaskivuo T; Huhtaniemi IT
Nat Genet; 1997 Feb; 15(2):205-6. PubMed ID: 9020851
[TBL] [Abstract][Full Text] [Related]
24. Population-based genetic analysis in infertile men reveals novel mutations of ADAD family members in patients with impaired spermatogenesis.
Dai S; Liu M; Liu M; Jiang C; Yang Y; Han H; Yang Y; Jiang X; Shen Y
Hum Mol Genet; 2023 May; 32(11):1814-1825. PubMed ID: 36708028
[TBL] [Abstract][Full Text] [Related]
25. The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans.
Wyrwoll MJ; Gaasbeek CM; Golubickaite I; Stakaitis R; Oud MS; Nagirnaja L; Dion C; Sindi EB; Leitch HG; Jayasena CN; Sironen A; Dicke AK; Rotte N; Stallmeyer B; Kliesch S; Grangeiro CHP; Araujo TF; Lasko P; ; D'Hauwers K; Smits RM; Ramos L; Xavier MJ; Conrad DF; Almstrup K; Veltman JA; Tüttelmann F; van der Heijden GW
Am J Hum Genet; 2022 Oct; 109(10):1850-1866. PubMed ID: 36150389
[TBL] [Abstract][Full Text] [Related]
26. Clinical, genetic, biochemical, and testicular biopsy findings among 1,213 men evaluated for infertility.
Olesen IA; Andersson AM; Aksglaede L; Skakkebaek NE; Rajpert-de Meyts E; Joergensen N; Juul A
Fertil Steril; 2017 Jan; 107(1):74-82.e7. PubMed ID: 27793385
[TBL] [Abstract][Full Text] [Related]
27. A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
Okutman O; Muller J; Skory V; Garnier JM; Gaucherot A; Baert Y; Lamour V; Serdarogullari M; Gultomruk M; Röpke A; Kliesch S; Herbepin V; Aknin I; Benkhalifa M; Teletin M; Bakircioglu E; Goossens E; Charlet-Berguerand N; Bahceci M; Tüttelmann F; Viville S
J Assist Reprod Genet; 2017 May; 34(5):683-694. PubMed ID: 28401488
[TBL] [Abstract][Full Text] [Related]
28. Expression of DAZ (deleted in azoospermia), DAZL1 (DAZ-like) and protamine-2 in testis and its application for diagnosis of spermatogenesis in non-obstructive azoospermia.
Lee JH; Lee DR; Yoon SJ; Chai YG; Roh SI; Yoon HS
Mol Hum Reprod; 1998 Sep; 4(9):827-34. PubMed ID: 9783841
[TBL] [Abstract][Full Text] [Related]
29. Selective ablation of Ppp1cc gene in testicular germ cells causes oligo-teratozoospermia and infertility in mice.
Sinha N; Puri P; Nairn AC; Vijayaraghavan S
Biol Reprod; 2013 Nov; 89(5):128. PubMed ID: 24089200
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. DNA damage in round spermatids of mice with a targeted disruption of the Pp1cgamma gene and in testicular biopsies of patients with non-obstructive azoospermia.
Jurisicova A; Lopes S; Meriano J; Oppedisano L; Casper RF; Varmuza S
Mol Hum Reprod; 1999 Apr; 5(4):323-30. PubMed ID: 10321803
[TBL] [Abstract][Full Text] [Related]
32. New insights into the expression profile of MicroRNA-34c and P53 in infertile men spermatozoa and testicular tissue.
Rahbar S; Novin MG; Alizadeh E; Shahnazi V; Pashaei-Asl F; AsrBadr YA; Farzadi L; Ebrahimie E; Pashaiasl M
Cell Mol Biol (Noisy-le-grand); 2017 Aug; 63(8):77-83. PubMed ID: 28886318
[TBL] [Abstract][Full Text] [Related]
33. Changes in the expression profile of the meiosis-involved mismatch repair genes in impaired human spermatogenesis.
Terribas E; Bonache S; García-Arévalo M; Sánchez J; Franco E; Bassas L; Larriba S
J Androl; 2010; 31(4):346-57. PubMed ID: 20075417
[TBL] [Abstract][Full Text] [Related]
34. An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family.
Tu C; Wang Y; Nie H; Meng L; Wang W; Li Y; Li D; Zhang H; Lu G; Lin G; Tan YQ; Du J
Clin Genet; 2020 May; 97(5):741-746. PubMed ID: 32017041
[TBL] [Abstract][Full Text] [Related]
35. Distribution of heat-shock protein 60 immunoreactivity in testes of infertile men.
Werner A; Meinhardt A; Seitz J; Bergmann M
Cell Tissue Res; 1997 Jun; 288(3):539-44. PubMed ID: 9134866
[TBL] [Abstract][Full Text] [Related]
36. Truncating mutations in TAF4B and ZMYND15 causing recessive azoospermia.
Ayhan Ö; Balkan M; Guven A; Hazan R; Atar M; Tok A; Tolun A
J Med Genet; 2014 Apr; 51(4):239-44. PubMed ID: 24431330
[TBL] [Abstract][Full Text] [Related]
37. CHD7 missense variants and clinical characteristics of Chinese males with infertility.
Li L; Wang R; Yu Y; Zhang H; Jiang Y; Yang X; Liu R
Mol Genet Genomic Med; 2020 Sep; 8(9):e1372. PubMed ID: 32573075
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Androgen receptor roles in spermatogenesis and fertility: lessons from testicular cell-specific androgen receptor knockout mice.
Wang RS; Yeh S; Tzeng CR; Chang C
Endocr Rev; 2009 Apr; 30(2):119-32. PubMed ID: 19176467
[TBL] [Abstract][Full Text] [Related]
40. Altered gene expression signature of early stages of the germ line supports the pre-meiotic origin of human spermatogenic failure.
Bonache S; Algaba F; Franco E; Bassas L; Larriba S
Andrology; 2014 Jul; 2(4):596-606. PubMed ID: 24803180
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
