216 related articles for article (PubMed ID: 26199321)
1. Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
Okutman O; Muller J; Baert Y; Serdarogullari M; Gultomruk M; Piton A; Rombaut C; Benkhalifa M; Teletin M; Skory V; Bakircioglu E; Goossens E; Bahceci M; Viville S
Hum Mol Genet; 2015 Oct; 24(19):5581-8. PubMed ID: 26199321
[TBL] [Abstract][Full Text] [Related]
2. A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest.
Okutman O; Boivin M; Muller J; Charlet-Berguerand N; Viville S
Hum Reprod; 2023 Feb; 38(2):306-314. PubMed ID: 36524333
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.
Riera-Escamilla A; Enguita-Marruedo A; Moreno-Mendoza D; Chianese C; Sleddens-Linkels E; Contini E; Benelli M; Natali A; Colpi GM; Ruiz-Castañé E; Maggi M; Baarends WM; Krausz C
Hum Reprod; 2019 Jun; 34(6):978-988. PubMed ID: 31125047
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest.
van der Bijl N; Röpke A; Biswas U; Wöste M; Jessberger R; Kliesch S; Friedrich C; Tüttelmann F
Hum Reprod; 2019 Nov; 34(11):2112-2119. PubMed ID: 31682730
[TBL] [Abstract][Full Text] [Related]
6. Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.
Wyrwoll MJ; Temel ŞG; Nagirnaja L; Oud MS; Lopes AM; van der Heijden GW; Heald JS; Rotte N; Wistuba J; Wöste M; Ledig S; Krenz H; Smits RM; Carvalho F; Gonçalves J; Fietz D; Türkgenç B; Ergören MC; Çetinkaya M; Başar M; Kahraman S; McEleny K; Xavier MJ; Turner H; Pilatz A; Röpke A; Dugas M; Kliesch S; Neuhaus N; ; Aston KI; Conrad DF; Veltman JA; Friedrich C; Tüttelmann F
Am J Hum Genet; 2020 Aug; 107(2):342-351. PubMed ID: 32673564
[TBL] [Abstract][Full Text] [Related]
7. Case study of a patient with cryptozoospermia associated with a recessive
Wang X; Jin HR; Cui YQ; Chen J; Sha YW; Gao ZL
Asian J Androl; 2018; 20(1):101-102. PubMed ID: 28303806
[No Abstract] [Full Text] [Related]
8. Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure.
Clavijo RI; Arora H; Gibbs E; Cohen S; Griswold A; Bakircioglu E; Bademci G; Tekin M; Ramasamy R
Urology; 2018 Oct; 120():86-89. PubMed ID: 29966603
[TBL] [Abstract][Full Text] [Related]
9. Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.
Wu Y; Li Y; Murtaza G; Zhou J; Jiao Y; Gong C; Hu C; Han Q; Zhang H; Zhang Y; Shi B; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Sep; 36(10):2793-2804. PubMed ID: 34392356
[TBL] [Abstract][Full Text] [Related]
10. Genomic study of
Qureshi S; Hardy JJ; Pombar C; Berman AJ; Malcher A; Gingrich T; Hvasta R; Kuong J; Munyoki S; Hwang K; Orwig KE; Ahmed J; Olszewska M; Kurpisz M; Conrad DF; Jaseem Khan M; Yatsenko AN
Front Genet; 2023; 14():1134849. PubMed ID: 37234866
[No Abstract] [Full Text] [Related]
11. 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]
12. An exonic insertion within Tex14 gene causes spermatogenic arrest in pigs.
Sironen A; Uimari P; Venhoranta H; Andersson M; Vilkki J
BMC Genomics; 2011 Dec; 12():591. PubMed ID: 22136159
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Point-of-care whole-exome sequencing of idiopathic male infertility.
Fakhro KA; Elbardisi H; Arafa M; Robay A; Rodriguez-Flores JL; Al-Shakaki A; Syed N; Mezey JG; Abi Khalil C; Malek JA; Al-Ansari A; Al Said S; Crystal RG
Genet Med; 2018 Nov; 20(11):1365-1373. PubMed ID: 29790874
[TBL] [Abstract][Full Text] [Related]
15. A homozygous FANCM frameshift pathogenic variant causes male infertility.
Yin H; Ma H; Hussain S; Zhang H; Xie X; Jiang L; Jiang X; Iqbal F; Bukhari I; Jiang H; Ali A; Zhong L; Li T; Fan S; Zhang B; Gao J; Li Y; Nazish J; Khan T; Khan M; Zubair M; Hao Q; Fang H; Huang J; Huleihel M; Sha J; Pandita TK; Zhang Y; Shi Q
Genet Med; 2019 Jan; 21(1):62-70. PubMed ID: 29895858
[TBL] [Abstract][Full Text] [Related]
16. Genetic variants in TEX15 gene conferred susceptibility to spermatogenic failure in the Chinese Han population.
Ruan J; He XJ; Du WD; Chen G; Zhou Y; Xu S; Zuo XB; Fang LB; Cao YX; Zhang XJ
Reprod Sci; 2012 Nov; 19(11):1190-6. PubMed ID: 22581801
[TBL] [Abstract][Full Text] [Related]
17. Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alström syndrome.
Katagiri S; Yoshitake K; Akahori M; Hayashi T; Furuno M; Nishino J; Ikeo K; Tsuneoka H; Iwata T
Mol Vis; 2013; 19():2393-406. PubMed ID: 24319333
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Whole Exome Sequencing Identifies a Rare Nonsense Mutation in FAM47C as a Possible Cause of Severe Oligospermia in Brothers With Varicocele.
Chertman W; Arora H; Griswold AJ; Lopategui DM; Ramasamy R
Urology; 2019 Jul; 129():71-73. PubMed ID: 30922974
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
