493 related articles for article (PubMed ID: 31985809)
1. Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia.
Oud MS; Okutman Ö; Hendricks LAJ; de Vries PF; Houston BJ; Vissers LELM; O'Bryan MK; Ramos L; Chemes HE; Viville S; Veltman JA
Hum Reprod; 2020 Jan; 35(1):240-252. PubMed ID: 31985809
[TBL] [Abstract][Full Text] [Related]
2. Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player.
Celse T; Cazin C; Mietton F; Martinez G; Martinez D; Thierry-Mieg N; Septier A; Guillemain C; Beurois J; Clergeau A; Mustapha SFB; Kharouf M; Zoghmar A; Chargui A; Papaxanthos A; Dorphin B; Foliguet B; Triki C; Sifer C; Lauton D; Tachdjian G; Schuler G; Lejeune H; Puechberty J; Bessonnat J; Pasquier L; Mery L; Poulain M; Chaabouni M; Sermondade N; Cabry R; Benbouhadja S; Veau S; Frapsauce C; Mitchell V; Achard V; Satre V; Hennebicq S; Zouari R; Arnoult C; Kherraf ZE; Coutton C; Ray PF
Hum Genet; 2021 Jan; 140(1):43-57. PubMed ID: 33108537
[TBL] [Abstract][Full Text] [Related]
3. Loss of SPACA1 function causes autosomal recessive globozoospermia by damaging the acrosome-acroplaxome complex.
Chen P; Saiyin H; Shi R; Liu B; Han X; Gao Y; Ye X; Zhang X; Sun Y
Hum Reprod; 2021 Aug; 36(9):2587-2596. PubMed ID: 34172998
[TBL] [Abstract][Full Text] [Related]
4. Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects.
Li Y; Wang Y; Wen Y; Zhang T; Wang X; Jiang C; Zheng R; Zhou F; Chen D; Yang Y; Shen Y
Hum Reprod; 2021 Dec; 37(1):152-177. PubMed ID: 34791246
[TBL] [Abstract][Full Text] [Related]
5. MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia.
Coutton C; Zouari R; Abada F; Ben Khelifa M; Merdassi G; Triki C; Escalier D; Hesters L; Mitchell V; Levy R; Sermondade N; Boitrelle F; Vialard F; Satre V; Hennebicq S; Jouk PS; Arnoult C; Lunardi J; Ray PF
Hum Reprod; 2012 Aug; 27(8):2549-58. PubMed ID: 22627659
[TBL] [Abstract][Full Text] [Related]
6. Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders.
Oud MS; Houston BJ; Volozonoka L; Mastrorosa FK; Holt GS; Alobaidi BKS; deVries PF; Astuti G; Ramos L; Mclachlan RI; O'Bryan MK; Veltman JA; Chemes HE; Sheth H
Hum Reprod; 2021 Aug; 36(9):2597-2611. PubMed ID: 34089056
[TBL] [Abstract][Full Text] [Related]
7. Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia.
Ghédir H; Ibala-Romdhane S; Okutman O; Viot G; Saad A; Viville S
Mol Hum Reprod; 2016 Jan; 22(1):35-45. PubMed ID: 26516168
[TBL] [Abstract][Full Text] [Related]
8. DPY19L2 gene mutations are a major cause of globozoospermia: identification of three novel point mutations.
Zhu F; Gong F; Lin G; Lu G
Mol Hum Reprod; 2013 Jun; 19(6):395-404. PubMed ID: 23512994
[TBL] [Abstract][Full Text] [Related]
9. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
Amiri-Yekta A; Coutton C; Kherraf ZE; Karaouzène T; Le Tanno P; Sanati MH; Sabbaghian M; Almadani N; Sadighi Gilani MA; Hosseini SH; Bahrami S; Daneshipour A; Bini M; Arnoult C; Colombo R; Gourabi H; Ray PF
Hum Reprod; 2016 Dec; 31(12):2872-2880. PubMed ID: 27798045
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Effects of
Olszewska M; Malcher A; Stokowy T; Pollock N; Berman AJ; Budkiewicz S; Kamieniczna M; Jackowiak H; Suszynska-Zajczyk J; Jedrzejczak P; Yatsenko AN; Kurpisz M
Hum Reprod Open; 2024; 2024(2):hoae020. PubMed ID: 38650655
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Teratozoospermia: spotlight on the main genetic actors in the human.
Coutton C; Escoffier J; Martinez G; Arnoult C; Ray PF
Hum Reprod Update; 2015; 21(4):455-85. PubMed ID: 25888788
[TBL] [Abstract][Full Text] [Related]
14. Globozoospermia: A Case Report and Systematic Review of Literature.
Crafa A; Condorelli RA; La Vignera S; Calogero AE; Cannarella R
World J Mens Health; 2023 Jan; 41(1):49-80. PubMed ID: 36047070
[TBL] [Abstract][Full Text] [Related]
15. Identification of a novel deletion mutation in
Li YZ; Wu RF; Zhu XS; Liu WS; Ye YY; Lu ZX; Li N
Mol Cytogenet; 2020; 13():24. PubMed ID: 32582379
[TBL] [Abstract][Full Text] [Related]
16. Deletion of ACTRT1 is associated with male infertility as sperm acrosomal ultrastructural defects and fertilization failure in human.
Zhang Q; Jin H; Long S; Tang X; Li J; Liu W; Han W; Liao H; Fu T; Huang G; Chen S; Lin T
Hum Reprod; 2024 May; 39(5):880-891. PubMed ID: 38414365
[TBL] [Abstract][Full Text] [Related]
17. DPY19L2 deletion as a major cause of globozoospermia.
Koscinski I; Elinati E; Fossard C; Redin C; Muller J; Velez de la Calle J; Schmitt F; Ben Khelifa M; Ray PF; Kilani Z; Barratt CL; Viville S
Am J Hum Genet; 2011 Mar; 88(3):344-50. PubMed ID: 21397063
[TBL] [Abstract][Full Text] [Related]
18. Genome-wide compound heterozygote analysis highlights DPY19L2 alleles in a non-consanguineous Spanish family with total globozoospermia.
López-Rodrigo O; Bossini-Castillo L; Carmona FD; Bassas L; Larriba S
Reprod Biomed Online; 2022 Aug; 45(2):332-340. PubMed ID: 35610156
[TBL] [Abstract][Full Text] [Related]
19. Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella.
Martinez G; Kherraf ZE; Zouari R; Fourati Ben Mustapha S; Saut A; Pernet-Gallay K; Bertrand A; Bidart M; Hograindleur JP; Amiri-Yekta A; Kharouf M; Karaouzène T; Thierry-Mieg N; Dacheux-Deschamps D; Satre V; Bonhivers M; Touré A; Arnoult C; Ray PF; Coutton C
Hum Reprod; 2018 Oct; 33(10):1973-1984. PubMed ID: 30137358
[TBL] [Abstract][Full Text] [Related]
20. Embryos derived from couples with consanguineous marriages with globozoospermia should be screened for gender or DPY19L2 deletion.
Ghazavi F; Peymani M; Hashemi MS; Ghaedi K; Nasr-Esfahani MH
Andrologia; 2019 May; 51(4):e13221. PubMed ID: 30584989
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
