These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 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]
    of 11.