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 *

190 related articles for article (PubMed ID: 37234866)

  • 1. 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]  

  • 2. 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]  

  • 3. Contribution of
    Guzmán-Jiménez A; González-Muñoz S; Cerván-Martín M; Rivera-Egea R; Garrido N; Luján S; Santos-Ribeiro S; Castilla JA; Gonzalvo MC; Clavero A; Vicente FJ; Maldonado V; Villegas-Salmerón J; Burgos M; Jiménez R; Pinto MG; Pereira I; Nunes J; Sánchez-Curbelo J; López-Rodrigo O; Pereira-Caetano I; Marques PI; Carvalho F; Barros A; Bassas L; Seixas S; Gonçalves J; Lopes AM; Larriba S; Palomino-Morales RJ; Carmona FD; Bossini-Castillo L; ;
    Front Cell Dev Biol; 2022; 10():1089782. PubMed ID: 36589743
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.
    Salas-Huetos A; Tüttelmann F; Wyrwoll MJ; Kliesch S; Lopes AM; Goncalves J; Boyden SE; Wöste M; Hotaling JM; ; Nagirnaja L; Conrad DF; Carrell DT; Aston KI
    Hum Genet; 2021 Jan; 140(1):217-227. PubMed ID: 33211200
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes.
    Ghieh F; Barbotin AL; Swierkowski-Blanchard N; Leroy C; Fortemps J; Gerault C; Hue C; Mambu Mambueni H; Jaillard S; Albert M; Bailly M; Izard V; Molina-Gomes D; Marcelli F; Prasivoravong J; Serazin V; Dieudonne MN; Delcroix M; Garchon HJ; Louboutin A; Mandon-Pepin B; Ferlicot S; Vialard F
    Hum Reprod; 2022 May; 37(6):1334-1350. PubMed ID: 35413094
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Toward clinical exomes in diagnostics and management of male infertility.
    Lillepea K; Juchnewitsch AG; Kasak L; Valkna A; Dutta A; Pomm K; Poolamets O; Nagirnaja L; Tamp E; Mahyari E; Vihljajev V; Tjagur S; Papadimitriou S; Riera-Escamilla A; Versbraegen N; Farnetani G; Castillo-Madeen H; Sütt M; Kübarsepp V; Tennisberg S; Korrovits P; Krausz C; Aston KI; Lenaerts T; Conrad DF; Punab M; Laan M
    Am J Hum Genet; 2024 May; 111(5):877-895. PubMed ID: 38614076
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure.
    Hardy JJ; Wyrwoll MJ; Mcfadden W; Malcher A; Rotte N; Pollock NC; Munyoki S; Veroli MV; Houston BJ; Xavier MJ; Kasak L; Punab M; Laan M; Kliesch S; Schlegel P; Jaffe T; Hwang K; Vukina J; Brieño-Enríquez MA; Orwig K; Yanowitz J; Buszczak M; Veltman JA; Oud M; Nagirnaja L; Olszewska M; O'Bryan MK; Conrad DF; Kurpisz M; Tüttelmann F; Yatsenko AN;
    Hum Genet; 2021 Aug; 140(8):1169-1182. PubMed ID: 33963445
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes.
    Wyrwoll MJ; van Walree ES; Hamer G; Rotte N; Motazacker MM; Meijers-Heijboer H; Alders M; Meißner A; Kaminsky E; Wöste M; Krallmann C; Kliesch S; Hunt TJ; Clark AT; Silber S; Stallmeyer B; Friedrich C; van Pelt AMM; Mathijssen IB; Tüttelmann F
    Hum Reprod; 2021 Dec; 37(1):178-189. PubMed ID: 34755185
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Genomic testing for copy number and single nucleotide variants in spermatogenic failure.
    Hardy J; Pollock N; Gingrich T; Sweet P; Ramesh A; Kuong J; Basar A; Jiang H; Hwang K; Vukina J; Jaffe T; Olszewska M; Kurpisz M; Yatsenko AN
    J Assist Reprod Genet; 2022 Sep; 39(9):2103-2114. PubMed ID: 35849255
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Bi-allelic
    Yao C; Yang C; Zhao L; Li P; Tian R; Chen H; Guo Y; Huang Y; Zhi E; Zhai J; Sun H; Zhang J; Hong Y; Zhang L; Ji Z; Zhang F; Zhou Z; Li Z
    J Med Genet; 2021 Oct; 58(10):679-686. PubMed ID: 32900840
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia.
    Li P; Ji Z; Zhi E; Zhang Y; Han S; Zhao L; Tian R; Chen H; Huang Y; Zhang J; Chen H; Zhao F; Zhou Z; Li Z; Yao C
    Reprod Biol Endocrinol; 2022 Jan; 20(1):21. PubMed ID: 35090489
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.