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 *

230 related articles for article (PubMed ID: 31916078)

  • 1. 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]  

  • 2. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
    Fan S; Jiao Y; Khan R; Jiang X; Javed AR; Ali A; Zhang H; Zhou J; Naeem M; Murtaza G; Li Y; Yang G; Zaman Q; Zubair M; Guan H; Zhang X; Ma H; Jiang H; Ali H; Dil S; Shah W; Ahmad N; Zhang Y; Shi Q
    Am J Hum Genet; 2021 Feb; 108(2):324-336. PubMed ID: 33508233
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia.
    Maor-Sagie E; Cinnamon Y; Yaacov B; Shaag A; Goldsmidt H; Zenvirt S; Laufer N; Richler C; Frumkin A
    J Assist Reprod Genet; 2015 Jun; 32(6):887-91. PubMed ID: 25899990
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia.
    Hou D; Yao C; Xu B; Luo W; Ke H; Li Z; Qin Y; Guo T
    J Clin Endocrinol Metab; 2022 Feb; 107(3):724-734. PubMed ID: 34718620
    [TBL] [Abstract][Full Text] [Related]  

  • 5.
    He WB; Tu CF; Liu Q; Meng LL; Yuan SM; Luo AX; He FS; Shen J; Li W; Du J; Zhong CG; Lu GX; Lin G; Fan LQ; Tan YQ
    J Med Genet; 2018 Mar; 55(3):198-204. PubMed ID: 29331980
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial primary ovarian insufficiency associated with an SYCE1 point mutation: defective meiosis elucidated in humanized mice.
    Hernández-López D; Geisinger A; Trovero MF; Santiñaque FF; Brauer M; Folle GA; Benavente R; Rodríguez-Casuriaga R
    Mol Hum Reprod; 2020 Jul; 26(7):485-497. PubMed ID: 32402064
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia.
    Huang Y; Tian R; Xu J; Ji Z; Zhang Y; Zhao L; Yang C; Li P; Zhi E; Bai H; Han S; Luo J; Zhao J; Zhang J; Zhou Z; Li Z; Yao C
    BMC Med Genomics; 2022 Jun; 15(1):137. PubMed ID: 35718780
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel exon mutation in SYCE1 gene is associated with non-obstructive azoospermia.
    Feng K; Ge H; Chen H; Cui C; Zhang S; Zhang C; Meng L; Guo H; Zhang L
    J Cell Mol Med; 2022 Feb; 26(4):1245-1252. PubMed ID: 35023261
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency.
    de Vries L; Behar DM; Smirin-Yosef P; Lagovsky I; Tzur S; Basel-Vanagaite L
    J Clin Endocrinol Metab; 2014 Oct; 99(10):E2129-32. PubMed ID: 25062452
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. STAG3 homozygous missense variant causes primary ovarian insufficiency and male non-obstructive azoospermia.
    Jaillard S; McElreavy K; Robevska G; Akloul L; Ghieh F; Sreenivasan R; Beaumont M; Bashamboo A; Bignon-Topalovic J; Neyroud AS; Bell K; Veron-Gastard E; Launay E; van den Bergen J; Nouyou B; Vialard F; Belaud-Rotureau MA; Ayers KL; Odent S; Ravel C; Tucker EJ; Sinclair AH
    Mol Hum Reprod; 2020 Sep; 26(9):665-677. PubMed ID: 32634216
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest.
    Gershoni M; Hauser R; Barda S; Lehavi O; Arama E; Pietrokovski S; Kleiman SE
    Hum Reprod; 2019 Apr; 34(4):666-671. PubMed ID: 30838384
    [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. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. A homozygous missense variant in YTHDC2 induces azoospermia in two siblings.
    Tian S; Faheem M; Satti HS; Xiao J; Zhang F; Khan TN; Liu C
    Mol Genet Genomics; 2024 Sep; 299(1):84. PubMed ID: 39223386
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.