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 *

181 related articles for article (PubMed ID: 34595750)

  • 1. A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia.
    Wu H; Zhang X; Shen Q; Liu Y; Gao Y; Wang G; Lv M; Hua R; Xu Y; Zhou P; Wei Z; Tao F; He X; Cao Y; Liu M
    Clin Genet; 2022 Jan; 101(1):55-64. PubMed ID: 34595750
    [TBL] [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. 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]  

  • 4. A novel homozygous FBXO43 mutation associated with male infertility and teratozoospermia in a consanguineous Chinese family.
    Ma Y; Xie N; Xie D; Sun L; Li S; Li P; Li Y; Li J; Dong Z; Xie X
    Fertil Steril; 2019 May; 111(5):909-917.e1. PubMed ID: 30878252
    [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. 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]  

  • 7. FBXO43 variants in patients with female infertility characterized by early embryonic arrest.
    Wang W; Wang W; Xu Y; Shi J; Fu J; Chen B; Mu J; Zhang Z; Zhao L; Lin J; Du J; Li Q; He L; Jin L; Sun X; Wang L; Sang Q
    Hum Reprod; 2021 Jul; 36(8):2392-2402. PubMed ID: 34052850
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 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. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. A pathogenic DMC1 frameshift mutation causes nonobstructive azoospermia but not primary ovarian insufficiency in humans.
    Cao D; Shi F; Guo C; Liu Y; Lin Z; Zhang J; Li RHW; Yao Y; Liu K; Ng EHY; Yeung WSB; Wang T
    Mol Hum Reprod; 2021 Sep; 27(9):. PubMed ID: 34515795
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia.
    Tang D; Lv M; Gao Y; Cheng H; Li K; Xu C; Geng H; Li G; Shen Q; Wang C; He X; Cao Y
    Reprod Biol Endocrinol; 2021 Aug; 19(1):129. PubMed ID: 34429122
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.