BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

282 related articles for article (PubMed ID: 35090489)

  • 1. 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]  

  • 2. 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]  

  • 3.
    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]  

  • 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. 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. 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]  

  • 7. 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]  

  • 8. A novel homozygous mutation in the meiotic gene
    Tang D; Xu C; Geng H; Gao Y; Cheng H; Ni X; He X; Cao Y
    Am J Transl Res; 2020; 12(12):8185-8191. PubMed ID: 33437391
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A novel homozygote nonsense variant of MSH4 leads to primary ovarian insufficiency and non-obstructive azoospermia.
    Hashemi Sheikhshabani S; Ghafouri-Fard S; Hosseini E; Omrani MD
    Mol Biol Rep; 2024 Jan; 51(1):68. PubMed ID: 38175272
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A homozygous frameshift variant in SYCP2 caused meiotic arrest and non-obstructive azoospermia.
    Xu J; Sun Y; Zhang Y; Ou N; Bai H; Zhao J; Xu S; Luo J; Han S; Li P; Tian R; Zhi E; Huang Y; Zhang J; Liu G; Li Z; Yao C
    Clin Genet; 2023 Nov; 104(5):577-581. PubMed ID: 37337432
    [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. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia.
    Zhang Y; Li N; Ji Z; Bai H; Ou N; Tian R; Li P; Zhi E; Huang Y; Zhao J; Han Y; Zhang J; Zhou Y; Li Z; Yao C
    J Hum Genet; 2023 Jun; 68(6):383-392. PubMed ID: 36759719
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia.
    Zhu X; Hu K; Cheng H; Wu H; Li K; Gao Y; Lv M; Xu C; Geng H; Shen Q; Cao Y; He X; Tang D; Guo R
    Clin Genet; 2024 Jan; 105(1):99-105. PubMed ID: 37715646
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Bi-allelic SPATA22 variants cause premature ovarian insufficiency and nonobstructive azoospermia due to meiotic arrest.
    Yao C; Hou D; Ji Z; Pang D; Li P; Tian R; Zhang Y; Ou N; Bai H; Zhi E; Huang Y; Qin Y; Zhao J; Wang C; Zhou Z; Guo T; Li Z
    Clin Genet; 2022 May; 101(5-6):507-516. PubMed ID: 35285020
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.