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 *

151 related articles for article (PubMed ID: 34976027)

  • 1. Novel Bi-Allelic Variants of
    Zhang Y; Li P; Liu N; Jing T; Ji Z; Yang C; Zhao L; Tian R; Chen H; Huang Y; Zhi E; Ou N; Bai H; Zhou Y; Li Z; Yao C
    Front Genet; 2021; 12():799886. PubMed ID: 34976027
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. FANCM Gene Variants in a Male Diagnosed with Sertoli Cell-Only Syndrome and Diffuse Astrocytoma.
    Klarić ML; Marić T; Žunić L; Trgovec-Greif L; Rokić F; Fiolić A; Šorgić AM; Ježek D; Vugrek O; Jakovčević A; Barbalić M; Belužić R; Katušić Bojanac A
    Genes (Basel); 2024 May; 15(6):. PubMed ID: 38927643
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
    Tang D; Li K; Geng H; Xu C; Lv M; Gao Y; Wang G; Yu H; Shao Z; Shen Q; Jiang H; Zhang X; He X; Cao Y
    Reprod Biol Endocrinol; 2022 Apr; 20(1):63. PubMed ID: 35366911
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Over-expression of hsa_circ_0000116 in patients with non-obstructive azoospermia and its predictive value in testicular sperm retrieval.
    Lv MQ; Zhou L; Ge P; Li YX; Zhang J; Zhou DX
    Andrology; 2020 Nov; 8(6):1834-1843. PubMed ID: 32735753
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A novel splicing mutation in helicase for meiosis 1 leads to non-obstructive azoospermia.
    Yao L; Ge Y; Du T; Chen T; Ma J; Song N
    J Assist Reprod Genet; 2023 Oct; 40(10):2493-2498. PubMed ID: 37574498
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Sertoli cells from non-obstructive azoospermia and obstructive azoospermia patients show distinct morphology, Raman spectrum and biochemical phenotype.
    Ma M; Yang S; Zhang Z; Li P; Gong Y; Liu L; Zhu Y; Tian R; Liu Y; Wang X; Liu F; He L; Liu Y; Yang H; Li Z; He Z
    Hum Reprod; 2013 Jul; 28(7):1863-73. PubMed ID: 23503944
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification and Functional Investigation of Novel Heterozygous
    Murtaza G; Yang L; Khan I; Unar A; Khan M; Huan Z; Khan R; Shi Q
    Genet Test Mol Biomarkers; 2021 Oct; 25(10):654-659. PubMed ID: 34672775
    [No Abstract]   [Full Text] [Related]  

  • 17. Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.
    Wang W; Meng L; He J; Su L; Li Y; Tan C; Xu X; Nie H; Zhang H; Du J; Lu G; Luo M; Lin G; Tu C; Tan YQ
    Mol Hum Reprod; 2022 May; 28(6):. PubMed ID: 35485979
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Discrimination and characterization of Sertoli cell-only syndrome in non-obstructive azoospermia using cell-free seminal DDX4.
    Yu Q; Gu X; Shang X; Li H; Xiong C
    Reprod Biomed Online; 2016 Aug; 33(2):189-96. PubMed ID: 27211570
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Expression of testicular androgen receptor in non-obstructive azoospermia and its change after hormonal therapy.
    Kato Y; Shiraishi K; Matsuyama H
    Andrology; 2014 Sep; 2(5):734-40. PubMed ID: 24919724
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.