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 *

255 related articles for article (PubMed ID: 32111475)

  • 21. Novel STAG3 variant associated with primary ovarian insufficiency and non-obstructive azoospermia in an Iranian consanguineous family.
    Akbari A; Zoha Tabatabaei S; Salehi N; Padidar K; Almadani N; Ali Sadighi Gilani M; Mashayekhi M; Motevaseli E; Totonchi M
    Gene; 2022 May; 821():146281. PubMed ID: 35176428
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Screening for the microdeletions of azoospermia factor on the Y chromosome in male infertile patients from Guangzhou].
    Liu YF; Ou JP; Zhou CQ; Wang Q; Wang ZL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Oct; 24(5):564-6. PubMed ID: 17922428
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. [Association of FASL-844 polymorphism with the risk of idiopathic azoospermia and severe oligozoospermia].
    Wang W; Lu NX; Xia YA; Wang XR; Zhang W; Song NH; Wei M; Su JT
    Zhonghua Nan Ke Xue; 2007 Apr; 13(4):302-5. PubMed ID: 17491259
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.
    Li L; Sha YW; Su ZY; Mei LB; Ji ZY; Zhang Q; Lin SB; Wang X; Qiu PP; Li P; Yin C
    Gene; 2018 Jan; 639():106-110. PubMed ID: 29017965
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association of TUSC1 and DPF3 gene polymorphisms with male infertility.
    Sato Y; Hasegawa C; Tajima A; Nozawa S; Yoshiike M; Koh E; Kanaya J; Namiki M; Matsumiya K; Tsujimura A; Komatsu K; Itoh N; Eguchi J; Yamauchi A; Iwamoto T
    J Assist Reprod Genet; 2018 Feb; 35(2):257-263. PubMed ID: 28975488
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Association of DAZL A260G and A386G polymorphisms with oligozoospermia- or azoospermia-induced male infertility: A meta-analysis].
    Chen XY; Chen P; Xu C; Zhang XH
    Zhonghua Nan Ke Xue; 2015 Apr; 21(4):345-56. PubMed ID: 26027104
    [TBL] [Abstract][Full Text] [Related]  

  • 28. XPC gene polymorphisms and risk of idiopathic azoospermia or oligozoospermia in a Chinese population.
    Liang J; Gu A; Xia Y; Wu B; Lu N; Wang W; Lu C; Zheng Q; Wang S; Wang X
    Int J Androl; 2009 Jun; 32(3):235-41. PubMed ID: 18067564
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. A Novel Frameshift Microdeletion of the TEX12 Gene Caused Infertility in Two Brothers with Nonobstructive Azoospermia.
    Bui MD; Luong TLA; Tran HD; Duong TTH; Nguyen TN; Nguyen DT; Nguyen TD; Nong VH
    Reprod Sci; 2023 Sep; 30(9):2876-2881. PubMed ID: 37012491
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.
    Chen S; Wang G; Zheng X; Ge S; Dai Y; Ping P; Chen X; Liu G; Zhang J; Yang Y; Zhang X; Zhong A; Zhu Y; Chu Q; Huang Y; Zhang Y; Shen C; Yuan Y; Yuan Q; Pei X; Cheng CY; Sun F
    Hum Mol Genet; 2020 Aug; 29(14):2451-2459. PubMed ID: 32469048
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Male infertility in Northeast China: a cytogenetic study of 135 patients with non-obstructive azoospermia and severe oligozoospermia.
    Zhang ZB; Jiang YT; Yun X; Yang X; Wang RX; Dai RL; Liu RZ
    J Assist Reprod Genet; 2012 Jan; 29(1):83-7. PubMed ID: 22089261
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of a Homozygous Mutation of CCDC40 in a Chinese Infertile Man with MMAF and PCD-like Phenotypes.
    Liu Z; Wang C; Ni F; Li T; Yang F; Wei H; Li T; Huang C; Wang J; Wang B
    Genet Test Mol Biomarkers; 2024 Aug; 28(8):337-341. PubMed ID: 38837151
    [No Abstract]   [Full Text] [Related]  

  • 35. Genetic screening for chromosomal abnormalities and Y chromosome microdeletions in Chinese infertile men.
    Fu L; Xiong DK; Ding XP; Li C; Zhang LY; Ding M; Nie SS; Quan Q
    J Assist Reprod Genet; 2012 Jun; 29(6):521-7. PubMed ID: 22415247
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Single nucleotide polymorphism C677T in the methylenetetrahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligozoospermia.
    A ZC; Yang Y; Zhang SZ; Li N; Zhang W
    Asian J Androl; 2007 Jan; 9(1):57-62. PubMed ID: 16888682
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family.
    Ben Khelifa M; Ghieh F; Boudjenah R; Hue C; Fauvert D; Dard R; Garchon HJ; Vialard F
    Hum Reprod; 2018 Jun; 33(6):1034-1037. PubMed ID: 29659827
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.
    Sha Y; Zheng L; Ji Z; Mei L; Ding L; Lin S; Wang X; Yang X; Li P
    BMC Med Genet; 2018 Apr; 19(1):63. PubMed ID: 29661171
    [TBL] [Abstract][Full Text] [Related]  

  • 39. From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the
    Kherraf ZE; Cazin C; Lestrade F; Muronova J; Coutton C; Arnoult C; Thierry-Mieg N; Ray PF
    Asian J Androl; 2022; 24(3):243-247. PubMed ID: 35017390
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 13.