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 *

184 related articles for article (PubMed ID: 34595750)

  • 21. 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]  

  • 22. 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]  

  • 23. Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermia.
    Ramasamy R; Bakırcıoğlu ME; Cengiz C; Karaca E; Scovell J; Jhangiani SN; Akdemir ZC; Bainbridge M; Yu Y; Huff C; Gibbs RA; Lupski JR; Lamb DJ
    Fertil Steril; 2015 Aug; 104(2):286-91. PubMed ID: 25956372
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination.
    Li Y; Wu Y; Zhou J; Zhang H; Zhang Y; Ma H; Jiang X; Shi Q
    Hum Reprod; 2021 Apr; 36(5):1436-1445. PubMed ID: 33713115
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans.
    Wu H; Zhang X; Hua R; Li Y; Cheng L; Li K; Liu Y; Gao Y; Shen Q; Wang G; Lv M; Xu Y; He X; Cao Y; Liu M
    Hum Genet; 2022 Nov; 141(11):1795-1809. PubMed ID: 35587281
    [TBL] [Abstract][Full Text] [Related]  

  • 26. X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
    Khan MJ; Pollock N; Jiang H; Castro C; Nazli R; Ahmed J; Basit S; Rajkovic A; Yatsenko AN
    Sci Rep; 2018 Nov; 8(1):16280. PubMed ID: 30389958
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes.
    Gershoni M; Hauser R; Yogev L; Lehavi O; Azem F; Yavetz H; Pietrokovski S; Kleiman SE
    Genet Med; 2017 Sep; 19(9):998-1006. PubMed ID: 28206990
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans.
    Tan YQ; Tu C; Meng L; Yuan S; Sjaarda C; Luo A; Du J; Li W; Gong F; Zhong C; Deng HX; Lu G; Liang P; Lin G
    Genet Med; 2019 May; 21(5):1209-1217. PubMed ID: 31048812
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. 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]  

  • 32. Genetics of Azoospermia.
    Cioppi F; Rosta V; Krausz C
    Int J Mol Sci; 2021 Mar; 22(6):. PubMed ID: 33806855
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A Homozygous Loss-of-Function Mutation in
    Gong C; Abbas T; Muhammad Z; Zhou J; Khan R; Ma H; Zhang H; Shi Q; Shi B
    Int J Mol Sci; 2022 Jun; 23(12):. PubMed ID: 35742973
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pathogenic variants of ATG4D in infertile men with non-obstructive azoospermia identified using whole-exome sequencing.
    Sha Y; Liu W; Wei X; Zhu X; Tang B; Zhang X; Yang X; Wang Y; Wang X
    Clin Genet; 2021 Sep; 100(3):280-291. PubMed ID: 33988247
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. 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]  

  • 38. A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia.
    Luo C; Chen Z; Meng L; Tan C; He W; Tu C; Du J; Lu GX; Lin G; Tan YQ; Hu TY
    Clin Genet; 2024 Jul; 106(1):27-36. PubMed ID: 38342987
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 10.