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 *

155 related articles for article (PubMed ID: 36068176)

  • 21. Single nucleotide polymorphisms of the gonadotrophin-regulated testicular helicase (GRTH) gene may be associated with the human spermatogenesis impairment.
    A Z; Zhang S; Yang Y; Ma Y; Lin L; Zhang W
    Hum Reprod; 2006 Mar; 21(3):755-9. PubMed ID: 16293649
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. AZF deletions in Indian populations: original study and meta-analyses.
    Waseem AS; Singh V; Makker GC; Trivedi S; Mishra G; Singh K; Rajender S
    J Assist Reprod Genet; 2020 Feb; 37(2):459-469. PubMed ID: 31919744
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia.
    Simoni M; Gromoll J; Dworniczak B; Rolf C; Abshagen K; Kamischke A; Carani C; Meschede D; Behre HM; Horst J; Nieschlag E
    Fertil Steril; 1997 Mar; 67(3):542-7. PubMed ID: 9091344
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Linking human Dead end 1 (DND1) variants to male infertility employing zebrafish embryos.
    Westerich KJ; Reinecke S; Emich J; Wyrwoll MJ; Stallmeyer B; Meyer M; Oud MS; Fietz D; Pilatz A; Kliesch S; Reichman-Fried M; Tarbashevich K; Limon T; Stehling M; Friedrich C; Tüttelmann F; Raz E
    Hum Reprod; 2023 Apr; 38(4):655-670. PubMed ID: 36807972
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia.
    Tu C; Meng L; Nie H; Yuan S; Wang W; Du J; Lu G; Lin G; Tan YQ
    Fertil Steril; 2020 Mar; 113(3):561-568. PubMed ID: 32111475
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Androgen receptor CAG gene polymorphism in men with azoospermia and oligozoospermia in Ukraine].
    Fesaĭ OA; Kravchenko SA; Tyrkus MIa; Makukh GV; Zinchenko VM; Strelko GV; Livshits LA
    Tsitol Genet; 2009; 43(6):45-51. PubMed ID: 20458976
    [TBL] [Abstract][Full Text] [Related]  

  • 29. SPANX gene variation in fertile and infertile males.
    Hansen S; Eichler EE; Fullerton SM; Carrell D
    Syst Biol Reprod Med; 2010 Feb; 55():18-26. PubMed ID: 20073942
    [TBL] [Abstract][Full Text] [Related]  

  • 30. SPATA16 promoter hypermethylation and downregulation in male infertility.
    Sujit KM; Pallavi S; Singh V; Andrabi SW; Trivedi S; Sankhwar SN; Gupta G; Rajender S
    Andrologia; 2022 Nov; 54(10):e14548. PubMed ID: 36177775
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Exosomal microRNAs in seminal plasma are markers of the origin of azoospermia and can predict the presence of sperm in testicular tissue.
    Barceló M; Mata A; Bassas L; Larriba S
    Hum Reprod; 2018 Jun; 33(6):1087-1098. PubMed ID: 29635626
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia.
    Yi S; Wang W; Su L; Meng L; Li Y; Tan C; Liu Q; Zhang H; Fan L; Lu G; Hu L; Du J; Lin G; Tan YQ; Tu C; Zhang Q
    Mol Hum Reprod; 2024 Feb; 30(2):. PubMed ID: 38258527
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.
    Cerván-Martín M; Bossini-Castillo L; Guzmán-Jiménez A; Rivera-Egea R; Garrido N; Lujan S; Romeu G; Santos-Ribeiro S; ; ; Castilla JA; Gonzalvo MDC; Clavero A; Maldonado V; Vicente FJ; Burgos M; Jiménez R; González-Muñoz S; Sánchez-Curbelo J; López-Rodrigo O; Pereira-Caetano I; Marques PI; Carvalho F; Barros A; Bassas L; Seixas S; Gonçalves J; Larriba S; Lopes AM; Palomino-Morales RJ; Carmona FD
    Andrology; 2022 Oct; 10(7):1339-1350. PubMed ID: 35752927
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. Basonuclin 1 deficiency causes testicular premature aging: BNC1 cooperates with TAF7L to regulate spermatogenesis.
    Li JY; Liu YF; Xu HY; Zhang JY; Lv PP; Liu ME; Ying YY; Qian YQ; Li K; Li C; Huang Y; Xu GF; Ding GL; Mao YC; Xu CM; Liu XM; Sheng JZ; Zhang D; Huang HF
    J Mol Cell Biol; 2020 Jan; 12(1):71-83. PubMed ID: 31065688
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Analysis of Y chromosome microdeletion in non-obstructive male infertile patients with azoospermia and severe oligozoospermia].
    Ting-Ting H; Xian-Ping D; Xia W; Jing R; Li-Yuan Z
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2013 Mar; 44(2):188-92. PubMed ID: 23745252
    [TBL] [Abstract][Full Text] [Related]  

  • 38. TTY2 genes deletions as genetic risk factor of male infertility.
    Shaveisi-Zadeh F; Alibakhshi R; Asgari R; Rostami-Far Z; Bakhtiari M; Abdi H; Movafagh A; Mirfakhraie R
    Cell Mol Biol (Noisy-le-grand); 2017 Feb; 63(2):57-61. PubMed ID: 28364784
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Mutation of KLHL-10 in idiopathic infertile males with azoospermia, oligospermia or asthenospermia].
    Qiu QM; Liu G; Li WN; Shi QW; Zhu FX; Lu GX
    Zhonghua Nan Ke Xue; 2009 Nov; 15(11):974-9. PubMed ID: 20218307
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Four Single Nucleotide Polymorphisms in INSR, SLC6A14, TAS2R38, and OR2W3 Genes in Association with Idiopathic Infertility in Persian Men.
    Siasi E; Aleyasin A
    J Reprod Med; 2016; 61(3-4):145-52. PubMed ID: 27172637
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.