BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

286 related articles for article (PubMed ID: 27798098)

  • 41. Identification of transcriptome characteristics of granulosa cells and the possible role of UBE2C in the pathogenesis of premature ovarian insufficiency.
    Liu D; Guan X; Liu W; Jia Y; Zhou H; Xi C; Zhao M; Fang Y; Wu L; Li K
    J Ovarian Res; 2023 Oct; 16(1):203. PubMed ID: 37848988
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Mutational analysis of theFAM175A gene in patients with premature ovarian insufficiency.
    Xu X; Zhang Y; Zhao S; Bian Y; Ning Y; Qin Y
    Reprod Biomed Online; 2019 Jun; 38(6):943-950. PubMed ID: 31000350
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure.
    Qin Y; Jiao X; Dalgleish R; Vujovic S; Li J; Simpson JL; Al-Azzawi F; Chen ZJ
    Fertil Steril; 2014 Apr; 101(4):1104-1109.e6. PubMed ID: 24524832
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mutations in eIF4ENIF1 are associated with primary ovarian insufficiency.
    Kasippillai T; MacArthur DG; Kirby A; Thomas B; Lambalk CB; Daly MJ; Welt CK
    J Clin Endocrinol Metab; 2013 Sep; 98(9):E1534-9. PubMed ID: 23902945
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Premature ovarian failure in nobox-deficient mice is caused by defects in somatic cell invasion and germ cell cyst breakdown.
    Lechowska A; Bilinski S; Choi Y; Shin Y; Kloc M; Rajkovic A
    J Assist Reprod Genet; 2011 Jul; 28(7):583-9. PubMed ID: 21369782
    [TBL] [Abstract][Full Text] [Related]  

  • 46. ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure.
    Delcour C; Amazit L; Patino LC; Magnin F; Fagart J; Delemer B; Young J; Laissue P; Binart N; Beau I
    Genet Med; 2019 Apr; 21(4):930-938. PubMed ID: 30224786
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice.
    Li G; Yang X; Wang L; Pan Y; Chen S; Shang L; Zhang Y; Wu Y; Zhou Z; Chen Q; Zhang X; Zhang L; Wang Y; Li J; Jin L; Wu Y; Zhang X; Zhang F
    J Med Genet; 2022 Jun; 59(6):579-588. PubMed ID: 33888552
    [TBL] [Abstract][Full Text] [Related]  

  • 48. FOXL2 impairment in human disease.
    Verdin H; De Baere E
    Horm Res Paediatr; 2012; 77(1):2-11. PubMed ID: 22248822
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A novel FOXL2 gene mutation and BMP15 variants in a woman with primary ovarian insufficiency and blepharophimosis-ptosis-epicanthus inversus syndrome.
    Settas N; Anapliotou M; Kanavakis E; Fryssira H; Sofocleous C; Dacou-Voutetakis C; Chrousos GP; Voutetakis A
    Menopause; 2015 Nov; 22(11):1264-8. PubMed ID: 25988799
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Rare variants in FANCA induce premature ovarian insufficiency.
    Yang X; Zhang X; Jiao J; Zhang F; Pan Y; Wang Q; Chen Q; Cai B; Tang S; Zhou Z; Chen S; Yin H; Fu W; Luo Y; Li D; Li G; Shang L; Yang J; Jin L; Shi Q; Wu Y
    Hum Genet; 2019 Dec; 138(11-12):1227-1236. PubMed ID: 31535215
    [TBL] [Abstract][Full Text] [Related]  

  • 51. miR-21 and Pellino-1 Expression Profiling in Autoimmune Premature Ovarian Insufficiency.
    Li X; Xie J; Wang Q; Cai H; Xie C; Fu X
    J Immunol Res; 2020; 2020():3582648. PubMed ID: 32352018
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Oxidative stress and ATPase6 mutation is associated with primary ovarian insufficiency.
    Venkatesh S; Kumar M; Sharma A; Kriplani A; Ammini AC; Talwar P; Agarwal A; Dada R
    Arch Gynecol Obstet; 2010 Sep; 282(3):313-8. PubMed ID: 20361200
    [TBL] [Abstract][Full Text] [Related]  

  • 53. NR5A1 (SF-1) mutations are not a major cause of primary ovarian insufficiency.
    Voican A; Bachelot A; Bouligand J; Francou B; Dulon J; Lombès M; Touraine P; Guiochon-Mantel A
    J Clin Endocrinol Metab; 2013 May; 98(5):E1017-21. PubMed ID: 23543655
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause.
    Chen Q; Ke H; Luo X; Wang L; Wu Y; Tang S; Li J; Jin L; Zhang F; Qin Y; Chen X
    Hum Mol Genet; 2020 Sep; 29(16):2698-2707. PubMed ID: 32716490
    [TBL] [Abstract][Full Text] [Related]  

  • 55. NOBOX does right for the follicle reserve: insights into premature ovarian failure.
    Albertini DF
    J Assist Reprod Genet; 2011 Jul; 28(7):567-8. PubMed ID: 21822584
    [No Abstract]   [Full Text] [Related]  

  • 56. FANCL gene mutations in premature ovarian insufficiency.
    Yang Y; Guo T; Liu R; Ke H; Xu W; Zhao S; Qin Y
    Hum Mutat; 2020 May; 41(5):1033-1041. PubMed ID: 32048394
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Reduced Foxo3a, FoxL2, and p27 mRNA expression in human ovarian tissue in premature ovarian insufficiency.
    Thanatsis N; Kaponis A; Koika V; Georgopoulos NA; Decavalas GO
    Hormones (Athens); 2019 Dec; 18(4):409-415. PubMed ID: 31637660
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A novel homozygous 1-bp deletion in the NOBOX gene in two Brazilian sisters with primary ovarian failure.
    França MM; Funari MFA; Lerario AM; Nishi MY; Pita CC; Fontenele EGP; Mendonca BB
    Endocrine; 2017 Dec; 58(3):442-447. PubMed ID: 29067606
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Mutations in MSH5 in primary ovarian insufficiency.
    Guo T; Zhao S; Zhao S; Chen M; Li G; Jiao X; Wang Z; Zhao Y; Qin Y; Gao F; Chen ZJ
    Hum Mol Genet; 2017 Apr; 26(8):1452-1457. PubMed ID: 28175301
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A kaleidoscopic view of ovarian genes associated with premature ovarian insufficiency and senescence.
    Yang Q; Mumusoglu S; Qin Y; Sun Y; Hsueh AJ
    FASEB J; 2021 Aug; 35(8):e21753. PubMed ID: 34233068
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.