BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

238 related articles for article (PubMed ID: 27802094)

  • 21. Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability.
    AlAsiri S; Basit S; Wood-Trageser MA; Yatsenko SA; Jeffries EP; Surti U; Ketterer DM; Afzal S; Ramzan K; Faiyaz-Ul Haque M; Jiang H; Trakselis MA; Rajkovic A
    J Clin Invest; 2015 Jan; 125(1):258-62. PubMed ID: 25437880
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.
    Jolly A; Bayram Y; Turan S; Aycan Z; Tos T; Abali ZY; Hacihamdioglu B; Coban Akdemir ZH; Hijazi H; Bas S; Atay Z; Guran T; Abali S; Bas F; Darendeliler F; Colombo R; Barakat TS; Rinne T; White JJ; Yesil G; Gezdirici A; Gulec EY; Karaca E; Pehlivan D; Jhangiani SN; Muzny DM; Poyrazoglu S; Bereket A; Gibbs RA; Posey JE; Lupski JR
    J Clin Endocrinol Metab; 2019 Aug; 104(8):3049-3067. PubMed ID: 31042289
    [TBL] [Abstract][Full Text] [Related]  

  • 23. MCM8-9 complex promotes resection of double-strand break ends by MRE11-RAD50-NBS1 complex.
    Lee KY; Im JS; Shibata E; Park J; Handa N; Kowalczykowski SC; Dutta A
    Nat Commun; 2015 Jul; 6():7744. PubMed ID: 26215093
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The MCM8/9 complex: A recent recruit to the roster of helicases involved in genome maintenance.
    Griffin WC; Trakselis MA
    DNA Repair (Amst); 2019 Apr; 76():1-10. PubMed ID: 30743181
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Control of homologous recombination by the HROB-MCM8-MCM9 pathway.
    Hustedt N; Saito Y; Zimmermann M; Álvarez-Quilón A; Setiaputra D; Adam S; McEwan A; Yuan JY; Olivieri M; Zhao Y; Kanemaki MT; Jurisicova A; Durocher D
    Genes Dev; 2019 Oct; 33(19-20):1397-1415. PubMed ID: 31467087
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutated MCM9 is associated with predisposition to hereditary mixed polyposis and colorectal cancer in addition to primary ovarian failure.
    Goldberg Y; Halpern N; Hubert A; Adler SN; Cohen S; Plesser-Duvdevani M; Pappo O; Shaag A; Meiner V
    Cancer Genet; 2015 Dec; 208(12):621-4. PubMed ID: 26806154
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Inhibiting the MCM8-9 complex selectively sensitizes cancer cells to cisplatin and olaparib.
    Morii I; Iwabuchi Y; Mori S; Suekuni M; Natsume T; Yoshida K; Sugimoto N; Kanemaki MT; Fujita M
    Cancer Sci; 2019 Mar; 110(3):1044-1053. PubMed ID: 30648820
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mcm8 and Mcm9 form a dimeric complex in Xenopus laevis egg extract that is not essential for DNA replication initiation.
    Gambus A; Blow JJ
    Cell Cycle; 2013 Apr; 12(8):1225-32. PubMed ID: 23518502
    [TBL] [Abstract][Full Text] [Related]  

  • 29. MCM8- and MCM9-deficient mice reveal gametogenesis defects and genome instability due to impaired homologous recombination.
    Lutzmann M; Grey C; Traver S; Ganier O; Maya-Mendoza A; Ranisavljevic N; Bernex F; Nishiyama A; Montel N; Gavois E; Forichon L; de Massy B; Méchali M
    Mol Cell; 2012 Aug; 47(4):523-34. PubMed ID: 22771120
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Heterozygous FMN2 missense variant found in a family case of premature ovarian insufficiency.
    Li J; Peng T; Wang L; Long P; Quan R; Tan H; Zeng M; Wu X; Yang J; Xiao H; Shi X
    J Ovarian Res; 2022 Feb; 15(1):31. PubMed ID: 35227295
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency.
    Bestetti I; Barbieri C; Sironi A; Specchia V; Yatsenko SA; De Donno MD; Caslini C; Gentilini D; Crippa M; Larizza L; Marozzi A; Rajkovic A; Toniolo D; Bozzetti MP; Finelli P
    Hum Reprod; 2021 Oct; 36(11):2975-2991. PubMed ID: 34480478
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetics of primary ovarian insufficiency: new developments and opportunities.
    Qin Y; Jiao X; Simpson JL; Chen ZJ
    Hum Reprod Update; 2015; 21(6):787-808. PubMed ID: 26243799
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention.
    Liu H; Wei X; Sha Y; Liu W; Gao H; Lin J; Li Y; Tang Y; Wang Y; Wang Y; Su Z
    J Ovarian Res; 2020 Sep; 13(1):114. PubMed ID: 32962729
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Causal and Candidate Gene Variants in a Large Cohort of Women With Primary Ovarian Insufficiency.
    Gorsi B; Hernandez E; Moore MB; Moriwaki M; Chow CY; Coelho E; Taylor E; Lu C; Walker A; Touraine P; Nelson LM; Cooper AR; Mardis ER; Rajkovic A; Yandell M; Welt CK
    J Clin Endocrinol Metab; 2022 Feb; 107(3):685-714. PubMed ID: 34718612
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Crystal structure of the winged-helix domain of MCM8.
    Zeng H; Li J; Xu H; Li H; Liu Y
    Biochem Biophys Res Commun; 2020 Jun; 526(4):993-998. PubMed ID: 32295713
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Role of
    Potorac I; Laterre M; Malaise O; Nechifor V; Fasquelle C; Colleye O; Detrembleur N; Verdin H; Symoens S; De Baere E; Daly AF; Bours V; Pétrossians P; Pintiaux A
    J Clin Med; 2023 Jan; 12(3):. PubMed ID: 36769638
    [TBL] [Abstract][Full Text] [Related]  

  • 37. AMH mutations with reduced in vitro bioactivity are related to premature ovarian insufficiency.
    Alvaro Mercadal B; Imbert R; Demeestere I; Gervy C; De Leener A; Englert Y; Costagliola S; Delbaere A
    Hum Reprod; 2015 May; 30(5):1196-202. PubMed ID: 25750103
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pathogenic germline MCM9 variants are rare in Australian Lynch-like syndrome patients.
    Liu Q; Hesson LB; Nunez AC; Packham D; Hawkins NJ; Ward RL; Sloane MA
    Cancer Genet; 2016 Nov; 209(11):497-500. PubMed ID: 27886675
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetics of ovarian insufficiency and defects of folliculogenesis.
    França MM; Mendonca BB
    Best Pract Res Clin Endocrinol Metab; 2022 Jan; 36(1):101594. PubMed ID: 34794894
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of new variants and candidate genes in women with familial premature ovarian insufficiency using whole-exome sequencing.
    Morales R; Lledo B; Ortiz JA; Lozano FM; Garcia EM; Bernabeu A; Fuentes A; Bernabeu R
    J Assist Reprod Genet; 2022 Nov; 39(11):2595-2605. PubMed ID: 36208357
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.