BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 31815884)

  • 1. Germline MUTYH Mutation in a Pediatric Cancer Survivor Developing a Secondary Malignancy.
    Lavergne V; Sabnis A; Tupule A; Davidson PR; Kline C; Matthay K; Nicolaides T; Goldsby R; Braunstein S; Fogh SE; Sneed PK; Menzel P; Nakamura A; DuBois SG; Haas-Kogan DA; Nakamura JL
    J Pediatr Hematol Oncol; 2020 Oct; 42(7):e647-e654. PubMed ID: 31815884
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Somatic and Germline
    Sherborne AL; Lavergne V; Yu K; Lee L; Davidson PR; Mazor T; Smirnoff IV; Horvai AE; Loh M; DuBois SG; Goldsby RE; Neglia JP; Hammond S; Robison LL; Wustrack R; Costello JF; Nakamura AO; Shannon KM; Bhatia S; Nakamura JL
    Clin Cancer Res; 2017 Apr; 23(7):1852-1861. PubMed ID: 27683180
    [No Abstract]   [Full Text] [Related]  

  • 3. Monoallelic deleterious MUTYH germline variants as a driver for tumorigenesis.
    Barreiro RAS; Sabbaga J; Rossi BM; Achatz MIW; Bettoni F; Camargo AA; Asprino PF; A F Galante P
    J Pathol; 2022 Feb; 256(2):214-222. PubMed ID: 34816434
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
    Lejeune S; Guillemot F; Triboulet JP; Cattan S; Mouton C; ; Porchet N; Manouvrier S; Buisine MP
    Hum Mutat; 2006 Oct; 27(10):1064. PubMed ID: 16941501
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genetic basis of subsequent malignant neoplasms].
    Yoshida M; Kato M
    Rinsho Ketsueki; 2020; 61(9):1174-1178. PubMed ID: 33162513
    [TBL] [Abstract][Full Text] [Related]  

  • 6. First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
    Morak M; Massdorf T; Sykora H; Kerscher M; Holinski-Feder E
    Eur J Cancer; 2011 May; 47(7):1046-55. PubMed ID: 21195604
    [TBL] [Abstract][Full Text] [Related]  

  • 7. NTHL1 and MUTYH polyposis syndromes: two sides of the same coin?
    Weren RD; Ligtenberg MJ; Geurts van Kessel A; De Voer RM; Hoogerbrugge N; Kuiper RP
    J Pathol; 2018 Feb; 244(2):135-142. PubMed ID: 29105096
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary.
    Papp J; Kovacs ME; Matrai Z; Orosz E; Kásler M; Børresen-Dale AL; Olah E
    Fam Cancer; 2016 Jan; 15(1):85-97. PubMed ID: 26446593
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations.
    Ngeow J; Stanuch K; Mester JL; Barnholtz-Sloan JS; Eng C
    J Clin Oncol; 2014 Jun; 32(17):1818-24. PubMed ID: 24778394
    [TBL] [Abstract][Full Text] [Related]  

  • 10. c.1227_1228dupGG (p.Glu410Glyfs), a frequent variant in Tunisian patients with MUTYH associated polyposis.
    Kdissa A; Brusgaard K; Ksiaa M; Golli L; Hallara O; Ousager LB; Manoubi W; Seghaier RB; Adala L; Halleb Y; Saad A; Hmila F; Gribaa M
    Cancer Genet; 2020 Jan; 240():45-53. PubMed ID: 31739127
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of a New Germline Variant in the MUTYH DNA Glycosylase Gene with Colorectal Adenoma Transformation into Malignancy.
    Mahasneh A; Al-Shaheri FN; BaniHani MN
    Iran Biomed J; 2019 Nov; 23(6):412-22. PubMed ID: 31104418
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prevalence of pathogenic variants in cancer-predisposing genes in second cancer after childhood solid cancers.
    Yoshida M; Nakabayashi K; Yang W; Sato-Otsubo A; Tsujimoto SI; Ogata-Kawata H; Kawai T; Ishiwata K; Sakamoto M; Okamura K; Yoshida K; Shirai R; Osumi T; Kiyotani C; Shioda Y; Terashima K; Ishimaru S; Yuza Y; Takagi M; Arakawa Y; Imamura T; Hasegawa D; Inoue A; Yoshioka T; Ito S; Tomizawa D; Koh K; Matsumoto K; Kiyokawa N; Ogawa S; Manabe A; Niwa A; Hata K; Yang JJ; Kato M
    Cancer Med; 2023 May; 12(10):11264-11273. PubMed ID: 37021926
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pathologic findings in breast, fallopian tube, and ovary specimens in non-BRCA hereditary breast and/or ovarian cancer syndromes: a study of 18 patients with deleterious germline mutations in RAD51C, BARD1, BRIP1, PALB2, MUTYH, or CHEK2.
    Schoolmeester JK; Moyer AM; Goodenberger ML; Keeney GL; Carter JM; Bakkum-Gamez JN
    Hum Pathol; 2017 Dec; 70():14-26. PubMed ID: 28709830
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Germline Genetic Features of Young Individuals With Colorectal Cancer.
    Stoffel EM; Koeppe E; Everett J; Ulintz P; Kiel M; Osborne J; Williams L; Hanson K; Gruber SB; Rozek LS
    Gastroenterology; 2018 Mar; 154(4):897-905.e1. PubMed ID: 29146522
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA.
    Schrader KA; Cheng DT; Joseph V; Prasad M; Walsh M; Zehir A; Ni A; Thomas T; Benayed R; Ashraf A; Lincoln A; Arcila M; Stadler Z; Solit D; Hyman DM; Zhang L; Klimstra D; Ladanyi M; Offit K; Berger M; Robson M
    JAMA Oncol; 2016 Jan; 2(1):104-11. PubMed ID: 26556299
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Subsequent neoplasms in childhood cancer survivors.
    Zichová A; Eckschlager T; Ganevová M; Malinová B; Lukš A; Kruseová J
    Cancer Epidemiol; 2020 Oct; 68():101779. PubMed ID: 32682319
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distinct functional consequences of MUTYH variants associated with colorectal cancer: Damaged DNA affinity, glycosylase activity and interaction with PCNA and Hus1.
    Brinkmeyer MK; David SS
    DNA Repair (Amst); 2015 Oct; 34():39-51. PubMed ID: 26377631
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Base excision repair deficiency signatures implicate germline and somatic
    Thibodeau ML; Zhao EY; Reisle C; Ch'ng C; Wong HL; Shen Y; Jones MR; Lim HJ; Young S; Cremin C; Pleasance E; Zhang W; Holt R; Eirew P; Karasinska J; Kalloger SE; Taylor G; Majounie E; Bonakdar M; Zong Z; Bleile D; Chiu R; Birol I; Gelmon K; Lohrisch C; Mungall KL; Mungall AJ; Moore R; Ma YP; Fok A; Yip S; Karsan A; Huntsman D; Schaeffer DF; Laskin J; Marra MA; Renouf DJ; Jones SJM; Schrader KA
    Cold Spring Harb Mol Case Stud; 2019 Apr; 5(2):. PubMed ID: 30833417
    [TBL] [Abstract][Full Text] [Related]  

  • 19. No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
    Steinke V; Rahner N; Morak M; Keller G; Schackert HK; Görgens H; Schmiegel W; Royer-Pokora B; Dietmaier W; Kloor M; Engel C; Propping P; Aretz S;
    Eur J Hum Genet; 2008 May; 16(5):587-92. PubMed ID: 18301448
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MUTYH and the mismatch repair system: partners in crime?
    Niessen RC; Sijmons RH; Ou J; Olthof SG; Osinga J; Ligtenberg MJ; Hogervorst FB; Weiss MM; Tops CM; Hes FJ; de Bock GH; Buys CH; Kleibeuker JH; Hofstra RM
    Hum Genet; 2006 Mar; 119(1-2):206-11. PubMed ID: 16408224
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.