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 *

162 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. 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]  

  • 13. 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]  

  • 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 9.