BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Colorectal cancer AND MUTYH, MYH, 4595, ENSG00000132781, hMYH, MGC4416, MYHbeta
559 results:

  • 1. FSHing for DNA Damage: Key Features of MutY Detection of 8-Oxoguanine:Adenine Mismatches.
    Majumdar C; Demir M; Merrill SR; Hashemian M; David SS
    Acc Chem Res; 2024 Apr; 57(7):1019-1031. PubMed ID: 38471078
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. Pan-cancer Interrogation of
    Paller CJ; Tukachinsky H; Maertens A; Decker B; Sampson JR; Cheadle JP; Antonarakis ES
    JCO Precis Oncol; 2024 Feb; 8():e2300251. PubMed ID: 38394468
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Oxidative stress accelerates intestinal tumorigenesis by enhancing 8-oxoguanine-mediated mutagenesis in mutyh-deficient mice.
    Ohno M; Takano N; Hidaka K; Sasaki F; Yamauchi K; Aoki Y; Nohmi T; Nakabeppu Y; Nakatsu Y; Tsuzuki T
    Genome Res; 2024 Feb; 34(1):47-56. PubMed ID: 38290979
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  • 4. [Results of Endoscopic Screening and Therapy of the Duodenum in mutyh-associated Polyposis].
    Haas S; Strassburg CP; Nattermann J; Hueneburg R
    Zentralbl Chir; 2023 Dec; 148(6):502-507. PubMed ID: 37995714
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. The Diagnostic Yield of Genetic Testing in Patients With Multiple colorectal Adenomas: A Specialist Center Cohort Study.
    Mak S; Alexander JL; Clark SK; Hawkins M; Cuthill V; Latchford A; Monahan KJ
    Clin Transl Gastroenterol; 2024 Jan; 15(1):e00645. PubMed ID: 37856205
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. Whole exome germline sequencing in early-onset prostate cancer patients: Genomic findings and clinical outcomes.
    Siegelmann-Danieli N; Neiman V; Bareket-Samish A; Berger R; Peretz A; Alapi H; Tsur E; Patalon T; Beller D; Rimler G; Chodick G; Shohat M
    Prostate; 2024 Jan; 84(1):39-46. PubMed ID: 37842866
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Colibactin mutational signatures in NTHL1 tumor syndrome and mutyh associated polyposis patients.
    Terlouw D; Boot A; Ducarmon QR; Nooij S; Jessurun MA; van Leerdam ME; Tops CM; Langers AMJ; Morreau H; van Wezel T; Nielsen M
    Genes Chromosomes Cancer; 2024 Jan; 63(1):e23208. PubMed ID: 37795928
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. A one-stop approach to diagnosing hereditary colorectal cancer in the Chinese population.
    Li C; Song W; Xu Y; Guo T; Zhou X; Liu F; Xu Y
    J Gastroenterol Hepatol; 2023 Nov; 38(11):1980-1987. PubMed ID: 37749864
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. Increased KRAS G12C Prevalence, High Tumor Mutational Burden, and Specific Mutational Signatures Are Associated With mutyh Mutations: A Pan-cancer Analysis.
    Disel U; Sivakumar S; Pham T; Fleischmann Z; Anu RI; Sokol ES; Kurzrock R
    Oncologist; 2024 Feb; 29(2):e213-e223. PubMed ID: 37589222
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. First report of medulloblastoma in a patient with mutyh-associated polyposis.
    Villy MC; Warcoin M; Filser M; Buecher B; Golmard L; Suybeng V; Schwartz M; Bieche I; Vacher S; Laurence V; Bourdeaut F; Bernier M; Gutman T; Stoppa-Lyonnet D; Masliah-Planchon J; Colas C
    Neuropathol Appl Neurobiol; 2023 Aug; 49(4):e12929. PubMed ID: 37524406
    [TBL] [Abstract] [Full Text] [Related]  

  • 11. Uncommon variants detected via hereditary cancer panel and suggestions for genetic counseling.
    Özdemir Z; Çevik E; Öksüzoğlu ÖBÇ; Doğan M; Ateş Ö; Esin E; Bilgetekin İ; Demirci U; Köseoğlu Ç; Topal A; Karadurmuş N; Erdem HB; Bahsi T
    Mutat Res; 2023; 827():111831. PubMed ID: 37453313
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. MBD4-associated neoplasia syndrome: screening of cases with suggestive phenotypes.
    Terradas M; Gonzalez-Abuin N; García-Mulero S; Viana-Errasti J; Aiza G; Piulats JM; Brunet J; Capellá G; Valle L
    Eur J Hum Genet; 2023 Oct; 31(10):1185-1189. PubMed ID: 37402954
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
    Sherwood K; Ward JC; Soriano I; Martin L; Campbell A; Rahbari R; Kafetzopoulos I; Sproul D; Green A; Sampson JR; Donaldson A; Ong KR; Heinimann K; Nielsen M; Thomas H; Latchford A; Palles C; Tomlinson I
    Nat Commun; 2023 Jun; 14(1):3636. PubMed ID: 37336879
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. Clinical Multigene Panel Testing Identifies Racial and Ethnic Differences in Germline Pathogenic Variants Among Patients With Early-Onset colorectal cancer.
    Seagle HM; Keller SR; Tavtigian SV; Horton C; Holowatyj AN
    J Clin Oncol; 2023 Sep; 41(26):4279-4289. PubMed ID: 37319387
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. Investigating the prevalence of pathogenic variants in Saudi Arabian patients with familial cancer using a multigene next generation sequencing panel.
    AlHarbi M; Mobark NA; AlJabarat WAR; ElBardis H; AlSolme E; Hamdan AB; AlFakeeh AH; AlMushawah F; AlHarthi F; AlSharm AA; Balbaid AAO; AlJohani N; Zhou AY; Robinson HA; Alqahtani SA; Abedalthagafi M
    Oncotarget; 2023 Jun; 14():580-594. PubMed ID: 37306523
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. Evolutionary Origin of
    Xiao F; Li J; Lagniton PNP; Kou SH; Lei H; Tam B; Wang SM
    Biomolecules; 2023 Feb; 13(3):. PubMed ID: 36979362
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. Genotype-Phenotype Correlations in Autosomal Dominant and Recessive APC Mutation-Negative colorectal Adenomatous Polyposis.
    Zhu LH; Dong J; Li WL; Kou ZY; Yang J
    Dig Dis Sci; 2023 Jul; 68(7):2799-2810. PubMed ID: 36862359
    [TBL] [Abstract] [Full Text] [Related]  

  • 18. [Surgical strategies for hereditary colorectal cancer].
    Kelm M; Wiegering A; Germer CT; Flemming S
    Chirurgie (Heidelb); 2023 May; 94(5):412-416. PubMed ID: 36856815
    [TBL] [Abstract] [Full Text] [Related]  

  • 19. Genetic Predisposition to colorectal cancer: How Many and Which Genes to Test?
    Rebuzzi F; Ulivi P; Tedaldi G
    Int J Mol Sci; 2023 Jan; 24(3):. PubMed ID: 36768460
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. High prevalence of mutyh associated polyposis among minority populations in Israel, due to rare founder pathogenic variants.
    Reznick Levi G; Goldberg Y; Segev H; Maza I; Gorelik Y; Laish I; Levi Z; Kedar I; Naftali Nathan S; Sharon Swartzman N; Abu Freha N; Paritsky M; Rennert G; Baris Feldman H; Paperna T; Weiss K; Half EE
    Dig Liver Dis; 2023 Jul; 55(7):880-887. PubMed ID: 36740502
    [TBL] [Abstract] [Full Text] [Related]  


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