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Journal Abstract Search

200 related items for PubMed ID: 33087284

  • 1. NTHL1 in genomic integrity, aging and cancer.
    Das L, Quintana VG, Sweasy JB.
    DNA Repair (Amst); 2020 Sep; 93():102920. PubMed ID: 33087284
    [Abstract] [Full Text] [Related]

  • 2. Defective repair capacity of variant proteins of the DNA glycosylase NTHL1 for 5-hydroxyuracil, an oxidation product of cytosine.
    Shinmura K, Kato H, Kawanishi Y, Goto M, Tao H, Yoshimura K, Nakamura S, Misawa K, Sugimura H.
    Free Radic Biol Med; 2019 Feb 01; 131():264-273. PubMed ID: 30552997
    [Abstract] [Full Text] [Related]

  • 3. 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 01; 244(2):135-142. PubMed ID: 29105096
    [Abstract] [Full Text] [Related]

  • 4. Polymorphic variant Asp239Tyr of human DNA glycosylase NTHL1 is inactive for removal of a variety of oxidatively-induced DNA base lesions from genomic DNA.
    Kant M, Quintana V, Coskun E, Jaruga P, Lloyd RS, Sweasy JB, Dizdaroglu M.
    DNA Repair (Amst); 2022 Sep 01; 117():103372. PubMed ID: 35870279
    [Abstract] [Full Text] [Related]

  • 5. Overexpression of the base excision repair NTHL1 glycosylase causes genomic instability and early cellular hallmarks of cancer.
    Limpose KL, Trego KS, Li Z, Leung SW, Sarker AH, Shah JA, Ramalingam SS, Werner EM, Dynan WS, Cooper PK, Corbett AH, Doetsch PW.
    Nucleic Acids Res; 2018 May 18; 46(9):4515-4532. PubMed ID: 29522130
    [Abstract] [Full Text] [Related]

  • 6. Mouse Embryonic Fibroblasts Isolated From Nthl1 D227Y Knockin Mice Exhibit Defective DNA Repair and Increased Genome Instability.
    Marsden CG, Das L, Nottoli TP, Kathe SD, Doublié S, Wallace SS, Sweasy JB.
    DNA Repair (Amst); 2022 Jan 18; 109():103247. PubMed ID: 34826736
    [Abstract] [Full Text] [Related]

  • 7. MUTYH-associated polyposis--from defect in base excision repair to clinical genetic testing.
    Cheadle JP, Sampson JR.
    DNA Repair (Amst); 2007 Mar 01; 6(3):274-9. PubMed ID: 17161978
    [Abstract] [Full Text] [Related]

  • 8. NTHL1-associate polyposis: first Australian case report.
    Groves A, Gleeson M, Spigelman AD.
    Fam Cancer; 2019 Apr 01; 18(2):179-182. PubMed ID: 30859360
    [Abstract] [Full Text] [Related]

  • 9. NTHL1 defines novel cancer syndrome.
    Kuiper RP, Hoogerbrugge N.
    Oncotarget; 2015 Oct 27; 6(33):34069-70. PubMed ID: 26431160
    [No Abstract] [Full Text] [Related]

  • 10. A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.
    Weren RD, Ligtenberg MJ, Kets CM, de Voer RM, Verwiel ET, Spruijt L, van Zelst-Stams WA, Jongmans MC, Gilissen C, Hehir-Kwa JY, Hoischen A, Shendure J, Boyle EA, Kamping EJ, Nagtegaal ID, Tops BB, Nagengast FM, Geurts van Kessel A, van Krieken JH, Kuiper RP, Hoogerbrugge N.
    Nat Genet; 2015 Jun 27; 47(6):668-71. PubMed ID: 25938944
    [Abstract] [Full Text] [Related]

  • 11. Evaluation of NTHL1, NEIL1, NEIL2, MPG, TDG, UNG and SMUG1 genes in familial colorectal cancer predisposition.
    Broderick P, Bagratuni T, Vijayakrishnan J, Lubbe S, Chandler I, Houlston RS.
    BMC Cancer; 2006 Oct 09; 6():243. PubMed ID: 17029639
    [Abstract] [Full Text] [Related]

  • 12. NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas.
    Belhadj S, Quintana I, Mur P, Munoz-Torres PM, Alonso MH, Navarro M, Terradas M, Piñol V, Brunet J, Moreno V, Lázaro C, Capellá G, Valle L.
    Sci Rep; 2019 Jun 21; 9(1):9020. PubMed ID: 31227763
    [Abstract] [Full Text] [Related]

  • 13. Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.
    Grolleman JE, de Voer RM, Elsayed FA, Nielsen M, Weren RDA, Palles C, Ligtenberg MJL, Vos JR, Ten Broeke SW, de Miranda NFCC, Kuiper RA, Kamping EJ, Jansen EAM, Vink-Börger ME, Popp I, Lang A, Spier I, Hüneburg R, James PA, Li N, Staninova M, Lindsay H, Cockburn D, Spasic-Boskovic O, Clendenning M, Sweet K, Capellá G, Sjursen W, Høberg-Vetti H, Jongmans MC, Neveling K, Geurts van Kessel A, Morreau H, Hes FJ, Sijmons RH, Schackert HK, Ruiz-Ponte C, Dymerska D, Lubinski J, Rivera B, Foulkes WD, Tomlinson IP, Valle L, Buchanan DD, Kenwrick S, Adlard J, Dimovski AJ, Campbell IG, Aretz S, Schindler D, van Wezel T, Hoogerbrugge N, Kuiper RP.
    Cancer Cell; 2019 Feb 11; 35(2):256-266.e5. PubMed ID: 30753826
    [Abstract] [Full Text] [Related]

  • 14. Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.
    Boulouard F, Kasper E, Buisine MP, Lienard G, Vasseur S, Manase S, Bahuau M, Barouk Simonet E, Bubien V, Coulet F, Cusin V, Dhooge M, Golmard L, Goussot V, Hamzaoui N, Lacaze E, Lejeune S, Mauillon J, Beaumont MP, Pinson S, Tlemsani C, Toulas C, Rey JM, Uhrhammer N, Bougeard G, Frebourg T, Houdayer C, Baert-Desurmont S.
    Clin Genet; 2021 May 11; 99(5):662-672. PubMed ID: 33454955
    [Abstract] [Full Text] [Related]

  • 15. Monoallelic NTHL1 Loss-of-Function Variants and Risk of Polyposis and Colorectal Cancer.
    Elsayed FA, Grolleman JE, Ragunathan A, NTHL1 study group, Buchanan DD, van Wezel T, de Voer RM.
    Gastroenterology; 2020 Dec 11; 159(6):2241-2243.e6. PubMed ID: 32860789
    [No Abstract] [Full Text] [Related]

  • 16. Oxidative Damage in Sporadic Colorectal Cancer: Molecular Mapping of Base Excision Repair Glycosylases MUTYH and hOGG1 in Colorectal Cancer Patients.
    Kavec MJ, Urbanova M, Makovicky P, Opattová A, Tomasova K, Kroupa M, Kostovcikova K, Siskova A, Navvabi N, Schneiderova M, Vymetalkova V, Vodickova L, Vodicka P.
    Int J Mol Sci; 2022 May 20; 23(10):. PubMed ID: 35628513
    [Abstract] [Full Text] [Related]

  • 17. Unraveling novel mRNA transcripts of the human DNA N-glycosylase 1 (NTHL1) gene with the implementation of an innovative targeted DNA-seq assay.
    Diamantopoulos MA, Adamopoulos PG, Tsiakanikas P, Nisotakis T, Skourou PC, Scorilas A.
    Gene; 2024 Dec 20; 930():148856. PubMed ID: 39147115
    [Abstract] [Full Text] [Related]

  • 18. NTHL1 Gene Mutations in Polish Polyposis Patients-Weighty Player or Vague Background?
    Grot N, Kaczmarek-Ryś M, Lis-Tanaś E, Kryszczyńska A, Nowakowska D, Jakubiuk-Tomaszuk A, Paszkowski J, Banasiewicz T, Hryhorowicz S, Pławski A.
    Int J Mol Sci; 2023 Sep 26; 24(19):. PubMed ID: 37834005
    [Abstract] [Full Text] [Related]

  • 19. Oxidative Damage in Sporadic Colorectal Cancer: Molecular Mapping of Base Excision Repair Glycosylases in Colorectal Cancer Patients.
    Vodicka P, Urbanova M, Makovicky P, Tomasova K, Kroupa M, Stetina R, Opattova A, Kostovcikova K, Siskova A, Schneiderova M, Vymetalkova V, Vodickova L.
    Int J Mol Sci; 2020 Apr 02; 21(7):. PubMed ID: 32252452
    [Abstract] [Full Text] [Related]

  • 20. Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer.
    Drost J, van Boxtel R, Blokzijl F, Mizutani T, Sasaki N, Sasselli V, de Ligt J, Behjati S, Grolleman JE, van Wezel T, Nik-Zainal S, Kuiper RP, Cuppen E, Clevers H.
    Science; 2017 Oct 13; 358(6360):234-238. PubMed ID: 28912133
    [Abstract] [Full Text] [Related]

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