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Journal Abstract Search

188 related items for PubMed ID: 30552997

  • 1. 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
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  • 2. 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
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  • 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 09; 244(2):135-142. PubMed ID: 29105096
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  • 4. NTHL1 in genomic integrity, aging and cancer.
    Das L, Quintana VG, Sweasy JB.
    DNA Repair (Amst); 2020 Sep 09; 93():102920. PubMed ID: 33087284
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  • 5. 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 09; 117():103372. PubMed ID: 35870279
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  • 6. 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
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  • 8. Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohort.
    Khan N, Lipsa A, Arunachal G, Ramadwar M, Sarin R.
    Sci Rep; 2017 May 22; 7(1):2214. PubMed ID: 28533537
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  • 9. Different organization of base excision repair of uracil in DNA in nuclei and mitochondria and selective upregulation of mitochondrial uracil-DNA glycosylase after oxidative stress.
    Akbari M, Otterlei M, Peña-Diaz J, Krokan HE.
    Neuroscience; 2007 Apr 14; 145(4):1201-12. PubMed ID: 17101234
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  • 10. 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 14; 99(5):662-672. PubMed ID: 33454955
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  • 14. 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 14; 47(6):668-71. PubMed ID: 25938944
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  • 16. 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
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  • 17. NEIL1 is the major DNA glycosylase that processes 5-hydroxyuracil in the proximity of a DNA single-strand break.
    Parsons JL, Kavli B, Slupphaug G, Dianov GL.
    Biochemistry; 2007 Apr 03; 46(13):4158-63. PubMed ID: 17348689
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  • 19. 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
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