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Journal Abstract Search

240 related items for PubMed ID: 27713038

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  • 3. 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; 47(6):668-71. PubMed ID: 25938944
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  • 4. Update on genetic predisposition to colorectal cancer and polyposis.
    Valle L, de Voer RM, Goldberg Y, Sjursen W, Försti A, Ruiz-Ponte C, Caldés T, Garré P, Olsen MF, Nordling M, Castellvi-Bel S, Hemminki K.
    Mol Aspects Med; 2019 Oct; 69():10-26. PubMed ID: 30862463
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  • 5. NTHL1-associate polyposis: first Australian case report.
    Groves A, Gleeson M, Spigelman AD.
    Fam Cancer; 2019 Apr; 18(2):179-182. PubMed ID: 30859360
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  • 6. The role of inherited genetic variants in colorectal polyposis syndromes.
    Short E, Sampson J.
    Adv Genet; 2019 Apr; 103():183-217. PubMed ID: 30904095
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  • 10. 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
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  • 12. 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; 99(5):662-672. PubMed ID: 33454955
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  • 18. 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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  • 19. Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer.
    Bellido F, Sowada N, Mur P, Lázaro C, Pons T, Valdés-Mas R, Pineda M, Aiza G, Iglesias S, Soto JL, Urioste M, Caldés T, Balbín M, Blay P, Rueda D, Durán M, Valencia A, Moreno V, Brunet J, Blanco I, Navarro M, Calin GA, Borck G, Puente XS, Capellá G, Valle L.
    Gastroenterology; 2018 Jan 09; 154(1):181-194.e20. PubMed ID: 28912018
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  • 20. 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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