BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 26559593)

  • 1. Biallelic NTHL1 Mutations in a Woman with Multiple Primary Tumors.
    Rivera B; Castellsagué E; Bah I; van Kempen LC; Foulkes WD
    N Engl J Med; 2015 Nov; 373(20):1985-6. PubMed ID: 26559593
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 9(1):9020. PubMed ID: 31227763
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Extending the clinical phenotype associated with biallelic NTHL1 germline mutations.
    Fostira F; Kontopodis E; Apostolou P; Fragkaki M; Androulakis N; Yannoukakos D; Konstantopoulou I; Saloustros E
    Clin Genet; 2018 Dec; 94(6):588-589. PubMed ID: 30248171
    [No Abstract]   [Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 35(2):256-266.e5. PubMed ID: 30753826
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 131():264-273. PubMed ID: 30552997
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prevalence and Characterization of Biallelic and Monoallelic
    Salo-Mullen EE; Maio A; Mukherjee S; Bandlamudi C; Shia J; Kemel Y; Cadoo KA; Liu Y; Carlo M; Ranganathan M; Kane S; Srinivasan P; Chavan SS; Donoghue MTA; Bourque C; Sheehan M; Tejada PR; Patel Z; Arnold AG; Kennedy JA; Amoroso K; Breen K; Catchings A; Sacca R; Marcell V; Markowitz AJ; Latham A; Walsh M; Misyura M; Ceyhan-Birsoy O; Solit DB; Berger MF; Robson ME; Taylor BS; Offit K; Mandelker D; Stadler ZK
    JCO Precis Oncol; 2021; 5():. PubMed ID: 34250384
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Validation of Recently Proposed Colorectal Cancer Susceptibility Gene Variants in an Analysis of Families and Patients-a Systematic Review.
    Broderick P; Dobbins SE; Chubb D; Kinnersley B; Dunlop MG; Tomlinson I; Houlston RS
    Gastroenterology; 2017 Jan; 152(1):75-77.e4. PubMed ID: 27713038
    [TBL] [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; 47(6):668-71. PubMed ID: 25938944
    [TBL] [Abstract][Full Text] [Related]  

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

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

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

  • 14. Intestinal and extraintestinal neoplasms in patients with NTHL1 tumor syndrome: a systematic review.
    Beck SH; Jelsig AM; Yassin HM; Lindberg LJ; Wadt KAW; Karstensen JG
    Fam Cancer; 2022 Oct; 21(4):453-462. PubMed ID: 35292903
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    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; 24(19):. PubMed ID: 37834005
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Six case reports of NTHL1-associated tumor syndrome further support it as a multi-tumor predisposition syndrome.
    Weatherill CB; Burke SA; Haskins CG; Berry DK; Homer JP; Demeure MJ; Darabi S
    Clin Genet; 2023 Feb; 103(2):231-235. PubMed ID: 36196035
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Germline MUTYH (MYH) mutations in Portuguese individuals with multiple colorectal adenomas.
    Isidro G; Laranjeira F; Pires A; Leite J; Regateiro F; Castro e Sousa F; Soares J; Castro C; Giria J; Brito MJ; Medeira A; Teixeira R; Morna H; Gaspar I; Marinho C; Jorge R; Brehm A; Ramos JS; Boavida MG
    Hum Mutat; 2004 Oct; 24(4):353-4. PubMed ID: 15366000
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Case of Multiple Adenomatous Colon Polyps and Meningiomas.
    Liu K; Kupfer SS; Jain R
    Gastroenterology; 2021 Sep; 161(3):811-813. PubMed ID: 33417938
    [No Abstract]   [Full Text] [Related]  

  • 20. Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition.
    Kumpula T; Tervasmäki A; Mantere T; Koivuluoma S; Huilaja L; Tasanen K; Winqvist R; de Voer RM; Pylkäs K
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1493. PubMed ID: 32949222
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.