212 related articles for article (PubMed ID: 33454955)
1. 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]
2. 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
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
Adam R; Spier I; Zhao B; Kloth M; Marquez J; Hinrichsen I; Kirfel J; Tafazzoli A; Horpaopan S; Uhlhaas S; Stienen D; Friedrichs N; Altmüller J; Laner A; Holzapfel S; Peters S; Kayser K; Thiele H; Holinski-Feder E; Marra G; Kristiansen G; Nöthen MM; Büttner R; Möslein G; Betz RC; Brieger A; Lifton RP; Aretz S
Am J Hum Genet; 2016 Aug; 99(2):337-51. PubMed ID: 27476653
[TBL] [Abstract][Full Text] [Related]
12. The role of inherited genetic variants in colorectal polyposis syndromes.
Short E; Sampson J
Adv Genet; 2019; 103():183-217. PubMed ID: 30904095
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Contribution to colonic polyposis of recently proposed predisposing genes and assessment of the prevalence of NTHL1- and MSH3-associated polyposes.
Terradas M; Munoz-Torres PM; Belhadj S; Aiza G; Navarro M; Brunet J; Capellá G; Valle L
Hum Mutat; 2019 Nov; 40(11):1910-1923. PubMed ID: 31243857
[TBL] [Abstract][Full Text] [Related]
15. POLE, POLD1, and NTHL1: the last but not the least hereditary cancer-predisposing genes.
Magrin L; Fanale D; Brando C; Fiorino A; Corsini LR; Sciacchitano R; Filorizzo C; Dimino A; Russo A; Bazan V
Oncogene; 2021 Oct; 40(40):5893-5901. PubMed ID: 34363023
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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; 7(1):2214. PubMed ID: 28533537
[TBL] [Abstract][Full Text] [Related]
18. 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]
19.
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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
