458 related articles for article (PubMed ID: 25938944)
1. 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]
2. 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]
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; 244(2):135-142. PubMed ID: 29105096
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
Lejeune S; Guillemot F; Triboulet JP; Cattan S; Mouton C; ; Porchet N; Manouvrier S; Buisine MP
Hum Mutat; 2006 Oct; 27(10):1064. PubMed ID: 16941501
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
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.
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]
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
[TBL] [Abstract][Full Text] [Related]
13. The first mutations in the MYH gene reported in Moroccan colon cancer patients.
Laarabi FZ; Cherkaoui Jaouad I; Baert-Desurmont S; Ouldim K; Ibrahimi A; Kanouni N; Frebourg T; Sefiani A
Gene; 2012 Mar; 496(1):55-8. PubMed ID: 22266422
[TBL] [Abstract][Full Text] [Related]
14. Germline MYH mutations in a clinic-based series of Canadian multiple colorectal adenoma patients.
Croitoru ME; Cleary SP; Berk T; Di Nicola N; Kopolovic I; Bapat B; Gallinger S
J Surg Oncol; 2007 May; 95(6):499-506. PubMed ID: 17219385
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Hereditary forms of colorectal adenomatous polyposis].
Kohoutová M; Stekrová J; Sulová M; Zidková K; Kleibl Z; Vandrovcová J; Kebrdlová V; Kotlas J; Jirásek V
Cas Lek Cesk; 2006; 145(6):475-9. PubMed ID: 16836001
[TBL] [Abstract][Full Text] [Related]
17. Increased MUTYH mutation frequency among Dutch families with breast cancer and colorectal cancer.
Wasielewski M; Out AA; Vermeulen J; Nielsen M; van den Ouweland A; Tops CM; Wijnen JT; Vasen HF; Weiss MM; Klijn JG; Devilee P; Hes FJ; Schutte M
Breast Cancer Res Treat; 2010 Dec; 124(3):635-41. PubMed ID: 20191381
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
Spier I; Kerick M; Drichel D; Horpaopan S; Altmüller J; Laner A; Holzapfel S; Peters S; Adam R; Zhao B; Becker T; Lifton RP; Holinski-Feder E; Perner S; Thiele H; Nöthen MM; Hoffmann P; Timmermann B; Schweiger MR; Aretz S
Fam Cancer; 2016 Apr; 15(2):281-8. PubMed ID: 26780541
[TBL] [Abstract][Full Text] [Related]
20. Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.
Nielsen M; Hes FJ; Nagengast FM; Weiss MM; Mathus-Vliegen EM; Morreau H; Breuning MH; Wijnen JT; Tops CM; Vasen HF
Clin Genet; 2007 May; 71(5):427-33. PubMed ID: 17489848
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
