These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
557 related articles for article (PubMed ID: 27165003)
1. The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer. Esteban-Jurado C; Franch-Expósito S; Muñoz J; Ocaña T; Carballal S; López-Cerón M; Cuatrecasas M; Vila-Casadesús M; Lozano JJ; Serra E; Beltran S; Brea-Fernández A; Ruiz-Ponte C; Castells A; Bujanda L; Garre P; Caldés T; Cubiella J; Balaguer F; Castellví-Bel S Eur J Hum Genet; 2016 Oct; 24(10):1501-5. PubMed ID: 27165003 [TBL] [Abstract][Full Text] [Related]
2. Evaluation of Fanconi Anemia genes in familial breast cancer predisposition. Seal S; Barfoot R; Jayatilake H; Smith P; Renwick A; Bascombe L; McGuffog L; Evans DG; Eccles D; Easton DF; Stratton MR; Rahman N; Cancer Res; 2003 Dec; 63(24):8596-9. PubMed ID: 14695169 [TBL] [Abstract][Full Text] [Related]
3. Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50. Chandrasekharappa SC; Chinn SB; Donovan FX; Chowdhury NI; Kamat A; Adeyemo AA; Thomas JW; Vemulapalli M; Hussey CS; Reid HH; Mullikin JC; Wei Q; Sturgis EM Cancer; 2017 Oct; 123(20):3943-3954. PubMed ID: 28678401 [TBL] [Abstract][Full Text] [Related]
4. Germline mutations in a DNA repair pathway are associated with familial colorectal cancer. Xu P; Sun D; Gao Y; Jiang Y; Zhong M; Zhao G; Chen J; Wang Z; Liu Q; Hong J; Chen H; Chen YX; Fang JY JCI Insight; 2021 Sep; 6(18):. PubMed ID: 34549727 [TBL] [Abstract][Full Text] [Related]
5. Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition. García MJ; Fernández V; Osorio A; Barroso A; Fernández F; Urioste M; Benítez J Carcinogenesis; 2009 Nov; 30(11):1898-902. PubMed ID: 19737859 [TBL] [Abstract][Full Text] [Related]
6. Frequency of heterozygous germline pathogenic variants in genes for Fanconi anemia in patients with non-BRCA1/BRCA2 breast cancer: a meta-analysis. Alter BP; Best AF Breast Cancer Res Treat; 2020 Jul; 182(2):465-476. PubMed ID: 32488392 [TBL] [Abstract][Full Text] [Related]
7. Analysis of a FANCE Splice Isoform in Regard to DNA Repair. Bouffard F; Plourde K; Bélanger S; Ouellette G; Labrie Y; Durocher F J Mol Biol; 2015 Sep; 427(19):3056-73. PubMed ID: 26277624 [TBL] [Abstract][Full Text] [Related]
8. Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1. Hussain S; Witt E; Huber PA; Medhurst AL; Ashworth A; Mathew CG Hum Mol Genet; 2003 Oct; 12(19):2503-10. PubMed ID: 12915460 [TBL] [Abstract][Full Text] [Related]
9. FANCC, FANCE, and FANCD2 form a ternary complex essential to the integrity of the Fanconi anemia DNA damage response pathway. Gordon SM; Alon N; Buchwald M J Biol Chem; 2005 Oct; 280(43):36118-25. PubMed ID: 16127171 [TBL] [Abstract][Full Text] [Related]
10. 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; 154(1):181-194.e20. PubMed ID: 28912018 [TBL] [Abstract][Full Text] [Related]
12. Homozygous loss of function BRCA1 variant causing a Fanconi-anemia-like phenotype, a clinical report and review of previous patients. Freire BL; Homma TK; Funari MFA; Lerario AM; Leal AM; Velloso EDRP; Malaquias AC; Jorge AAL Eur J Med Genet; 2018 Mar; 61(3):130-133. PubMed ID: 29133208 [TBL] [Abstract][Full Text] [Related]
13. Martín-Morales L; Garre P; Lorca V; Cazorla M; Llovet P; Bando I; García-Barberan V; González-Morales ML; Esteban-Jurado C; de la Hoya M; Castellví-Bel S; Caldés T Cancer Prev Res (Phila); 2021 Feb; 14(2):185-194. PubMed ID: 33115781 [TBL] [Abstract][Full Text] [Related]
14. The genetics of FANCC and FANCG in familial pancreatic cancer. Rogers CD; van der Heijden MS; Brune K; Yeo CJ; Hruban RH; Kern SE; Goggins M Cancer Biol Ther; 2004 Feb; 3(2):167-9. PubMed ID: 14726700 [TBL] [Abstract][Full Text] [Related]
15. Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype. Sawyer SL; Tian L; Kähkönen M; Schwartzentruber J; Kircher M; ; ; Majewski J; Dyment DA; Innes AM; Boycott KM; Moreau LA; Moilanen JS; Greenberg RA Cancer Discov; 2015 Feb; 5(2):135-42. PubMed ID: 25472942 [TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of Fanconi anemia and mismatch repair genes in patients with colorectal carcinoma. Colombino M; Avallone A; Izzo F; Tatangelo F; Budroni M; Cossu A; Galimi F; Comella P; Botti G; Sini MC; Tanda F; Palmieri G; Oncol Rep; 2011 Apr; 25(4):899-904. PubMed ID: 21286667 [TBL] [Abstract][Full Text] [Related]
17. Mutational analysis of the breast cancer susceptibility gene BRIP1 /BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families. Guénard F; Labrie Y; Ouellette G; Joly Beauparlant C; Simard J; ; Durocher F J Hum Genet; 2008; 53(7):579. PubMed ID: 18414782 [TBL] [Abstract][Full Text] [Related]
18. Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies. Bogliolo M; Pujol R; Aza-Carmona M; Muñoz-Subirana N; Rodriguez-Santiago B; Casado JA; Rio P; Bauser C; Reina-Castillón J; Lopez-Sanchez M; Gonzalez-Quereda L; Gallano P; Catalá A; Ruiz-Llobet A; Badell I; Diaz-Heredia C; Hladun R; Senent L; Argiles B; Bergua Burgues JM; Bañez F; Arrizabalaga B; López Almaraz R; Lopez M; Figuera Á; Molinés A; Pérez de Soto I; Hernando I; Muñoz JA; Del Rosario Marin M; Balmaña J; Stjepanovic N; Carrasco E; Cuesta I; Cosuelo JM; Regueiro A; Moraleda Jimenez J; Galera-Miñarro AM; Rosiñol L; Carrió A; Beléndez-Bieler C; Escudero Soto A; Cela E; de la Mata G; Fernández-Delgado R; Garcia-Pardos MC; Sáez-Villaverde R; Barragaño M; Portugal R; Lendinez F; Hernadez I; Vagace JM; Tapia M; Nieto J; Garcia M; Gonzalez M; Vicho C; Galvez E; Valiente A; Antelo ML; Ancliff P; Garcia F; Dopazo J; Sevilla J; Paprotka T; Pérez-Jurado LA; Bueren J; Surralles J J Med Genet; 2020 Apr; 57(4):258-268. PubMed ID: 31586946 [TBL] [Abstract][Full Text] [Related]
19. Functional analysis of Fanconi anemia mutations in China. Li N; Ding L; Li B; Wang J; D'Andrea AD; Chen J Exp Hematol; 2018 Oct; 66():32-41.e8. PubMed ID: 30031030 [TBL] [Abstract][Full Text] [Related]