359 related articles for article (PubMed ID: 12893777)
1. Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice.
Houghtaling S; Timmers C; Noll M; Finegold MJ; Jones SN; Meyn MS; Grompe M
Genes Dev; 2003 Aug; 17(16):2021-35. PubMed ID: 12893777
[TBL] [Abstract][Full Text] [Related]
2. Fanconi anemia group A and C double-mutant mice: functional evidence for a multi-protein Fanconi anemia complex.
Noll M; Battaile KP; Bateman R; Lax TP; Rathbun K; Reifsteck C; Bagby G; Finegold M; Olson S; Grompe M
Exp Hematol; 2002 Jul; 30(7):679-88. PubMed ID: 12135664
[TBL] [Abstract][Full Text] [Related]
3. Heterozygosity for p53 (Trp53+/-) accelerates epithelial tumor formation in fanconi anemia complementation group D2 (Fancd2) knockout mice.
Houghtaling S; Granville L; Akkari Y; Torimaru Y; Olson S; Finegold M; Grompe M
Cancer Res; 2005 Jan; 65(1):85-91. PubMed ID: 15665282
[TBL] [Abstract][Full Text] [Related]
4. Genomic instability in mice is greater in Fanconi anemia caused by deficiency of Fancd2 than Fancg.
Reliene R; Yamamoto ML; Rao PN; Schiestl RH
Cancer Res; 2010 Dec; 70(23):9703-10. PubMed ID: 21118969
[TBL] [Abstract][Full Text] [Related]
5. Severe Fanconi Anemia phenotypes in Fancd2 depletion mice.
Yang Q; Xie H; Zhong Y; Li D; Ke X; Ying H; Yu B; Zhang T
Biochem Biophys Res Commun; 2019 Jun; 514(3):713-719. PubMed ID: 31078270
[TBL] [Abstract][Full Text] [Related]
6. Function of the Fanconi anemia pathway in Fanconi anemia complementation group F and D1 cells.
Siddique MA; Nakanishi K; Taniguchi T; Grompe M; D'Andrea AD
Exp Hematol; 2001 Dec; 29(12):1448-55. PubMed ID: 11750104
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Embryonic lethality after combined inactivation of Fancd2 and Mlh1 in mice.
van de Vrugt HJ; Eaton L; Hanlon Newell A; Al-Dhalimy M; Liskay RM; Olson SB; Grompe M
Cancer Res; 2009 Dec; 69(24):9431-8. PubMed ID: 19934329
[TBL] [Abstract][Full Text] [Related]
9. FANCD2, FANCJ and BRCA2 cooperate to promote replication fork recovery independently of the Fanconi Anemia core complex.
Raghunandan M; Chaudhury I; Kelich SL; Hanenberg H; Sobeck A
Cell Cycle; 2015; 14(3):342-53. PubMed ID: 25659033
[TBL] [Abstract][Full Text] [Related]
10. Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes.
Yamashita T; Nakahata T
Int J Hematol; 2001 Jul; 74(1):33-41. PubMed ID: 11530803
[TBL] [Abstract][Full Text] [Related]
11. FANCD2 monoubiquitination and activation by hexavalent chromium [Cr(VI)] exposure: activation is not required for repair of Cr(VI)-induced DSBs.
Vilcheck SK; Ceryak S; O'Brien TJ; Patierno SR
Mutat Res; 2006 Nov; 610(1-2):21-30. PubMed ID: 16893675
[TBL] [Abstract][Full Text] [Related]
12. A Fanci knockout mouse model reveals common and distinct functions for FANCI and FANCD2.
Dubois EL; Guitton-Sert L; Béliveau M; Parmar K; Chagraoui J; Vignard J; Pauty J; Caron MC; Coulombe Y; Buisson R; Jacquet K; Gamblin C; Gao Y; Laprise P; Lebel M; Sauvageau G; D d'Andrea A; Masson JY
Nucleic Acids Res; 2019 Aug; 47(14):7532-7547. PubMed ID: 31219578
[TBL] [Abstract][Full Text] [Related]
13. Inactivation of murine Usp1 results in genomic instability and a Fanconi anemia phenotype.
Kim JM; Parmar K; Huang M; Weinstock DM; Ruit CA; Kutok JL; D'Andrea AD
Dev Cell; 2009 Feb; 16(2):314-20. PubMed ID: 19217432
[TBL] [Abstract][Full Text] [Related]
14. siRNA depletion of BRCA1, but not BRCA2, causes increased genome instability in Fanconi anemia cells.
Bruun D; Folias A; Akkari Y; Cox Y; Olson S; Moses R
DNA Repair (Amst); 2003 Sep; 2(9):1007-13. PubMed ID: 12967657
[TBL] [Abstract][Full Text] [Related]
15. Heterogeneous activation of the Fanconi anemia pathway by patient-derived FANCA mutants.
Adachi D; Oda T; Yagasaki H; Nakasato K; Taniguchi T; D'Andrea AD; Asano S; Yamashita T
Hum Mol Genet; 2002 Dec; 11(25):3125-34. PubMed ID: 12444097
[TBL] [Abstract][Full Text] [Related]
16. Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2.
Godthelp BC; van Buul PP; Jaspers NG; Elghalbzouri-Maghrani E; van Duijn-Goedhart A; Arwert F; Joenje H; Zdzienicka MZ
Mutat Res; 2006 Oct; 601(1-2):191-201. PubMed ID: 16920162
[TBL] [Abstract][Full Text] [Related]
17. Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.
Godthelp BC; Wiegant WW; Waisfisz Q; Medhurst AL; Arwert F; Joenje H; Zdzienicka MZ
Mutat Res; 2006 Feb; 594(1-2):39-48. PubMed ID: 16154163
[TBL] [Abstract][Full Text] [Related]
18. Gene-specific selection against experimental fanconi anemia gene inactivation in human cancer.
Gallmeier E; Hucl T; Calhoun ES; Cunningham SC; Bunz F; Brody JR; Kern SE
Cancer Biol Ther; 2007 May; 6(5):654-60. PubMed ID: 17387268
[TBL] [Abstract][Full Text] [Related]
19. Functional interaction between the Fanconi Anemia D2 protein and proliferating cell nuclear antigen (PCNA) via a conserved putative PCNA interaction motif.
Howlett NG; Harney JA; Rego MA; Kolling FW; Glover TW
J Biol Chem; 2009 Oct; 284(42):28935-42. PubMed ID: 19704162
[TBL] [Abstract][Full Text] [Related]
20. Compromised repair of radiation-induced DNA double-strand breaks in Fanconi anemia fibroblasts in G2.
Zahnreich S; Weber B; Rösch G; Schindler D; Schmidberger H
DNA Repair (Amst); 2020 Dec; 96():102992. PubMed ID: 33069004
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]