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Items: 1 to 20 of 50

1.

FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3.

Wilson JB, Yamamoto K, Marriott AS, Hussain S, Sung P, Hoatlin ME, Mathew CG, Takata M, Thompson LH, Kupfer GM, Jones NJ.

Oncogene. 2008 Jun 12;27(26):3641-52. doi: 10.1038/sj.onc.1211034.

PMID:
18212739
2.

ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage.

Matsuoka S, Ballif BA, Smogorzewska A, McDonald ER 3rd, Hurov KE, Luo J, Bakalarski CE, Zhao Z, Solimini N, Lerenthal Y, Shiloh Y, Gygi SP, Elledge SJ.

Science. 2007 May 25;316(5828):1160-6.

3.

Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair.

Smogorzewska A, Matsuoka S, Vinciguerra P, McDonald ER 3rd, Hurov KE, Luo J, Ballif BA, Gygi SP, Hofmann K, D'Andrea AD, Elledge SJ.

Cell. 2007 Apr 20;129(2):289-301.

4.

FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway.

Ling C, Ishiai M, Ali AM, Medhurst AL, Neveling K, Kalb R, Yan Z, Xue Y, Oostra AB, Auerbach AD, Hoatlin ME, Schindler D, Joenje H, de Winter JP, Takata M, Meetei AR, Wang W.

EMBO J. 2007 Apr 18;26(8):2104-14.

5.

Chk1-mediated phosphorylation of FANCE is required for the Fanconi anemia/BRCA pathway.

Wang X, Kennedy RD, Ray K, Stuckert P, Ellenberger T, D'Andrea AD.

Mol Cell Biol. 2007 Apr;27(8):3098-108.

6.

Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.

Ciccia A, Ling C, Coulthard R, Yan Z, Xue Y, Meetei AR, Laghmani el H, Joenje H, McDonald N, de Winter JP, Wang W, West SC.

Mol Cell. 2007 Feb 9;25(3):331-43.

7.

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.

Xia B, Dorsman JC, Ameziane N, de Vries Y, Rooimans MA, Sheng Q, Pals G, Errami A, Gluckman E, Llera J, Wang W, Livingston DM, Joenje H, de Winter JP.

Nat Genet. 2007 Feb;39(2):159-61.

PMID:
17200672
8.

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.

Reid S, Schindler D, Hanenberg H, Barker K, Hanks S, Kalb R, Neveling K, Kelly P, Seal S, Freund M, Wurm M, Batish SD, Lach FP, Yetgin S, Neitzel H, Ariffin H, Tischkowitz M, Mathew CG, Auerbach AD, Rahman N.

Nat Genet. 2007 Feb;39(2):162-4.

PMID:
17200671
9.

Phosphorylation of FANCD2 on two novel sites is required for mitomycin C resistance.

Ho GP, Margossian S, Taniguchi T, D'Andrea AD.

Mol Cell Biol. 2006 Sep;26(18):7005-15.

10.

Molecular pathogenesis of Fanconi anemia: recent progress.

Taniguchi T, D'Andrea AD.

Blood. 2006 Jun 1;107(11):4223-33. Review.

11.

Molecular pathogenesis of Fanconi anemia.

Collins N, Kupfer GM.

Int J Hematol. 2005 Oct;82(3):176-83. Review.

PMID:
16207587
12.

A FancD2-monoubiquitin fusion reveals hidden functions of Fanconi anemia core complex in DNA repair.

Matsushita N, Kitao H, Ishiai M, Nagashima N, Hirano S, Okawa K, Ohta T, Yu DS, McHugh PJ, Hickson ID, Venkitaraman AR, Kurumizaka H, Takata M.

Mol Cell. 2005 Sep 16;19(6):841-7.

13.

BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ.

Litman R, Peng M, Jin Z, Zhang F, Zhang J, Powell S, Andreassen PR, Cantor SB.

Cancer Cell. 2005 Sep;8(3):255-65.

14.

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.

Levitus M, Waisfisz Q, Godthelp BC, de Vries Y, Hussain S, Wiegant WW, Elghalbzouri-Maghrani E, Steltenpool J, Rooimans MA, Pals G, Arwert F, Mathew CG, Zdzienicka MZ, Hiom K, De Winter JP, Joenje H.

Nat Genet. 2005 Sep;37(9):934-5.

PMID:
16116423
15.

A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.

Meetei AR, Medhurst AL, Ling C, Xue Y, Singh TR, Bier P, Steltenpool J, Stone S, Dokal I, Mathew CG, Hoatlin M, Joenje H, de Winter JP, Wang W.

Nat Genet. 2005 Sep;37(9):958-63.

16.

The deubiquitinating enzyme USP1 regulates the Fanconi anemia pathway.

Nijman SM, Huang TT, Dirac AM, Brummelkamp TR, Kerkhoven RM, D'Andrea AD, Bernards R.

Mol Cell. 2005 Feb 4;17(3):331-9.

17.

Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair.

Nakanishi K, Yang YG, Pierce AJ, Taniguchi T, Digweed M, D'Andrea AD, Wang ZQ, Jasin M.

Proc Natl Acad Sci U S A. 2005 Jan 25;102(4):1110-5.

18.

The DNA damage response: sensing and signaling.

McGowan CH, Russell P.

Curr Opin Cell Biol. 2004 Dec;16(6):629-33. Review.

PMID:
15530773
19.

X-linked inheritance of Fanconi anemia complementation group B.

Meetei AR, Levitus M, Xue Y, Medhurst AL, Zwaan M, Ling C, Rooimans MA, Bier P, Hoatlin M, Pals G, de Winter JP, Wang W, Joenje H.

Nat Genet. 2004 Nov;36(11):1219-24.

PMID:
15502827
20.

ATR-dependent phosphorylation of ATRIP in response to genotoxic stress.

Itakura E, Umeda K, Sekoguchi E, Takata H, Ohsumi M, Matsuura A.

Biochem Biophys Res Commun. 2004 Oct 29;323(4):1197-202.

PMID:
15451423
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