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Items: 1 to 20 of 160

1.

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype.

Stoepker C, Hain K, Schuster B, Hilhorst-Hofstee Y, Rooimans MA, Steltenpool J, Oostra AB, Eirich K, Korthof ET, Nieuwint AW, Jaspers NG, Bettecken T, Joenje H, Schindler D, Rouse J, de Winter JP.

Nat Genet. 2011 Feb;43(2):138-41. doi: 10.1038/ng.751. Epub 2011 Jan 16.

PMID:
21240277
2.

Mutations of the SLX4 gene in Fanconi anemia.

Kim Y, Lach FP, Desetty R, Hanenberg H, Auerbach AD, Smogorzewska A.

Nat Genet. 2011 Feb;43(2):142-6. doi: 10.1038/ng.750. Epub 2011 Jan 16.

3.

RAD51C: a novel cancer susceptibility gene is linked to Fanconi anemia and breast cancer.

Somyajit K, Subramanya S, Nagaraju G.

Carcinogenesis. 2010 Dec;31(12):2031-8. doi: 10.1093/carcin/bgq210. Epub 2010 Oct 15. Review.

4.

A new nuclease member of the FAN club.

Huang M, D'Andrea AD.

Nat Struct Mol Biol. 2010 Aug;17(8):926-8. doi: 10.1038/nsmb0810-926.

5.

FANCJ/BRIP1 recruitment and regulation of FANCD2 in DNA damage responses.

Zhang F, Fan Q, Ren K, Auerbach AD, Andreassen PR.

Chromosoma. 2010 Dec;119(6):637-49. doi: 10.1007/s00412-010-0285-6. Epub 2010 Jul 31.

6.

Rad18-mediated translesion synthesis of bulky DNA adducts is coupled to activation of the Fanconi anemia DNA repair pathway.

Song IY, Palle K, Gurkar A, Tateishi S, Kupfer GM, Vaziri C.

J Biol Chem. 2010 Oct 8;285(41):31525-36. doi: 10.1074/jbc.M110.138206. Epub 2010 Jul 30.

7.

The FANCM/FAAP24 complex is required for the DNA interstrand crosslink-induced checkpoint response.

Huang M, Kim JM, Shiotani B, Yang K, Zou L, D'Andrea AD.

Mol Cell. 2010 Jul 30;39(2):259-68. doi: 10.1016/j.molcel.2010.07.005.

8.

Translesion DNA synthesis polymerases in DNA interstrand crosslink repair.

Ho TV, Schärer OD.

Environ Mol Mutagen. 2010 Jul;51(6):552-66. doi: 10.1002/em.20573. Review.

PMID:
20658647
9.

Assessing the link between BACH1/FANCJ and MLH1 in DNA crosslink repair.

Cantor SB, Xie J.

Environ Mol Mutagen. 2010 Jul;51(6):500-7. doi: 10.1002/em.20568. Review.

PMID:
20658644
10.

Preventing nonhomologous end joining suppresses DNA repair defects of Fanconi anemia.

Adamo A, Collis SJ, Adelman CA, Silva N, Horejsi Z, Ward JD, Martinez-Perez E, Boulton SJ, La Volpe A.

Mol Cell. 2010 Jul 9;39(1):25-35. doi: 10.1016/j.molcel.2010.06.026.

11.

Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.

Alter BP, Giri N, Savage SA, Peters JA, Loud JT, Leathwood L, Carr AG, Greene MH, Rosenberg PS.

Br J Haematol. 2010 Jul;150(2):179-88. doi: 10.1111/j.1365-2141.2010.08212.x. Epub 2010 Apr 30.

12.

Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1.

Parmar K, Kim J, Sykes SM, Shimamura A, Stuckert P, Zhu K, Hamilton A, Deloach MK, Kutok JL, Akashi K, Gilliland DG, D'andrea A.

Stem Cells. 2010 Jul;28(7):1186-95. doi: 10.1002/stem.437.

13.

Several tetratricopeptide repeat (TPR) motifs of FANCG are required for assembly of the BRCA2/D1-D2-G-X3 complex, FANCD2 monoubiquitylation and phleomycin resistance.

Wilson JB, Blom E, Cunningham R, Xiao Y, Kupfer GM, Jones NJ.

Mutat Res. 2010 Jul 7;689(1-2):12-20. doi: 10.1016/j.mrfmmm.2010.04.003. Epub 2010 May 5.

14.

Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry.

Tamary H, Nishri D, Yacobovich J, Zilber R, Dgany O, Krasnov T, Aviner S, Stepensky P, Ravel-Vilk S, Bitan M, Kaplinsky C, Ben Barak A, Elhasid R, Kapelusnik J, Koren A, Levin C, Attias D, Laor R, Yaniv I, Rosenberg PS, Alter BP.

Haematologica. 2010 Aug;95(8):1300-7. doi: 10.3324/haematol.2009.018119. Epub 2010 Apr 30.

15.

Pathophysiology and management of inherited bone marrow failure syndromes.

Shimamura A, Alter BP.

Blood Rev. 2010 May;24(3):101-22. doi: 10.1016/j.blre.2010.03.002. Epub 2010 Apr 24. Review. Erratum in: Blood Rev. 2010 Jul-Sep;24(4-5):201.

16.

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.

Meindl A, Hellebrand H, Wiek C, Erven V, Wappenschmidt B, Niederacher D, Freund M, Lichtner P, Hartmann L, Schaal H, Ramser J, Honisch E, Kubisch C, Wichmann HE, Kast K, Deissler H, Engel C, Müller-Myhsok B, Neveling K, Kiechle M, Mathew CG, Schindler D, Schmutzler RK, Hanenberg H.

Nat Genet. 2010 May;42(5):410-4. doi: 10.1038/ng.569. Epub 2010 Apr 18.

PMID:
20400964
17.

Mutation of the RAD51C gene in a Fanconi anemia-like disorder.

Vaz F, Hanenberg H, Schuster B, Barker K, Wiek C, Erven V, Neveling K, Endt D, Kesterton I, Autore F, Fraternali F, Freund M, Hartmann L, Grimwade D, Roberts RG, Schaal H, Mohammed S, Rahman N, Schindler D, Mathew CG.

Nat Genet. 2010 May;42(5):406-9. doi: 10.1038/ng.570. Epub 2010 Apr 18.

PMID:
20400963
18.

Haematopoeitic cell transplantation for Fanconi anaemia - when and how?

MacMillan ML, Wagner JE.

Br J Haematol. 2010 Apr;149(1):14-21. doi: 10.1111/j.1365-2141.2010.08078.x. Epub 2010 Feb 5. Review.

PMID:
20136826
19.

FANCM connects the genome instability disorders Bloom's Syndrome and Fanconi Anemia.

Deans AJ, West SC.

Mol Cell. 2009 Dec 25;36(6):943-53. doi: 10.1016/j.molcel.2009.12.006.

20.

Diagnosis of myelodysplastic syndrome among a cohort of 119 patients with fanconi anemia: morphologic and cytogenetic characteristics.

Cioc AM, Wagner JE, MacMillan ML, DeFor T, Hirsch B.

Am J Clin Pathol. 2010 Jan;133(1):92-100. doi: 10.1309/AJCP7W9VMJENZOVG.

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