-
1
-
-
33744481750
-
Molecular pathogenesis of Fanconi anemia: Recent progress
-
Taniguchi T, D'Andrea AD. Molecular pathogenesis of Fanconi anemia: recent progress. Blood 2006;107:4223-33.
-
(2006)
Blood
, vol.107
, pp. 4223-4233
-
-
Taniguchi, T.1
D'Andrea, A.D.2
-
2
-
-
0031052108
-
Bloom's syndrome. XX. The first 100 cancers
-
German J. Bloom's syndrome. XX. The first 100 cancers. Cancer Genet Cytogenet 1997;93:100-6.
-
(1997)
Cancer Genet Cytogenet
, vol.93
, pp. 100-106
-
-
German, J.1
-
3
-
-
0033513587
-
Inactivation of ataxia telangiectasia mutated gene in B-cell chronic lymphocytic leukaemia
-
Stankovic T, Weber P, Stewart G, Bedenham T, Murray J, Byrd P, et al. Inactivation of ataxia telangiectasia mutated gene in B-cell chronic lymphocytic leukaemia. The Lancet 1999;353:26-9.
-
(1999)
The Lancet
, vol.353
, pp. 26-29
-
-
Stankovic, T.1
Weber, P.2
Stewart, G.3
Bedenham, T.4
Murray, J.5
Byrd, P.6
-
4
-
-
0035328489
-
Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL)
-
Varon R, Reis A, Henze G, von Einsiedel HG, Sperling K, Seeger K. Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL). Canc Res 2001;61:3570-2.
-
(2001)
Canc Res
, vol.61
, pp. 3570-3572
-
-
Varon, R.1
Reis, A.2
Henze, G.3
von Einsiedel, H.G.4
Sperling, K.5
Seeger, K.6
-
5
-
-
0033166623
-
Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient
-
Riballo E, Critchlow SE, Teo S-H, Doherty AJ, Priestley A, Broughton B, et al. Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient. Curr Biol 1999;9:699-704.
-
(1999)
Curr Biol
, vol.9
, pp. 699-704
-
-
Riballo, E.1
Critchlow, S.E.2
Teo, S.-H.3
Doherty, A.J.4
Priestley, A.5
Broughton, B.6
-
6
-
-
0036733355
-
The therapeutic potential of Poly (ADP-ribose) Polymerase inhibitors
-
Virag S, Szabo C. The therapeutic potential of Poly (ADP-ribose) Polymerase inhibitors. Pharm Rev 2002;54:375-429.
-
(2002)
Pharm Rev
, vol.54
, pp. 375-429
-
-
Virag, S.1
Szabo, C.2
-
7
-
-
17244375049
-
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase
-
Bryant HE, Schultz N, Thomas HD, Parker KM, Flower D, Lopez E, et al. Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase. Nature 2005;434:913-7.
-
(2005)
Nature
, vol.434
, pp. 913-917
-
-
Bryant, H.E.1
Schultz, N.2
Thomas, H.D.3
Parker, K.M.4
Flower, D.5
Lopez, E.6
-
8
-
-
17244373777
-
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
-
Farmer H, McCabe N, Lord CJ, Tutt ANJ, Johnson DA, Knights C, et al. Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature 2005;434:917-21.
-
(2005)
Nature
, vol.434
, pp. 917-921
-
-
Farmer, H.1
McCabe, N.2
Lord, C.J.3
Tutt, A.N.J.4
Johnson, D.A.5
Knights, C.6
-
9
-
-
33645532464
-
Inhibition of poly (ADP-ribose) polymerase activates ATM which is required for subsequent homologous recombination repair
-
Bryant HE, Helleday T. Inhibition of poly (ADP-ribose) polymerase activates ATM which is required for subsequent homologous recombination repair. Nucl Acid Res 2006;34:1685-91.
-
(2006)
Nucl Acid Res
, vol.34
, pp. 1685-1691
-
-
Bryant, H.E.1
Helleday, T.2
-
10
-
-
85047695296
-
Increased error-prone non homologous DNA End-Joining - A proposed mechanism of Chromosomal instability in Bloom's syndrome
-
Gaymes TJ, North PS, Brady N, Hickson ID, Mufti GJ, Rassool FV. Increased error-prone non homologous DNA End-Joining - A proposed mechanism of Chromosomal instability in Bloom's syndrome. Oncogene 2002;21:2525-33.
-
(2002)
Oncogene
, vol.21
, pp. 2525-2533
-
-
Gaymes, T.J.1
North, P.S.2
Brady, N.3
Hickson, I.D.4
Mufti, G.J.5
Rassool, F.V.6
-
11
-
-
33748427812
-
Histone deacetylase inhibitors (HDI) induce DNA damage and repair: A mechanism for HDI dependent apoptosis in leukemia cells
-
Gaymes TJ, Orr S, Mufti GJ, Rassool FV. Histone deacetylase inhibitors (HDI) induce DNA damage and repair: a mechanism for HDI dependent apoptosis in leukemia cells. Mol Cancer Res 2006;4:563-73.
-
(2006)
Mol Cancer Res
, vol.4
, pp. 563-573
-
-
Gaymes, T.J.1
Orr, S.2
Mufti, G.J.3
Rassool, F.V.4
-
12
-
-
0037447303
-
Increased error-prone NHEJ activity in myeloid leukemias is associated with DNA damage at sites that recruit key non-homologous end-joining proteins
-
Brady N, Gaymes TJ, Cheung M, Mufti GJ, Rassool FV. Increased error-prone NHEJ activity in myeloid leukemias is associated with DNA damage at sites that recruit key non-homologous end-joining proteins. Cancer Res 2003;63:1798-805.
-
(2003)
Cancer Res
, vol.63
, pp. 1798-1805
-
-
Brady, N.1
Gaymes, T.J.2
Cheung, M.3
Mufti, G.J.4
Rassool, F.V.5
-
13
-
-
1542713417
-
Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia
-
Tischkowitz MD, Morgan NV, Grimwade D, Eddy C, Ball S, Vorechovsky I, et al. Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia. Leukemia 2004;18:420-5.
-
(2004)
Leukemia
, vol.18
, pp. 420-425
-
-
Tischkowitz, M.D.1
Morgan, N.V.2
Grimwade, D.3
Eddy, C.4
Ball, S.5
Vorechovsky, I.6
-
14
-
-
0036336280
-
Analysis of the Fanconi anaemia complentation group A gene in acute myeloid leukemia
-
Condie A, Powles RL, Hudson CD, Shepherd V, Bevan S, Yuille MR, et al. Analysis of the Fanconi anaemia complentation group A gene in acute myeloid leukemia. Leuk Lymphoma 2002;43:1849-53.
-
(2002)
Leuk Lymphoma
, vol.43
, pp. 1849-1853
-
-
Condie, A.1
Powles, R.L.2
Hudson, C.D.3
Shepherd, V.4
Bevan, S.5
Yuille, M.R.6
-
15
-
-
19944411110
-
Fanconi Anemia protein FANCD2 promotes immunoglobulin gene conversion and DNA repair through a mechanism related to homologous recombination
-
Yamamoto K, Hirano S, Ishiai M, Morishima K, Kitao H, Namikoshi K, et al. Fanconi Anemia protein FANCD2 promotes immunoglobulin gene conversion and DNA repair through a mechanism related to homologous recombination. Mol Cell Biol 2005;25:34-43
-
(2005)
Mol Cell Biol
, vol.25
, pp. 34-43
-
-
Yamamoto, K.1
Hirano, S.2
Ishiai, M.3
Morishima, K.4
Kitao, H.5
Namikoshi, K.6
-
16
-
-
12844286052
-
Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair
-
Nakanishi K, Yang Y-G, Pierce AJ, Taniguchi T, Digweed M, D'Andrea AD, et al. Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair. Proc Natl Acad Sci USA 2005;102:1110-5.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 1110-1115
-
-
Nakanishi, K.1
Yang, Y.-G.2
Pierce, A.J.3
Taniguchi, T.4
Digweed, M.5
D'Andrea, A.D.6
-
17
-
-
0037123768
-
Convergence of the fanconi anemia and ataxia telangiectasia signaling pathways
-
Taniguchi T, Garcia-Higuera I, Xu B, Andreassen PR, Gregory RC, Kim ST, et al. Convergence of the fanconi anemia and ataxia telangiectasia signaling pathways. Cell 2002;109:459-72.
-
(2002)
Cell
, vol.109
, pp. 459-472
-
-
Taniguchi, T.1
Garcia-Higuera, I.2
Xu, B.3
Andreassen, P.R.4
Gregory, R.C.5
Kim, S.T.6
-
18
-
-
0032522789
-
RecQ helicase, in concert with RecA and SSB proteins, initiates and disrupts DNA recombination
-
Harmon FG, Kowalczykowski SC. RecQ helicase, in concert with RecA and SSB proteins, initiates and disrupts DNA recombination. Genes Dev 1998;12:1134-44.
-
(1998)
Genes Dev
, vol.12
, pp. 1134-1144
-
-
Harmon, F.G.1
Kowalczykowski, S.C.2
-
19
-
-
0347987856
-
The Bloom's syndrome helicase suppresses crossing over during homologous recombination
-
Wu L, Hickson ID. The Bloom's syndrome helicase suppresses crossing over during homologous recombination. Nature 2003;18:870-4.
-
(2003)
Nature
, vol.18
, pp. 870-874
-
-
Wu, L.1
Hickson, I.D.2
-
20
-
-
0033119701
-
Defending genome integrity during DNA replication: A proposed role for RecQ family helicases
-
Chakraverty RK, Hickson ID. Defending genome integrity during DNA replication: a proposed role for RecQ family helicases. Bioessays 1999;21:286-94.
-
(1999)
Bioessays
, vol.21
, pp. 286-294
-
-
Chakraverty, R.K.1
Hickson, I.D.2
-
21
-
-
0037195937
-
A DNA double-strand break repair defect in Fanconi anemia
-
Donahue SL, Campbell C. A DNA double-strand break repair defect in Fanconi anemia. J Biol Chem 2002;277:46243-7.
-
(2002)
J Biol Chem
, vol.277
, pp. 46243-46247
-
-
Donahue, S.L.1
Campbell, C.2
-
22
-
-
34548312368
-
Tip60 is a haplo-insufficient tumour suppressor required for an oncogene-induced DNA damage response
-
Gorrini C, Squatrito M, Luise C, Syed N, Perna D, Wark L, et al. Tip60 is a haplo-insufficient tumour suppressor required for an oncogene-induced DNA damage response. Nature 2007;448:1063-7.
-
(2007)
Nature
, vol.448
, pp. 1063-1067
-
-
Gorrini, C.1
Squatrito, M.2
Luise, C.3
Syed, N.4
Perna, D.5
Wark, L.6
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