-
1
-
-
0035474694
-
Fanconi anemia and DNA repair
-
Grompe, M. & D'Andrea, A. Fanconi anemia and DNA repair. Hum. Mol. Genet. 10, 2253-2259 (2001).
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2253-2259
-
-
Grompe, M.1
D'Andrea, A.2
-
2
-
-
0035379611
-
The emerging genetic and molecular basis of Fanconi anaemia
-
Joenje, H. & Patel, K. J. The emerging genetic and molecular basis of Fanconi anaemia. Nature Rev. Genet. 2, 446-457 (2001).
-
(2001)
Nature Rev. Genet.
, vol.2
, pp. 446-457
-
-
Joenje, H.1
Patel, K.J.2
-
3
-
-
0028837378
-
Fanconi anemia
-
Auerbach, A. D. Fanconi anemia. Dermatol. Clin. 13, 41-49 (1995).
-
(1995)
Dermatol. Clin.
, vol.13
, pp. 41-49
-
-
Auerbach, A.D.1
-
4
-
-
0029861118
-
Fanconi anemia and malignancies
-
Alter, B. P. Fanconi anemia and malignancies. Am. J. Hematol. 53, 99-110 (1996).
-
(1996)
Am. J. Hematol.
, vol.53
, pp. 99-110
-
-
Alter, B.P.1
-
5
-
-
0037306904
-
Cancer incidence in persons with Fanconi's anemia
-
5 Sept (doi:10.1182/blood-2002-05-1498)
-
Rosenberg, P. S., Greene, M. H. & Alter B. P. Cancer incidence in persons with Fanconi's anemia. Blood 5 Sept 2002 (doi:10.1182/blood-2002-05-1498).
-
(2002)
Blood
-
-
Rosenberg, P.S.1
Greene, M.H.2
Alter, B.P.3
-
6
-
-
0030884238
-
Molecular biology of Fanconi anemia: Implications for diagnosis and therapy
-
D'Andrea, A. D. & Grompe, M. Molecular biology of Fanconi anemia: implications for diagnosis and therapy. Blood 90, 1725-1736 (1997).
-
(1997)
Blood
, vol.90
, pp. 1725-1736
-
-
D'Andrea, A.D.1
Grompe, M.2
-
7
-
-
0022353392
-
Endogenous blockage and delay of the chromosome cycle despite normal recruitment and growth phase explain poor proliferation and frequent edomitosis in Fanconi anemia cells
-
Kubbies, M., Schindler, D., Hoehn, H., Schinzel, A. & Rabinovitch, P. S. Endogenous blockage and delay of the chromosome cycle despite normal recruitment and growth phase explain poor proliferation and frequent edomitosis in Fanconi anemia cells. Am. J. Hum. Genet. 37, 1022-1030 (1985).
-
(1985)
Am. J. Hum. Genet.
, vol.37
, pp. 1022-1030
-
-
Kubbies, M.1
Schindler, D.2
Hoehn, H.3
Schinzel, A.4
Rabinovitch, P.S.5
-
8
-
-
0020067168
-
Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment
-
Kaiser, T. N. et al. Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment. Cytometry 2, 291-297 (1982).
-
(1982)
Cytometry
, vol.2
, pp. 291-297
-
-
Kaiser, T.N.1
-
9
-
-
0035691754
-
The 4N cell cycle delay in Fanconi anemia reflects growth arrest in late S phase
-
Akkan, Y. M. et al. The 4N cell cycle delay in Fanconi anemia reflects growth arrest in late S phase. Mol. Genet. Metab. 74, 403-412 (2001).
-
(2001)
Mol. Genet. Metab.
, vol.74
, pp. 403-412
-
-
Akkan, Y.M.1
-
10
-
-
0027861014
-
Fanconi anemia diagnosis and the diepoxybutane (DEB) test
-
Auerbach, A. D. Fanconi anemia diagnosis and the diepoxybutane (DEB) test. Exp. Hematol. 21, 731-733 (1993).
-
(1993)
Exp. Hematol.
, vol.21
, pp. 731-733
-
-
Auerbach, A.D.1
-
11
-
-
0032796554
-
Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism
-
Waisfisz, Q. et al. Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism. Nature Genet. 22, 379-383 (1999).
-
(1999)
Nature Genet.
, vol.22
, pp. 379-383
-
-
Waisfisz, Q.1
-
12
-
-
7344253051
-
Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transfer
-
Pulsipher, M. et al. Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transfer. Mol. Med. 4, 468-479 (1998).
-
(1998)
Mol. Med.
, vol.4
, pp. 468-479
-
-
Pulsipher, M.1
-
13
-
-
18444378426
-
Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool
-
Hanenberg, H. et al. Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool. Exp. Hematol. 30, 410-420 (2002).
-
(2002)
Exp. Hematol.
, vol.30
, pp. 410-420
-
-
Hanenberg, H.1
-
14
-
-
0028125830
-
Evaluation of granulocyte-macrophage colony-stimulating factor for treatment of pancytopenia in children with fanconi anemia
-
Guinan, E. C., Lopez, K. D., Huhn, R. D., Felser, J. M. & Nathan, D. G. Evaluation of granulocyte-macrophage colony-stimulating factor for treatment of pancytopenia in children with fanconi anemia. J. Pediatr. 124, 144-150 (1994).
-
(1994)
J. Pediatr.
, vol.124
, pp. 144-150
-
-
Guinan, E.C.1
Lopez, K.D.2
Huhn, R.D.3
Felser, J.M.4
Nathan, D.G.5
-
15
-
-
0030071799
-
Unrelated donor bone marrow transplantation for Fanconi anemia
-
Davies, S. M. et al. Unrelated donor bone marrow transplantation for Fanconi anemia. Bone Marrow Transplant. 17, 43-47 (1996).
-
(1996)
Bone Marrow Transplant.
, vol.17
, pp. 43-47
-
-
Davies, S.M.1
-
16
-
-
0025563311
-
Transplantation of embilical cord blood in Fanconi's anemia
-
Gluckman, E. et al. Transplantation of embilical cord blood in Fanconi's anemia. Nouvelle Revue Francaise d Hematologie 32, 423-425 (1990).
-
(1990)
Nouvelle Revue Francaise d Hematologie
, vol.32
, pp. 423-425
-
-
Gluckman, E.1
-
17
-
-
0027325335
-
Umbilical cord blood stem cell transplantation
-
Wagner, J. E. Umbilical cord blood stem cell transplantation. Am. J. Pedatr. Hematol. Oncol. 15, 169-174 (1993).
-
(1993)
Am. J. Pedatr. Hematol. Oncol.
, vol.15
, pp. 169-174
-
-
Wagner, J.E.1
-
18
-
-
17744367210
-
Prompt and durable hematopoietic reconstitution by unrelated cord blood transplantation in a child with Fanconi anemia
-
Yoshimasu, T. et al. Prompt and durable hematopoietic reconstitution by unrelated cord blood transplantation in a child with Fanconi anemia. Bone Marrow Transplant. 27, 767-769 (2001).
-
(2001)
Bone Marrow Transplant.
, vol.27
, pp. 767-769
-
-
Yoshimasu, T.1
-
19
-
-
0035958352
-
Preimplantation diagnosis for Fanconi anemia combined with HLA matching
-
Vedinsky, Y., Rechitsky, S., Schoolcraft, W., Strom, C. & Kuliev, A. Preimplantation diagnosis for Fanconi anemia combined with HLA matching. JAMA 285, 3130-3133 (2001).
-
(2001)
JAMA
, vol.285
, pp. 3130-3133
-
-
Vedinsky, Y.1
Rechitsky, S.2
Schoolcraft, W.3
Strom, C.4
Kuliev, A.5
-
20
-
-
0033588822
-
Engraftment of hematopoietic progenitor cells transduced with the Fanconi anemia group C gene (FANCC)
-
Liu, J. M. et al. Engraftment of hematopoietic progenitor cells transduced with the Fanconi anemia group C gene (FANCC). Hum. Gene Ther. 10, 2337-2346 (1999).
-
(1999)
Hum. Gene Ther.
, vol.10
, pp. 2337-2346
-
-
Liu, J.M.1
-
21
-
-
0031580604
-
Retroviral mediated gene transfer of the Fanconi anemia complementation group C gene to hematopoietic progenitors of group C patients
-
Liu, J. M. et al. Retroviral mediated gene transfer of the Fanconi anemia complementation group C gene to hematopoietic progenitors of group C patients. Hum. Gene Ther. 8, 1715-1730 (1997).
-
(1997)
Hum. Gene Ther.
, vol.8
, pp. 1715-1730
-
-
Liu, J.M.1
-
22
-
-
0026521238
-
Cloning of cDNAs for Fanconi's anaemia by functional complementation
-
Strathdee, C. A., Gavish, H., Shannon, W. R. & Buchwald, M. Cloning of cDNAs for Fanconi's anaemia by functional complementation. Nature 356, 763-767 (1992). Describes the first successful cloning of a Fanconi anemia cDNA, by functional complementation of an FA-C lymphoblast line. A similar strategy was subsequently used for the cloning of the FANCA, FANCG, FANCF and FANCE cDNAs.
-
(1992)
Nature
, vol.356
, pp. 763-767
-
-
Strathdee, C.A.1
Gavish, H.2
Shannon, W.R.3
Buchwald, M.4
-
23
-
-
0029827550
-
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
-
Lo Ten Foe, J. R. et al. Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA. Nature Genet. 14, 320-323 (1996).
-
(1996)
Nature Genet.
, vol.14
, pp. 320-323
-
-
Lo Ten Foe, J.R.1
-
24
-
-
0033759693
-
Isolation of a cDNA representing the fanconi anemia complementation group E gene
-
de Winter, J. P. et al. Isolation of a cDNA representing the fanconi anemia complementation group E gene. Am. J. Hum. Genet. 67, 1306-1308 (2000).
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1306-1308
-
-
De Winter, J.P.1
-
25
-
-
0033989248
-
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM
-
de Winter, J. P. et al. The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM. Nature Genet. 24, 15-16 (2000).
-
(2000)
Nature Genet.
, vol.24
, pp. 15-16
-
-
De Winter, J.P.1
-
26
-
-
17344363009
-
The Fanconi anaemia group G gene FANCG is identical with XRCC9
-
de Winter, J. R. et al. The Fanconi anaemia group G gene FANCG is identical with XRCC9. Nature Genet. 20, 281-283 (1998).
-
(1998)
Nature Genet.
, vol.20
, pp. 281-283
-
-
De Winter, J.R.1
-
27
-
-
0030293337
-
Positional Cloning of the Fanconi anaemia group A gene. The Fanconi anaemia/breast cancer consortium
-
Positional Cloning of the Fanconi anaemia group A gene. The Fanconi anaemia/breast cancer consortium. Nature Genet. 14, 324-328 (1996).
-
(1996)
Nature Genet.
, vol.14
, pp. 324-328
-
-
-
28
-
-
17744394476
-
Positional cloning of a novel Fanconi anemia gene, FANCD2
-
Timmers, C. et al. Positional cloning of a novel Fanconi anemia gene, FANCD2. Mol. Cell 7, 241-248 (2001). Describes the position cloning of the Fanconi anaemia gene, FANCD2. This paper also shows that the FANCD2 cDNA can functionally complement the mitomycin C sensitivity of FA-D2 cells.
-
(2001)
Mol. Cell
, vol.7
, pp. 241-248
-
-
Timmers, C.1
-
29
-
-
0028292273
-
The Ashkenazi Jewish Fanconi anemia mutation: Incidence among patients and carrier frequency in the at-risk population
-
Whitney, M. A., Jakobs, P., Kaback, M., Moses, R. E. & Grompe, M. The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population. Hum. Mutat. 3, 339-341 (1994).
-
(1994)
Hum. Mutat.
, vol.3
, pp. 339-341
-
-
Whitney, M.A.1
Jakobs, P.2
Kaback, M.3
Moses, R.E.4
Grompe, M.5
-
30
-
-
0028858123
-
Carrier frequency of the IVS4 + 4 A→T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population
-
Vedander, P. C. et al. Carrier frequency of the IVS4 + 4 A→T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population. Blood 86, 4034-4038 (1995).
-
(1995)
Blood
, vol.86
, pp. 4034-4038
-
-
Vedander, P.C.1
-
31
-
-
0034672154
-
Association of complementation group and mutation type with clinical outcome in fanconi anemia
-
Faivre, L. et al. Association of complementation group and mutation type with clinical outcome in fanconi anemia. Blood 96, 4064-4070 (2000).
-
(2000)
Blood
, vol.96
, pp. 4064-4070
-
-
Faivre, L.1
-
32
-
-
0030960336
-
Phenotypic consequences of mutations in the Fanconi anemia FAC gene: An International Fanconi Anemia Registry study
-
Gillio, A. P., Verlander, P. C., Batish, S. D., Giampietro, P. F. & Auerbach, A. D. Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry study. Blood 90, 105-110 (1997).
-
(1997)
Blood
, vol.90
, pp. 105-110
-
-
Gillio, A.P.1
Verlander, P.C.2
Batish, S.D.3
Giampietro, P.F.4
Auerbach, A.D.5
-
33
-
-
24244442661
-
Cloning and characterization of the zebrafish homologue of the Fanconi anemia protein, FANCD2
-
Liu, T. et al. Cloning and characterization of the zebrafish homologue of the Fanconi anemia protein, FANCD2. Blood 100, 43a (2002).
-
(2002)
Blood
, vol.100
-
-
Liu, T.1
-
34
-
-
0030292447
-
Fanconi anaemia forges a novel pathway
-
D'Andrea, A. D. Fanconi anaemia forges a novel pathway. Nature Genet. 14, 240-242 (1996).
-
(1996)
Nature Genet.
, vol.14
, pp. 240-242
-
-
D'Andrea, A.D.1
-
35
-
-
0031831253
-
Fanconi's anemia: What have we learned from the genes so far?
-
Carreau, M. & Buchwald, M. Fanconi's anemia: what have we learned from the genes so far? Mol. Med. Today 4, 201-206 (1998).
-
(1998)
Mol. Med. Today
, vol.4
, pp. 201-206
-
-
Carreau, M.1
Buchwald, M.2
-
36
-
-
0030667925
-
The Fanconi anaemia proteins, FAA and FAC, interact to form a nuclear complex
-
Kupfer, G. M., Naf, D., Suliman, A., Pulsipher, M. & D'Andrea, A. D. The Fanconi anaemia proteins, FAA and FAC, interact to form a nuclear complex. Nature Genet. 17, 487-490 (1997).
-
(1997)
Nature Genet.
, vol.17
, pp. 487-490
-
-
Kupfer, G.M.1
Naf, D.2
Suliman, A.3
Pulsipher, M.4
D'Andrea, A.D.5
-
37
-
-
0033000911
-
Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex
-
Garcia-Higuera, I., Kuang, Y., Naf, D., Wasik, J. & D'Andrea, A. D. Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex. Mol. Cell. Biol. 19, 4866-4873 (1999).
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 4866-4873
-
-
Garcia-Higuera, I.1
Kuang, Y.2
Naf, D.3
Wasik, J.4
D'Andrea, A.D.5
-
38
-
-
0032573229
-
The Fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation
-
Yamashita, T. et al. The Fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation. Proc. Natl. Acad. Sci. USA 95, 13085-13090 (1998).
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 13085-13090
-
-
Yamashita, T.1
-
39
-
-
0034326299
-
The fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG
-
de Winter, J. P. et al. The fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG. Hum. Mol. Genet. 9, 2665-2674 (2000). Shows that the FANCC, FANCG, FANCA and FANCF proteins accumulate as a complex in the nucleus of normal human cells, supporting the concept of an FA pathway.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2665-2674
-
-
De Winter, J.P.1
-
40
-
-
0035864856
-
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway
-
Medhurst, A. L., Huber, P. A., Waisfisz, Q., de Winter, J. P. & Mathew, C. G. Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway. Hum. Mol. Genet. 10, 423-429 (2001).
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 423-429
-
-
Medhurst, A.L.1
Huber, P.A.2
Waisfisz, Q.3
De Winter, J.P.4
Mathew, C.G.5
-
41
-
-
0034329325
-
The fanconi anemia proteins FANCA and FANCG stabilize each other and promote the nuclear accumulation of the fanconi anemia complex
-
Garcia-Higuera, I., Kuang, Y., Denham, J. & D'Andrea, A. D. The fanconi anemia proteins FANCA and FANCG stabilize each other and promote the nuclear accumulation of the fanconi anemia complex. Blood 96, 3224-3230 (2000).
-
(2000)
Blood
, vol.96
, pp. 3224-3230
-
-
Garcia-Higuera, I.1
Kuang, Y.2
Denham, J.3
D'Andrea, A.D.4
-
42
-
-
0035968325
-
Fanconi anemia proteins localize to chromatin and the nuclear matrix in a DNA damage- and cell cycle-regulated manner
-
Qiao, F., Moss, A. & Kupfer, G. M. Fanconi anemia proteins localize to chromatin and the nuclear matrix in a DNA damage- and cell cycle-regulated manner. J. Biol. Chem. 276, 23391-23396 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 23391-23396
-
-
Qiao, F.1
Moss, A.2
Kupfer, G.M.3
-
43
-
-
18444384217
-
FANCE: The link between Fanconi anaemia complex assembly and activity
-
Pace, P. et al. FANCE: the link between Fanconi anaemia complex assembly and activity. EMBO J. 21, 3414-3423 (2002). Shows that the FANCE gene is a component of the FA complex, is required for the accumulation of FANCC in the nucleus, and provides a functional connection between the FA complex and FANCD2.
-
(2002)
EMBO J.
, vol.21
, pp. 3414-3423
-
-
Pace, P.1
-
44
-
-
0034948865
-
Functional analysis of patient-derived mutations in the Fanconi anemia gene, FANCG/XRCC9
-
Nakanishi, K. et al. Functional analysis of patient-derived mutations in the Fanconi anemia gene, FANCG/XRCC9. Exp. Hematol. 29, 842-849 (2001).
-
(2001)
Exp. Hematol.
, vol.29
, pp. 842-849
-
-
Nakanishi, K.1
-
45
-
-
0035105291
-
Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway
-
Garcia-Higuera, I. et al. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. Mol. Cell 7, 249-262 (2001). Shows that six cloned FA proteins (A, C, D2, E, F and G) interact in a common pathway, resulting in the monoubiquitylation of FANCD2 and its targeting to BRCA1-containing nuclear foci.
-
(2001)
Mol. Cell
, vol.7
, pp. 249-262
-
-
Garcia-Higuera, I.1
-
46
-
-
0036785375
-
S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51
-
Taniguchi, T. et al. S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51. Blood 100, 2414-2420 (2002).
-
(2002)
Blood
, vol.100
, pp. 2414-2420
-
-
Taniguchi, T.1
-
47
-
-
0034655991
-
BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures
-
Wang, Y. et al. BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures. Genes Dev. 14, 927-939 (2000).
-
(2000)
Genes Dev.
, vol.14
, pp. 927-939
-
-
Wang, Y.1
-
48
-
-
0033613222
-
RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination
-
Lorick, K. L. et al. RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination. Proc. Natl. Acad. Sci. USA 96, 11364-11369 (1999).
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 11364-11369
-
-
Lorick, K.L.1
-
49
-
-
0031990269
-
Involvement of Brca2 in DNA repair
-
Patel, K. J. et al. Involvement of Brca2 in DNA repair. Mol. Cell 1, 347-357 (1998).
-
(1998)
Mol. Cell
, vol.1
, pp. 347-357
-
-
Patel, K.J.1
-
50
-
-
0036136316
-
Brca2 (XRCC11) deficiency results in radioresistant DNA synthesis and a higher frequency of spontaneous deletions
-
Kraakman-van der Zwet, M. et al. Brca2 (XRCC11) deficiency results in radioresistant DNA synthesis and a higher frequency of spontaneous deletions. Mol. Cell. Biol. 22, 669-679 (2002).
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 669-679
-
-
Kraakman-van der Zwet, M.1
-
51
-
-
0036174445
-
Cancer susceptibility of mice with a homozygous deletion in the COOH-terminal domain of the Brca2 gene
-
McAllister, K. A. et al. Cancer susceptibility of mice with a homozygous deletion in the COOH-terminal domain of the Brca2 gene. Cancer Res. 62, 990-994 (2002).
-
(2002)
Cancer Res.
, vol.62
, pp. 990-994
-
-
McAllister, K.A.1
-
52
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi anemia
-
Howlett, N. G. et al. Biallelic inactivation of BRCA2 in Fanconi anemia. Science 297, 606-609 (2002). Shows that some rare FA patients have biallelic inactivation of the BRCA2 gene. Cells from FA-D1 cells can be functionally complemented with the BRCA2 gene.
-
(2002)
Science
, vol.297
, pp. 606-609
-
-
Howlett, N.G.1
-
53
-
-
0036312426
-
Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia
-
Digweed, M. et al. Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia. Carcinogenesis 23, 1121-1126 (2002).
-
(2002)
Carcinogenesis
, vol.23
, pp. 1121-1126
-
-
Digweed, M.1
-
54
-
-
0036799765
-
BRCA1 interacts directly with the Fanconi anemia protein, FANCA
-
Folias, A. et al. BRCA1 interacts directly with the Fanconi anemia protein, FANCA. Hum. Mol. Genet. 11, 2591-2597 (2002).
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2591-2597
-
-
Folias, A.1
-
55
-
-
24244444920
-
Regulated interaction of the Fanconi anemia protein, FANCD2, with damaged chromatin
-
Margossian, S. et al. Regulated interaction of the Fanconi anemia protein, FANCD2, with damaged chromatin. Blood 100, 9a (2002).
-
(2002)
Blood
, vol.100
-
-
Margossian, S.1
-
56
-
-
0031760462
-
Deubiquitinating enzymes: A new class of biological regulators
-
D'Andrea, A. D. & Pellman, D. Deubiquitinating enzymes: A new class of biological regulators. Crit. Rev. Biochem. Mol. 33, 337-352 (1998).
-
(1998)
Crit. Rev. Biochem. Mol.
, vol.33
, pp. 337-352
-
-
D'Andrea, A.D.1
Pellman, D.2
-
57
-
-
0035184902
-
The inherited basis of human radiosensitivity
-
Gatti, R. A The inherited basis of human radiosensitivity. Acta Oncol. 40, 702-711 (2001).
-
(2001)
Acta Oncol.
, vol.40
, pp. 702-711
-
-
Gatti, R.A.1
-
58
-
-
0036223483
-
Radiosensitivity in Fanconi's anemia patients
-
Alter, B. P. Radiosensitivity in Fanconi's anemia patients. Radiother. Oncol. 62, 345-347 (2002).
-
(2002)
Radiother. Oncol.
, vol.62
, pp. 345-347
-
-
Alter, B.P.1
-
59
-
-
0003433577
-
-
(eds Nickoloff, J. A. & Hoekstra, M.) (Humana Press, Totowa, New Jersey)
-
Khanna, K. et al. in DNA Damage and Repair (eds Nickoloff, J. A. & Hoekstra, M.) 395-442 (Humana Press, Totowa, New Jersey, 1999).
-
(1999)
DNA Damage and Repair
, pp. 395-442
-
-
Khanna, K.1
-
60
-
-
0032508504
-
Enhance phosphorylation of p53 by ATM in response to DNA damage
-
Banin, S. et al. Enhance phosphorylation of p53 by ATM in response to DNA damage. Science 281, 1674-1677 (1998).
-
(1998)
Science
, vol.281
, pp. 1674-1677
-
-
Banin, S.1
-
61
-
-
0032508608
-
Activation of the ATM kinase by ionizing radiation and phosphorylation of p53
-
Canman, C. E. et al. Activation of the ATM kinase by ionizing radiation and phosphorylation of p53. Science 281, 1677-1679 (1998).
-
(1998)
Science
, vol.281
, pp. 1677-1679
-
-
Canman, C.E.1
-
62
-
-
0034611728
-
ATM phosphorylates p95/nbs1 in an S-phase checkpoint pathway
-
Lim, D. S. et al. ATM phosphorylates p95/nbs1 in an S-phase checkpoint pathway. Nature 404, 613-617 (2000).
-
(2000)
Nature
, vol.404
, pp. 613-617
-
-
Lim, D.S.1
-
63
-
-
0034106722
-
ATM-dependent phosphorylation of nibrin in response to radiation exposure
-
Gatei, M. et al. ATM-dependent phosphorylation of nibrin in response to radiation exposure. Nature Genet. 25, 115-119 (2000).
-
(2000)
Nature Genet.
, vol.25
, pp. 115-119
-
-
Gatei, M.1
-
64
-
-
0033527717
-
Requirement of ATM-dependent phosphorylation of Brca1 in the DNA damage response to double-strand breaks
-
Cortez, D., Wang, Y., Qin, J. & Elledge, S. J. Requirement of ATM-dependent phosphorylation of Brca1 in the DNA damage response to double-strand breaks. Science 286, 1162-1166 (1999).
-
(1999)
Science
, vol.286
, pp. 1162-1166
-
-
Cortez, D.1
Wang, Y.2
Qin, J.3
Elledge, S.J.4
-
65
-
-
0037123768
-
Convergence of the fanconi anemia and ataxia telangiectasia signaling pathways
-
Taniguchi, T. et al. Convergence of the fanconi anemia and ataxia telangiectasia signaling pathways. Cell 109, 459-472 (2002). Shows that the FANCD2 protein undergoes two discrete post-translational modifications - an ATM-dependent phosphorylation and an FA-complex-dependent monoubiquitylation. Each modification activates a different cellular function.
-
(2002)
Cell
, vol.109
, pp. 459-472
-
-
Taniguchi, T.1
-
66
-
-
0035032649
-
Involvement of Brca1 in S-phase and G(2)-phase checkpoints after ionizing irradiation
-
Xu, B., Kim, S. & Kastan, M. B. Involvement of Brca1 in S-phase and G(2)-phase checkpoints after ionizing irradiation. Mol. Cell. Biol. 21, 3445-3450 (2001).
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 3445-3450
-
-
Xu, B.1
Kim, S.2
Kastan, M.B.3
-
67
-
-
0035253615
-
ATM and ATR: Networking cellular responses to DNA damage
-
Shiloh, Y. ATM and ATR: networking cellular responses to DNA damage. Curr. Opin. Genet. Dev. 11, 71-77 (2001).
-
(2001)
Curr. Opin. Genet. Dev.
, vol.11
, pp. 71-77
-
-
Shiloh, Y.1
-
68
-
-
0033179360
-
Chromosomal breakage syndromes
-
Carney, J. P. Chromosomal breakage syndromes. Curr. Opin. Immunol. 11, 443-447 (1999).
-
(1999)
Curr. Opin. Immunol.
, vol.11
, pp. 443-447
-
-
Carney, J.P.1
-
69
-
-
0034020464
-
The Mre11 complex and ATM: Collaborating to navigate S phase
-
Petrini, J. H. The Mre11 complex and ATM: collaborating to navigate S phase. Curr. Opin. Cell Biol. 12, 293-296 (2000).
-
(2000)
Curr. Opin. Cell Biol.
, vol.12
, pp. 293-296
-
-
Petrini, J.H.1
-
70
-
-
0032721091
-
The Mre11-Rad50-Xrs2 protein complex facilitates homologous recombination-based double-strand break repair in Saccharomyces cerevisiae
-
Bressan, D. A., Baxter, B. K. & Petrini, J. H. The Mre11-Rad50-Xrs2 protein complex facilitates homologous recombination-based double-strand break repair in Saccharomyces cerevisiae. Mol. Cell. Biol. 19, 7681-7687 (1999).
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 7681-7687
-
-
Bressan, D.A.1
Baxter, B.K.2
Petrini, J.H.3
-
71
-
-
0034616915
-
Independence of R/M/N focus formation and the presence of intact BRCA1
-
Wu, X. et al. Independence of R/M/N focus formation and the presence of intact BRCA1. Science 289, 11 (2000).
-
(2000)
Science
, vol.289
, pp. 11
-
-
Wu, X.1
-
72
-
-
0036215992
-
Nijmegen breakage syndrome: Clinical characteristics and mutation analysis in eight unrelated Russian families
-
Resnick, I. B. et al. Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian families. J. Pediatr. 140, 355-361 (2002).
-
(2002)
J. Pediatr.
, vol.140
, pp. 355-361
-
-
Resnick, I.B.1
-
73
-
-
4544280871
-
Interaction of FANCD2 and NBS1 in the DNA damage response
-
-/- cells have mitomycin C sensitivity, similar to the defect observed in FA cells. Moreover, NBS1 and FANCD2 interact in an S-phase checkpoint function and in repair of DNA crosslinks.
-
(2002)
Nature Cell. Biol.
, vol.4
, pp. 913-920
-
-
Nakanishi, K.1
-
74
-
-
0037114696
-
A novel diagnostic screen for defects in the Fanconi anemia pathway
-
29 Aug [epub ahead of print]
-
Shimamura, A. et al. A novel diagnostic screen for defects in the Fanconi anemia pathway. Blood 29 Aug 2002 [epub ahead of print].
-
(2002)
Blood
-
-
Shimamura, A.1
-
75
-
-
13344278020
-
Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia
-
Chen, M. et al. Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia. Nature Genet. 12, 448-451 (1996).
-
(1996)
Nature Genet.
, vol.12
, pp. 448-451
-
-
Chen, M.1
-
76
-
-
8944258558
-
Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene
-
Whitney, M. A. et al. Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene. Blood 88, 49-58 (1996). Describes a knockout of the murine Fancc gene. Primary cells isolated from the knockout animal have chromosome instability and γ-interferon hypersensitivity.
-
(1996)
Blood
, vol.88
, pp. 49-58
-
-
Whitney, M.A.1
-
77
-
-
0036329775
-
Fanconi anemia group A and C double-mutant mice. Functional evidence for a multi-protein Fanconi anemia complex
-
Noll, M. et al. Fanconi anemia group A and C double-mutant mice. Functional evidence for a multi-protein Fanconi anemia complex. Exp. Hematol. 30, 679-688 (2002).
-
(2002)
Exp. Hematol.
, vol.30
, pp. 679-688
-
-
Noll, M.1
-
78
-
-
0037105463
-
In vitro phenotypic correction of hematopoietic progenitors from Fanconi anemia group A knockout mice
-
Rio, P. et al. In vitro phenotypic correction of hematopoietic progenitors from Fanconi anemia group A knockout mice. Blood 100, 2032-2039 (2002).
-
(2002)
Blood
, vol.100
, pp. 2032-2039
-
-
Rio, P.1
-
79
-
-
0035760285
-
Targeted disruption of the murine Fanconi anemia gene, Fancg/Xrcc9
-
Yang, Y. et al. Targeted disruption of the murine Fanconi anemia gene, Fancg/Xrcc9. Blood 96, 3435-3440 (2001).
-
(2001)
Blood
, vol.96
, pp. 3435-3440
-
-
Yang, Y.1
-
80
-
-
0036472292
-
Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice
-
Koomen, M. et al. Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice. Hum. Mol. Genet. 11, 273-281 (2002).
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 273-281
-
-
Koomen, M.1
-
81
-
-
0033168321
-
Loss of FancC function results in decreased hematopoietic stem cell repopulating ability
-
Haneline, L. S. et al. Loss of FancC function results in decreased hematopoietic stem cell repopulating ability. Blood 94, 1-8 (1999).
-
(1999)
Blood
, vol.94
, pp. 1-8
-
-
Haneline, L.S.1
-
82
-
-
0032101030
-
-/- mice
-
-/- mice. Blood 91, 4092-4098 (1998).
-
(1998)
Blood
, vol.91
, pp. 4092-4098
-
-
Haneline, L.S.1
-
83
-
-
0030845529
-
Inactivation of the Fanconi anemia group C gene augments interferon-gamma-induced apoptotic responses in hematopoietic cells
-
Rathbun, R. K. et al. Inactivation of the Fanconi anemia group C gene augments interferon-gamma-induced apoptotic responses in hematopoietic cells. Blood 90, 974-985 (1997).
-
(1997)
Blood
, vol.90
, pp. 974-985
-
-
Rathbun, R.K.1
-
84
-
-
0034672372
-
Interferon-gamma-induced apoptotic responses of fanconi anemia group C hematopoietic progenitor cells involve caspase 8-dependent activation of caspase 3 family members
-
Rathbun, R. K. et al. Interferon-gamma-induced apoptotic responses of fanconi anemia group C hematopoietic progenitor cells involve caspase 8-dependent activation of caspase 3 family members. Blood 96, 4204-4211 (2000).
-
(2000)
Blood
, vol.96
, pp. 4204-4211
-
-
Rathbun, R.K.1
-
85
-
-
0032523198
-
Bone marrow failure in the Fanconi anemia group C mouse model after DNA damage
-
Carreau, M. et al. Bone marrow failure in the Fanconi anemia group C mouse model after DNA damage. Blood 91, 2737-2744 (1998).
-
(1998)
Blood
, vol.91
, pp. 2737-2744
-
-
Carreau, M.1
-
86
-
-
0034981121
-
Preclinical protocol for in vivo selection of hematopoietic stem cells conected by gene therapy in Fanconi anemia group C
-
Noll, M., Bateman, R. L., D'Andrea, A. D. & Grompe, M. Preclinical protocol for in vivo selection of hematopoietic stem cells conected by gene therapy in Fanconi anemia group C. Mol. Ther. 3, 14-23 (2001).
-
(2001)
Mol. Ther.
, vol.3
, pp. 14-23
-
-
Noll, M.1
Bateman, R.L.2
D'Andrea, A.D.3
Grompe, M.4
-
87
-
-
0033567909
-
In vivo selection of wild-type hematopoietic stem cells in a murine model of Fanconi anemia
-
Battalle, K. P. et al. In vivo selection of wild-type hematopoietic stem cells in a murine model of Fanconi anemia. Blood 94, 2151-2158 (1999).
-
(1999)
Blood
, vol.94
, pp. 2151-2158
-
-
Battalle, K.P.1
-
88
-
-
0030659153
-
Tumorgenesis and a DNA repair defect in mice with a truncating Brca2 mutation
-
Connor, F. et al. Tumorgenesis and a DNA repair defect in mice with a truncating Brca2 mutation. Nature Genet. 17, 423-430 (1997).
-
(1997)
Nature Genet.
, vol.17
, pp. 423-430
-
-
Connor, F.1
-
89
-
-
0035811590
-
Development of mammary adenocarcinomas by tissue-specific knockout of Brca2 in mice
-
Ludwig, T., Fisher, P., Murty, V. & Efstratiadis, A. Development of mammary adenocarcinomas by tissue-specific knockout of Brca2 in mice. Oncogene 20, 3937-3948 (2001).
-
(2001)
Oncogene
, vol.20
, pp. 3937-3948
-
-
Ludwig, T.1
Fisher, P.2
Murty, V.3
Efstratiadis, A.4
-
90
-
-
0030924656
-
Targeted mutations of breast cancer susceptibility gene homologs in mice: Lethal phenotypes of Brca1, Brca2, Brca1/Brca2, Brca1/p53, and Brca2/p53 nullizygous embryos
-
Ludwig, T., Chapman, D. L., Papaioannou, V. E. & Efstratiadis, A. Targeted mutations of breast cancer susceptibility gene homologs in mice: lethal phenotypes of Brca1, Brca2, Brca1/Brca2, Brca1/p53, and Brca2/p53 nullizygous embryos. Genes Dev. 11, 1226-1241 (1997).
-
(1997)
Genes Dev.
, vol.11
, pp. 1226-1241
-
-
Ludwig, T.1
Chapman, D.L.2
Papaioannou, V.E.3
Efstratiadis, A.4
-
91
-
-
0033501050
-
Disruption of muREC2/RAD51L1 in mice results in early embryonic lethality which can be partially rescued in a p53(-/-) background
-
Shu, Z., Smith, S., Wang, L., Rice, M. C. & Kmiec, E. B. Disruption of muREC2/RAD51L1 in mice results in early embryonic lethality which can be partially rescued in a p53(-/-) background. Mol. Cell. Biol. 19, 8686-8693 (1999).
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 8686-8693
-
-
Shu, Z.1
Smith, S.2
Wang, L.3
Rice, M.C.4
Kmiec, E.B.5
-
92
-
-
0029784528
-
Inactivation of the mouse Brca1 gene leads to failure in the morphogenesis of the egg cylinder in early postimplantation development
-
Liu, C. Y., Flesken-Nikitin, A., Li, S., Zeng, Y. & Lee, W. H. Inactivation of the mouse Brca1 gene leads to failure in the morphogenesis of the egg cylinder in early postimplantation development. Genes Dev. 10, 1835-1843 (1996).
-
(1996)
Genes Dev.
, vol.10
, pp. 1835-1843
-
-
Liu, C.Y.1
Flesken-Nikitin, A.2
Li, S.3
Zeng, Y.4
Lee, W.H.5
-
93
-
-
0032542216
-
A targeted disruption of the murine Brca1 gene causes gamma-irradiation hypersensitivity and genetic instability
-
Shen, S. X. et al. A targeted disruption of the murine Brca1 gene causes gamma-irradiation hypersensitivity and genetic instability. Oncogene 17, 3115-3124 (1998).
-
(1998)
Oncogene
, vol.17
, pp. 3115-3124
-
-
Shen, S.X.1
-
94
-
-
0019407454
-
Radioresistant DNA synthesis: An intrinsic feature of ataxia telangiectasia
-
Painter, R. B. Radioresistant DNA synthesis: an intrinsic feature of ataxia telangiectasia. Mutat. Res. 84, 183-190 (1981).
-
(1981)
Mutat. Res.
, vol.84
, pp. 183-190
-
-
Painter, R.B.1
-
95
-
-
0034332550
-
Damage-resistant DNA synthesis in fanconi anemia cells treated with a DNA cross-linking agent
-
Centurion, S. A., Kuo, H. R. & Lambert, W. C. Damage-resistant DNA synthesis in fanconi anemia cells treated with a DNA cross-linking agent. Exp. Cell Res. 260, 216-221 (2000).
-
(2000)
Exp. Cell Res.
, vol.260
, pp. 216-221
-
-
Centurion, S.A.1
Kuo, H.R.2
Lambert, W.C.3
-
96
-
-
0034331336
-
Arrest of S-phase progression is impaired in fanconi anemia cells
-
Sala-Trepat, M. et al. Arrest of S-phase progression is impaired in fanconi anemia cells. Exp. Cell Res. 260, 208-215 (2000).
-
(2000)
Exp. Cell Res.
, vol.260
, pp. 208-215
-
-
Sala-Trepat, M.1
-
97
-
-
0033780760
-
DNA replication is required to elicit cellular responses to psoralen-induced DNA interstrand cross-links
-
Akkari, Y. M., Bateman, R. L., Relfsteck, C. A., Olson, S. B. & Grompe, M. DNA replication is required to elicit cellular responses to psoralen-induced DNA interstrand cross-links. Mol. Cell. Biol. 20, 8283-8289 (2000). Shows that DNA crosslinks cause a cellular arrest in S phase. The data indicate that crosslink repair is mediated by homologous recombination repair in S phase.
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 8283-8289
-
-
Akkari, Y.M.1
Bateman, R.L.2
Relfsteck, C.A.3
Olson, S.B.4
Grompe, M.5
-
98
-
-
0031835895
-
The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome
-
Escarceller, M., Rousset, S., Moustacchi, E. & Papadopoulo, D. The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome. Somatic Cell Mol. Genet. 23, 401-411 (1997).
-
(1997)
Somatic Cell Mol. Genet.
, vol.23
, pp. 401-411
-
-
Escarceller, M.1
Rousset, S.2
Moustacchi, E.3
Papadopoulo, D.4
-
99
-
-
0035937735
-
Defecient DNA end joining activity in extracts from fanconi anemia fibroblasts
-
Lundberg, R., Mavinakere, M. & Campbell, C. Defecient DNA end joining activity in extracts from fanconi anemia fibroblasts. J. Biol. Chem. 276, 9543-9549 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 9543-9549
-
-
Lundberg, R.1
Mavinakere, M.2
Campbell, C.3
-
100
-
-
0032486086
-
Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining
-
Escarceller, M. et al. Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining. J. Mol. Biol. 279, 375-385 (1998).
-
(1998)
J. Mol. Biol.
, vol.279
, pp. 375-385
-
-
Escarceller, M.1
-
101
-
-
0034638924
-
DNA polymerase stalling, sister chromatid recombination and the BRCA genes
-
Scully, R., Puget, N. & Vlasakova, K. DNA polymerase stalling, sister chromatid recombination and the BRCA genes. Oncogene 19, 6176-6183 (2000).
-
(2000)
Oncogene
, vol.19
, pp. 6176-6183
-
-
Scully, R.1
Puget, N.2
Vlasakova, K.3
-
102
-
-
0035099044
-
BRCA2 is required for homology-directed repair of chromosomal breaks
-
Moynahan, M. E., Pierce, A. J. & Jasin, M. BRCA2 is required for homology-directed repair of chromosomal breaks. Mol. Cell. 7, 263-272 (2001).
-
(2001)
Mol. Cell.
, vol.7
, pp. 263-272
-
-
Moynahan, M.E.1
Pierce, A.J.2
Jasin, M.3
-
103
-
-
0035801472
-
Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences
-
-/- cells have an underlying defect in homologous recombination repair and in sister-chromatid exchange.
-
(2001)
EMBO J.
, vol.20
, pp. 4704-4716
-
-
Tutt, A.1
-
104
-
-
0036673956
-
Deficiency in BRCA2 leads to increase in non-conservative homologous recombination
-
Larminat, F., Germanier M., Papouli, E. & Defais, M. Deficiency in BRCA2 leads to increase in non-conservative homologous recombination. Oncogene 21, 5188-5192 (2002).
-
(2002)
Oncogene
, vol.21
, pp. 5188-5192
-
-
Larminat, F.1
Germanier, M.2
Papouli, E.3
Defais, M.4
-
105
-
-
0031466027
-
RAD51 interacts with the evolutionary conserved BRC motifs in the human breast cancer susceptibility gene Brca2
-
Wong, A. K., Pero, R., Ormonde, P. A., Tavtigian, S. V. & Bartel, P. L. RAD51 interacts with the evolutionary conserved BRC motifs in the human breast cancer susceptibility gene Brca2. J. Biol. Chem. 272, 31941-31944 (1997).
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 31941-31944
-
-
Wong, A.K.1
Pero, R.2
Ormonde, P.A.3
Tavtigian, S.V.4
Bartel, P.L.5
-
106
-
-
0037072620
-
Cancer: BRCA2 enters the fray
-
Wilson, J. H. & Elledge, S. J. Cancer: BRCA2 enters the fray. Science 297, 1822-1823 (2002).
-
(2002)
Science
, vol.297
, pp. 1822-1823
-
-
Wilson, J.H.1
Elledge, S.J.2
-
107
-
-
18544372595
-
BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure
-
Yang, H. et al. BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure Science 297, 1837-1848 (2002). Describes the first crystal structure for a domain of a Fanconi anaemia protein, BRCA2/FANCD2. This paper also shows that the carboxyl terminus of the protein has a regulated interaction with DNA.
-
(2002)
Science
, vol.297
, pp. 1837-1848
-
-
Yang, H.1
-
108
-
-
0030850047
-
Dynamic changes of BRCA1 subnuclear location and phosphorylation state are initiated by DNA damage
-
Scully, R. et al. Dynamic changes of BRCA1 subnuclear location and phosphorylation state are initiated by DNA damage. Cell 90, 425-435 (1997).
-
(1997)
Cell
, vol.90
, pp. 425-435
-
-
Scully, R.1
-
109
-
-
0033368701
-
Meiotic chromosomes: Integrating structure and function
-
Zickler, D. & Kleckner, N. Meiotic chromosomes: integrating structure and function. Annu. Rev. Genet. 33, 603-754 (1999).
-
(1999)
Annu. Rev. Genet.
, vol.33
, pp. 603-754
-
-
Zickler, D.1
Kleckner, N.2
-
110
-
-
0033213392
-
Brca1 controls homology-directed DNA repair
-
Moynahan, M. E., Chiu, J. W., Koller, B. H. & Jasin, M. Brca1 controls homology-directed DNA repair. Mol. Cell 4, 511-518 (1999).
-
(1999)
Mol. Cell
, vol.4
, pp. 511-518
-
-
Moynahan, M.E.1
Chiu, J.W.2
Koller, B.H.3
Jasin, M.4
-
111
-
-
0035874894
-
Homology-directed DNA repair, mitomycin-C resistance, and chromosome stability is restored with correction of a Brca1 mutation
-
Moynahan, M. E., Cui, T. Y. & Jasin, M. Homology-directed DNA repair, mitomycin-C resistance, and chromosome stability is restored with correction of a Brca1 mutation. Cancer Res. 61, 4842-4850 (2001).
-
(2001)
Cancer Res.
, vol.61
, pp. 4842-4850
-
-
Moynahan, M.E.1
Cui, T.Y.2
Jasin, M.3
-
112
-
-
0142206321
-
The involvement of Fanconi Anemia proteins in homologous genetic recombination
-
Meyn, S., D'Andrea, A., Grompe, M. & Wang, W. The involvement of Fanconi Anemia proteins in homologous genetic recombination. Am. J. Hum. Genet. 69, 750 (2001).
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 750
-
-
Meyn, S.1
D'Andrea, A.2
Grompe, M.3
Wang, W.4
-
113
-
-
0030854142
-
Elevated homologous recombination activity in fanconi anemia fibroblasts
-
Thyagarajan, B. & Campbell, C. Elevated homologous recombination activity in fanconi anemia fibroblasts. J. Biol. Chem. 272, 23328-23333 (1997).
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 23328-23333
-
-
Thyagarajan, B.1
Campbell, C.2
-
114
-
-
0025059685
-
Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus
-
Papadopoulo, D., Guillouf, C., Mohrenweiser, H. & Moustacchi, E. Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus. Proc. Natl Acad. Sci. USA 87, 8383-8387 (1990).
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 8383-8387
-
-
Papadopoulo, D.1
Guillouf, C.2
Mohrenweiser, H.3
Moustacchi, E.4
-
115
-
-
0027249768
-
Frequencies of HPRT lymphocytes and glycophorin A variants erythrocytes in Fanconi anemia patients, their parents and control donors
-
Sala-Trepat, M., Boyse, J., Richard, P., Papadopoulo, D. & Moustacchi, E. Frequencies of HPRT lymphocytes and glycophorin A variants erythrocytes in Fanconi anemia patients, their parents and control donors. Mut. Res. 289, 115-126 (1993).
-
(1993)
Mut. Res.
, vol.289
, pp. 115-126
-
-
Sala-Trepat, M.1
Boyse, J.2
Richard, P.3
Papadopoulo, D.4
Moustacchi, E.5
-
116
-
-
0033385037
-
Molecular spectra of HPRT deletion mutations in circulating T-lymphocytes in Fanconi anemia patients
-
Laquerbe, A., Sala-Trepat, M., Vives, C., Escarceller, M. & Papadopoulo, D. Molecular spectra of HPRT deletion mutations in circulating T-lymphocytes in Fanconi anemia patients. Mutat. Res. 431, 341-350 (1999).
-
(1999)
Mutat. Res.
, vol.431
, pp. 341-350
-
-
Laquerbe, A.1
Sala-Trepat, M.2
Vives, C.3
Escarceller, M.4
Papadopoulo, D.5
-
117
-
-
0035436539
-
Repair of DNA interstrand crosslinks: Molecular mechanisms and clinical relevance
-
McHugh, P. J., Spanswick, V. J. & Hartley, J. A. Repair of DNA interstrand crosslinks: molecular mechanisms and clinical relevance. Lancet Oncol. 2, 483-490 (2001).
-
(2001)
Lancet Oncol.
, vol.2
, pp. 483-490
-
-
McHugh, P.J.1
Spanswick, V.J.2
Hartley, J.A.3
-
118
-
-
0035132725
-
Involvement of nucleotide excision repair in a recombination-independent and error-prone pathway of DNA interstrand cross-link repair
-
Wang, X. et al. Involvement of nucleotide excision repair in a recombination-independent and error-prone pathway of DNA interstrand cross-link repair. Mol. Cell. Biol. 21, 713-720 (2001).
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 713-720
-
-
Wang, X.1
-
119
-
-
0030667311
-
Initiation of DNA interstrand cross-link repair in humans: The nucleotide excision repair system makes dual incisions 5′ to the cross-linked base and removes a 22- to 28-nucleotide-long damage-free strand
-
Bessho, T., Mu, D. & Sancar, A. Initiation of DNA interstrand cross-link repair in humans: the nucleotide excision repair system makes dual incisions 5′ to the cross-linked base and removes a 22- to 28-nucleotide-long damage-free strand. Mol. Cell. Biol. 17, 6822-6830 (1997).
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 6822-6830
-
-
Bessho, T.1
Mu, D.2
Sancar, A.3
-
120
-
-
0033781210
-
Defining the roles of nucleotide excision repair and recombination in the repair of DNA interstrand cross-links in mammalian cells
-
De Silva, I. U., McHugh, P. J., Clingen, P. H. & Hartley, J. A. Defining the roles of nucleotide excision repair and recombination in the repair of DNA interstrand cross-links in mammalian cells. Mol. Cell. Biol. 20, 7980-7990 (2000).
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 7980-7990
-
-
De Silva, I.U.1
McHugh, P.J.2
Clingen, P.H.3
Hartley, J.A.4
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