-
1
-
-
0035379611
-
The emerging genetic and molecular basis of Fanconi anaemia
-
Joenje, H. and Patel, K.J. (2001) The emerging genetic and molecular basis of Fanconi anaemia. Nat. Rev. Genet., 2, 446-459.
-
(2001)
Nat. Rev. Genet
, vol.2
, pp. 446-459
-
-
Joenje, H.1
Patel, K.J.2
-
2
-
-
29144506137
-
The Fanconi anemia/BRCA pathway: New faces in the crowd
-
Kennedy, R.D. and D'Andrea, A.D. (2005) The Fanconi anemia/BRCA pathway: new faces in the crowd. Genes Dev., 19, 2925-2940.
-
(2005)
Genes Dev
, vol.19
, pp. 2925-2940
-
-
Kennedy, R.D.1
D'Andrea, A.D.2
-
3
-
-
34548759123
-
Emergence of a DNA-damage response network consisting of Fanconi anemia and BRCA proteins
-
doi:10.1038/nrg2159
-
Wang, W. (2007) Emergence of a DNA-damage response network consisting of Fanconi anemia and BRCA proteins. Nat. Rev. Genet., 8, doi:10.1038/nrg2159.
-
(2007)
Nat. Rev. Genet
, vol.8
-
-
Wang, W.1
-
4
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi anemia
-
Howlett, N.G., Taniguchi, T., Olson, S., Cox, B., Waisfisz, Q., De Die-Smulders, C., Persky, N., Grompe, M., Joenje, H., Pals, G. et al. (2002) Biallelic inactivation of BRCA2 in Fanconi anemia. Science 297, 606-609.
-
(2002)
Science
, vol.297
, pp. 606-609
-
-
Howlett, N.G.1
Taniguchi, T.2
Olson, S.3
Cox, B.4
Waisfisz, Q.5
De Die-Smulders, C.6
Persky, N.7
Grompe, M.8
Joenje, H.9
Pals, G.10
-
5
-
-
25144457604
-
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
-
Levitus, M., Waisfisz, Q., Godthelp, B.C., de Vries, Y., Hussain, S., Wiegant, W.W., Elghalbzouri-Maghrani, E., Steltenpool, J., Rooimans, M.A., Pals, G. et al. (2005) The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nat. Genet., 37, 934-935.
-
(2005)
Nat. Genet
, vol.37
, pp. 934-935
-
-
Levitus, M.1
Waisfisz, Q.2
Godthelp, B.C.3
de Vries, Y.4
Hussain, S.5
Wiegant, W.W.6
Elghalbzouri-Maghrani, E.7
Steltenpool, J.8
Rooimans, M.A.9
Pals, G.10
-
6
-
-
25144497571
-
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
-
Levran, O., Attwooll, C., Henry, R.T., Milton, K.L., Neveling, K., Rio, P., Batish, S.D., Kalb, R., Velleuer, E., Barral, S. et al. (2005) The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. Nat. Genet., 37, 931-933.
-
(2005)
Nat. Genet
, vol.37
, pp. 931-933
-
-
Levran, O.1
Attwooll, C.2
Henry, R.T.3
Milton, K.L.4
Neveling, K.5
Rio, P.6
Batish, S.D.7
Kalb, R.8
Velleuer, E.9
Barral, S.10
-
7
-
-
24944575242
-
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, P.R. and Cantor, S.b. (2005) BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ. Cancer Cell, 8, 255-265.
-
(2005)
Cancer Cell
, vol.8
, pp. 255-265
-
-
Litman, R.1
Peng, M.2
Jin, Z.3
Zhang, F.4
Zhang, J.5
Powell, S.6
Andreassen, P.R.7
Cantor, S.B.8
-
8
-
-
33846601829
-
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
-
Xia, B., Dorsman, J.C., Ameziane, N., de Vries, Y., Rooimans, M.A., Sheng, Q., Pals, G., Errami, A., Gluckman, E., Llera, J. et al. (2007) Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Nat. Genet., 39, 159-161.
-
(2007)
Nat. Genet
, vol.39
, pp. 159-161
-
-
Xia, B.1
Dorsman, J.C.2
Ameziane, N.3
de Vries, Y.4
Rooimans, M.A.5
Sheng, Q.6
Pals, G.7
Errami, A.8
Gluckman, E.9
Llera, J.10
-
9
-
-
33846569450
-
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. et al. (2007) Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat. Genet., 39, 162-164.
-
(2007)
Nat. Genet
, vol.39
, pp. 162-164
-
-
Reid, S.1
Schindler, D.2
Hanenberg, H.3
Barker, K.4
Hanks, S.5
Kalb, R.6
Neveling, K.7
Kelly, P.8
Seal, S.9
Freund, M.10
-
10
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
Rahman, N., Seal, S., Thompson, D., Kelly, P., Renwick, A., Elliott, A., Reid, S., Spanova, K., Barfoot, R., Chagtai, T. et al. (2007) PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat. Genet., 39, 165-167.
-
(2007)
Nat. Genet
, vol.39
, pp. 165-167
-
-
Rahman, N.1
Seal, S.2
Thompson, D.3
Kelly, P.4
Renwick, A.5
Elliott, A.6
Reid, S.7
Spanova, K.8
Barfoot, R.9
Chagtai, T.10
-
11
-
-
34249857115
-
Analysis of PALB2/FANCN-associated breast cancer families
-
Tischkowitz, M., Xia, B., Sabbaghian, N., Reis-Filho, J.S., Hamel, N., Li, G., van Beers, E.H., Li, L., Khalil, T., Ouenneville, L.A. et al. (2007) Analysis of PALB2/FANCN-associated breast cancer families. Proc. Natl Acad. Sci. USA, 104, 6788-6793.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 6788-6793
-
-
Tischkowitz, M.1
Xia, B.2
Sabbaghian, N.3
Reis-Filho, J.S.4
Hamel, N.5
Li, G.6
van Beers, E.H.7
Li, L.8
Khalil, T.9
Ouenneville, L.A.10
-
12
-
-
33847227378
-
A recurrent mutation in PALB2 in Finnish cancer families
-
Erkko, H., Xia, B., Nikkila, J., Schleutker, J., Syrjakoski, K., Mannermaa, A., Kallioniemi, A., Pylkas, K., Karppinen, S.M., Rapakko, K. et al. (2007) A recurrent mutation in PALB2 in Finnish cancer families. Nature, 446, 316-319.
-
(2007)
Nature
, vol.446
, pp. 316-319
-
-
Erkko, H.1
Xia, B.2
Nikkila, J.3
Schleutker, J.4
Syrjakoski, K.5
Mannermaa, A.6
Kallioniemi, A.7
Pylkas, K.8
Karppinen, S.M.9
Rapakko, K.10
-
13
-
-
0141484612
-
A novel ubiquitin ligase is deficient in Fanconi anemia
-
Meetei, A.R., de Winter, J.P., Medhurst, A.L., Wallisch, M., Waisfisz, Q., van de Vrugt, H.J., Oostra, A.B., Yan, Z., Ling, C., Bishop, C.E. et al. (2003) A novel ubiquitin ligase is deficient in Fanconi anemia. Nat. Genet., 35, 165-170.
-
(2003)
Nat. Genet
, vol.35
, pp. 165-170
-
-
Meetei, A.R.1
de Winter, J.P.2
Medhurst, A.L.3
Wallisch, M.4
Waisfisz, Q.5
van de Vrugt, H.J.6
Oostra, A.B.7
Yan, Z.8
Ling, C.9
Bishop, C.E.10
-
14
-
-
10944239213
-
X-linked inheritance of Fanconi anemia complementation group B
-
Meetei, A.R., Levitus, M., Xue, Y., Medhurst, A.L., Zwaan, M., Ling, C., Rooimans, M.A., Bier, P., Hoatlin, M., Pals, G. et al. (2004) X-linked inheritance of Fanconi anemia complementation group B. Nat. Genet., 36, 1219-1224.
-
(2004)
Nat. Genet
, vol.36
, pp. 1219-1224
-
-
Meetei, A.R.1
Levitus, M.2
Xue, Y.3
Medhurst, A.L.4
Zwaan, M.5
Ling, C.6
Rooimans, M.A.7
Bier, P.8
Hoatlin, M.9
Pals, G.10
-
15
-
-
25144449181
-
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
-
Meetei, A.R., Medhurst, A.L., Ling, C., Xue, Y., Singh, T.R., Bier, P., Steltenpool, J., Stone, S., Dokal, I., Mathew, C.G. et al. (2005) A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nat. Genet., 37, 958-963.
-
(2005)
Nat. Genet
, vol.37
, pp. 958-963
-
-
Meetei, A.R.1
Medhurst, A.L.2
Ling, C.3
Xue, Y.4
Singh, T.R.5
Bier, P.6
Steltenpool, J.7
Stone, S.8
Dokal, I.9
Mathew, C.G.10
-
16
-
-
34247110291
-
Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair
-
Smogorzewska, A., Matsuoka, S., Vinciguerra, P., McDonald, E.R., III, Hurov, K.E., Luo, J., Ballif, B.A., Gygi, S.P., Hofmann, K., D'Andrea, A.D. et al. (2007) Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair. Cell, 129, 289-301.
-
(2007)
Cell
, vol.129
, pp. 289-301
-
-
Smogorzewska, A.1
Matsuoka, S.2
Vinciguerra, P.3
McDonald III, E.R.4
Hurov, K.E.5
Luo, J.6
Ballif, B.A.7
Gygi, S.P.8
Hofmann, K.9
D'Andrea, A.D.10
-
17
-
-
34249281152
-
FANCI is a second monoubiquitinated member of the Fanconi anemia pathway
-
Sims, A.E., Spiteri, E., Sims, R.J., III, Arita, A.G., Lach, F.P., Landers, T., Wurm, M., Freund, M., Neveling, K., Hanenberg, H. et al. (2007) FANCI is a second monoubiquitinated member of the Fanconi anemia pathway. Nat. Struct. Mol. Biol, 14, 564-567.
-
(2007)
Nat. Struct. Mol. Biol
, vol.14
, pp. 564-567
-
-
Sims, A.E.1
Spiteri, E.2
Sims III, R.J.3
Arita, A.G.4
Lach, F.P.5
Landers, T.6
Wurm, M.7
Freund, M.8
Neveling, K.9
Hanenberg, H.10
-
18
-
-
0035105291
-
Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway
-
Garcia-Higuera, I., Taniguchi, T., Ganesan, S., Meyn, M.S., Timmers, C., Hejna, J., Grompe, M. and D'Andrea, A.D. (2001) Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. Mol. Cell, 7, 249-262.
-
(2001)
Mol. Cell
, vol.7
, pp. 249-262
-
-
Garcia-Higuera, I.1
Taniguchi, T.2
Ganesan, S.3
Meyn, M.S.4
Timmers, C.5
Hejna, J.6
Grompe, M.7
D'Andrea, A.D.8
-
19
-
-
33947167388
-
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability
-
Bogliolo, M., Lyakhovich, A., Callen, E., Castella, M., Cappelli, E., Ramirez, M.J., Creus, A., Marcos, R., Kalb, R., Neveling, K. et al. (2007) Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability. EMBO J, 26, 1340-1351.
-
(2007)
EMBO J
, vol.26
, pp. 1340-1351
-
-
Bogliolo, M.1
Lyakhovich, A.2
Callen, E.3
Castella, M.4
Cappelli, E.5
Ramirez, M.J.6
Creus, A.7
Marcos, R.8
Kalb, R.9
Neveling, K.10
-
20
-
-
26944499485
-
The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway
-
Mosedale, G., Niedzwiedz, W., Alpi, A., Perrina, F., Pereira-Leal, J.B., Johnson, M., Langevin, F., Pace, P. and Patel, K.J. (2005) The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway. Nat. Struct. Mol. Biol. 12, 763-771.
-
(2005)
Nat. Struct. Mol. Biol
, vol.12
, pp. 763-771
-
-
Mosedale, G.1
Niedzwiedz, W.2
Alpi, A.3
Perrina, F.4
Pereira-Leal, J.B.5
Johnson, M.6
Langevin, F.7
Pace, P.8
Patel, K.J.9
-
21
-
-
33846799430
-
Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM
-
Ciccia, A., Ling, C., Coulthard, R., Yan, Z., Xue, Y., Meetei, A.R., Laghmani el, H., Joenje, H., McDonald, N., de Winter, J.P. et al. (2007) Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM. Mol. Cell, 25, 331-343.
-
(2007)
Mol. Cell
, vol.25
, pp. 331-343
-
-
Ciccia, A.1
Ling, C.2
Coulthard, R.3
Yan, Z.4
Xue, Y.5
Meetei, A.R.6
Laghmani el, H.7
Joenje, H.8
McDonald, N.9
de Winter, J.P.10
-
22
-
-
11144225798
-
Cooperation of the N-terminal helicase and C-terminal endonuclease activities of archaeal Hef protein in processing stalled replication forks
-
Komori, K., Hidaka, M., Horiuchi, T., Fujikane, R., Shinagawa, H. and Ishino, Y. (2004) Cooperation of the N-terminal helicase and C-terminal endonuclease activities of archaeal Hef protein in processing stalled replication forks. J. Biol. Chem., 279, 53175-53185.
-
(2004)
J. Biol. Chem
, vol.279
, pp. 53175-53185
-
-
Komori, K.1
Hidaka, M.2
Horiuchi, T.3
Fujikane, R.4
Shinagawa, H.5
Ishino, Y.6
-
23
-
-
12444336898
-
X-ray and biochemical anatomy of an archaeal XPF/Rad1/Mus81 family nuclease: Similarity between its endonuclease domain and restriction enzymes
-
Nishino, T., Komori, K., Ishino, Y. and Morikawa, K. (2003) X-ray and biochemical anatomy of an archaeal XPF/Rad1/Mus81 family nuclease: similarity between its endonuclease domain and restriction enzymes. Structure (Camb.), 11, 445-457.
-
(2003)
Structure (Camb.)
, vol.11
, pp. 445-457
-
-
Nishino, T.1
Komori, K.2
Ishino, Y.3
Morikawa, K.4
-
24
-
-
38349050087
-
The Fanconi anemia protein FANCM can promote branch migration of Holliday junctions and replication forks
-
Gari, K., Decaillet, C., Stasiak, A.Z., Stasiak, A. and Constantinou, A. (2008) The Fanconi anemia protein FANCM can promote branch migration of Holliday junctions and replication forks. Mol. Cell, 29, 141-148.
-
(2008)
Mol. Cell
, vol.29
, pp. 141-148
-
-
Gari, K.1
Decaillet, C.2
Stasiak, A.Z.3
Stasiak, A.4
Constantinou, A.5
-
25
-
-
33746715608
-
Rad54 protein promotes branch migration of Holliday junctions
-
Bugreev, D.V., Mazina, O.M. and Mazin, A.V. (2006) Rad54 protein promotes branch migration of Holliday junctions. Nature, 442 590-593.
-
(2006)
Nature
, vol.442
, pp. 590-593
-
-
Bugreev, D.V.1
Mazina, O.M.2
Mazin, A.V.3
-
26
-
-
0026651978
-
Ethidium bromide provides a simple tool for identifying genuine DNA-independent protein associations
-
Lai, J.S. and Herr, W. (1992) Ethidium bromide provides a simple tool for identifying genuine DNA-independent protein associations. Proc. Natl Acad. Sci. USA, 89, 6958-6962.
-
(1992)
Proc. Natl Acad. Sci. USA
, vol.89
, pp. 6958-6962
-
-
Lai, J.S.1
Herr, W.2
-
27
-
-
0033864250
-
Promotion of Rad51-dependent D-loop formation by yeast recombination factor Rdh54/ Tid1
-
Petukhova, G., Sung, P. and Klein, H. (2000) Promotion of Rad51-dependent D-loop formation by yeast recombination factor Rdh54/ Tid1. Genes Dev., 14, 2206-2215.
-
(2000)
Genes Dev
, vol.14
, pp. 2206-2215
-
-
Petukhova, G.1
Sung, P.2
Klein, H.3
-
28
-
-
0033635247
-
Superhelicity-driven homologous DNA pairing by yeast recombination factors Rad51 and Rad54
-
Van Komen, S., Petukhova, G., Sigurdsson, S., Stratton, S. and Sung, P. (2000) Superhelicity-driven homologous DNA pairing by yeast recombination factors Rad51 and Rad54. Mol. Cell, 6, 563-572.
-
(2000)
Mol. Cell
, vol.6
, pp. 563-572
-
-
Van Komen, S.1
Petukhova, G.2
Sigurdsson, S.3
Stratton, S.4
Sung, P.5
-
29
-
-
0035902524
-
The architecture of the human Rad54-DNA complex provides evidence for protein translocation along DNA
-
Ristic, D., Wyman, C., Paulusma, C. and Kanaar, R. (2001) The architecture of the human Rad54-DNA complex provides evidence for protein translocation along DNA. Proc. Natl Acad. Sci. USA, 98 8454-8460.
-
(2001)
Proc. Natl Acad. Sci. USA
, vol.98
, pp. 8454-8460
-
-
Ristic, D.1
Wyman, C.2
Paulusma, C.3
Kanaar, R.4
-
30
-
-
0038100136
-
Rad54p is a chromatin remodeling enzyme required for heteroduplex DNA joint formation with chromatin
-
Jaskelioff, M., Van Komen, S., Krebs, J.E., Sung, P. and Peterson, C.L. (2003) Rad54p is a chromatin remodeling enzyme required for heteroduplex DNA joint formation with chromatin. J. Biol. Chem., 278, 9212-9218.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 9212-9218
-
-
Jaskelioff, M.1
Van Komen, S.2
Krebs, J.E.3
Sung, P.4
Peterson, C.L.5
-
31
-
-
33745498749
-
Visualization of Rad54, a chromatin remodeling protein, translocating on single DNA molecules
-
Amitani, I., Baskin, R.J. and Kowalczykowski, S.C. (2006) Visualization of Rad54, a chromatin remodeling protein, translocating on single DNA molecules. Mol. Cell, 23, 143-148.
-
(2006)
Mol. Cell
, vol.23
, pp. 143-148
-
-
Amitani, I.1
Baskin, R.J.2
Kowalczykowski, S.C.3
-
32
-
-
34547136691
-
Interactions of hRad54 protein with branched DNA molecules
-
Mazina, O.M., Rossi, M.J., Thoma, N.H. and Mazin, A.V. (2007) Interactions of hRad54 protein with branched DNA molecules. J. Biol. Chem., 282, 21068-21080.
-
(2007)
J. Biol. Chem
, vol.282
, pp. 21068-21080
-
-
Mazina, O.M.1
Rossi, M.J.2
Thoma, N.H.3
Mazin, A.V.4
-
33
-
-
0026633047
-
ATP-dependent branch migration of Holliday junctions promoted by the RuvA and RuvB proteins of E. coli
-
Tsaneva, I.R., Muller, B. and West, S.C. (1992) ATP-dependent branch migration of Holliday junctions promoted by the RuvA and RuvB proteins of E. coli. Cell, 69, 1171-1180.
-
(1992)
Cell
, vol.69
, pp. 1171-1180
-
-
Tsaneva, I.R.1
Muller, B.2
West, S.C.3
-
34
-
-
0027397630
-
Dissociation of synthetic Holliday junctions by E. coli RecG protein
-
Lloyd, R.G. and Sharples, G.J. (1993) Dissociation of synthetic Holliday junctions by E. coli RecG protein. EMBO J, 12, 17-22.
-
(1993)
EMBO J
, vol.12
, pp. 17-22
-
-
Lloyd, R.G.1
Sharples, G.J.2
-
35
-
-
0034612333
-
The Bloom's syndrome gene product promotes branch migration of Holliday junctions
-
Karow, J.K., Constantinou, A., Li, J.L., West, S.C. and Hickson, I.D. (2000) The Bloom's syndrome gene product promotes branch migration of Holliday junctions. Proc. Natl Acad. Sci. USA, 97, 6504-6508.
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 6504-6508
-
-
Karow, J.K.1
Constantinou, A.2
Li, J.L.3
West, S.C.4
Hickson, I.D.5
-
36
-
-
0034231844
-
Werner's syndrome protein (WRN) migrates Holliday junctions and co- localizes with RPA upon replication arrest
-
Constantinou, A., Tarsounas, M., Karow, J.K., Brosh, R.M., Bohr, V.A., Hickson, I.D. and West, S.C. (2000) Werner's syndrome protein (WRN) migrates Holliday junctions and co- localizes with RPA upon replication arrest. EMBO Rep., 1, 80-84.
-
(2000)
EMBO Rep
, vol.1
, pp. 80-84
-
-
Constantinou, A.1
Tarsounas, M.2
Karow, J.K.3
Brosh, R.M.4
Bohr, V.A.5
Hickson, I.D.6
West, S.C.7
-
37
-
-
0036683338
-
Genome stability and the processing of damaged replication forks by RecG
-
McGlynn, P. and Lloyd, R.G. (2002) Genome stability and the processing of damaged replication forks by RecG. Trends Genet., 18, 413-419.
-
(2002)
Trends Genet
, vol.18
, pp. 413-419
-
-
McGlynn, P.1
Lloyd, R.G.2
-
38
-
-
33751426143
-
DNA helicases required for homologous recombination and repair of damaged replication forks
-
Wu, L. and Hickson, I.D. (2006) DNA helicases required for homologous recombination and repair of damaged replication forks. Annu. Rev. Genet., 40, 279-306.
-
(2006)
Annu. Rev. Genet
, vol.40
, pp. 279-306
-
-
Wu, L.1
Hickson, I.D.2
-
39
-
-
2442572065
-
Yeast MPH1 gene functions in an error-free DNA damage bypass pathway that requires genes from homologous recombination, but not from postreplicative repair
-
Schurer, K.A., Rudolph, C., Ulrich, H.D. and Kramer, W. (2004) Yeast MPH1 gene functions in an error-free DNA damage bypass pathway that requires genes from homologous recombination, but not from postreplicative repair. Genetics, 166, 1673-1686.
-
(2004)
Genetics
, vol.166
, pp. 1673-1686
-
-
Schurer, K.A.1
Rudolph, C.2
Ulrich, H.D.3
Kramer, W.4
-
40
-
-
0030982261
-
Reduced X-ray resistance and homologous recombination frequencies in a RAD54-/- mutant of the chicken DT40 cell line
-
Bezzubova, O., Silbergleit, A., Yamaguchi-Iwai, Y., Takeda, S. and Buerstedde, J.M. (1997) Reduced X-ray resistance and homologous recombination frequencies in a RAD54-/- mutant of the chicken DT40 cell line. Cell, 89, 185-193.
-
(1997)
Cell
, vol.89
, pp. 185-193
-
-
Bezzubova, O.1
Silbergleit, A.2
Yamaguchi-Iwai, Y.3
Takeda, S.4
Buerstedde, J.M.5
-
41
-
-
0030948789
-
Disruption of mouse RAD54 reduces ionizing radiation resistance and homologous recombination
-
Essers, J., Hendriks, R.W., Swagemakers, S.M., Troelstra, C., de Wit, J., Bootsma, D., Hoeijmakers, J.H. and Kanaar, R. (1997) Disruption of mouse RAD54 reduces ionizing radiation resistance and homologous recombination. Cell, 89, 195-204.
-
(1997)
Cell
, vol.89
, pp. 195-204
-
-
Essers, J.1
Hendriks, R.W.2
Swagemakers, S.M.3
Troelstra, C.4
de Wit, J.5
Bootsma, D.6
Hoeijmakers, J.H.7
Kanaar, R.8
-
42
-
-
25144492769
-
Unraveling the Fanconi anemia-DNA repair connection
-
Thompson, L.H. (2005) Unraveling the Fanconi anemia-DNA repair connection. Nat. Genet., 37, 921-922.
-
(2005)
Nat. Genet
, vol.37
, pp. 921-922
-
-
Thompson, L.H.1
-
43
-
-
33747352774
-
The Bloom's syndrome helicase can promote the regression of a model replication fork
-
Ralf, C., Hickson, I.D. and Wu, L. (2006) The Bloom's syndrome helicase can promote the regression of a model replication fork. J. Biol. Chem., 281, 22839-22846.
-
(2006)
J. Biol. Chem
, vol.281
, pp. 22839-22846
-
-
Ralf, C.1
Hickson, I.D.2
Wu, L.3
-
44
-
-
24944461145
-
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, D.S., McHugh, P.J., Hickson, I.D. et al. (2005) A FancD2-monoubiquitin fusion reveals hidden functions of Fanconi anemia core complex in DNA repair. Mol. Cell, 19, 841-847.
-
(2005)
Mol. Cell
, vol.19
, pp. 841-847
-
-
Matsushita, N.1
Kitao, H.2
Ishiai, M.3
Nagashima, N.4
Hirano, S.5
Okawa, K.6
Ohta, T.7
Yu, D.S.8
McHugh, P.J.9
Hickson, I.D.10
-
45
-
-
33749146108
-
DNA unwinding and protein displacement by superfamily 1 and superfamily 2 helicases
-
Mackintosh, S.G. and Raney, K.D. (2006) DNA unwinding and protein displacement by superfamily 1 and superfamily 2 helicases. Nucleic Acids Res., 34, 4154-4159.
-
(2006)
Nucleic Acids Res
, vol.34
, pp. 4154-4159
-
-
Mackintosh, S.G.1
Raney, K.D.2
-
46
-
-
34247208998
-
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway
-
Ling, C., Ishiai, M., Ali, A.M., Medhurst, A.L., Neveling, K., Kalb, R., Yan, Z., Xue, Y., Oostra, A.B., Auerbach, A.D. et al. (2007) FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway. EMBO J., 26, 2104-2114.
-
(2007)
EMBO J
, vol.26
, pp. 2104-2114
-
-
Ling, C.1
Ishiai, M.2
Ali, A.M.3
Medhurst, A.L.4
Neveling, K.5
Kalb, R.6
Yan, Z.7
Xue, Y.8
Oostra, A.B.9
Auerbach, A.D.10
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