-
1
-
-
0033780760
-
DNA replication is required To elicit cellular responses to psoralen-induced DNA interstrand cross-links
-
Akkari Y.M.N., Bateman R.L., Reifsteck 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. 2000, 20:8283-8289.
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 8283-8289
-
-
Akkari, Y.M.N.1
Bateman, R.L.2
Reifsteck, C.A.3
Olson, S.B.4
Grompe, M.5
-
2
-
-
33846415079
-
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2
-
Alter B.P., Rosenberg P.S., Brody L.C. Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2. J.Med. Genet. 2007, 44:1-9.
-
(2007)
J.Med. Genet.
, vol.44
, pp. 1-9
-
-
Alter, B.P.1
Rosenberg, P.S.2
Brody, L.C.3
-
3
-
-
67650451108
-
Fanconi anemia and its diagnosis
-
Auerbach A.D. Fanconi anemia and its diagnosis. Mutat. Res. 2009, 668:4-10.
-
(2009)
Mutat. Res.
, vol.668
, pp. 4-10
-
-
Auerbach, A.D.1
-
4
-
-
84875220657
-
Human RECQ1 promotes restart of replication forks reversed by DNA topoisomerase I inhibition
-
Berti M., Ray Chaudhuri A., Thangavel S., Gomathinayagam S., Kenig S., Vujanovic M., Odreman F., Glatter T., Graziano S., Mendoza-Maldonado R., et al. Human RECQ1 promotes restart of replication forks reversed by DNA topoisomerase I inhibition. Nat. Struct. Mol. Biol. 2013, 20:347-354.
-
(2013)
Nat. Struct. Mol. Biol.
, vol.20
, pp. 347-354
-
-
Berti, M.1
Ray Chaudhuri, A.2
Thangavel, S.3
Gomathinayagam, S.4
Kenig, S.5
Vujanovic, M.6
Odreman, F.7
Glatter, T.8
Graziano, S.9
Mendoza-Maldonado, R.10
-
5
-
-
84877584276
-
Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia
-
Bogliolo M., Schuster B., Stoepker C., Derkunt B., Su Y., Raams A., Trujillo J.P., Minguillón J., Ramírez M.J., Pujol R., et al. Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia. Am. J. Hum. Genet. 2013, 92:800-806.
-
(2013)
Am. J. Hum. Genet.
, vol.92
, pp. 800-806
-
-
Bogliolo, M.1
Schuster, B.2
Stoepker, C.3
Derkunt, B.4
Su, Y.5
Raams, A.6
Trujillo, J.P.7
Minguillón, J.8
Ramírez, M.J.9
Pujol, R.10
-
6
-
-
32644466860
-
Roles of ATP binding and ATP hydrolysis in human Rad51 recombinase function
-
Chi P., Van Komen S., Sehorn M.G., Sigurdsson S., Sung P. Roles of ATP binding and ATP hydrolysis in human Rad51 recombinase function. DNA Repair (Amst.) 2006, 5:381-391.
-
(2006)
DNA Repair (Amst.)
, vol.5
, pp. 381-391
-
-
Chi, P.1
Van Komen, S.2
Sehorn, M.G.3
Sigurdsson, S.4
Sung, P.5
-
7
-
-
84885024085
-
Advances in understanding the complex mechanisms of DNA interstrand cross-link repair
-
Clauson C., Schärer O.D., Niedernhofer L. Advances in understanding the complex mechanisms of DNA interstrand cross-link repair. Cold Spring Harb. Perspect. Med. 2013, 3:a012732.
-
(2013)
Cold Spring Harb. Perspect. Med.
, vol.3
, pp. a012732
-
-
Clauson, C.1
Schärer, O.D.2
Niedernhofer, L.3
-
8
-
-
84930092326
-
Germline RECQL mutations are associated with breast cancer susceptibility
-
Cybulski C., Carrot-Zhang J., Kluźniak W., Rivera B., Kashyap A., Wokołorczyk D., Giroux S., Nadaf J., Hamel N., Zhang S., et al. Germline RECQL mutations are associated with breast cancer susceptibility. Nat. Genet. 2015, 47:643-646.
-
(2015)
Nat. Genet.
, vol.47
, pp. 643-646
-
-
Cybulski, C.1
Carrot-Zhang, J.2
Kluźniak, W.3
Rivera, B.4
Kashyap, A.5
Wokołorczyk, D.6
Giroux, S.7
Nadaf, J.8
Hamel, N.9
Zhang, S.10
-
9
-
-
84857049860
-
RAD51 haploinsufficiency causes congenital mirror movements in humans
-
Depienne C., Bouteiller D., Méneret A., Billot S., Groppa S., Klebe S., Charbonnier-Beaupel F., Corvol J.C., Saraiva J.P., Brueggemann N., et al. RAD51 haploinsufficiency causes congenital mirror movements in humans. Am. J. Hum. Genet. 2012, 90:301-307.
-
(2012)
Am. J. Hum. Genet.
, vol.90
, pp. 301-307
-
-
Depienne, C.1
Bouteiller, D.2
Méneret, A.3
Billot, S.4
Groppa, S.5
Klebe, S.6
Charbonnier-Beaupel, F.7
Corvol, J.C.8
Saraiva, J.P.9
Brueggemann, N.10
-
10
-
-
38349008365
-
A forward chemical genetic screen reveals an inhibitor of the Mre11-Rad50-Nbs1 complex
-
Dupré A., Boyer-Chatenet L., Sattler R.M., Modi A.P., Lee J.H., Nicolette M.L., Kopelovich L., Jasin M., Baer R., Paull T.T., Gautier J. A forward chemical genetic screen reveals an inhibitor of the Mre11-Rad50-Nbs1 complex. Nat. Chem. Biol. 2008, 4:119-125.
-
(2008)
Nat. Chem. Biol.
, vol.4
, pp. 119-125
-
-
Dupré, A.1
Boyer-Chatenet, L.2
Sattler, R.M.3
Modi, A.P.4
Lee, J.H.5
Nicolette, M.L.6
Kopelovich, L.7
Jasin, M.8
Baer, R.9
Paull, T.T.10
Gautier, J.11
-
12
-
-
84890531796
-
RAD51 deficiency disrupts the corticospinal lateralization of motor control
-
Gallea C., Popa T., Hubsch C., Valabregue R., Brochard V., Kundu P., Schmitt B., Bardinet E., Bertasi E., Flamand-Roze C., et al. RAD51 deficiency disrupts the corticospinal lateralization of motor control. Brain 2013, 136:3333-3346.
-
(2013)
Brain
, vol.136
, pp. 3333-3346
-
-
Gallea, C.1
Popa, T.2
Hubsch, C.3
Valabregue, R.4
Brochard, V.5
Kundu, P.6
Schmitt, B.7
Bardinet, E.8
Bertasi, E.9
Flamand-Roze, C.10
-
13
-
-
84866952680
-
Genotoxic consequences of endogenous aldehydes on mouse haematopoietic stem cell function
-
Garaycoechea J.I., Crossan G.P., Langevin F., Daly M., Arends M.J., Patel K.J. Genotoxic consequences of endogenous aldehydes on mouse haematopoietic stem cell function. Nature 2012, 489:571-575.
-
(2012)
Nature
, vol.489
, pp. 571-575
-
-
Garaycoechea, J.I.1
Crossan, G.P.2
Langevin, F.3
Daly, M.4
Arends, M.J.5
Patel, K.J.6
-
14
-
-
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., D'Andrea A.D. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. Mol. Cell 2001, 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
-
15
-
-
60249099583
-
Corrected structure of mirin, a small-molecule inhibitor of the Mre11-Rad50-Nbs1 complex
-
Garner K.M., Pletnev A.A., Eastman A. Corrected structure of mirin, a small-molecule inhibitor of the Mre11-Rad50-Nbs1 complex. Nat. Chem. Biol. 2009, 5:129-130.
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 129-130
-
-
Garner, K.M.1
Pletnev, A.A.2
Eastman, A.3
-
16
-
-
84885855405
-
Human GEN1 and the SLX4-associated nucleases MUS81 and SLX1 are essential for the resolution of replication-induced Holliday junctions
-
Garner E., Kim Y., Lach F.P., Kottemann M.C., Smogorzewska A. Human GEN1 and the SLX4-associated nucleases MUS81 and SLX1 are essential for the resolution of replication-induced Holliday junctions. Cell Rep. 2013, 5:207-215.
-
(2013)
Cell Rep.
, vol.5
, pp. 207-215
-
-
Garner, E.1
Kim, Y.2
Lach, F.P.3
Kottemann, M.C.4
Smogorzewska, A.5
-
17
-
-
78549251695
-
Rad51 protects nascent DNA from Mre11-dependent degradation and promotes continuous DNA synthesis
-
Hashimoto Y., Ray Chaudhuri A., Lopes M., Costanzo V. Rad51 protects nascent DNA from Mre11-dependent degradation and promotes continuous DNA synthesis. Nat. Struct. Mol. Biol. 2010, 17:1305-1311.
-
(2010)
Nat. Struct. Mol. Biol.
, vol.17
, pp. 1305-1311
-
-
Hashimoto, Y.1
Ray Chaudhuri, A.2
Lopes, M.3
Costanzo, V.4
-
18
-
-
58849096231
-
Direct imaging of human Rad51 nucleoprotein dynamics on individual DNA molecules
-
Hilario J., Amitani I., Baskin R.J., Kowalczykowski S.C. Direct imaging of human Rad51 nucleoprotein dynamics on individual DNA molecules. Proc. Natl. Acad. Sci. USA 2009, 106:361-368.
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 361-368
-
-
Hilario, J.1
Amitani, I.2
Baskin, R.J.3
Kowalczykowski, S.C.4
-
19
-
-
84938667462
-
Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia
-
Hira A., Yoshida K., Sato K., Okuno Y., Shiraishi Y., Chiba K., Tanaka H., Miyano S., Shimamoto A., Tahara H., et al. Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia. Am. J. Hum. Genet. 2015, 96:1001-1007.
-
(2015)
Am. J. Hum. Genet.
, vol.96
, pp. 1001-1007
-
-
Hira, A.1
Yoshida, K.2
Sato, K.3
Okuno, Y.4
Shiraishi, Y.5
Chiba, K.6
Tanaka, H.7
Miyano, S.8
Shimamoto, A.9
Tahara, H.10
-
20
-
-
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. Biallelic inactivation of BRCA2 in Fanconi anemia. Science 2002, 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
-
21
-
-
84902096048
-
Development and applications of CRISPR-Cas9 for genome engineering
-
Hsu P.D., Lander E.S., Zhang F. Development and applications of CRISPR-Cas9 for genome engineering. Cell 2014, 157:1262-1278.
-
(2014)
Cell
, vol.157
, pp. 1262-1278
-
-
Hsu, P.D.1
Lander, E.S.2
Zhang, F.3
-
22
-
-
0038154016
-
The human Bloom syndrome gene suppresses the DNA replication and repair defects of yeast dna2 mutants
-
Imamura O., Campbell J.L. The human Bloom syndrome gene suppresses the DNA replication and repair defects of yeast dna2 mutants. Proc. Natl. Acad. Sci. USA 2003, 100:8193-8198.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 8193-8198
-
-
Imamura, O.1
Campbell, J.L.2
-
23
-
-
77957975815
-
Purified human BRCA2 stimulates RAD51-mediated recombination
-
Jensen R.B., Carreira A., Kowalczykowski S.C. Purified human BRCA2 stimulates RAD51-mediated recombination. Nature 2010, 467:678-683.
-
(2010)
Nature
, vol.467
, pp. 678-683
-
-
Jensen, R.B.1
Carreira, A.2
Kowalczykowski, S.C.3
-
24
-
-
84869485349
-
DNA2 and EXO1 in replication-coupled, homology-directed repair and in the interplay between HDR and the FA/BRCA network
-
Karanja K.K., Cox S.W., Duxin J.P., Stewart S.A., Campbell J.L. DNA2 and EXO1 in replication-coupled, homology-directed repair and in the interplay between HDR and the FA/BRCA network. Cell Cycle 2012, 11:3983-3996.
-
(2012)
Cell Cycle
, vol.11
, pp. 3983-3996
-
-
Karanja, K.K.1
Cox, S.W.2
Duxin, J.P.3
Stewart, S.A.4
Campbell, J.L.5
-
25
-
-
84900559537
-
Preventing over-resection by DNA2 helicase/nuclease suppresses repair defects in Fanconi anemia cells
-
Karanja K.K., Lee E.H., Hendrickson E.A., Campbell J.L. Preventing over-resection by DNA2 helicase/nuclease suppresses repair defects in Fanconi anemia cells. Cell Cycle 2014, 13:1540-1550.
-
(2014)
Cell Cycle
, vol.13
, pp. 1540-1550
-
-
Karanja, K.K.1
Lee, E.H.2
Hendrickson, E.A.3
Campbell, J.L.4
-
26
-
-
84877580404
-
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia
-
Kashiyama K., Nakazawa Y., Pilz D.T., Guo C., Shimada M., Sasaki K., Fawcett H., Wing J.F., Lewin S.O., Carr L., et al. Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia. Am. J. Hum. Genet. 2013, 92:807-819.
-
(2013)
Am. J. Hum. Genet.
, vol.92
, pp. 807-819
-
-
Kashiyama, K.1
Nakazawa, Y.2
Pilz, D.T.3
Guo, C.4
Shimada, M.5
Sasaki, K.6
Fawcett, H.7
Wing, J.F.8
Lewin, S.O.9
Carr, L.10
-
27
-
-
84872082435
-
Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4
-
Kim Y., Spitz G.S., Veturi U., Lach F.P., Auerbach A.D., Smogorzewska A. Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4. Blood 2013, 121:54-63.
-
(2013)
Blood
, vol.121
, pp. 54-63
-
-
Kim, Y.1
Spitz, G.S.2
Veturi, U.3
Lach, F.P.4
Auerbach, A.D.5
Smogorzewska, A.6
-
28
-
-
84899991195
-
XPF-ERCC1 acts in unhooking DNA interstrand crosslinks in cooperation with FANCD2 and FANCP/SLX4
-
Klein Douwel D., Boonen R.A., Long D.T., Szypowska A.A., Raschle M., Walter J.C., Knipscheer P. XPF-ERCC1 acts in unhooking DNA interstrand crosslinks in cooperation with FANCD2 and FANCP/SLX4. Mol. Cell 2014, 54:460-471.
-
(2014)
Mol. Cell
, vol.54
, pp. 460-471
-
-
Klein Douwel, D.1
Boonen, R.A.2
Long, D.T.3
Szypowska, A.A.4
Raschle, M.5
Walter, J.C.6
Knipscheer, P.7
-
29
-
-
72949123930
-
The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair
-
Knipscheer P., Räschle M., Smogorzewska A., Enoiu M., Ho T.V., Schärer O.D., Elledge S.J., Walter J.C. The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair. Science 2009, 326:1698-1701.
-
(2009)
Science
, vol.326
, pp. 1698-1701
-
-
Knipscheer, P.1
Räschle, M.2
Smogorzewska, A.3
Enoiu, M.4
Ho, T.V.5
Schärer, O.D.6
Elledge, S.J.7
Walter, J.C.8
-
30
-
-
84872578210
-
Fanconi anaemia and the repair of Watson and Crick DNA crosslinks
-
Kottemann M.C., Smogorzewska A. Fanconi anaemia and the repair of Watson and Crick DNA crosslinks. Nature 2013, 493:356-363.
-
(2013)
Nature
, vol.493
, pp. 356-363
-
-
Kottemann, M.C.1
Smogorzewska, A.2
-
31
-
-
0024318225
-
Biochemical events essential to the recombination activity of Escherichia coli RecA protein. II. Co-dominant effects of RecA142 protein on wild-type RecA protein function
-
Kowalczykowski S.C., Krupp R.A. Biochemical events essential to the recombination activity of Escherichia coli RecA protein. II. Co-dominant effects of RecA142 protein on wild-type RecA protein function. J.Mol. Biol. 1989, 207:735-747.
-
(1989)
J.Mol. Biol.
, vol.207
, pp. 735-747
-
-
Kowalczykowski, S.C.1
Krupp, R.A.2
-
32
-
-
79960037006
-
Fancd2 counteracts the toxic effects of naturally produced aldehydes in mice
-
Langevin F., Crossan G.P., Rosado I.V., Arends M.J., Patel K.J. Fancd2 counteracts the toxic effects of naturally produced aldehydes in mice. Nature 2011, 475:53-58.
-
(2011)
Nature
, vol.475
, pp. 53-58
-
-
Langevin, F.1
Crossan, G.P.2
Rosado, I.V.3
Arends, M.J.4
Patel, K.J.5
-
33
-
-
0027379579
-
Negative co-dominant inhibition of recA protein function. Biochemical properties of the recA1, recA13 and recA56 proteins and the effect of recA56 protein on the activities of the wild-type recA protein function invitro
-
Lauder S.D., Kowalczykowski S.C. Negative co-dominant inhibition of recA protein function. Biochemical properties of the recA1, recA13 and recA56 proteins and the effect of recA56 protein on the activities of the wild-type recA protein function invitro. J.Mol. Biol. 1993, 234:72-86.
-
(1993)
J.Mol. Biol.
, vol.234
, pp. 72-86
-
-
Lauder, S.D.1
Kowalczykowski, S.C.2
-
34
-
-
77957804215
-
Human BRCA2 protein promotes RAD51 filament formation on RPA-covered single-stranded DNA
-
Liu J., Doty T., Gibson B., Heyer W.D. Human BRCA2 protein promotes RAD51 filament formation on RPA-covered single-stranded DNA. Nat. Struct. Mol. Biol. 2010, 17:1260-1262.
-
(2010)
Nat. Struct. Mol. Biol.
, vol.17
, pp. 1260-1262
-
-
Liu, J.1
Doty, T.2
Gibson, B.3
Heyer, W.D.4
-
35
-
-
79959843168
-
Mechanism of RAD51-dependent DNA interstrand cross-link repair
-
Long D.T., Räschle M., Joukov V., Walter J.C. Mechanism of RAD51-dependent DNA interstrand cross-link repair. Science 2011, 333:84-87.
-
(2011)
Science
, vol.333
, pp. 84-87
-
-
Long, D.T.1
Räschle, M.2
Joukov, V.3
Walter, J.C.4
-
36
-
-
0022429092
-
Interaction of recA protein with single-stranded DNA. Quantitative aspects of binding affinity modulation by nucleotide cofactors
-
Menetski J.P., Kowalczykowski S.C. Interaction of recA protein with single-stranded DNA. Quantitative aspects of binding affinity modulation by nucleotide cofactors. J.Mol. Biol. 1985, 181:281-295.
-
(1985)
J.Mol. Biol.
, vol.181
, pp. 281-295
-
-
Menetski, J.P.1
Kowalczykowski, S.C.2
-
37
-
-
77649131406
-
Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesis
-
Moynahan M.E., Jasin M. Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesis. Nat. Rev. Mol. Cell Biol. 2010, 11:196-207.
-
(2010)
Nat. Rev. Mol. Cell Biol.
, vol.11
, pp. 196-207
-
-
Moynahan, M.E.1
Jasin, M.2
-
38
-
-
79951688343
-
BLM-DNA2-RPA-MRN and EXO1-BLM-RPA-MRN constitute two DNA end resection machineries for human DNA break repair
-
Nimonkar A.V., Genschel J., Kinoshita E., Polaczek P., Campbell J.L., Wyman C., Modrich P., Kowalczykowski S.C. BLM-DNA2-RPA-MRN and EXO1-BLM-RPA-MRN constitute two DNA end resection machineries for human DNA break repair. Genes Dev. 2011, 25:350-362.
-
(2011)
Genes Dev.
, vol.25
, pp. 350-362
-
-
Nimonkar, A.V.1
Genschel, J.2
Kinoshita, E.3
Polaczek, P.4
Campbell, J.L.5
Wyman, C.6
Modrich, P.7
Kowalczykowski, S.C.8
-
39
-
-
84856015503
-
Hereditary ovarian cancer: beyond the usual suspects
-
Pennington K.P., Swisher E.M. Hereditary ovarian cancer: beyond the usual suspects. Gynecol. Oncol. 2012, 124:347-353.
-
(2012)
Gynecol. Oncol.
, vol.124
, pp. 347-353
-
-
Pennington, K.P.1
Swisher, E.M.2
-
40
-
-
76849109722
-
Hydroxyurea-stalled replication forks become progressively inactivated and require two different RAD51-mediated pathways for restart and repair
-
Petermann E., Orta M.L., Issaeva N., Schultz N., Helleday T. Hydroxyurea-stalled replication forks become progressively inactivated and require two different RAD51-mediated pathways for restart and repair. Mol. Cell 2010, 37:492-502.
-
(2010)
Mol. Cell
, vol.37
, pp. 492-502
-
-
Petermann, E.1
Orta, M.L.2
Issaeva, N.3
Schultz, N.4
Helleday, T.5
-
41
-
-
0029095108
-
Isolation and characterization of the human MRE11 homologue
-
Petrini J.H., Walsh M.E., DiMare C., Chen X.N., Korenberg J.R., Weaver D.T. Isolation and characterization of the human MRE11 homologue. Genomics 1995, 29:80-86.
-
(1995)
Genomics
, vol.29
, pp. 80-86
-
-
Petrini, J.H.1
Walsh, M.E.2
DiMare, C.3
Chen, X.N.4
Korenberg, J.R.5
Weaver, D.T.6
-
42
-
-
0033569684
-
XRCC3 promotes homology-directed repair of DNA damage in mammalian cells
-
Pierce A.J., Johnson R.D., Thompson L.H., Jasin M. XRCC3 promotes homology-directed repair of DNA damage in mammalian cells. Genes Dev. 1999, 13:2633-2638.
-
(1999)
Genes Dev.
, vol.13
, pp. 2633-2638
-
-
Pierce, A.J.1
Johnson, R.D.2
Thompson, L.H.3
Jasin, M.4
-
43
-
-
51549098159
-
Mechanism of replication-coupled DNA interstrand crosslink repair
-
Räschle M., Knipscheer P., Enoiu M., Angelov T., Sun J., Griffith J.D., Ellenberger T.E., Schärer O.D., Walter J.C. Mechanism of replication-coupled DNA interstrand crosslink repair. Cell 2008, 134:969-980.
-
(2008)
Cell
, vol.134
, pp. 969-980
-
-
Räschle, M.1
Knipscheer, P.2
Enoiu, M.3
Angelov, T.4
Sun, J.5
Griffith, J.D.6
Ellenberger, T.E.7
Schärer, O.D.8
Walter, J.C.9
-
44
-
-
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. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat. Genet. 2007, 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
-
45
-
-
84937525461
-
Deficiency of UBE2T, the E2 ubiquitin ligase necessary for FANCD2 and FANCI ubiquitination, causes FA-T subtype of Fanconi anemia
-
Rickman K.A., Lach F.P., Abhyankar A., Donovan F.X., Sanborn E.M., Kennedy J.A., Sougnez C., Gabriel S.B., Elemento O., Chandrasekharappa S.C., et al. Deficiency of UBE2T, the E2 ubiquitin ligase necessary for FANCD2 and FANCI ubiquitination, causes FA-T subtype of Fanconi anemia. Cell Rep. 2015, 12:35-41.
-
(2015)
Cell Rep.
, vol.12
, pp. 35-41
-
-
Rickman, K.A.1
Lach, F.P.2
Abhyankar, A.3
Donovan, F.X.4
Sanborn, E.M.5
Kennedy, J.A.6
Sougnez, C.7
Gabriel, S.B.8
Elemento, O.9
Chandrasekharappa, S.C.10
-
46
-
-
50649100744
-
Mechanism of eukaryotic homologous recombination
-
San Filippo J., Sung P., Klein H. Mechanism of eukaryotic homologous recombination. Annu. Rev. Biochem. 2008, 77:229-257.
-
(2008)
Annu. Rev. Biochem.
, vol.77
, pp. 229-257
-
-
San Filippo, J.1
Sung, P.2
Klein, H.3
-
47
-
-
84926505383
-
Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype
-
Sawyer S.L., Tian L., Kähkönen M., Schwartzentruber J., Kircher M., Majewski J., Dyment D.A., Innes A.M., Boycott K.M., Moreau L.A., et al. Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype. Cancer Discov. 2015, 5:135-142.
-
(2015)
Cancer Discov.
, vol.5
, pp. 135-142
-
-
Sawyer, S.L.1
Tian, L.2
Kähkönen, M.3
Schwartzentruber, J.4
Kircher, M.5
Majewski, J.6
Dyment, D.A.7
Innes, A.M.8
Boycott, K.M.9
Moreau, L.A.10
-
48
-
-
79955799175
-
Double-strand break repair-independent role for BRCA2 in blocking stalled replication fork degradation by MRE11
-
Schlacher K., Christ N., Siaud N., Egashira A., Wu H., Jasin M. Double-strand break repair-independent role for BRCA2 in blocking stalled replication fork degradation by MRE11. Cell 2011, 145:529-542.
-
(2011)
Cell
, vol.145
, pp. 529-542
-
-
Schlacher, K.1
Christ, N.2
Siaud, N.3
Egashira, A.4
Wu, H.5
Jasin, M.6
-
49
-
-
84863753191
-
A distinct replication fork protection pathway connects Fanconi anemia tumor suppressors to RAD51-BRCA1/2
-
Schlacher K., Wu H., Jasin M. A distinct replication fork protection pathway connects Fanconi anemia tumor suppressors to RAD51-BRCA1/2. Cancer Cell 2012, 22:106-116.
-
(2012)
Cancer Cell
, vol.22
, pp. 106-116
-
-
Schlacher, K.1
Wu, H.2
Jasin, M.3
-
50
-
-
82855169525
-
Orchestrating the nucleases involved in DNA interstrand cross-link (ICL) repair
-
Sengerová B., Wang A.T., McHugh P.J. Orchestrating the nucleases involved in DNA interstrand cross-link (ICL) repair. Cell Cycle 2011, 10:3999-4008.
-
(2011)
Cell Cycle
, vol.10
, pp. 3999-4008
-
-
Sengerová, B.1
Wang, A.T.2
McHugh, P.J.3
-
51
-
-
33847228012
-
RECQL, a member of the RecQ family of DNA helicases, suppresses chromosomal instability
-
Sharma S., Stumpo D.J., Balajee A.S., Bock C.B., Lansdorp P.M., Brosh R.M., Blackshear P.J. RECQL, a member of the RecQ family of DNA helicases, suppresses chromosomal instability. Mol. Cell. Biol. 2007, 27:1784-1794.
-
(2007)
Mol. Cell. Biol.
, vol.27
, pp. 1784-1794
-
-
Sharma, S.1
Stumpo, D.J.2
Balajee, A.S.3
Bock, C.B.4
Lansdorp, P.M.5
Brosh, R.M.6
Blackshear, P.J.7
-
52
-
-
34247110291
-
Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair
-
Smogorzewska A., Matsuoka S., Vinciguerra P., McDonald E.R., Hurov K.E., Luo J., Ballif B.A., Gygi S.P., Hofmann K., D'Andrea A.D., Elledge S.J. Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair. Cell 2007, 129:289-301.
-
(2007)
Cell
, vol.129
, pp. 289-301
-
-
Smogorzewska, A.1
Matsuoka, S.2
Vinciguerra, P.3
McDonald, 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
Elledge, S.J.11
-
53
-
-
84907584670
-
DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells
-
Sturzenegger A., Burdova K., Kanagaraj R., Levikova M., Pinto C., Cejka P., Janscak P. DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells. J.Biol. Chem. 2014, 289:27314-27326.
-
(2014)
J.Biol. Chem.
, vol.289
, pp. 27314-27326
-
-
Sturzenegger, A.1
Burdova, K.2
Kanagaraj, R.3
Levikova, M.4
Pinto, C.5
Cejka, P.6
Janscak, P.7
-
54
-
-
0031004885
-
A single-stranded DNA-binding protein is needed for efficient presynaptic complex formation by the Saccharomyces cerevisiae Rad51 protein
-
Sugiyama T., Zaitseva E.M., Kowalczykowski S.C. A single-stranded DNA-binding protein is needed for efficient presynaptic complex formation by the Saccharomyces cerevisiae Rad51 protein. J.Biol. Chem. 1997, 272:7940-7945.
-
(1997)
J.Biol. Chem.
, vol.272
, pp. 7940-7945
-
-
Sugiyama, T.1
Zaitseva, E.M.2
Kowalczykowski, S.C.3
-
55
-
-
84930534513
-
Mutations in RECQL Gene Are Associated with Predisposition to Breast Cancer
-
Sun J., Wang Y., Xia Y., Xu Y., Ouyang T., Li J., Wang T., Fan Z., Fan T., Lin B., et al. Mutations in RECQL Gene Are Associated with Predisposition to Breast Cancer. PLoS Genet. 2015, 11:e1005228.
-
(2015)
PLoS Genet.
, vol.11
, pp. e1005228
-
-
Sun, J.1
Wang, Y.2
Xia, Y.3
Xu, Y.4
Ouyang, T.5
Li, J.6
Wang, T.7
Fan, Z.8
Fan, T.9
Lin, B.10
-
56
-
-
0029112483
-
DNA strand exchange mediated by a RAD51-ssDNA nucleoprotein filament with polarity opposite to that of RecA
-
Sung P., Robberson D.L. DNA strand exchange mediated by a RAD51-ssDNA nucleoprotein filament with polarity opposite to that of RecA. Cell 1995, 82:453-461.
-
(1995)
Cell
, vol.82
, pp. 453-461
-
-
Sung, P.1
Robberson, D.L.2
-
57
-
-
84905493192
-
End resection at double-strand breaks: mechanism and regulation
-
Symington L.S. End resection at double-strand breaks: mechanism and regulation. Cold Spring Harb. Perspect. Biol. 2014, 6:a016436.
-
(2014)
Cold Spring Harb. Perspect. Biol.
, vol.6
, pp. a016436
-
-
Symington, L.S.1
-
58
-
-
80755187806
-
Double-strand break end resection and repair pathway choice
-
Symington L.S., Gautier J. Double-strand break end resection and repair pathway choice. Annu. Rev. Genet. 2011, 45:247-271.
-
(2011)
Annu. Rev. Genet.
, vol.45
, pp. 247-271
-
-
Symington, L.S.1
Gautier, J.2
-
59
-
-
0033846527
-
The Rad51 paralog Rad51B promotes homologous recombinational repair
-
Takata M., Sasaki M.S., Sonoda E., Fukushima T., Morrison C., Albala J.S., Swagemakers S.M., Kanaar R., Thompson L.H., Takeda S. The Rad51 paralog Rad51B promotes homologous recombinational repair. Mol. Cell. Biol. 2000, 20:6476-6482.
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 6476-6482
-
-
Takata, M.1
Sasaki, M.S.2
Sonoda, E.3
Fukushima, T.4
Morrison, C.5
Albala, J.S.6
Swagemakers, S.M.7
Kanaar, R.8
Thompson, L.H.9
Takeda, S.10
-
60
-
-
84924873531
-
DNA2 drives processing and restart of reversed replication forks in human cells
-
Thangavel S., Berti M., Levikova M., Pinto C., Gomathinayagam S., Vujanovic M., Zellweger R., Moore H., Lee E.H., Hendrickson E.A., et al. DNA2 drives processing and restart of reversed replication forks in human cells. J.Cell Biol. 2015, 208:545-562.
-
(2015)
J.Cell Biol.
, vol.208
, pp. 545-562
-
-
Thangavel, S.1
Berti, M.2
Levikova, M.3
Pinto, C.4
Gomathinayagam, S.5
Vujanovic, M.6
Zellweger, R.7
Moore, H.8
Lee, E.H.9
Hendrickson, E.A.10
-
61
-
-
0029987450
-
Targeted disruption of the Rad51 gene leads to lethality in embryonic mice
-
Tsuzuki T., Fujii Y., Sakumi K., Tominaga Y., Nakao K., Sekiguchi M., Matsushiro A., Yoshimura Y., Morita T. Targeted disruption of the Rad51 gene leads to lethality in embryonic mice. Proc. Natl. Acad. Sci. USA 1996, 93:6236-6240.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 6236-6240
-
-
Tsuzuki, T.1
Fujii, Y.2
Sakumi, K.3
Tominaga, Y.4
Nakao, K.5
Sekiguchi, M.6
Matsushiro, A.7
Yoshimura, Y.8
Morita, T.9
-
62
-
-
77951747926
-
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., et al. Mutation of the RAD51C gene in a Fanconi anemia-like disorder. Nat. Genet. 2010, 42:406-409.
-
(2010)
Nat. Genet.
, vol.42
, pp. 406-409
-
-
Vaz, F.1
Hanenberg, H.2
Schuster, B.3
Barker, K.4
Wiek, C.5
Erven, V.6
Neveling, K.7
Endt, D.8
Kesterton, I.9
Autore, F.10
-
63
-
-
65149095154
-
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder
-
Waltes R., Kalb R., Gatei M., Kijas A.W., Stumm M., Sobeck A., Wieland B., Varon R., Lerenthal Y., Lavin M.F., et al. Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder. Am. J. Hum. Genet. 2009, 84:605-616.
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 605-616
-
-
Waltes, R.1
Kalb, R.2
Gatei, M.3
Kijas, A.W.4
Stumm, M.5
Sobeck, A.6
Wieland, B.7
Varon, R.8
Lerenthal, Y.9
Lavin, M.F.10
-
64
-
-
84920942368
-
SnapShot: Fanconi anemia and associated proteins
-
Wang A.T., Smogorzewska A. SnapShot: Fanconi anemia and associated proteins. Cell 2015, 160:354-354.e1.
-
(2015)
Cell
, vol.160
, pp. 354-354.e1
-
-
Wang, A.T.1
Smogorzewska, A.2
-
65
-
-
80052440005
-
Human SNM1A and XPF-ERCC1 collaborate to initiate DNA interstrand cross-link repair
-
Wang A.T., Sengerová B., Cattell E., Inagawa T., Hartley J.M., Kiakos K., Burgess-Brown N.A., Swift L.P., Enzlin J.H., Schofield C.J., et al. Human SNM1A and XPF-ERCC1 collaborate to initiate DNA interstrand cross-link repair. Genes Dev. 2011, 25:1859-1870.
-
(2011)
Genes Dev.
, vol.25
, pp. 1859-1870
-
-
Wang, A.T.1
Sengerová, B.2
Cattell, E.3
Inagawa, T.4
Hartley, J.M.5
Kiakos, K.6
Burgess-Brown, N.A.7
Swift, L.P.8
Enzlin, J.H.9
Schofield, C.J.10
-
66
-
-
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. Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Nat. Genet. 2007, 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
-
67
-
-
0030749867
-
Conditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cells
-
Xiao Y., Weaver D.T. Conditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cells. Nucleic Acids Res. 1997, 25:2985-2991.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 2985-2991
-
-
Xiao, Y.1
Weaver, D.T.2
-
68
-
-
84861888851
-
Mre11-dependent degradation of stalled DNA replication forks is prevented by BRCA2 and PARP1
-
Ying S., Hamdy F.C., Helleday T. Mre11-dependent degradation of stalled DNA replication forks is prevented by BRCA2 and PARP1. Cancer Res. 2012, 72:2814-2821.
-
(2012)
Cancer Res.
, vol.72
, pp. 2814-2821
-
-
Ying, S.1
Hamdy, F.C.2
Helleday, T.3
-
69
-
-
84924911767
-
Rad51-mediated replication fork reversal is a global response to genotoxic treatments in human cells
-
Zellweger R., Dalcher D., Mutreja K., Berti M., Schmid J.A., Herrador R., Vindigni A., Lopes M. Rad51-mediated replication fork reversal is a global response to genotoxic treatments in human cells. J.Cell Biol. 2015, 208:563-579.
-
(2015)
J.Cell Biol.
, vol.208
, pp. 563-579
-
-
Zellweger, R.1
Dalcher, D.2
Mutreja, K.3
Berti, M.4
Schmid, J.A.5
Herrador, R.6
Vindigni, A.7
Lopes, M.8
-
70
-
-
84902112143
-
Mechanism and regulation of incisions during DNA interstrand cross-link repair
-
Zhang J., Walter J.C. Mechanism and regulation of incisions during DNA interstrand cross-link repair. DNA Repair (Amst) 2014, 19:135-142.
-
(2014)
DNA Repair (Amst)
, vol.19
, pp. 135-142
-
-
Zhang, J.1
Walter, J.C.2
-
71
-
-
84864413963
-
FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair
-
Zhou W., Otto E.A., Cluckey A., Airik R., Hurd T.W., Chaki M., Diaz K., Lach F.P., Bennett G.R., Gee H.Y., et al. FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair. Nat. Genet. 2012, 44:910-915.
-
(2012)
Nat. Genet.
, vol.44
, pp. 910-915
-
-
Zhou, W.1
Otto, E.A.2
Cluckey, A.3
Airik, R.4
Hurd, T.W.5
Chaki, M.6
Diaz, K.7
Lach, F.P.8
Bennett, G.R.9
Gee, H.Y.10
|