-
1
-
-
84863670930
-
Regulation of DNA cross-link repair by the Fanconi anemia/BRCA pathway
-
Kim H, D'Andrea AD, (2012) Regulation of DNA cross-link repair by the Fanconi anemia/BRCA pathway. Genes Dev 26: 1393-1408.
-
(2012)
Genes Dev
, vol.26
, pp. 1393-1408
-
-
Kim, H.1
D'Andrea, A.D.2
-
2
-
-
84872578210
-
Fanconi anaemia and the repair of Watson and Crick DNA crosslinks
-
Kottemann MC, Smogorzewska A, (2013) Fanconi anaemia and the repair of Watson and Crick DNA crosslinks. Nature 493: 356-363.
-
(2013)
Nature
, vol.493
, pp. 356-363
-
-
Kottemann, M.C.1
Smogorzewska, A.2
-
3
-
-
84877584276
-
Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia
-
Bogliolo M, Schuster B, Stoepker C, Derkunt B, Su Y, et al. (2013) Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia. Am J Hum Genet 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
-
4
-
-
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 DT, Guo C, Shimada M, et al. (2013) Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia. Am J Hum Genet 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
-
5
-
-
72949123930
-
The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair
-
Knipscheer P, Raschle M, Smogorzewska A, Enoiu M, Ho TV, et al. (2009) The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair. Science 326: 1698-1701.
-
(2009)
Science
, vol.326
, pp. 1698-1701
-
-
Knipscheer, P.1
Raschle, M.2
Smogorzewska, A.3
Enoiu, M.4
Ho, T.V.5
-
6
-
-
0035105291
-
Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway
-
Garcia-Higuera I, Taniguchi T, Ganesan S, Meyn MS, Timmers C, et al. (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
-
7
-
-
67650569540
-
Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M
-
Singh TR, Bakker ST, Agarwal S, Jansen M, Grassman E, et al. (2009) Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M. Blood 114: 174-180.
-
(2009)
Blood
, vol.114
, pp. 174-180
-
-
Singh, T.R.1
Bakker, S.T.2
Agarwal, S.3
Jansen, M.4
Grassman, E.5
-
8
-
-
46749106037
-
Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24
-
Kim JM, Kee Y, Gurtan A, D'Andrea AD, (2008) Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24. Blood 111: 5215-5222.
-
(2008)
Blood
, vol.111
, pp. 5215-5222
-
-
Kim, J.M.1
Kee, Y.2
Gurtan, A.3
D'Andrea, A.D.4
-
9
-
-
4043133287
-
ATR couples FANCD2 monoubiquitination to the DNA-damage response
-
Andreassen PR, D'Andrea AD, Taniguchi T, (2004) ATR couples FANCD2 monoubiquitination to the DNA-damage response. Genes Dev 18: 1958-1963.
-
(2004)
Genes Dev
, vol.18
, pp. 1958-1963
-
-
Andreassen, P.R.1
D'Andrea, A.D.2
Taniguchi, T.3
-
10
-
-
2942705849
-
Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin
-
Wang X, Andreassen PR, D'Andrea AD, (2004) Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin. Mol Cell Biol 24: 5850-5862.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 5850-5862
-
-
Wang, X.1
Andreassen, P.R.2
D'Andrea, A.D.3
-
11
-
-
84876861783
-
FANCM and FAAP24 maintain genome stability via cooperative as well as unique functions
-
Wang Y, Leung JW, Jiang Y, Lowery MG, Do H, et al. (2013) FANCM and FAAP24 maintain genome stability via cooperative as well as unique functions. Mol Cell 49: 997-1009.
-
(2013)
Mol Cell
, vol.49
, pp. 997-1009
-
-
Wang, Y.1
Leung, J.W.2
Jiang, Y.3
Lowery, M.G.4
Do, H.5
-
12
-
-
38349050087
-
The Fanconi anemia protein FANCM can promote branch migration of Holliday junctions and replication forks
-
Gari K, Decaillet C, Stasiak AZ, Stasiak A, 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
-
13
-
-
0025881472
-
Fanconi's anaemia and pregnancy
-
Alter BP, Frissora CL, Halperin DS, Freedman MH, Chitkara U, et al. (1991) Fanconi's anaemia and pregnancy. Br J Haematol 77: 410-418.
-
(1991)
Br J Haematol
, vol.77
, pp. 410-418
-
-
Alter, B.P.1
Frissora, C.L.2
Halperin, D.S.3
Freedman, M.H.4
Chitkara, U.5
-
14
-
-
67650451108
-
Fanconi anemia and its diagnosis
-
Auerbach AD, (2009) Fanconi anemia and its diagnosis. Mutat Res 668: 4-10.
-
(2009)
Mutat Res
, vol.668
, pp. 4-10
-
-
Auerbach, A.D.1
-
15
-
-
0037112817
-
A novel gene, Pog, is necessary for primordial germ cell proliferation in the mouse and underlies the germ cell deficient mutation, gcd
-
Agoulnik AI, Lu B, Zhu Q, Truong C, Ty MT, et al. (2002) A novel gene, Pog, is necessary for primordial germ cell proliferation in the mouse and underlies the germ cell deficient mutation, gcd. Hum Mol Genet 11: 3047-3053.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 3047-3053
-
-
Agoulnik, A.I.1
Lu, B.2
Zhu, Q.3
Truong, C.4
Ty, M.T.5
-
16
-
-
82755194916
-
Fancf-deficient mice are prone to develop ovarian tumours
-
Bakker ST, van de Vrugt HJ, Visser JA, Delzenne-Goette E, van der Wal A, et al. (2012) Fancf-deficient mice are prone to develop ovarian tumours. J Pathol 226: 28-39.
-
(2012)
J Pathol
, vol.226
, pp. 28-39
-
-
Bakker, S.T.1
van de Vrugt, H.J.2
Visser, J.A.3
Delzenne-Goette, E.4
van der Wal, A.5
-
18
-
-
69449102249
-
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M
-
Bakker ST, van de Vrugt HJ, Rooimans MA, Oostra AB, Steltenpool J, et al. (2009) Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M. Hum Mol Genet 18: 3484-3495.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3484-3495
-
-
Bakker, S.T.1
van de Vrugt, H.J.2
Rooimans, M.A.3
Oostra, A.B.4
Steltenpool, J.5
-
19
-
-
79251624412
-
Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia
-
Crossan GP, van der Weyden L, Rosado IV, Langevin F, Gaillard PH, et al. (2011) Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia. Nat Genet 43: 147-152.
-
(2011)
Nat Genet
, vol.43
, pp. 147-152
-
-
Crossan, G.P.1
van der Weyden, L.2
Rosado, I.V.3
Langevin, F.4
Gaillard, P.H.5
-
20
-
-
8944258558
-
Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene
-
Whitney MA, Royle G, Low MJ, Kelly MA, Axthelm MK, et al. (1996) 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)
Blood
, vol.88
, pp. 49-58
-
-
Whitney, M.A.1
Royle, G.2
Low, M.J.3
Kelly, M.A.4
Axthelm, M.K.5
-
21
-
-
0042921156
-
Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia
-
Wong JC, Alon N, McKerlie C, Huang JR, Meyn MS, et al. (2003) Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia. Hum Mol Genet 12: 2063-2076.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2063-2076
-
-
Wong, J.C.1
Alon, N.2
McKerlie, C.3
Huang, J.R.4
Meyn, M.S.5
-
22
-
-
0042519602
-
Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice
-
Houghtaling S, Timmers C, Noll M, Finegold MJ, Jones SN, et al. (2003) Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice. Genes Dev 17: 2021-2035.
-
(2003)
Genes Dev
, vol.17
, pp. 2021-2035
-
-
Houghtaling, S.1
Timmers, C.2
Noll, M.3
Finegold, M.J.4
Jones, S.N.5
-
23
-
-
0033851758
-
Fanconi anemia complementation group C is required for proliferation of murine primordial germ cells
-
Nadler JJ, Braun RE, (2000) Fanconi anemia complementation group C is required for proliferation of murine primordial germ cells. Genesis 27: 117-123.
-
(2000)
Genesis
, vol.27
, pp. 117-123
-
-
Nadler, J.J.1
Braun, R.E.2
-
24
-
-
79959725029
-
Variation in genome-wide mutation rates within and between human families
-
Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, et al. (2011) Variation in genome-wide mutation rates within and between human families. Nat Genet 43: 712-714.
-
(2011)
Nat Genet
, vol.43
, pp. 712-714
-
-
Conrad, D.F.1
Keebler, J.E.2
DePristo, M.A.3
Lindsay, S.J.4
Zhang, Y.5
-
25
-
-
0030985103
-
The natural somatic mutation frequency and human carcinogenesis
-
Simpson AJ, (1997) The natural somatic mutation frequency and human carcinogenesis. Adv Cancer Res 71: 209-240.
-
(1997)
Adv Cancer Res
, vol.71
, pp. 209-240
-
-
Simpson, A.J.1
-
26
-
-
0033679966
-
A conserved checkpoint pathway mediates DNA damage-induced apoptosis and cell cycle arrest in C. elegans
-
Gartner A, Milstein S, Ahmed S, Hodgkin J, Hengartner MO, (2000) A conserved checkpoint pathway mediates DNA damage-induced apoptosis and cell cycle arrest in C. elegans. Mol Cell 5: 435-443.
-
(2000)
Mol Cell
, vol.5
, pp. 435-443
-
-
Gartner, A.1
Milstein, S.2
Ahmed, S.3
Hodgkin, J.4
Hengartner, M.O.5
-
27
-
-
0037356808
-
Phenotype-based identification of mouse chromosome instability mutants
-
Shima N, Hartford SA, Duffy T, Wilson LA, Schimenti KJ, et al. (2003) Phenotype-based identification of mouse chromosome instability mutants. Genetics 163: 1031-1040.
-
(2003)
Genetics
, vol.163
, pp. 1031-1040
-
-
Shima, N.1
Hartford, S.A.2
Duffy, T.3
Wilson, L.A.4
Schimenti, K.J.5
-
28
-
-
33644656566
-
Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse
-
Moran JL, Bolton AD, Tran PV, Brown A, Dwyer ND, et al. (2006) Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse. Genome Res 16: 436-440.
-
(2006)
Genome Res
, vol.16
, pp. 436-440
-
-
Moran, J.L.1
Bolton, A.D.2
Tran, P.V.3
Brown, A.4
Dwyer, N.D.5
-
29
-
-
11244249864
-
Synapsis or silence
-
Schimenti J, (2005) Synapsis or silence. Nat Genet 37: 11-13.
-
(2005)
Nat Genet
, vol.37
, pp. 11-13
-
-
Schimenti, J.1
-
30
-
-
57949087168
-
Development of germ cells in the mouse
-
Durcova-Hills G, Capel B, (2008) Development of germ cells in the mouse. Curr Top Dev Biol 83: 185-212.
-
(2008)
Curr Top Dev Biol
, vol.83
, pp. 185-212
-
-
Durcova-Hills, G.1
Capel, B.2
-
31
-
-
0019393572
-
Proliferation and migration of primordial germ cells during compensatory growth in mouse embryos
-
Tam PP, Snow MH, (1981) Proliferation and migration of primordial germ cells during compensatory growth in mouse embryos. J Embryol Exp Morphol 64: 133-147.
-
(1981)
J Embryol Exp Morphol
, vol.64
, pp. 133-147
-
-
Tam, P.P.1
Snow, M.H.2
-
32
-
-
78650845164
-
Primordial germ cell proliferation is impaired in Fused Toes mutant embryos
-
Kim B, Kim Y, Sakuma R, Hui CC, Ruther U, et al. (2011) Primordial germ cell proliferation is impaired in Fused Toes mutant embryos. Dev Biol 349: 417-426.
-
(2011)
Dev Biol
, vol.349
, pp. 417-426
-
-
Kim, B.1
Kim, Y.2
Sakuma, R.3
Hui, C.C.4
Ruther, U.5
-
33
-
-
0030860488
-
p53-induced p21 controls DNA replication
-
Waga S, Li R, Stillman B, (1997) p53-induced p21 controls DNA replication. Leukemia 11 (Suppl 3):: 321-323.
-
(1997)
Leukemia
, vol.11
, Issue.SUPPL. 3
, pp. 321-323
-
-
Waga, S.1
Li, R.2
Stillman, B.3
-
34
-
-
0027359827
-
WAF1, a potential mediator of p53 tumor suppression
-
el-Deiry WS, Tokino T, Velculescu VE, Levy DB, Parsons R, et al. (1993) WAF1, a potential mediator of p53 tumor suppression. Cell 75: 817-825.
-
(1993)
Cell
, vol.75
, pp. 817-825
-
-
El-Deiry, W.S.1
Tokino, T.2
Velculescu, V.E.3
Levy, D.B.4
Parsons, R.5
-
35
-
-
0027496935
-
The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases
-
Harper JW, Adami GR, Wei N, Keyomarsi K, Elledge SJ, (1993) The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases. Cell 75: 805-816.
-
(1993)
Cell
, vol.75
, pp. 805-816
-
-
Harper, J.W.1
Adami, G.R.2
Wei, N.3
Keyomarsi, K.4
Elledge, S.J.5
-
36
-
-
0027717617
-
p21 is a universal inhibitor of cyclin kinases
-
Xiong Y, Hannon GJ, Zhang H, Casso D, Kobayashi R, et al. (1993) p21 is a universal inhibitor of cyclin kinases. Nature 366: 701-704.
-
(1993)
Nature
, vol.366
, pp. 701-704
-
-
Xiong, Y.1
Hannon, G.J.2
Zhang, H.3
Casso, D.4
Kobayashi, R.5
-
37
-
-
84894353718
-
DNA damage response: three levels of DNA repair regulation
-
Sirbu BM, Cortez D, (2013) DNA damage response: three levels of DNA repair regulation. Cold Spring Harb Perspect Biol 5: a012724.
-
(2013)
Cold Spring Harb Perspect Biol
, vol.5
-
-
Sirbu, B.M.1
Cortez, D.2
-
38
-
-
33947278974
-
Genome maintenance defects in cultured cells and mice following partial inactivation of the essential cell cycle checkpoint gene Hus1
-
Levitt PS, Zhu M, Cassano A, Yazinski SA, Liu H, et al. (2007) Genome maintenance defects in cultured cells and mice following partial inactivation of the essential cell cycle checkpoint gene Hus1. Mol Cell Biol 27: 2189-2201.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 2189-2201
-
-
Levitt, P.S.1
Zhu, M.2
Cassano, A.3
Yazinski, S.A.4
Liu, H.5
-
39
-
-
0036724625
-
Chk2 is a tumor suppressor that regulates apoptosis in both an ataxia telangiectasia mutated (ATM)-dependent and an ATM-independent manner
-
Hirao A, Cheung A, Duncan G, Girard PM, Elia AJ, et al. (2002) Chk2 is a tumor suppressor that regulates apoptosis in both an ataxia telangiectasia mutated (ATM)-dependent and an ATM-independent manner. Mol Cell Biol 22: 6521-6532.
-
(2002)
Mol Cell Biol
, vol.22
, pp. 6521-6532
-
-
Hirao, A.1
Cheung, A.2
Duncan, G.3
Girard, P.M.4
Elia, A.J.5
-
40
-
-
84893119595
-
Reversal of female infertility by Chk2 ablation reveals the oocyte DNA damage checkpoint pathway
-
Bolcun-Filas E, Rinaldi VD, White ME, Schimenti JC, (2014) Reversal of female infertility by Chk2 ablation reveals the oocyte DNA damage checkpoint pathway. Science 343: 533-536.
-
(2014)
Science
, vol.343
, pp. 533-536
-
-
Bolcun-Filas, E.1
Rinaldi, V.D.2
White, M.E.3
Schimenti, J.C.4
-
41
-
-
84860263013
-
The structure of the FANCM-MHF complex reveals physical features for functional assembly
-
Tao Y, Jin C, Li X, Qi S, Chu L, et al. (2012) The structure of the FANCM-MHF complex reveals physical features for functional assembly. Nat Commun 3: 782.
-
(2012)
Nat Commun
, vol.3
, pp. 782
-
-
Tao, Y.1
Jin, C.2
Li, X.3
Qi, S.4
Chu, L.5
-
42
-
-
82555188036
-
Human MutS and FANCM complexes function as redundant DNA damage sensors in the Fanconi Anemia pathway
-
Huang M, Kennedy R, Ali AM, Moreau LA, Meetei AR, et al. (2011) Human MutS and FANCM complexes function as redundant DNA damage sensors in the Fanconi Anemia pathway. DNA Repair (Amst) 10: 1203-1212.
-
(2011)
DNA Repair (Amst)
, vol.10
, pp. 1203-1212
-
-
Huang, M.1
Kennedy, R.2
Ali, A.M.3
Moreau, L.A.4
Meetei, A.R.5
-
43
-
-
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 JB, et al. (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
-
44
-
-
25144449181
-
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
-
Meetei AR, Medhurst AL, Ling C, Xue Y, Singh TR, 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
-
45
-
-
84862602750
-
FANCM limits meiotic crossovers
-
Crismani W, Girard C, Froger N, Pradillo M, Santos JL, et al. (2012) FANCM limits meiotic crossovers. Science 336: 1588-1590.
-
(2012)
Science
, vol.336
, pp. 1588-1590
-
-
Crismani, W.1
Girard, C.2
Froger, N.3
Pradillo, M.4
Santos, J.L.5
-
46
-
-
84861675090
-
The Fanconi anemia ortholog FANCM ensures ordered homologous recombination in both somatic and meiotic cells in Arabidopsis
-
Knoll A, Higgins JD, Seeliger K, Reha SJ, Dangel NJ, et al. (2012) The Fanconi anemia ortholog FANCM ensures ordered homologous recombination in both somatic and meiotic cells in Arabidopsis. Plant Cell 24: 1448-1464.
-
(2012)
Plant Cell
, vol.24
, pp. 1448-1464
-
-
Knoll, A.1
Higgins, J.D.2
Seeliger, K.3
Reha, S.J.4
Dangel, N.J.5
-
47
-
-
84862603467
-
The fission yeast FANCM ortholog directs non-crossover recombination during meiosis
-
Lorenz A, Osman F, Sun W, Nandi S, Steinacher R, et al. (2012) The fission yeast FANCM ortholog directs non-crossover recombination during meiosis. Science 336: 1585-1588.
-
(2012)
Science
, vol.336
, pp. 1585-1588
-
-
Lorenz, A.1
Osman, F.2
Sun, W.3
Nandi, S.4
Steinacher, R.5
-
48
-
-
84887204233
-
The DNA translocase FANCM/MHF promotes replication traverse of DNA interstrand crosslinks
-
Huang J, Liu S, Bellani MA, Thazhathveetil AK, Ling C, et al. (2013) The DNA translocase FANCM/MHF promotes replication traverse of DNA interstrand crosslinks. Mol Cell 52: 434-446.
-
(2013)
Mol Cell
, vol.52
, pp. 434-446
-
-
Huang, J.1
Liu, S.2
Bellani, M.A.3
Thazhathveetil, A.K.4
Ling, C.5
-
49
-
-
25144449181
-
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
-
Meetei AR, Medhurst AL, Ling C, Xue Y, Singh TR, et al. (2005) A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nature genetics 37: 958-963.
-
(2005)
Nature Genetics
, vol.37
, pp. 958-963
-
-
Meetei, A.R.1
Medhurst, A.L.2
Ling, C.3
Xue, Y.4
Singh, T.R.5
-
50
-
-
84859255818
-
The DNA translocase activity of FANCM protects stalled replication forks
-
Blackford AN, Schwab RA, Nieminuszczy J, Deans AJ, West SC, et al. (2012) The DNA translocase activity of FANCM protects stalled replication forks. Human molecular genetics 21: 2005-2016.
-
(2012)
Human Molecular Genetics
, vol.21
, pp. 2005-2016
-
-
Blackford, A.N.1
Schwab, R.A.2
Nieminuszczy, J.3
Deans, A.J.4
West, S.C.5
-
51
-
-
70350007132
-
The Fanconi anemia protein FANCM is controlled by FANCD2 and the ATR/ATM pathways
-
Sobeck A, Stone S, Landais I, de Graaf B, Hoatlin ME, (2009) The Fanconi anemia protein FANCM is controlled by FANCD2 and the ATR/ATM pathways. J Biol Chem 284: 25560-25568.
-
(2009)
J Biol Chem
, vol.284
, pp. 25560-25568
-
-
Sobeck, A.1
Stone, S.2
Landais, I.3
de Graaf, B.4
Hoatlin, M.E.5
-
52
-
-
34248184445
-
Fanconi anemia pathway-deficient tumor cells are hypersensitive to inhibition of ataxia telangiectasia mutated
-
Kennedy RD, Chen CC, Stuckert P, Archila EM, De la Vega MA, et al. (2007) Fanconi anemia pathway-deficient tumor cells are hypersensitive to inhibition of ataxia telangiectasia mutated. J Clin Invest 117: 1440-1449.
-
(2007)
J Clin Invest
, vol.117
, pp. 1440-1449
-
-
Kennedy, R.D.1
Chen, C.C.2
Stuckert, P.3
Archila, E.M.4
De la Vega, M.A.5
-
53
-
-
84873824707
-
Targeting the fanconi anemia pathway to identify tailored anticancer therapeutics
-
Jenkins C, Kan J, Hoatlin ME, (2012) Targeting the fanconi anemia pathway to identify tailored anticancer therapeutics. Anemia 2012: 481583.
-
(2012)
Anemia
, vol.2012
, pp. 481583
-
-
Jenkins, C.1
Kan, J.2
Hoatlin, M.E.3
-
54
-
-
74549187963
-
Monoketone analogs of curcumin, a new class of Fanconi anemia pathway inhibitors
-
Landais I, Hiddingh S, McCarroll M, Yang C, Sun A, et al. (2009) Monoketone analogs of curcumin, a new class of Fanconi anemia pathway inhibitors. Mol Cancer 8: 133.
-
(2009)
Mol Cancer
, vol.8
, pp. 133
-
-
Landais, I.1
Hiddingh, S.2
McCarroll, M.3
Yang, C.4
Sun, A.5
-
55
-
-
65349103899
-
Blinded by the Light: The Growing Complexity of p53
-
Vousden KH, Prives C, (2009) Blinded by the Light: The Growing Complexity of p53. Cell 137: 413-431.
-
(2009)
Cell
, vol.137
, pp. 413-431
-
-
Vousden, K.H.1
Prives, C.2
-
56
-
-
79953801997
-
Loss of p53 partially rescues embryonic development of Palb2 knockout mice but does not foster haploinsufficiency of Palb2 in tumour suppression
-
Bouwman P, Drost R, Klijn C, Pieterse M, van der Gulden H, et al. (2011) Loss of p53 partially rescues embryonic development of Palb2 knockout mice but does not foster haploinsufficiency of Palb2 in tumour suppression. J Pathol 224: 10-21.
-
(2011)
J Pathol
, vol.224
, pp. 10-21
-
-
Bouwman, P.1
Drost, R.2
Klijn, C.3
Pieterse, M.4
van der Gulden, H.5
-
57
-
-
33847350610
-
RAD51C deficiency in mice results in early prophase I arrest in males and sister chromatid separation at metaphase II in females
-
Kuznetsov S, Pellegrini M, Shuda K, Fernandez-Capetillo O, Liu Y, et al. (2007) RAD51C deficiency in mice results in early prophase I arrest in males and sister chromatid separation at metaphase II in females. J Cell Biol 176: 581-592.
-
(2007)
J Cell Biol
, vol.176
, pp. 581-592
-
-
Kuznetsov, S.1
Pellegrini, M.2
Shuda, K.3
Fernandez-Capetillo, O.4
Liu, Y.5
-
58
-
-
84863625900
-
Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells
-
Ceccaldi R, Parmar K, Mouly E, Delord M, Kim JM, et al. (2012) Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells. Cell Stem Cell 11: 36-49.
-
(2012)
Cell Stem Cell
, vol.11
, pp. 36-49
-
-
Ceccaldi, R.1
Parmar, K.2
Mouly, E.3
Delord, M.4
Kim, J.M.5
-
59
-
-
77957334868
-
Sex reversal in zebrafish fancl mutants is caused by Tp53-mediated germ cell apoptosis
-
Rodriguez-Mari A, Canestro C, Bremiller RA, Nguyen-Johnson A, Asakawa K, et al. (2010) Sex reversal in zebrafish fancl mutants is caused by Tp53-mediated germ cell apoptosis. PLoS Genet 6: e1001034.
-
(2010)
PLoS Genet
, vol.6
-
-
Rodriguez-Mari, A.1
Canestro, C.2
Bremiller, R.A.3
Nguyen-Johnson, A.4
Asakawa, K.5
-
60
-
-
14144256740
-
Distinct DNA-damage-dependent and -independent responses drive the loss of oocytes in recombination-defective mouse mutants
-
Di Giacomo M, Barchi M, Baudat F, Edelmann W, Keeney S, et al. (2005) Distinct DNA-damage-dependent and-independent responses drive the loss of oocytes in recombination-defective mouse mutants. PNAS 102: 737-742.
-
(2005)
PNAS
, vol.102
, pp. 737-742
-
-
Di Giacomo, M.1
Barchi, M.2
Baudat, F.3
Edelmann, W.4
Keeney, S.5
-
61
-
-
84885870096
-
HELQ promotes RAD51 paralogue-dependent repair to avert germ cell loss and tumorigenesis
-
Adelman CA, Lolo RL, Birkbak NJ, Murina O, Matsuzaki K, et al. (2013) HELQ promotes RAD51 paralogue-dependent repair to avert germ cell loss and tumorigenesis. Nature 502: 381-384.
-
(2013)
Nature
, vol.502
, pp. 381-384
-
-
Adelman, C.A.1
Lolo, R.L.2
Birkbak, N.J.3
Murina, O.4
Matsuzaki, K.5
-
62
-
-
84890400906
-
Helq acts in parallel to Fancc to suppress replication-associated genome instability
-
Luebben SW, Kawabata T, Akre MK, Lee WL, Johnson CS, et al. (2013) Helq acts in parallel to Fancc to suppress replication-associated genome instability. Nucleic Acids Res 41: 10283-10297.
-
(2013)
Nucleic Acids Res
, vol.41
, pp. 10283-10297
-
-
Luebben, S.W.1
Kawabata, T.2
Akre, M.K.3
Lee, W.L.4
Johnson, C.S.5
-
63
-
-
80055085862
-
Minichromosome maintenance helicase paralog MCM9 is dispensible for DNA replication but functions in germ-line stem cells and tumor suppression
-
Hartford SA, Luo Y, Southard TL, Min IM, Lis JT, et al. (2011) Minichromosome maintenance helicase paralog MCM9 is dispensible for DNA replication but functions in germ-line stem cells and tumor suppression. Proc Natl Acad Sci U S A 108: 17702-17707.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 17702-17707
-
-
Hartford, S.A.1
Luo, Y.2
Southard, T.L.3
Min, I.M.4
Lis, J.T.5
-
64
-
-
0042476570
-
Pin1 regulates the timing of mammalian primordial germ cell proliferation
-
Atchison FW, Capel B, Means AR, (2003) Pin1 regulates the timing of mammalian primordial germ cell proliferation. Development 130: 3579-3586.
-
(2003)
Development
, vol.130
, pp. 3579-3586
-
-
Atchison, F.W.1
Capel, B.2
Means, A.R.3
-
65
-
-
84876240946
-
The REV7 subunit of DNA polymerase zeta is essential for primordial germ cell maintenance in the mouse
-
Watanabe N, Mii S, Asai N, Asai M, Niimi K, et al. (2013) The REV7 subunit of DNA polymerase zeta is essential for primordial germ cell maintenance in the mouse. J Biol Chem 288: 10459-10471.
-
(2013)
J Biol Chem
, vol.288
, pp. 10459-10471
-
-
Watanabe, N.1
Mii, S.2
Asai, N.3
Asai, M.4
Niimi, K.5
-
66
-
-
84893708527
-
A Missense Mutation in Rev7 Disrupts Formation of Polzeta, Impairing Mouse Development and Repair of Genotoxic Agent-induced DNA Lesions
-
Khalaj M, Abbasi A, Yamanishi H, Akiyama K, Wakitani S, et al. (2014) A Missense Mutation in Rev7 Disrupts Formation of Polzeta, Impairing Mouse Development and Repair of Genotoxic Agent-induced DNA Lesions. J Biol Chem 289: 3811-3824.
-
(2014)
J Biol Chem
, vol.289
, pp. 3811-3824
-
-
Khalaj, M.1
Abbasi, A.2
Yamanishi, H.3
Akiyama, K.4
Wakitani, S.5
-
67
-
-
84884201492
-
Human DNA helicase HELQ participates in DNA interstrand crosslink tolerance with ATR and RAD51 paralogs
-
Takata K, Reh S, Tomida J, Person MD, Wood RD, (2013) Human DNA helicase HELQ participates in DNA interstrand crosslink tolerance with ATR and RAD51 paralogs. Nat Commun 4: 2338.
-
(2013)
Nat Commun
, vol.4
, pp. 2338
-
-
Takata, K.1
Reh, S.2
Tomida, J.3
Person, M.D.4
Wood, R.D.5
-
68
-
-
84876234845
-
The MCM8-MCM9 complex promotes RAD51 recruitment at DNA damage sites to facilitate homologous recombination
-
Park J, Long DT, Lee KY, Abbas T, Shibata E, et al. (2013) The MCM8-MCM9 complex promotes RAD51 recruitment at DNA damage sites to facilitate homologous recombination. Mol Cell Biol 33: 1632-1644.
-
(2013)
Mol Cell Biol
, vol.33
, pp. 1632-1644
-
-
Park, J.1
Long, D.T.2
Lee, K.Y.3
Abbas, T.4
Shibata, E.5
-
69
-
-
84865368229
-
MCM8- and MCM9-deficient mice reveal gametogenesis defects and genome instability due to impaired homologous recombination
-
Lutzmann M, Grey C, Traver S, Ganier O, Maya-Mendoza A, et al. (2012) MCM8- and MCM9-deficient mice reveal gametogenesis defects and genome instability due to impaired homologous recombination. Mol Cell 47: 523-534.
-
(2012)
Mol Cell
, vol.47
, pp. 523-534
-
-
Lutzmann, M.1
Grey, C.2
Traver, S.3
Ganier, O.4
Maya-Mendoza, A.5
-
70
-
-
84865353862
-
Mcm8 and Mcm9 form a complex that functions in homologous recombination repair induced by DNA interstrand crosslinks
-
Nishimura K, Ishiai M, Horikawa K, Fukagawa T, Takata M, et al. (2012) Mcm8 and Mcm9 form a complex that functions in homologous recombination repair induced by DNA interstrand crosslinks. Mol Cell 47: 511-522.
-
(2012)
Mol Cell
, vol.47
, pp. 511-522
-
-
Nishimura, K.1
Ishiai, M.2
Horikawa, K.3
Fukagawa, T.4
Takata, M.5
-
71
-
-
78650144544
-
Evidence that meiotic sex chromosome inactivation is essential for male fertility
-
Royo H, Polikiewicz G, Mahadevaiah SK, Prosser H, Mitchell M, et al. (2010) Evidence that meiotic sex chromosome inactivation is essential for male fertility. Current Biol 20: 2117-2123.
-
(2010)
Current Biol
, vol.20
, pp. 2117-2123
-
-
Royo, H.1
Polikiewicz, G.2
Mahadevaiah, S.K.3
Prosser, H.4
Mitchell, M.5
-
72
-
-
31344442810
-
Differential contributions of mammalian Rad54 paralogs to recombination, DNA damage repair, and meiosis
-
Wesoly J, Agarwal S, Sigurdsson S, Bussen W, Van Komen S, et al. (2006) Differential contributions of mammalian Rad54 paralogs to recombination, DNA damage repair, and meiosis. Mol Cell Biol 26: 976-989.
-
(2006)
Mol Cell Biol
, vol.26
, pp. 976-989
-
-
Wesoly, J.1
Agarwal, S.2
Sigurdsson, S.3
Bussen, W.4
Van Komen, S.5
-
73
-
-
67650095306
-
Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells
-
Raya A, Rodriguez-Piza I, Guenechea G, Vassena R, Navarro S, et al. (2009) Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells. Nature 460: 53-59.
-
(2009)
Nature
, vol.460
, pp. 53-59
-
-
Raya, A.1
Rodriguez-Piza, I.2
Guenechea, G.3
Vassena, R.4
Navarro, S.5
-
74
-
-
84861912972
-
Overcoming reprogramming resistance of Fanconi anemia cells
-
Muller LUW, Milsom MD, Harris CE, Vyas R, Brumme KM, et al. (2012) Overcoming reprogramming resistance of Fanconi anemia cells. Blood 119: 5449-5457.
-
(2012)
Blood
, vol.119
, pp. 5449-5457
-
-
Muller, L.U.W.1
Milsom, M.D.2
Harris, C.E.3
Vyas, R.4
Brumme, K.M.5
-
75
-
-
1542609301
-
Forward genetic screens for meiotic and mitotic recombination-defective mutants in mice
-
Reinholdt L, Ashley T, Schimenti J, Shima N, (2004) Forward genetic screens for meiotic and mitotic recombination-defective mutants in mice. Methods Mol Biol 262: 87-107.
-
(2004)
Methods Mol Biol
, vol.262
, pp. 87-107
-
-
Reinholdt, L.1
Ashley, T.2
Schimenti, J.3
Shima, N.4
-
76
-
-
0037260993
-
BayGenomics: a resource of insertional mutations in mouse embryonic stem cells
-
Stryke D, Kawamoto M, Huang CC, Johns SJ, King LA, et al. (2003) BayGenomics: a resource of insertional mutations in mouse embryonic stem cells. Nucleic Acids Res 31: 278-281.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 278-281
-
-
Stryke, D.1
Kawamoto, M.2
Huang, C.C.3
Johns, S.J.4
King, L.A.5
-
77
-
-
21444451785
-
Conditional inactivation of the mouse Hus1 cell cycle checkpoint gene
-
Levitt PS, Liu H, Manning C, Weiss RS, (2005) Conditional inactivation of the mouse Hus1 cell cycle checkpoint gene. Genomics 86: 212-224.
-
(2005)
Genomics
, vol.86
, pp. 212-224
-
-
Levitt, P.S.1
Liu, H.2
Manning, C.3
Weiss, R.S.4
-
78
-
-
0029097759
-
Radiation-induced cell cycle arrest compromised by p21 deficiency
-
Brugarolas J, Chandrasekaran C, Gordon JI, Beach D, Jacks T, et al. (1995) Radiation-induced cell cycle arrest compromised by p21 deficiency. Nature 377: 552-557.
-
(1995)
Nature
, vol.377
, pp. 552-557
-
-
Brugarolas, J.1
Chandrasekaran, C.2
Gordon, J.I.3
Beach, D.4
Jacks, T.5
-
79
-
-
0028118111
-
Tumor spectrum analysis in p53-mutant mice
-
Jacks T, Remington L, Williams BO, Schmitt EM, Halachmi S, et al. (1994) Tumor spectrum analysis in p53-mutant mice. Curr Biol 4: 1-7.
-
(1994)
Curr Biol
, vol.4
, pp. 1-7
-
-
Jacks, T.1
Remington, L.2
Williams, B.O.3
Schmitt, E.M.4
Halachmi, S.5
-
80
-
-
0029848286
-
Pleiotropic defects in ataxia-telangiectasia protein-deficient mice
-
Elson A, Wang Y, Daugherty CJ, Morton CC, Zhou F, et al. (1996) Pleiotropic defects in ataxia-telangiectasia protein-deficient mice. Proc Natl Acad Sci U S A 93: 13084-13089.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 13084-13089
-
-
Elson, A.1
Wang, Y.2
Daugherty, C.J.3
Morton, C.C.4
Zhou, F.5
-
81
-
-
8644233355
-
The mouse genomic instability mutation chaos1 is an allele of Polq that exhibits genetic interaction with Atm
-
Shima N, Munroe RJ, Schimenti JC, (2004) The mouse genomic instability mutation chaos1 is an allele of Polq that exhibits genetic interaction with Atm. Mol Cell Biol 24: 10381-10389.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 10381-10389
-
-
Shima, N.1
Munroe, R.J.2
Schimenti, J.C.3
-
82
-
-
33746784295
-
The mouse gcd2 mutation causes primordial germ cell depletion
-
Reinholdt LG, Munroe RJ, Kamdar S, Schimenti JC, (2006) The mouse gcd2 mutation causes primordial germ cell depletion. Mech Dev 123: 559-569.
-
(2006)
Mech Dev
, vol.123
, pp. 559-569
-
-
Reinholdt, L.G.1
Munroe, R.J.2
Kamdar, S.3
Schimenti, J.C.4
-
83
-
-
0025147087
-
Primordial germ cells in the mouse embryo during gastrulation
-
Ginsburg M, Snow MH, McLaren A, (1990) Primordial germ cells in the mouse embryo during gastrulation. Development 110: 521-528.
-
(1990)
Development
, vol.110
, pp. 521-528
-
-
Ginsburg, M.1
Snow, M.H.2
McLaren, A.3
-
84
-
-
33750806537
-
Premeiotic germ cell defect in seminiferous tubules of Atm-null testis
-
Takubo K, Hirao A, Ohmura M, Azuma M, Arai F, et al. (2006) Premeiotic germ cell defect in seminiferous tubules of Atm-null testis. Biochem Biophys Res Commun 351: 993-998.
-
(2006)
Biochem Biophys Res Commun
, vol.351
, pp. 993-998
-
-
Takubo, K.1
Hirao, A.2
Ohmura, M.3
Azuma, M.4
Arai, F.5
|