-
1
-
-
0035379611
-
The emerging genetic and molecular basis of Fanconi anaemia
-
DOI 10.1038/35076590
-
Joenje H, Patel KJ (2001) The emerging genetic and molecular basis of Fanconi anaemia. Nat Rev Genet 2:446-457. (Pubitemid 33673411)
-
(2001)
Nature Reviews Genetics
, vol.2
, Issue.6
, pp. 446-457
-
-
Joenje, H.1
Patel, K.J.2
-
2
-
-
29144506137
-
The Fanconi Anemia/BRCA pathway: New faces in the crowd
-
DOI 10.1101/gad.1370505
-
Kennedy RD, D'Andrea AD (2005) The Fanconi anemia/BRCA pathway: New faces in the crowd. Genes Dev 19:2925-2940. (Pubitemid 41798109)
-
(2005)
Genes and Development
, vol.19
, Issue.24
, pp. 2925-2940
-
-
Kennedy, R.D.1
D'Andrea, A.D.2
-
3
-
-
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
-
4
-
-
34247208998
-
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway
-
DOI 10.1038/sj.emboj.7601666, PII 7601666
-
Ling C, et al. (2007) FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway. EMBO J 26:2104-2114. (Pubitemid 46625801)
-
(2007)
EMBO Journal
, vol.26
, Issue.8
, 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
Hoatlin, M.E.11
Schindler, D.12
Joenje, H.13
De Winter, J.P.14
Takata, M.15
Meetei, A.R.16
Wang, W.17
-
5
-
-
29244489543
-
Fanconi anemia (cross)linked to DNA repair
-
DOI 10.1016/j.cell.2005.12.009, PII S0092867405013917
-
Niedernhofer LJ, Lalai AS, Hoeijmakers JH (2005) Fanconi anemia (cross)linked to DNA repair. Cell 123:1191-1198. (Pubitemid 41821778)
-
(2005)
Cell
, vol.123
, Issue.7
, pp. 1191-1198
-
-
Niedernhofer, L.J.1
Lalai, A.S.2
Hoeijmakers, J.H.J.3
-
6
-
-
33747883762
-
Dedicated to the core: Understanding the Fanconi anemia complex
-
DOI 10.1016/j.dnarep.2006.05.009, PII S1568786406001492, Mechanisms of Chromosomal Translocations
-
Gurtan AM, D'Andrea AD (2006) Dedicated to the core: Understanding the Fanconi anemia complex. DNA Repair (Amst) 5:1119-1125. (Pubitemid 44291606)
-
(2006)
DNA Repair
, vol.5
, Issue.9-10
, pp. 1119-1125
-
-
Gurtan, A.M.1
D'Andrea, A.D.2
-
7
-
-
77955889790
-
Expanded roles of the Fanconi anemia pathway in preserving genomic stability
-
Kee Y, D'Andrea AD (2010) Expanded roles of the Fanconi anemia pathway in preserving genomic stability. Genes Dev 24:1680-1694.
-
(2010)
Genes Dev
, vol.24
, pp. 1680-1694
-
-
Kee, Y.1
D'Andrea, A.D.2
-
8
-
-
34247110291
-
Identification of the FANCI Protein, a Monoubiquitinated FANCD2 Paralog Required for DNA Repair
-
DOI 10.1016/j.cell.2007.03.009, PII S0092867407003200
-
Smogorzewska A, et al. (2007) Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair. Cell 129:289-301. (Pubitemid 46584733)
-
(2007)
Cell
, vol.129
, Issue.2
, 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
Elledge, S.J.11
-
9
-
-
0035105291
-
Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway
-
DOI 10.1016/S1097-2765(01)00173-3
-
Garcia-Higuera I, et al. (2001) Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. Mol Cell 7:249-262. (Pubitemid 32206493)
-
(2001)
Molecular Cell
, vol.7
, Issue.2
, 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
-
10
-
-
34249281152
-
FANCI is a second monoubiquitinated member of the Fanconi anemia pathway
-
DOI 10.1038/nsmb1252, PII NSMB1252
-
Sims AE, et al. (2007) FANCI is a second monoubiquitinated member of the Fanconi anemia pathway. Nat Struct Mol Biol 14:564-567. (Pubitemid 46871814)
-
(2007)
Nature Structural and Molecular Biology
, vol.14
, Issue.6
, 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
Auerbach, A.D.11
Huang, T.T.12
-
11
-
-
34249332276
-
Identification of the Fanconi anemia complementation group I gene, FANCI
-
Dorsman JC, et al. (2007) Identification of the Fanconi anemia complementation group I gene, FANCI. Cell Oncol 29:211-218. (Pubitemid 46855710)
-
(2007)
Cellular Oncology
, vol.29
, Issue.3
, pp. 211-218
-
-
Dorsman, J.C.1
Levitus, M.2
Rockx, D.3
Rooimans, M.A.4
Oostra, A.B.5
Haitjema, A.6
Bakker, S.T.7
Steltenpool, J.8
Schuler, D.9
Mohan, S.10
Schindler, D.11
Arwert, F.12
Pals, G.13
Mathew, C.G.14
Waisfisz, Q.15
De Winter, J.P.16
Joenje, H.17
-
12
-
-
77954279611
-
Deficiency of FANCD2-associated nuclease KIAA1018/FAN1 sensitizes cells to interstrand crosslinking agents
-
Kratz K, et al. (2010) Deficiency of FANCD2-associated nuclease KIAA1018/FAN1 sensitizes cells to interstrand crosslinking agents. Cell 142:77-88.
-
(2010)
Cell
, vol.142
, pp. 77-88
-
-
Kratz, K.1
-
13
-
-
77955290719
-
FAN1 acts with FANCI-FANCD2 to promote DNA interstrand cross-link repair
-
Liu T, Ghosal G, Yuan J, Chen J, Huang J (2010) FAN1 acts with FANCI-FANCD2 to promote DNA interstrand cross-link repair. Science 329:693-696.
-
(2010)
Science
, vol.329
, pp. 693-696
-
-
Liu, T.1
Ghosal, G.2
Yuan, J.3
Chen, J.4
Huang, J.5
-
14
-
-
77954274685
-
Identification of KIAA1018/FAN1, a DNA repair nuclease recruited to DNA damage by monoubiquitinated FANCD2
-
MacKay C, et al. (2010) Identification of KIAA1018/FAN1, a DNA repair nuclease recruited to DNA damage by monoubiquitinated FANCD2. Cell 142:65-76.
-
(2010)
Cell
, vol.142
, pp. 65-76
-
-
MacKay, C.1
-
15
-
-
77954286076
-
A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair
-
Smogorzewska A, et al. (2010) A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair. Mol Cell 39:36-47.
-
(2010)
Mol Cell
, vol.39
, pp. 36-47
-
-
Smogorzewska, A.1
-
16
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi anemia
-
DOI 10.1126/science.1073834
-
Howlett NG, et al. (2002) Biallelic inactivation of BRCA2 in Fanconi anemia. Science 297:606-609. (Pubitemid 34815345)
-
(2002)
Science
, vol.297
, Issue.5581
, 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
Ikeda, H.11
Fox, E.A.12
D'Andrea, A.D.13
-
17
-
-
33846601829
-
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
-
DOI 10.1038/ng1942, PII NG1942
-
Xia B, et al. (2007) Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Nat Genet 39:159-161. (Pubitemid 46184344)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, 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
Wang, W.11
Livingston, D.M.12
Joenje, H.13
De Winter, J.P.14
-
18
-
-
33846569450
-
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
-
DOI 10.1038/ng1947, PII NG1947
-
Reid S, et al. (2007) Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat Genet 39:162-164. (Pubitemid 46184345)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, 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
Wurm, M.11
Batish, S.D.12
Lach, F.P.13
Yetgin, S.14
Neitzel, H.15
Ariffin, H.16
Tischkowitz, M.17
Mathew, C.G.18
Auerbach, A.D.19
Rahman, N.20
more..
-
19
-
-
24944575242
-
BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ
-
DOI 10.1016/j.ccr.2005.08.004, PII S153561080500262X
-
Litman R, et al. (2005) BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ. Cancer Cell 8:255-265. (Pubitemid 41317595)
-
(2005)
Cancer Cell
, vol.8
, Issue.3
, 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
-
20
-
-
69749106825
-
Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication
-
Shen X, et al. (2009) Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication. Mol Cell 35:716-723.
-
(2009)
Mol Cell
, vol.35
, pp. 716-723
-
-
Shen, X.1
-
21
-
-
79251632658
-
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype
-
Stoepker C, et al. (2011) SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype. Nat Genet 43:138-141.
-
(2011)
Nat Genet
, vol.43
, pp. 138-141
-
-
Stoepker, C.1
-
22
-
-
79251624412
-
Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia
-
Sanger Mouse Genetics Project
-
Crossan GP, et al.; Sanger Mouse Genetics Project (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
-
23
-
-
77951747926
-
Mutation of the RAD51C gene in a Fanconi anemia-like disorder
-
Vaz F, et al. (2010) Mutation of the RAD51C gene in a Fanconi anemia-like disorder. Nat Genet 42:406-409.
-
(2010)
Nat Genet
, vol.42
, pp. 406-409
-
-
Vaz, F.1
-
24
-
-
25144457604
-
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
-
DOI 10.1038/ng1625, PII NG1625
-
Levitus M, et al. (2005) The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nat Genet 37:934-935. (Pubitemid 43086148)
-
(2005)
Nature Genetics
, vol.37
, Issue.9
, 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
Arwert, F.11
Mathew, C.G.12
Zdzienicka, M.Z.13
Hiom, K.14
De Winter, J.P.15
Joenje, H.16
-
25
-
-
25144497571
-
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
-
DOI 10.1038/ng1624, PII NG1624
-
Levran O, et al. (2005) The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. Nat Genet 37:931-933. (Pubitemid 43086147)
-
(2005)
Nature Genetics
, vol.37
, Issue.9
, 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
Ott, J.11
Petrini, J.12
Schindler, D.13
Hanenberg, H.14
Auerbach, A.D.15
-
26
-
-
77958499239
-
RAD18-mediated ubiquitination of PCNA activates the Fanconi anemia DNA repair network
-
Geng L, Huntoon CJ, Karnitz LM (2010) RAD18-mediated ubiquitination of PCNA activates the Fanconi anemia DNA repair network. J Cell Biol 191:249-257.
-
(2010)
J Cell Biol
, vol.191
, pp. 249-257
-
-
Geng, L.1
Huntoon, C.J.2
Karnitz, L.M.3
-
27
-
-
33744481750
-
Molecular pathogenesis of Fanconi anemia: Recent progress
-
DOI 10.1182/blood-2005-10-4240
-
Taniguchi T, D'Andrea AD (2006) Molecular pathogenesis of Fanconi anemia: Recent progress. Blood 107:4223-4233. (Pubitemid 43801344)
-
(2006)
Blood
, vol.107
, Issue.11
, pp. 4223-4233
-
-
Taniguchi, T.1
D'Andrea, A.D.2
-
28
-
-
34247577746
-
The Fanconi Family Adds a Fraternal Twin
-
DOI 10.1016/j.devcel.2007.04.008, PII S1534580707001554
-
Grompe M, van de Vrugt H (2007) The Fanconi family adds a fraternal twin. Dev Cell 12:661-662. (Pubitemid 46671150)
-
(2007)
Developmental Cell
, vol.12
, Issue.5
, pp. 661-662
-
-
Grompe, M.1
Van de, V.H.2
-
29
-
-
50849117845
-
Loss of homologous recombination or non-homologous end-joining leads to radial formation following DNA interstrand crosslink damage
-
Hanlon Newell AE, et al. (2008) Loss of homologous recombination or non-homologous end-joining leads to radial formation following DNA interstrand crosslink damage. Cytogenet Genome Res 121:174-180.
-
(2008)
Cytogenet Genome Res
, vol.121
, pp. 174-180
-
-
Hanlon Newell, A.E.1
-
30
-
-
4544355937
-
The Fanconi anemia gene product FANCF is a flexible adaptor protein
-
DOI 10.1074/jbc.M407034200
-
Léveillé F, et al. (2004) The Fanconi anemia gene product FANCF is a flexible adaptor protein. J Biol Chem 279:39421-39430. (Pubitemid 39258207)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.38
, pp. 39421-39430
-
-
Leveille, F.1
Blom, E.2
Medhurst, A.L.3
Bier, P.4
Laghmani, E.H.5
Johnson, M.6
Rooimans, M.A.7
Sobeck, A.8
Waisfisz, Q.9
Arwert, F.10
Patel, K.J.11
Hoatlin, M.E.12
Joenje, H.13
De Winter, J.P.14
-
31
-
-
0034650934
-
Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2- hybrid system
-
Reuter T, Herterich S, Bernhard O, Hoehn H, Gross HJ (2000) Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system. Blood 95:719-720. (Pubitemid 30041693)
-
(2000)
Blood
, vol.95
, Issue.2
, pp. 719-720
-
-
Reuter, T.1
Herterich, S.2
Bernhard, O.3
Hoehn, H.4
Gross, H.J.5
-
32
-
-
0033000911
-
Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex
-
Garcia-Higuera I, Kuang Y, Näf D, Wasik J, D'Andrea AD (1999) Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex. Mol Cell Biol 19:4866-4873. (Pubitemid 29289525)
-
(1999)
Molecular and Cellular Biology
, vol.19
, Issue.7
, pp. 4866-4873
-
-
Garcia-Higuera, I.1
Kuang, Y.2
Naf, D.3
Wasik, J.4
D'Andrea, A.D.5
-
33
-
-
33846799430
-
Identification of FAAP24, a Fanconi Anemia Core Complex Protein that Interacts with FANCM
-
DOI 10.1016/j.molcel.2007.01.003, PII S109727650700007X
-
Ciccia A, et al. (2007) Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM. Mol Cell 25:331-343. (Pubitemid 46206138)
-
(2007)
Molecular Cell
, vol.25
, Issue.3
, pp. 331-343
-
-
Ciccia, A.1
Ling, C.2
Coulthard, R.3
Yan, Z.4
Xue, Y.5
Meetei, A.R.6
Laghmani, E.H.7
Joenje, H.8
McDonald, N.9
De Winter, J.P.10
Wang, W.11
West, S.C.12
-
34
-
-
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 AD (2000) 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)
Blood
, vol.96
, pp. 3224-3230
-
-
Garcia-Higuera, I.1
Kuang, Y.2
Denham, J.3
D'Andrea, A.D.4
-
35
-
-
69449102249
-
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M
-
Bakker ST, 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
-
36
-
-
79955580794
-
Involvement of SLX4 in interstrand cross-link repair is regulated by the Fanconi anemia pathway
-
Yamamoto KN, et al. (2011) Involvement of SLX4 in interstrand cross-link repair is regulated by the Fanconi anemia pathway. Proc Natl Acad Sci USA 108:6492-6496.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 6492-6496
-
-
Yamamoto, K.N.1
-
37
-
-
79955968976
-
The E3 ubiquitin ligase RAD18 regulates ubiquitylation and chromatin loading of FANCD2 and FANCI
-
Williams SA, Longerich S, Sung P, Vaziri C, Kupfer GM (2011) The E3 ubiquitin ligase RAD18 regulates ubiquitylation and chromatin loading of FANCD2 and FANCI. Blood 117:5078-5087.
-
(2011)
Blood
, vol.117
, pp. 5078-5087
-
-
Williams, S.A.1
Longerich, S.2
Sung, P.3
Vaziri, C.4
Kupfer, G.M.5
-
38
-
-
79958705572
-
SET nuclear oncogene associates with microcephalin/MCPH1 and regulates chromosome condensation
-
Leung JW, et al. (2011) SET nuclear oncogene associates with microcephalin/MCPH1 and regulates chromosome condensation. J Biol Chem 286:21393-21400.
-
(2011)
J Biol Chem
, vol.286
, pp. 21393-21400
-
-
Leung, J.W.1
-
39
-
-
38749142157
-
Epitope tagging of endogenous proteins for genome-wide ChIP-chip studies
-
DOI 10.1038/nmeth1170, PII NMETH1170
-
Zhang X, et al. (2008) Epitope tagging of endogenous proteins for genome-wide ChIP-chip studies. Nat Methods 5:163-165. (Pubitemid 351181743)
-
(2008)
Nature Methods
, vol.5
, Issue.2
, pp. 163-165
-
-
Zhang, X.1
Guo, C.2
Chen, Y.3
Shulha, H.P.4
Schnetz, M.P.5
LaFramboise, T.6
Bartels, C.F.7
Markowitz, S.8
Weng, Z.9
Scacheri, P.C.10
Wang, Z.11
|