-
1
-
-
34548759123
-
Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins
-
Wang W. Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins. Nat Rev Genet 2007, 8:735-748.
-
(2007)
Nat Rev Genet
, vol.8
, pp. 735-748
-
-
Wang, W.1
-
2
-
-
77952600845
-
Susceptibility pathways in Fanconi's anemia and breast cancer
-
10.1056/NEJMra0809889, 3069698, 20484397
-
D'Andrea AD. Susceptibility pathways in Fanconi's anemia and breast cancer. N Engl J Med 2010, 362:1909-1919. 10.1056/NEJMra0809889, 3069698, 20484397.
-
(2010)
N Engl J Med
, vol.362
, pp. 1909-1919
-
-
D'Andrea, A.D.1
-
3
-
-
77951720395
-
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
-
10.1038/ng.569, 20400964
-
Meindl A, Hellebrand H, Wiek C, Erven V, Wappenschmidt B, Niederacher D, Freund M, Lichtner P, Hartmann L, Schaal H, Ramser J, Honisch E, Kubisch C, Wichmann HE, Kast K, Deissler H, Engel C, Muller-Myhsok B, Neveling K, Kiechle M, Mathew CG, Schindler D, Schmutzler RK, Hanenberg H. Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. Nat Genet 2010, 42:410-414. 10.1038/ng.569, 20400964.
-
(2010)
Nat Genet
, vol.42
, pp. 410-414
-
-
Meindl, A.1
Hellebrand, H.2
Wiek, C.3
Erven, V.4
Wappenschmidt, B.5
Niederacher, D.6
Freund, M.7
Lichtner, P.8
Hartmann, L.9
Schaal, H.10
Ramser, J.11
Honisch, E.12
Kubisch, C.13
Wichmann, H.E.14
Kast, K.15
Deissler, H.16
Engel, C.17
Muller-Myhsok, B.18
Neveling, K.19
Kiechle, M.20
Mathew, C.G.21
Schindler, D.22
Schmutzler, R.K.23
Hanenberg, H.24
more..
-
4
-
-
77951747926
-
Mutation of the RAD51C gene in a Fanconi anemia-like disorder
-
10.1038/ng.570, 20400963
-
Vaz F, Hanenberg H, Schuster B, Barker K, Wiek C, Erven V, Neveling K, Endt D, Kesterton I, Autore F, Fraternali F, Freund M, Hartmann L, Grimwade D, Roberts RG, Schaal H, Mohammed S, Rahman N, Schindler D, Mathew CG. Mutation of the RAD51C gene in a Fanconi anemia-like disorder. Nat Genet 2010, 42:406-409. 10.1038/ng.570, 20400963.
-
(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
Fraternali, F.11
Freund, M.12
Hartmann, L.13
Grimwade, D.14
Roberts, R.G.15
Schaal, H.16
Mohammed, S.17
Rahman, N.18
Schindler, D.19
Mathew, C.G.20
more..
-
5
-
-
79251624412
-
Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia
-
10.1038/ng.752, 21240276
-
Crossan GP, van der Weyden L, Rosado IV, Langevin F, Gaillard PH, McIntyre RE, Gallagher F, Kettunen MI, Lewis DY, Brindle K, Arends MJ, Adams DJ, Patel KJ. Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia. Nat Genet 2011, 43:147-152. 10.1038/ng.752, 21240276.
-
(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
McIntyre, R.E.6
Gallagher, F.7
Kettunen, M.I.8
Lewis, D.Y.9
Brindle, K.10
Arends, M.J.11
Adams, D.J.12
Patel, K.J.13
-
6
-
-
79251611165
-
Mutations of the SLX4 gene in Fanconi anemia
-
10.1038/ng.750, 21240275
-
Kim Y, Lach FP, Desetty R, Hanenberg H, Auerbach AD, Smogorzewska A. Mutations of the SLX4 gene in Fanconi anemia. Nat Genet 2011, 43:142-146. 10.1038/ng.750, 21240275.
-
(2011)
Nat Genet
, vol.43
, pp. 142-146
-
-
Kim, Y.1
Lach, F.P.2
Desetty, R.3
Hanenberg, H.4
Auerbach, A.D.5
Smogorzewska, A.6
-
7
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi anemia
-
10.1126/science.1073834, 12065746
-
Howlett NG, Taniguchi T, Olson S, Cox B, Waisfisz Q, De Die-Smulders C, Persky N, Grompe M, Joenje H, Pals G, Ikeda H, Fox EA, D'Andrea AD. Biallelic inactivation of BRCA2 in Fanconi anemia. Science 2002, 297:606-609. 10.1126/science.1073834, 12065746.
-
(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
Ikeda, H.11
Fox, E.A.12
D'Andrea, A.D.13
-
8
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
10.1038/378789a0, 8524414
-
Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, Collins N, Gregory S, Gumbs C, Micklem G. Identification of the breast cancer susceptibility gene BRCA2. Nature 1995, 378:789-792. 10.1038/378789a0, 8524414.
-
(1995)
Nature
, vol.378
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
Swift, S.4
Seal, S.5
Mangion, J.6
Collins, N.7
Gregory, S.8
Gumbs, C.9
Micklem, G.10
-
9
-
-
25144497571
-
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
-
10.1038/ng1624, 16116424
-
Levran O, Attwooll C, Henry RT, Milton KL, Neveling K, Rio P, Batish SD, Kalb R, Velleuer E, Barral S, Ott J, Petrini J, Schindler D, Hanenberg H, Auerbach AD. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. Nat Genet 2005, 37:931-933. 10.1038/ng1624, 16116424.
-
(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
Ott, J.11
Petrini, J.12
Schindler, D.13
Hanenberg, H.14
Auerbach, A.D.15
-
10
-
-
25144457604
-
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
-
10.1038/ng1625, 16116423
-
Levitus M, Waisfisz Q, Godthelp BC, de Vries Y, Hussain S, Wiegant WW, Elghalbzouri-Maghrani E, Steltenpool J, Rooimans MA, Pals G, Arwert F, Mathew CG, Zdzienicka MZ, Hiom K, De Winter JP, Joenje H. The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nat Genet 2005, 37:934-935. 10.1038/ng1625, 16116423.
-
(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
Arwert, F.11
Mathew, C.G.12
Zdzienicka, M.Z.13
Hiom, K.14
De Winter, J.P.15
Joenje, H.16
-
11
-
-
24944575242
-
BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ
-
10.1016/j.ccr.2005.08.004, 16153896
-
Litman R, Peng M, Jin Z, Zhang F, Zhang J, Powell S, Andreassen PR, Cantor SB. BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ. Cancer Cell 2005, 8:255-265. 10.1016/j.ccr.2005.08.004, 16153896.
-
(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
-
12
-
-
33750465216
-
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
-
10.1038/ng1902, 17033622
-
Seal S, Thompson D, Renwick A, Elliott A, Kelly P, Barfoot R, Chagtai T, Jayatilake H, Ahmed M, Spanova K, North B, McGuffog L, Evans DG, Eccles D, Easton DF, Stratton MR, Rahman N. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet 2006, 38:1239-1241. 10.1038/ng1902, 17033622.
-
(2006)
Nat Genet
, vol.38
, pp. 1239-1241
-
-
Seal, S.1
Thompson, D.2
Renwick, A.3
Elliott, A.4
Kelly, P.5
Barfoot, R.6
Chagtai, T.7
Jayatilake, H.8
Ahmed, M.9
Spanova, K.10
North, B.11
McGuffog, L.12
Evans, D.G.13
Eccles, D.14
Easton, D.F.15
Stratton, M.R.16
Rahman, N.17
-
13
-
-
33847227378
-
A recurrent mutation in PALB2 in Finnish cancer families
-
10.1038/nature05609, 17287723
-
Erkko H, Xia B, Nikkila J, Schleutker J, Syrjakoski K, Mannermaa A, Kallioniemi A, Pylkas K, Karppinen SM, Rapakko K, Miron A, Sheng Q, Li G, Mattila H, Bell DW, Haber DA, Grip M, Reiman M, Jukkola-Vuorinen A, Mustonen A, Kere J, Aaltonen LA, Kosma VM, Kataja V, Soini Y, Drapkin RI, Livingston DM, Winqvist R. A recurrent mutation in PALB2 in Finnish cancer families. Nature 2007, 446:316-319. 10.1038/nature05609, 17287723.
-
(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
Miron, A.11
Sheng, Q.12
Li, G.13
Mattila, H.14
Bell, D.W.15
Haber, D.A.16
Grip, M.17
Reiman, M.18
Jukkola-Vuorinen, A.19
Mustonen, A.20
Kere, J.21
Aaltonen, L.A.22
Kosma, V.M.23
Kataja, V.24
Soini, Y.25
Drapkin, R.I.26
Livingston, D.M.27
Winqvist, R.28
more..
-
14
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
10.1038/ng1959, 2871593, 17200668
-
Rahman N, Seal S, Thompson D, Kelly P, Renwick A, Elliott A, Reid S, Spanova K, Barfoot R, Chagtai T, Jayatilake H, McGuffog L, Hanks S, Evans DG, Eccles D, Easton DF, Stratton MR. PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat Genet 2007, 39:165-167. 10.1038/ng1959, 2871593, 17200668.
-
(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
Jayatilake, H.11
McGuffog, L.12
Hanks, S.13
Evans, D.G.14
Eccles, D.15
Easton, D.F.16
Stratton, M.R.17
-
15
-
-
33846569450
-
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
-
10.1038/ng1947, 17200671
-
Reid S, Schindler D, Hanenberg H, Barker K, Hanks S, Kalb R, Neveling K, Kelly P, Seal S, Freund M, Wurm M, Batish SD, Lach FP, Yetgin S, Neitzel H, Ariffin H, Tischkowitz M, Mathew CG, Auerbach AD, Rahman N. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat Genet 2007, 39:162-164. 10.1038/ng1947, 17200671.
-
(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
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..
-
16
-
-
36749002743
-
RAD51 135G→C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies
-
10.1086/522611, 2276351, 17999359, Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers Study (GEMO)
-
Antoniou AC, Sinilnikova OM, Simard J, Léoné M, Dumont M, Neuhausen SL, Struewing JP, Stoppa-Lyonnet D, Barjhoux L, Hughes DJ, Coupier I, Belotti M, Lasset C, Bonadona V, Bignon YJ, Rebbeck TR, Wagner T, Lynch HT, Domchek SM, Nathanson KL, Garber JE, Weitzel J, Narod SA, Tomlinson G, Olopade OI, Godwin A, Isaacs C, Jakubowska A, Lubinski J, et al. Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers Study (GEMO) RAD51 135G→C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies. Am J Hum Genet 2007, 81:1186-1200. 10.1086/522611, 2276351, 17999359, Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers Study (GEMO).
-
(2007)
Am J Hum Genet
, vol.81
, pp. 1186-1200
-
-
Antoniou, A.C.1
Sinilnikova, O.M.2
Simard, J.3
Léoné, M.4
Dumont, M.5
Neuhausen, S.L.6
Struewing, J.P.7
Stoppa-Lyonnet, D.8
Barjhoux, L.9
Hughes, D.J.10
Coupier, I.11
Belotti, M.12
Lasset, C.13
Bonadona, V.14
Bignon, Y.J.15
Rebbeck, T.R.16
Wagner, T.17
Lynch, H.T.18
Domchek, S.M.19
Nathanson, K.L.20
Garber, J.E.21
Weitzel, J.22
Narod, S.A.23
Tomlinson, G.24
Olopade, O.I.25
Godwin, A.26
Isaacs, C.27
Jakubowska, A.28
Lubinski, J.29
more..
-
17
-
-
0031472370
-
Association of BRCA1 with Rad51 in mitotic and meiotic cells
-
10.1016/S0092-8674(00)81847-4, 9008167
-
Scully R, Chen J, Plug A, Xiao Y, Weaver D, Feunteun J, Ashley T, Livingston DM. Association of BRCA1 with Rad51 in mitotic and meiotic cells. Cell 1997, 88:265-275. 10.1016/S0092-8674(00)81847-4, 9008167.
-
(1997)
Cell
, vol.88
, pp. 265-275
-
-
Scully, R.1
Chen, J.2
Plug, A.3
Xiao, Y.4
Weaver, D.5
Feunteun, J.6
Ashley, T.7
Livingston, D.M.8
-
18
-
-
0030933762
-
Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2
-
10.1038/386804a0, 9126738
-
Sharan SK, Morimatsu M, Albrecht U, Lim DS, Regel E, Dinh C, Sands A, Eichele G, Hasty P, Bradley A. Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2. Nature 1997, 386:804-810. 10.1038/386804a0, 9126738.
-
(1997)
Nature
, vol.386
, pp. 804-810
-
-
Sharan, S.K.1
Morimatsu, M.2
Albrecht, U.3
Lim, D.S.4
Regel, E.5
Dinh, C.6
Sands, A.7
Eichele, G.8
Hasty, P.9
Bradley, A.10
-
19
-
-
36949026476
-
BRCA2: a universal recombinase regulator
-
10.1038/sj.onc.1210870, 18066084
-
Thorslund T, West SC. BRCA2: a universal recombinase regulator. Oncogene 2007, 26:7720-7730. 10.1038/sj.onc.1210870, 18066084.
-
(2007)
Oncogene
, vol.26
, pp. 7720-7730
-
-
Thorslund, T.1
West, S.C.2
-
20
-
-
63049094474
-
Monoubiquitylation in the Fanconi anemia DNA damage response pathway
-
Alpi AF, Patel KJ. Monoubiquitylation in the Fanconi anemia DNA damage response pathway. DNA Repair (Amst) 2009, 8:430-435.
-
(2009)
DNA Repair (Amst)
, vol.8
, pp. 430-435
-
-
Alpi, A.F.1
Patel, K.J.2
-
21
-
-
77951181795
-
MRG15 binds directly to PALB2 and stimulates homology-directed repair of chromosomal breaks
-
10.1242/jcs.060178, 2844321, 20332121
-
Hayakawa T, Zhang F, Hayakawa N, Ohtani Y, Shinmyozu K, Nakayama J, Andreassen PR. MRG15 binds directly to PALB2 and stimulates homology-directed repair of chromosomal breaks. J Cell Sci 2010, 123:1124-1130. 10.1242/jcs.060178, 2844321, 20332121.
-
(2010)
J Cell Sci
, vol.123
, pp. 1124-1130
-
-
Hayakawa, T.1
Zhang, F.2
Hayakawa, N.3
Ohtani, Y.4
Shinmyozu, K.5
Nakayama, J.6
Andreassen, P.R.7
-
22
-
-
69249088889
-
MRG15 is a novel PALB2 interacting factor involved in homologous recombination
-
10.1074/jbc.C109.023937, 2755835, 19553677
-
Sy SM, Huen MS, Chen J. MRG15 is a novel PALB2 interacting factor involved in homologous recombination. J Biol Chem 2009, 284:21127-21131. 10.1074/jbc.C109.023937, 2755835, 19553677.
-
(2009)
J Biol Chem
, vol.284
, pp. 21127-21131
-
-
Sy, S.M.1
Huen, M.S.2
Chen, J.3
-
23
-
-
35349024501
-
Network modeling links breast cancer susceptibility and centrosome dysfunction
-
10.1038/ng.2007.2, 17922014
-
Pujana MA, Han JD, Starita LM, Stevens KN, Tewari M, Ahn JS, Rennert G, Moreno V, Kirchhoff T, Gold B, Assmann V, Elshamy WM, Rual JF, Levine D, Rozek LS, Gelman RS, Gunsalus KC, Greenberg RA, Sobhian B, Bertin N, Venkatesan K, Ayivi-Guedehoussou N, Sole X, Hernandez P, Lazaro C, Nathanson KL, Weber BL, Cusick ME, Hill DE, Offit K, et al. Network modeling links breast cancer susceptibility and centrosome dysfunction. Nat Genet 2007, 39:1338-1349. 10.1038/ng.2007.2, 17922014.
-
(2007)
Nat Genet
, vol.39
, pp. 1338-1349
-
-
Pujana, M.A.1
Han, J.D.2
Starita, L.M.3
Stevens, K.N.4
Tewari, M.5
Ahn, J.S.6
Rennert, G.7
Moreno, V.8
Kirchhoff, T.9
Gold, B.10
Assmann, V.11
Elshamy, W.M.12
Rual, J.F.13
Levine, D.14
Rozek, L.S.15
Gelman, R.S.16
Gunsalus, K.C.17
Greenberg, R.A.18
Sobhian, B.19
Bertin, N.20
Venkatesan, K.21
Ayivi-Guedehoussou, N.22
Sole, X.23
Hernandez, P.24
Lazaro, C.25
Nathanson, K.L.26
Weber, B.L.27
Cusick, M.E.28
Hill, D.E.29
Offit, K.30
more..
-
24
-
-
48649096489
-
A protein domain-based interactome network for C. elegans early embryogenesis
-
10.1016/j.cell.2008.07.009, 2596478, 18692475
-
Boxem M, Maliga Z, Klitgord N, Li N, Lemmens I, Mana M, de Lichtervelde L, Mul JD, van de Peut D, Devos M, Simonis N, Yildirim MA, Cokol M, Kao HL, de Smet AS, Wang H, Schlaitz AL, Hao T, Milstein S, Fan C, Tipsword M, Drew K, Galli M, Rhrissorrakrai K, Drechsel D, Koller D, Roth FP, Iakoucheva LM, Dunker AK, Bonneau R, et al. A protein domain-based interactome network for C. elegans early embryogenesis. Cell 2008, 134:534-545. 10.1016/j.cell.2008.07.009, 2596478, 18692475.
-
(2008)
Cell
, vol.134
, pp. 534-545
-
-
Boxem, M.1
Maliga, Z.2
Klitgord, N.3
Li, N.4
Lemmens, I.5
Mana, M.6
de Lichtervelde, L.7
Mul, J.D.8
van de Peut, D.9
Devos, M.10
Simonis, N.11
Yildirim, M.A.12
Cokol, M.13
Kao, H.L.14
de Smet, A.S.15
Wang, H.16
Schlaitz, A.L.17
Hao, T.18
Milstein, S.19
Fan, C.20
Tipsword, M.21
Drew, K.22
Galli, M.23
Rhrissorrakrai, K.24
Drechsel, D.25
Koller, D.26
Roth, F.P.27
Iakoucheva, L.M.28
Dunker, A.K.29
Bonneau, R.30
more..
-
25
-
-
38549146894
-
The Pfam protein families database
-
10.1093/nar/gkn226, 2238907, 18039703
-
Finn RD, Tate J, Mistry J, Coggill PC, Sammut SJ, Hotz HR, Ceric G, Forslund K, Eddy SR, Sonnhammer EL, Bateman A. The Pfam protein families database. Nucleic Acids Res 2008, 36:D281-D288. 10.1093/nar/gkn226, 2238907, 18039703.
-
(2008)
Nucleic Acids Res
, vol.36
-
-
Finn, R.D.1
Tate, J.2
Mistry, J.3
Coggill, P.C.4
Sammut, S.J.5
Hotz, H.R.6
Ceric, G.7
Forslund, K.8
Eddy, S.R.9
Sonnhammer, E.L.10
Bateman, A.11
-
26
-
-
22744437069
-
Natively disordered proteins: functions and predictions
-
10.2165/00822942-200403020-00005, 15693736
-
Romero P, Obradovic Z, Dunker AK. Natively disordered proteins: functions and predictions. Appl Bioinformatics 2004, 3:105-113. 10.2165/00822942-200403020-00005, 15693736.
-
(2004)
Appl Bioinformatics
, vol.3
, pp. 105-113
-
-
Romero, P.1
Obradovic, Z.2
Dunker, A.K.3
-
27
-
-
0034854563
-
High-throughput yeast two-hybrid assays for large-scale protein interaction mapping
-
10.1006/meth.2001.1190, 11403578
-
Walhout AJ, Vidal M. High-throughput yeast two-hybrid assays for large-scale protein interaction mapping. Methods 2001, 24:297-306. 10.1006/meth.2001.1190, 11403578.
-
(2001)
Methods
, vol.24
, pp. 297-306
-
-
Walhout, A.J.1
Vidal, M.2
-
28
-
-
1542345539
-
Increasing specificity in high-throughput yeast two-hybrid experiments
-
10.1016/j.ymeth.2003.10.001, 15003598
-
Vidalain PO, Boxem M, Ge H, Li S, Vidal M. Increasing specificity in high-throughput yeast two-hybrid experiments. Methods 2004, 32:363-370. 10.1016/j.ymeth.2003.10.001, 15003598.
-
(2004)
Methods
, vol.32
, pp. 363-370
-
-
Vidalain, P.O.1
Boxem, M.2
Ge, H.3
Li, S.4
Vidal, M.5
-
29
-
-
11144358198
-
A gene atlas of the mouse and human protein-encoding transcriptomes
-
10.1073/pnas.0400782101, 395923, 15075390
-
Su AI, Wiltshire T, Batalov S, Lapp H, Ching KA, Block D, Zhang J, Soden R, Hayakawa M, Kreiman G, Cooke MP, Walker JR, Hogenesch JB. A gene atlas of the mouse and human protein-encoding transcriptomes. Proc Natl Acad Sci USA 2004, 101:6062-6067. 10.1073/pnas.0400782101, 395923, 15075390.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 6062-6067
-
-
Su, A.I.1
Wiltshire, T.2
Batalov, S.3
Lapp, H.4
Ching, K.A.5
Block, D.6
Zhang, J.7
Soden, R.8
Hayakawa, M.9
Kreiman, G.10
Cooke, M.P.11
Walker, J.R.12
Hogenesch, J.B.13
-
30
-
-
39149098464
-
Nuclear translocation of hypoxia-inducible factors (HIFs): involvement of the classical importin a/b pathway
-
10.1016/j.bbamcr.2007.12.006, 18187047
-
Depping R, Steinhoff A, Schindler SG, Friedrich B, Fagerlund R, Metzen E, Hartmann E, Kohler M. Nuclear translocation of hypoxia-inducible factors (HIFs): involvement of the classical importin a/b pathway. Biochim Biophys Acta 2008, 1783:394-404. 10.1016/j.bbamcr.2007.12.006, 18187047.
-
(2008)
Biochim Biophys Acta
, vol.1783
, pp. 394-404
-
-
Depping, R.1
Steinhoff, A.2
Schindler, S.G.3
Friedrich, B.4
Fagerlund, R.5
Metzen, E.6
Hartmann, E.7
Kohler, M.8
-
31
-
-
65849476475
-
MRG15, a component of HAT and HDAC complexes, is essential for proliferation and differentiation of neural precursor cells
-
10.1002/jnr.21976, 2913448, 19115414
-
Chen M, Takano-Maruyama M, Pereira-Smith OM, Gaufo GO, Tominaga K. MRG15, a component of HAT and HDAC complexes, is essential for proliferation and differentiation of neural precursor cells. J Neurosci Res 2009, 87:1522-1531. 10.1002/jnr.21976, 2913448, 19115414.
-
(2009)
J Neurosci Res
, vol.87
, pp. 1522-1531
-
-
Chen, M.1
Takano-Maruyama, M.2
Pereira-Smith, O.M.3
Gaufo, G.O.4
Tominaga, K.5
-
32
-
-
35548941765
-
Mrg15 null and heterozygous mouse embryonic fibroblasts exhibit DNA-repair defects post exposure to gamma ionizing radiation
-
10.1016/j.febslet.2007.10.017, 2132445, 17961556
-
Garcia SN, Kirtane BM, Podlutsky AJ, Pereira-Smith OM, Tominaga K. Mrg15 null and heterozygous mouse embryonic fibroblasts exhibit DNA-repair defects post exposure to gamma ionizing radiation. FEBS Lett 2007, 581:5275-5281. 10.1016/j.febslet.2007.10.017, 2132445, 17961556.
-
(2007)
FEBS Lett
, vol.581
, pp. 5275-5281
-
-
Garcia, S.N.1
Kirtane, B.M.2
Podlutsky, A.J.3
Pereira-Smith, O.M.4
Tominaga, K.5
-
33
-
-
84860105218
-
MRG15 regulates embryonic development and cell proliferation
-
10.1128/MCB.25.8.2924-2937.2005, 1069611, 15798182
-
Tominaga K, Kirtane B, Jackson JG, Ikeno Y, Ikeda T, Hawks C, Smith JR, Matzuk MM, Pereira-Smith OM. MRG15 regulates embryonic development and cell proliferation. Mol Cell Biol 2005, 25:2924-2937. 10.1128/MCB.25.8.2924-2937.2005, 1069611, 15798182.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 2924-2937
-
-
Tominaga, K.1
Kirtane, B.2
Jackson, J.G.3
Ikeno, Y.4
Ikeda, T.5
Hawks, C.6
Smith, J.R.7
Matzuk, M.M.8
Pereira-Smith, O.M.9
-
34
-
-
0037184965
-
MRG15, a novel chromodomain protein, is present in two distinct multiprotein complexes involved in transcriptional activation
-
10.1074/jbc.M203839200, 12397079
-
Pardo PS, Leung JK, Lucchesi JC, Pereira-Smith OM. MRG15, a novel chromodomain protein, is present in two distinct multiprotein complexes involved in transcriptional activation. J Biol Chem 2002, 277:50860-50866. 10.1074/jbc.M203839200, 12397079.
-
(2002)
J Biol Chem
, vol.277
, pp. 50860-50866
-
-
Pardo, P.S.1
Leung, J.K.2
Lucchesi, J.C.3
Pereira-Smith, O.M.4
-
35
-
-
38449085292
-
Maintenance of C. elegans
-
Stiernagle T. Maintenance of C. elegans. WormBook 2006, 1:1-11.
-
(2006)
WormBook
, vol.1
, pp. 1-11
-
-
Stiernagle, T.1
-
36
-
-
0033990048
-
Primer3 on the WWW for general users and for biologist programmers
-
Rozen S, Skaletsky H. Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol 2000, 132:365-386.
-
(2000)
Methods Mol Biol
, vol.132
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.2
-
37
-
-
71049194443
-
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
-
10.1093/hmg/ddp372, 2782243, 19656774
-
Antoniou AC, Sinilnikova OM, McGuffog L, Healey S, Nevanlinna H, Heikkinen T, Simard J, Spurdle AB, Beesley J, Chen X, Neuhausen SL, Ding YC, Couch FJ, Wang X, Fredericksen Z, Peterlongo P, Peissel B, Bonanni B, Viel A, Bernard L, Radice P, Szabo CI, Foretova L, Zikan M, Claes K, Greene MH, Mai PL, Rennert G, Lejbkowicz F, Andrulis IL, et al. Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. Hum Mol Genet 2009, 18:4442-4456. 10.1093/hmg/ddp372, 2782243, 19656774.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 4442-4456
-
-
Antoniou, A.C.1
Sinilnikova, O.M.2
McGuffog, L.3
Healey, S.4
Nevanlinna, H.5
Heikkinen, T.6
Simard, J.7
Spurdle, A.B.8
Beesley, J.9
Chen, X.10
Neuhausen, S.L.11
Ding, Y.C.12
Couch, F.J.13
Wang, X.14
Fredericksen, Z.15
Peterlongo, P.16
Peissel, B.17
Bonanni, B.18
Viel, A.19
Bernard, L.20
Radice, P.21
Szabo, C.I.22
Foretova, L.23
Zikan, M.24
Claes, K.25
Greene, M.H.26
Mai, P.L.27
Rennert, G.28
Lejbkowicz, F.29
Andrulis, I.L.30
more..
-
38
-
-
84860398653
-
CIMBA
-
CIMBA. , http://www.srl.cam.ac.uk/consortia/cimba/eligibility/eligibility.html
-
-
-
-
39
-
-
21344437509
-
A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes
-
10.1002/gepi.20074, 15880399
-
Antoniou AC, Goldgar DE, Andrieu N, Chang-Claude J, Brohet R, Rookus MA, Easton DF. A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes. Genet Epidemiol 2005, 29:1-11. 10.1002/gepi.20074, 15880399.
-
(2005)
Genet Epidemiol
, vol.29
, pp. 1-11
-
-
Antoniou, A.C.1
Goldgar, D.E.2
Andrieu, N.3
Chang-Claude, J.4
Brohet, R.5
Rookus, M.A.6
Easton, D.F.7
-
40
-
-
18544389716
-
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
-
10.1038/ng879, 11967536
-
Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, et al. Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet 2002, 31:55-59. 10.1038/ng879, 11967536.
-
(2002)
Nat Genet
, vol.31
, pp. 55-59
-
-
Meijers-Heijboer, H.1
van den Ouweland, A.2
Klijn, J.3
Wasielewski, M.4
de Snoo, A.5
Oldenburg, R.6
Hollestelle, A.7
Houben, M.8
Crepin, E.9
van Veghel-Plandsoen, M.10
Elstrodt, F.11
van Duijn, C.12
Bartels, C.13
Meijers, C.14
Schutte, M.15
McGuffog, L.16
Thompson, D.17
Easton, D.18
Sodha, N.19
Seal, S.20
Barfoot, R.21
Mangion, J.22
Chang-Claude, J.23
Eccles, D.24
Eeles, R.25
Evans, D.G.26
Houlston, R.27
Murday, V.28
Narod, S.29
Peretz, T.30
more..
-
41
-
-
1542358787
-
Prediction and functional analysis of native disorder in proteins from the three kingdoms of life
-
10.1016/j.jmb.2004.02.002, 15019783
-
Ward JJ, Sodhi JS, McGuffin LJ, Buxton BF, Jones DT. Prediction and functional analysis of native disorder in proteins from the three kingdoms of life. J Mol Biol 2004, 337:635-645. 10.1016/j.jmb.2004.02.002, 15019783.
-
(2004)
J Mol Biol
, vol.337
, pp. 635-645
-
-
Ward, J.J.1
Sodhi, J.S.2
McGuffin, L.J.3
Buxton, B.F.4
Jones, D.T.5
-
42
-
-
34548448958
-
Inferring function using patterns of native disorder in proteins
-
10.1371/journal.pcbi.0030162, 1950950, 17722973
-
Lobley A, Swindells MB, Orengo CA, Jones DT. Inferring function using patterns of native disorder in proteins. PLoS Comput Biol 2007, 3:e162. 10.1371/journal.pcbi.0030162, 1950950, 17722973.
-
(2007)
PLoS Comput Biol
, vol.3
-
-
Lobley, A.1
Swindells, M.B.2
Orengo, C.A.3
Jones, D.T.4
-
43
-
-
0035504589
-
Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1
-
10.1093/nar/29.21.4378, 60193, 11691925
-
Pedrazzi G, Perrera C, Blaser H, Kuster P, Marra G, Davies SL, Ryu GH, Freire R, Hickson ID, Jiricny J, Stagljar I. Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1. Nucleic Acids Res 2001, 29:4378-4386. 10.1093/nar/29.21.4378, 60193, 11691925.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 4378-4386
-
-
Pedrazzi, G.1
Perrera, C.2
Blaser, H.3
Kuster, P.4
Marra, G.5
Davies, S.L.6
Ryu, G.H.7
Freire, R.8
Hickson, I.D.9
Jiricny, J.10
Stagljar, I.11
-
44
-
-
0028304833
-
Formation of a ternary complex by human XPA, ERCC1, and ERCC4(XPF) excision repair proteins
-
10.1073/pnas.91.11.5017, 43921, 8197175
-
Park CH, Sancar A. Formation of a ternary complex by human XPA, ERCC1, and ERCC4(XPF) excision repair proteins. Proc Natl Acad Sci USA 1994, 91:5017-5021. 10.1073/pnas.91.11.5017, 43921, 8197175.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 5017-5021
-
-
Park, C.H.1
Sancar, A.2
-
45
-
-
0038642027
-
A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome
-
10.1128/MCB.23.10.3417-3426.2003, 164758, 12724401
-
Meetei AR, Sechi S, Wallisch M, Yang D, Young MK, Joenje H, Hoatlin ME, Wang W. A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome. Mol Cell Biol 2003, 23:3417-3426. 10.1128/MCB.23.10.3417-3426.2003, 164758, 12724401.
-
(2003)
Mol Cell Biol
, vol.23
, pp. 3417-3426
-
-
Meetei, A.R.1
Sechi, S.2
Wallisch, M.3
Yang, D.4
Young, M.K.5
Joenje, H.6
Hoatlin, M.E.7
Wang, W.8
-
46
-
-
27144530248
-
Towards a proteome-scale map of the human protein-protein interaction network
-
10.1038/nature04209, 16189514
-
Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, et al. Towards a proteome-scale map of the human protein-protein interaction network. Nature 2005, 437:1173-1178. 10.1038/nature04209, 16189514.
-
(2005)
Nature
, vol.437
, pp. 1173-1178
-
-
Rual, J.F.1
Venkatesan, K.2
Hao, T.3
Hirozane-Kishikawa, T.4
Dricot, A.5
Li, N.6
Berriz, G.F.7
Gibbons, F.D.8
Dreze, M.9
Ayivi-Guedehoussou, N.10
Klitgord, N.11
Simon, C.12
Boxem, M.13
Milstein, S.14
Rosenberg, J.15
Goldberg, D.S.16
Zhang, L.V.17
Wong, S.L.18
Franklin, G.19
Li, S.20
Albala, J.S.21
Lim, J.22
Fraughton, C.23
Llamosas, E.24
Cevik, S.25
Bex, C.26
Lamesch, P.27
Sikorski, R.S.28
Vandenhaute, J.29
Zoghbi, H.Y.30
more..
-
47
-
-
67649634849
-
Defining the human deubiquitinating enzyme interaction landscape
-
10.1016/j.cell.2009.04.042, 2716422, 19615732
-
Sowa ME, Bennett EJ, Gygi SP, Harper JW. Defining the human deubiquitinating enzyme interaction landscape. Cell 2009, 138:389-403. 10.1016/j.cell.2009.04.042, 2716422, 19615732.
-
(2009)
Cell
, vol.138
, pp. 389-403
-
-
Sowa, M.E.1
Bennett, E.J.2
Gygi, S.P.3
Harper, J.W.4
-
48
-
-
70349183714
-
Histone chaperones ASF1 and NAP1 differentially modulate removal of active histone marks by LID-RPD3 complexes during NOTCH silencing
-
10.1016/j.molcel.2009.07.020, 19782028
-
Moshkin YM, Kan TW, Goodfellow H, Bezstarosti K, Maeda RK, Pilyugin M, Karch F, Bray SJ, Demmers JA, Verrijzer CP. Histone chaperones ASF1 and NAP1 differentially modulate removal of active histone marks by LID-RPD3 complexes during NOTCH silencing. Mol Cell 2009, 35:782-793. 10.1016/j.molcel.2009.07.020, 19782028.
-
(2009)
Mol Cell
, vol.35
, pp. 782-793
-
-
Moshkin, Y.M.1
Kan, T.W.2
Goodfellow, H.3
Bezstarosti, K.4
Maeda, R.K.5
Pilyugin, M.6
Karch, F.7
Bray, S.J.8
Demmers, J.A.9
Verrijzer, C.P.10
-
49
-
-
34147217542
-
Functional dissection of protein complexes involved in yeast chromosome biology using a genetic interaction map
-
10.1038/nature05649, 17314980
-
Collins SR, Miller KM, Maas NL, Roguev A, Fillingham J, Chu CS, Schuldiner M, Gebbia M, Recht J, Shales M, Ding H, Xu H, Han J, Ingvarsdottir K, Cheng B, Andrews B, Boone C, Berger SL, Hieter P, Zhang Z, Brown GW, Ingles CJ, Emili A, Allis CD, Toczyski DP, Weissman JS, Greenblatt JF, Krogan NJ. Functional dissection of protein complexes involved in yeast chromosome biology using a genetic interaction map. Nature 2007, 446:806-810. 10.1038/nature05649, 17314980.
-
(2007)
Nature
, vol.446
, pp. 806-810
-
-
Collins, S.R.1
Miller, K.M.2
Maas, N.L.3
Roguev, A.4
Fillingham, J.5
Chu, C.S.6
Schuldiner, M.7
Gebbia, M.8
Recht, J.9
Shales, M.10
Ding, H.11
Xu, H.12
Han, J.13
Ingvarsdottir, K.14
Cheng, B.15
Andrews, B.16
Boone, C.17
Berger, S.L.18
Hieter, P.19
Zhang, Z.20
Brown, G.W.21
Ingles, C.J.22
Emili, A.23
Allis, C.D.24
Toczyski, D.P.25
Weissman, J.S.26
Greenblatt, J.F.27
Krogan, N.J.28
more..
-
50
-
-
44349180746
-
Topoisomerase IIIα is required for normal proliferation and telomere stability in alternative lengthening of telomeres
-
2396391, 18418389
-
Temime-Smaali N, Guittat L, Wenner T, Bayart E, Douarre C, Gomez D, Giraud-Panis MJ, Londono-Vallejo A, Gilson E, Amor-Gueret M, Riou JF. Topoisomerase IIIα is required for normal proliferation and telomere stability in alternative lengthening of telomeres. Embo J 2008, 27:1513-1524. 2396391, 18418389.
-
(2008)
Embo J
, vol.27
, pp. 1513-1524
-
-
Temime-Smaali, N.1
Guittat, L.2
Wenner, T.3
Bayart, E.4
Douarre, C.5
Gomez, D.6
Giraud-Panis, M.J.7
Londono-Vallejo, A.8
Gilson, E.9
Amor-Gueret, M.10
Riou, J.F.11
-
51
-
-
0029040211
-
A novel gene, translin, encodes a recombination hotspot binding protein associated with chromosomal translocations
-
10.1038/ng0695-167, 7663511
-
Aoki K, Suzuki K, Sugano T, Tasaka T, Nakahara K, Kuge O, Omori A, Kasai M. A novel gene, translin, encodes a recombination hotspot binding protein associated with chromosomal translocations. Nat Genet 1995, 10:167-174. 10.1038/ng0695-167, 7663511.
-
(1995)
Nat Genet
, vol.10
, pp. 167-174
-
-
Aoki, K.1
Suzuki, K.2
Sugano, T.3
Tasaka, T.4
Nakahara, K.5
Kuge, O.6
Omori, A.7
Kasai, M.8
-
52
-
-
8544273217
-
The human protein translin specifically binds single-stranded microsatellite repeats, d(GT)n, and G-strand telomeric repeats, d(TTAGGG)n: a study of the binding parameters
-
10.1016/j.jmb.2004.09.095, 15544804
-
Jacob E, Pucshansky L, Zeruya E, Baran N, Manor H. The human protein translin specifically binds single-stranded microsatellite repeats, d(GT)n, and G-strand telomeric repeats, d(TTAGGG)n: a study of the binding parameters. J Mol Biol 2004, 344:939-950. 10.1016/j.jmb.2004.09.095, 15544804.
-
(2004)
J Mol Biol
, vol.344
, pp. 939-950
-
-
Jacob, E.1
Pucshansky, L.2
Zeruya, E.3
Baran, N.4
Manor, H.5
-
53
-
-
77954700065
-
Biological roles of translin and translin-associated factor-X: RNA metabolism comes to the fore
-
10.1042/BJ20100273, 20578993
-
Jaendling A, McFarlane RJ. Biological roles of translin and translin-associated factor-X: RNA metabolism comes to the fore. Biochem J 2010, 429:225-234. 10.1042/BJ20100273, 20578993.
-
(2010)
Biochem J
, vol.429
, pp. 225-234
-
-
Jaendling, A.1
McFarlane, R.J.2
-
54
-
-
0033052012
-
Accelerated telomere shortening and telomerase activation in Fanconi's anaemia
-
10.1046/j.1365-2141.1999.01445.x, 10554797
-
Leteurtre F, Li X, Guardiola P, Le Roux G, Sergere JC, Richard P, Carosella ED, Gluckman E. Accelerated telomere shortening and telomerase activation in Fanconi's anaemia. Br J Haematol 1999, 105:883-893. 10.1046/j.1365-2141.1999.01445.x, 10554797.
-
(1999)
Br J Haematol
, vol.105
, pp. 883-893
-
-
Leteurtre, F.1
Li, X.2
Guardiola, P.3
Le Roux, G.4
Sergere, J.C.5
Richard, P.6
Carosella, E.D.7
Gluckman, E.8
-
55
-
-
0032525092
-
Progressive telomere shortening in aplastic anemia
-
Ball SE, Gibson FM, Rizzo S, Tooze JA, Marsh JC, Gordon-Smith EC. Progressive telomere shortening in aplastic anemia. Blood 1998, 91:3582-3592.
-
(1998)
Blood
, vol.91
, pp. 3582-3592
-
-
Ball, S.E.1
Gibson, F.M.2
Rizzo, S.3
Tooze, J.A.4
Marsh, J.C.5
Gordon-Smith, E.C.6
-
56
-
-
0037084889
-
Breaks at telomeres and TRF2-independent end fusions in Fanconi anemia
-
10.1093/hmg/11.4.439, 11854176
-
Callén E, Samper E, Ramírez MJ, Creus A, Marcos R, Ortega JJ, Olivé T, Badell I, Blasco MA, Surrallés J. Breaks at telomeres and TRF2-independent end fusions in Fanconi anemia. Hum Mol Genet 2002, 11:439-444. 10.1093/hmg/11.4.439, 11854176.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 439-444
-
-
Callén, E.1
Samper, E.2
Ramírez, M.J.3
Creus, A.4
Marcos, R.5
Ortega, J.J.6
Olivé, T.7
Badell, I.8
Blasco, M.A.9
Surrallés, J.10
-
57
-
-
64549109258
-
A role for monoubiquitinated FANCD2 at telomeres in ALT cells
-
10.1093/nar/gkn995, 2665210, 19129235
-
Fan Q, Zhang F, Barrett B, Ren K, Andreassen PR. A role for monoubiquitinated FANCD2 at telomeres in ALT cells. Nucleic Acids Res 2009, 37:1740-1754. 10.1093/nar/gkn995, 2665210, 19129235.
-
(2009)
Nucleic Acids Res
, vol.37
, pp. 1740-1754
-
-
Fan, Q.1
Zhang, F.2
Barrett, B.3
Ren, K.4
Andreassen, P.R.5
-
58
-
-
10244229101
-
Telomere dynamics in Fancg-deficient mouse and human cells
-
10.1182/blood-2003-10-3626, 15319283
-
Franco S, van de Vrugt HJ, Fernández P, Aracil M, Arwert F, Blasco MA. Telomere dynamics in Fancg-deficient mouse and human cells. Blood 2004, 104:3927-3935. 10.1182/blood-2003-10-3626, 15319283.
-
(2004)
Blood
, vol.104
, pp. 3927-3935
-
-
Franco, S.1
van de Vrugt, H.J.2
Fernández, P.3
Aracil, M.4
Arwert, F.5
Blasco, M.A.6
-
59
-
-
77950536222
-
FANCC suppresses short telomere-initiated telomere sister chromatid exchange
-
10.1093/hmg/ddp556, 2816614, 20022886
-
Rhee DB, Wang Y, Mizesko M, Zhou F, Haneline L, Liu Y. FANCC suppresses short telomere-initiated telomere sister chromatid exchange. Hum Mol Genet 2010, 19:879-887. 10.1093/hmg/ddp556, 2816614, 20022886.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 879-887
-
-
Rhee, D.B.1
Wang, Y.2
Mizesko, M.3
Zhou, F.4
Haneline, L.5
Liu, Y.6
-
60
-
-
33745200945
-
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2
-
10.1016/j.molcel.2006.05.022, 16793542
-
Xia B, Sheng Q, Nakanishi K, Ohashi A, Wu J, Christ N, Liu X, Jasin M, Couch FJ, Livingston DM. Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2. Mol Cell 2006, 22:719-729. 10.1016/j.molcel.2006.05.022, 16793542.
-
(2006)
Mol Cell
, vol.22
, pp. 719-729
-
-
Xia, B.1
Sheng, Q.2
Nakanishi, K.3
Ohashi, A.4
Wu, J.5
Christ, N.6
Liu, X.7
Jasin, M.8
Couch, F.J.9
Livingston, D.M.10
-
61
-
-
16244407723
-
RAD-51-dependent and -independent roles of a Caenorhabditis elegans BRCA2-related protein during DNA double-strand break repair
-
10.1128/MCB.25.8.3127-3139.2005, 1069622, 15798199
-
Martin JS, Winkelmann N, Petalcorin MI, McIlwraith MJ, Boulton SJ. RAD-51-dependent and -independent roles of a Caenorhabditis elegans BRCA2-related protein during DNA double-strand break repair. Mol Cell Biol 2005, 25:3127-3139. 10.1128/MCB.25.8.3127-3139.2005, 1069622, 15798199.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 3127-3139
-
-
Martin, J.S.1
Winkelmann, N.2
Petalcorin, M.I.3
McIlwraith, M.J.4
Boulton, S.J.5
-
62
-
-
63449092932
-
Essential role of brc-2 in chromosome integrity of germ cells in C. elegans
-
Ko E, Lee J, Lee H. Essential role of brc-2 in chromosome integrity of germ cells in C. elegans. Mol Cells 2008, 26:590-594.
-
(2008)
Mol Cells
, vol.26
, pp. 590-594
-
-
Ko, E.1
Lee, J.2
Lee, H.3
-
63
-
-
0036011242
-
MRG-1, a mortality factor-related chromodomain protein, is required maternally for primordial germ cells to initiate mitotic proliferation in C. elegans
-
10.1016/S0925-4773(02)00058-8, 12175490
-
Fujita M, Takasaki T, Nakajima N, Kawano T, Shimura Y, Sakamoto H. MRG-1, a mortality factor-related chromodomain protein, is required maternally for primordial germ cells to initiate mitotic proliferation in C. elegans. Mech Dev 2002, 114:61-69. 10.1016/S0925-4773(02)00058-8, 12175490.
-
(2002)
Mech Dev
, vol.114
, pp. 61-69
-
-
Fujita, M.1
Takasaki, T.2
Nakajima, N.3
Kawano, T.4
Shimura, Y.5
Sakamoto, H.6
-
64
-
-
33947319151
-
MRG-1, an autosome-associated protein, silences X-linked genes and protects germline immortality in Caenorhabditis elegans
-
10.1242/dev.02771, 2435364, 17215300
-
Takasaki T, Liu Z, Habara Y, Nishiwaki K, Nakayama J, Inoue K, Sakamoto H, Strome S. MRG-1, an autosome-associated protein, silences X-linked genes and protects germline immortality in Caenorhabditis elegans. Development 2007, 134:757-767. 10.1242/dev.02771, 2435364, 17215300.
-
(2007)
Development
, vol.134
, pp. 757-767
-
-
Takasaki, T.1
Liu, Z.2
Habara, Y.3
Nishiwaki, K.4
Nakayama, J.5
Inoue, K.6
Sakamoto, H.7
Strome, S.8
-
65
-
-
78650568796
-
Mutation analysis of the gene encoding the PALB2-binding protein MRG15 in BRCA1/2-negative breast cancer families
-
10.1038/jhg.2010.112, 20844547
-
Rio Frio T, Haanpaa M, Pouchet C, Pylkas K, Vuorela M, Tischkowitz M, Winqvist R, Foulkes WD. Mutation analysis of the gene encoding the PALB2-binding protein MRG15 in BRCA1/2-negative breast cancer families. J Hum Genet 2010, 55:842-843. 10.1038/jhg.2010.112, 20844547.
-
(2010)
J Hum Genet
, vol.55
, pp. 842-843
-
-
Rio Frio, T.1
Haanpaa, M.2
Pouchet, C.3
Pylkas, K.4
Vuorela, M.5
Tischkowitz, M.6
Winqvist, R.7
Foulkes, W.D.8
-
66
-
-
64849092309
-
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene
-
10.1126/science.1171202, 2684332, 19264984
-
Jones S, Hruban RH, Kamiyama M, Borges M, Zhang X, Parsons DW, Lin JC, Palmisano E, Brune K, Jaffee EM, Iacobuzio-Donahue CA, Maitra A, Parmigiani G, Kern SE, Velculescu VE, Kinzler KW, Vogelstein B, Eshleman JR, Goggins M, Klein AP. Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene. Science 2009, 324:217. 10.1126/science.1171202, 2684332, 19264984.
-
(2009)
Science
, vol.324
, pp. 217
-
-
Jones, S.1
Hruban, R.H.2
Kamiyama, M.3
Borges, M.4
Zhang, X.5
Parsons, D.W.6
Lin, J.C.7
Palmisano, E.8
Brune, K.9
Jaffee, E.M.10
Iacobuzio-Donahue, C.A.11
Maitra, A.12
Parmigiani, G.13
Kern, S.E.14
Velculescu, V.E.15
Kinzler, K.W.16
Vogelstein, B.17
Eshleman, J.R.18
Goggins, M.19
Klein, A.P.20
more..
-
67
-
-
34250001297
-
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
-
10.1038/ng2075, 17529973
-
Hunter DJ, Kraft P, Jacobs KB, Cox DG, Yeager M, Hankinson SE, Wacholder S, Wang Z, Welch R, Hutchinson A, Wang J, Yu K, Chatterjee N, Orr N, Willett WC, Colditz GA, Ziegler RG, Berg CD, Buys SS, McCarty CA, Feigelson HS, Calle EE, Thun MJ, Hayes RB, Tucker M, Gerhard DS, Fraumeni JF, Hoover RN, Thomas G, Chanock SJ. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet 2007, 39:870-874. 10.1038/ng2075, 17529973.
-
(2007)
Nat Genet
, vol.39
, pp. 870-874
-
-
Hunter, D.J.1
Kraft, P.2
Jacobs, K.B.3
Cox, D.G.4
Yeager, M.5
Hankinson, S.E.6
Wacholder, S.7
Wang, Z.8
Welch, R.9
Hutchinson, A.10
Wang, J.11
Yu, K.12
Chatterjee, N.13
Orr, N.14
Willett, W.C.15
Colditz, G.A.16
Ziegler, R.G.17
Berg, C.D.18
Buys, S.S.19
McCarty, C.A.20
Feigelson, H.S.21
Calle, E.E.22
Thun, M.J.23
Hayes, R.B.24
Tucker, M.25
Gerhard, D.S.26
Fraumeni, J.F.27
Hoover, R.N.28
Thomas, G.29
Chanock, S.J.30
more..
-
68
-
-
78449270064
-
Identification of susceptibility loci in a mouse model of KRASG12D-driven pancreatic cancer
-
10.1158/0008-5472.CAN-09-3980, 20959479
-
Jorgenson TC, Williams BR, Wendland A, Bilger A, Sandgren EP, Drinkwater NR. Identification of susceptibility loci in a mouse model of KRASG12D-driven pancreatic cancer. Cancer Res 2010, 70:8398-8406. 10.1158/0008-5472.CAN-09-3980, 20959479.
-
(2010)
Cancer Res
, vol.70
, pp. 8398-8406
-
-
Jorgenson, T.C.1
Williams, B.R.2
Wendland, A.3
Bilger, A.4
Sandgren, E.P.5
Drinkwater, N.R.6
-
69
-
-
41649097333
-
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers
-
10.1016/j.ajhg.2008.02.008, 2427217, 18355772
-
Antoniou AC, Spurdle AB, Sinilnikova OM, Healey S, Pooley KA, Schmutzler RK, Versmold B, Engel C, Meindl A, Arnold N, Hofmann W, Sutter C, Niederacher D, Deissler H, Caldes T, Kampjarvi K, Nevanlinna H, Simard J, Beesley J, Chen X, Neuhausen SL, Rebbeck TR, Wagner T, Lynch HT, Isaacs C, Weitzel J, Ganz PA, Daly MB, Tomlinson G, Olopade OI, et al. Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. Am J Hum Genet 2008, 82:937-948. 10.1016/j.ajhg.2008.02.008, 2427217, 18355772.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 937-948
-
-
Antoniou, A.C.1
Spurdle, A.B.2
Sinilnikova, O.M.3
Healey, S.4
Pooley, K.A.5
Schmutzler, R.K.6
Versmold, B.7
Engel, C.8
Meindl, A.9
Arnold, N.10
Hofmann, W.11
Sutter, C.12
Niederacher, D.13
Deissler, H.14
Caldes, T.15
Kampjarvi, K.16
Nevanlinna, H.17
Simard, J.18
Beesley, J.19
Chen, X.20
Neuhausen, S.L.21
Rebbeck, T.R.22
Wagner, T.23
Lynch, H.T.24
Isaacs, C.25
Weitzel, J.26
Ganz, P.A.27
Daly, M.B.28
Tomlinson, G.29
Olopade, O.I.30
more..
|