-
1
-
-
10244239321
-
Life with 6000 genes
-
Galibert F, Hoheisel JD, Jacq C, Johnston M, Louis EJ, Mewes HW, Murakami Y, Philippsen P, Tettelin H, Oliver SG. Life with 6000 genes. Science 1996; 274:546-67.
-
(1996)
Science
, vol.274
, pp. 546-567
-
-
Galibert, F.1
Hoheisel, J.D.2
Jacq, C.3
Johnston, M.4
Louis, E.J.5
Mewes, H.W.6
Murakami, Y.7
Philippsen, P.8
Tettelin, H.9
Oliver, S.G.10
-
2
-
-
0035861532
-
Systematic genetic analysis with ordered arrays of yeast deletion mutants
-
Tong AH, Evangelista M, Parsons AB, Xu H, Bader GD, Pagé N, Robinson M, Raghibizadeh S, Hogue CW, Bussey H, Andrews B, Tyers M, Boone C. Systematic genetic analysis with ordered arrays of yeast deletion mutants. Science 2001; 294:2364-8.
-
(2001)
Science
, vol.294
, pp. 2364-2368
-
-
Tong, A.H.1
Evangelista, M.2
Parsons, A.B.3
Xu, H.4
Bader, G.D.5
Pagé, N.6
Robinson, M.7
Raghibizadeh, S.8
Hogue, C.W.9
Bussey, H.10
Andrews, B.11
Tyers, M.12
Boone, C.13
-
3
-
-
10744230485
-
-
Tong AH, Lesage G, Bader GD, Ding H, Xu H, Xin X, Young J, Berriz GF, Brost RL, Chang M, Chen Y, Cheng X, Chua G, Friesen H, Goldberg DS, Haynes J, Humphries C, He G, Hussein S, Ke L, Krogan N, Li Z, Levinson JN, Lu H, Ménard P, Munyana C, Parsons AB, Ryan O, Tonikian R, Roberts T, Sdicu AM, Shapiro J, Sheikh B, Suter B, Wong SL, Zhang LV, Zhu H, Burd CG, Munro S, Sander C, Rine J, Greenblatt J, Peter M, Bretscher A, Bell G, Roth FP, Brown GW, Andrews B, Bussey H, Boone C. Global mapping of the yeast genetic interaction network. Science 2004; 303:808-13.
-
Tong AH, Lesage G, Bader GD, Ding H, Xu H, Xin X, Young J, Berriz GF, Brost RL, Chang M, Chen Y, Cheng X, Chua G, Friesen H, Goldberg DS, Haynes J, Humphries C, He G, Hussein S, Ke L, Krogan N, Li Z, Levinson JN, Lu H, Ménard P, Munyana C, Parsons AB, Ryan O, Tonikian R, Roberts T, Sdicu AM, Shapiro J, Sheikh B, Suter B, Wong SL, Zhang LV, Zhu H, Burd CG, Munro S, Sander C, Rine J, Greenblatt J, Peter M, Bretscher A, Bell G, Roth FP, Brown GW, Andrews B, Bussey H, Boone C. Global mapping of the yeast genetic interaction network. Science 2004; 303:808-13.
-
-
-
-
4
-
-
33644778778
-
A DNA integrity network in the yeast Saccharomyces cerevisiae
-
Pan X, Ye P, Yuan DS, Wang X, Bader JS, Boeke DE. A DNA integrity network in the yeast Saccharomyces cerevisiae. Cell 2006; 124:1069-81.
-
(2006)
Cell
, vol.124
, pp. 1069-1081
-
-
Pan, X.1
Ye, P.2
Yuan, D.S.3
Wang, X.4
Bader, J.S.5
Boeke, D.E.6
-
5
-
-
0028033989
-
The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: A potential eukaryotic reverse gyrase
-
Gangloff S, McDonald JP, Bendixen C, Arthur L, Rothstein R. The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase. Mol Cell Biol 1994; 14:8391-8.
-
(1994)
Mol Cell Biol
, vol.14
, pp. 8391-8398
-
-
Gangloff, S.1
McDonald, J.P.2
Bendixen, C.3
Arthur, L.4
Rothstein, R.5
-
6
-
-
0030994386
-
+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest
-
+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest. EMBO J 1997; 16:2682-92.
-
(1997)
EMBO J
, vol.16
, pp. 2682-2692
-
-
Stewart, E.1
Chapman, C.R.2
Al-Khodairy, F.3
Carr, A.M.4
Enoch, T.5
-
7
-
-
0033046015
-
Evolution of the RECQ family of helicases: A drosophila homolog, Dmblm, is similar to the human bloom syndrome gene
-
Kusano K, Berres ME, Engels WR. Evolution of the RECQ family of helicases: A drosophila homolog, Dmblm, is similar to the human bloom syndrome gene. Genetics 1999; 151:1027-39.
-
(1999)
Genetics
, vol.151
, pp. 1027-1039
-
-
Kusano, K.1
Berres, M.E.2
Engels, W.R.3
-
8
-
-
0032535661
-
Cloning of two new human helicase genes of the RecQ family: Biological significance of multiple species in higher eukaryotes
-
Kitao S, Ohsugi I, Ichikawa K, Goto M, Furuichi Y, Shimamoto A. Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes. Genomics 1998; 54:443-52.
-
(1998)
Genomics
, vol.54
, pp. 443-452
-
-
Kitao, S.1
Ohsugi, I.2
Ichikawa, K.3
Goto, M.4
Furuichi, Y.5
Shimamoto, A.6
-
9
-
-
36749085205
-
Two closely related RecQ helicases have antagonistic roles in homologous recombination and DNA repair in Arabidopsis thaliana
-
Hartung F, Suer S, Puchta H. Two closely related RecQ helicases have antagonistic roles in homologous recombination and DNA repair in Arabidopsis thaliana. Proc Natl Acad Sci USA 2007; 104:18836-41.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 18836-18841
-
-
Hartung, F.1
Suer, S.2
Puchta, H.3
-
10
-
-
33645851036
-
The archaeal Hjm helicase has recQ-like functions, and may be involved in repair of stalled replication fork
-
Fujikane R, Shinagawa H, Ishino Y. The archaeal Hjm helicase has recQ-like functions, and may be involved in repair of stalled replication fork. Genes Cells 2006; 11:99-110.
-
(2006)
Genes Cells
, vol.11
, pp. 99-110
-
-
Fujikane, R.1
Shinagawa, H.2
Ishino, Y.3
-
11
-
-
33846604202
-
Systematic pathway analysis using high-resolution fitness profiling of combinatorial gene deletions
-
St Onge RP, Mani R, Oh J, Proctor M, Fung E, Davis RW, Nislow C, Roth FP, Giaever G. Systematic pathway analysis using high-resolution fitness profiling of combinatorial gene deletions. Nat Genet 2007; 39:199-206.
-
(2007)
Nat Genet
, vol.39
, pp. 199-206
-
-
St Onge, R.P.1
Mani, R.2
Oh, J.3
Proctor, M.4
Fung, E.5
Davis, R.W.6
Nislow, C.7
Roth, F.P.8
Giaever, G.9
-
12
-
-
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, Bier P, Steltenpool J, Stone S, Dokal I, Mathew CG, Hoatlin M, Joenje H, de Winter JP, Wang W. A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nat Genet 2005; 37:958-63.
-
(2005)
Nat Genet
, vol.37
, pp. 958-963
-
-
Meetei, A.R.1
Medhurst, A.L.2
Ling, C.3
Xue, Y.4
Singh, T.R.5
Bier, P.6
Steltenpool, J.7
Stone, S.8
Dokal, I.9
Mathew, C.G.10
Hoatlin, M.11
Joenje, H.12
de Winter, J.P.13
Wang, W.14
-
13
-
-
0021792806
-
The recQ gene of Escherichia coli K12: Molecular cloning and isolation of insertion mutants
-
Nakayama K, Irino N, Nakayama H. The recQ gene of Escherichia coli K12: molecular cloning and isolation of insertion mutants. Mol Gen Genet 1985; 200:266-71.
-
(1985)
Mol Gen Genet
, vol.200
, pp. 266-271
-
-
Nakayama, K.1
Irino, N.2
Nakayama, H.3
-
14
-
-
0034176335
-
Initiation of genetic recombination and recombination-dependent replication
-
Kowalczykowski SC. Initiation of genetic recombination and recombination-dependent replication. Trends Biochem Sci 2000; 25:156-65.
-
(2000)
Trends Biochem Sci
, vol.25
, pp. 156-165
-
-
Kowalczykowski, S.C.1
-
15
-
-
0030888233
-
RecQ DNA helicase is a suppressor of illegitimate recombination in Escherichia coli
-
Hanada K, Ukita T, Kohno Y, Saito K, Kato J, Ikeda H. RecQ DNA helicase is a suppressor of illegitimate recombination in Escherichia coli. Proc Natl Acad Sci USA 1997; 94:3860-5.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 3860-3865
-
-
Hanada, K.1
Ukita, T.2
Kohno, Y.3
Saito, K.4
Kato, J.5
Ikeda, H.6
-
16
-
-
0021185614
-
Isolation and genetic characterization of a thymineless death-resistant mutant of Escherichia coli K12: Identification of a new mutation (recQ1) that blocks the RecF recombination pathway
-
Nakayama H, Nakayama K, Nakayama R, Irino N, Nakayama Y, Hanawalt PC. Isolation and genetic characterization of a thymineless death-resistant mutant of Escherichia coli K12: identification of a new mutation (recQ1) that blocks the RecF recombination pathway. Mol Gen Genet 1984; 195:474-80.
-
(1984)
Mol Gen Genet
, vol.195
, pp. 474-480
-
-
Nakayama, H.1
Nakayama, K.2
Nakayama, R.3
Irino, N.4
Nakayama, Y.5
Hanawalt, P.C.6
-
17
-
-
0028061993
-
Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli RecQ helicase and localization of the gene at chromosome 12p12
-
Seki M, Miyazawa H, Tada S, Yanagisawa J, Yamaoka T, Hoshino S, Ozawa K, Eki T, Nogami M, Okumura K, Taguchi H, Hanaoka F, Enomoto T. Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli RecQ helicase and localization of the gene at chromosome 12p12. Nucleic Acids Res 1994; 22:4566-73.
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 4566-4573
-
-
Seki, M.1
Miyazawa, H.2
Tada, S.3
Yanagisawa, J.4
Yamaoka, T.5
Hoshino, S.6
Ozawa, K.7
Eki, T.8
Nogami, M.9
Okumura, K.10
Taguchi, H.11
Hanaoka, F.12
Enomoto, T.13
-
18
-
-
0027942415
-
Cloning and characterization of RECQL, a potential human homologue of the Escherichia coli DNA helicase RecQ
-
Puranam KL, Blackshear PJ. Cloning and characterization of RECQL, a potential human homologue of the Escherichia coli DNA helicase RecQ. J Biol Chem 1994; 269:29838-45.
-
(1994)
J Biol Chem
, vol.269
, pp. 29838-29845
-
-
Puranam, K.L.1
Blackshear, P.J.2
-
19
-
-
0026728155
-
Alteration of a DNA-dependent ATPase activity in xeroderma pigmentosum complementation group C cells
-
Yanagisawa J, Seki M, Ui M, Enomoto T. Alteration of a DNA-dependent ATPase activity in xeroderma pigmentosum complementation group C cells. J Biol Chem 1992; 267:3585-8.
-
(1992)
J Biol Chem
, vol.267
, pp. 3585-3588
-
-
Yanagisawa, J.1
Seki, M.2
Ui, M.3
Enomoto, T.4
-
20
-
-
0028294269
-
Purification of two DNA-dependent adenosinetriphosphatases having DNA helicase activity from HeLa cells and comparison of the properties of the two enzymes
-
Seki M, Yanagisawa J, Kohda T, Sonoyama T, Ui M, Enomoto T. Purification of two DNA-dependent adenosinetriphosphatases having DNA helicase activity from HeLa cells and comparison of the properties of the two enzymes. J Biochem 1994; 115:523-31.
-
(1994)
J Biochem
, vol.115
, pp. 523-531
-
-
Seki, M.1
Yanagisawa, J.2
Kohda, T.3
Sonoyama, T.4
Ui, M.5
Enomoto, T.6
-
21
-
-
0035050472
-
Functions of RecQ family helicases: Possible involvement of Bloom's and Werner's syndrome gene products in guarding genome integrity during DNA replication
-
Enomoto T. Functions of RecQ family helicases: possible involvement of Bloom's and Werner's syndrome gene products in guarding genome integrity during DNA replication. J Biochem 2001; 129:501-7.
-
(2001)
J Biochem
, vol.129
, pp. 501-507
-
-
Enomoto, T.1
-
22
-
-
0028785586
-
The Bloom's syndrome gene product is homologous to RecQ helicases
-
Ellis NA, Groden J, Ye TZ, Straughen J, Lennon DJ, Ciocci S, Proytcheva M, German J. The Bloom's syndrome gene product is homologous to RecQ helicases. Cell 1995; 83:655-66.
-
(1995)
Cell
, vol.83
, pp. 655-666
-
-
Ellis, N.A.1
Groden, J.2
Ye, T.Z.3
Straughen, J.4
Lennon, D.J.5
Ciocci, S.6
Proytcheva, M.7
German, J.8
-
23
-
-
15844409553
-
Positional cloning of the Werner's syndrome gene
-
Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD. Positional cloning of the Werner's syndrome gene. Science 1996; 272:258-62.
-
(1996)
Science
, vol.272
, pp. 258-262
-
-
Yu, C.E.1
Oshima, J.2
Fu, Y.H.3
Wijsman, E.M.4
Hisama, F.5
Alisch, R.6
Matthews, S.7
Nakura, J.8
Miki, T.9
Ouais, S.10
Martin, G.M.11
Mulligan, J.12
Schellenberg, G.D.13
-
24
-
-
0027331383
-
Bloom syndrome: A mendelian prototype of somatic mutational disease
-
German J. Bloom syndrome: a mendelian prototype of somatic mutational disease. Medicine 1993; 72:393-406.
-
(1993)
Medicine
, vol.72
, pp. 393-406
-
-
German, J.1
-
25
-
-
0025302748
-
An abnormal profile of DNA replication intermediates in Bloom's syndrome
-
Lönn U, Lönn S, Nylen U, Winblad G, German J. An abnormal profile of DNA replication intermediates in Bloom's syndrome. Cancer Res 1990; 50:3141-5.
-
(1990)
Cancer Res
, vol.50
, pp. 3141-3145
-
-
Lönn, U.1
Lönn, S.2
Nylen, U.3
Winblad, G.4
German, J.5
-
26
-
-
0013907774
-
Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process
-
Epstein CJ, Martin GM, Schultz AL, Motulsky AG. Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process. Medicine 1966; 45:177-221.
-
(1966)
Medicine
, vol.45
, pp. 177-221
-
-
Epstein, C.J.1
Martin, G.M.2
Schultz, A.L.3
Motulsky, A.G.4
-
27
-
-
0017549976
-
Cellular aging - clonal senescence. A review (Part I)
-
Martin GM. Cellular aging - clonal senescence. A review (Part I). Am J Pathol 1977; 89:484-511.
-
(1977)
Am J Pathol
, vol.89
, pp. 484-511
-
-
Martin, G.M.1
-
28
-
-
0024465870
-
Mutator phenotype of Werner syndrome is characterized by extensive deletions
-
Fukuchi K, Martin GM, Monnat RJ Jr. Mutator phenotype of Werner syndrome is characterized by extensive deletions. Proc Natl Acad Sci USA 1989; 86:5893-7.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 5893-5897
-
-
Fukuchi, K.1
Martin, G.M.2
Monnat Jr., R.J.3
-
29
-
-
0032535661
-
Cloning of two new human helicase genes of the RecQ family: Biological significance of multiple species in higher eukaryotes
-
Kitao S, Ohsugi I, Ichikawa K, Goto M, Furuichi Y, Shimamoto A. Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes. Genomics 1998; 54:443-52.
-
(1998)
Genomics
, vol.54
, pp. 443-452
-
-
Kitao, S.1
Ohsugi, I.2
Ichikawa, K.3
Goto, M.4
Furuichi, Y.5
Shimamoto, A.6
-
30
-
-
0032939991
-
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome
-
Kitao S, Shimamoto A, Goto M, Miller RW, Smithson WA, Lindor NM, Furuichi Y. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. Nat Genet 1999; 22:82-4.
-
(1999)
Nat Genet
, vol.22
, pp. 82-84
-
-
Kitao, S.1
Shimamoto, A.2
Goto, M.3
Miller, R.W.4
Smithson, W.A.5
Lindor, N.M.6
Furuichi, Y.7
-
31
-
-
0034737004
-
Rothmund-Thomson syndrome due to RECQ4 helicase mutations: Report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome
-
Lindor NM, Furuichi Y, Kitao S, Shimamoto A, Arndt C, Jalal S. Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome. Am J Med Genet 2000; 90:223-8.
-
(2000)
Am J Med Genet
, vol.90
, pp. 223-228
-
-
Lindor, N.M.1
Furuichi, Y.2
Kitao, S.3
Shimamoto, A.4
Arndt, C.5
Jalal, S.6
-
32
-
-
0242609126
-
Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases
-
Siitonen HA, Kopra O, Kääriäinen H, Haravuori H, Winter RM, Säämänen AM, Peltonen L, Kestilä M. Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases. Hum Mol Genet 2003; 12:2837-44.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2837-2844
-
-
Siitonen, H.A.1
Kopra, O.2
Kääriäinen, H.3
Haravuori, H.4
Winter, R.M.5
Säämänen, A.M.6
Peltonen, L.7
Kestilä, M.8
-
33
-
-
30344442461
-
Rothmund-Thomson syndrome and RECQL4 defect: Splitting and lumping
-
Larizza L, Magnani I, Roversi G. Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping. Cancer Lett 2006; 232:107-20.
-
(2006)
Cancer Lett
, vol.232
, pp. 107-120
-
-
Larizza, L.1
Magnani, I.2
Roversi, G.3
-
34
-
-
32944476196
-
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene
-
Van Maldergem L, Siitonen HA, Jalkh N, Chouery E, De Roy M, Delague V, Muenke M, Jabs EW, Cai J, Wang LL, Plon SE, Fourneau C, Kestilä M, Gillerot Y, Mégarbané A, Verloes A. Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene. J Med Genet 2006; 43:148-52.
-
(2006)
J Med Genet
, vol.43
, pp. 148-152
-
-
Van Maldergem, L.1
Siitonen, H.A.2
Jalkh, N.3
Chouery, E.4
De Roy, M.5
Delague, V.6
Muenke, M.7
Jabs, E.W.8
Cai, J.9
Wang, L.L.10
Plon, S.E.11
Fourneau, C.12
Kestilä, M.13
Gillerot, Y.14
Mégarbané, A.15
Verloes, A.16
-
35
-
-
20444380748
-
Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome
-
Sangrithi MN, Bernal JA, Madine M, Philpott A, Lee J, Dunphy WG, Venkitaraman AR. Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome. Cell 2005; 121:887-98.
-
(2005)
Cell
, vol.121
, pp. 887-898
-
-
Sangrithi, M.N.1
Bernal, J.A.2
Madine, M.3
Philpott, A.4
Lee, J.5
Dunphy, W.G.6
Venkitaraman, A.R.7
-
36
-
-
33645814832
-
Single nucleotide polymorphisms of RecQ1, RAD54L and ATM genes are associated with reduced survival of pancreatic cancer
-
Li D, Frazier M, Evans DB, Hess KR, Crane CH, Jiao L, Abbruzzese JL. Single nucleotide polymorphisms of RecQ1, RAD54L and ATM genes are associated with reduced survival of pancreatic cancer. J Clin Oncol 2006; 24:1720-8.
-
(2006)
J Clin Oncol
, vol.24
, pp. 1720-1728
-
-
Li, D.1
Frazier, M.2
Evans, D.B.3
Hess, K.R.4
Crane, C.H.5
Jiao, L.6
Abbruzzese, J.L.7
-
37
-
-
36849013079
-
RECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filaments
-
Hu Y, Raynard S, Sehorn MG, Lu X, Bussen W, Zheng L, Stark JM, Barnes EL, Chi P, Janscak P, Jasin M, Vogel H, Sung P, Luo G. RECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filaments. Genes Dev 2007; 21:3073-84.
-
(2007)
Genes Dev
, vol.21
, pp. 3073-3084
-
-
Hu, Y.1
Raynard, S.2
Sehorn, M.G.3
Lu, X.4
Bussen, W.5
Zheng, L.6
Stark, J.M.7
Barnes, E.L.8
Chi, P.9
Janscak, P.10
Jasin, M.11
Vogel, H.12
Sung, P.13
Luo, G.14
-
38
-
-
0141567744
-
RecQ helicases: Suppressors of tumorigenesis and premature aging
-
Bachrati CZ, Hickson ID. RecQ helicases: suppressors of tumorigenesis and premature aging. Biochem J 2003; 374:577-606.
-
(2003)
Biochem J
, vol.374
, pp. 577-606
-
-
Bachrati, C.Z.1
Hickson, I.D.2
-
39
-
-
24044521924
-
Current advances in unraveling the function of the Werner syndrome protein
-
Ozgenc A, Loeb LA. Current advances in unraveling the function of the Werner syndrome protein. Mutat Res 2005; 577:237-51.
-
(2005)
Mutat Res
, vol.577
, pp. 237-251
-
-
Ozgenc, A.1
Loeb, L.A.2
-
41
-
-
33749117158
-
RecQ helicases: Lessons from model organisms
-
Cobb JA, Bjergbaek L. RecQ helicases: lessons from model organisms. Nucleic Acids Res 2006; 34:4106-14.
-
(2006)
Nucleic Acids Res
, vol.34
, pp. 4106-4114
-
-
Cobb, J.A.1
Bjergbaek, L.2
-
42
-
-
34249946979
-
Role of the BLM helicase in replication fork management
-
Wu L. Role of the BLM helicase in replication fork management. DNA Repair 2007; 6:936-44.
-
(2007)
DNA Repair
, vol.6
, pp. 936-944
-
-
Wu, L.1
-
43
-
-
34548321123
-
Molecular genetics of RecQ helicase disorders
-
Hanada K, Hickson ID. Molecular genetics of RecQ helicase disorders. Cell Mol Life Sci 2007; 64:2306-22.
-
(2007)
Cell Mol Life Sci
, vol.64
, pp. 2306-2322
-
-
Hanada, K.1
Hickson, I.D.2
-
44
-
-
38049075962
-
Human premature aging, DNA repair and RecQ helicases
-
Brosh RM Jr, Bohr VA. Human premature aging, DNA repair and RecQ helicases. Nucleic Acids Res 2007; 35:7527-44.
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 7527-7544
-
-
Brosh Jr, R.M.1
Bohr, V.A.2
-
45
-
-
38949094875
-
Telomere ResQue and preservation - roles for the Werner syndrome protein and other RecQ helicases
-
Opresko PL. Telomere ResQue and preservation - roles for the Werner syndrome protein and other RecQ helicases. Mech Ageing Dev 2008; 129:79-90.
-
(2008)
Mech Ageing Dev
, vol.129
, pp. 79-90
-
-
Opresko, P.L.1
-
46
-
-
45449110194
-
Homologous recombination and maintenance of genome integrity: Cancer and aging through the prism of human RecQ helicases
-
Ouyang KJ, Woo LL, Ellis NA. Homologous recombination and maintenance of genome integrity: Cancer and aging through the prism of human RecQ helicases. Mech Ageing Dev 2008; 129:425-40.
-
(2008)
Mech Ageing Dev
, vol.129
, pp. 425-440
-
-
Ouyang, K.J.1
Woo, L.L.2
Ellis, N.A.3
-
47
-
-
30344477373
-
Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome
-
Macris MA, Krejci L, Bussen W, Shimamoto A, Sung P. Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome. DNA Repair 2006; 5:172-80.
-
(2006)
DNA Repair
, vol.5
, pp. 172-180
-
-
Macris, M.A.1
Krejci, L.2
Bussen, W.3
Shimamoto, A.4
Sung, P.5
-
48
-
-
0030686496
-
The Bloom's syndrome gene product is a 3′-5′ DNA helicase
-
Karow JK, Chakraverty RK, Hickson ID. The Bloom's syndrome gene product is a 3′-5′ DNA helicase. J Biol Chem 1997; 272:30611-4.
-
(1997)
J Biol Chem
, vol.272
, pp. 30611-30614
-
-
Karow, J.K.1
Chakraverty, R.K.2
Hickson, I.D.3
-
49
-
-
0030751354
-
The Werner syndrome protein is a DNA helicase
-
Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA. The Werner syndrome protein is a DNA helicase. Nat Genet 1997; 17:100-3.
-
(1997)
Nat Genet
, vol.17
, pp. 100-103
-
-
Gray, M.D.1
Shen, J.C.2
Kamath-Loeb, A.S.3
Blank, A.4
Sopher, B.L.5
Martin, G.M.6
Oshima, J.7
Loeb, L.A.8
-
50
-
-
3543007196
-
Human RECQ5β, a protein with DNA helicase and strand-annealing activities in a single polypeptide
-
Garcia PL, Liu Y, Jiricny J, West SC, Janscak P. Human RECQ5β, a protein with DNA helicase and strand-annealing activities in a single polypeptide. EMBO J 2004; 23:2882-91.
-
(2004)
EMBO J
, vol.23
, pp. 2882-2891
-
-
Garcia, P.L.1
Liu, Y.2
Jiricny, J.3
West, S.C.4
Janscak, P.5
-
51
-
-
33750980979
-
Human RECQ5β helicase promotes strand exchange on synthetic DNA structures resembling a stalled replication fork
-
Kanagaraj R, Saydam N, Garcia PL, Zheng L, Janscak P. Human RECQ5β helicase promotes strand exchange on synthetic DNA structures resembling a stalled replication fork. Nucleic Acids Res 2006; 34:5217-31.
-
(2006)
Nucleic Acids Res
, vol.34
, pp. 5217-5231
-
-
Kanagaraj, R.1
Saydam, N.2
Garcia, P.L.3
Zheng, L.4
Janscak, P.5
-
52
-
-
0035393720
-
The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases
-
Mohaghegh P, Karow JK, Brosh RM Jr, Bohr VA, Hickson ID. The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases. Nucleic Acids Res 2001; 29:2843-9.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 2843-2849
-
-
Mohaghegh, P.1
Karow, J.K.2
Brosh Jr, R.M.3
Bohr, V.A.4
Hickson, I.D.5
-
53
-
-
0037189485
-
Biochemical characterization of the DNA substrate specificity of Werner syndrome helicase
-
Brosh RM Jr, Waheed J, Sommers JA. Biochemical characterization of the DNA substrate specificity of Werner syndrome helicase. J Biol Chem 2002; 277:23236-45.
-
(2002)
J Biol Chem
, vol.277
, pp. 23236-23245
-
-
Brosh Jr, R.M.1
Waheed, J.2
Sommers, J.A.3
-
54
-
-
23044517287
-
Biochemical analysis of the DNA unwinding and strand annealing activities catalyzed by human RECQ1
-
Sharma S, Sommers JA, Choudhary S, Faulkner JK, Cui S, Andreoli L, Muzzolini L, Vindigni A, Brosh RM Jr. Biochemical analysis of the DNA unwinding and strand annealing activities catalyzed by human RECQ1. J Biol Chem 2005; 280:28072-84.
-
(2005)
J Biol Chem
, vol.280
, pp. 28072-28084
-
-
Sharma, S.1
Sommers, J.A.2
Choudhary, S.3
Faulkner, J.K.4
Cui, S.5
Andreoli, L.6
Muzzolini, L.7
Vindigni, A.8
Brosh Jr., R.M.9
-
55
-
-
0037137177
-
The Werner syndrome helicase/exonuclease (WRN) disrupts and degrades D-loops in vitro
-
Orren DK, Theodore S, Machwe A. The Werner syndrome helicase/exonuclease (WRN) disrupts and degrades D-loops in vitro. Biochemistry 2002; 41:13483-8.
-
(2002)
Biochemistry
, vol.41
, pp. 13483-13488
-
-
Orren, D.K.1
Theodore, S.2
Machwe, A.3
-
56
-
-
33646843592
-
Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase
-
Bachrati CZ, Borts RH, Hickson ID. Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase. Nucleic Acids Res 2006; 34:2269-79.
-
(2006)
Nucleic Acids Res
, vol.34
, pp. 2269-2279
-
-
Bachrati, C.Z.1
Borts, R.H.2
Hickson, I.D.3
-
57
-
-
28544438312
-
Identification of RecQL1 as a Holliday junction processing enzyme in human cell lines
-
LeRoy G, Carroll R, Kyin S, Seki M, Cole MD. Identification of RecQL1 as a Holliday junction processing enzyme in human cell lines. Nucleic Acids Res 2005; 33:6251-7.
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 6251-6257
-
-
LeRoy, G.1
Carroll, R.2
Kyin, S.3
Seki, M.4
Cole, M.D.5
-
58
-
-
22444447945
-
The Bloom's syndrome helicase promotes the annealing of complementary single-stranded DNA
-
Cheok CF, Wu L, Garcia PL, Janscak P, Hickson ID. The Bloom's syndrome helicase promotes the annealing of complementary single-stranded DNA. Nucleic Acids Res 2005; 33:3932-41.
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 3932-3941
-
-
Cheok, C.F.1
Wu, L.2
Garcia, P.L.3
Janscak, P.4
Hickson, I.D.5
-
59
-
-
33751581731
-
The Werner and Bloom syndrome proteins catalyze regression of a model replication fork
-
Machwe A, Xiao L, Groden J, Orren DK. The Werner and Bloom syndrome proteins catalyze regression of a model replication fork. Biochemistry 2006; 45:13939-46.
-
(2006)
Biochemistry
, vol.45
, pp. 13939-13946
-
-
Machwe, A.1
Xiao, L.2
Groden, J.3
Orren, D.K.4
-
60
-
-
33747352774
-
The Bloom's syndrome helicase can promote the regression of a model replication fork
-
Ralf C, Hickson ID, Wu L. The Bloom's syndrome helicase can promote the regression of a model replication fork. J Biol Chem 2006; 281:22839-46.
-
(2006)
J Biol Chem
, vol.281
, pp. 22839-22846
-
-
Ralf, C.1
Hickson, I.D.2
Wu, L.3
-
62
-
-
0035880025
-
Unwinding the molecular basis of the Werner syndrome
-
Shen J, Loeb LA. Unwinding the molecular basis of the Werner syndrome. Mech Ageing Dev 2001; 122:921-44.
-
(2001)
Mech Ageing Dev
, vol.122
, pp. 921-944
-
-
Shen, J.1
Loeb, L.A.2
-
63
-
-
49649099084
-
The human recq helicases, blm and recq1, display distinct DNA substrate specificities
-
Popuri V, Bachrati CZ, Muzzolini L, Mosedale G, Costantini S, Giacomini E, Hickson ID, Vindigni A. The human recq helicases, blm and recq1, display distinct DNA substrate specificities. J Biol Chem 2008; 283:17766-76.
-
(2008)
J Biol Chem
, vol.283
, pp. 17766-17776
-
-
Popuri, V.1
Bachrati, C.Z.2
Muzzolini, L.3
Mosedale, G.4
Costantini, S.5
Giacomini, E.6
Hickson, I.D.7
Vindigni, A.8
-
64
-
-
0028033989
-
The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: A potential eukaryotic reverse gyrase
-
Gangloff S, McDonald JP, Bendixen C, Arthur L, Rothstein R. The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase. Mol Cell Biol 1994; 14:8391-8.
-
(1994)
Mol Cell Biol
, vol.14
, pp. 8391-8398
-
-
Gangloff, S.1
McDonald, J.P.2
Bendixen, C.3
Arthur, L.4
Rothstein, R.5
-
65
-
-
0034089029
-
Bipartite structure of the SGS1 DNA helicase in Saccharomyces cerevisiae
-
Mullen JR, Kaliraman V, Brill SJ. Bipartite structure of the SGS1 DNA helicase in Saccharomyces cerevisiae. Genetics 2000; 154:1101-14.
-
(2000)
Genetics
, vol.154
, pp. 1101-1114
-
-
Mullen, J.R.1
Kaliraman, V.2
Brill, S.J.3
-
66
-
-
0035937840
-
Mapping the DNA topoisomerase III binding domain of the Sgs1 DNA helicase
-
Fricke WM, Kaliraman V, Brill SJ. Mapping the DNA topoisomerase III binding domain of the Sgs1 DNA helicase. J Biol Chem 2001; 276:8848-55.
-
(2001)
J Biol Chem
, vol.276
, pp. 8848-8855
-
-
Fricke, W.M.1
Kaliraman, V.2
Brill, S.J.3
-
67
-
-
0034882238
-
The N-terminal region of Sgs1, which interacts with Top3, is required for complementation of MMS sensitivity and suppression of hyper-recombination in sgs1 disruptants
-
Ui A, Satoh Y, Onoda F, Miyajima A, Seki M, Enomoto T. The N-terminal region of Sgs1, which interacts with Top3, is required for complementation of MMS sensitivity and suppression of hyper-recombination in sgs1 disruptants. Mol Genet Genomics 2001; 265:837-50.
-
(2001)
Mol Genet Genomics
, vol.265
, pp. 837-850
-
-
Ui, A.1
Satoh, Y.2
Onoda, F.3
Miyajima, A.4
Seki, M.5
Enomoto, T.6
-
68
-
-
0033570217
-
Topoisomerase III is essential for accurate nuclear division in Schizosaccharomyces pombe
-
Goodwin A, Wang SW, Toda T, Norbury C, Hickson ID. Topoisomerase III is essential for accurate nuclear division in Schizosaccharomyces pombe. Nucleic Acids Res 1999; 27:4050-8.
-
(1999)
Nucleic Acids Res
, vol.27
, pp. 4050-4058
-
-
Goodwin, A.1
Wang, S.W.2
Toda, T.3
Norbury, C.4
Hickson, I.D.5
-
69
-
-
0029986401
-
Human TOP3: A single-copy gene encoding DNA topoisomerase III
-
Hanai R, Caron PR, Wang JC. Human TOP3: a single-copy gene encoding DNA topoisomerase III. Proc Natl Acad Sci USA 1996; 93:3653-7.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 3653-3657
-
-
Hanai, R.1
Caron, P.R.2
Wang, J.C.3
-
70
-
-
0032582667
-
Cloning of cDNA encoding a novel mouse DNA topoisomerase III (Topo IIIβ) possessing negatively supercoiled DNA relaxing activity, whose message is highly expressed in the testis
-
Seki T, Seki M, Onodera R, Katada T, Enomoto T. Cloning of cDNA encoding a novel mouse DNA topoisomerase III (Topo IIIβ) possessing negatively supercoiled DNA relaxing activity, whose message is highly expressed in the testis. J Biol Chem 1998; 273:28553-6.
-
(1998)
J Biol Chem
, vol.273
, pp. 28553-28556
-
-
Seki, T.1
Seki, M.2
Onodera, R.3
Katada, T.4
Enomoto, T.5
-
71
-
-
0032477804
-
Mammalian DNA topoisomerase IIIα is essential in early embryogenesis
-
Li W, Wang JC. Mammalian DNA topoisomerase IIIα is essential in early embryogenesis. Proc Natl Acad Sci USA 1998; 95:1010-3.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 1010-1013
-
-
Li, W.1
Wang, J.C.2
-
72
-
-
0035826797
-
Mice lacking DNA topoisomerase IIIβ develop to maturity but show a reduced mean lifespan
-
Kwan KY, Wang JC. Mice lacking DNA topoisomerase IIIβ develop to maturity but show a reduced mean lifespan. Proc Natl Acad Sci USA 2001; 98:5717-21.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 5717-5721
-
-
Kwan, K.Y.1
Wang, J.C.2
-
73
-
-
0034737641
-
The Bloom's syndrome gene product interacts with topoisomerase III
-
Wu L, Davies SL, North PS, Goulaouic H, Riou JF, Turley H, Gatter KC, Hickson ID. The Bloom's syndrome gene product interacts with topoisomerase III. J Biol Chem 2000; 275:9636-44.
-
(2000)
J Biol Chem
, vol.275
, pp. 9636-9644
-
-
Wu, L.1
Davies, S.L.2
North, P.S.3
Goulaouic, H.4
Riou, J.F.5
Turley, H.6
Gatter, K.C.7
Hickson, I.D.8
-
74
-
-
0034164070
-
Human RecQ5β, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerases 3α and 3β
-
Shimamoto A, Nishikawa K, Kitao S, Furuichi Y. Human RecQ5β, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerases 3α and 3β. Nucleic Acids Res 2000; 28:1647-55.
-
(2000)
Nucleic Acids Res
, vol.28
, pp. 1647-1655
-
-
Shimamoto, A.1
Nishikawa, K.2
Kitao, S.3
Furuichi, Y.4
-
75
-
-
0034162770
-
Association of the Bloom syndrome protein with topoisomerase IIIα in somatic and meiotic cells
-
Johnson FB, Lombard DB, Neff NF, Mastrangelo MA, Dewolf W, Ellis NA, Marciniak RA, Yin Y, Jaenisch R and Guarente L. Association of the Bloom syndrome protein with topoisomerase IIIα in somatic and meiotic cells. Cancer Res 2000; 60:1162-7.
-
(2000)
Cancer Res
, vol.60
, pp. 1162-1167
-
-
Johnson, F.B.1
Lombard, D.B.2
Neff, N.F.3
Mastrangelo, M.A.4
Dewolf, W.5
Ellis, N.A.6
Marciniak, R.A.7
Yin, Y.8
Jaenisch, R.9
Guarente, L.10
-
76
-
-
33746966063
-
Bloom helicase and DNA topoisomerase IIIα are involved in the dissolution of sister chromatids
-
Seki M, Nakagawa T, Seki T, Kato G, Tada S, Takahashi Y, Yoshimura A, Kobayashi T, Aoki A, Otsuki M, Habermann FA, Tanabe H, Ishii Y, Enomoto T. Bloom helicase and DNA topoisomerase IIIα are involved in the dissolution of sister chromatids. Mol Cell Biol 2006; 26:6299-307.
-
(2006)
Mol Cell Biol
, vol.26
, pp. 6299-6307
-
-
Seki, M.1
Nakagawa, T.2
Seki, T.3
Kato, G.4
Tada, S.5
Takahashi, Y.6
Yoshimura, A.7
Kobayashi, T.8
Aoki, A.9
Otsuki, M.10
Habermann, F.A.11
Tanabe, H.12
Ishii, Y.13
Enomoto, T.14
-
77
-
-
0347987856
-
The Bloom's syndrome helicase suppresses crossing over during homologous recombination
-
Wu L, Hickson ID. The Bloom's syndrome helicase suppresses crossing over during homologous recombination. Nature 2003; 426:870-4.
-
(2003)
Nature
, vol.426
, pp. 870-874
-
-
Wu, L.1
Hickson, I.D.2
-
78
-
-
17844386117
-
BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity
-
Yin J, Sobeck A, Xu C, Meetei AR, Hoatlin M, Li L, Wang W. BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity. EMBO J 2005; 24:1465-76.
-
(2005)
EMBO J
, vol.24
, pp. 1465-1476
-
-
Yin, J.1
Sobeck, A.2
Xu, C.3
Meetei, A.R.4
Hoatlin, M.5
Li, L.6
Wang, W.7
-
79
-
-
33645242115
-
BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates
-
Wu L, Bachrati CZ, Ou J, Xu C, Yin J, Chang M, Wang W, Li L, Brown GW, Hickson ID. BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates. Proc Natl Acad Sci USA 2006; 103:4068-73.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 4068-4073
-
-
Wu, L.1
Bachrati, C.Z.2
Ou, J.3
Xu, C.4
Yin, J.5
Chang, M.6
Wang, W.7
Li, L.8
Brown, G.W.9
Hickson, I.D.10
-
80
-
-
35748981213
-
Holliday junction processing activity of the BLM-Topo IIIα-BLAP75 complex
-
Bussen W, Raynard S, Busygina V, Singh AK, Sung P. Holliday junction processing activity of the BLM-Topo IIIα-BLAP75 complex. J Biol Chem 2007; 282:31484-92.
-
(2007)
J Biol Chem
, vol.282
, pp. 31484-31492
-
-
Bussen, W.1
Raynard, S.2
Busygina, V.3
Singh, A.K.4
Sung, P.5
-
81
-
-
23044449199
-
The HRDC domain of BLM is required for the dissolution of double Holliday junctions
-
Wu L, Chan KL, Ralf C, Bernstein DA, Garcia PL, Bohr VA, Vindigni A, Janscak P, Keck JL, Hickson ID. The HRDC domain of BLM is required for the dissolution of double Holliday junctions. EMBO J 2005; 24:2679-87.
-
(2005)
EMBO J
, vol.24
, pp. 2679-2687
-
-
Wu, L.1
Chan, K.L.2
Ralf, C.3
Bernstein, D.A.4
Garcia, P.L.5
Bohr, V.A.6
Vindigni, A.7
Janscak, P.8
Keck, J.L.9
Hickson, I.D.10
-
82
-
-
0001262820
-
Mitotic spindle pulls but fails to separate chromosomes in type II DNA topoisomerase mutants: Uncoordinated mitosis
-
Uemura T, Tanagida M. Mitotic spindle pulls but fails to separate chromosomes in type II DNA topoisomerase mutants: uncoordinated mitosis. EMBO J 1986; 5:1003-10.
-
(1986)
EMBO J
, vol.5
, pp. 1003-1010
-
-
Uemura, T.1
Tanagida, M.2
-
83
-
-
0022400533
-
DNA topoisomerase II is required at the time of mitosis in yeast
-
Holm C, Goto T, Wang JC, Botstein D. DNA topoisomerase II is required at the time of mitosis in yeast. Cell 1985; 41:553-63.
-
(1985)
Cell
, vol.41
, pp. 553-563
-
-
Holm, C.1
Goto, T.2
Wang, J.C.3
Botstein, D.4
-
84
-
-
1842480104
-
Functional compatibility between isoform α and β of type II DNA topoisomerase
-
Sakaguchi A, Kikuchi A. Functional compatibility between isoform α and β of type II DNA topoisomerase. J Cell Sci 2004; 117:1047-54.
-
(2004)
J Cell Sci
, vol.117
, pp. 1047-1054
-
-
Sakaguchi, A.1
Kikuchi, A.2
-
85
-
-
0028589156
-
Topoisomerase III, but not topoisomerase I, can support nascent chain elongation during theta-type DNA replication
-
Hiasa H, Marians KJ. Topoisomerase III, but not topoisomerase I, can support nascent chain elongation during theta-type DNA replication. J Biol Chem 1994; 269:32655-9.
-
(1994)
J Biol Chem
, vol.269
, pp. 32655-32659
-
-
Hiasa, H.1
Marians, K.J.2
-
86
-
-
34547192058
-
BLM is required for faithful chromosome segregation and its localization defines a class of ultrafine anaphase bridges
-
Chan KL, North PS, Hickson ID. BLM is required for faithful chromosome segregation and its localization defines a class of ultrafine anaphase bridges. EMBO J 2007; 26:3397-409.
-
(2007)
EMBO J
, vol.26
, pp. 3397-3409
-
-
Chan, K.L.1
North, P.S.2
Hickson, I.D.3
-
87
-
-
0034600976
-
Possible association of BLM in decreasing DNA double strand breaks during DNA replication
-
Wang W, Seki M, Narita Y, Sonoda E, Takeda S, Yamada K, Masuko T, Katada T, Enomoto T. Possible association of BLM in decreasing DNA double strand breaks during DNA replication. EMBO J 2000; 19:3428-35.
-
(2000)
EMBO J
, vol.19
, pp. 3428-3435
-
-
Wang, W.1
Seki, M.2
Narita, Y.3
Sonoda, E.4
Takeda, S.5
Yamada, K.6
Masuko, T.7
Katada, T.8
Enomoto, T.9
-
88
-
-
17644410077
-
Recql5 and Blm RecQ DNA helicases have nonredundant roles in suppressing crossovers
-
Hu Y, Lu X, Barnes E, Yan M, Lou H, Luo G. Recql5 and Blm RecQ DNA helicases have nonredundant roles in suppressing crossovers. Mol Cell Biol 2005; 25:3431-42.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 3431-3442
-
-
Hu, Y.1
Lu, X.2
Barnes, E.3
Yan, M.4
Lou, H.5
Luo, G.6
-
89
-
-
0037965769
-
Functional relation among RecQ family helicases RecQL1, RecQL5 and BLM in cell growth and sister chromatid exchange formation
-
Wang W, Seki M, Narita Y, Nakagawa T, Yoshimura A, Otsuki M, Kawabe Y, Tada S, Yagi H, Ishii Y, Enomoto T. Functional relation among RecQ family helicases RecQL1, RecQL5 and BLM in cell growth and sister chromatid exchange formation. Mol Cell Biol 2003; 23:3527-35.
-
(2003)
Mol Cell Biol
, vol.23
, pp. 3527-3535
-
-
Wang, W.1
Seki, M.2
Narita, Y.3
Nakagawa, T.4
Yoshimura, A.5
Otsuki, M.6
Kawabe, Y.7
Tada, S.8
Yagi, H.9
Ishii, Y.10
Enomoto, T.11
-
90
-
-
39149114123
-
Analyses of functional interaction between RECQL1, RECQL5 and BLM which physically interact with DNA topoisomerase IIIα
-
Otsuki M, Seki M, Inoue E, Abe T, Narita Y, Yoshimura A, Tada S, Ishii Y, Enomoto T. Analyses of functional interaction between RECQL1, RECQL5 and BLM which physically interact with DNA topoisomerase IIIα. Biochim Biophys Acta 2008; 1782:75-81.
-
(2008)
Biochim Biophys Acta
, vol.1782
, pp. 75-81
-
-
Otsuki, M.1
Seki, M.2
Inoue, E.3
Abe, T.4
Narita, Y.5
Yoshimura, A.6
Tada, S.7
Ishii, Y.8
Enomoto, T.9
-
91
-
-
33847228012
-
-
Sharma S, Stumpo DJ, Balajee AS, Bock CB, Lansdorp PM, Brosh RM Jr, Blackshear PJ. RECQL, a member of the RecQ family of DNA helicases, suppresses chromosomal instability. Mol Cell Biol 2007; 27:1784-94.
-
Sharma S, Stumpo DJ, Balajee AS, Bock CB, Lansdorp PM, Brosh RM Jr, Blackshear PJ. RECQL, a member of the RecQ family of DNA helicases, suppresses chromosomal instability. Mol Cell Biol 2007; 27:1784-94.
-
-
-
-
92
-
-
29544437558
-
Multiple mechanisms control chromosome integrity after replication fork uncoupling and restart at irreparable UV lesions
-
Lopes M, Foiani M, Sogo JM. Multiple mechanisms control chromosome integrity after replication fork uncoupling and restart at irreparable UV lesions. Mol Cell 2006; 21:15-27.
-
(2006)
Mol Cell
, vol.21
, pp. 15-27
-
-
Lopes, M.1
Foiani, M.2
Sogo, J.M.3
-
93
-
-
35348941829
-
Functional interactions between BLM and XRCC3 in the cell
-
Otsuki M, Seki M, Inoue E, Yoshimura A, Kato G, Yamanouchi S, Kawabe Y, Tada S, Shinohara A, Komura J, Ono T, Takeda S, Ishii Y, Enomoto T. Functional interactions between BLM and XRCC3 in the cell. J Cell Biol 2007; 179:53-63.
-
(2007)
J Cell Biol
, vol.179
, pp. 53-63
-
-
Otsuki, M.1
Seki, M.2
Inoue, E.3
Yoshimura, A.4
Kato, G.5
Yamanouchi, S.6
Kawabe, Y.7
Tada, S.8
Shinohara, A.9
Komura, J.10
Ono, T.11
Takeda, S.12
Ishii, Y.13
Enomoto, T.14
-
94
-
-
0035363706
-
Evidence for BLM and Topoisomerase IIIα interaction in genomic stability
-
Hu P, Beresten SF, van Brabant AJ, Ye TZ, Pandolfi PP, Johnson FB, Guarente L, Ellis NA. Evidence for BLM and Topoisomerase IIIα interaction in genomic stability. Hum Mol Genet 2001; 10:1287-98.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1287-1298
-
-
Hu, P.1
Beresten, S.F.2
van Brabant, A.J.3
Ye, T.Z.4
Pandolfi, P.P.5
Johnson, F.B.6
Guarente, L.7
Ellis, N.A.8
-
95
-
-
1342306874
-
The absence of a functional relationship between ATM and BLM, the components of BASC, in DT40 cells
-
Wang W, Seki M, Otsuki M, Tada S, Takao N, Yamamoto K, Hayashi M, Honma M, Enomoto T. The absence of a functional relationship between ATM and BLM, the components of BASC, in DT40 cells. Biochim Biophys Acta 2004; 1688:137-44.
-
(2004)
Biochim Biophys Acta
, vol.1688
, pp. 137-144
-
-
Wang, W.1
Seki, M.2
Otsuki, M.3
Tada, S.4
Takao, N.5
Yamamoto, K.6
Hayashi, M.7
Honma, M.8
Enomoto, T.9
-
96
-
-
36849029846
-
Novel pro- and anti-recombination activities of the Bloom's syndrome helicase
-
Bugreev DV, Yu X, Egelman EH, Mazin AV. Novel pro- and anti-recombination activities of the Bloom's syndrome helicase. Genes Dev 2007; 21:3085-94.
-
(2007)
Genes Dev
, vol.21
, pp. 3085-3094
-
-
Bugreev, D.V.1
Yu, X.2
Egelman, E.H.3
Mazin, A.V.4
-
97
-
-
0037673941
-
DNA helicase Srs2 disrupts the Rad51 presynaptic filament
-
Krejci L, Van Komen S, Li Y, Villemain J, Reddy MS, Klein H, Ellenberger T, Sung P. DNA helicase Srs2 disrupts the Rad51 presynaptic filament. Nature 2003; 423:305-9.
-
(2003)
Nature
, vol.423
, pp. 305-309
-
-
Krejci, L.1
Van Komen, S.2
Li, Y.3
Villemain, J.4
Reddy, M.S.5
Klein, H.6
Ellenberger, T.7
Sung, P.8
-
98
-
-
0034119866
-
Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases
-
Gangloff S, Soustelle C, Fabre F. Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases. Nat Genet 2000; 25:192-4.
-
(2000)
Nat Genet
, vol.25
, pp. 192-194
-
-
Gangloff, S.1
Soustelle, C.2
Fabre, F.3
-
99
-
-
24344508122
-
Role of the Schizosaccharomyces pombe F-Box DNA helicase in processing recombination intermediates
-
Morishita T, Furukawa F, Sakaguchi C, Toda T, Carr AM, Iwasaki H, Shinagawa H. Role of the Schizosaccharomyces pombe F-Box DNA helicase in processing recombination intermediates. Mol Cell Biol 2005; 25:8074-83.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 8074-8083
-
-
Morishita, T.1
Furukawa, F.2
Sakaguchi, C.3
Toda, T.4
Carr, A.M.5
Iwasaki, H.6
Shinagawa, H.7
-
100
-
-
34147220115
-
Cooperative roles of vertebrate Fbh1 and Blm DNA helicases in avoidance of crossovers during recombination initiated by replication fork collapse
-
Kohzaki M, Hatanaka A, Sonoda E, Yamazoe M, Kikuchi K, Vu Trung N, Szüts D, Sale JE, Shinagawa H, Watanabe M, Takeda S. Cooperative roles of vertebrate Fbh1 and Blm DNA helicases in avoidance of crossovers during recombination initiated by replication fork collapse. Mol Cell Biol 2007; 2812-20.
-
(2007)
Mol Cell Biol
, pp. 2812-2820
-
-
Kohzaki, M.1
Hatanaka, A.2
Sonoda, E.3
Yamazoe, M.4
Kikuchi, K.5
Vu Trung, N.6
Szüts, D.7
Sale, J.E.8
Shinagawa, H.9
Watanabe, M.10
Takeda, S.11
-
101
-
-
0017065529
-
Study of mitomycin C-induced chromosomal exchange
-
Huttner KM, Ruddle FH. Study of mitomycin C-induced chromosomal exchange. Chromosoma 1976; 56:1-13.
-
(1976)
Chromosoma
, vol.56
, pp. 1-13
-
-
Huttner, K.M.1
Ruddle, F.H.2
-
102
-
-
0019865496
-
Mitotic crossing-over and segregation in man
-
Therman E, Kuhn EM. Mitotic crossing-over and segregation in man. Hum Genet 1981; 59:93-100.
-
(1981)
Hum Genet
, vol.59
, pp. 93-100
-
-
Therman, E.1
Kuhn, E.M.2
-
103
-
-
17444391598
-
A genetic screen for top3 suppressors in Saccharomyces cerevisiae identifies SHU1, SHU2, PSY3 and CSM2: Four genes involved in error-free DNA repair
-
Shor E, Weinstein J, Rothstein R. A genetic screen for top3 suppressors in Saccharomyces cerevisiae identifies SHU1, SHU2, PSY3 and CSM2: four genes involved in error-free DNA repair. Genetics 2005; 169:1275-89.
-
(2005)
Genetics
, vol.169
, pp. 1275-1289
-
-
Shor, E.1
Weinstein, J.2
Rothstein, R.3
-
104
-
-
0347416973
-
Branch migrating sister chromatid junctions form at replication origins through Rad51/Rad52-independent mechanisms
-
Lopes M, Cotta-Ramusino C, Liberi G, Foiani M. Branch migrating sister chromatid junctions form at replication origins through Rad51/Rad52-independent mechanisms. Mol Cell 2003; 12:1499-510.
-
(2003)
Mol Cell
, vol.12
, pp. 1499-1510
-
-
Lopes, M.1
Cotta-Ramusino, C.2
Liberi, G.3
Foiani, M.4
-
105
-
-
0017298802
-
A model for replication repair in mammalian cells
-
Higgins NP, Kato K, Strauss B. A model for replication repair in mammalian cells. J Mol Biol 1976; 101:417-25.
-
(1976)
J Mol Biol
, vol.101
, pp. 417-425
-
-
Higgins, N.P.1
Kato, K.2
Strauss, B.3
-
106
-
-
0037178740
-
Fork reversal and ssDNA accumulation at stalled replication forks owing to checkpoint defects
-
Sogo JM, Lopes M, Foiani M. Fork reversal and ssDNA accumulation at stalled replication forks owing to checkpoint defects. Science 2002; 297:599-602.
-
(2002)
Science
, vol.297
, pp. 599-602
-
-
Sogo, J.M.1
Lopes, M.2
Foiani, M.3
-
107
-
-
19944432787
-
Rad51-dependent DNA structures accumulate at damaged replication forks in sgs1 mutants defective in the yeast ortholog of BLM RecQ helicase
-
Liberi G, Maffioletti G, Lucca C, Chiolo I, Baryshnikova A, Cotta-Ramusino C, Lopes M, Pellicioli A, Haber JE, Foiani M. Rad51-dependent DNA structures accumulate at damaged replication forks in sgs1 mutants defective in the yeast ortholog of BLM RecQ helicase. Genes Dev 2005; 19:339-50.
-
(2005)
Genes Dev
, vol.19
, pp. 339-350
-
-
Liberi, G.1
Maffioletti, G.2
Lucca, C.3
Chiolo, I.4
Baryshnikova, A.5
Cotta-Ramusino, C.6
Lopes, M.7
Pellicioli, A.8
Haber, J.E.9
Foiani, M.10
-
108
-
-
42049116919
-
The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest
-
Sidorova JM, Li N, Folch A, Monnat RJ Jr. The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest. Cell Cycle 2008; 7:796-807.
-
(2008)
Cell Cycle
, vol.7
, pp. 796-807
-
-
Sidorova, J.M.1
Li, N.2
Folch, A.3
Monnat Jr., R.J.4
-
109
-
-
10344256183
-
Defective telomere lagging strand synthesis in cells lacking WRN helicase activity
-
Crabbe L, Verdun RE, Haggblom CI, Karlseder J. Defective telomere lagging strand synthesis in cells lacking WRN helicase activity. Science 2004; 306:1951-3.
-
(2004)
Science
, vol.306
, pp. 1951-1953
-
-
Crabbe, L.1
Verdun, R.E.2
Haggblom, C.I.3
Karlseder, J.4
-
110
-
-
33750309123
-
Role for RAD18 in homologous recombination in DT40 cells
-
Szüts D, Simpson LJ, Kabani S, Yamazoe M, Sale JE. Role for RAD18 in homologous recombination in DT40 cells. Mol Cell Biol 2006; 26:8032-41.
-
(2006)
Mol Cell Biol
, vol.26
, pp. 8032-8041
-
-
Szüts, D.1
Simpson, L.J.2
Kabani, S.3
Yamazoe, M.4
Sale, J.E.5
-
111
-
-
0038642027
-
A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome
-
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; 23:3417-26.
-
(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
-
112
-
-
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; 8:735-48.
-
(2007)
Nat Rev Genet
, vol.8
, pp. 735-748
-
-
Wang, W.1
-
113
-
-
19944411110
-
Fanconi anemia protein FANCD2 promotes immunoglobulin gene conversion and DNA repair through a mechanism related to homologous recombination
-
Yamamoto K, Hirano S, Ishiai M, Morishima K, Kitao H, Namikoshi K, Kimura M, Matsushita N, Arakawa H, Buerstedde JM, Komatsu K, Thompson LH, Takata M. Fanconi anemia protein FANCD2 promotes immunoglobulin gene conversion and DNA repair through a mechanism related to homologous recombination. Mol Cell Biol 2005; 25:34-43.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 34-43
-
-
Yamamoto, K.1
Hirano, S.2
Ishiai, M.3
Morishima, K.4
Kitao, H.5
Namikoshi, K.6
Kimura, M.7
Matsushita, N.8
Arakawa, H.9
Buerstedde, J.M.10
Komatsu, K.11
Thompson, L.H.12
Takata, M.13
-
114
-
-
13444270410
-
Functional relationships of FANCC to homologous recombination, translesion synthesis and BLM
-
Hirano S, Yamamoto K, Ishiai M, Yamazoe M, Seki M, Matsushita N, Ohzeki M, Yamashita YM, Arakawa H, Buerstedde JM, Enomoto T, Takeda S, Thompson LH, Takata M. Functional relationships of FANCC to homologous recombination, translesion synthesis and BLM. EMBO J 2005; 24:418-27.
-
(2005)
EMBO J
, vol.24
, pp. 418-427
-
-
Hirano, S.1
Yamamoto, K.2
Ishiai, M.3
Yamazoe, M.4
Seki, M.5
Matsushita, N.6
Ohzeki, M.7
Yamashita, Y.M.8
Arakawa, H.9
Buerstedde, J.M.10
Enomoto, T.11
Takeda, S.12
Thompson, L.H.13
Takata, M.14
-
115
-
-
17944373792
-
Rad52 partially substitutes for the Rad51 paralog XRCC3 in maintaining chromosomal integrity in vertebrate cells
-
Fujimori A, Tachiiri S, Sonoda E, Thompson LH, Dhar PK, Hiraoka M, Takeda S, Zhang Y, Reth M, Takata M. Rad52 partially substitutes for the Rad51 paralog XRCC3 in maintaining chromosomal integrity in vertebrate cells. EMBO J 2001; 20:5513-20.
-
(2001)
EMBO J
, vol.20
, pp. 5513-5520
-
-
Fujimori, A.1
Tachiiri, S.2
Sonoda, E.3
Thompson, L.H.4
Dhar, P.K.5
Hiraoka, M.6
Takeda, S.7
Zhang, Y.8
Reth, M.9
Takata, M.10
-
116
-
-
0141480945
-
WRN interacts physically and functionally with the recombination mediator protein RAD52
-
Baynton K, Otterlei M, Bjørås M, von Kobbe C, Bohr VA, Seeberg E. WRN interacts physically and functionally with the recombination mediator protein RAD52. J Biol Chem 2003; 278:36476-86.
-
(2003)
J Biol Chem
, vol.278
, pp. 36476-36486
-
-
Baynton, K.1
Otterlei, M.2
Bjørås, M.3
von Kobbe, C.4
Bohr, V.A.5
Seeberg, E.6
-
117
-
-
34547525678
-
Werner syndrome protein interacts functionally with translesion DNA polymerases
-
Kamath-Loeb AS, Lan L, Nakajima S, Yasui A, Loeb LA. Werner syndrome protein interacts functionally with translesion DNA polymerases. Proc Natl Acad Sci USA 2007; 104:10394-9.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 10394-10399
-
-
Kamath-Loeb, A.S.1
Lan, L.2
Nakajima, S.3
Yasui, A.4
Loeb, L.A.5
-
118
-
-
39549114273
-
DNA repair synthesis facilitates RAD52-mediated second-end capture during DSB repair
-
McIlwraith MJ, West SC. DNA repair synthesis facilitates RAD52-mediated second-end capture during DSB repair. Mol Cell 2008; 29:510-6.
-
(2008)
Mol Cell
, vol.29
, pp. 510-516
-
-
McIlwraith, M.J.1
West, S.C.2
|