-
1
-
-
0028785586
-
The Bloom's syndrome gene product is homologous to RecQ helicases
-
Ellis N.A., Gordon J., Ye T.Z., Straughen J., Lennon D.J., Ciocci S., Proytcheva M., German J. The Bloom's syndrome gene product is homologous to RecQ helicases. Cell 1995, 83:655-666.
-
(1995)
Cell
, vol.83
, pp. 655-666
-
-
Ellis, N.A.1
Gordon, J.2
Ye, T.Z.3
Straughen, J.4
Lennon, D.J.5
Ciocci, S.6
Proytcheva, M.7
German, J.8
-
2
-
-
15844409553
-
Positional cloning of the Werner's syndrome gene
-
Yu C.E., Oshima J., Fu Y.H., Wijsman E.M., Hisama F., Alisch R., Matthews S., Nakura J., Miki T., Ouais S., Martin G.M., Mulligan J., Schellenberg G.D. Positional cloning of the Werner's syndrome gene. Science 1996, 272:258-262.
-
(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
-
3
-
-
0032939991
-
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome
-
Kitao S., Shimamoto A., Goto M., Miller R.W., Smithson W.A., Lindor N.M., Furuichi Y. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. Nat. Genet. 1999, 22:82-84.
-
(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
-
4
-
-
62049085034
-
Dual DNA unwinding activities of the Rothmund-Thomson syndrome protein, RECQ4
-
Xu X., Liu Y. Dual DNA unwinding activities of the Rothmund-Thomson syndrome protein, RECQ4. EMBO J. 2009, 28:568-577.
-
(2009)
EMBO J.
, vol.28
, pp. 568-577
-
-
Xu, X.1
Liu, Y.2
-
5
-
-
70449732463
-
DNA helicase activity in purified human RECQL4 protein
-
Suzuki T., Kohno T., Ishimi Y. DNA helicase activity in purified human RECQL4 protein. J. Biochem. 2009, 146:327-335.
-
(2009)
J. Biochem.
, vol.146
, pp. 327-335
-
-
Suzuki, T.1
Kohno, T.2
Ishimi, Y.3
-
7
-
-
0032736140
-
Rothmond-Thomson syndrome responsible gene, RECQL4: genomic structure and products
-
Kitao S., Lindor N.M., Shiratori M., Furuichi Y., Shimamoto A. Rothmond-Thomson syndrome responsible gene, RECQL4: genomic structure and products. Genomics 1999, 61:268-276.
-
(1999)
Genomics
, vol.61
, pp. 268-276
-
-
Kitao, S.1
Lindor, N.M.2
Shiratori, M.3
Furuichi, Y.4
Shimamoto, A.5
-
8
-
-
58349104333
-
The mutation spectrum in RECQL4 diseases
-
Siitonen H.A., Sotkasiira J., Biervliet M., Benmansour A., Capri Y., Cormier-Daire V., Crandall B., Hannula-Jouppi K., Hennekam R., Herzog D., Keymolen K., Lipsanen-Nyman M., Miny P., Plon S.E., Riedl S., Sarkar A., Vargas F.R., Verloes A., Wang L.L., Kaariainen H., Kestila M. The mutation spectrum in RECQL4 diseases. Eur. J. Hum. Genet. 2009, 17:151-158.
-
(2009)
Eur. J. Hum. Genet.
, vol.17
, pp. 151-158
-
-
Siitonen, H.A.1
Sotkasiira, J.2
Biervliet, M.3
Benmansour, A.4
Capri, Y.5
Cormier-Daire, V.6
Crandall, B.7
Hannula-Jouppi, K.8
Hennekam, R.9
Herzog, D.10
Keymolen, K.11
Lipsanen-Nyman, M.12
Miny, P.13
Plon, S.E.14
Riedl, S.15
Sarkar, A.16
Vargas, F.R.17
Verloes, A.18
Wang, L.L.19
Kaariainen, H.20
Kestila, M.21
more..
-
9
-
-
34247102690
-
The molecular role of the Rothmund-Thomson-, RAPADILINO- and Baller-Gerold-gene product, RECQL4: recent progress
-
Dietschy T., Shevelev I., Stagljar I. The molecular role of the Rothmund-Thomson-, RAPADILINO- and Baller-Gerold-gene product, RECQL4: recent progress. Cell. Mol. Life Sci. 2007, 64796-64802.
-
(2007)
Cell. Mol. Life Sci.
, pp. 64796-64802
-
-
Dietschy, T.1
Shevelev, I.2
Stagljar, I.3
-
10
-
-
0036233108
-
Preparation of the gene targeted knockout mice for human premature aging diseases, Werner syndrome, and Rothmund-Thomson syndrome caused by the mutation of DNA helicases
-
Ichikawa K., Noda T., Furuichi Y. Preparation of the gene targeted knockout mice for human premature aging diseases, Werner syndrome, and Rothmund-Thomson syndrome caused by the mutation of DNA helicases. Nippon Yakugaku Zasshi 2002, 119:219-226.
-
(2002)
Nippon Yakugaku Zasshi
, vol.119
, pp. 219-226
-
-
Ichikawa, K.1
Noda, T.2
Furuichi, Y.3
-
11
-
-
10744225050
-
Growth retardation and skin abnormalities of the Recql4-deficient mouse
-
Hoki Y., Araki R., Fujimori A., Ohhata T., Koseki H., Fukumura R., Nakamura M., Takahashi H., Noda Y., Kito S., Abe M. Growth retardation and skin abnormalities of the Recql4-deficient mouse. Hum. Mol. Genet. 2003, 12:2293-2299.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2293-2299
-
-
Hoki, Y.1
Araki, R.2
Fujimori, A.3
Ohhata, T.4
Koseki, H.5
Fukumura, R.6
Nakamura, M.7
Takahashi, H.8
Noda, Y.9
Kito, S.10
Abe, M.11
-
12
-
-
15544389502
-
Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome
-
Mann M.B., Hodges C.A., Barnes E., Vogel H., Hassold T.J., Lou G. Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome. Hum. Mol. Genet. 2005, 14:813-825.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 813-825
-
-
Mann, M.B.1
Hodges, C.A.2
Barnes, E.3
Vogel, H.4
Hassold, T.J.5
Lou, G.6
-
13
-
-
20444380748
-
Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome
-
Sangrithi M.N., Bernal J.A., Madine M., Philpott A., Lee J., Dunphy W.G., Venkitaraman A.R. Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome. Cell 2005, 121:887-898.
-
(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
-
14
-
-
33745471225
-
The N-terminal noncatalytic region of Xenopus RecQ4 is required for chromatin binding of DNA polymerase α in the initiation of DNA replication
-
Matsuno K., Kumano M., Kubota Y., Hashimoto Y., Takisawa H. The N-terminal noncatalytic region of Xenopus RecQ4 is required for chromatin binding of DNA polymerase α in the initiation of DNA replication. Mol. Cell. Biol. 2006, 26:4843-4852.
-
(2006)
Mol. Cell. Biol.
, vol.26
, pp. 4843-4852
-
-
Matsuno, K.1
Kumano, M.2
Kubota, Y.3
Hashimoto, Y.4
Takisawa, H.5
-
15
-
-
0037034048
-
S-Cdk-dependent phosphorylation of Sld2 essential for chromosomal DNA replication in budding yeast
-
Masumoto H., Muramatsu S., Kamimura Y., Araki H. S-Cdk-dependent phosphorylation of Sld2 essential for chromosomal DNA replication in budding yeast. Nature 2002, 415:651-655.
-
(2002)
Nature
, vol.415
, pp. 651-655
-
-
Masumoto, H.1
Muramatsu, S.2
Kamimura, Y.3
Araki, H.4
-
16
-
-
70350573964
-
MCM10 mediates RECQ4 association with MCM2-7 helicase complex during DNA replication
-
Xu X., Rochette P.J., Feyissa E.A., Su T.V., Liu Y. MCM10 mediates RECQ4 association with MCM2-7 helicase complex during DNA replication. EMBO J. 2009, 28:3005-3014.
-
(2009)
EMBO J.
, vol.28
, pp. 3005-3014
-
-
Xu, X.1
Rochette, P.J.2
Feyissa, E.A.3
Su, T.V.4
Liu, Y.5
-
17
-
-
77749330814
-
Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation
-
Thangavel S., Mendoza-Maldonado R., Tissino E., Sidorova J.M., Yin J., Wang W., Monnat R.J., Falasci A., Vindigni A. Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation. Mol. Cell. Biol. 2010, 30:1382-1396.
-
(2010)
Mol. Cell. Biol.
, vol.30
, pp. 1382-1396
-
-
Thangavel, S.1
Mendoza-Maldonado, R.2
Tissino, E.3
Sidorova, J.M.4
Yin, J.5
Wang, W.6
Monnat, R.J.7
Falasci, A.8
Vindigni, A.9
-
18
-
-
53649102650
-
Drosophila homologue of the Rothmund-Thomson syndrome gene: essential function in DNA replication during development
-
Wu J., Capp C., Feng L., Hsieh T.S. Drosophila homologue of the Rothmund-Thomson syndrome gene: essential function in DNA replication during development. Dev. Biol. 2008, 323:130-142.
-
(2008)
Dev. Biol.
, vol.323
, pp. 130-142
-
-
Wu, J.1
Capp, C.2
Feng, L.3
Hsieh, T.S.4
-
19
-
-
71449108720
-
Drosophila RecQ4 has a 3'-5' DNA helicase activity that is essential for viability
-
Capp C., Wu J., Hsieh T.S. Drosophila RecQ4 has a 3'-5' DNA helicase activity that is essential for viability. J. Biol. Chem. 2009, 284:30845-30852.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 30845-30852
-
-
Capp, C.1
Wu, J.2
Hsieh, T.S.3
-
20
-
-
33947309418
-
Possible involvement of RecQL4 in the repair of double-strand DNA breaks in Xenopus egg extracts
-
Kumata Y., Tada S., Yamanada Y., Tsuyama T., Kobayashi T., Dong Y.P., Ikegami K., Murofushi H., Seki M., Enomoto T. Possible involvement of RecQL4 in the repair of double-strand DNA breaks in Xenopus egg extracts. Biochim. Biophys. Acta 2007, 1773:556-564.
-
(2007)
Biochim. Biophys. Acta
, vol.1773
, pp. 556-564
-
-
Kumata, Y.1
Tada, S.2
Yamanada, Y.3
Tsuyama, T.4
Kobayashi, T.5
Dong, Y.P.6
Ikegami, K.7
Murofushi, H.8
Seki, M.9
Enomoto, T.10
-
21
-
-
27144460601
-
The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability
-
Petkovic M., Dietschy T., Freire R., Jiao R., Stagljar I. The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability. J. Cell Sci. 2005, 118:4261-4269.
-
(2005)
J. Cell Sci.
, vol.118
, pp. 4261-4269
-
-
Petkovic, M.1
Dietschy, T.2
Freire, R.3
Jiao, R.4
Stagljar, I.5
-
22
-
-
77956707391
-
The involvement of human RECQL4 in DNA double strand break repair
-
Singh D.K., Karmakar P., Aamann M., Schurman S.H., May A., Croteau D.L., Burks L., Plon S.E., Bohr V.A. The involvement of human RECQL4 in DNA double strand break repair. Aging Cell 2010, 9:358-371.
-
(2010)
Aging Cell
, vol.9
, pp. 358-371
-
-
Singh, D.K.1
Karmakar, P.2
Aamann, M.3
Schurman, S.H.4
May, A.5
Croteau, D.L.6
Burks, L.7
Plon, S.E.8
Bohr, V.A.9
-
23
-
-
69449097526
-
Direct and indirect roles of RECQL4 in modulating base excision repair capacity
-
Schurman S.H., Hedayati M., Wang Z., Singh D.K., Speina E., Zhang Y., Becker K., Macris M., Sung P., Wilson D.M., Croteau D.L., Bohr V.A. Direct and indirect roles of RECQL4 in modulating base excision repair capacity. Hum. Mol. Genet. 2009, 18:3470-3483.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3470-3483
-
-
Schurman, S.H.1
Hedayati, M.2
Wang, Z.3
Singh, D.K.4
Speina, E.5
Zhang, Y.6
Becker, K.7
Macris, M.8
Sung, P.9
Wilson, D.M.10
Croteau, D.L.11
Bohr, V.A.12
-
24
-
-
57649198428
-
RecQ4 facilitates UV light-induced DNA damage repair through interaction with nucleotide excision repair factor xeroderma pigmentosum group A (XPA)
-
Fan W., Luo J. RecQ4 facilitates UV light-induced DNA damage repair through interaction with nucleotide excision repair factor xeroderma pigmentosum group A (XPA). J. Biol. Chem. 2008, 283:29037-29044.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 29037-29044
-
-
Fan, W.1
Luo, J.2
-
25
-
-
45049086666
-
Sensitivity of RECQL4-deficient fibroblasts from Rothmund-Thomson syndrome patients to genotoxic agents
-
Jin W., Liu H., Zhang Y., Otta S.K., Plon S.E., Wang L.L. Sensitivity of RECQL4-deficient fibroblasts from Rothmund-Thomson syndrome patients to genotoxic agents. Hum. Genet. 2008, 123:643-653.
-
(2008)
Hum. Genet.
, vol.123
, pp. 643-653
-
-
Jin, W.1
Liu, H.2
Zhang, Y.3
Otta, S.K.4
Plon, S.E.5
Wang, L.L.6
-
26
-
-
49249109473
-
Identification of new RECQL4 mutations in Caucasian Rothmund-Thomson patients and analysis of sensitivity to a wide range of genotoxic agents
-
Cabral R.E., Queille S., Bodemer C., de Prost Y., Neto J.B., Sarasin A., Daya-Grosjean L. Identification of new RECQL4 mutations in Caucasian Rothmund-Thomson patients and analysis of sensitivity to a wide range of genotoxic agents. Mutat. Res. 2008, 643:41-47.
-
(2008)
Mutat. Res.
, vol.643
, pp. 41-47
-
-
Cabral, R.E.1
Queille, S.2
Bodemer, C.3
de Prost, Y.4
Neto, J.B.5
Sarasin, A.6
Daya-Grosjean, L.7
-
27
-
-
0026720075
-
Tight control of gene expression in mammalian cells by tetracycline-responsive promoters
-
Gossen M., Bujard H. Tight control of gene expression in mammalian cells by tetracycline-responsive promoters. Proc. Natl Acad. Sci. USA 1992, 89:5547-5551.
-
(1992)
Proc. Natl Acad. Sci. USA
, vol.89
, pp. 5547-5551
-
-
Gossen, M.1
Bujard, H.2
-
28
-
-
33746966063
-
Bloom helicase and DNA topoisomerase III alpha 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 F.A., Tanabe H., Ishii Y., Enomoto T. Bloom helicase and DNA topoisomerase III alpha are involved in the dissolution of sister chromatids. Mol. Cell. Biol. 2006, 26:6299-6307.
-
(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
-
29
-
-
52149121819
-
KU70/80, DNA-PKcs, and Artemis are essential for the rapid induction of apoptosis after massive DSB formation
-
Abe T., Ishiai M., Hosono Y., Yoshimura A., Tada S., Adachi N., Koyama H., Takata M., Takeda S., Enomoto T., Seki M. KU70/80, DNA-PKcs, and Artemis are essential for the rapid induction of apoptosis after massive DSB formation. Cell. Signal. 2008, 20:1978-1985.
-
(2008)
Cell. Signal.
, vol.20
, pp. 1978-1985
-
-
Abe, T.1
Ishiai, M.2
Hosono, Y.3
Yoshimura, A.4
Tada, S.5
Adachi, N.6
Koyama, H.7
Takata, M.8
Takeda, S.9
Enomoto, T.10
Seki, M.11
|