-
1
-
-
0030691121
-
Hierarchical deterioration of body systems in Werner's syndrome: Implications for normal ageing
-
Goto, M. Hierarchical deterioration of body systems in Werner's syndrome: implications for normal ageing. Mech. Ageing Dev. 98, 239-254 (1997).
-
(1997)
Mech. Ageing Dev.
, vol.98
, pp. 239-254
-
-
Goto, M.1
-
2
-
-
0037530653
-
Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process
-
Opresko, P.L., Cheng, W.H., von Kobbe, C., Harrigan, J.A. & Bohr, V.A. Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process. Carcinogenesis 24, 791-802 (2003).
-
(2003)
Carcinogenesis
, vol.24
, pp. 791-802
-
-
Opresko, P.L.1
Cheng, W.H.2
Von Kobbe, C.3
Harrigan, J.A.4
Bohr, V.A.5
-
3
-
-
15844409553
-
Positional cloning of the Werner's syndrome gene
-
Yu, C.E. et al. Positional cloning of the Werner's syndrome gene. Science 272, 258-262 (1996).
-
(1996)
Science
, vol.272
, pp. 258-262
-
-
Yu, C.E.1
-
4
-
-
0037107539
-
A nucleolar targeting sequence in the Werner syndrome protein resides within residues 949-1092
-
von Kobbe, C. & Bohr, V.A. A nucleolar targeting sequence in the Werner syndrome protein resides within residues 949-1092. J. Cell Sci. 115, 3901-3907 (2002).
-
(2002)
J. Cell Sci.
, vol.115
, pp. 3901-3907
-
-
Von Kobbe, C.1
Bohr, V.A.2
-
5
-
-
0031204917
-
Impaired nuclear localization of defective DNA helicases in Werner's syndrome
-
Matsumoto, T., Shimamoto, A., Goto, M. & Furuichi, Y. Impaired nuclear localization of defective DNA helicases in Werner's syndrome. Nat. Genet. 16, 335-336 (1997).
-
(1997)
Nat. Genet.
, vol.16
, pp. 335-336
-
-
Matsumoto, T.1
Shimamoto, A.2
Goto, M.3
Furuichi, Y.4
-
6
-
-
0034650238
-
WRN helicase expression in Werner syndrome cell lines
-
Moser, M.J. et al. WRN helicase expression in Werner syndrome cell lines. Nucleic Acids Res. 28, 648-654 (2000).
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 648-654
-
-
Moser, M.J.1
-
7
-
-
0032848570
-
Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products
-
Goto, M. et al. Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products. Hum. Genet. 105, 301-307 (1999).
-
(1999)
Hum. Genet.
, vol.105
, pp. 301-307
-
-
Goto, M.1
-
8
-
-
0037364415
-
RecQ helicases: Caretakers of the genome
-
Hickson, I.D. RecQ helicases: caretakers of the genome. Nat. Rev. Cancer 3, 169-178 (2003).
-
(2003)
Nat. Rev. Cancer
, vol.3
, pp. 169-178
-
-
Hickson, I.D.1
-
9
-
-
0031574363
-
The proofreading domain of Escherichia coli DNA polymerase I and other DNA and/or RNA exonuclease domains
-
Moser, M.J., Holley, W.R., Chatterjee, A. & Mian, I.S. The proofreading domain of Escherichia coli DNA polymerase I and other DNA and/or RNA exonuclease domains. Nucleic Acids Res. 25, 5110-5118 (1997).
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 5110-5118
-
-
Moser, M.J.1
Holley, W.R.2
Chatterjee, A.3
Mian, I.S.4
-
10
-
-
0030915681
-
Positionally cloned human disease genes: Patterns of evolutionary conservation and functional motifs
-
Mushegian, A.R., Bassett, D.E., Jr., Boguski, M.S., Bork, P. & Koonin, E.V. Positionally cloned human disease genes: patterns of evolutionary conservation and functional motifs. Proc. Natl. Acad. Sci. USA 94, 5831-5836 (1997).
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 5831-5836
-
-
Mushegian, A.R.1
Bassett Jr., D.E.2
Boguski, M.S.3
Bork, P.4
Koonin, E.V.5
-
11
-
-
0031686571
-
The premature ageing syndrome protein, WRN, is a 3′ → 5′ exonuclease
-
Huang, S. et al. The premature ageing syndrome protein, WRN, is a 3′ → 5′ exonuclease. Nat. Genet. 20, 114-116 (1998).
-
(1998)
Nat. Genet.
, vol.20
, pp. 114-116
-
-
Huang, S.1
-
12
-
-
0347362703
-
Werner syndrome protein contains three structure-specific DNA binding domains
-
von Kobbe, C., Thoma, N.H., Czyzewski, B.K., Pavletich, N.P. & Bohr, V.A. Werner syndrome protein contains three structure-specific DNA binding domains. J. Biol. Chem. 278, 52997-53006 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 52997-53006
-
-
Von Kobbe, C.1
Thoma, N.H.2
Czyzewski, B.K.3
Pavletich, N.P.4
Bohr, V.A.5
-
13
-
-
0035976963
-
Coordinate action of the helicase and 3′ to 5′ exonuclease of Werner syndrome protein
-
Opresko, P.L., Laine, J.P., Brosh, R.M., Jr., Seidman, M.M. & Bohr, V.A. Coordinate action of the helicase and 3′ to 5′ exonuclease of Werner syndrome protein. J. Biol. Chem. 276, 44677-44687 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 44677-44687
-
-
Opresko, P.L.1
Laine, J.P.2
Brosh Jr., R.M.3
Seidman, M.M.4
Bohr, V.A.5
-
14
-
-
4344649442
-
The Werner syndrome protein at the crossroads of DNA repair and apoptosis
-
Comai, L. & Li, B. The Werner syndrome protein at the crossroads of DNA repair and apoptosis. Mech. Ageing Dev. 125, 521-528 (2004).
-
(2004)
Mech. Ageing Dev.
, vol.125
, pp. 521-528
-
-
Comai, L.1
Li, B.2
-
15
-
-
2442660468
-
Linkage between Werner syndrome protein and the Mre11 complex via Nbs1
-
Cheng, W.H. et al. Linkage between Werner syndrome protein and the Mre11 complex via Nbs1. J. Biol. Chem. 279, 21169-21176 (2004).
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 21169-21176
-
-
Cheng, W.H.1
-
16
-
-
0035851181
-
Werner syndrome protein is regulated and phosphorylated by DNA-dependent protein kinase
-
Yannone, S.M. et al. Werner syndrome protein is regulated and phosphorylated by DNA-dependent protein kinase. J. Biol. Chem. 276, 38242-38248 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 38242-38248
-
-
Yannone, S.M.1
-
17
-
-
0141480945
-
WRN interacts physically and functionally with the recombination mediator protein RAD52
-
Baynton, K. et al. WRN interacts physically and functionally with the recombination mediator protein RAD52. J. Biol. Chem. 278, 36476-36486 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 36476-36486
-
-
Baynton, K.1
-
18
-
-
0035009356
-
Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51
-
Sakamoto, S. et al. Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51. Genes Cells 6, 421-430 (2001).
-
(2001)
Genes Cells
, vol.6
, pp. 421-430
-
-
Sakamoto, S.1
-
19
-
-
0034655912
-
Ku complex interacts with and stimulates the Werner protein
-
Cooper, M.P. et al. Ku complex interacts with and stimulates the Werner protein. Genes Dev. 14, 907-912 (2000).
-
(2000)
Genes Dev.
, vol.14
, pp. 907-912
-
-
Cooper, M.P.1
-
20
-
-
0034665971
-
Functional interaction between Ku and the werner syndrome protein in DNA end processing
-
Li, B. & Comai, L. Functional interaction between Ku and the werner syndrome protein in DNA end processing. J. Biol. Chem. 275, 39800 (2000).
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 39800
-
-
Li, B.1
Comai, L.2
-
21
-
-
0035339672
-
A functional interaction of Ku with Werner exonuclease facilitates digestion of damaged DNA
-
Orren, D.K. et al. A functional interaction of Ku with Werner exonuclease facilitates digestion of damaged DNA. Nucleic Acids Res. 29, 1926-1934 (2001).
-
(2001)
Nucleic Acids Res.
, vol.29
, pp. 1926-1934
-
-
Orren, D.K.1
-
22
-
-
0035971076
-
Requirements for the nucleolytic processing of DNA ends by the Werner syndrome protein-Ku70/80 complex
-
Li, B. & Comai, L. Requirements for the nucleolytic processing of DNA ends by the Werner syndrome protein-Ku70/80 complex. J. Biol. Chem. 276, 9896-9902 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 9896-9902
-
-
Li, B.1
Comai, L.2
-
23
-
-
0036714151
-
Displacement of DNA-PKcs from DNA ends by the Werner syndrome protein
-
Li, B. & Comai, L. Displacement of DNA-PKcs from DNA ends by the Werner syndrome protein. Nucleic Acids Res. 30, 3653-3661 (2002).
-
(2002)
Nucleic Acids Res.
, vol.30
, pp. 3653-3661
-
-
Li, B.1
Comai, L.2
-
24
-
-
0037166306
-
Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation
-
Karmakar, P. et al. Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation. J. Biol. Chem. 277, 18291-18302 (2002).
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 18291-18302
-
-
Karmakar, P.1
-
25
-
-
1842791545
-
Identification and biochemical characterization of a Werner's syndrome protein complex with Ku70/80 and poly (ADP-ribose) polymerase-1
-
Li, B., Navarro, S., Kasahara, N. & Comai, L. Identification and biochemical characterization of a Werner's syndrome protein complex with Ku70/80 and poly (ADP-ribose) polymerase-1. J. Biol. Chem. 279, 13659-13667 (2004).
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 13659-13667
-
-
Li, B.1
Navarro, S.2
Kasahara, N.3
Comai, L.4
-
26
-
-
0026019625
-
Structural basis for the 3′-5′ exonuclease activity of Escherichia coli DNA polymerase I: A two metal ion mechanism
-
Beese, L.S. & Steitz, T.A. Structural basis for the 3′-5′ exonuclease activity of Escherichia coli DNA polymerase I: a two metal ion mechanism. EMBO J. 10, 25-33 (1991).
-
(1991)
EMBO J.
, vol.10
, pp. 25-33
-
-
Beese, L.S.1
Steitz, T.A.2
-
27
-
-
0033531970
-
Human glutathione transferase A4-4 crystal structures and mutagenesis reveal the basis of high catalytic efficiency with toxic lipid peroxidation products
-
Bruns, C.M., Hubatsch, I., Ridderstrom, M., Mannervik, B. & Tainer, J.A. Human glutathione transferase A4-4 crystal structures and mutagenesis reveal the basis of high catalytic efficiency with toxic lipid peroxidation products. J. Mol. Biol. 288, 427-439 (1999).
-
(1999)
J. Mol. Biol.
, vol.288
, pp. 427-439
-
-
Bruns, C.M.1
Hubatsch, I.2
Ridderstrom, M.3
Mannervik, B.4
Tainer, J.A.5
-
28
-
-
0033485840
-
Structural elucidation of the binding and inhibitory properties of lanthanide (III) ions at the 3′-5′ exonucleolytic active site of the Klenow fragment
-
Brautigam, C.A., Aschheim, K. & Steitz, T.A. Structural elucidation of the binding and inhibitory properties of lanthanide (III) ions at the 3′-5′ exonucleolytic active site of the Klenow fragment. Chem. Biol. 6, 901-908 (1999).
-
(1999)
Chem. Biol.
, vol.6
, pp. 901-908
-
-
Brautigam, C.A.1
Aschheim, K.2
Steitz, T.A.3
-
29
-
-
0032571245
-
Structural principles for the inhibition of the 3′-5′ exonuclease activity of Escherichia coli DNA polymerase I by phosphorothioates
-
Brautigam, C.A. & Steitz, T.A. Structural principles for the inhibition of the 3′-5′ exonuclease activity of Escherichia coli DNA polymerase I by phosphorothioates. J. Mol. Biol. 277, 363-377 (1998).
-
(1998)
J. Mol. Biol.
, vol.277
, pp. 363-377
-
-
Brautigam, C.A.1
Steitz, T.A.2
-
30
-
-
0029666424
-
Crystal structures of an NH2-terminal fragment of T4 DNA polymerase and its complexes with single-stranded DNA and with divalent metal ions
-
Wang, J., Yu, P., Lin, T.C., Konigsberg, W.H. & Steitz, T.A. Crystal structures of an NH2-terminal fragment of T4 DNA polymerase and its complexes with single-stranded DNA and with divalent metal ions. Biochemistry 35, 8110-8119 (1996).
-
(1996)
Biochemistry
, vol.35
, pp. 8110-8119
-
-
Wang, J.1
Yu, P.2
Lin, T.C.3
Konigsberg, W.H.4
Steitz, T.A.5
-
31
-
-
0032518398
-
Crystal structure of a bacteriophage T7 DNA replication complex at 2.2 A resolution
-
Doublie, S., Tabor, S., Long, A.M., Richardson, C.C. & Ellenberger, T. Crystal structure of a bacteriophage T7 DNA replication complex at 2.2 A resolution. Nature 391, 251-258 (1998).
-
(1998)
Nature
, vol.391
, pp. 251-258
-
-
Doublie, S.1
Tabor, S.2
Long, A.M.3
Richardson, C.C.4
Ellenberger, T.5
-
32
-
-
0033616725
-
Crystal structure of a thermostable type B DNA polymerase from Thermococcus gorgonarius
-
Hopfner, K.P. et al. Crystal structure of a thermostable type B DNA polymerase from Thermococcus gorgonarius. Proc. Natl. Acad. Sci. USA 96, 3600-3605 (1999).
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 3600-3605
-
-
Hopfner, K.P.1
-
33
-
-
11244258888
-
The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834C
-
Kamath-Loeb, A.S., Welcsh, P., Waite, M., Adman, E.T. & Loeb, L.A. The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834C. J. Biol. Chem. 279, 55499-55505 (2004).
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 55499-55505
-
-
Kamath-Loeb, A.S.1
Welcsh, P.2
Waite, M.3
Adman, E.T.4
Loeb, L.A.5
-
34
-
-
0141865522
-
High-resolution structure of the E. coli RecQ helicase catalytic core
-
Bernstein, D.A., Zittel, M.C. & Keck, J.L. High-resolution structure of the E. coli RecQ helicase catalytic core. EMBO J. 22, 4910-4921 (2003).
-
(2003)
EMBO J.
, vol.22
, pp. 4910-4921
-
-
Bernstein, D.A.1
Zittel, M.C.2
Keck, J.L.3
-
35
-
-
0037081095
-
Lack of WRN results in extensive deletion at nonhomologous joining ends
-
Oshima, J., Huang, S., Pae, C., Campisi, J. & Schiestl, R.H. Lack of WRN results in extensive deletion at nonhomologous joining ends. Cancer Res. 62, 547-551 (2002).
-
(2002)
Cancer Res.
, vol.62
, pp. 547-551
-
-
Oshima, J.1
Huang, S.2
Pae, C.3
Campisi, J.4
Schiestl, R.H.5
-
36
-
-
10344256183
-
Defective telomere lagging strand synthesis in cells lacking WRN helicase activity
-
Crabbe, L., Verdun, R.E., Haggblom, C.I. & Karlseder, J. Defective telomere lagging strand synthesis in cells lacking WRN helicase activity. Science 306, 1951-1953 (2004).
-
(2004)
Science
, vol.306
, pp. 1951-1953
-
-
Crabbe, L.1
Verdun, R.E.2
Haggblom, C.I.3
Karlseder, J.4
-
37
-
-
27644443332
-
Elevated telomere-telomere recombination in WRN-deficient, telomere dysfunctional cells promotes escape from senescence and engagement of the ALT pathway
-
Laud, P.R. et al. Elevated telomere-telomere recombination in WRN-deficient, telomere dysfunctional cells promotes escape from senescence and engagement of the ALT pathway. Genes Dev. 19, 2560-2570 (2005).
-
(2005)
Genes Dev.
, vol.19
, pp. 2560-2570
-
-
Laud, P.R.1
-
38
-
-
0032502886
-
Rejoining of DNA by the RAG1 and RAG2 proteins
-
Melek, M., Gellert, M. & van Gent, D.C. Rejoining of DNA by the RAG1 and RAG2 proteins. Science 280, 301-303 (1998).
-
(1998)
Science
, vol.280
, pp. 301-303
-
-
Melek, M.1
Gellert, M.2
Van Gent, D.C.3
-
39
-
-
0036206462
-
Different types of V(D)J recombination and end-joining defects in DNA double-strand break repair mutant mammalian cells
-
Verkaik, N.S. et al. Different types of V(D)J recombination and end-joining defects in DNA double-strand break repair mutant mammalian cells. Eur. J. Immunol. 32, 701-709 (2002).
-
(2002)
Eur. J. Immunol.
, vol.32
, pp. 701-709
-
-
Verkaik, N.S.1
-
40
-
-
0037038362
-
Nbs1 is essential for DNA repair by homologous recombination in higher vertebrate cells
-
Tauchi, H. et al. Nbs1 is essential for DNA repair by homologous recombination in higher vertebrate cells. Nature 420, 93-98 (2002).
-
(2002)
Nature
, vol.420
, pp. 93-98
-
-
Tauchi, H.1
-
41
-
-
0141740425
-
WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair
-
Chen, L. et al. WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair. Aging Cell 2, 191-199 (2003).
-
(2003)
Aging Cell
, vol.2
, pp. 191-199
-
-
Chen, L.1
-
42
-
-
27144551710
-
Accumulation of Werner protein at DNA double-strand breaks in human cells
-
Lan, L. et al. Accumulation of Werner protein at DNA double-strand breaks in human cells. J. Cell Sci. 118, 4153-4162 (2005).
-
(2005)
J. Cell Sci.
, vol.118
, pp. 4153-4162
-
-
Lan, L.1
-
43
-
-
4344706812
-
Werner syndrome protein - Unwinding function to explain disease
-
Monnat, R.J., Jr. & Saintigny, Y. Werner syndrome protein - unwinding function to explain disease. Sci. Aging Knowledge Environ. 2004, re3 (2004).
-
(2004)
Sci. Aging Knowledge Environ.
, vol.2004
-
-
Monnat Jr., R.J.1
Saintigny, Y.2
-
44
-
-
1842685207
-
The Werner syndrome protein has separable recombination and survival functions
-
Swanson, C., Saintigny, Y., Emond, M.J. & Monnat, R.J., Jr. The Werner syndrome protein has separable recombination and survival functions. DNA Repair (Amst.) 3, 475-482 (2004).
-
(2004)
DNA Repair (Amst.)
, vol.3
, pp. 475-482
-
-
Swanson, C.1
Saintigny, Y.2
Emond, M.J.3
Monnat Jr., R.J.4
-
46
-
-
0034660246
-
Characterization of the human and mouse WRN 3′ → 5′ exonuclease
-
Huang, S. et al. Characterization of the human and mouse WRN 3′ → 5′ exonuclease. Nucleic Acids Res. 28, 2396-2405 (2000).
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 2396-2405
-
-
Huang, S.1
-
47
-
-
0033519722
-
Oligomeric ring structure of the Bloom's syndrome helicase
-
Karow, J.K., Newman, R.H., Freemont, P.S. & Hickson, I.D. Oligomeric ring structure of the Bloom's syndrome helicase. Curr. Biol. 9, 597-600 (1999).
-
(1999)
Curr. Biol.
, vol.9
, pp. 597-600
-
-
Karow, J.K.1
Newman, R.H.2
Freemont, P.S.3
Hickson, I.D.4
-
48
-
-
0037022821
-
A minimal exonuclease domain of WRN forms a hexamer on DNA and possesses both 3′ - 5′ exonuclease and 5′-protruding strand endonuclease activities
-
Xue, Y. et al. A minimal exonuclease domain of WRN forms a hexamer on DNA and possesses both 3′ - 5′ exonuclease and 5′-protruding strand endonuclease activities. Biochemistry 41, 2901-2912 (2002).
-
(2002)
Biochemistry
, vol.41
, pp. 2901-2912
-
-
Xue, Y.1
-
49
-
-
0035833552
-
Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair
-
Walker, J.R., Corpina, R.A. & Goldberg, J. Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair. Nature 412, 607-614 (2001).
-
(2001)
Nature
, vol.412
, pp. 607-614
-
-
Walker, J.R.1
Corpina, R.A.2
Goldberg, J.3
-
50
-
-
3242880580
-
Structure and function of the double-strand break repair machinery
-
Shin, D.S., Chahwan, C., Huffman, J.L. & Tainer, J.A. Structure and function of the double-strand break repair machinery. DNA Repair (Amst.) 3, 863-873 (2004).
-
(2004)
DNA Repair (Amst.)
, vol.3
, pp. 863-873
-
-
Shin, D.S.1
Chahwan, C.2
Huffman, J.L.3
Tainer, J.A.4
|