-
1
-
-
69249209608
-
RecQ helicases: multifunctional genome caretakers
-
Chu WK, Hickson ID, (2009) RecQ helicases: multifunctional genome caretakers. Nature reviews Cancer 9: 644-654.
-
(2009)
Nature Reviews Cancer
, vol.9
, pp. 644-654
-
-
Chu, W.K.1
Hickson, I.D.2
-
2
-
-
78649467087
-
Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology
-
Monnat RJ Jr, (2010) Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology. Seminars in cancer biology 20: 329-339.
-
(2010)
Seminars in Cancer Biology
, vol.20
, pp. 329-339
-
-
Monnat Jr., R.J.1
-
3
-
-
0031686571
-
The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease
-
Huang S, Li B, Gray MD, Oshima J, Mian IS, et al. (1998) The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease. Nat Genet 20: 114-116.
-
(1998)
Nat Genet
, vol.20
, pp. 114-116
-
-
Huang, S.1
Li, B.2
Gray, M.D.3
Oshima, J.4
Mian, I.S.5
-
4
-
-
0032545515
-
Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide
-
Shen JC, Gray MD, Oshima J, Kamath-Loeb AS, Fry M, et al. (1998) Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide. J Biol Chem 273: 34139-34144.
-
(1998)
J Biol Chem
, vol.273
, pp. 34139-34144
-
-
Shen, J.C.1
Gray, M.D.2
Oshima, J.3
Kamath-Loeb, A.S.4
Fry, M.5
-
5
-
-
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, (1966) Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process. Medicine 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
-
6
-
-
55749095542
-
The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis
-
Muftuoglu M, Oshima J, von Kobbe C, Cheng WH, Leistritz DF, et al. (2008) The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis. Human genetics 124: 369-377.
-
(2008)
Human Genetics
, vol.124
, pp. 369-377
-
-
Muftuoglu, M.1
Oshima, J.2
von Kobbe, C.3
Cheng, W.H.4
Leistritz, D.F.5
-
7
-
-
2542499623
-
Clinical features of Bloom syndrome and function of the causative gene, BLM helicase
-
Kaneko H, Kondo N, (2004) Clinical features of Bloom syndrome and function of the causative gene, BLM helicase. Expert review of molecular diagnostics 4: 393-401.
-
(2004)
Expert Review of Molecular Diagnostics
, vol.4
, pp. 393-401
-
-
Kaneko, H.1
Kondo, N.2
-
8
-
-
0001542940
-
Chromosomal Breakage in a Rare and Probably Genetically Determined Syndrome of Man
-
German J, Archibald R, Bloom D, (1965) Chromosomal Breakage in a Rare and Probably Genetically Determined Syndrome of Man. Science 148: 506-507.
-
(1965)
Science
, vol.148
, pp. 506-507
-
-
German, J.1
Archibald, R.2
Bloom, D.3
-
9
-
-
76749168005
-
Roles of Werner syndrome protein in protection of genome integrity
-
Rossi ML, Ghosh AK, Bohr VA, (2010) Roles of Werner syndrome protein in protection of genome integrity. DNA repair 9: 331-344.
-
(2010)
DNA Repair
, vol.9
, pp. 331-344
-
-
Rossi, M.L.1
Ghosh, A.K.2
Bohr, V.A.3
-
11
-
-
0035393720
-
The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases
-
Mohaghegh P, Karow JK, Brosh RM Jr, Jr, Bohr VA, Hickson ID, (2001) The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases. Nucleic Acids Res 29: 2843-2849.
-
(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
-
12
-
-
0033617316
-
Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n
-
Fry M, Loeb LA, (1999) Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n. J Biol Chem 274: 12797-12802.
-
(1999)
J Biol Chem
, vol.274
, pp. 12797-12802
-
-
Fry, M.1
Loeb, L.A.2
-
13
-
-
0032538453
-
The Bloom's syndrome helicase unwinds G4 DNA
-
Sun H, Karow JK, Hickson ID, Maizels N, (1998) The Bloom's syndrome helicase unwinds G4 DNA. J Biol Chem 273: 27587-27592.
-
(1998)
J Biol Chem
, vol.273
, pp. 27587-27592
-
-
Sun, H.1
Karow, J.K.2
Hickson, I.D.3
Maizels, N.4
-
14
-
-
33646843592
-
Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase
-
Bachrati CZ, Borts RH, Hickson ID, (2006) Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase. Nucleic Acids Res 34: 2269-2279.
-
(2006)
Nucleic Acids Res
, vol.34
, pp. 2269-2279
-
-
Bachrati, C.Z.1
Borts, R.H.2
Hickson, I.D.3
-
15
-
-
54349099705
-
RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability
-
Xu D, Guo R, Sobeck A, Bachrati CZ, Yang J, et al. (2008) RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability. Genes < development 22: 2843-2855.
-
(2008)
Genes < Development
, vol.22
, pp. 2843-2855
-
-
Xu, D.1
Guo, R.2
Sobeck, A.3
Bachrati, C.Z.4
Yang, J.5
-
16
-
-
54349114671
-
BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome
-
Singh TR, Ali AM, Busygina V, Raynard S, Fan Q, et al. (2008) BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome. Genes < development 22: 2856-2868.
-
(2008)
Genes < Development
, vol.22
, pp. 2856-2868
-
-
Singh, T.R.1
Ali, A.M.2
Busygina, V.3
Raynard, S.4
Fan, Q.5
-
17
-
-
77954382263
-
Human topoisomerase IIIalpha is a single-stranded DNA decatenase that is stimulated by BLM and RMI1
-
Yang J, Bachrati CZ, Ou J, Hickson ID, Brown GW, (2010) Human topoisomerase IIIalpha is a single-stranded DNA decatenase that is stimulated by BLM and RMI1. The Journal of biological chemistry 285: 21426-21436.
-
(2010)
The Journal of Biological Chemistry
, vol.285
, pp. 21426-21436
-
-
Yang, J.1
Bachrati, C.Z.2
Ou, J.3
Hickson, I.D.4
Brown, G.W.5
-
18
-
-
0030751354
-
The Werner syndrome protein is a DNA helicase
-
Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, et al. (1997) The Werner syndrome protein is a DNA helicase. Nature genetics 17: 100-103.
-
(1997)
Nature Genetics
, 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
-
20
-
-
0003855149
-
Short Protocol in Molecular Biology
-
Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K, (2002) Short Protocol in Molecular Biology. pp. 8-7 to 8-11.
-
(2002)
-
-
Ausubel, F.M.1
Brent, R.2
Kingston, R.E.3
Moore, D.D.4
Seidman, J.G.5
Smith, J.A.6
Struhl, K.7
-
21
-
-
11244258888
-
The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834C
-
Kamath-Loeb AS, Welcsh P, Waite M, Adman ET, Loeb LA, (2004) The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834C. The Journal of biological chemistry 279: 55499-55505.
-
(2004)
The Journal of Biological Chemistry
, vol.279
, pp. 55499-55505
-
-
Kamath-Loeb, A.S.1
Welcsh, P.2
Waite, M.3
Adman, E.T.4
Loeb, L.A.5
-
22
-
-
0031047969
-
Purification and characterization of qTBP42, a new single-stranded and quadruplex telomeric DNA-binding protein from rat hepatocytes
-
Sarig G, Weisman-Shomer P, Erlitzki R, Fry M, (1997) Purification and characterization of qTBP42, a new single-stranded and quadruplex telomeric DNA-binding protein from rat hepatocytes. J Biol Chem 272: 4474-4482.
-
(1997)
J Biol Chem
, vol.272
, pp. 4474-4482
-
-
Sarig, G.1
Weisman-Shomer, P.2
Erlitzki, R.3
Fry, M.4
-
23
-
-
0034695638
-
Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins
-
Weisman-Shomer P, Naot Y, Fry M, (2000) Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins. J Biol Chem 275: 2231-2238.
-
(2000)
J Biol Chem
, vol.275
, pp. 2231-2238
-
-
Weisman-Shomer, P.1
Naot, Y.2
Fry, M.3
-
24
-
-
0033135161
-
The Saccharomyces cerevisiae Sgs1 helicase efficiently unwinds G-G paired DNAs
-
Sun H, Bennett RJ, Maizels N, (1999) The Saccharomyces cerevisiae Sgs1 helicase efficiently unwinds G-G paired DNAs. Nucleic Acids Res 27: 1978-1984.
-
(1999)
Nucleic Acids Res
, vol.27
, pp. 1978-1984
-
-
Sun, H.1
Bennett, R.J.2
Maizels, N.3
-
25
-
-
0031589543
-
Telomeric and tetraplex DNA binding properties of qTBP42: a homologue of the CArG box binding protein CBF-A
-
Sarig G, Weisman-Shomer P, Fry M, (1997) Telomeric and tetraplex DNA binding properties of qTBP42: a homologue of the CArG box binding protein CBF-A. Biochem Biophys Res Commun 237: 617-623.
-
(1997)
Biochem Biophys Res Commun
, vol.237
, pp. 617-623
-
-
Sarig, G.1
Weisman-Shomer, P.2
Fry, M.3
-
26
-
-
54049147388
-
The Werner syndrome protein binds replication fork and holliday junction DNAs as an oligomer
-
Compton SA, Tolun G, Kamath-Loeb AS, Loeb LA, Griffith JD, (2008) The Werner syndrome protein binds replication fork and holliday junction DNAs as an oligomer. The Journal of biological chemistry 283: 24478-24483.
-
(2008)
The Journal of Biological Chemistry
, vol.283
, pp. 24478-24483
-
-
Compton, S.A.1
Tolun, G.2
Kamath-Loeb, A.S.3
Loeb, L.A.4
Griffith, J.D.5
-
27
-
-
0037106470
-
G4 DNA unwinding by BLM and Sgs1p: substrate specificity and substrate-specific inhibition
-
Huber MD, Lee DC, Maizels N, (2002) G4 DNA unwinding by BLM and Sgs1p: substrate specificity and substrate-specific inhibition. Nucleic Acids Res 30: 3954-3961.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 3954-3961
-
-
Huber, M.D.1
Lee, D.C.2
Maizels, N.3
-
28
-
-
33646100776
-
A conserved G4 DNA binding domain in RecQ family helicases
-
Huber MD, Duquette ML, Shiels JC, Maizels N, (2006) A conserved G4 DNA binding domain in RecQ family helicases. J Mol Biol 358: 1071-1080.
-
(2006)
J Mol Biol
, vol.358
, pp. 1071-1080
-
-
Huber, M.D.1
Duquette, M.L.2
Shiels, J.C.3
Maizels, N.4
-
29
-
-
0034655991
-
BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures
-
Wang Y, Cortez D, Yazdi P, Neff N, Elledge SJ, et al. (2000) BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures. Genes < development 14: 927-939.
-
(2000)
Genes < Development
, vol.14
, pp. 927-939
-
-
Wang, Y.1
Cortez, D.2
Yazdi, P.3
Neff, N.4
Elledge, S.J.5
-
30
-
-
79951813659
-
Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome
-
Suhasini AN, Rawtani NA, Wu Y, Sommers JA, Sharma S, et al. (2011) Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome. The EMBO journal 30: 692-705.
-
(2011)
The EMBO Journal
, vol.30
, pp. 692-705
-
-
Suhasini, A.N.1
Rawtani, N.A.2
Wu, Y.3
Sommers, J.A.4
Sharma, S.5
|