-
1
-
-
0034578446
-
Dna helicases, genomic instability, and human genetic disease
-
AJ van Brabant, R Stan, NA Ellis. DNA helicases, genomic instability, and human genetic disease. Annu Rev of Genomics Hum Genet 1:409-459, 2000.
-
(2000)
Annu Rev of Genomics Hum Genet
, vol.1
, pp. 409-459
-
-
Van Brabant, A.J.R.1
Stan Ellis, N.A.2
-
2
-
-
84944972302
-
Congenital telangiectatic erythema resembling lupus erythematosus in dwarfs
-
D Bloom. Congenital telangiectatic erythema resembling lupus erythematosus in dwarfs. Am J Dis Child 88:754-758, 1954.
-
(1954)
Am J Dis Child
, vol.88
, pp. 754-758
-
-
Bloom, D.1
-
3
-
-
0002715953
-
Bloom syndrome
-
CR Scriver, AL Beaudet, WS Sly, D Valle, eds. New York: McGraw-Hill
-
J German, NA Ellis. Bloom syndrome. In: Metabolic and Molecular Basis of Inherited Disease. CR Scriver, AL Beaudet, WS Sly, D Valle, eds. New York: McGraw-Hill, 2000, pp 733-752.
-
(2000)
Metabolic and Molecular Basis of Inherited Disease
, pp. 733-752
-
-
German, J.1
Ellis, N.A.2
-
5
-
-
0021941956
-
Mitotic chiasmata, gene density, and oncogenes
-
EM Kuhn, E Therman, C Denniston. Mitotic chiasmata, gene density, and oncogenes. Hum Genet 70:1-5, 1985.
-
(1985)
Hum Genet
, vol.70
, pp. 1-5
-
-
Kuhn, E.M.E.1
Therman Denniston, C.2
-
6
-
-
0346351375
-
A manyfold increase in sister chromatid exchanges in bloom’s syndrome lymphocytes
-
RS Chaganti, S Schonberg, J German. A manyfold increase in sister chromatid exchanges in Bloom’s syndrome lymphocytes. Proc Natl Acad Sci USA 71:4508-4512, 1974.
-
(1974)
Proc Natl Acad Sci USA
, vol.71
, pp. 4508-4512
-
-
Chaganti, R.S.S.1
Schonberg German, J.2
-
7
-
-
3142544243
-
Evidence for increased in vivo mutation and somatic recombination in bloom syndrome
-
RG Langlois, WL Bigbee, RH Jensen, J German. Evidence for increased in vivo mutation and somatic recombination in Bloom syndrome. Proc Natl Acad Sci USA 86:670-674, 1989.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 670-674
-
-
Langlois, R.1
Bigbee, R.H.2
Jensen German, J.3
-
8
-
-
0024325920
-
Frequency of variant erythrocytes at the glycophorin-a locus in two bloom’s syndrome patients
-
S Kyoizumi, N Nakamura, H Takebe, K Tatsumi, J German, M Akiyama. Frequency of variant erythrocytes at the glycophorin-A locus in two Bloom’s syndrome patients. Mutat Res 214:215-222, 1989.
-
(1989)
Mutat Res
, vol.214
, pp. 215-222
-
-
Kyoizumi, S.N.1
Nakamura, H.2
Takebe, K.3
Tatsumi, J.4
German Akiyama, M.5
-
9
-
-
0020619254
-
Bloom syndrome: Evidence for an increased mutation frequency in vivo
-
Vijayalaxmi, HJ Evans, JH Ray, J German. Bloom syndrome: evidence for an increased mutation frequency in vivo. Science 221:851-853, 1983.
-
(1983)
Science
, vol.221
, pp. 851-853
-
-
Vijayalaxmi, H.J.1
Evans, J.H.2
Ray German, J.3
-
10
-
-
0028223554
-
Increased rate of spontaneous mitotic recombination in t lymphocytes from a bloom syndrome patient using a flow-cytometric assay at hla-a locus
-
Y Kusunoki, T Hayashi, Y Hirai, J Kushiro, K Tatsumi, T Kurihara, M Zghal, et al. Increased rate of spontaneous mitotic recombination in T lymphocytes from a Bloom syndrome patient using a flow-cytometric assay at HLA-A locus. Jpn J Cancer Res 85:610-618, 1994.
-
(1994)
Jpn J Cancer Res
, vol.85
, pp. 610-618
-
-
Kusunoki, Y.T.1
Hayashi, Y.2
Hirai, J.3
Kushiro, K.4
Tatsumi, T.5
Kurihara Zghal, M.6
-
11
-
-
0029915524
-
Large deletions at the hprt locus associated with the mutator phenotype in a bloom’s syndrome lymphoblastoid cell line
-
A Tachibana, K Tatsumi, T Masui, T Kato. Large deletions at the HPRT locus associated with the mutator phenotype in a Bloom’s syndrome lymphoblastoid cell line. Mol Carcinog 17:41-47, 1996.
-
(1996)
Mol Carcinog
, vol.17
, pp. 41-47
-
-
Tachibana, A.K.1
Tatsumi, T.2
Masui Kato, T.3
-
12
-
-
0027051362
-
Bloom’s syndrome. Xviii. Hypermutability at a tandem-repeat locus
-
J Groden, J German. Bloom’s syndrome. XVIII. Hypermutability at a tandem-repeat locus. Hum Genet 90:360-367, 1992.
-
(1992)
Hum Genet
, vol.90
, pp. 360-367
-
-
Groden, J.1
German, J.2
-
13
-
-
0025362253
-
Molecular evidence that homologous recombination occurs in proliferating human somatic cells
-
J Groden, Y Nakamura, J German. Molecular evidence that homologous recombination occurs in proliferating human somatic cells. Proc Natl Acad Sci USA 87: 4315-4319, 1990.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 4315-4319
-
-
Groden, J.Y.1
Nakamura German, J.2
-
14
-
-
0019570997
-
Elevated spontaneous mutation rate in bloom syndrome fibroblasts
-
ST Warren, RA Schultz, CC Change, MH Wade, JE Trosko. Elevated spontaneous mutation rate in Bloom syndrome fibroblasts. Proc Natl Acad Sci USA 78:3133-3137, 1981.
-
(1981)
Proc Natl Acad Sci USA
, vol.78
, pp. 3133-3137
-
-
Warren, S.1
Schultz, C.C.2
Change, M.H.3
Wade Trosko, J.E.4
-
15
-
-
0019168989
-
Diphtheria toxin resistance in human fibroblast cell strains from normal and cancer-prone individuals
-
RS Gupta, S Goldstein. Diphtheria toxin resistance in human fibroblast cell strains from normal and cancer-prone individuals. Mutat Res 73:331-338, 1980.
-
(1980)
Mutat Res
, vol.73
, pp. 331-338
-
-
Gupta, R.S.1
Goldstein, S.2
-
16
-
-
0021997395
-
Elevated spontaneous mutation rate in sv40-transformed werner syndrome fibroblast cell lines
-
K Fukuchi, K Tanaka, J Nakura, Y Kumahara, T Uchida, Y Okada. Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines. Somat Cell Mol Genet 11:303-308, 1985.
-
(1985)
Somat Cell Mol Genet
, vol.11
, pp. 303-308
-
-
Fukuchi, K.K.1
Tanaka, J.2
Nakura, Y.3
Kumahara, T.4
Uchida Okada, Y.5
-
17
-
-
0031751941
-
Vivo somatic mutations in werner’s syndrome
-
S Kyoizumi, Y Kusunoki, T Seyama, A Hatamochi, M Goto. In vivo somatic mutations in Werner’s syndrome. Hum Genet 103:405-410, 1998.
-
(1998)
Hum Genet
, vol.103
, pp. 405-410
-
-
Kyoizumi, S.Y.1
Kusunoki, T.2
Seyama Hatamochi, A.3
Goto, M.4
-
18
-
-
0034194139
-
Genetic instability and hematologic disease risk in werner syndrome patients and heterozygotes
-
MJ Moser, WL Bigbee, SG Grant, MJ Emond, RG Langlois, RH Jensen, J Oshima, RJ Monnat Jr. Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes. Cancer Res 60:2492-2496, 2000.
-
(2000)
Cancer Res
, vol.60
, pp. 2492-2496
-
-
Moser, M.1
Bigbee, S.G.2
Grant, M.J.3
Emond, R.G.4
Langlois, R.H.5
Jensen, J.6
Oshima Monnat, R.J.7
-
19
-
-
0016678691
-
Variegated translocation mosaicism in human skin fibroblast cultures
-
H Hoehn, EM Bryant, K Au, TH Norwood, H Boman, GM Martin. Variegated translocation mosaicism in human skin fibroblast cultures. Cytogenet Cell Genet 15:282-298, 1975.
-
(1975)
Cytogenet Cell Genet
, vol.15
, pp. 282-298
-
-
Hoehn, K.A.1
Norwood, T.H.H.2
Boman Martin, G.M.3
-
20
-
-
0020460340
-
Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with werner’s syndrome
-
S Scappaticci, D Cerimele, M Fraccaro. Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner’s syndrome. Hum Genet 62:16-24, 1982.
-
(1982)
Hum Genet
, vol.62
, pp. 16-24
-
-
Scappaticci, S.D.1
Cerimele Fraccaro, M.2
-
21
-
-
0034486160
-
Spectral karyotyping of werner syndrome fibroblast cultures
-
R Melcher, R von Golitschek, C Steinlein, D Schindler, H Neitzel, K Kainer, M Schmid, H Hoehn. Spectral karyotyping of Werner syndrome fibroblast cultures. Cytogenet Cell Genet 91:180-185, 2000.
-
(2000)
Cytogenet Cell Genet
, vol.91
, pp. 180-185
-
-
Melcher, R.R.1
Von Golitschek, C.2
Steinlein, D.3
Schindler, H.4
Neitzel, K.5
Kainer, M.6
Schmid Hoehn, H.7
-
22
-
-
0018873418
-
Studies on the ultraviolet light sensitivity of bloom’s syndrome fibroblasts
-
AB Krepinsky, AJ Rainbow, JA Heddle. Studies on the ultraviolet light sensitivity of Bloom’s syndrome fibroblasts. Mutat Res 69:357-368, 1980.
-
(1980)
Mutat Res
, vol.69
, pp. 357-368
-
-
Krepinsky, A.1
Rainbow Heddle, J.A.2
-
23
-
-
0019352718
-
Dna repair in bloom’s syndrome fibroblasts after uv irradiation or treatment with mitomycin c
-
K Ishizaki, T Yagi, M Inoue, O Nikaido, H Takebe. DNA repair in Bloom’s syndrome fibroblasts after UV irradiation or treatment with mitomycin C. Mutat Res 80:213-219, 1981.
-
(1981)
Mutat Res
, vol.80
, pp. 213-219
-
-
Ishizaki, K.T.1
Yagi, M.2
Inoue, O.3
Nikaido Takebe, H.4
-
24
-
-
0018286806
-
Sensitivity of bloom’s syndrome lymphocytes to ethyl methanesulfonate
-
AB Krepinsky, JA Heddle, J German. Sensitivity of Bloom’s syndrome lymphocytes to ethyl methanesulfonate. Hum Genet 50:151-156, 1979.
-
(1979)
Hum Genet
, vol.50
, pp. 151-156
-
-
Krepinsky, A.1
Heddle German, J.2
-
25
-
-
0023201158
-
Hypersensitivity of bloom’s syndrome fibroblasts to n-ethyl-n-nitrosourea
-
T Kurihara, M Inoue, K Tatsumi. Hypersensitivity of Bloom’s syndrome fibroblasts to N-ethyl-N-nitrosourea. Mutat Res 184:147-151, 1987.
-
(1987)
Mutat Res
, vol.184
, pp. 147-151
-
-
Kurihara, T.M.1
Inoue Tatsumi, K.2
-
26
-
-
0031453968
-
An apoptosis-inducing genotoxin differentiates heterozygotic carriers for werner helicase mutations from wild-type and homozygous mutants
-
CE Ogburn, J Oshima, M Poot, R Chen, KE Hunt, KA Gollahon, PS Rabinovitch, GM Martin. An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants. Hum Genet 101:121-125, 1997.
-
(1997)
Hum Genet
, vol.101
, pp. 121-125
-
-
Ogburn, C.E.J.1
Oshima, M.2
Poot, R.3
Chen, K.E.4
Hunt, K.A.5
Gollahon, P.S.6
Rabinovitch Martin, G.M.7
-
27
-
-
0033010781
-
Werner syndrome lymphoblastoid cells are sensitive to camptothecin-induced apoptosis in s-phase
-
M Poot, KA Gollahon, PS Rabinovitch. Werner syndrome lymphoblastoid cells are sensitive to camptothecin-induced apoptosis in S-phase. Hum Genet 104:10-14, 1999.
-
(1999)
Hum Genet
, vol.104
, pp. 10-14
-
-
Poot, M.K.1
Gollahon Rabinovitch, P.S.2
-
28
-
-
0035349905
-
Werner syndrome cells are sensitive to dna cross-linking drugs
-
M Poot, JS Yom, SH Whang, JT Kato, KA Gollahon, PS Rabinovitch. Werner syndrome cells are sensitive to DNA cross-linking drugs. FASEB J 15:1224-1226, 2001.
-
(2001)
FASEB J
, vol.15
, pp. 1224-1226
-
-
Poot, M.J.1
Yom, S.H.2
Whang, J.T.3
Kato, K.A.4
Gollahon Rabinovitch, P.S.5
-
29
-
-
0024591985
-
Bloom syndrome. Xii. Report from the registry for 1987
-
J German, E Passarge. Bloom syndrome. XII. Report from the Registry for 1987. Clin Genet 35:57-69, 1989.
-
(1989)
Clin Genet
, vol.35
, pp. 57-69
-
-
German, J.1
Passarge, E.2
-
30
-
-
0014486220
-
Bloom’s syndrome. I. Genetical and clinical observations in the first twenty-seven patients
-
J German. Bloom’s syndrome. I. Genetical and clinical observations in the first twenty-seven patients. Am J Hum Genet 21:196-227, 1969.
-
(1969)
Am J Hum Genet
, vol.21
, pp. 196-227
-
-
German, J.1
-
31
-
-
0023943610
-
Bloom syndrome: A single complementation group defines patients of diverse ethnic origin
-
R Weksberg, C Smith, L Anson-Cartwright, K Maloney. Bloom syndrome: a single complementation group defines patients of diverse ethnic origin. Am J Hum Genet 42:816-824, 1988.
-
(1988)
Am J Hum Genet
, vol.42
, pp. 816-824
-
-
Weksberg, R.C.1
Smith, L.2
Anson-Cartwright Maloney, K.3
-
32
-
-
0026732784
-
Elevated sister chromatid exchange phenotype of bloom syndrome cells is complemented by human chromosome 15
-
LD McDaniel, RA Schultz. Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15. Proc Natl Acad Sci USA 89:7968-7972, 1992.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 7968-7972
-
-
McDaniel, L.D.1
Schultz, R.A.2
-
33
-
-
0028355717
-
Bloom syndrome: An analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1
-
J German, AM Roe, M Leppert, NA Ellis. Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1. Proc Natl Acad Sci USA 91:6669-6673, 1994.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6669-6673
-
-
German, J.A.1
Roe, M.2
Leppert Ellis, N.A.3
-
34
-
-
3042945232
-
Bloom’s syndrome. Viii. Review of clinical and genetic aspects
-
RM Goodman, AG Motulsky, eds. New York: Raven Press
-
J German. Bloom’s syndrome. VIII. Review of clinical and genetic aspects. In Genetic Diseases among Ashkenazi Jews. RM Goodman, AG Motulsky, eds. New York: Raven Press, 1979, pp 121-139.
-
(1979)
Genetic Diseases among Ashkenazi Jews
, pp. 121-139
-
-
German, J.1
-
35
-
-
0028108115
-
Linkage disequilibrium between the fes, d15s127, and blm loci in ashkenazi jews with bloom syndrome
-
NA Ellis, AM Roe, J Kozloski, M Proytcheva, C Falk, J German. Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome. Am J Hum Genet 55:453-460, 1994.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 453-460
-
-
Ellis, N.1
Roe, J.2
Kozloski, M.3
Proytcheva, C.4
Falk German, J.5
-
36
-
-
0028785586
-
The bloom’s syndrome gene product is homologous to recq helicases
-
NA Ellis, J Groden, T-Z Ye, J Straughen, DJ Lennon, S Ciocci, M Proytcheva, J German. The Bloom’s syndrome gene product is homologous to RecQ helicases. Cell 83:655-666, 1995.
-
(1995)
Cell
, vol.83
, pp. 655-666
-
-
Ellis, N.A.J.1
Groden, T.-Z.2
Ye, J.3
Straughen, D.J.4
Lennon, S.5
Ciocci, M.6
Proytcheva German, J.7
-
38
-
-
0017748038
-
Bloom syndrome. Iv. Sister-chro-matid exchanges in lymphocytes
-
J German, S Schonberg, E Louie, RSK Chaganti. Bloom syndrome. IV. Sister-chro-matid exchanges in lymphocytes. Am J Hum Genet 29: 248-255, 1977.
-
(1977)
Am J Hum Genet
, vol.29
, pp. 248-255
-
-
German, J.S.1
Schonberg, E.2
Louie Chaganti, R.3
-
39
-
-
0029986276
-
Bloom’s syndrome. Xix. Cytogenetic and population evidence for genetic heterogeneity
-
J German, NA Ellis, M Proytcheva. Bloom’s syndrome. XIX. Cytogenetic and population evidence for genetic heterogeneity. Clin Genet 49:223-231, 1996.
-
(1996)
Clin Genet
, vol.49
, pp. 223-231
-
-
German, J.N.1
Ellis Proytcheva, M.2
-
40
-
-
0028859379
-
Somatic intragenic recombination within the mutated locus blm can correct the high-sce phenotype of bloom syndrome cells
-
NA Ellis, DJ Lennon, M Proytcheva, B Alhadeff, EE Henderson, J German. Somatic intragenic recombination within the mutated locus BLM can correct the high-SCE phenotype of Bloom syndrome cells. Am J Hum Genet 57:1019-1027, 1995.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1019-1027
-
-
Ellis, N.1
Lennon, M.2
Proytcheva, B.3
Alhadeff, E.E.4
Henderson German, J.5
-
41
-
-
0027221506
-
A genetic analysis of the werner syndrome region on human chromosome 8p
-
W Thomas, M Rubenstein, M Goto, D Drayna. A genetic analysis of the Werner syndrome region on human chromosome 8p. Genomics 16:685-690, 1993.
-
(1993)
Genomics
, vol.16
, pp. 685-690
-
-
Thomas, W.M.1
Rubenstein, M.2
Goto Drayna, D.3
-
42
-
-
0026588296
-
Homozygosity mapping and werner’s syndrome
-
GD Schellenberg, GM Martin, EM Wijsman, J Nakura, T Miki, T Ogihara. Homozygosity mapping and Werner’s syndrome. Lancet 339:1002, 1992.
-
(1992)
Lancet
, vol.339
, pp. 1002
-
-
Schellenberg, G.1
Martin, E.M.2
Wijsman, J.3
Nakura, T.4
Miki Ogihara, T.5
-
43
-
-
0028128738
-
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and werner syndrome
-
CE Yu, J Oshima, KA Goddard, T Miki, J Nakura, T Ogihara, M Poot, H Hoehn, M Fraccaro, C Piussan, et al. Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome. Am J Hum Genet 55: 356-364, 1994.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 356-364
-
-
Yu, C.E.J.1
Oshima, K.A.2
Goddard, T.3
Miki, J.4
Nakura, T.5
Ogihara, M.6
Poot, H.7
Hoehn, M.8
Fraccaro Piussan, C.9
-
44
-
-
0033028692
-
Wrn mutations in werner syndrome
-
MJ Moser, J Oshima, RJ Monnat Jr. WRN mutations in Werner syndrome. Hum Mutat 13:271-279, 1999.
-
(1999)
Hum Mutat
, vol.13
, pp. 271-279
-
-
Mj Moser, J.1
OshimaMonnat, R.J.2
-
45
-
-
15844409553
-
Positional cloning of the werner’s syndrome gene
-
CE Yu, J Oshima, YH Fu, EM Wijsman, F Hisama, R Alisch, S Matthews, J Nakura, T Miki, S Ouais, GM Martin, J Mulligan, GD Schellenberg. Positional cloning of the Werner’s syndrome gene. Science 272:258-262, 1996.
-
(1996)
Science
, vol.272
, pp. 258-262
-
-
Yu Oshima Fu, J.Y.H.1
Wijsman, E.M.F.2
Hisama, R.3
Alisch, S.4
Matthews, J.5
Nakura, T.6
Miki, S.7
Ouais, G.M.8
Martin, J.9
Mulligan Schellenberg, G.D.10
-
46
-
-
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
-
H Nakayama, K Nakayama, R Nakayama, N Irino, Y Nakayama, PC Hanawalt. 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 195:474-480, 1984.
-
(1984)
Mol Gen Genet
, vol.195
, pp. 474-480
-
-
Nakayama, H.K.1
Nakayama, R.2
Nakayama, N.3
Irino, Y.4
Nakayama Hanawalt, P.C.5
-
47
-
-
0028033989
-
The yeast type i topoisomerase top3 interacts with sgs1, a dna helicase homolog: A potential eukaryotic reverse gyrase
-
S Gangloff, JP McDonald, C Bendixen, L Arthur, R Rothstein. The yeast type I topoisomerase top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase. Mol Cell Biol 14:8391-8398, 1994.
-
(1994)
Mol Cell Biol
, vol.14
, pp. 8391-8398
-
-
Gangloff, S.J.1
McDonald, C.2
Bendixen, L.3
Arthur Rothstein, R.4
-
48
-
-
0030994386
-
Rqh1 +, a fission yeast gene related to the bloom’s and werner’s syndrome genes, is required for reversible s phase arrest
-
E Stewart, CR Chapman, F Al-Khodairy, AM Carr, T Enoch. rqh1 +, A fission yeast gene related to the Bloom’s and Werner’s syndrome genes, is required for reversible S phase arrest. EMBO J 16:2682-2692, 1997.
-
(1997)
EMBO J
, vol.16
, pp. 2682-2692
-
-
Stewart, E.C.1
Chapman, F.2
Al-Khodairy, A.M.3
Carr Enoch, T.4
-
49
-
-
0033046015
-
Engels. Evolution of the recq family of heliacases: A drosophila homolog, dmblm, is similar to the human bloom syndrome gene
-
K Kusano, ME Berres, WR Engels. Evolution of the RECQ family of heliacases: a drosophila homolog, Dmblm, is similar to the human Bloom syndrome gene. Genetics 151:1027-1039, 1999.
-
(1999)
Genetics
, vol.151
, pp. 1027-1039
-
-
K Kusano, M.E.1
Berres, W.R.2
-
50
-
-
0034326274
-
Molecular characterisation of recq homologues in arabidopsis thaliana
-
F Hartung, H Plchova, H Puchta. Molecular characterisation of RecQ homologues in Arabidopsis thaliana. Nucleic Acids Res 28:4275-4282, 2000.
-
(2000)
Nucleic Acids Res
, vol.28
, pp. 4275-4282
-
-
Hartung, F.H.1
Plchova Puchta, H.2
-
51
-
-
0035809934
-
Evidence for a replication function of ffa-1, the xenopus orthologue of werner syndrome protein
-
CY Chen, J Graham, H Yan. Evidence for a replication function of FFA-1, the Xenopus orthologue of Werner syndrome protein. J Cell Biol 152:985-996, 2001.
-
(2001)
J Cell Biol
, vol.152
, pp. 985-996
-
-
Chen, C.Y.J.1
Graham Yan, H.2
-
52
-
-
0034667907
-
The function of xenopus bloom’s syndrome protein homolog (xblm) in dna replication
-
S Liao, J Graham, H Yan. The function of Xenopus Bloom’s syndrome protein homolog (xBLM) in DNA replication. Genes Dev 14:2570-2575, 2000.
-
(2000)
Genes Dev
, vol.14
, pp. 2570-2575
-
-
Liao, S.J.1
Graham Yan, H.2
-
53
-
-
0034600976
-
Possible association of blm in decreasing dna double strand breaks during dna replication
-
W Wang, M Seki, Y Narita, E Sonoda, S Takeda, K Yamada, T Masuko, T Katada, T Enomoto. Possible association of BLM in decreasing DNA double strand breaks during DNA replication. EMBO J 19:3428-3435, 2000.
-
(2000)
EMBO J
, vol.19
, pp. 3428-3435
-
-
Wang, W.M.1
Seki, Y.2
Narita, E.3
Sonoda, S.4
Takeda, K.5
Yamada, T.6
Masuko, T.7
Katada Enomoto, T.8
-
54
-
-
0032570031
-
Cloning of two isoforms of mouse dna helicase q1/recql cdna; alpha form is expressed ubiquitously and beta form specifically in the testis
-
WS Wang, M Seki, T Yamaoka, T Seki, S Tada, T Katada, H Fujimoto, T Enomoto. Cloning of two isoforms of mouse DNA helicase Q1/RecQL cDNA; alpha form is expressed ubiquitously and beta form specifically in the testis. Biochim Biophys Acta 1443:198-202, 1998.
-
(1998)
Biochim Biophys Acta
, vol.1443
, pp. 198-202
-
-
Wang, W.S.M.1
Seki, T.2
Yamaoka, T.3
Seki, S.4
Tada, T.5
Katada, H.6
Fujimoto Enomoto, T.7
-
55
-
-
0032213939
-
Stage-specific apoptosis, developmental delay, and embryonic lethality in mice homozygous for a targeted disruption in the murine bloom’s syndrome gene
-
N Chester, F Kuo, C Kozak, CD O’Hara, P Leder. Stage-specific apoptosis, developmental delay, and embryonic lethality in mice homozygous for a targeted disruption in the murine Bloom’s syndrome gene. Genes Dev 12:3382-3393, 1998.
-
(1998)
Genes Dev
, vol.12
, pp. 3382-3393
-
-
Chester, N.F.1
Kuo, C.2
Kozak, C.D.3
O’Hara Leder, P.4
-
56
-
-
0033667704
-
Cancer predisposition caused by elevated mitotic recombination in bloom mice
-
G Luo, IM Santoro, LD McDaniel, I Nishijima, M Mills, H Youssoufian, H Vogel, RA Schultz, A Bradley. Cancer predisposition caused by elevated mitotic recombination in Bloom mice. Nat Genet 26:424-429, 2000.
-
(2000)
Nat Genet
, vol.26
, pp. 424-429
-
-
Luo, G.I.1
Santoro, L.D.2
McDaniel, I.3
Nishijima, M.4
Mills, H.5
Youssoufian, H.6
Vogel, R.A.7
Schultz Bradley, A.8
-
57
-
-
0032573157
-
A deletion within the murine werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity
-
M Lebel, P Leder. A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity. Proc Natl Acad Sci USA 95:13097-13102, 1998.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 13097-13102
-
-
Lebel, M.1
Leder, P.2
-
58
-
-
0033978881
-
Cellular werner phenotypes in mice expressing a putative dominant-negative human wrn gene
-
L Wang, CE Ogburn, CB Ware, WC Ladiges, H Youssoufian, GM Martin, J Os-hima. Cellular Werner phenotypes in mice expressing a putative dominant-negative human WRN gene. Genetics 154:357-362, 2000.
-
(2000)
Genetics
, vol.154
, pp. 357-362
-
-
Wang, L.C.1
Ogburn, C.B.2
Ware, W.C.3
Ladiges, H.4
Youssoufian, G.M.5
Martin, J.6
-
59
-
-
0034739792
-
Cloning, genomic structure and chromosomal localization of the gene encoding mouse dna helicase recq helicase protein-like 4
-
T Ohhata, R Araki, R Fukumura, A Kuroiwa, Y Matsuda, K Tatsumi, M Abe. Cloning, genomic structure and chromosomal localization of the gene encoding mouse DNA helicase RecQ helicase protein-like 4. Gene 261:251-258, 2000.
-
(2000)
Gene
, vol.261
, pp. 251-258
-
-
Ohhata, T.R.1
Araki, R.2
Fukumura, A.3
Kuroiwa, Y.4
Matsuda, K.5
Tatsumi Abe, M.6
-
60
-
-
0027942415
-
Pj blackshear.Cloning and characterization of recql, a potential human homologue of the escherichia coli dna helicase recq
-
KL Puranam, PJ Blackshear.Cloning and characterization of RECQL, a potential human homologue of the Escherichia coli DNA helicase RecQ. J Biol Chem 269:29838-29845, 1994.
-
(1994)
J Biol Chem
, vol.269
, pp. 29838-29845
-
-
Puranam, K.L.1
-
61
-
-
0028061993
-
Molecular cloning of cdna encoding human dna helicase q1 which has homology to escherichia coli rec q helicase and localization of the gene at chromosome l2pl2
-
M Seki, H Miyazawa, S Tada, J Yanagisawa, T Yamaoka, S Hoshino, K Ozawa, T Eki. Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli Rec Q helicase and localization of the gene at chromosome l2pl2. Nucleic Acids Res 22:4566-4573, 1994.
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 4566-4573
-
-
Seki, M.H.1
Miyazawa, S.2
Tada, J.3
Yanagisawa, T.4
Yamaoka, S.5
Hoshino, K.6
Ozawa Eki, T.7
-
62
-
-
0032736140
-
Rothmund-thomson syndrome responsible gene, recql4: Genomic structure and products
-
M Nogami, K Okumura, S Kitao, NM Lindor, M Shiratori, Y Furuichi, A Shi-mamoto S. Rothmund-Thomson syndrome responsible gene, RECQL4: genomic structure and products. Genomics 61:268-276, 1999.
-
(1999)
Genomics
, vol.61
, pp. 268-276
-
-
Nogami, M.K.1
Okumura, S.2
Kitao, N.M.3
Lindor, M.4
Shiratori, Y.5
Furuichi, A.6
Shi-Mamoto, S.7
-
63
-
-
0032939991
-
Mutations in recql4 cause a subset of cases of rothmund-thomson syndrome
-
S Kitao, A Shimamoto, M Goto, RW Miller, WA Smithson, NM Lindor, Y Furuichi. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. Nat Genet 22:82-84, 1999.
-
(1999)
Nat Genet
, vol.22
, pp. 82-84
-
-
Kitao, S.A.1
Shimamoto, M.2
Goto, R.W.3
Miller, W.A.4
Smithson, N.M.5
Lindor Furuichi, Y.6
-
64
-
-
0032535661
-
Cloning of two new human helicase genes of the recq family: Biological significance of multiple species in higher eukaryotes
-
S Kitao, I Ohsugi, K Ichikawa, M Goto, Y Furuichi, A Shimamoto. Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes. Genomics 54:443-452, 1998.
-
(1998)
Genomics
, vol.54
, pp. 443-452
-
-
Kitao, S.I.1
Ohsugi, K.2
Ichikawa, M.3
Goto, Y.4
Furuichi Shimamoto, A.5
-
65
-
-
0032964641
-
The dna helicase activity of blm is necessary for the correction of the genomic instability of bloom syndrome cells
-
NF Neff, NA Ellis, TZ Ye, J Noonan, K Huang, M Sanz, M Proytcheva. The DNA helicase activity of BLM is necessary for the correction of the genomic instability of bloom syndrome cells. Mol Biol Cell 10:665-676, 1999.
-
(1999)
Mol Biol Cell
, vol.10
, pp. 665-676
-
-
Neff, N.1
Ellis, T.Z.2
Ye, J.3
Noonan, K.4
Huang, M.5
Sanz Proytcheva, M.6
-
66
-
-
0032547953
-
Point mutations causing bloom’s syndrome abolish atpase and dna helicase activities of the blm protein
-
A Bahr, F De Graeve, C Kedinger, B Chatton. Point mutations causing Bloom’s syndrome abolish ATPase and DNA helicase activities of the BLM protein. Oncogene 17:2565-2571, 1998.
-
(1998)
Oncogene
, vol.17
, pp. 2565-2571
-
-
Bahr, A.F.1
De Graeve, C.2
Kedinger Chatton, B.3
-
67
-
-
0030697336
-
A putative nucleic acid-binding domain in bloom’s and werner’s syndrome helicases
-
V Morozov, AR Mushegian, EV Koonin, P Bork. A putative nucleic acid-binding domain in Bloom’s and Werner’s syndrome helicases. Trends Biochem Sci 22: 417-418, 1997.
-
(1997)
Trends Biochem Sci
, vol.22
, pp. 417-418
-
-
Morozov, V.A.1
Mushegian, E.V.2
Koonin Bork, P.3
-
68
-
-
0031576552
-
Blm (the causative gene of bloom syndrome) protein translocation into the nucleus by a nuclear localization signal
-
H Kaneko, KO Orii, E Matsui, N Shimozawa, T Fukao, T Matsumoto, A Shi-mamoto, Y Furuichi, S Hayakawa, K Kasahara, N Kondo. BLM (the causative gene of Bloom syndrome) protein translocation into the nucleus by a nuclear localization signal. Biochem Biophys Res Commun 240:348-353, 1997.
-
(1997)
Biochem Biophys Res Commun
, vol.240
, pp. 348-353
-
-
Kaneko, H.K.1
Orii, E.2
Matsui, N.3
Shimozawa, T.4
Fukao, T.5
Matsumoto, A.6
Shi-Mamoto, Y.7
Furuichi, S.8
Hayakawa, K.9
Kasahara Kondo, N.10
-
69
-
-
0031686571
-
The premature ageing syndrome protein, wrn, is a 3′→5′ exonuclease
-
S Huang, B Li, MD Gray, J Oshima, IS Mian, J Campisi. 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
Li, B.2
Gray, M.D.3
Oshima, J.4
Mian, I.S.5
Campisi, J.6
-
70
-
-
0032545515
-
Werner syndrome protein. I. Dna helicase and dna exonuclease reside on the same polypeptide
-
JC Shen, MD Gray, J Oshima, AS Kamath-Loeb, M Fry, LA Loeb. Werner syndrome protein. I. DNA helicase and DNA exonuclease reside on the same polypeptide. J Biol Chem 273:34139-34144, 1998.
-
(1998)
J Biol Chem
, vol.273
, pp. 34139-34144
-
-
Shen, J.1
Gray, J.2
Oshima, A.S.3
Kamath-Loeb, M.4
Fry Loeb, L.A.5
-
71
-
-
0030686496
-
The bloom’s syndrome gene product is a 3'-5' dna helicase
-
JK Karow, RK Chakraverty, ID Hickson. The Bloom’s syndrome gene product is a 3'-5' DNA helicase. J Biol Chem 272:30611-30614, 1997.
-
(1997)
J Biol Chem
, vol.272
, pp. 30611-30614
-
-
Karow, J.1
Chakraverty Hickson, I.D.2
-
72
-
-
0032538453
-
The bloom’s syndrome helicase unwinds g4 dna
-
H Sun, JK Karow, ID Hickson, N Maizels. The Bloom’s syndrome helicase unwinds G4 DNA. J Biol Chem 273:27587-27592, 1998.
-
(1998)
J Biol Chem
, vol.273
, pp. 27587-27592
-
-
Sun, H.J.1
Karow, I.D.2
Hickson Maizels, N.3
-
73
-
-
0035793552
-
Unwinding of a dna triple helix by the werner and bloom syndrome helicases
-
RM Brosh Jr, A Majumdar, S Desai, ID Hickson, VA Bohr, MM Seidman. Unwinding of a DNA triple helix by the Werner and Bloom syndrome helicases. J Biol Chem 276:3024-3030, 2001.
-
(2001)
J Biol Chem
, vol.276
, pp. 3024-3030
-
-
Brosh, R.M.A.1
Majumdar, S.2
Desai, I.D.3
Hickson, V.A.4
Bohr Seidman, M.M.5
-
74
-
-
0034612333
-
The bloom’s syndrome gene product promotes branch migration of holliday junctions
-
JK Karow, A Constantinou, JL Li, SC West, ID Hickson. The Bloom’s syndrome gene product promotes branch migration of Holliday junctions. Proc Natl Acad Sci USA 97:6504-6508, 2000.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 6504-6508
-
-
Karow, J.K.A.1
Constantinou, J.L.2
Li, S.C.3
West Hickson, I.D.4
-
75
-
-
0034727684
-
Binding and melting of d-loops by the bloom syndrome helicase
-
AJ van Brabant, T Ye, M Sanz, J German, NA Ellis, WK Holloman. Binding and melting of D-loops by the bloom syndrome helicase. Biochemistry 39: 14617-14625, 2000.
-
(2000)
Biochemistry
, vol.39
, pp. 14617-14625
-
-
Van Brabant, A.J.T.1
Ye, M.2
Sanz, J.3
German, N.A.4
Ellis Holloman, W.K.5
-
76
-
-
0033617316
-
Human werner syndrome dna helicase unwinds tetrahelical structures of the fragile x syndrome repeat sequence d(Cgg)n
-
M Fry, LA Loeb. 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.
-
(1999)
J Biol Chem
, vol.274
, pp. 12797-12802
-
-
Fry, M.1
Loeb, L.A.2
-
77
-
-
0035393720
-
The bloom’s and werner’s syndrome proteins are dna structure-specific helicases
-
P Mohaghegh, JK Karow, RM Jr Brosh Jr, VA Bohr, ID Hickson. The Bloom’s and Werner’s syndrome proteins are DNA structure-specific helicases. Nucleic Acids Res 29:2843-2849, 2001.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 2843-2849
-
-
Mohaghegh, P.1
Karow, J.K.2
Brosh, R.M.3
Bohr, V.A.4
Hickson, I.D.5
-
78
-
-
0345680627
-
Transfection of blm into cultured bloom syndrome cells reduces the sister-chromatid exchange rate toward normal
-
NA Ellis, M Proytcheva, MM Sanz, TZ Ye, J German. Transfection of BLM into cultured Bloom syndrome cells reduces the sister-chromatid exchange rate toward normal. Am J Hum Genet 65:1368-1374, 1999.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1368-1374
-
-
Ellis, N.A.M.1
Proytcheva, M.M.2
Sanz, T.Z.3
Ye German, J.4
-
79
-
-
0033598931
-
A role for pml and the nuclear body in genomic stability
-
S Zhong, P Hu, TZ Ye, R Stan, NA Ellis, PP Pandolfi. A role for PML and the nuclear body in genomic stability. Oncogene 18:7941-7942, 1999.
-
(1999)
Oncogene
, vol.18
, pp. 7941-7942
-
-
Zhong Hu, P.1
Ye, T.Z.R.2
Stan, N.A.3
Ellis Pandolfi, P.P.4
-
80
-
-
0032231606
-
Structure, organization, and dynamics of promyelocytic leukemia protein nuclear bodies
-
M Hodges, C Tissot, K Howe, D Grimwade, PS Freemont. Structure, organization, and dynamics of promyelocytic leukemia protein nuclear bodies. Am J Hum Genet 63:297-304, 1998.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 297-304
-
-
Hodges, M.C.1
Tissot, K.2
Howe, D.3
Grimwade Freemont, P.S.4
-
81
-
-
0035060774
-
Oncogenes and tumor suppressors in the molecular pathogenesis of acute promyelocytic leukemia
-
PP Pandolfi. Oncogenes and tumor suppressors in the molecular pathogenesis of acute promyelocytic leukemia. Hum Mol Genet 10:769-775, 2001.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 769-775
-
-
Pandolfi, P.P.1
-
82
-
-
0034186133
-
The transcriptional role of pml and the nuclear body
-
S Zhong, P Salomoni, PP Pandolfi. The transcriptional role of PML and the nuclear body. Nat Cell Biol 2:85-90, 2000.
-
(2000)
Nat Cell Biol
, vol.2
, pp. 85-90
-
-
Zhong, S.P.1
Salomoni Pandolfi, P.P.2
-
83
-
-
0032143446
-
Nuclear domain 10, the site of dna virus transcription and replication
-
GG Maul. Nuclear domain 10, the site of DNA virus transcription and replication. Bioessays 20:660-667, 1998.
-
(1998)
Bioessays
, vol.20
, pp. 660-667
-
-
Maul, M.1
-
84
-
-
0032721540
-
Pml is critical for nd10 formation and recruits the pml-interacting protein daxx to this nuclear structure when modified by sumo-1
-
AM Ishov, AG Sotnikov, D Negorev, OV Vladimirova, N Neff, T Kamitani, ET Yeh, JF Strauss 3rd, GG Maul. PML is critical for ND10 formation and recruits the PML-interacting protein daxx to this nuclear structure when modified by SUMO-1. J Cell Biol 147:221-234, 1999.
-
(1999)
J Cell Biol
, vol.147
, pp. 221-234
-
-
Ishov, A.1
Sotnikov, D.2
Negorev, O.V.3
Vladimirova, N.4
Neff, T.5
Kamitani, E.T.6
Yeh, J.F.7
Strauss Maul, G.G.8
-
85
-
-
0032760273
-
Localization of the bloom syndrome helicase to punctate nuclear structures and the nuclear matrix and regulation during the cell cycle: Comparison with the werner’s syndrome helicase
-
V Gharibyan, H Youssoufian. Localization of the Bloom syndrome helicase to punctate nuclear structures and the nuclear matrix and regulation during the cell cycle: comparison with the Werner’s syndrome helicase. Mol Carcinog 26:261-273, 1999.
-
(1999)
Mol Carcinog
, vol.26
, pp. 261-273
-
-
Gharibyan, V.1
Youssoufian, H.2
-
86
-
-
0034713244
-
Cell cycle regulation of the endogenous wild type bloom’s syndrome dna helicase
-
S Dutertre, M Ababou, R Onclercq, J Delic, B Chatton, C Jaulin, M Amor-Gueret. Cell cycle regulation of the endogenous wild type Bloom’s syndrome DNA helicase. Oncogene 19:2731-2738, 2000.
-
(2000)
Oncogene
, vol.19
, pp. 2731-2738
-
-
Dutertre, S.M.1
Ababou, R.2
Onclercq, J.3
Delic, B.4
Chatton, C.5
Jaulin Amor-Gueret, M.6
-
87
-
-
0034726966
-
Differential regulation of human recq family helicases in cell transformation and cell cycle
-
T Kawabe, N Tsuyama, S Kitao, K Nishikawa, A Shimamoto, M Shiratori, T Matsumoto, K Anno, T Sato, Y Mitsui, et al. Differential regulation of human RecQ family helicases in cell transformation and cell cycle. Oncogene 19:4764-4772, 2000.
-
(2000)
Oncogene
, vol.19
, pp. 4764-4772
-
-
Kawabe, T.N.1
Tsuyama, S.2
Kitao, K.3
Nishikawa, A.4
Shimamoto, M.5
Shiratori, T.6
Matsumoto, K.7
Anno, T.8
Sato Mitsui, Y.9
-
88
-
-
0034489683
-
Blm, the bloom’s syndrome protein, varies during the cell cycle in its amount, distribution, and colocalization with other nuclear proteins
-
MM Sanz, M Proytcheva, NA Ellis, WK Holloman, J German. BLM, the Bloom’s syndrome protein, varies during the cell cycle in its amount, distribution, and colocalization with other nuclear proteins. Cytogenet Cell Genet 91:217-223, 2000.
-
(2000)
Cytogenet Cell Genet
, vol.91
, pp. 217-223
-
-
Sanz, M.M.1
Proytcheva, M.N.2
Ellis, W.K.3
Holloman German, J.4
-
89
-
-
0034619757
-
Atm-dependent phosphorylation and accumulation of endogenous blm protein in response to ionizing radiation
-
M Ababou, S Dutertre, Y Lecluse, R Onclercq, B Chatton, M Amor-Gueret. ATM-dependent phosphorylation and accumulation of endogenous BLM protein in response to ionizing radiation. Oncogene 19:5955-5963, 2000.
-
(2000)
Oncogene
, vol.19
, pp. 5955-5963
-
-
Ababou, M.S.1
Dutertre, Y.2
Lecluse, R.3
Onclercq, B.4
Chatton Amor-Gueret, M.5
-
90
-
-
0034523266
-
Sumo—nonclassical ubiquitin
-
F Melchior. SUMO—nonclassical ubiquitin. Annu Rev Cell Dev Biol 16:591-626, 2000.
-
(2000)
Annu Rev Cell Dev Biol
, vol.16
, pp. 591-626
-
-
Melchior, F.1
-
91
-
-
0034705319
-
Sumo-1 modification of mdm2 prevents its self-ubiquitination and increases mdm2 ability to ubiquitinate p53
-
T Buschmann, SY Fuchs, CG Lee, ZQ Pan, Z Ronai. SUMO-1 modification of Mdm2 prevents its self-ubiquitination and increases Mdm2 ability to ubiquitinate p53. Cell 101:753-762, 2000.
-
(2000)
Cell
, vol.101
, pp. 753-762
-
-
Buschmann, T.S.1
Fuchs, C.G.2
Lee, Z.Q.3
Pan Ronai, Z.4
-
92
-
-
0343776952
-
Role of sumo-l-modified pml in nuclear body formation
-
S Zhong, S Muller, S Ronchetti, PS Freemont, A Dejean, PP Pandolfi. Role of SUMO-l-modified PML in nuclear body formation. Blood 95:2748-2752, 2000.
-
(2000)
Blood
, vol.95
, pp. 2748-2752
-
-
Zhong, S.S.1
Muller, S.2
Ronchetti, P.S.3
Freemont, A.4
Dejean Pandolfi, P.P.5
-
94
-
-
0033545238
-
Detection by epitope-defined monoclonal antibodies of werner dna helicases in the nucleoplasm and their upregulation by cell transformation and immortalization
-
M Shiratori, S Sakamoto, N Suzuki, Y Tokutake, Y Kawabe, T Enomoto, M Sugimoto, M Goto, T Matsumoto, Y Furuichi. Detection by epitope-defined monoclonal antibodies of Werner DNA helicases in the nucleoplasm and their upregulation by cell transformation and immortalization. J Cell Biol 144:1-9, 1999.
-
(1999)
J Cell Biol
, vol.144
, pp. 1-9
-
-
Shiratori, M.S.1
Sakamoto, N.2
Suzuki, Y.3
Tokutake, Y.4
Kawabe, T.5
Enomoto, M.6
Sugimoto, M.7
Goto, T.8
Matsumoto Furuichi, Y.9
-
95
-
-
0032146147
-
Werner helicase is localized to transcriptionally active nucleoli of cycling cells
-
MD Gray, L Wang, H Youssoufian, GM Martin, J Oshima. Werner helicase is localized to transcriptionally active nucleoli of cycling cells. Exp Cell Res 242: 487-494, 1998.
-
(1998)
Exp Cell Res
, vol.242
, pp. 487-494
-
-
Gray, M.D.L.1
Wang, H.2
Youssoufian, G.M.3
Martin Oshima, J.4
-
96
-
-
0034647556
-
Covalent modification of the werner’s syndrome gene product with the ubiquitin-related protein, sumo-1
-
Y Kawabe, M Seki, T Seki, WS Wang, O Imamura, Y Furuichi, H Saitoh, T Enomoto. Covalent modification of the Werner’s syndrome gene product with the ubiquitin-related protein, SUMO-1. J Biol Chem 275:20963-20966, 2000.
-
(2000)
J Biol Chem
, vol.275
, pp. 20963-20966
-
-
Kawabe, Y.M.1
Seki, T.2
Seki, W.S.3
Wang, O.4
Imamura, Y.5
Furuichi, H.6
Saitoh Enomoto, T.7
-
97
-
-
0034666241
-
Telomere repeat dna forms a large non-covalent complex with unique cohesive properties which is dissociated by werner syndrome dna helicase in the presence of replication protein a
-
I Ohsugi, Y Tokutake, N Suzuki, T Ide, M Sugimoto, Y Furuichi. Telomere repeat DNA forms a large non-covalent complex with unique cohesive properties which is dissociated by Werner syndrome DNA helicase in the presence of replication protein A. Nucleic Acids Res 28:3642-3648, 2000.
-
(2000)
Nucleic Acids Res
, vol.28
, pp. 3642-3648
-
-
Ohsugi, I.Y.1
Tokutake, N.2
Suzuki, T.3
Ide, M.4
Sugimoto Furuichi, Y.5
-
98
-
-
0033199695
-
Telomerase-negative immortalized human cells contain a novel type of promyelo-cytic leukemia (pml) body
-
TR Yeager, AA Neumann, A Englezou, LI Huschtscha, JR Noble, RR Reddel. Telomerase-negative immortalized human cells contain a novel type of promyelo-cytic leukemia (PML) body. Cancer Res 59:4175-4179, 1999.
-
(1999)
Cancer Res
, vol.59
, pp. 4175-4179
-
-
Yeager, T.1
Neumann, A.2
Englezou, L.I.3
Huschtscha, J.R.4
Noble Reddel, R.R.5
-
99
-
-
0033519722
-
Oligomeric ring structure of the bloom’s syndrome helicase
-
JK Karow, RH Newman, PS Freemont, ID Hickson. 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.1
Newman, P.S.2
Freemont Hickson, I.D.3
-
100
-
-
0033230396
-
Purification of overexpressed hexahistidine-tagged blm n431 as oligomeric complexes
-
SF Beresten, R Stan, AJ van Brabant, T Ye, S Naureckiene, NA Ellis. Purification of overexpressed hexahistidine-tagged BLM N431 as oligomeric complexes. Protein Expr Purif 17:239-248, 1999.
-
(1999)
Protein Expr Purif
, vol.17
, pp. 239-248
-
-
Beresten, S.F.R.1
Stan, A.J.2
Van Brabant, T.3
Ye, S.4
Naureckiene Ellis, N.A.5
-
101
-
-
0034660246
-
Characterization of the human and mouse wrn 3'—5' exonuclease
-
S Huang, S Beresten, B Li, J Oshima, NA Ellis, J Campisi. 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.S.1
Beresten, B.2
Li, J.3
Oshima, N.A.4
Ellis Campisi, J.5
-
102
-
-
0034604545
-
Replication protein a physically interacts with the bloom’s syndrome protein and stimulates its helicase activity
-
RM Brosh Jr, JL Li, MK Kenny, JK Karow, MP Cooper, RP Kureekattil, ID Hickson, VA Bohr. Replication protein A physically interacts with the Bloom’s syndrome protein and stimulates its helicase activity. J Biol Chem 275:23500-23508, 2000.
-
(2000)
J Biol Chem
, vol.275
, pp. 23500-23508
-
-
Brosh, R.1
Li, M.K.2
Kenny, J.K.3
Karow, M.P.4
Cooper, R.P.5
Kureekattil, I.D.6
Hickson Bohr, V.A.7
-
103
-
-
0034231844
-
Werner’s syndrome protein (Wrn) migrates holliday junctions and co-localizes with rpa upon replication arrest
-
A Constantinou, M Tarsounas, JK Karow, RM Brosh, VA Bohr, ID Hickson, SC West. Werner’s syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest. EMBO Rep 1:80-84, 2000.
-
(2000)
EMBO Rep
, vol.1
, pp. 80-84
-
-
Constantinou, A.M.1
Tarsounas, J.K.2
Karow, R.M.3
Brosh, V.A.4
Bohr, I.D.5
Hickson West, S.C.6
-
104
-
-
0030014783
-
Dna topoisomerases
-
JC Wang. DNA topoisomerases. Annu Rev Biochem 65:635-692, 1996.
-
(1996)
Annu Rev Biochem
, vol.65
, pp. 635-692
-
-
Wang, J.C.1
-
105
-
-
0024324482
-
A hyper-recombination mutation in s. Cerevisiae identifies a novel eukaryotic topoisomerase
-
JW Wallis, G Chrebet, G Brodsky, M Rolfe, R Rothstein. A hyper-recombination mutation in S. Cerevisiae identifies a novel eukaryotic topoisomerase. Cell 58: 409-419, 1989.
-
(1989)
Cell
, vol.58
, pp. 409-419
-
-
Wallis, J.W.G.1
Chrebet, G.2
Brodsky, M.3
Rolfe Rothstein, R.4
-
106
-
-
0028033989
-
The yeast type i topoisomerase tops interacts with sgsl, a dna helicase homolog: A potential eukaryotic reverse gyrase
-
S Gangloff, JP McDonald, C Bendixen, L Arthur, R Rothstein. The yeast type I topoisomerase TopS interacts with Sgsl, a DNA helicase homolog: a potential eukaryotic reverse gyrase. Mol Cell Biol 14:8391-8398, 1994.
-
(1994)
Mol Cell Biol
, vol.14
, pp. 8391-8398
-
-
Gangloff, S.J.1
McDonald, C.2
Bendixen, L.3
Arthur Rothstein, R.4
-
107
-
-
0034282385
-
Interaction between yeast sgsl helicase and dna topoisomerase iii
-
RJ Bennett, MF Noirot-Gros, JC Wang JC. Interaction between yeast sgsl helicase and DNA topoisomerase III. J Biol Chem 275:26898-26905, 2000.
-
(2000)
J Biol Chem
, vol.275
, pp. 26898-26905
-
-
Bennett, R.1
Noirot-Gros JC, J.C.2
-
108
-
-
0033652754
-
Genetic analysis of the saccharomyces cerevisiae sgsl helicase defines an essential function for the sgsl-tops complex in the absence of srs2 or top1. mol gen genet 264:89-97, 2000. Wm fricke, v kaliraman, sj brill. Mapping the dna topoisomerase iii binding domain of the sgsl dna helicase
-
M Duno, B Thomsen, O Westergaard, L Krejci, C Bendixen. Genetic analysis of the Saccharomyces cerevisiae Sgsl helicase defines an essential function for the Sgsl-TopS complex in the absence of SRS2 or TOP1. Mol Gen Genet 264:89-97, 2000. WM Fricke, V Kaliraman, SJ Brill. Mapping the DNA topoisomerase III binding domain of the Sgsl DNA helicase. J Biol Chem 276:8848-8855, 2001.
-
(2001)
J Biol Chem
, vol.276
, pp. 8848-8855
-
-
Duno, M.B.1
Thomsen, O.2
Westergaard, L.3
Krejci Bendixen, C.4
-
109
-
-
0029657781
-
Sgs1, a homologue of the bloom’s and werner’s syndrome genes, is required for maintenance of genome stability in saccharomyces cerevisiae
-
PM Watt, ID Hickson, RH Borts, EJ Louis. SGS1, a homologue of the Bloom’s and Werner’s syndrome genes, is required for maintenance of genome stability in Saccharomyces cerevisiae. Genetics 144:935-945, 1996.
-
(1996)
Genetics
, vol.144
, pp. 935-945
-
-
Watt, P.1
Hickson, R.H.2
Borts Louis, E.J.3
-
110
-
-
0034737641
-
The bloom’s syndrome gene product interacts with topoisomerase iii
-
L Wu, SL Davies, PS North, H Goulaouic, JF Riou, H Turley, KC Gatter, ID Hickson. The Bloom’s syndrome gene product interacts with topoisomerase III. J Biol Chem 275:9636-9644, 2000.
-
(2000)
J Biol Chem
, vol.275
, pp. 9636-9644
-
-
Wu, L.S.1
Davies, P.S.2
North, H.3
Goulaouic, J.F.4
Riou, H.5
Turley, K.C.6
Gatter Hickson, I.D.7
-
111
-
-
0034162770
-
Association of the bloom syndrome protein with topoisomerase iiialpha in somatic and meiotic cells
-
FB Johnson, DB Lombard, NF Neff, MA Mastrangelo, W Dewolf, NA Ellis, RA Marciniak, Y Yin, R Jaenisch, L Guarente. Association of the Bloom syndrome protein with topoisomerase IIIalpha in somatic and meiotic cells. Cancer Res 60:11621167, 2000.
-
(2000)
Cancer Res
, pp. 60
-
-
Johnson, F.1
Lombard, N.F.2
Neff, M.A.3
Mastrangelo, W.4
Dewolf, N.A.5
Ellis, R.A.6
Marciniak, Y.7
Yin, R.8
Jaenisch Guarente, L.9
-
112
-
-
0035363706
-
Evidence for blm and topoisomerase iiialpha interaction in genomic stability
-
P Hu, SF Beresten, AJ van Brabant, TZ Ye, PP Pandolfi, FB Johnson, L Guarente, NA Ellis. Evidence for BLM and topoisomerase IIIalpha interaction in genomic stability. Hum Mol Genet 10:1287-1298, 2001.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1287-1298
-
-
Hu, P.S.1
Beresten, A.J.2
Van Brabant, T.Z.3
Ye, P.P.4
Pandolfi, F.B.5
Johnson, L.6
Guarente Ellis, N.A.7
-
113
-
-
0035949560
-
Association of yeast dna topoisomerase iii and sgs1 dna helicase: Studies of fusion proteins
-
RJ Bennett, JC Wang. Association of yeast DNA topoisomerase III and Sgs1 DNA helicase: studies of fusion proteins. Proc Natl Acad Sci USA 98:11108-11113, 2001.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 11108-11113
-
-
Bennett, R.J.1
Wang, J.C.2
-
114
-
-
0035897415
-
Regulation and localization of the bloom syndrome protein in response to dna damage
-
O Bischof, SH Kim, J Irving, S Beresten, NA Ellis, J Campisi. Regulation and localization of the Bloom syndrome protein in response to DNA damage. J Cell Biol 153:367-380, 2001.
-
(2001)
J Cell Biol
, vol.153
, pp. 367-380
-
-
Bischof, O.S.1
Kim, J.2
Irving, S.3
Beresten, N.A.4
Ellis Campisi, J.5
-
115
-
-
0035377356
-
Potential role for the blm helicase in re-combinational repair via a conserved interaction with rad51
-
L Wu, SL Davies, NC Levitt, ID Hickson. Potential role for the BLM helicase in re-combinational repair via a conserved interaction with RAD51. J Biol Chem 276:19375-19381, 2001.
-
(2001)
J Biol Chem
, vol.276
, pp. 19375-19381
-
-
Wu, L.S.1
Davies, N.C.2
Levitt Hickson, I.D.3
-
116
-
-
0035839467
-
The bloom’s syndrome protein (blm) interacts with mlh1 but is not required for dna mismatch repair
-
G Langland, J Kordich, J Creaney, KH Goss, K Lillard-Wetherell, K Bebenek, TA Kunkel, J Groden. The Bloom’s syndrome protein (BLM) interacts with MLH1 but is not required for DNA mismatch repair. J Biol Chem 276:30031-30035, 2001.
-
(2001)
J Biol Chem
, vol.276
, pp. 30031-30035
-
-
Langland, G.J.1
Kordich, J.2
Creaney, K.H.3
Goss, K.4
Lillard-Wetherell, K.5
Bebenek, T.A.6
Kunkel Groden, J.7
-
117
-
-
0033728483
-
The werner syndrome protein contributes to induction of p53 by dna damage
-
G Blander, N Zalle, JF Leal, RL Bar-Or, CE Yu, M Oren. The Werner syndrome protein contributes to induction of p53 by DNA damage. FASEB J 14:2138-2140, 2000.
-
(2000)
FASEB J
, vol.14
, pp. 2138-2140
-
-
Blander, G.N.1
Zalle, J.F.2
Leal, C.Y.3
Oren, M.4
-
118
-
-
0035980070
-
Functional interaction of p53 and blm dna helicase in apoptosis
-
XW Wang, A Tseng, NA Ellis, EA Spillare, SP Linke, AI Robles, H Seker, Q Yang, P Hu, S Beresten, NA Bemmels, S Garfield, CC Harris. Functional interaction of p53 and BLM DNA helicase in apoptosis. J Biol Chem 276:32948-32955, 2001.
-
(2001)
J Biol Chem
, vol.276
, pp. 32948-32955
-
-
Wang, X.W.1
Tseng, A.2
Ellis, N.A.3
Spillare, E.A.4
Linke, S.P.5
Robles, A.I.6
Sekhar, H.7
Yang, Q.8
Hu, P.9
Beresten, S.10
Bemmels, N.A.11
Garfield, C.C.12
Harris, C.C.13
-
119
-
-
0035860775
-
P53 modulates the exonuclease activity of werner syndrome protein
-
RM Jr, P Karmakar, JA Sommers, Q Yang, XW Wang, EA Spillare, CC Harris, VA Bohr. p53 Modulates the exonuclease activity of werner syndrome protein. J Biol Chem 276:35093-35102, 2001.
-
(2001)
J Biol Chem
, vol.276
, pp. 35093-35102
-
-
Karmakar, J.A.1
Sommers, Q.2
Yang, X.W.3
Wang, E.A.4
Spillare, C.C.5
Harris Bohr, V.A.6
-
120
-
-
0034665971
-
Functional interaction between ku and the werner syndrome protein in dna end processing
-
B Li, L Comai. Functional interaction between Ku and the werner syndrome protein in DNA end processing. J Biol Chem 275:28349-28352, 2000.
-
(2000)
J Biol Chem
, vol.275
, pp. 28349-28352
-
-
Li, B.1
Comai, L.2
-
121
-
-
0034655912
-
Ku complex interacts with and stimulates the werner protein
-
MP Cooper, A Machwe, DK Orren, RM Brosh, D Ramsden, VA Bohr. Ku complex interacts with and stimulates the Werner protein. Genes Dev 14:907-912, 2001.
-
(2001)
Genes Dev
, vol.14
, pp. 907-912
-
-
Cooper, M.P.A.1
Machwe, D.K.2
Orren, R.M.3
Brosh, D.4
Ramsden Bohr, V.A.5
-
122
-
-
0035844242
-
Interactions between the werner syndrome helicase and dna polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(cgg)n trinucleotide repeat sequence
-
AS Kamath-Loeb, LA Loeb, E Johansson, PM Burgers, M Fry. Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)n trinucleotide repeat sequence. J Biol Chem 276:16439-16446, 2001.
-
(2001)
J Biol Chem
, vol.276
, pp. 16439-16446
-
-
Kamath-Loeb, A.1
Loeb, E.2
Johansson, P.M.3
Burgers Fry, M.4
-
123
-
-
0034633732
-
Werner protein recruits dna polymerase delta to the nucleolus
-
AM Szekely, YH Chen, C Zhang, J Oshima, SM Weissman. Werner protein recruits DNA polymerase delta to the nucleolus. Proc Natl Acad Sci USA 97:11365-11370, 2000.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 11365-11370
-
-
Szekely, A.1
Chen, C.2
Zhang, J.3
Oshima Weissman, S.M.4
-
124
-
-
0035233133
-
Completion of base excision repair by mammalian dna ligases
-
AE Tomkinson, L Chen, Z Dong, JB Leppard, DS Levin, ZB Mackey, TA Motycka. Completion of base excision repair by mammalian DNA ligases. Prog Nucleic Acid Res Mol Biol 68:151-164, 2001.
-
(2001)
Prog Nucleic Acid Res Mol Biol
, vol.68
, pp. 151-164
-
-
Tomkinson, A.E.L.1
Chen, Z.2
Dong, J.B.3
Leppard, D.S.4
Levin, Z.B.5
Mackey Motycka, T.A.6
-
125
-
-
0026758489
-
Construction of human xrcc1 minigenes that fully correct the cho dna repair mutant em9
-
KW Caldecott, JD Tucker, LH Thompson. Construction of human XRCC1 minigenes that fully correct the CHO DNA repair mutant EM9. Nucleic Acids Res 20:4575-4579, 1992.
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 4575-4579
-
-
Caldecott, K.1
Tucker Thompson, L.H.2
-
127
-
-
3142546346
-
A retarded rate of dna chain growth in bloom’s syndrome
-
R Hand, J German. A retarded rate of DNA chain growth in Bloom’s syndrome. Proc Natl Acad Sci USA 72:758-762, 1975.
-
(1975)
Proc Natl Acad Sci USA
, vol.72
, pp. 758-762
-
-
Hand, R.1
German, J.2
-
128
-
-
0025302748
-
An abnormal profile of dna replication intermediates in bloom’s syndrome
-
U Lonn, S Lonn, U Nylen, G Winblad, J German. An abnormal profile of DNA replication intermediates in Bloom’s syndrome. Cancer Res 50:3141-3145, 1990.
-
(1990)
Cancer Res
, vol.50
, pp. 3141-3145
-
-
Lonn, U.S.1
Lonn, U.2
Nylen, G.3
Winblad German, J.4
-
129
-
-
0018822521
-
Effects of inhibitors of dna synthesis on spontaneous and ultraviolet light-induced sister-chromatid exchanges in chinese hamster cells
-
Y Ishii, MA Bender. Effects of inhibitors of DNA synthesis on spontaneous and ultraviolet light-induced sister-chromatid exchanges in Chinese hamster cells. Mutat Res 79:19-32, 1980.
-
(1980)
Mutat Res
, vol.79
, pp. 19-32
-
-
Ishii, Y.1
Bender, M.A.2
-
130
-
-
0025800372
-
Dna topoisomerases: Why so many?
-
JC Wang. DNA topoisomerases: why so many? J Biol Chem 266:6659-6662, 1991.
-
(1991)
J Biol Chem
, vol.266
, pp. 6659-6662
-
-
Wang, J.C.1
-
131
-
-
0023712287
-
Identification of a potent decatenating enzyme from escherichia coli
-
RJ DiGate, KJ Marians. Identification of a potent decatenating enzyme from Escherichia coli. J Biol Chem 263:13366-73, 1988.
-
(1988)
J Biol Chem
, vol.263
, pp. 13366-13373
-
-
DiGate, R.J.1
Marians, K.J.2
-
132
-
-
0026795617
-
Identification of the yeast top3 gene product as a single strand-specific dna topoisomerase
-
RA Kim, JC Wang. Identification of the yeast TOP3 gene product as a single strand-specific DNA topoisomerase. J Biol Chem 267:17178-17185, 1992.
-
(1992)
J Biol Chem
, vol.267
, pp. 17178-17185
-
-
Kim, R.A.1
Wang, J.C.2
-
133
-
-
0033564431
-
Purification and characterization of human dna topoisomerase iiialpha
-
H Goulaouic, T Roulon, O Flamand, L Grondard, F Lavelle, JF Riou. Purification and characterization of human DNA topoisomerase IIIalpha. Nucleic Acids Res 27:2443-2450, 1999.
-
(1999)
Nucleic Acids Res
, vol.27
, pp. 2443-2450
-
-
Goulaouic, H.T.1
Roulon, O.2
Flamand, L.3
Grondard, F.4
Lavelle Riou, J.F.5
-
134
-
-
0033031935
-
Recq helicase and topoisomerase iii comprise a novel dna strand passage function: A conserved mechanism for control of dna recombination
-
FG Harmon, RJ DiGate, SC Kowalczykowski. RecQ helicase and topoisomerase III comprise a novel DNA strand passage function: a conserved mechanism for control of DNA recombination. Mol Cell 3:611-620, 1999.
-
(1999)
Mol Cell
, vol.3
, pp. 611-620
-
-
Harmon, F.1
Digate Kowalczykowski, S.C.2
-
135
-
-
0026704435
-
Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (hprt) gene deletions
-
RJ Monnat Jr, AF Hackmann, TA Chiaverotti. Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletions. Genomics 13:777-787, 1992.
-
(1992)
Genomics
, vol.13
, pp. 777-787
-
-
Monnat, R.1
Hackmann Chiaverotti, T.A.2
-
136
-
-
0035970893
-
Sterility of drosophila with mutations in the bloom syndrome gene—complementation by ku70
-
K Kusano, DM Johnson-Schlitz, WR Engels. Sterility of Drosophila with mutations in the Bloom syndrome gene—complementation by Ku70. Science 291:2600-2602, 2001.
-
(2001)
Science
, vol.291
, pp. 2600-2602
-
-
Kusano, K.D.1
Johnson-Schlitz Engels, W.R.2
-
137
-
-
0035812848
-
Sp-ring for sumo: News functions bloom for a ubiquitin-like protein
-
M Hochstrasser, SP-RING for SUMO: News functions bloom for a ubiquitin-like protein. Cell 107:5-8 (2001).
-
(2001)
Cell
, vol.107
, pp. 5-8
-
-
Hochstrasser, M.1
-
138
-
-
0035865143
-
The saccharomyces cerevisiae wrn homolog sqs1p participates in telomere maintenance in cells lacking telomerase
-
FB Johnson, RA Marciniak, M McVey, SA Stewart, WC Hahn, L Guarente. The Saccharomyces cerevisiae WRN homolog Sqs1p participates in telomere maintenance in cells lacking telomerase. EMBO J 20:905-913 (2001).
-
(2001)
EMBO J
, vol.20
, pp. 905-913
-
-
Johnson, F.1
Marciniak, M.2
McVey, S.A.3
Stewart, W.C.4
Hahn Guarente, L.5
-
139
-
-
0035504589
-
Direct association of bloom’s syndrome gene product with the human mismatch repair protein mlh1
-
G Pedrazzi, C Perrera, H Blaser, P Kuster, G Marra, S Davies, G-H Ryu, R Freira, I Hickson, J Jixicny, I Stagljar. Direct association of Bloom’s syndrome gene product with the human mismatch repair protein MLH1. Nucleic Acids Res 29:4378-4386 (2001).
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 4378-4386
-
-
Pedrazzi, G.C.1
Perrera, H.2
Blaser, P.3
Kuster, G.4
Marra, S.5
Davies, G.-H.6
Ryu, R.7
Freira, I.8
Hickson, J.9
Jixicny Stagljar, I.10
|