-
1
-
-
0022858295
-
Diminished response of Werner's syndrome fibroblasts to growth factors PDGF and FGF
-
Bauer E.A., Silverman N., Busiek D.F., Kronberger A., Deuel T.F. Diminished response of Werner's syndrome fibroblasts to growth factors PDGF and FGF. Science. 234:1986;1240-1243.
-
(1986)
Science
, vol.234
, pp. 1240-1243
-
-
Bauer, E.A.1
Silverman, N.2
Busiek, D.F.3
Kronberger, A.4
Deuel, T.F.5
-
2
-
-
0030829431
-
Mismatch repair in extracts of Werner syndrome cell lines
-
Bennett S.E., Umar A., Oshima J., Monnat R.J. Jr, Kunkel T.A. Mismatch repair in extracts of Werner syndrome cell lines. Cancer Res. 57:1997;2956-2960.
-
(1997)
Cancer Res
, vol.57
, pp. 2956-2960
-
-
Bennett, S.E.1
Umar, A.2
Oshima, J.3
Monnat R.J., Jr.4
Kunkel, T.A.5
-
3
-
-
0013907774
-
Werner's syndrome: A review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process
-
Epstein C.J., Martin G.M., Schultz A.L., Motulsky A.G. Werner's syndrome A review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process . Medicine. 45:1966;177-222.
-
(1966)
Medicine
, vol.45
, pp. 177-222
-
-
Epstein, C.J.1
Martin, G.M.2
Schultz, A.L.3
Motulsky, A.G.4
-
4
-
-
0017668626
-
A retarded rate of DNA replication and normal level of DNA repair in Werner's syndrome fibroblasts in culture
-
Fujiwara Y., Higashikawa T., Tatsumi M. A retarded rate of DNA replication and normal level of DNA repair in Werner's syndrome fibroblasts in culture. J. Cell. Physiol. 92:1977;365-374.
-
(1977)
J. Cell. Physiol.
, vol.92
, pp. 365-374
-
-
Fujiwara, Y.1
Higashikawa, T.2
Tatsumi, M.3
-
5
-
-
0021997395
-
Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines
-
Fukuchi K., Tanaka K., Nakura J., Kumahara Y., Uchida T., Okada Y. Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines. Somat. Cell Mol. Genet. 11:1985;303-308.
-
(1985)
Somat. Cell Mol. Genet.
, vol.11
, pp. 303-308
-
-
Fukuchi, K.1
Tanaka, K.2
Nakura, J.3
Kumahara, Y.4
Uchida, T.5
Okada, Y.6
-
6
-
-
0024465870
-
Mutator phenotype of Werner syndrome is characterized by extensive deletions
-
Fukuchi K., Martin G.M., Monnat R.J. Jr. Mutator phenotype of Werner syndrome is characterized by extensive deletions. Proc. Natl. Acad. Sci. USA. 86:1989;5893-5897.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 5893-5897
-
-
Fukuchi, K.1
Martin, G.M.2
Monnat R.J., Jr.3
-
7
-
-
0025169778
-
Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients
-
Fukuchi K., Tanaka K., Kumahara Y., Marumo K., Pride M.B., Martin G.M., Monnat R.J. Jr. Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients. Hum. Genet. 84:1990;249-252.
-
(1990)
Hum. Genet.
, vol.84
, pp. 249-252
-
-
Fukuchi, K.1
Tanaka, K.2
Kumahara, Y.3
Marumo, K.4
Pride, M.B.5
Martin, G.M.6
Monnat R.J., Jr.7
-
9
-
-
0031018953
-
Analysis of helicase gene mutations in Japanese Werner's syndrome patients
-
Goto M., Imamura O., Kuromitsu J., Matsumoto T., Yamabe Y., Tokutake Y., Suzuki N., Mason B., Drayna D., Sugawara M., Sugimoto M., Furuichi Y. Analysis of helicase gene mutations in Japanese Werner's syndrome patients. Hum. Genet. 99:1997;191-193.
-
(1997)
Hum. Genet.
, vol.99
, pp. 191-193
-
-
Goto, M.1
Imamura, O.2
Kuromitsu, J.3
Matsumoto, T.4
Yamabe, Y.5
Tokutake, Y.6
Suzuki, N.7
Mason, B.8
Drayna, D.9
Sugawara, M.10
Sugimoto, M.11
Furuichi, Y.12
-
10
-
-
0030751354
-
The Werner syndrome protein is a DNA helicase
-
Gray M.D., Shen J.C., Kamath-Loeb A.S., Blank A., Sopher B.L., Martin G.M., Oshima J., Loeb L.A. The Werner syndrome protein is a DNA helicase. Nat. Genet. 17:1997;100-103.
-
(1997)
Nat. Genet.
, vol.17
, pp. 100-103
-
-
Gray, M.D.1
Shen, J.C.2
Kamath-Loeb, A.S.3
Blank, A.4
Sopher, B.L.5
Martin, G.M.6
Oshima, J.7
Loeb, L.A.8
-
11
-
-
0020538765
-
Decrease in the average size of replicons in a Werner syndrome cell line by Simian virus 40 infection
-
Hanaoka F., Takeuchi F., Matsumura T., Goto M., Miyamoto T., Yamada M. Decrease in the average size of replicons in a Werner syndrome cell line by Simian virus 40 infection. Exp. Cell Res. 144:1983;463-467.
-
(1983)
Exp. Cell Res.
, vol.144
, pp. 463-467
-
-
Hanaoka, F.1
Takeuchi, F.2
Matsumura, T.3
Goto, M.4
Miyamoto, T.5
Yamada, M.6
-
12
-
-
0027496935
-
The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases
-
Harper J.W., Adami G.R., Wei N., Keyomarsi K., Elledge S.J. The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases. Cell. 75:1993;805-816.
-
(1993)
Cell
, vol.75
, pp. 805-816
-
-
Harper, J.W.1
Adami, G.R.2
Wei, N.3
Keyomarsi, K.4
Elledge, S.J.5
-
13
-
-
0018195078
-
Normal level of unscheduled DNA synthesis in Werner's syndrome fibroblasts in culture
-
Higashikawa T., Fujiwara Y. Normal level of unscheduled DNA synthesis in Werner's syndrome fibroblasts in culture. Exp. Cell Res. 113:1978;438-442.
-
(1978)
Exp. Cell Res.
, vol.113
, pp. 438-442
-
-
Higashikawa, T.1
Fujiwara, Y.2
-
14
-
-
0022551258
-
Functional dissection of a eukaryotic transcriptional activator protein, GCN4 of yeast
-
Hope I.A., Struhl K. Functional dissection of a eukaryotic transcriptional activator protein, GCN4 of yeast. Cell. 46:1986;885-894.
-
(1986)
Cell
, vol.46
, pp. 885-894
-
-
Hope, I.A.1
Struhl, K.2
-
16
-
-
0029144441
-
Differential regulation of plasminogen activator and inhibitor gene transcription by the tumor suppressor p53
-
Kunz C., Pebler S., Otte J., Von Der Ahe D. Differential regulation of plasminogen activator and inhibitor gene transcription by the tumor suppressor p53. Nucleic Acids Res. 23:1995;3710-3717.
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 3710-3717
-
-
Kunz, C.1
Pebler, S.2
Otte, J.3
Von Der Ahe, D.4
-
17
-
-
0029922445
-
Identification of gene sequences overexpressed in senescent and Werner syndrome human fibroblasts
-
Lecka-Czernik B., Moerman E.J., Jones R.A., Goldstein S. Identification of gene sequences overexpressed in senescent and Werner syndrome human fibroblasts. Exp. Gerontol. 31:1996;159-174.
-
(1996)
Exp. Gerontol.
, vol.31
, pp. 159-174
-
-
Lecka-Czernik, B.1
Moerman, E.J.2
Jones, R.A.3
Goldstein, S.4
-
18
-
-
0023652389
-
Deletion analysis of GAL4 defines two transcriptional activating segments
-
Ma J., Ptashne M. Deletion analysis of GAL4 defines two transcriptional activating segments. Cell. 48:1987;847-853.
-
(1987)
Cell
, vol.48
, pp. 847-853
-
-
Ma, J.1
Ptashne, M.2
-
19
-
-
0029834445
-
The human cut homeodomain protein can repress gene expression by two distinct mechanisms: Active repression and competition for binding site occupancy
-
Mailly F., Berube G., Harada R., Mao P.L., Phillips S., Nepveu A. The human cut homeodomain protein can repress gene expression by two distinct mechanisms Active repression and competition for binding site occupancy . Mol. Cell. Biol. 16:1996;5346-5357.
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 5346-5357
-
-
Mailly, F.1
Berube, G.2
Harada, R.3
Mao, P.L.4
Phillips, S.5
Nepveu, A.6
-
20
-
-
0014816132
-
Replicative life-span of cultivated human cells: Effects of donor's age, tissue and genotype
-
Martin G.M., Sprague C.A., Epstein C.J. Replicative life-span of cultivated human cells Effects of donor's age, tissue and genotype . Lab. Invest. 23:1970;86-92.
-
(1970)
Lab. Invest.
, vol.23
, pp. 86-92
-
-
Martin, G.M.1
Sprague, C.A.2
Epstein, C.J.3
-
21
-
-
0030872571
-
Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: Genetic epidemiology in the Japanese population
-
Matsumoto T., Imamura O., Yamabe Y., Kuromitsu J., Tokutake Y., Shimamoto A., Suzuki N., Satoh M., Kitao S., Ichikawa K., Kataoka H., Sugawara K., Thomas W., Mason B., Tsuchihashi Z., Drayna D., Sugawara M., Sugimoto M., Furuichi Y., Goto M. Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure Genetic epidemiology in the Japanese population . Hum. Genet. 100:1997;123-130.
-
(1997)
Hum. Genet.
, vol.100
, pp. 123-130
-
-
Matsumoto, T.1
Imamura, O.2
Yamabe, Y.3
Kuromitsu, J.4
Tokutake, Y.5
Shimamoto, A.6
Suzuki, N.7
Satoh, M.8
Kitao, S.9
Ichikawa, K.10
Kataoka, H.11
Sugawara, K.12
Thomas, W.13
Mason, B.14
Tsuchihashi, Z.15
Drayna, D.16
Sugawara, M.17
Sugimoto, M.18
Furuichi, Y.19
Goto, M.20
more..
-
22
-
-
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. 16:1997;335-336.
-
(1997)
Nat. Genet.
, vol.16
, pp. 335-336
-
-
Matsumoto, T.1
Shimamoto, A.2
Goto, M.3
Furuichi, Y.4
-
23
-
-
0030836805
-
Comparative sequence analysis of ribonucleases HII, III, II PH and D
-
Mian I.S. Comparative sequence analysis of ribonucleases HII, III, II PH and D. Nucleic Acids Res. 25:1997;3187-3195.
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 3187-3195
-
-
Mian, I.S.1
-
24
-
-
0030697336
-
A putative nucleic acid-binding domain in Bloom's and Werner's syndrome helicases
-
Morozov V., Mushegian A.R., Koonin E.V., Bork P. A putative nucleic acid-binding domain in Bloom's and Werner's syndrome helicases. Trends Biochem. Sci. 22:1997;417-418.
-
(1997)
Trends Biochem. Sci.
, vol.22
, pp. 417-418
-
-
Morozov, V.1
Mushegian, A.R.2
Koonin, E.V.3
Bork, P.4
-
25
-
-
0025866760
-
Diverse gene sequences are overexpressed in Werner syndrome fibroblasts undergoing premature replicative senescence
-
Murano S., Thweatt R., Shmookler-Reis R.J., Jones R.A., Moerman E.J., Goldstein S. Diverse gene sequences are overexpressed in Werner syndrome fibroblasts undergoing premature replicative senescence. Mol. Cell. Biol. 11:1991;3905-3914.
-
(1991)
Mol. Cell. Biol.
, vol.11
, pp. 3905-3914
-
-
Murano, S.1
Thweatt, R.2
Shmookler-Reis, R.J.3
Jones, R.A.4
Moerman, E.J.5
Goldstein, S.6
-
26
-
-
0019948063
-
Werner's syndrome: Twenty-four cases with a review of the Japanese medical literature
-
Murata K., Nakashima H. Werner's syndrome Twenty-four cases with a review of the Japanese medical literature . J. Am. Geriatr. Soc. 30:1982;303-308.
-
(1982)
J. Am. Geriatr. Soc.
, vol.30
, pp. 303-308
-
-
Murata, K.1
Nakashima, H.2
-
27
-
-
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. 94:1997;5831-5836.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 5831-5836
-
-
Mushegian, A.R.1
Bassett D.E., Jr.2
Boguski, M.S.3
Bork, P.4
Koonin, E.V.5
-
28
-
-
0028079995
-
Homozygosity mapping of the Werner syndrome locus (WRN)
-
Nakura J., Wijsman E.M., Miki T., Kamino K., Yu C.E., Oshima J., Fukuchi K., Weber J.L., Piussan C., Melaragno M.I., Epstein C.J., Scappaticci S., Fraccaro M., Matsumura T., Murano S., Yoshida S., Fujiwara Y., Saida T., Ogihara T., Martin G.M., Schellenberg G.D. Homozygosity mapping of the Werner syndrome locus (WRN). Genomics. 23:1994;600-608.
-
(1994)
Genomics
, vol.23
, pp. 600-608
-
-
Nakura, J.1
Wijsman, E.M.2
Miki, T.3
Kamino, K.4
Yu, C.E.5
Oshima, J.6
Fukuchi, K.7
Weber, J.L.8
Piussan, C.9
Melaragno, M.I.10
Epstein, C.J.11
Scappaticci, S.12
Fraccaro, M.13
Matsumura, T.14
Murano, S.15
Yoshida, S.16
Fujiwara, Y.17
Saida, T.18
Ogihara, T.19
Martin, G.M.20
Schellenberg, G.D.21
more..
-
29
-
-
0030586959
-
Narrowing the position of the Werner syndrome locus by homozygosity analysis: Extension of homozygosity analysis
-
Nakura J., Miki T., Ye L., Mitsuda M., Zhao Y., Kihara K., Yu C.E., Oshima J., Fukuchi K., Wijsman E.M., Schellenberg G.D., Martin G.M., Murano S., Hashimoto K., Fujiwara Y., Ogihara T. Narrowing the position of the Werner syndrome locus by homozygosity analysis Extension of homozygosity analysis . Genomics. 36:1996;130-141.
-
(1996)
Genomics
, vol.36
, pp. 130-141
-
-
Nakura, J.1
Miki, T.2
Ye, L.3
Mitsuda, M.4
Zhao, Y.5
Kihara, K.6
Yu, C.E.7
Oshima, J.8
Fukuchi, K.9
Wijsman, E.M.10
Schellenberg, G.D.11
Martin, G.M.12
Murano, S.13
Hashimoto, K.14
Fujiwara, Y.15
Ogihara, T.16
-
30
-
-
10544231878
-
Homozygous and compound heterozygous mutations at the Werner locus
-
Oshima J., Yu C.E., Puissan C., Klein G., Jabkowski J., Balci S., Miki T., Nakura J., Ogihara T., Ells J., Smith M.A.C., Melagno M.I., Fraccaro M., Scappatici S., Matthews J., Ouais S., Jarzebowicz A., Schellenberg G.D., Martin G.M. Homozygous and compound heterozygous mutations at the Werner locus. Hum. Mol. Genet. 5:1996;1909-1913.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1909-1913
-
-
Oshima, J.1
Yu, C.E.2
Puissan, C.3
Klein, G.4
Jabkowski, J.5
Balci, S.6
Miki, T.7
Nakura, J.8
Ogihara, T.9
Ells, J.10
Smith, M.A.C.11
Melagno, M.I.12
Fraccaro, M.13
Scappatici, S.14
Matthews, J.15
Ouais, S.16
Jarzebowicz, A.17
Schellenberg, G.D.18
Martin, G.M.19
-
31
-
-
0019444282
-
Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts
-
Salk D., Bryan E., Au K., Hoehn H., Martin G.M. Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts. Hum. Genet. 58:1981;310-316.
-
(1981)
Hum. Genet.
, vol.58
, pp. 310-316
-
-
Salk, D.1
Bryan, E.2
Au, K.3
Hoehn, H.4
Martin, G.M.5
-
32
-
-
0020455613
-
Werner's syndrome: A review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations
-
Salk D. Werner's syndrome A review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations . Hum. Genet. 62:1982;1-15.
-
(1982)
Hum. Genet.
, vol.62
, pp. 1-15
-
-
Salk, D.1
-
33
-
-
0026588296
-
Homozygosity mapping and Werner's syndrome
-
Schellenberg G.D., Martin G.M., Wijsman E.M., Nakura J., Miki T., Ogihara T. Homozygosity mapping and Werner's syndrome. Lancet. 339:1992;1002.
-
(1992)
Lancet
, vol.339
, pp. 1002
-
-
Schellenberg, G.D.1
Martin, G.M.2
Wijsman, E.M.3
Nakura, J.4
Miki, T.5
Ogihara, T.6
-
34
-
-
0030757524
-
DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system
-
Suzuki N., Shimamoto A., Imamura O., Kuromitsu J., Kitao S., Goto J., Furuichi Y. DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system. Nucleic Acids Res. 25:1997;2973-2978.
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 2973-2978
-
-
Suzuki, N.1
Shimamoto, A.2
Imamura, O.3
Kuromitsu, J.4
Kitao, S.5
Goto, J.6
Furuichi, Y.7
-
35
-
-
0020306698
-
Prolongation of S phase and whole cell cycle in Werner's syndrome fibroblasts
-
Takeuchi F., Hanaoka F., Goto M., Yamada M. Prolongation of S phase and whole cell cycle in Werner's syndrome fibroblasts. Exp. Gerontol. 17:1982;473-480.
-
(1982)
Exp. Gerontol.
, vol.17
, pp. 473-480
-
-
Takeuchi, F.1
Hanaoka, F.2
Goto, M.3
Yamada, M.4
-
36
-
-
0019979019
-
Altered frequency of initiation sites of DNA replication in Werner's syndrome cells
-
Takeuchi F., Hanaoka F., Goto M., Akaoka I., Hori T., Yamada M., Miyamoto T. Altered frequency of initiation sites of DNA replication in Werner's syndrome cells. Hum. Genet. 60:1982;365-368.
-
(1982)
Hum. Genet.
, vol.60
, pp. 365-368
-
-
Takeuchi, F.1
Hanaoka, F.2
Goto, M.3
Akaoka, I.4
Hori, T.5
Yamada, M.6
Miyamoto, T.7
-
37
-
-
0018641508
-
Increase in DNA synthesis in Werner's syndrome cells by hybridization with normal human diploid and HeLa cells
-
Tanaka K., Nakazawa T., Okada Y., Kumahara Y. Increase in DNA synthesis in Werner's syndrome cells by hybridization with normal human diploid and HeLa cells. Exp. Cell Res. 123:1979;261-267.
-
(1979)
Exp. Cell Res.
, vol.123
, pp. 261-267
-
-
Tanaka, K.1
Nakazawa, T.2
Okada, Y.3
Kumahara, Y.4
-
38
-
-
0019011091
-
Roles of nuclear and cytoplasmic environments in the retarded DNA synthesis in Werner syndrome cells
-
Tanaka K., Nakazawa T., Okada Y., Kumahara Y. Roles of nuclear and cytoplasmic environments in the retarded DNA synthesis in Werner syndrome cells. Exp. Cell Res. 127:1980;185-190.
-
(1980)
Exp. Cell Res.
, vol.127
, pp. 185-190
-
-
Tanaka, K.1
Nakazawa, T.2
Okada, Y.3
Kumahara, Y.4
-
39
-
-
0022308353
-
Cell fusion studies in the Werner syndrome
-
Tanaka K., Yamamura K., Fukuchi K., Kawai K., Kumahara Y. Cell fusion studies in the Werner syndrome. Adv. Exp. Med. Biol. 190:1985;341-351.
-
(1985)
Adv. Exp. Med. Biol.
, vol.190
, pp. 341-351
-
-
Tanaka, K.1
Yamamura, K.2
Fukuchi, K.3
Kawai, K.4
Kumahara, Y.5
-
40
-
-
0029944713
-
DNA repair fine structure in Werner's syndrome cell lines. Exp. Cell Res. 224, 272-278, 1996. Werner's syndrome gene
-
Webb D.K., Evans M.K., Bohr V.A. DNA repair fine structure in Werner's syndrome cell lines. Exp. Cell Res. 224, 272-278, 1996. Werner's syndrome gene. Science. 272:1996;258-262.
-
(1996)
Science
, vol.272
, pp. 258-262
-
-
Webb, D.K.1
Evans, M.K.2
Bohr, V.A.3
-
41
-
-
17344379792
-
Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population
-
Ye L., Miki T., Nakura J., Oshima J., Kamino K., Rakugi H., Ikegami H., Higaki J., Edland S.D., Martin G.M., Ogihara T. Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population. Am. J. Med. Genet. 68:1997;494-498.
-
(1997)
Am. J. Med. Genet.
, vol.68
, pp. 494-498
-
-
Ye, L.1
Miki, T.2
Nakura, J.3
Oshima, J.4
Kamino, K.5
Rakugi, H.6
Ikegami, H.7
Higaki, J.8
Edland, S.D.9
Martin, G.M.10
Ogihara, T.11
-
42
-
-
0345577740
-
-
Positional cloning of the 1996
-
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., and Schellenberg, G.D., , Positional cloning of the 1996.
-
-
-
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
-
43
-
-
16944366241
-
And , The Werner's Syndrome Collaborative Group. Mutations in the consensus helicase domains of the Werner syndrome gene
-
Yu C.E., Oshima J., Wijsman E.M., Nakura J., Miki T., Puissan C., Matthews S., Fu Y.H., Mulligan J., Martin G.M., Schellenberg G.D. and , The Werner's Syndrome Collaborative Group. Mutations in the consensus helicase domains of the Werner syndrome gene. Am. J. Hum. Genet. 60:1997;330-341.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 330-341
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Yu, C.E.1
Oshima, J.2
Wijsman, E.M.3
Nakura, J.4
Miki, T.5
Puissan, C.6
Matthews, S.7
Fu, Y.H.8
Mulligan, J.9
Martin, G.M.10
Schellenberg, G.D.11
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