-
1
-
-
0023150972
-
A case of Werner's syndrome associated with bladder cancer
-
1 Arima, K., K. Tsukamoto, N. Hori, Y. Sugimura, H. Tochigi, J. Kawamura, M. Goto: A case of Werner's syndrome associated with bladder cancer. Hinyokika Kiyo. 33 (1987), 269-274.
-
(1987)
Hinyokika Kiyo
, vol.33
, pp. 269-274
-
-
Arima, K.1
Tsukamoto, K.2
Hori, N.3
Sugimura, Y.4
Tochigi, H.5
Kawamura, J.6
Goto, M.7
-
2
-
-
0023147671
-
Cardiovaskular features of the Werner syndrome
-
2 Cohen, J. L., E. N. Arnett, E. N. Kolodyn, W. C. Robert: Cardiovaskular features of the Werner syndrome. Amer. J. Cardiol. 59 (1987), 493-495.
-
(1987)
Amer. J. Cardiol.
, vol.59
, pp. 493-495
-
-
Cohen, J.L.1
Arnett, E.N.2
Kolodyn, E.N.3
Robert, W.C.4
-
3
-
-
0030861685
-
DNA helicases in inherited human disorders
-
3 Ellis, N. A., DNA helicases in inherited human disorders. Curr. Opin. Genet. Dev. 7 ( 1997), 354-363.
-
(1997)
Curr. Opin. Genet. Dev.
, vol.7
, pp. 354-363
-
-
Ellis, N.A.1
-
4
-
-
0013907774
-
Werner's syndrome: A review of its symptomatology, natural history, pathological features, genetics and relationship to the natural aging process
-
4 Epstein, C. J., G. M. Martin, A. L. Schulz, A. G. Motulsky: Werner's syndrome: a review of its symptomatology, natural history, pathological features, genetics and relationship to the natural aging process. Medicine 45 (1966), 177-221.
-
(1966)
Medicine
, vol.45
, pp. 177-221
-
-
Epstein, C.J.1
Martin, G.M.2
Schulz, A.L.3
Motulsky, A.G.4
-
5
-
-
0017668626
-
A retarded rate of DNA replication and normal level of DNA repair in Werner's syndrome fibroblasts in culture
-
5 Fujiwara, Y., T. Higashikawa, M. Tatsumi: 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
-
6
-
-
0024465870
-
Mutator phenotype of Werner syndrome is characterized by extensive deletions
-
published erratum appears in Proc. Natl. Acad. Sci. 1989 Oct.; 86 (20): 7994
-
6 Fukuchi, K., G. M. Martin, R. J. Monnat Jr.: Mutator phenotype of Werner syndrome is characterized by extensive deletions [published erratum appears in Proc. Natl. Acad. Sci. 1989 Oct.; 86 (20): 7994]. Proc. Nat. Acad. Sci. 86 (1989), 5893-5897.
-
(1989)
Proc. Nat. Acad. Sci.
, vol.86
, pp. 5893-5897
-
-
Fukuchi, K.1
Martin, G.M.2
Monnat R.J., Jr.3
-
7
-
-
0021997395
-
Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines
-
7 Fukuchi, K., K, Tanaka, J. Nakura, Y. Kumahara, T. Uchida, Y. Okada: Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines. Somat. cell molec. Gen. 11 (1985), 303-308.
-
(1985)
Somat. Cell Molec. Gen.
, vol.11
, pp. 303-308
-
-
Fukuchi, K.1
Tanaka, K.2
Nakura, J.3
Kumahara, Y.4
Uchida, T.5
Okada, Y.6
-
8
-
-
0025105188
-
Werner's syndrome: A molecular genetic hypothesis
-
8 Goldstein, S., S. Murano, R. J. Shmookler: Werner's syndrome: a molecular genetic hypothesis. J. Gerontol. 45 (1990), 3-8.
-
(1990)
J. Gerontol.
, vol.45
, pp. 3-8
-
-
Goldstein, S.1
Murano, S.2
Shmookler, R.J.3
-
9
-
-
0019507754
-
Family analysis of Werner's syndrome: A survey of 42 Japanese families with review of the literature
-
9 Goto, M., K. Tanimoto, Y. Horichi, T. Sasazuki: Family analysis of Werner's syndrome: A survey of 42 Japanese families with review of the literature. Clin. Genet. 19 (1981), 8-15.
-
(1981)
Clin. Genet.
, vol.19
, pp. 8-15
-
-
Goto, M.1
Tanimoto, K.2
Horichi, Y.3
Sasazuki, T.4
-
10
-
-
33846289198
-
Excess of rare cancers in Werner's syndrome (adult progeria)
-
10 Goto, M., R. W. Miller, Y. Ishikawa, H. Sugano: Excess of rare cancers in Werner's syndrome (adult progeria). Cancer Epidemiol. Bio. Prevent. 5 (1996), 239-246.
-
(1996)
Cancer Epidemiol. Bio. Prevent.
, vol.5
, pp. 239-246
-
-
Goto, M.1
Miller, R.W.2
Ishikawa, Y.3
Sugano, H.4
-
11
-
-
0018119113
-
Werner's syndrome: Analysi of 15 cases with review of the Japanese literature
-
11 Goto, M., Y. Horiuchi, K. Tanimoto, T. Ishii, H. Nakashima: Werner's syndrome: Analysis of 15 cases with review of the Japanese literature. J. Amer. Geriat. Soc. 26 (1978), 341-347.
-
(1978)
J. Amer. Geriat. Soc.
, vol.26
, pp. 341-347
-
-
Goto, M.1
Horiuchi, Y.2
Tanimoto, K.3
Ishii, T.4
Nakashima, H.5
-
12
-
-
0020028472
-
Werner's syndrome with associated malignant neoplasms
-
12 Hrabko, R. P., H. Milgrom, R. A. Schwartz: Werner's syndrome with associated malignant neoplasms. Arch. Dermatol. 118 (1982), 106-108.
-
(1982)
Arch. Dermatol.
, vol.118
, pp. 106-108
-
-
Hrabko, R.P.1
Milgrom, H.2
Schwartz, R.A.3
-
13
-
-
0022317420
-
Clinical endocrine and metabolic aspects of the werner's syndrome compared with those of normal aging
-
13 Imura, H., Y. Nakao, H. Kuzuya, M. Okamoto, M. Okamoto, K. Yamada: Clinical endocrine and metabolic aspects of the Werner's syndrome compared with those of normal aging. Advanc. exp. Med. Biol. 190 (1985), 171-185.
-
(1985)
Advanc. Exp. Med. Biol.
, vol.190
, pp. 171-185
-
-
Imura, H.1
Nakao, Y.2
Kuzuya, H.3
Okamoto, M.4
Okamoto, M.5
Yamada, K.6
-
14
-
-
0014816132
-
Replicative life-span of cultivated human cells. Effects of donor's age, tissue, and genotype
-
14 Martin, G. M., C. A. Sprague, C. J. Epstein: 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
-
15
-
-
0029896027
-
Premature aging in Werner's syndrome spares the central nervous system
-
15 Postiglione, A., A. Soricelli, E. M. Covelli, N. lazzatte, A. Ruocco: Premature aging in Werner's syndrome spares the central nervous system. Neurobiol. of Aging 17 (1996), 325-330.
-
(1996)
Neurobiol. of Aging
, vol.17
, pp. 325-330
-
-
Postiglione, A.1
Soricelli, A.2
Covelli, E.M.3
Lazzatte, N.4
Ruocco, A.5
-
16
-
-
0023199962
-
Bladder carcinoma with Werner syndrome
-
16 Saeki, H., O. Yamaguchi, S. Kondo, G. Ishizuka, T. Morita, Y. Koizumi: Bladder carcinoma with Werner syndrome. Urology 30 (1987), 494-495.
-
(1987)
Urology
, vol.30
, pp. 494-495
-
-
Saeki, H.1
Yamaguchi, O.2
Kondo, S.3
Ishizuka, G.4
Morita, T.5
Koizumi, Y.6
-
17
-
-
0019440557
-
Cytogenetics of Werner's syndrome cultured skin fibroblasts: Variegated translocation mosaicism
-
17 Salk, D., K. Au, H. Hoehn, G. M. Martin: Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism. Cytogenet. Cell Genet. 30 (1981), 92-107.
-
(1981)
Cytogenet. Cell Genet.
, vol.30
, pp. 92-107
-
-
Salk, D.1
Au, K.2
Hoehn, H.3
Martin, G.M.4
-
18
-
-
0020455613
-
Werner's syndrome. A review of recent research with analysis of connective tissue metabolism, growth control of cultivated cells and chromosomal aberrations
-
18 Salk, D.: Werner's syndrome. A review of recent research with analysis of connective tissue metabolism, growth control of cultivated cells and chromosomal aberrations. Hum. Genet. 62 (1982), 1-15.
-
(1982)
Hum. Genet.
, vol.62
, pp. 1-15
-
-
Salk, D.1
-
19
-
-
0020460340
-
Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's syndrome
-
19 Scappaticci, S., D. Cerimele, M. Fraccaro: Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's syndrome. Hum. Genet. 62 (1982), 16-24.
-
(1982)
Hum. Genet.
, vol.62
, pp. 16-24
-
-
Scappaticci, S.1
Cerimele, D.2
Fraccaro, M.3
-
20
-
-
0019979019
-
Altered frequency of initiations sites of DNA replication in Werner's syndrome cells
-
20 Takeuchi, F., F. Hanaoka, M. Goto, I. Akaoka, T. Hori, M. Yamada, T. Miyamoto: Altered frequency of initiations 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
-
21
-
-
0001078903
-
Werner's syndrome (progeria of the adult) and Rothmund's syndrome: Two types of closely related heredofamilial atrophic dermatoses with juvenile catarracts and endocrine features; a critical study with five new cases
-
21 Thannhauser, S. J.: Werner's syndrome (progeria of the adult) and Rothmund's syndrome: two types of closely related heredofamilial atrophic dermatoses with juvenile catarracts and endocrine features; a critical study with five new cases. Ann. intern. Med. 23 ( 1945), 559-626.
-
(1945)
Ann. Intern. Med.
, vol.23
, pp. 559-626
-
-
Thannhauser, S.J.1
-
22
-
-
0004183888
-
Über katarakt in verbindung mit sklerodermie (inaugural-dissertation), universität kiel: Schmidt und klaunig, 1904; in englischer sprache: On cataract in conjunction with scleroderma
-
22 Werner, O.: Über Katarakt in Verbindung mit Sklerodermie (Inaugural-Dissertation), Universität Kiel: Schmidt und Klaunig, 1904; in englischer Sprache: On cataract in conjunction with scleroderma. Advanc. Exp. Med. Biol. 190 (1985), 1-14.
-
(1985)
Advanc. Exp. Med. Biol.
, vol.190
, pp. 1-14
-
-
Werner, O.1
-
23
-
-
15844409553
-
Positional cloning of the Werner's syndrome gene
-
23 Yu, C. E., J. Oshima, Y. H. Fu, E. M. Wijsman, F. Hisama, R. Alisch, S. Matthews, J. Nakura, T. Miki, S. Quais, G. M. Martin, J. Mulligan, G. D. Schellenberg: Positional cloning of the Werner's syndrome gene. Science 272 (1996), 258-262.
-
(1996)
Science
, vol.272
, pp. 258-262
-
-
Yu, C.E.1
Oshima, J.2
Fu, Y.H.3
Wijsman, E.M.4
Hisama, F.5
Alisch, R.6
Matthews, S.7
Nakura, J.8
Miki, T.9
Quais, S.10
Martin, G.M.11
Mulligan, J.12
Schellenberg, G.D.13
|