-
1
-
-
0016775933
-
Retinoblastoma—a clinical survey and its genetic implications
-
Aheme, G. E. S., and Roberts, D. F. Retinoblastoma—a clinical survey and its genetic implications. Clin. Genet., 8: 275–290, 1975.
-
(1975)
Clin. Genet.
, vol.8
, pp. 275-290
-
-
Aheme, G.E.S.1
Roberts, D.F.2
-
2
-
-
0017156289
-
Relation of DNA repair processes to pathological ageing of the nervous system in xeroderma pigmentosum
-
Andrews, A. D., Barrett, S. F. and Robbins, J. H. Relation of DNA repair processes to pathological ageing of the nervous system in xeroderma pigmentosum. Lancet, 1:1318-1320,1976.
-
(1976)
Lancet
, vol.1
, pp. 1318-1320
-
-
Andrews, A.D.1
Barrett, S.F.2
Robbins, J.H.3
-
3
-
-
0000439206
-
Mutagenicity testing with V79 Chinese hamster cells
-
B. Kilbey et al. (eds.), Amsterdam: Elsevier/North Holland
-
Arlett. C. F. Mutagenicity testing with V79 Chinese hamster cells. In: B. Kilbey et al. (eds.), Handbook of Mutagenicity Test Procedures, pp. 175–192. Amsterdam: Elsevier/North Holland, 1977.
-
(1977)
Handbook of Mutagenicity Test Procedures
, pp. 175-192
-
-
Arlett, C.F.1
-
4
-
-
0016727657
-
The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet light irradiation
-
Arlett, C. F., Harcourt, S. A., and Broughton, B. C. The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet light irradiation. Mutat. Res., 33: 341–346, 1975.
-
(1975)
Mutat. Res.
, vol.33
, pp. 341-346
-
-
Arlett, C.F.1
Harcourt, S.A.2
Broughton, B.C.3
-
5
-
-
0018104594
-
A human subject with a new defect in repair of ultraviolet damage
-
Arlett, C. F., Lehmann, A. R., Giannelli, F., and Ramsay. C. A. A human subject with a new defect in repair of ultraviolet damage. J. Invest. Dermatol., 70:173-177, 1978.
-
(1978)
J. Invest. Dermatol.
, vol.70
, pp. 173-177
-
-
Arlett, C.F.1
Lehmann, A.R.2
Giannelli, F.3
Ramsay, C.A.4
-
6
-
-
78651043982
-
Ataxia telangiectasia. A familial syndrome of progressive cerebellar ataxia, oculocutaneous telangiectasia and frequent pulmonary infection
-
Boder, E., and Sedgwick, R. P. Ataxia telangiectasia. A familial syndrome of progressive cerebellar ataxia, oculocutaneous telangiectasia and frequent pulmonary infection. Pediatrics, 21: 526–554, 1958.
-
(1958)
Pediatrics
, pp. 526-554
-
-
Boder, E.1
Sedgwick, R.P.2
-
7
-
-
84965839935
-
Bacterial reaction to radiation
-
Bridges, B. A. Bacterial reaction to radiation. Shildon, England; Meadowfield Press, 1976.
-
(1976)
Shildon
-
-
Bridges, B.A.1
-
8
-
-
0017326267
-
Repair deficient and radiation sensitive human cell variants
-
Bridges, B. A., Arlett. C. F., Lehmann, A. R., Taylor, A. M. R., and Harnden, D. G. Repair deficient and radiation sensitive human cell variants. Stud. Biophys., 61: 65–70, 1977.
-
(1977)
Stud. Biophys.
, vol.61
, pp. 65-70
-
-
Bridges, B.A.1
Arlett, C.F.2
Lehmann, A.R.3
Taylor, A.M.R.4
Harnden, D.G.5
-
9
-
-
0014906887
-
DNA repair and radiation sensitivity in human (xeroderma pigmentosum) cells
-
Cleaver, J. E. DNA repair and radiation sensitivity in human (xeroderma pigmentosum) cells. Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med., 18: 557–565, 1970.
-
(1970)
Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med.
, vol.18
, pp. 557-565
-
-
Cleaver, J.E.1
-
10
-
-
0017864466
-
Ataxia telangiectasia: The evaluation of radiosensitivity in cultured skin fibroblasts as a diagnostic test
-
Cox, R., Hosking, G. P., and Wilson, J. Ataxia telangiectasia: The evaluation of radiosensitivity in cultured skin fibroblasts as a diagnostic test. Arch. Dis. Child., 53. 386–390, 1978.
-
(1978)
Arch. Dis. Child.
, vol.53
, pp. 386-390
-
-
Cox, R.1
Hosking, G.P.2
Wilson, J.3
-
11
-
-
0016296256
-
Changes in radiosensitivity during the in vitro growth of diploid human fibroblasts
-
Cox, R., and Masson, W. K. Changes in radiosensitivity during the in vitro growth of diploid human fibroblasts. Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med., 26. 193–196, 1974.
-
(1974)
Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med.
, vol.26
, pp. 193-196
-
-
Cox, R.1
Masson, W.K.2
-
12
-
-
0015319601
-
The Hutchinson-Gilford progeria syndrome
-
De Busk, F. L. The Hutchinson-Gilford progeria syndrome. J. Pediatr., 80: 697–724, 1972.
-
(1972)
J. Pediatr.
, vol.80
, pp. 697-724
-
-
De Busk, F.L.1
-
13
-
-
0013907774
-
Werner's syndrome
-
Epstein, C. J. Martin, G. M., Schultz, A. L., and Motulsky, A. G. Werner's syndrome. Medicine (Baltimore), 45: 177–221, 1966.
-
(1966)
Medicine
, vol.45
, pp. 177-221
-
-
Epstein, C.J.1
Martin, G.M.2
Schultz, A.L.3
Motulsky, A.G.4
-
14
-
-
84915290516
-
Multiple self-healing squamous epithelioma
-
Baltimore: Williams and Wilkins.
-
Ferguson-Smith, M. A., Wallace. D. C., James. Z. H., and Renwick, J. H. Multiple self-healing squamous epithelioma. In: D. Bergsma (ed.), Third Conference on the Clinical Delineation of Birth Defects, Vol. 12, pp. 157–163. Baltimore: Williams and Wilkins. 1972.
-
(1972)
Third Conference on the Clinical Delineation of Birth Defects
, vol.12
, pp. 157-163
-
-
Ferguson-Smith, M.A.1
Wallace, D.C.2
James, Z.H.3
Renwick, J.H.4
-
15
-
-
0001455199
-
Survival after treatment with EMS, y-rays and mitomycin C of skin fibroblasts from patients with Fanconi's anaemia
-
Finkelberg, R., Thompson, M., and Siminovitch, L. Survival after treatment with EMS, y-rays and mitomycin C of skin fibroblasts from patients with Fanconi's anaemia. Am. J. Hum. Genet., 26: A30, 1975.
-
(1975)
Am. J. Hum. Genet.
, vol.26
-
-
Finkelberg, R.1
Thompson, M.2
Siminovitch, L.3
-
16
-
-
0014486220
-
Genetical and clinical observations in the first twenty-seven patients
-
German, J. 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
-
17
-
-
0017357401
-
Ultraviolet light sensitivity and delayed DNA-chain maturation in Bloom's syndrome fibroblasts
-
Giannelli, F., Benson, P. F., Pawsey, S. A., and Polani, P. E. Ultraviolet light sensitivity and delayed DNA-chain maturation in Bloom's syndrome fibroblasts. Nature (Lond.), 265: 466–469, 1977.
-
(1977)
Nature
, vol.265
, pp. 466-469
-
-
Giannelli, F.1
Benson, P.F.2
Pawsey, S.A.3
Polani, P.E.4
-
18
-
-
5744230671
-
Ataxia telangiectasia syndrome: Cytogenetic and cancer aspects
-
New York: John Wiley & Sons, Inc.
-
Harnden, D. G. Ataxia telangiectasia syndrome: Cytogenetic and cancer aspects. In: J. German (ed.), Chromosomes and Cancer, pp. 619–636. New York: John Wiley & Sons, Inc., 1974.
-
(1974)
Chromosomes and Cancer
, pp. 619-636
-
-
Harnden, D.G.1
-
19
-
-
84965839604
-
The effects of radiation on the chromosomes of patients susceptible to cancer
-
Edinburgh, Scotland:
-
Harnden, D. G., and Taylor, A. M. R. The effects of radiation on the chromosomes of patients susceptible to cancer. In: H. J. Evans and D. C. Lloyd (eds.). Mutagen-induced Chromosome Damage in Man. pp. 52–61. Edinburgh, Scotland: 1978.
-
(1978)
Mutagen-induced Chromosome Damage in Man
, pp. 52-61
-
-
Harnden, D.G.1
Taylor, A.M.R.2
-
20
-
-
0017724485
-
DNA repair enzymes in ataxia telangiectasia and Bloom's syndrome fibroblasts
-
Inoue, T., Hirano, K. Yokoiyama, A., Kada, T., and Kato, H. DNA repair enzymes in ataxia telangiectasia and Bloom's syndrome fibroblasts. Biochim. Biophys. Acta, 479: 497–500, 1977.
-
(1977)
Biochim. Biophys. Acta
, vol.479
, pp. 497-500
-
-
Inoue, T.1
Hirano, K.2
Yokoiyama, A.3
Kada, T.4
Kato, H.5
-
21
-
-
84933353579
-
Ataxia telangiectasia: Characterization of heterozygotes
-
New York:
-
Lavin, M. F., Chen, P. C., and Kidson. C. Ataxia telangiectasia: Characterization of heterozygotes. In: P. C. Hanawalt, E. C. Friedberg, and C. F. Fox (eds.), DNA Repair Mechanisms, ICN-UCLA Symposia on Molecular and Cellular Biology, Vol. 9, pp. 651–654. New York: 1978.
-
(1978)
ICN-UCLA Symposia on Molecular and Cellular Biology
, vol.9
, pp. 651-654
-
-
Lavin, M.F.1
Chen, P.C.2
Kidson, C.3
-
22
-
-
0017736229
-
Repair of UV damage in a variety of human fibroblast cell strains
-
Lehmann, A. R., Kirk-Bell, S., Arlett, C. F., Harcourt, S. A., and Hall-Smith, P. Repair of UV damage in a variety of human fibroblast cell strains. Cancer Res., 37: 904–910. 1977.
-
(1977)
, vol.37
, pp. 904-910
-
-
Lehmann, A.R.1
Kirk-Bell, S.2
Arlett, C.F.3
Harcourt, S.A.4
Hall-Smith, P.5
-
23
-
-
0002886691
-
Human skin fibroblasts
-
New York: Academic Press, Inc.
-
Martin, G. M. Human skin fibroblasts. In: P. F. Kruse and M. K. Paterson (eds.). Tissue Culture—Methods and Applications, pp. 39–43. New York: Academic Press, Inc., 1973.
-
(1973)
Tissue Culture—Methods and Applications
, pp. 39-43
-
-
Martin, G.M.1
-
24
-
-
84909574888
-
Ataxia telangiectasia; an inherited human disease involving radiosensitivity
-
New York:
-
Paterson, M. C., Smith, B. P., Knight, P. A., and Anderson, A. K. Ataxia telangiectasia; an inherited human disease involving radiosensitivity, malignancy and defective DNA repair. In: A. Castellani (ed.), Research in Photobiology, pp. 207–218. New York: Plenum Publishing Corp., 1977.
-
(1977)
Research in Photobiology
, pp. 207-218
-
-
Paterson, M.C.1
Smith, B.P.2
Knight, P.A.3
Anderson, A.K.4
-
25
-
-
0017280394
-
Defective Excision Repair of gamma ray-damaged DNA in human
-
Paterson, M. C., Smith, B. P., Lohman, P. H. M., Anderson, A. K., and Fishman, L. Defective Excision Repair of gamma ray-damaged DNA in human (ataxia telangiectasia) fibroblasts. Nature (Lond.), 260: 444–447, 1976.
-
(1976)
Nature
, vol.260
, pp. 444-447
-
-
Paterson, M.C.1
Smith, B.P.2
Lohman, P.H.M.3
Anderson, A.K.4
Fishman, L.5
-
26
-
-
0013516337
-
Cytogenetic studies of ataxia telangiectasia
-
Rary, J. M., Bender, M. A., and Kelly, T. E. Cytogenetic studies of ataxia telangiectasia. Am. J. Hum. Genet., 26: 1974.
-
(1974)
Am. J. Hum. Genet.
, vol.26
-
-
Rary, J.M.1
Bender, M.A.2
Kelly, T.E.3
-
27
-
-
0014314284
-
Basal cell nevus syndrome
-
Rater, C. J., Seike, A. C., and van Epps, E. F. Basal cell nevus syndrome. Am. J. Roentgenol., 103: 589–594, 1968.
-
(1968)
Am. J. Roentgenol.
, vol.103
, pp. 589-594
-
-
Rater, C.J.1
Seike, A.C.2
van Epps, E.F.3
-
28
-
-
0015982924
-
Xeroderma pigmentosum: An inherited disease with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair
-
Robbins, J. H., Kraemer, K. H., Lutzner, M. A., Festoff, B. W., and Coon, H. G. Xeroderma pigmentosum: An inherited disease with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair. Ann. Intern. Med., 80: 221–248, 1974.
-
(1974)
Ann. Intern. Med.
, pp. 221-248
-
-
Robbins, J.H.1
Kraemer, K.H.2
Lutzner, M.A.3
Festoff, B.W.4
Coon, H.G.5
-
29
-
-
84965806406
-
-
Oxford, England:
-
Rook, A., Wilkinson, D. S., and Ebling, F. J. G. (eds.). Textbook of Dermatology, Ed. 2. Oxford, England: Blackwell Scientific Publications, 1972.
-
(1972)
Blackwell Scientific Publications
-
-
Rook, A.1
Wilkinson, D.S.2
Ebling, F.J.G.3
-
30
-
-
0017653212
-
Cockayne syndrome—cellular sensitivity to ultraviolet light
-
Schmickel, R. D., Chu, E. H. Y., Trosko, J. E., and Chang, C. C. Cockayne syndrome—cellular sensitivity to ultraviolet light. Pediatrics, 60: 135–139, 1977.
-
(1977)
Pediatrics
, vol.60
, pp. 135-139
-
-
Schmickel, R.D.1
Trosko, J.E.2
Chu, E.H.Y.3
Chang, C.C.4
-
31
-
-
0017154482
-
Malignant disease in heterozygous carriers. Natl. Found. March Dimes Birth Defects Orig
-
Swift, M. Malignant disease in heterozygous carriers. Natl. Found. March Dimes Birth Defects Orig. Artie. Ser., 12: 133–144, 1976.
-
(1976)
Artie. Ser.
, vol.12
, pp. 133-144
-
-
Swift, M.1
-
32
-
-
0016786321
-
Ataxia telangiectasia a human mutant with abnormal radiation sensitivity
-
Taylor, A. M. R., Harnden. D. G., Arlett, C. F., Harcourt, S. A., Lehmann, A. R., Stevens, S., and Bridges, B. A. Ataxia telangiectasia a human mutant with abnormal radiation sensitivity. Nature (Lond.), 258: 427–429, 1975.
-
(1975)
Nature
, vol.258
, pp. 427-429
-
-
Taylor, A.M.R.1
Harnden, D.G.2
Arlett, C.F.3
Harcourt, S.A.4
Lehmann, A.R.5
Stevens, S.6
Bridges, B.A.7
-
33
-
-
0017325660
-
Skin fibroblasts from a D-deletion type retinoblastoma patient are abnormally X-ray sensitive
-
Weichselbaum, R. R., Nove, J., and Little, J. B. Skin fibroblasts from a D-deletion type retinoblastoma patient are abnormally X-ray sensitive. Nature (Lond.), 266: 726–727, 1977.
-
(1977)
Nature
, vol.266
, pp. 726-727
-
-
Weichselbaum, R.R.1
Nove, J.2
Little, J.B.3
-
34
-
-
0018890926
-
X-Ray sensitivity of fifty-three human diploid fibroblast cell strains from patients with characterized genetic disorders
-
Weichselbaum, R. R., Nove, J., and Little, J. B. X-Ray sensitivity of fifty-three human diploid fibroblast cell strains from patients with characterized genetic disorders. Cancer Res., 40; 920–925, 1980.
-
(1980)
Cancer Res.
, vol.40
, pp. 920-925
-
-
Weichselbaum, R.R.1
Nove, J.2
Little, J.B.3
|