128 related articles for article (PubMed ID: 6878899)
1. In vitro radiosensitivity of fibroblasts derived from patients with retinoblastoma and abnormalities of chromosome 13.
Weichselbaum RR; Nichols WW; Albert DM; Little JB
Retina; 1983; 3(2):126-30. PubMed ID: 6878899
[TBL] [Abstract][Full Text] [Related]
2. An in vitro investigation of x-ray sensitivity in fibroblasts from patients with retinoblastoma.
Weichselbaum R; Albert DM; Cassady JR; Little JB
Invest Ophthalmol Vis Sci; 1983 Jul; 24(7):958-61. PubMed ID: 6862797
[TBL] [Abstract][Full Text] [Related]
3. Radiosensitivity of fibroblasts from patients with retinoblastoma and chromosome-13 anomalies.
Ejima Y; Sasaki MS; Utsumi H; Kaneko A; Tanooka H
Mutat Res; 1982 Feb; 103(2):177-84. PubMed ID: 7057793
[TBL] [Abstract][Full Text] [Related]
4. Retinoblastoma, chromosome 13, and in vitro cellular radiosensitivity.
Nove J; Little JB; Weichselbaum RR; Nichols WW; Hoffman E
Cytogenet Cell Genet; 1979; 24(3):176-84. PubMed ID: 477414
[TBL] [Abstract][Full Text] [Related]
5. Abnormalities of human chromosome 13 and in vitro radiosensitivity; a study of 19 fibroblast strains.
Nove J; Nichols WW; Weichselbaum RR; Little JB
Mutat Res; 1981 Nov; 84(1):157-67. PubMed ID: 7329430
[TBL] [Abstract][Full Text] [Related]
6. Sister chromatid exchanges and chromosome aberrations in fibroblasts from patients with retinoblastoma.
Takabayashi T; Lin MS; Wilson MG
Hum Genet; 1983; 63(4):317-9. PubMed ID: 6862435
[TBL] [Abstract][Full Text] [Related]
7. Repair of potentially lethal X-ray damage in fibroblasts derived from patients with hereditary and D-deletion retinoblastoma.
Weichselbaum RR; Tomkinson K; Little JB
Int J Radiat Biol Relat Stud Phys Chem Med; 1985 Apr; 47(4):445-56. PubMed ID: 3872857
[TBL] [Abstract][Full Text] [Related]
8. X-ray, UV and chemical mutagen sensitivities of skin fibroblasts from patients with familial and chromosome 13q- retinoblastomas.
Fujiwara Y; Miyazaki N; Kano Y; Takahashi T; Kaneko A
J Radiat Res; 1981 Dec; 22(4):472-6. PubMed ID: 7338842
[No Abstract] [Full Text] [Related]
9. New findings in the chromosome 13 long-arm deletion syndrome and retinoblastoma.
Weichselbaum RR; Zakov ZN; Albert DM; Friedman AH; Nove J; Little JB
Ophthalmology; 1979 Jun; 86(6):1191-201. PubMed ID: 118416
[TBL] [Abstract][Full Text] [Related]
10. An in vitro investigation of genetic susceptibility to cancer in diploid fibroblasts from retinoblastoma patients.
Weichselbaum RR; Nove J; Albert D; Little JB
Teratog Carcinog Mutagen; 1980; 1(2):171-9. PubMed ID: 6119809
[TBL] [Abstract][Full Text] [Related]
11. Retinoblastoma with 13q- chromosomal deletion associated with maternal paracentric inversion of 13q.
Sparkes RS; Muller H; Klisak I
Science; 1979 Mar; 203(4384):1027-9. PubMed ID: 424728
[TBL] [Abstract][Full Text] [Related]
12. Multiple karyotypic changes in retinoblastoma tumor cells: presence of normal chromosome No. 13 in most tumors.
Gardner HA; Gallie BL; Knight LA; Phillips RA
Cancer Genet Cytogenet; 1982 Jul; 6(3):201-11. PubMed ID: 7116318
[TBL] [Abstract][Full Text] [Related]
13. Cellular studies on retinoblastoma.
Morten JE
Int J Radiat Biol Relat Stud Phys Chem Med; 1986 Mar; 49(3):485-93. PubMed ID: 2937750
[TBL] [Abstract][Full Text] [Related]
14. Comparison of kinetics of X-ray-induced cell killing in normal, ataxia telangiectasia and hereditary retinoblastoma fibroblasts.
Nagasawa H; Little JB
Mutat Res; 1983 May; 109(2):297-308. PubMed ID: 6843573
[TBL] [Abstract][Full Text] [Related]
15. Retinoblastoma and its association with a deletion in chromosome #13: a survey using high-resolution chromosome techniques.
Johnson MP; Ramsay N; Cervenka J; Wang N
Cancer Genet Cytogenet; 1982 May; 6(1):29-37. PubMed ID: 7104985
[TBL] [Abstract][Full Text] [Related]
16. Gene carrier detection in retinoblastoma.
Gallie BL
Ophthalmology; 1980 Jun; 87(6):591-5. PubMed ID: 7413148
[TBL] [Abstract][Full Text] [Related]
17. Radiation sensitivity of cell strains from families with genetic disorders predisposing to radiation-induced cancer.
Little JB; Nichols WW; Troilo P; Nagasawa H; Strong LC
Cancer Res; 1989 Sep; 49(17):4705-14. PubMed ID: 2758405
[TBL] [Abstract][Full Text] [Related]
18. X-ray sensitivity of fibroblasts from patients with hereditary retinoblastoma and their families.
Pledger JV; Craft AW; Bartlett K; Long DR
Br J Cancer; 1987 Jun; 55(6):617-21. PubMed ID: 3620303
[TBL] [Abstract][Full Text] [Related]
19. Chromosomal abnormalities in human retinoblastoma. A review.
Potluri VR; Helson L; Ellsworth RM; Reid T; Gilbert F
Cancer; 1986 Aug; 58(3):663-71. PubMed ID: 3524791
[TBL] [Abstract][Full Text] [Related]
20. G2-phase chromosomal radiosensitivity of primary fibroblasts from hereditary retinoblastoma family members and some apparently normal controls.
Wilson PF; Nagasawa H; Fitzek MM; Little JB; Bedford JS
Radiat Res; 2010 Jan; 173(1):62-70. PubMed ID: 20041760
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
