Cytogenetics of Bloom's syndrome

Cancer Genetics and Cytogenetics

Volumn 22, Issue 1, 1986, Pages 1-18

  Kuhn, Evelyn M ^a   Therman, Eeva ^b  

^a UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD AND HEMOPOIETIC SYSTEM; BLOOM SYNDROME; CARCINOGENESIS; CHROMOSOME ABERRATION; CHROMOSOME Q BAND; CONGENITAL DISORDER; HEREDITY; HISTOLOGY; HUMAN; HUMAN CELL; IMMUNE DEFICIENCY; IN VITRO STUDY; LYMPHATIC SYSTEM; LYMPHOCYTE; PRIORITY JOURNAL; SHORT SURVEY; SISTER CHROMATID EXCHANGE;

BLOOM SYNDROME; BONE MARROW; CELLS, CULTURED; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CROSSING OVER (GENETICS); FIBROBLASTS; GENETIC MARKERS; HUMAN; KARYOTYPING; LYMPHOCYTES; MITOSIS; ONCOGENES; PRECANCEROUS CONDITIONS; RISK; SISTER CHROMATID EXCHANGE; SUPPORT, NON-U.S. GOV'T;

EID: 0022467739     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/0165-4608(86)90132-9     Document Type: Review

References (73)

1. No increased chromosome breakage in three Bloom's syndrome heterozygotes
2. Spontaneous cell fusion and PCC formation in Bloom's syndrome
3. Cytogenetic investigations in a new case of Bloom's syndrome
4. The behavior of allocyclic chromosomes in Bloom's syndrome
5. Chromosome breakage and rejoining of sister chromatids in Bloom's syndrome
6. Localization by Q-banding of mitotic chiasmata in cases of Bloom's syndrome
7. Hot spots and functional organization of human chromosomes
8. A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes
9. Bloom's syndrome. IV. Sister chromatid exchanges in lymphocytes
10. Dimorphism of sister chromatid exchange in Bloom's syndrome B- and T-cell lines transformed with Epstein—Barr and adult T-cell leukemia viruses
11. Effect of cocultivation on sister chromatid exchange frequencies in Bloom's syndrome and normal fibroblast cells
12. Clastogenic activity from Bloom syndrome fibroblast cultures
13. Chromosome breakage factor in the plasma of two Bloom's syndrome patients
14. Bloom syndrome fibroblasts secrete a metabolite which enhances SCE rate in normal fibroblasts
15. Sister chromatid exchange in cells metabolically coupled to Bloom's syndrome cells
16. Suppression of the frequencies of sister chromatid exchanges in Bloom's syndrome fibroblasts by co-cultivation with Chinese hamster cells
17. Frequency of sister chromatid exchanges in Bloom's syndrome fibroblasts reduced by cocultivation with normal cells
18. Mutagen-induced sister chromatid exchange rate in Bloom's syndrome remains unaltered in the presence of Bloom corrective factor
19. Bloom's syndrome: In vitro correction of the sister chromatid exchange rate by normal cells
20. Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect
21. Normalization of sister chromatid exchange frequencies in Bloom's syndrome by euploid cell hybridization
22. High rate of sister chromatid exchanges of Bloom's syndrome chromosomes is corrected in rodent human somatic cell hybrids
23. Normalization by cell fusion of sister chromatid exchange in Bloom's syndrome lymphocytes
24. Correction of sister chromatid exchanges in Bloom's syndrome fibroblasts after fusion with cytoplasts from a Chinese hamster cell line
25. Effect of incubation temperature on the frequency of sister chromatid exchanges in Bloom's syndrome lymphocytes
26. Effects of temperature on sister chromatid exchange in Bloom syndrome cells
27. Analyses of bromodeoxyuridine-associated sister chromatid exchanges (SCEs) in Bloom syndrome based on cell fusion: Single and twin SCEs in endoreduplication
28. A retarded rate of DNA chain growth in Bloom's syndrome
29. Ultraviolet light sensitivity and delayed DNA-chain maturation in Bloom's syndrome fibroblasts
30. Quantitative replicon analysis of DNA synthesis in cancer-prone conditions and the defects in Bloom's syndrome
31. DNA fork displacement rates in Bloom's syndrome fibroblasts
32. Altered temporal expression of DNA repair in hypermutable Bloom's syndrome cells
33. Elevated spontaneous mutation rate in Bloom syndrome fibroblasts
34. Bloom's syndrome: evidence for an increased mutation frequency in vivo
35. Cytological demonstration of mitotic crossing-over in man
36. Bloom's syndrome. III. Analysis of the chromosome aberration characteristic of this disorder
37. The internal order of the interphase nucleus
38. Position of chromosomes in the human interphase nucleus
39. Mitotic recombination and segregation of satellites in Bloom's syndrome
40. Incidence and origin of symmetric and asymmetric dicentrics in Bloom's syndrome
41. A high incidence of mitotic chiasmata in endoreduplicated Bloom's syndrome cells
42. Mitotic chiasmata in human diplochromosomes
43. Mitotic crossing-over and segregation in man
44. Mitotic chiasmata and other quadriradials in mitomycin C-treated Bloom's syndrome lymphocytes
45. Effects of x-irradiation in G1 and G2 on Bloom's syndrome and normal chromosomes
46. Terminal association of homologous chromosomes at metaphase a new cytogenetic finding in Bloom's syndrome
47. Molecular evidence for genetic exchanges among ribosomal genes on nonhomologous chromosomes in man and apes
48. “Jumping” satellites in three generations: A warning for paternity tests and prenatal diagnosis
49. An unstable giant satellite associated with chromosomes 21 and 22 in the same individual
50. Questionable Bloom's syndrome in a negro girl
51. Leukemia in a black child with Bloom's syndrome
52. Apparently isodicentric but functionally monocentric X chromosome in man
53. A woman with multiple congenital anomalies mental retardation and mosaicism for an unusual translocation chromosome t(6;19)
54. Chromosomal rearrangements and protein structure
55. 2 gene
56. Mitotic crossing-over in man
57. Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement
58. Mitotic chiasmata, gene density, and oncogenes
59. Nonrandom localization of mitotic crossing-over in Bloom's syndrome
60. Origin of symmetrical triradial chromosomes in human cells
61. Cytogenetics of pregnancy wastage
62. Three main classes of constitutive heterochromatin in man: intercalary, Y-type and centric
63. Partial 11q trisomy syndrome
64. Characterization of Giemsa dark- and light-band DNA
65. Replication timing of genes and middle repetitive sequences
66. The chromosomal basis of human neoplasia
67. Metaphase chromosome anomaly: Association with drug resistance and cell-specific products
68. Mapping of human small nuclear RNA genes by in situ hybridization
69. Homogeneously staining chromosomal regions contain amplified copies of an abundantly expressed cellular oncogene (c-myc) in malignant neuroendocrine cells from a human colon carcinoma
70. Expression of recessive alleles by chromosomal mechanisms in retinoblastoma