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Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells.

作者信息

Auerbach A D, Wolman S R

出版信息

Nature. 1978 Jan 5;271(5640):69-71. doi: 10.1038/271069a0.

DOI:10.1038/271069a0
PMID:625326
Abstract
摘要

相似文献

1
Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells.
Nature. 1978 Jan 5;271(5640):69-71. doi: 10.1038/271069a0.
2
Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens.
Nature. 1976 Jun 10;261(5560):494-6. doi: 10.1038/261494a0.
3
Clinical and cytogenetic diversity in Fanconi's anaemia.范可尼贫血的临床和细胞遗传学多样性
J Med Genet. 1984 Jun;21(3):197-203. doi: 10.1136/jmg.21.3.197.
4
Fanconi's anemia--chromosome breakage studies in homozygotes and heterozygotes.范科尼贫血——纯合子和杂合子的染色体断裂研究
Cancer Genet Cytogenet. 1988 Jul 15;33(2):175-83. doi: 10.1016/0165-4608(88)90027-1.
5
Fanconi's anaemia in adults: study of three families.
Haematologica. 1977 Dec;62(6):615-28.
6
Fanconi's anaemia; chromosome breakage in a large African family.
Hereditas. 1980;93(2):255-60. doi: 10.1111/j.1601-5223.1980.tb01365.x.
7
Fanconi's anemia: terminal leukemia and "Forme fruste" in one family.
Clin Genet. 1979 Oct;16(4):260-8. doi: 10.1111/j.1399-0004.1979.tb00998.x.
8
[Chromosome abnormalities in bone marrow cells and peripheral lymphocytes in a patient with Fanconi's anemia].[范可尼贫血患者骨髓细胞和外周淋巴细胞中的染色体异常]
Minerva Med. 1981 Sep 22;72(35):2361-5.
9
Sensitivity to five mutagens in Fanconi's anemia as measured by the micronucleus method.
Cancer Res. 1978 Sep;38(9):2983-8.
10
[Fanconi's anemia: in vitro tests for the individualization of heterozygotes].[范科尼贫血：杂合子个体化的体外检测]
G Ital Med Lav. 1986 May-Jul;8(3-4):133-8.

引用本文的文献

1
Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype.使用血型糖蛋白A体细胞突变检测法快速、明确地鉴定范可尼贫血纯合子，无论其GPA基因型如何。
Am J Med Genet A. 2005 May 15;135(1):59-65. doi: 10.1002/ajmg.a.30687.
2
DNA repair dependent NAD+ metabolism is impaired in cells from patients with Fanconi's anemia.范可尼贫血患者细胞中依赖DNA修复的NAD+代谢受损。
EMBO J. 1983;2(3):303-7. doi: 10.1002/j.1460-2075.1983.tb01423.x.
3
Suppression of spontaneous and mitomycin C-induced chromosome aberrations in Fanconi's anemia by cell fusion with normal human fibroblasts.
通过与正常人成纤维细胞进行细胞融合抑制范科尼贫血中自发的和丝裂霉素C诱导的染色体畸变。
Hum Genet. 1980;55(2):223-6. doi: 10.1007/BF00291770.
4
Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect.布鲁姆综合征杂合子成纤维细胞的功能缺陷作为原发性缺陷的特异性表现。
Am J Hum Genet. 1981 Nov;33(6):928-34.
5
Reduced uptake and incorporation of 3H-thymidine in Fanconi anemia fibroblasts.范可尼贫血成纤维细胞中³H-胸腺嘧啶核苷摄取和掺入减少。
Hum Genet. 1981;57(3):296-9. doi: 10.1007/BF00278948.
6
The cell cycle of lymphocytes in Fanconi anemia.范可尼贫血中淋巴细胞的细胞周期
Hum Genet. 1982;62(4):327-32. doi: 10.1007/BF00304549.
7
Dna repair: pathways and defects.DNA修复：途径与缺陷
Eur J Pediatr. 1980 Dec;135(2):121-8. doi: 10.1007/BF00441631.
8
Sister chromatid exchange analysis.
Am J Hum Genet. 1980 May;32(3):297-313.
9
Cytogenetic toxicity of antitumor platinum compounds in Fanconi's anemia.抗肿瘤铂化合物对范可尼贫血的细胞遗传学毒性。
Hum Genet. 1982;61(3):228-30. doi: 10.1007/BF00296447.
10
Response of lymphocytes from Fanconi's anemia patients and their heterozygous relatives to 8-methoxy-psoralene in a cloning survival test system.范科尼贫血患者及其杂合子亲属的淋巴细胞在克隆存活测试系统中对8-甲氧基补骨脂素的反应。
Hum Genet. 1983;64(2):167-72. doi: 10.1007/BF00327118.