范科尼贫血的染色体特性及“体外”检查 - Suppr

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Chromosomal peculiarities and "in vitro" examinations in Fanconi's anaemia.

作者信息

Schuler D, Kiss A, Fábián F

出版信息

Humangenetik. 1969;7(4):314-22. doi: 10.1007/BF00283553.

DOI:10.1007/BF00283553

PMID:5365572

Abstract

摘要

相似文献

Chromosomal peculiarities and "in vitro" examinations in Fanconi's anaemia.范科尼贫血的染色体特性及“体外”检查

Humangenetik. 1969;7(4):314-22. doi: 10.1007/BF00283553.

[Chromosomal study of Fanconi's aplastic anemia. Apropos of 2 cases].

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Inherited aplastic anaemia with increased endoreduplications: a new syndrome of Fanconi's anaemia variant?伴有核内复制增加的遗传性再生障碍性贫血：范可尼贫血变异型的一种新综合征？

Br J Haematol. 1979 Jan;41(1):77-82. doi: 10.1111/j.1365-2141.1979.tb03683.x.

Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia.范科尼贫血中染色体畸变的氧依赖性

Nature. 1981 Mar 12;290(5802):142-3. doi: 10.1038/290142a0.

Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells.范科尼贫血：1例骨髓细胞存在显著染色体异常患者的报告。

J Med Genet. 1972 Dec;9(4):474-8. doi: 10.1136/jmg.9.4.474.

[Chromosomal anomalies in Fanconi's anemia (6 personal cases)].[范科尼贫血中的染色体异常（6例个人病例）]

Pediatrie. 1968 Mar;23(2):153-67.

Fanconi's anaemia; chromosome breakage in a large African family.

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Clinical and chromosome studies in Fanconi's aplastic anaemia.范科尼贫血的临床与染色体研究

J Med Genet. 1969 Mar;6(1):28-33. doi: 10.1136/jmg.6.1.28.

[Chromosome aberrations in Fanconi's aplastic anemia].

Pediatr Pol. 1985 Jan;60(1):87-9.

[Cytogenic and biochemical studies of 8 cases of Fanconi's anemia].

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引用本文的文献

Cytogenetics in Fanconi Anemia: The Importance of Follow-Up and the Search for New Biomarkers of Genomic Instability.范可尼贫血症的细胞遗传学：随访的重要性和寻找新的基因组不稳定性生物标志物。

Int J Mol Sci. 2022 Nov 15;23(22):14119. doi: 10.3390/ijms232214119.

Comparison of chromosome breakage in non-mosaic and mosaic patients with Fanconi anemia, relatives, and patients with other inherited bone marrow failure syndromes.非嵌合型和嵌合型范可尼贫血患者、亲属以及其他遗传性骨髓衰竭综合征患者的染色体断裂情况比较。

Cytogenet Genome Res. 2014;144(1):15-27. doi: 10.1159/000366251. Epub 2014 Sep 11.

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.

Genetic heterogeneity of Fanconi's anemia demonstrated by somatic cell hybrids.通过体细胞杂种证明的范可尼贫血的遗传异质性。

Hum Genet. 1980;56(1):81-4. doi: 10.1007/BF00281573.

Antagonistic effect of cocultivation on mitomycin C-induced aberration rate in cells of a patient with Fanconi's anemia and in Chinese hamster ovary cells.共培养对范可尼贫血患者细胞及中国仓鼠卵巢细胞中丝裂霉素C诱导的畸变率的拮抗作用。

Hum Genet. 1980;56(1):85-8. doi: 10.1007/BF00281574.

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.

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.

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.

The identification of fanconi anemia genotypes by clastogenic stress.通过致断裂应激鉴定范可尼贫血基因型

Am J Hum Genet. 1982 Sep;34(5):794-810.

Proliferative kinetics and mitomycin C-induced chromosome damage in Fanconi's anemia lymphocytes.范科尼贫血淋巴细胞的增殖动力学及丝裂霉素C诱导的染色体损伤

Hum Genet. 1983;63(1):19-23. doi: 10.1007/BF00285391.

本文引用的文献

Neonatal Aplastic Anaemia and Fanconi's Anaemia.新生儿再生障碍性贫血与范科尼贫血

Arch Dis Child. 1963 Feb;38(197):92-4. doi: 10.1136/adc.38.197.92.

Constitutional infantile panmyelopathy with multiple malformations Fanconi anemia.

Helv Paediatr Acta. 1952 Jun;7(3):299-308.

[FAMILIAL PANMYELOPATHY].[家族性全骨髓病]

Schweiz Med Wochenschr. 1964 Sep 19;94:1309-18.

PHYTOHAEMAGGLUTININ IN THE TREATMENT OF APLASTIC ANAEMIA.植物血凝素在再生障碍性贫血治疗中的应用

Lancet. 1965 May 29;1(7396):1164-5. doi: 10.1016/s0140-6736(65)91990-2.

PHYTOHAEMAGGLUTININ IN TREATMENT OF APLASTIC ANAEMIA.植物血凝素治疗再生障碍性贫血

Lancet. 1965 May 15;1(7394):1070-1. doi: 10.1016/s0140-6736(65)91348-6.

PHYTOHAEMAGGLUTININ IN TREATMENT OF APLASTIC ANAEMIA.植物血凝素治疗再生障碍性贫血

Lancet. 1965 May 1;1(7392):962. doi: 10.1016/s0140-6736(65)91296-1.

ENDOREDUPLICATION AND DISEASE.

Lancet. 1965 Apr 24;1(7391):915. doi: 10.1016/s0140-6736(65)92655-3.

CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN.人类一种罕见且可能由基因决定的综合征中的染色体断裂

Science. 1965 Apr 23;148(3669):506-7. doi: 10.1126/science.148.3669.506.

THE TREATMENT OF APLASTIC ANAEMIA WITH PHYTOHAEMAGGLUTININ.用植物血凝素治疗再生障碍性贫血

Lancet. 1964 Jun 20;1(7347):1345-9. doi: 10.1016/s0140-6736(64)92037-9.

The present status of the lymphocyte problem.淋巴细胞问题的现状。

Lancet. 1962 Jan 27;1(7222):206-11. doi: 10.1016/s0140-6736(62)91094-2.

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