(Q41711508)

English

Partial complementation of the Fanconi anemia defect upon transfection by heterologous DNA. Phenotypic dissociation of chromosomal and cellular hypersensitivity to DNA cross-linking agents

scientific article published on December 1990

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scholarly article

1 reference

Europe PubMed Central

7 October 2017

Partial complementation of the Fanconi anemia defect upon transfection by heterologous DNA. Phenotypic dissociation of chromosomal and cellular hypersensitivity to DNA cross-linking agents (English)

1 reference

Europe PubMed Central

7 October 2017

1 reference

based on heuristic

inferred from title

author name string

C Diatloff-Zito

1

1 reference

Europe PubMed Central

7 October 2017

F Rosselli

2

1 reference

Europe PubMed Central

7 October 2017

J Heddle

3

1 reference

Europe PubMed Central

7 October 2017

E Moustacchi

4

1 reference

Europe PubMed Central

7 October 2017

publication date

1 December 1990

1 reference

Europe PubMed Central

7 October 2017

1 reference

Europe PubMed Central

7 October 2017

86

1 reference

Europe PubMed Central

7 October 2017

2

1 reference

Europe PubMed Central

7 October 2017

151-161

1 reference

Europe PubMed Central

7 October 2017

https://scigraph.springernature.com/pub.10.1007/bf00197697

0 references

Human chromosome 15 confers partial complementation of phenotypes to xeroderma pigmentosum group F cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Measurement of micronuclei in lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fate of 8-methoxypsoralen-photoinduced DNA interstrand crosslinks in Fanconi's anemia cells of defined genetic complementation groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Co-recessive inheritance: a model for DNA repair, genetic disease and carcinogenesis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stable radioresistance in ataxia-telangiectasia cells containing DNA from normal human cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fanconi's anaemia: correlation of genetic complementation group with psoralen/UVA response.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensitivity to five mutagens in Fanconi's anemia as measured by the micronucleus method

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reaction of DNA with chemically or enzymatically activated mitomycin C: isolation and structure of the major covalent adduct

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on gene transfer and reversion to UV resistance in xeroderma pigmentosum cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of UV-resistant revertants from a xeroderma pigmentosum complementation group A cell line

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal response to DNA crosslinking agents of Fanconi anemia fibroblasts can be corrected by transfection with normal human DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cocultivation of Fanconi anemia cells and of mouse lymphoma mutants leads to interspecies complementation of chromosomal hypersensitivity to DNA cross-linking agents.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a HeLa mRNA fraction which can correct the DNA-repair defect in Fanconi anaemia fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutagenic response of Fanconi's anemia cells from a defined complementation group after treatment with photoactivated bifunctional psoralens

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of a human gene that regulates chromosome condensation and is essential for cell proliferation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). I. Clinical aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic cloning and preliminary characterization of the human thymidine kinase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth of cultured cells from patients with Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Susceptibility of Fanconi's anemia lymphoblasts to DNA-cross-linking and alkylating agents

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Repair of 4,5',8-trimethylpsoralen plus light-induced DNA damage in normal and Fanconi's anemia cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formal genetics of Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene transfer in lymphoid cells: expression of the Thy-1.2 antigen by Thy-1.1 BW5147 lymphoma cells transfected with unfractionated cellular DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two complementation groups of Fanconi's anemia differ in their phenotypic response to a DNA-crosslinking treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA semi-conservative synthesis in normal and Fanconi anemia fibroblasts following treatment with 8-methoxypsoralen and near ultraviolet light or with X-rays.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transfection of normal human and Chinese hamster DNA corrects diepoxybutane-induced chromosomal hypersensitivity of Fanconi anemia fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The production of micronuclei from chromosome aberrations in irradiated cultures of human lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic toxicity of antitumor platinum compounds in Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of a human DNA repair gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific cellular defects in patients with Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suppression of cytotoxic effect of mitomycin-C by superoxide dismutase in Fanconi's anemia and dyskeratosis congenita fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of gene transfer and reversion to mitomycin C resistance in Fanconi anemia cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of two complementation groups in Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic heterogeneity within the first complementation group of UV-sensitive mutants of Chinese hamster cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis by electron microscopy of the removal of psoralen-photoinduced DNA cross-links in normal and Fanconi's anemia fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of a mouse DNA repair gene that complements the defect of group-A xeroderma pigmentosum

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complementation of a DNA repair defect in xeroderma pigmentosum cells by transfer of human chromosome 9.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning and characterization of a mammalian excision repair gene that partially restores UV resistance to xeroderma pigmentosum complementation group D cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2265827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00197697

1 reference

Europe PubMed Central

7 October 2017

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0 references

1 reference

Europe PubMed Central

7 October 2017

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