Is Fanconi anemia caused by a defect in the processing of DNA damage? (Q52184525)

26 April 2018

review article

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title

Is Fanconi anemia caused by a defect in the processing of DNA damage? (English)

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26 April 2018

1 reference

Buchwald M

1

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26 April 2018

Moustacchi E

series ordinal

2

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26 April 2018

language of work or name

English

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publication date

1 August 1998

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26 April 2018

published in

Mutation Research

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26 April 2018

volume

408

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26 April 2018

issue

2

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26 April 2018

page(s)

75-90

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26 April 2018

Fanconi's anemia and malignancies

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When checkpoints fail

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Complementation groups: one or more per gene?

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Evidence for at least eight Fanconi anemia genes

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Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9

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Cloning of cDNAs for Fanconi's anaemia by functional complementation

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Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.

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Positional cloning of the Fanconi anaemia group A gene

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A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

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Abnormal lymphokine production: a novel feature of the genetic disease Fanconi anemia. I. Involvement of interleukin-6

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Tumor necrosis factor-alpha overproduction in Fanconi's anemia

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7 January 2021

Identification and chromosomal localization of a DNA fragment implicated in the partial correction of the Fanconi anemia group D cellular defect

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Isolation of an ubiquitously expressed cDNA encoding human dynamin II, a member of the large GTP-binding protein family

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Irreversible repression of DNA synthesis in Fanconi anemia cells is alleviated by the product of a novel cyclin-related gene

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Correction of radiation sensitivity in ataxia telangiectasia cells by a truncated I kappa B-alpha

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Overexpression of a truncated human topoisomerase III partially corrects multiple aspects of the ataxia-telangiectasia phenotype

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7 January 2021

Identification of two complementation groups in Fanconi anemia

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7 January 2021

Complementation group assignments in Fanconi anemia fibroblast cell lines from North America.

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7 January 2021

Fanconi anaemia complementation groups in Germany and The Netherlands. European Fanconi Anaemia Research group

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7 January 2021

In vitro effect of cyclophosphamide metabolites on chromosomes of Fanconi anaemia patients

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7 January 2021

Correction of the spontaneous and DEB-induced chromosomal aberrations in Fanconi anemia cells of the FA(C) complementation group by the FACC gene

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7 January 2021

Specific cellular defects in patients with Fanconi anemia

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7 January 2021

Chemical clastogenicity in lymphoid cell lines of chromosomal instability syndromes

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7 January 2021

Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations.

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7 January 2021

Multiplicity reactivation and mutagenesis of trimethylpsoralen-damaged herpes virus in normal and Fanconi's anaemia cells

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7 January 2021

Isolation and structure of a covalent cross-link adduct between mitomycin C and DNA

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7 January 2021

Recognition between mitomycin C and specific DNA sequences for cross-link formation

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7 January 2021

The sensitivity of Fanconi anaemia group C cells to apoptosis induced by mitomycin C is due to oxygen radical generation, not DNA crosslinking

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https://api.crossref.org/works/10.1016%2FS0921-8777%2898%2900024-X

7 January 2021

Cross-link repair in human cells and its possible defect in Fanconi's anemia cells

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7 January 2021

Defective repair of mitomycin C crosslinks in Fanconi's anemia and loss in confluent normal human and xeroderma pigmentosum cells

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7 January 2021

RecA-dependent incision of psoralen-crosslinked DNA by (A)BC excinuclease

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7 January 2021

The fate of 8-methoxypsoralen photoinduced crosslinks in nuclear and mitochondrial yeast DNA: comparison of wild-type and repair-deficient strains

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Pulsed-field gel electrophoresis analysis of the repair of psoralen plus UVA induced DNA photoadducts in Saccharomyces cerevisiae

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Psoralen Photoinactivation of Herpes Simplex Virus: Monoadduct and Cross-Link Repair by Xeroderma Pigmentosum and Fanconi's Anemia Cells

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Removal of psoralen monoadducts and crosslinks by human cell free extracts

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7 January 2021

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

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7 January 2021

Microinjection of normal cell extracts into Fanconi anemia fibroblasts corrects defective scheduled DNA synthesis recovery after 8-methoxypsoralen plus UVa treatment

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7 January 2021

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

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7 January 2021

Defective DNA endonuclease activities in Fanconi's anemia cells, complementation groups A and B

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7 January 2021

A damage-recognition protein which binds to DNA containing interstrand cross-links is absent or defective in Fanconi anemia, complementation group A, cells

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7 January 2021

Correction of the DNA repair defect in Fanconi anemia complementation groups A and D cells

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7 January 2021

Immunological probing of induction and repair of 8-methoxypsoralen photoadducts in DNA from Fanconi anemia and normal human fibroblasts: quantitative analysis by electron microscopy

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7 January 2021

6,4,4'-Trimethylangelicin photoadduct immunodetection in DNA: induction and repair in Fanconi's anemia and normal human fibroblasts

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7 January 2021

Repair analysis of mitomycin C-induced DNA crosslinking in ribosomal RNA genes in lymphoblastoid cells from Fanconi's anemia patients

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7 January 2021

Fanconi anaemia cells are not uniformly deficient in unhooking of DNA interstrand crosslinks, induced by mitomycin C or 8-methoxypsoralen plus UVA.

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7 January 2021

Induction and removal of interstrand crosslinks in the ribosomal RNA genes of lymphoblastoid cell lines from patients with Fanconi anemia

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7 January 2021

Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells

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7 January 2021

Reactivation of psoralen-reacted plasmid DNA in Fanconi anemia, xeroderma pigmentosum, and normal human fibroblast cells

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7 January 2021

The basal and the mutagen-induced levels of ADP-ribosyl transferase activity are not modified in Fanconi's anemia cells

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7 January 2021

No abnormalities in the NAD+ ADP-ribosyltransferase (polymerizing) gene of transformed cells from a Fanconi's anemia patient

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7 January 2021

Cell cycle effects of the DNA topoisomerase inhibitors camptothecin and m-AMSA in lymphoblastoid cell lines from patients with Fanconi anemia

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7 January 2021

Comparison of the effects of DNA topoisomerase inhibitors on lymphoblasts from normal and Fanconi anemia donors

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7 January 2021

Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus

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7 January 2021

HPRT gene expression differs in mutants derived from normal and Fanconi anemia cells: analysis of spontaneous and psoralen-photoinduced mutants

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7 January 2021

Molecular spectrum of mutations induced at the HPRT locus by a cross-linking agent in human cell lines with different repair capacities

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7 January 2021

The molecular mechanism underlying formation of deletions in Fanconi anemia cells may involve a site-specific recombination

1 reference

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7 January 2021

Mutagenic processing of psoralen monoadducts differ in normal and Fanconi anemia cells

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7 January 2021

Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining

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7 January 2021

Small polydispersed circular DNA (spcDNA) in human cells: association with genomic instability

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7 January 2021

Elevated homologous recombination activity in fanconi anemia fibroblasts

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7 January 2021

Mutagenesis by third-strand-directed psoralen adducts in repair-deficient human cells: high frequency and altered spectrum in a xeroderma pigmentosum variant

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7 January 2021

Mutational response of Fanconi anaemia cells to shuttle vector site-specific psoralen cross-links

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7 January 2021

Frequencies of HPRT- lymphocytes and glycophorin A variants erythrocytes in Fanconi anemia patients, their parents and control donors

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7 January 2021

The role of oxygen metabolism for the pathological phenotype of Fanconi anemia

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7 January 2021

Hypersensitivity to oxygen is a uniform and secondary defect in Fanconi anemia cells

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7 January 2021

Cell cycle defect in connection with oxygen and iron sensitivity in Fanconi anemia lymphoblastoid cells

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7 January 2021

Expression of the Fanconi anemia gene FAC in human cell lines: lack of effect of oxygen tension.

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7 January 2021

Increased formation of 8-hydroxydeoxyguanosine, an oxidative DNA damage, in lymphoblasts from Fanconi's anemia patients due to possible catalase deficiency

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7 January 2021

In vivo accumulation of 8-hydroxy-2'-deoxyguanosine in DNA correlates with release of reactive oxygen species in Fanconi's anaemia families

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7 January 2021

Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector

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7 January 2021

The cell cycle of lymphocytes in Fanconi anemia

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7 January 2021

Fanconi anemia. Chromosome breakage and cell cycle studies

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7 January 2021

G2 phase cell cycle disturbance as a manifestation of genetic cell damage

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7 January 2021

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

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7 January 2021

Decreased IL-1 beta and TNF alpha secretion in long-term bone marrow culture supernatant from Fanconi's anaemia patients

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7 January 2021

Apoptosis is not involved in the hypersensitivity of Fanconi anemia cells to mitomycin C

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7 January 2021

p53 activates Fanconi anemia group C gene expression

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7 January 2021

The Fanconi anemia polypeptide FACC is localized to the cytoplasm

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7 January 2021

Identification of Cytosolic Proteins That Bind to the Fanconi Anemia Complementation Group C Polypeptidein Vitro

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7 January 2021

The Fanconi anaemia proteins, FAA and FAC, interact to form a nuclear complex

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7 January 2021

MxA overexpression reveals a common genetic link in four Fanconi anemia complementation groups

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7 January 2021

Sequence variation in the Fanconi anemia gene FAA

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7 January 2021

DNA helicases in inherited human disorders

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7 January 2021

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Identifiers

DOI

1 reference

26 April 2018

PubMed ID

9739810

1 reference

26 April 2018