D. Papadopoulo

发表

Protein interaction mapping: a Drosophila case study.

R. Chanet, G. Faye, J. Girault, 2005, Genome research.

Genotoxic potential of psoralen cross-links versus monoadducts in normal human lymphoblasts.

D. Papadopoulo, E. Moustacchi, A. Laquerbe, 1995, Mutation research.

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

D. Papadopoulo, E. Moustacchi, J. Boyse, 1993, Mutation research.

Fidelity of DNA double-strand break repair in heterozygous cell lines harbouring BRCA1 missense mutations

D. Papadopoulo, D. Stoppa-Lyonnet, I. Coupier, 2004, Oncogene.

Relative efficiencies of three ultraviolet radiation wavelengths for cell killing and transformation in mouse cells in vitro.

D. Papadopoulo, R. Latarjet, B. Muel, 1983, International journal of radiation biology and related studies in physics, chemistry, and medicine.

Arrest of S-phase progression is impaired in Fanconi anemia cells.

D. Papadopoulo, E. Moustacchi, D. Rouillard, 2000, Experimental cell research.

Molecular spectra of HPRT deletion mutations in circulating T-lymphocytes in Fanconi anemia patients.

D. Papadopoulo, A. Laquerbe, M. Escarceller, 1999, Mutation research.

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

H. Mohrenweiser, D. Papadopoulo, C. Guillouf, 1990, Proceedings of the National Academy of Sciences of the United States of America.

A single mutated BRCA1 allele leads to impaired fidelity of double strand break end-joining

D. Papadopoulo, D. Stoppa-Lyonnet, J. Smith, 2002, Oncogene.

Decreased deletion mutation in radioadapted human lymphoblasts.

D. Papadopoulo, E. Moustacchi, O. Rigaud, 1993, Radiation research.

Abnormal rearrangements associated with V(D)J recombination in Fanconi anemia.

D. Papadopoulo, J. Andrau, N. Doyen, 1998, Journal of molecular biology.

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

D. Papadopoulo, C. Guillouf, E. Moustacchi, 1993, Mutation research.

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

D. Papadopoulo, C. Guillouf, E. Moustacchi, 1991, Somatic cell and molecular genetics.

Erratum: Protein interaction mapping: A Drosophila case study (Genome Research (2005) 15 (376-384))

Alain Vincent, Pierre Legrain, Bernard Jacq, 2005 .

Mutagenic effects photoinduced in normal human lymphoblasts by a monofunctional pyridopsoralen in comparison to 8-methoxypsoralen.

D. Papadopoulo, E. Moustacchi, Ethel Moustacchi, 1990, Mutation research.

Possible anti-recombinogenic role of Bloom's syndrome helicase in double-strand break processing.

C. Delteil, D. Papadopoulo, P. Calsou, 2003, Nucleic acids research.

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

D. Papadopoulo, E. Moustacchi, B. Porfirio, 1990, Cancer research.

Phenotypic and Genetic Heterogeneity in Fanconi Anemia, Fate of Cross-Links, and Correction of the Defect by DNA Transfection

D. Averbeck, D. Papadopoulo, E. Moustacchi, 1989 .

Protein interaction mapping: A Drosophila case study (vol 15, pg 376, 2005)

R. Chanet, G. Faye, C. Brun, 2005 .

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

D. Papadopoulo, C. Guillouf, E. Moustacchi, 1993, Mutagenesis.

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

P. Jeggo, S. Jackson, M. Buchwald, 1998, Journal of molecular biology.

Hypomutability inFanconi anemia cells isassociated withincreased deletion frequency attheHPRT locus

D. Papadopoulo, C. Guillouf, H. MOHRENWEISERt, 1990 .

Normal and benzo(a)pyrene-transformed fetal mouse brain cells

B. Coulomb, D. Papadopoulo, P. Benda, 1979, Acta Neuropathologica.

[Fanconi anemia: genes and function(s) revisited].

D. Papadopoulo, E. Moustacchi, 2005, Medecine sciences : M/S.

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

D. Averbeck, D. Papadopoulo, E. Moustacchi, 1987, Mutation research.

Genotoxic effects and DNA photoadducts induced in Chinese hamster V79 cells by 5-methoxypsoralen and 8-methoxypsoralen.

D. Averbeck, D. Papadopoulo, 1985, Mutation research.

Mutagenic effects of psoralens in yeast and V79 Chinese hamster cells.

D. Averbeck, D. Papadopoulo, I. Quinto, 1984, National Cancer Institute monograph.

Mutagenic effects of 3-carbethoxypsoralen and 8-methoxypsoralen plus 365-nm irradiation in mammalian cells.

D. Averbeck, D. Papadopoulo, F. Sagliocco, 1983, Mutation research.

Damage in Normal and Fanconi's Anemia Cell Lines ,8-Trimethylpsoralen plus Light-induced DNA ' Repair of 4,5

D. Averbeck, D. Papadopoulo, E. Moustacchi, 2015 .

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

M. Buchwald, D. Papadopoulo, E. Moustacchi, 1987, Human Genetics.

Processing of Photoinduced Cross-Links and Monoadducts in Human Cell DNA: Genetic and Molecular Features

D. Averbeck, D. Papadopoulo, E. Moustacchi, 1989 .

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

D. Averbeck, D. Papadopoulo, E. Moustacchi, 1988, Cancer research.

HIGH LEVELS OF 4,5′,8‐TRIMETHYLPSORALEN PHOTOINDUCED FURAN‐SIDE MONOADDUCTS CAN BLOCK CROSS‐LINK REMOVAL IN NORMAL HUMAN CELLS

D. Papadopoulo, E. Moustacchi, D. Averback, 1988, Photochemistry and photobiology.

Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency.

M. Cavazzana‐Calvo, D. Papadopoulo, G. de Saint Basile, 1993, The Journal of clinical investigation.

MUTAGENIC EFFECTS PHOTOINDUCED IN MAMMALIAN CELLS IN VITRO BY TWO MONOFUNCTIONAL PYRIDOPSORALENS

D. Averbeck, D. Papadopoulo, E. Moustacchi, 1986, Photochemistry and photobiology.

The fidelity of double strand breaks processing is impaired in complementation groups B and D of fanconi anemia, a genetic instability syndrome

D. Papadopoulo, E. Moustacchi, S. Rousset, 1997, Somatic cell and molecular genetics.

Establishment of normal diploid and malignant heteroploid cell lines from non-treated and benzo(a)pyrene treated hamster embryo cell cultures

D. Papadopoulo, S. Mann, P. Sabharwal, 1975, Experientia.

Effects of several dimethylbenzacridines on secondary hamster embryo cells: neoplastic transformation.

D. Papadopoulo, V. Poirier, P. Markovits, 1981, European journal of cancer.

Hamster cells, untreated and treated with chemical carcinogens, maintained in vitro for 2 1/2 years.

D. Papadopoulo, L. Chamaillard, P. Markovits, 1977, British Journal of Cancer.

Transformation of hamster embryo cells by 7-methyl benz(a)anthracene in vitro: tumorigenicity, chromosome pattern and spheroid formation.

D. Papadopoulo, S. Nocentini, L. Chamaillard, 1976, European journal of cancer.

Malignant transformation of hamster embryo cells in tissue culture by 7,10‐dimethyl benzo(c)acridine

D. Papadopoulo, A. Mazabraud, J. Coppey, 1974, International journal of cancer.

The influence of DNA double-strand break structure on end-joining in human cells.

D. Papadopoulo, C. Baldeyron, J. Smith, 2001, Nucleic acids research.

A Human Severe Combined Immunodeficiency (SCID) Condition with Increased Sensitivity to Ionizing Radiations and Impaired V(D)J Rearrangements Defines a New DNA Recombination/Repair Deficiency

A. Fischer, M. Cavazzana‐Calvo, D. Papadopoulo, 1998, The Journal of experimental medicine.

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

J. Fuscoe, D. Papadopoulo, E. Moustacchi, 1995, Proceedings of the National Academy of Sciences of the United States of America.

The Transcriptional Histone Acetyltransferase Cofactor TRRAP Associates with the MRN Repair Complex and Plays a Role in DNA Double-Strand Break Repair

Z. Herceg, L. Tora, D. Papadopoulo, 2006, Molecular and Cellular Biology.

Photochemotherapy using pyridopsoralens.

D. Averbeck, J. Blais, D. Papadopoulo, 1985, Biochimie.

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

D. Averbeck, D. Papadopoulo, E. Moustacchi, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Impact of DNA ligase IV on the fidelity of end joining in human cells.

M. Lieber, P. Jeggo, D. Papadopoulo, 2003, Nucleic acids research.

Decreased mutagenicity in Fanconi's anemia lymphoblasts following treatment with photoactivated psoralens.

D. Papadopoulo, C. Guillouf, E. Moustacchi, 1990, Progress in clinical and biological research.

The mutagenic processing of psoralen photolesions leaves a highly specific signature at an endogenous human locus.

D. Papadopoulo, C. Guillouf, E. Moustacchi, 1996, Journal of molecular biology.

Lack of detectable defect in DNA double‐strand break repair and DNA‐dependent protein kinase activity in radiosensitive human severe combined immunodeficiency fibroblasts

S. Jackson, M. Cavazzana‐Calvo, D. Papadopoulo, 1996, European journal of immunology.

The Mutagenic Processing of Psoralen Photolesions Leaves a Highly Specific Signature at an Endogenous Human Locus

D. Papadopoulo, C. Guillouf, E. Moustacchi, 1995 .

Normal and benzo(a)pyrene-transformed fetal mouse brain cells

D. Papadopoulo, M. Toga, M. Tripier, 1979, Acta Neuropathologica.

Normal and benzo(a)pyrene-transformed fetal mouse brain cell. I. Tumorigenicity and immunochemical detection of glial fibrillary acidic protein.

B. Coulomb, D. Papadopoulo, P. Benda, 1979, Acta neuropathologica.