المؤلفون: Denis Biard, Alexandre T. Vessoni, Annabel Quinet, Alain Sarasin, Davi Jardim Martins, Carlos Frederico Martins Menck, Anne Stary

المساهمون: Universidade de São Paulo = University of São Paulo (USP), Institut de Radiobiologie Cellulaire et Moléculaire (IRCM), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay, Intégrité du génome et cancers (IGC), École Pratique des Hautes Études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut Gustave Roussy (IGR)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), University of São Paulo (USP), Stabilité Génétique et Oncogenèse (UMR 8200), Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Nucleic Acids Research
Nucleic Acids Research, 2016, 44 (12), pp.5717-5731. ⟨10.1093/nar/gkw280⟩
Nucleic Acids Research, Oxford University Press, 2016, 44 (12), pp.5717-5731. ⟨10.1093/nar/gkw280⟩

مصطلحات موضوعية: DNA Replication, 0301 basic medicine, MESH: Human Cells, DNA Repair, Ultraviolet Rays, DNA repair, DNA polymerase, DNA damage, MESH: DNA Lesion, Genetic Vectors, DNA, Single-Stranded, Pyrimidine dimer, [SDV.CAN]Life Sciences [q-bio]/Cancer, DNA-Directed DNA Polymerase, Genome Integrity, Repair and Replication, Adenoviridae, S Phase, 03 medical and health sciences, Transduction, Genetic, Genetics, Postreplication repair, Humans, Cell Line, Transformed, MESH: Xeroderma Pigmentosum, MESH: DNA Damage, MESH: Translesion Synthesis, biology, Genome, Human, DNA replication, Nuclear Proteins, MESH: Ultraviolet, Fibroblasts, DNA Replication Fork, Nucleotidyltransferases, Cell biology, DNA-Binding Proteins, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Pyrimidine Dimers, biology.protein, REV1, MESH: Coronary Disease, Deoxyribodipyrimidine Photo-Lyase, DNA Damage

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5b6b3e6c5f04e7774ad3693216e7f7bTest
https://hal.science/hal-03679922/documentTest

المؤلفون: Nicolas Dupin, Nadem Soufir, Alain Sarasin, S. Regnier, Jean-Jacques Lacapère, M.-F. Avril, G. Hetet, D. Pham, Bernard Grandchamp, André Palangié, Agnes Bourillon, Isabelle Gorin, S. Jacobelli

المصدر: British Journal of Dermatology. 159:968-973

مصطلحات موضوعية: Skin Neoplasms, Xeroderma pigmentosum, DNA Repair, Mutation, Missense, Dermatology, Biology, Gene mutation, medicine.disease_cause, White People, Frameshift mutation, Neoplasms, Multiple Primary, Exon, medicine, Humans, Missense mutation, Survivors, Frameshift Mutation, Melanoma, Pigmentation disorder, Aged, 80 and over, Genetics, Xeroderma Pigmentosum, Mutation, medicine.disease, DNA-Binding Proteins, Phenotype, Cancer research, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca0d7813ca05d2cb6a73c1d059b513d7Test
https://doi.org/10.1111/j.1365-2133.2008.08791.xTest

المؤلفون: Alain Sarasin, Simone Benhamou

المصدر: American Journal of Epidemiology. 161:1-14

مصطلحات موضوعية: Genetics, Lung Neoplasms, Polymorphism, Genetic, Xeroderma pigmentosum, Genotype, Epidemiology, Haplotype, DNA Helicases, Exons, Biology, medicine.disease, DNA-Binding Proteins, Cancer research, medicine, Humans, ERCC2, Genetic Predisposition to Disease, Lung cancer, Genotyping Techniques, Transcription Factors, Xeroderma Pigmentosum Group D Protein, Nucleotide excision repair, Genetic association

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e63c99732919473992d5a9d4242a4975Test
https://doi.org/10.1093/aje/kwi018Test

المؤلفون: Alain Sarasin, Apuã C.M. Paquola, Renata M. A. Costa, Lydia Riou, Carlos Frederico Martins Menck

المصدر: Oncogene. 24:1359-1374

مصطلحات موضوعية: Cancer Research, Xeroderma pigmentosum, DNA Repair, Transcription, Genetic, Ultraviolet Rays, DNA repair, Trichothiodystrophy, Down-Regulation, Biology, Transfection, medicine.disease_cause, Cell Line, Neoplasms, Genetics, medicine, Humans, Allele, Cockayne Syndrome, Molecular Biology, Alleles, Oligonucleotide Array Sequence Analysis, Xeroderma Pigmentosum, Gene Expression Profiling, DNA Helicases, Syndrome, Fibroblasts, Cell cycle, medicine.disease, Isogenic human disease models, Molecular biology, Up-Regulation, DNA-Binding Proteins, Mutation, Hair Diseases, Carcinogenesis, Nucleotide excision repair

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c58cbe92010a6d4bbcb6d6de777598fTest
https://doi.org/10.1038/sj.onc.1208288Test

المؤلفون: Simone Benhamou, Alain Sarasin

المصدر: Mutagenesis. 17:463-469

مصطلحات موضوعية: Skin Neoplasms, Xeroderma pigmentosum, DNA Repair, DNA repair, Health, Toxicology and Mutagenesis, Population, Single-nucleotide polymorphism, Biology, Toxicology, Polymorphism, Single Nucleotide, Exon, Risk Factors, Neoplasms, Genetics, medicine, Humans, education, Gene, Genetics (clinical), Xeroderma Pigmentosum Group D Protein, Xeroderma Pigmentosum, education.field_of_study, Polymorphism, Genetic, Models, Genetic, Smoking, DNA Helicases, Proteins, Cancer, medicine.disease, DNA-Binding Proteins, Mutation, ERCC2, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::452857a81861a2b0beb08791af377a5dTest
https://doi.org/10.1093/mutage/17.6.463Test

المؤلفون: Anne Stary, Alain Sarasin, Osamu Nikaido, Mauro Mezzina, Lin Zeng, Alain Taieb, Lydia Riou, Odile Chevallier-Lagente, Geert Weeda

المساهمون: Molecular Genetics

المصدر: Human Molecular Genetics, 8(6), 1125-1133. Oxford University Press

مصطلحات موضوعية: Male, DNA, Complementary, Xeroderma pigmentosum, DNA Repair, Ultraviolet Rays, DNA repair, Recombinant Fusion Proteins, Trichothiodystrophy, Biology, Transfection, medicine.disease_cause, Cockayne syndrome, Genetics, medicine, Humans, Child, Cockayne Syndrome, Molecular Biology, Gene, Genetics (clinical), Cell Line, Transformed, Xeroderma Pigmentosum, Mutation, DNA Helicases, DNA, General Medicine, Middle Aged, medicine.disease, Molecular biology, DNA-Binding Proteins, Gene Expression Regulation, Pyrimidine Dimers, Child, Preschool, Transcription factor II H, Hair Diseases, Nucleotide excision repair

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11fa342c74773d11cce7fb4f217de4ecTest
https://doi.org/10.1093/hmg/8.6.1125Test

المؤلفون: Alain Sarasin, Tiziana Nardo, Veridiana Munford, Fernanda C. Cabral, Carlos Frederico Martins Menck, Clarissa Ribeiro Reily Rocha, Januário B. Cabral-Neto, Daniela T. Soltys, Miria Stefanini, Leticia K. Lerner, Tiago Antonio de Souza

المصدر: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

مصطلحات موضوعية: Male, Heterozygote, Xeroderma pigmentosum, Adolescent, DNA Repair, DNA repair, DNA damage, Cell Survival, Protein Conformation, Ultraviolet Rays, Molecular Sequence Data, Mutation, Missense, Biology, medicine.disease_cause, Cockayne syndrome, Cell Line, Young Adult, Genotype, Genetics, medicine, Humans, Amino Acid Sequence, Cloning, Molecular, Cockayne Syndrome, Gene, Genetics (clinical), Alleles, Mutation, Xeroderma Pigmentosum, Nuclear Proteins, MICROBIOLOGIA, Sequence Analysis, DNA, Fibroblasts, medicine.disease, Endonucleases, Molecular biology, DNA-Binding Proteins, Oxidative Stress, Phenotype, Female, Sequence Alignment, Brazil, Nucleotide excision repair, DNA Damage, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::074273beee3a518622375203fb9573ecTest
https://pubmed.ncbi.nlm.nih.gov/23255472Test

المؤلفون: Emilie Warrick, Alain Sarasin, Odile Chevallier, Marcela Del Rio, Thierry Magnaldo, Daniela Sartori, Fulvio Mavilio, Fernando Larcher, Françoise Bernerd, Marie-Françoise Avril, Marta García, Valérie Bergoglio, Corinne Chagnoleau, Jaime F. Angulo

المساهمون: L'Oréal Recherche France (L'Oréal Recherche), L'OREAL, Centre européen de recherche et d'enseignement des géosciences de l'environnement (CEREGE), Institut de Recherche pour le Développement (IRD)-Institut National de la Recherche Agronomique (INRA)-Aix Marseille Université (AMU)-Collège de France (CdF (institution))-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS), Etude des relations instabilité génétique et cancer (ERIGC), Centre National de la Recherche Scientifique (CNRS), Stabilité Génétique et Oncogenèse (UMR 8200), Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Centre National de la Recherche Scientifique (CNRS), Institut de pharmacologie et de biologie structurale (IPBS), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS), Généthon, Laboratoire de Génétique de la Radiosensibilité, Département de Radiobiologie et Radiopathologie, Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Hôpital Cochin [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Génomes et cancer (GC (FRE2939)), Epithelial Biomedicine Division [CIEMAT Madrid], Centro de Investigaciones Energéticas Medioambientales y Tecnológicas [Madrid] (CIEMAT), Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Collège de France (CdF)-Institut national des sciences de l'Univers (INSU - CNRS)-Aix Marseille Université (AMU)-Institut National de la Recherche Agronomique (INRA), GENETHON 3, CHU Cochin [AP-HP], Aix Marseille Université (AMU)-Institut national des sciences de l'Univers (INSU - CNRS)-Collège de France (CdF (institution))-Institut de Recherche pour le Développement (IRD)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Recherche Agronomique (INRA), Centre National de la Recherche Scientifique (CNRS)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées

المصدر: Molecular Therapy
Molecular Therapy, Cell Press, 2012, 20 (4), pp.798-807. ⟨10.1038/mt.2011.233⟩
Molecular Therapy, 2012, 20 (4), pp.798-807. ⟨10.1038/mt.2011.233⟩
Molecular Therapy, Nature Publishing Group, 2012, 20 (4), pp.798-807. ⟨10.1038/mt.2011.233⟩
e-Archivo. Repositorio Institucional de la Universidad Carlos III de Madrid
instname

مصطلحات موضوعية: Keratinocytes, [SDV]Life Sciences [q-bio], Human skin, 030207 dermatology & venereal diseases, 0302 clinical medicine, Drug Discovery, Cells, Cultured, ComputingMilieux_MISCELLANEOUS, Skin, 0303 health sciences, education.field_of_study, DNA-repair, Stem Cells, Group-C protein, Flow Cytometry, 3. Good health, DNA-Binding Proteins, Blotting, Southern, medicine.anatomical_structure, Blotting, Western, Epidermis, Genetic Therapy, Humans, Real-Time Polymerase Chain Reaction, Xeroderma Pigmentosum, Molecular Biology, Molecular Medicine, Genetics, Drug Discovery3003 Pharmaceutical Science, Pharmacology, Dystrioguc epidermolysis-bullosa, Original Article, Stem cell, Keratinocyte, Human epidermal-keratinocytes, Xeroderma pigmentosum, Retroviral vectors, Medicina, Population, Biology, 03 medical and health sciences, Long-term engraftement, Transduction, In-vivo assessment, medicine, education, Clonogenic assay, 030304 developmental biology, medicine.disease, Molecular biology, Epidermal Cells, Therapy, Skin cancer, Nucleotide excision repair, Nucleotide excision-repair

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e94f324583b71b0c2379856743affb73Test
https://hdl.handle.net/10016/18254Test

المؤلفون: Romina Zanier, Alain Sarasin, Delphine Briot, Filippo Rosselli, Jean-Antoine Dugas du Villard

المصدر: Oncogene. 23(29)

مصطلحات موضوعية: Cancer Research, Fanconi anemia, complementation group C, DNA Repair, DNA damage, DNA repair, Gene Expression, Cell Cycle Proteins, Biology, medicine.disease_cause, Gene product, Fanconi anemia, hemic and lymphatic diseases, Gene expression, Genetics, medicine, Humans, Myeloid Cells, ATP Binding Cassette Transporter, Subfamily B, Member 1, Molecular Biology, Gene, Oligonucleotide Array Sequence Analysis, Inflammation, Fanconi Anemia Complementation Group C Protein, NF-kappa B, Nuclear Proteins, Proteins, Cell Differentiation, medicine.disease, Molecular biology, Fanconi Anemia Complementation Group Proteins, DNA-Binding Proteins, Gene Expression Regulation, Mutation, Carcinogenesis

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3db4618d68fd7395a35743c909a4df65Test
https://pubmed.ncbi.nlm.nih.gov/15077170Test

المؤلفون: Odile Chevallier-Lagente, Florence Brellier, Catherine Arnaudeau-Bégard, Jan H.J. Hoeijmakers, Françoise Bernerd, Alain Sarasin, Thierry Magnaldo

المساهمون: Molecular Genetics

المصدر: Human Gene Therapy, 14(10), 983-996. Mary Ann Liebert Inc.

مصطلحات موضوعية: Keratinocytes, Xeroderma pigmentosum, DNA Repair, Cell Survival, DNA repair, Biology, Autosomal recessive trait, SDG 3 - Good Health and Well-being, Transduction, Genetic, Genetics, medicine, Humans, Child, Molecular Biology, Cells, Cultured, Skin, Xeroderma Pigmentosum, Transition (genetics), Integrin beta1, Genetic Complementation Test, Cancer, medicine.disease, DNA-Binding Proteins, Complementation, Child, Preschool, Cancer research, Molecular Medicine, Moloney murine leukemia virus, Skin cancer, Cell Division, Nucleotide excision repair

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a7d3c8247c07bc79d9e78932381c684Test
https://pure.eur.nl/en/publications/2f9bde05-1589-4919-9d81-5b9e31d9f5e7Test