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: Anne Stary, Alain Sarasin, Leon H.F. Mullenders

المصدر: Atlas of Genetics and Cytogenetics in Oncology and Haematology.

مصطلحات موضوعية: Cancer Research, Oncology, Chemistry, Genetics, Cancer research, Hematology, Nucleotide excision repair

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::5a46bbf922dbda9dfae732c3849c2020Test
https://doi.org/10.4267/2042/37743Test

المؤلفون: Anne Stary, Alain Sarasin

المصدر: Atlas of Genetics and Cytogenetics in Oncology and Haematology.

مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Xeroderma pigmentosum, integumentary system, nutritional and metabolic diseases, Hematology, Biology, medicine.disease, Molecular biology, Complementation group, chemistry.chemical_compound, Oncology, chemistry, medicine, skin and connective tissue diseases, Gene, DNA, Chromosome 13

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::dbf37b3821c56fd35417483cf20b6d50Test
https://doi.org/10.4267/2042/37753Test

المؤلفون: Alain Sarasin, Anne Stary

المصدر: Atlas of Genetics and Cytogenetics in Oncology and Haematology.

مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Xeroderma pigmentosum, integumentary system, nutritional and metabolic diseases, Hematology, Biology, medicine.disease, Molecular biology, Complementation group, chemistry.chemical_compound, Oncology, chemistry, medicine, skin and connective tissue diseases, Gene, DNA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::47231f87ef953c9747c903934c7b7469Test
https://doi.org/10.4267/2042/37808Test

المؤلفون: Hélène Dollfus, Victoria Murday, Pierre Sarda, E. Raffo, Patrick Edery, Alain Sarasin, Jacqueline Vigneron, D. Gubser-Mercati, Andrew R. Gennery, Karen Fieggen, Vincent Laugel, Valérie Drouin-Garraud, F. Sauvanaud, Dominique Martin-Coignard, Hubert Journel, Louise Brueton, John Tolmie, Marie-Claire Vincent, Alan R. Lehmann, Delphine Héron, Benoît Funalot, Stanislas Lyonnet, D. Pham, Jean-Marc Egly, Mustafa A. Salih, Sylvie Odent, U. Kristensen, E. Muñoz, Agnès Bloch-Zupan, Heather Fawcett, Edward S. Tobias, J. Sanchez del Pozo, Blanca Gener, Brigitte Chabrol, Lina M. Ramos, M. Durand, Cecile Dalloz, Zornitza Stark, K. Prescott, Laurent Pasquier, Mehrdad Noruzinia, Valérie Cormier-Daire

المساهمون: Service de génétique médicale, CHU Strasbourg-Hôpital de Hautepierre [Strasbourg], Institut de génétique et biologie moléculaire et cellulaire (IGBMC), Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de diagnostic génétique, CHU Strasbourg, Laboratoire de génétique moléculaire et génomique médicale [CHU Rennes], CHU Pontchaillou [Rennes], Service de Génétique Médicale [CHU Necker], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Department of Medical Genetics, Hospital de Cruces, Division of Developmental Medicine, Royal Hospital for Sick Children, Service de génétique, Centre Hospitalier Le Mans (CH Le Mans), Service de génétique [Rouen], CHU Rouen, Normandie Université (NU)-Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Génétique Médicale, Centre hospitalier Bretagne Atlantique (Morbihan) (CHBA)-Hôpital Chubert, Service de Pédiatrie [CHRU Nancy], Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy), Consultation de Génétique, Neurologie Pédiatrique, Hôpital neuchâtelois, Service de Neurologie [CHU Limoges], CHU Limoges, Biomolécules Thérapies anti-tumorales (EA4021), Université de Limoges (UNILIM)-Génomique, Environnement, Immunité, Santé, Thérapeutique (GEIST FR CNRS 3503), Department of Clinical Genetics, Birmingham Women's Hospital, Centro de Biología Molecular Severo Ochoa [Madrid] (CBMSO), Universidad Autónoma de Madrid (UAM)-Consejo Superior de Investigaciones Científicas [Madrid] (CSIC), Department Neurology, Hospital Clinic, Department of Pediatrics, Newcastle General Hospital, Division of Pediatric Neurology, King Saud University [Riyadh] (KSU), Department of Hematology, Tarbiat Modares University [Tehran], St James's University Hospital, Pediatric Hospital, Genetic Health Services Victoria, Groote Schuur and Red Cross Children's Hospital, Service de pédiatrie et neurologie pédiatrique, Université de la Méditerranée - Aix-Marseille 2-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE), Unité de Génétique Médicale et Foetopathologie, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Hôpital Arnaud de Villeneuve, Service de Génétique, Hospices Civils de Lyon (HCL), Reference Centre for Oral Manifestations of Rare Diseases, Hôpitaux Universitaires de Strasbourg, Centre for Genome Damage and Stability, University of Sussex, Génomes et cancer (GC (FRE2939)), Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Centre National de la Recherche Scientifique (CNRS), Institut de génétique et biologie moléculaire et cellulaire ( IGBMC ), Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ), Laboratoire de Génétique Moléculaire et Hormonologie, Hôpital Pontchaillou, Assistance publique - Hôpitaux de Paris (AP-HP)-CHU Necker - Enfants Malades [AP-HP], CH Le Mans, CHU Rouen-Université de Rouen Normandie ( UNIROUEN ), Normandie Université ( NU ) -Normandie Université ( NU ), Service de Génétique Cytogénétique et Embryologie [CHU Pitié-Salpêtrière], Assistance publique - Hôpitaux de Paris (AP-HP)-CHU Pitié-Salpêtrière [APHP], Centre Hospitalier Bretagne Atlantique-Hôpital Chubert, Centre Hospitalier Régional Universitaire de Nancy ( CHRU Nancy ), Biomolécules Thérapies anti-tumorales ( EA4021 ), Université de Limoges ( UNILIM ) -Génomique, Environnement, Immunité, Santé, Thérapeutique ( GEIST FR CNRS 3503 ), Centro de Biología Molecular Severo Ochoa ( CBMSO ), Universidad Autonoma de Madrid ( UAM ) -Consejo Superior de Investigaciones Científicas [Spain] ( CSIC ), King Saud University [Riyadh] ( KSU ), Tarbiat Modares University, Université de la Méditerranée - Aix-Marseille 2-Assistance Publique - Hôpitaux de Marseille ( APHM ) - Hôpital de la Timone [CHU - APHM] ( TIMONE ), Centre Hospitalier Régional Universitaire [Montpellier] ( CHRU Montpellier ) -Hôpital Arnaud de Villeneuve, Hospices Civils de Lyon ( HCL ), Génomes et cancer ( GC (FRE2939) ), Université Paris-Sud - Paris 11 ( UP11 ) -Institut Gustave Roussy ( IGR ) -Centre National de la Recherche Scientifique ( CNRS ), CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Universidad Autonoma de Madrid (UAM)-Consejo Superior de Investigaciones Científicas [Madrid] (CSIC), De Villemeur, Hervé

المصدر: Human Mutation
Human Mutation, 2010, 31 (2), pp.113-26. ⟨10.1002/humu.21154⟩
Human Mutation, Wiley, 2010, 31 (2), pp.113-26. 〈10.1002/humu.21154〉
Human Mutation, Wiley, 2010, 31 (2), pp.113-26. ⟨10.1002/humu.21154⟩

مصطلحات موضوعية: Molecular Sequence Data, Prenatal diagnosis, [SDV.GEN] Life Sciences [q-bio]/Genetics, Biology, medicine.disease_cause, Bioinformatics, Cockayne syndrome, 03 medical and health sciences, Structure-Activity Relationship, 0302 clinical medicine, [SDV.BDD] Life Sciences [q-bio]/Development Biology, Databases, Genetic, Genetics, medicine, Missense mutation, Coding region, Humans, Amino Acid Sequence, [ SDV.BDD ] Life Sciences [q-bio]/Development Biology, Cockayne Syndrome, Poly-ADP-Ribose Binding Proteins, Gene, [SDV.BDD]Life Sciences [q-bio]/Development Biology, Genetics (clinical), Genetic Association Studies, 030304 developmental biology, 0303 health sciences, Mutation, [SDV.GEN]Life Sciences [q-bio]/Genetics, Polymorphism, Genetic, DNA Helicases, medicine.disease, 3. Good health, ERCC8, DNA Repair Enzymes, ERCC6, [ SDV.GEN ] Life Sciences [q-bio]/Genetics, Sequence Alignment, 030217 neurology & neurosurgery, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::580207dd2444c2f96378e05a74ec87caTest
https://www.hal.inserm.fr/inserm-00436454Test

المؤلفون: Alain Sarasin, Carlos Frederico Martins Menck, Anne Stary

المصدر: Mutation Research/Environmental Mutagenesis and Related Subjects. 272:101-110

مصطلحات موضوعية: Herpesvirus 4, Human, Methylnitronitrosoguanidine, Base Sequence, Mutagenicity Tests, Base pair, Point mutation, Genetic Vectors, Molecular Sequence Data, lac operon, Locus (genetics), DNA, Simian virus 40, Biology, beta-Galactosidase, Toxicology, Molecular biology, Cell Line, Plasmid, Shuttle vector, Genetics, Humans, Low copy number, Gene, Plasmids

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a023a19f3dbc78320ba754723f6f4ecfTest
https://doi.org/10.1016/0165-1161Test(92)90038-n

المؤلفون: Michael R. James, André Cordier, Alain Sarasin, Denis S.F. Biard

المصدر: Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1130:68-74

مصطلحات موضوعية: Chloramphenicol O-Acetyltransferase, Isopropyl Thiogalactoside, Herpesvirus 4, Human, Transcription, Genetic, Operon, Genetic Vectors, Molecular Sequence Data, Biophysics, Repressor, lac operon, Biology, Lac repressor, Biochemistry, Cell Line, Structural Biology, Gene expression, Escherichia coli, Genetics, Humans, Promoter Regions, Genetic, Regulation of gene expression, Reporter gene, Base Sequence, Promoter, beta-Galactosidase, Molecular biology, Repressor Proteins, carbohydrates (lipids), Zinc, Gene Expression Regulation, Lac Operon, Cadmium, Plasmids

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca8db58cfc847624ecbd7ecef6088526Test
https://doi.org/10.1016/0167-4781Test(92)90463-a

المؤلفون: Andrew Collins, Jan H.J. Hoeijmakers, R. Montesano, Ethel Moustacchi, Miria Stefanini, Claude Backendorf, G.P. van der Schans, R.P.D. Fuchs, Małgorzata Z. Zdzienicka, Geoffrey P. Margison, Bryn A. Bridges, A.A. van Zeeland, L.H. Thompson, Christine A. Weber, Charles Allen Smith, Erling Seeberg, Alain Sarasin, Adayapalam T. Natarajan, Alan R. Lehmann, Miroslav Radman

المصدر: Mutation Research/DNA Repair. 273:1-28

مصطلحات موضوعية: Genetics, DNA repair, education, Local organization, Library science, Biology, Toxicology, Molecular Biology, Defective DNA repair

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d7d4148877648a87a5025ccc887007a9Test
https://doi.org/10.1016/0921-8777Test(92)90046-6

المؤلفون: Anne Stary, Alain Sarasin

المصدر: Nucleic Acids Research. 20:4269-4274

مصطلحات موضوعية: DNA Replication, Recombination, Genetic, Genetics, Base Sequence, Antigens, Polyomavirus Transforming, FLP-FRT recombination, Genetic Vectors, Molecular Sequence Data, Alu element, Simian virus 40, Biology, Origin of replication, chemistry.chemical_compound, Plasmid, Proviruses, chemistry, Humans, Ectopic recombination, In vitro recombination, Recombination, DNA, HeLa Cells, Plasmids, Repetitive Sequences, Nucleic Acid

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b54f6b011193081c9f5d565a9058426dTest
https://doi.org/10.1093/nar/20.16.4269Test

المؤلفون: Alain Sarasin, J. Armier, Vassiliki Pletsa, Alain Gentil, Soterios A. Kyrtopoulos, A. Margot

المصدر: Nucleic Acids Research. 20:4897-4901

مصطلحات موضوعية: Genetics, Mutation, Guanine, Mutagenesis, O-6-methylguanine-DNA methyltransferase, Biology, medicine.disease_cause, Molecular biology, chemistry.chemical_compound, Plasmid, chemistry, Shuttle vector, biology.protein, medicine, Mutation frequency, psychological phenomena and processes, Polymerase

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::940e88b2d89dd237349be4c559abb3b9Test
https://doi.org/10.1093/nar/20.18.4897Test