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1دورية أكاديمية
المؤلفون: Ayman Al Saati, Pierre Vande Perre, Julien Plenecassagnes, Julia Gilhodes, Nils Monselet, Bastien Cabarrou, Norbert Lignon, Thomas Filleron, Dominique Telly, Emilie Perello-Lestrade, Viviane Feillel, Anne Staub, Mathilde Martinez, Edith Chipoulet, Gaëlle Collet, Fabienne Thomas, Laurence Gladieff, Christine Toulas
المصدر: International Journal of Molecular Sciences, Vol 24, Iss 18, p 14348 (2023)
مصطلحات موضوعية: male breast cancer predisposition, large multigene panel sequencing, MBC-specific mutated profile, new genes potentially involved in MBC risk, Biology (General), QH301-705.5, Chemistry, QD1-999
وصف الملف: electronic resource
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المؤلفون: Julie Meilleroux, David Grand, Anne Cécile Brunac, Etienne Buscail, Marie Danjoux, Samira Icher, Anne Pascale Laurenty, Marion Jaffrelot, Edith Chipoulet, Delphine Bonnet, C. Maulat, Pierre Vande Perre, Eliane Mery, Janick Selves, Anne Staub, Rosine Guimbaud, Nadim Fares, Christine Toulas
المصدر: Modern Pathology. 35:427-437
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Pathology, medicine.medical_specialty, MLH1, medicine.disease_cause, DNA Mismatch Repair, complex mixtures, Pathology and Forensic Medicine, PMS2, Humans, Medicine, Mismatch Repair Endonuclease PMS2, Mutation, business.industry, Syndrome, Phenotype, digestive system diseases, MSH6, MutS Homolog 2 Protein, MSH2, Immunohistochemistry, Microsatellite Instability, DNA mismatch repair, Colorectal Neoplasms, MutL Protein Homolog 1, business
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المؤلفون: N Hamzaoui, Christine Toulas, Delphine Bonnet, P Vande Perre, Janick Selves, J S Hoffmann, A Siegfried, Rosine Guimbaud, Carole Corsini, Emmanuelle Uro-Coste, Edith Chipoulet
المصدر: Familial Cancer. 18:173-178
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Heterozygote, Cancer Research, Colorectal cancer, 030105 genetics & heredity, Germline, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Uterine cancer, Genetics, Humans, Medicine, Poly-ADP-Ribose Binding Proteins, Germ-Line Mutation, Genetics (clinical), Aged, Aged, 80 and over, Brain Neoplasms, business.industry, DNA Polymerase II, Middle Aged, medicine.disease, Human genetics, Pedigree, Giant-cell glioblastoma, Adenomatous Polyposis Coli, Oncology, Giant cell, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), Cancer research, Female, Colorectal Neoplasms, Glioblastoma, business
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المؤلفون: Christine Toulas, Caroline Delmas, Janick Selves, Rosine Guimbaud, Pascal Pujol, Anne-Françoise Tilkin-Mariamé, Stefania Millevoi, Gilles Favre, Françoise Fouque, Adrien Decorsière, Jean-Marc Rey, Edith Chipoulet, Stéphan Vagner
المساهمون: Centre de Recherches en Cancérologie de Toulouse (CRCT), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut Claudius Regaud, CRLCC Institut Claudius Regaud, Equipe 11-E.Moyal/C.Toulas, Service d'anatomie et cytologie pathologiques [Purpan], Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-CHU Toulouse [Toulouse]-Hôpital Purpan [Toulouse], CHU Toulouse [Toulouse], Département d'Oncologie Digestive [CHU Toulouse], Hôpital Arnaud de Villeneuve, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Biomarqueurs prédictifs et nouvelles stratégies moléculaires en thérapeutique anticancéreuse (U981), Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Gustave Roussy (IGR)-Université Paris-Sud - Paris 11 (UP11), Institut Gustave Roussy (IGR), Université Paris-Sud - Paris 11 (UP11), This work was supported by INSERM and FRM (Equipe FRM, soutenue par la Fondation Recherche Médicale to S.V.) and the Groupe de Recherche de l’Institut Claudius Regaud (F.F., C.T., S.M., S.V., R.G.). A.D. was a recipient of a studentship from ARC (Association pour la recherche sur le cancer) and FRM., The authors sincerely thank Thomas Filleron for his help in statistical analyses, Chantal Darnau, Pauline Dejean and Isabelle Gitlaw for their efficient technical assistance., Hôpital Arnaud de Villeneuve [CHRU Montpellier], Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-CHU Toulouse [Toulouse]
المصدر: Cell Cycle
Cell Cycle, Taylor & Francis, 2012, 11 (13), pp.2578-2580. ⟨10.4161/cc.20625⟩مصطلحات موضوعية: Polyadenylation, 0302 clinical medicine, MRNA polyadenylation, MESH: DNA-Binding Proteins/genetics, Gene Duplication, Gene duplication, 3' Untranslated Regions, ComputingMilieux_MISCELLANEOUS, Genetics, 0303 health sciences, MESH: Polymorphism, Single Nucleotide, MESH: Gene Duplication, MESH: 3' Untranslated Regions, Lynch syndrome, MESH: Polyadenylation, DNA-Binding Proteins, 030220 oncology & carcinogenesis, MESH: Cell Line, Tumor, MESH: Mutation, Base pair, MESH: HCT116 Cells, [SDV.CAN]Life Sciences [q-bio]/Cancer, Biology, MESH: DNA-Binding Proteins/metabolism, Polymorphism, Single Nucleotide, 03 medical and health sciences, MESH: Colorectal Neoplasms, Hereditary Nonpolyposis/metabolism, Cell Line, Tumor, medicine, Humans, RNA, Messenger, Molecular Biology, 030304 developmental biology, MESH: Humans, MESH: RNA, Messenger/metabolism, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, Cell Biology, MSH6, medicine.disease, HCT116 Cells, Colorectal Neoplasms, Hereditary Nonpolyposis, MESH: Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, MESH: HeLa Cells, Mutation, Developmental Biology, HeLa Cells
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المؤلفون: Delphine Bonnet, Bastien Cabarrou, Janick Selves, Christine Toulas, Thomas Filleron, Marie Danjoux, Rosine Guimbaud, Camille Herve, Anne Staub, Edith Chipoulet, Anne-Pascale Laurenty
المصدر: Journal of Clinical Oncology. 33:e14629-e14629
مصطلحات موضوعية: Oncology, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Mutation, medicine.medical_specialty, business.industry, Colorectal cancer, Microsatellite instability, Bioinformatics, medicine.disease, medicine.disease_cause, Phenotype, digestive system diseases, Lynch syndrome, Germline mutation, Internal medicine, DNA methylation, Medicine, DNA mismatch repair, business, neoplasms
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::5adce2a14ca30bd15aef28c8ea4c6074
https://doi.org/10.1200/jco.2015.33.15_suppl.e14629
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