المؤلفون: Cyril Burin des Roziers, Benjamin Dauriat, Michel Vidaud, Laurence Pacot, Hélène Dollfus, Catherine Yardin, Brigitte Gilbert-Dussardier, Camille Tlemsani, Audrey Coustier, Christian Derancourt, Audrey Briand-Suleau, Yvon-Gauthier Muller, Sophie Blesson, Eric Pasmant, Dominique Vidaud, Ingrid Laurendeau, Diana Rodriguez, Quentin Thomas, Laurence Faivre, Béatrice Parfait, Théodora Mayard

المساهمون: Service de Génétique et Biologie Moléculaires [CHU Cochin], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Cochin [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Institut Cochin (IC UM3 (UMR 8104 / U1016)), Centre National de la Recherche Scientifique (CNRS)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Lipides - Nutrition - Cancer [Dijon - U1231] (LNC), Université de Bourgogne (UB)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Maladies neurodéveloppementales et neurovasculaires (NeuroDiderot (UMR_S_1141 / U1141)), Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Régional Universitaire de Tours (CHRU TOURS), Centre de Référence pour les Affections Rares en Génétique Ophtalmologique (CARGO) et Service de Génétique Médicale, Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre [Strasbourg], Laboratoire de Génétique Médicale (LGM), Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre hospitalier universitaire de Poitiers (CHU Poitiers), Unité neurovasculaire et troubles cognitifs (Neuvacod), Université de Poitiers, Service d'Histologie, cytologie, cytogénétique, biologie cellulaire [CHU Limoges], CHU Limoges, XLIM (XLIM), Université de Limoges (UNILIM)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Virologie-Immunologie [Fort de France, Martinique] (EA 4537), Centre Hospitalier Universitaire de Martinique [Fort-de-France, Martinique], CHU Cochin [AP-HP], Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université de Bourgogne (UB)-Institut National de la Santé et de la Recherche Médicale (INSERM)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement, Centre Hospitalier Régional Universitaire de Tours (CHRU Tours), Yardin, catherine

المصدر: Genes
Volume 10
Issue 9
Genes, MDPI, 2019, 10 (9), pp.633. ⟨10.3390/genes10090633⟩
Genes, 2019, 10 (9), pp.633. ⟨10.3390/genes10090633⟩
Genes, Vol 10, Iss 9, p 633 (2019)

مصطلحات موضوعية: 0301 basic medicine, Mutation rate, medicine.medical_specialty, SPRED1, congenital, hereditary, and neonatal diseases and abnormalities, lcsh:QH426-470, [SDV]Life Sciences [q-bio], 030105 genetics & heredity, Biology, neurofibromatosis type 1, 03 medical and health sciences, Genetics, medicine, Neurofibromatosis, neoplasms, Genetics (clinical), Legius syndrome, Molecular pathology, Autosomal dominant trait, medicine.disease, Penetrance, NF1, eye diseases, 3. Good health, nervous system diseases, [SDV] Life Sciences [q-bio], lcsh:Genetics, 030104 developmental biology, Medical genetics, SPRED1 Gene, de novo variant

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::483d9e55fa46b0df3fe43d282e27a653Test

المؤلفون: Jason Whitt, J. Bart Rose, Renata Jaskula‐Stzul, Samuel Jang, Zviadi Aburjania, Herbert Chen

المصدر: The Oncologist. 23:900-911

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Cancer Diagnostics and Molecular Pathology, medicine.disease_cause, 03 medical and health sciences, 0302 clinical medicine, Vasculogenesis, Notch Family, Neoplasms, Animals, Humans, Medicine, Molecular Targeted Therapy, CADASIL, Receptor, Notch3, Gene, business.industry, Cancer, medicine.disease, Review article, 030104 developmental biology, Oncology, 030220 oncology & carcinogenesis, Cancer research, business, Carcinogenesis, Function (biology)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24e724d5b39726fba121a279c1112ae9Test
https://doi.org/10.1634/theoncologist.2017-0677Test

المؤلفون: Taekjin Choi, Jisub Park, Seung-Jae Lee, Sangok Kim, Yeongjun Jang, Jongho Kim, Jihae Seo, Yeajee Kwon, Sanghyuk Lee

المصدر: BMC Medical Genomics, Vol 11, Iss S2, Pp 95-103 (2018)
BMC Medical Genomics

مصطلحات موضوعية: 0301 basic medicine, lcsh:Internal medicine, lcsh:QH426-470, Computer science, medicine.medical_treatment, Information system, Targeted therapy, 03 medical and health sciences, Annotation, Neoplasms, Genomic medicine, Genetics, medicine, Humans, lcsh:RC31-1245, Genetics (clinical), Cancer, business.industry, Molecular pathology, Gene Expression Profiling, Precision medicine, Molecular Sequence Annotation, Genomics, medicine.disease, Data science, Personalized medicine, Human genetics, lcsh:Genetics, 030104 developmental biology, Oncology, business, Software, Signal Transduction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ffc7308504b24bc73fa4b5cf71aad8fTest
http://link.springer.com/article/10.1186/s12920-018-0347-9Test

المؤلفون: Henry O Ebili, Mohammad Ilyas, Susanti Susanti, Abid Sharif, James Hassall, Abutaleb Asiri, Joanne Field, Hersh A. Ham-Karim, Ausrine Nestarenkaite, Anca Oniscu, Wakkas Fadhil, Katherine Stafford, Balwir Matharoo-Ball, Efthymios Hadjimichael

المصدر: Journal of Clinical Pathology. 71:713-720

مصطلحات موضوعية: Proto-Oncogene Proteins B-raf, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, High Resolution Melting (HRM), Colorectal cancer, DNA Mutational Analysis, Biology, MLH1, Polymerase Chain Reaction, Workflow, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Predictive Value of Tests, Biomarkers, Tumor, medicine, Humans, Genetic Predisposition to Disease, Promoter Regions, Genetic, neoplasms, Microsatellite Instability (MSI), Molecular pathology, Gene Expression Profiling, Reproducibility of Results, nutritional and metabolic diseases, Microsatellite instability, General Medicine, Methylation, DNA Methylation, HCT116 Cells, Promoter methylation, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Molecular biology, digestive system diseases, Lynch syndrome, MSH6, Phenotype, BRAF mutation, 030104 developmental biology, MSH2, Lynch Syndrome, 030220 oncology & carcinogenesis, Mutation, Microsatellite Instability, MutL Protein Homolog 1

وصف الملف: PDF

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8a5b0c8a6830c08d913996a6ec02b20Test
https://doi.org/10.1136/jclinpath-2018-205013Test

المؤلفون: Ilaria Montagnani, Rodolfo Montironi, Francesca Castiglione, Antonio Lopez-Beltran, Liang Cheng, Maria Rosaria Raspollini, Guido Martignoni

المصدر: Journal of Clinical Pathology. 71:467-471

مصطلحات موضوعية: Male, 0301 basic medicine, Neuroblastoma RAS viral oncogene homolog, Tumour heterogeneity, DNA Mutational Analysis, Antineoplastic Agents, Gene mutation, medicine.disease_cause, Nephrectomy, Pathology and Forensic Medicine, Metastasis, Genetic Heterogeneity, 03 medical and health sciences, 0302 clinical medicine, Predictive Value of Tests, Biomarkers, Tumor, medicine, Humans, Genetic Predisposition to Disease, Molecular Targeted Therapy, Precision Medicine, Renal sinus, Carcinoma, Renal Cell, neoplasms, Molecular pathology, business.industry, General Medicine, Middle Aged, medicine.disease, Kidney Neoplasms, Clear cell renal cell carcinoma, Phenotype, 030104 developmental biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Mutation, Cancer research, KRAS, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3facab423a31b4be6c1888613fe7646eTest
https://doi.org/10.1136/jclinpath-2017-204931Test

المؤلفون: Yujun Liu, Shengwei Ye, Guangsheng Zhu, Huabin Wang, Wenjia Sun

المصدر: Medicine. 100:e27011

مصطلحات موضوعية: Pathology, medicine.medical_specialty, GiST, Sunitinib, Molecular pathology, business.industry, Skeletal muscle, Imatinib, General Medicine, medicine.disease, Metastasis, medicine.anatomical_structure, medicine, Immunohistochemistry, Stromal tumor, business, neoplasms, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::ea0af64f54be342194c830fd6effab86Test
https://doi.org/10.1097/md.0000000000027011Test

المؤلفون: Lewis R. Roberts, Robert Hullsiek, Lindsey A. Lee, Wendy A. Hudson, Barbara R. Tschida, Timothy P. Kuka, Michael A. Linden, Vincent W. Keng, Sandra Wagner, David A. Largaespada, Rachel A. Heuer, Pauline J. Beckmann, Nuri A. Temiz, Khalid Amin, Jesse D. Riordan, Joseph H. Nadeau, Ju Dong Yang, Adam J. Dupuy, Carlos A. Tierrablanca, Aaron L. Sarver

المصدر: Cancer Research. 77:6576-6588

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Pathology, medicine.medical_specialty, Molecular pathology, Fatty liver, Cancer, Context (language use), Biology, medicine.disease, Article, digestive system diseases, Insertional mutagenesis, 03 medical and health sciences, 030104 developmental biology, Oncology, Hepatocellular carcinoma, medicine, Cancer research, Steatosis, neoplasms, Genetic screen

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37cd0ca90ca0a637f8e3963106308c88Test
https://doi.org/10.1158/0008-5472.can-17-2281Test

المؤلفون: Kellie Kurasaki, Shumei Kato, Sadakatsu Ikeda, Razelle Kurzrock

المصدر: The Oncologist
The oncologist, vol 23, iss 2
Kato, S; Kurasaki, K; Ikeda, S; & Kurzrock, R. (2018). Rare Tumor Clinic: The University of California San Diego Moores Cancer Center Experience with a Precision Therapy Approach. ONCOLOGIST, 23(2), 171-178. doi: 10.1634/theoncologist.2017-0199. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/6rv4q83gTest

مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Gerontology, Cancer Research, medicine.medical_treatment, Medical Oncology, Ambulatory Care Facilities, Targeted therapy, 0302 clinical medicine, Neoplasms, Antineoplastic Combined Chemotherapy Protocols, Molecular Targeted Therapy, Precision Medicine, Protein analyses, Ameloblastoma, Cancer, Tumor, Hazard ratio, Genomics, Middle Aged, Prognosis, Combined Modality Therapy, 3. Good health, Survival Rate, Local, Lymphatic Metastasis, 030220 oncology & carcinogenesis, Female, Sarcoma, Biotechnology, Adult, medicine.medical_specialty, Cancer Diagnostics and Molecular Pathology, Liver tumor, Oncology and Carcinogenesis, Vaccine Related, 03 medical and health sciences, Rare Diseases, Clinical Research, Internal medicine, Genetics, medicine, Humans, Neoplasm Invasiveness, Oncology & Carcinogenesis, Retrospective Studies, Aged, Rare tumors, Neoplastic, Precision therapy, business.industry, Human Genome, Precision medicine, medicine.disease, Clinical trial, Neoplasm Recurrence, Orphan Drug, 030104 developmental biology, Gene Expression Regulation, Immunization, business, Biomarkers, Follow-Up Studies

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::330b996e0212ff6ca50adb1f12a3cff3Test
https://doi.org/10.1634/theoncologist.2017-0199Test

المؤلفون: Nancy Ann Oberheim Bush, Jessica Schulte, Tarik Tihan, Melike Pekmezci, Minh P. Nguyen, David R. Raleigh, Stephen T. Magill, Julieann C. Lee, Michael McDermott, Andrew W. Bollen, Nicholas Butowski, Arie Perry, Javier Villanueva-Meyer, David A. Solomon, Philip V. Theodosopoulos

المصدر: Neuro Oncol

مصطلحات موضوعية: Cancer Research, Mutation, MTOR Serine-Threonine Kinases, Molecular Pathology & Classification, Computational biology, Biology, medicine.disease, medicine.disease_cause, Meningioma, Oncology, PIK3CA gene, otorhinolaryngologic diseases, medicine, Neurology (clinical), Epigenetics, Akt1 gene, neoplasms

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afc1618494521ab223550d512555fbb0Test
https://doi.org/10.1093/neuonc/noaa215.715Test

المؤلفون: Giancarlo Troncone, Mauro Buono, Pasquale Pisapia, Christian Rolfo, Umberto Malapelle, Gianluca Russo, Rossella Tufano, Francesco Pepe

المساهمون: Malapelle, Umberto, Buono, Mauro, Pisapia, Pasquale, Russo, Gianluca, Tufano, Rossella, Pepe, Francesco, Rolfo, Christian, Troncone, Giancarlo

المصدر: Critical Reviews in Oncology/Hematology. 163:103394

مصطلحات موضوعية: 0301 basic medicine, Computational biology, DNA sequencing, Circulating Tumor DNA, 03 medical and health sciences, 0302 clinical medicine, Circulating tumor cell, Neoplasms, Biomarkers, Tumor, Humans, Medicine, Pathology, Molecular, Allele, Liquid biopsy, Molecular pathology, business.industry, High-Throughput Nucleotide Sequencing, Cancer, Hematology, medicine.disease, 030104 developmental biology, Oncology, Cell-free fetal DNA, 030220 oncology & carcinogenesis, Mutation, Cancer biomarkers, business, Mathematics

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22f356bd8deda3850e9955dfb139d80bTest
https://doi.org/10.1016/j.critrevonc.2021.103394Test