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المؤلفون: Jinming Yu, Jia Yang, Yongsheng Gao, Xingchen Ding, Jujie Sun, Tao Xin, Man Hu, Xianbin Zhang, Song Xue, Yufang Zhu, Shulun Nie, Zhaoqiu Chen, Dianbin Mu
المصدر: Radiation Oncology, Vol 16, Iss 1, Pp 1-11 (2021)
Radiation Oncology (London, England)مصطلحات موضوعية: Male, Patient-Specific Modeling, Microscopic extension, medicine.medical_treatment, R895-920, Macropathology, Medical physics. Medical radiology. Nuclear medicine, 0302 clinical medicine, High-grade glioma, Bayesian multivariate linear regression, Medicine, DNA Modification Methylases, RC254-282, medicine.diagnostic_test, Brain Neoplasms, Area under the curve, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Glioma, Middle Aged, Magnetic Resonance Imaging, Isocitrate Dehydrogenase, Isocitrate dehydrogenase, Oncology, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, Female, 03 medical and health sciences, Biomarkers, Tumor, Humans, Radiology, Nuclear Medicine and imaging, Neoplasm Staging, Receiver operating characteristic, Radiotherapy, business.industry, Tumor Suppressor Proteins, Research, Magnetic resonance imaging, medicine.disease, Radiation therapy, Clinical trial, DNA Repair Enzymes, Clinical target volume, ROC Curve, Predictive model, Mutation, business, Nuclear medicine, Chromosomes, Human, Pair 19, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5220203a67893fd2e8312937af247689Test
https://doaj.org/article/422c326f377f4f09bd8e3cb96fc53f01Test -
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المؤلفون: Xiaofeng Zhu, Craig L. Hanis, Hua Tang, Mengshi Zhou, Karen Y. He, Sharon L.R. Kardia, Heming Wang, Uli Broeckel, Richard S. Cooper, Xumin Ni, Susan Redline
المصدر: BMC Genomics, Vol 21, Iss 1, Pp 1-13 (2020)
BMC Genomicsمصطلحات موضوعية: Linkage disequilibrium, lcsh:QH426-470, lcsh:Biotechnology, ved/biology.organism_classification_rank.species, Population, Genome-wide association study, Biology, Genome, Polymorphism, Single Nucleotide, Fitness epistasis, Linkage Disequilibrium, Receptors, G-Protein-Coupled, 03 medical and health sciences, 0302 clinical medicine, lcsh:TP248.13-248.65, Genetics, Humans, Computer Simulation, Model organism, education, Gene, 030304 developmental biology, 0303 health sciences, education.field_of_study, Admixed population, ved/biology, Chromosomes, Human, Pair 10, Chromosome, Epistasis, Genetic, Diseases/traits, Black or African American, Co-evolution, lcsh:Genetics, Admixture linkage disequilibrium, Evolutionary biology, Chromosomes, Human, Pair 1, Epistasis, Genetic Fitness, 030217 neurology & neurosurgery, Biotechnology, Research Article, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28c8daf6dc8937676a8c5369f27b1baaTest
http://link.springer.com/article/10.1186/s12864-020-06874-7Test -
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المؤلفون: Emily Chia Yu Su, Sean Chun Chang Chen, Chung Ming Lo, Shih Hua Wang
المصدر: BMC Bioinformatics, Vol 20, Iss S19, Pp 1-11 (2019)
BMC Bioinformaticsمصطلحات موضوعية: RNA editing, 1p/19q Codeletion, Computational biology, Biology, lcsh:Computer applications to medicine. Medical informatics, Biochemistry, 03 medical and health sciences, 0302 clinical medicine, Structural Biology, Glioma, Machine learning, medicine, Humans, Gliomas, Molecular Biology, lcsh:QH301-705.5, 030304 developmental biology, Chromosome Aberrations, 0303 health sciences, Receiver operating characteristic, Brain Neoplasms, Research, Applied Mathematics, Cancer, medicine.disease, Classification, Prognosis, Computer Science Applications, Isocitrate dehydrogenase, lcsh:Biology (General), Chromosomes, Human, Pair 1, Mutation, Mutation (genetic algorithm), lcsh:R858-859.7, Neoplasm Grading, DNA microarray, Chromosomes, Human, Pair 19, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f3aab33e1c5d896cc4eb246a69654c3Test
https://doaj.org/article/5b649244e4044b36bab9daaecf0ba583Test -
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المصدر: BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
BMC Medical Geneticsمصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, lcsh:Internal medicine, lcsh:QH426-470, Preimplantation genetic testing for chromosomal structural rearrengements (PGT-SR), Prenatal diagnosis, Case Report, Biology, Translocation, Genetic, 03 medical and health sciences, 0302 clinical medicine, Pregnancy, Genetics, Homologous chromosome, medicine, Humans, lcsh:RC31-1245, Genetics (clinical), Preimplantation Diagnosis, Sex Chromosome Aberrations, Genetic testing, Parental iUPD (9), 030219 obstetrics & reproductive medicine, medicine.diagnostic_test, Cytogenetics, Infant, Newborn, Pregnancy Outcome, Karyotype, Uniparental Disomy, medicine.disease, Uniparental disomy, lcsh:Genetics, 030104 developmental biology, Phenotype, Chromosomes, Human, Pair 1, Amniocentesis, Mosaic Klinefelter syndrome, Female, Genomic imprinting, Comparative genomic hybridization, Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d39df930a8772123162b6f6608d73ce1Test
http://link.springer.com/article/10.1186/s12881-019-0897-5Test -
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المصدر: Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-5 (2019)
Journal of Medical Case Reportsمصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, IDH1, Axial skeleton, Oligodendroglioma, Brain tumor, lcsh:Medicine, Case Report, Bone Neoplasms, 030204 cardiovascular system & hematology, 03 medical and health sciences, 0302 clinical medicine, Surgical oncology, Biopsy, Medicine, Humans, Sequence Deletion, medicine.diagnostic_test, Base Sequence, business.industry, Brain Neoplasms, Bone metastases, lcsh:R, General Medicine, medicine.disease, Isocitrate Dehydrogenase, nervous system diseases, medicine.anatomical_structure, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, Anaplastic oligodendroglioma, Immunohistochemistry, Bone marrow, business, Metastatic oligodendroglioma
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb64b9a58424b927db0c0a3e2230ec3aTest
http://link.springer.com/article/10.1186/s13256-019-2061-4Test -
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المؤلفون: Ying Zhang, Zulifeiya Musha, Wenkui Lv, Jianzhong Yang, Xianhui Zhou, Yanmei Lu, Baopeng Tang, Ling Zhang, Bin Yang, Ping Fan, Yuanzheng Ye
المصدر: Lipids in Health and Disease, Vol 18, Iss 1, Pp 1-13 (2019)
Lipids in Health and Diseaseمصطلحات موضوعية: Adult, Male, China, Microarray, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Population, 030209 endocrinology & metabolism, Computational biology, 030204 cardiovascular system & hematology, Biology, Essential hypertension, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Ion binding, Gene expression, microRNA, Cell Adhesion, Ethnicity, medicine, Humans, education, Gene, lcsh:RC620-627, education.field_of_study, Ion Transport, Uyghur population, Microarray analysis techniques, Research, Biochemistry (medical), Chromosome Mapping, Molecular Sequence Annotation, Biomarker, Microarray Analysis, Prognosis, medicine.disease, MicroRNAs, lcsh:Nutritional diseases. Deficiency diseases, Early Diagnosis, Gene Expression Regulation, Chromosomes, Human, Pair 1, Case-Control Studies, Female, Chromosomes, Human, Pair 19, Biomarkers, Signal Transduction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1787a1ae2a8b4dfa4928c6e7b5263afTest
http://link.springer.com/article/10.1186/s12944-019-1028Test-1 -
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المؤلفون: Hongyang Lu, Lei Lei, Zhiming Jiang, Gu Zhang, Qiaoyuan Cheng
المصدر: World Journal of Surgical Oncology, Vol 16, Iss 1, Pp 1-6 (2018)
World Journal of Surgical Oncologyمصطلحات موضوعية: Male, 0301 basic medicine, Lung Neoplasms, Pulmonary carcinoid, 0302 clinical medicine, Surgical oncology, Promoter methylation, Medicine, MGMT methylation, Promoter Regions, Genetic, DNA Modification Methylases, medicine.diagnostic_test, Methylation, Middle Aged, Prognosis, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Oncology, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, Female, Chromosome Deletion, Large-cell neuroendocrine carcinoma, medicine.drug, Adult, China, lcsh:Surgery, 1p/19q co-deletion, Carcinoid Tumor, DNA methyltransferase, lcsh:RC254-282, Disease-Free Survival, 03 medical and health sciences, Humans, Lung cancer, neoplasms, Aged, Retrospective Studies, Temozolomide, business.industry, Tumor Suppressor Proteins, Research, lcsh:RD1-811, DNA Methylation, medicine.disease, Carcinoma, Neuroendocrine, DNA Repair Enzymes, 030104 developmental biology, Cancer research, Carcinoma, Large Cell, Surgery, Oligodendroglioma, business, Chromosomes, Human, Pair 19, Fluorescence in situ hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32b124f6475d17ec2f5f6d094098bb30Test
http://link.springer.com/article/10.1186/s12957-018-1413-7Test -
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المؤلفون: Gladitz, Josef, Klink, Barbara, Seifert, Michael
المصدر: Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-15 (2018)
Acta Neuropathologica Communicationsمصطلحات موضوعية: Male, Bioinformatics, Oligodendroglioma, Gene Dosage, 1p/19q co-deletion, Network inference, lcsh:RC346-429, Cancer genomics, Humans, lcsh:Neurology. Diseases of the nervous system, Brain Neoplasms, Research, Computational Biology, Network propagation, Isocitrate Dehydrogenase, Neoplasm Proteins, Gene Expression Regulation, Neoplastic, Succinate Dehydrogenase, Chromosomes, Human, Pair 1, Computational systems biology, Mutation, Vesicular Glutamate Transport Protein 1, Network biology, Female, Chromosome Deletion, Oligodendrogliomas, Chromosomes, Human, Pair 19, Metabolic Networks and Pathways, Signal Transduction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::27dcef995f45f3c06e70a1e9df694c99Test
http://link.springer.com/article/10.1186/s40478-018-0544-yTest -
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المؤلفون: Nikita Raje, Maxime Cadieux-Dion, Kristi Canty, Neil A. Miller, Elena Repnikova, Isabelle Thiffault, Emily G. Farrow, Lee Zellmer, Nicole P. Safina, Carol J Saunders, Kendra Engleman
المصدر: BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
BMC Medical Geneticsمصطلحات موضوعية: Male, 0301 basic medicine, Ectodermal dysplasia, Pathology, Case Report, 030105 genetics & heredity, Compound heterozygosity, AEC, Gene Frequency, Ectodermal Dysplasia, Cocoon syndrome, Eye Abnormalities, Genetics (clinical), Exome sequencing, Autosomal dominant trait, Microdeletion syndrome, I-kappa B Kinase, Pedigree, Cleft Palate, Phenotype, Chromosomes, Human, Pair 1, Child, Preschool, CHUK, Interferon Regulatory Factors, Chromosome Deletion, Heterozygote, medicine.medical_specialty, lcsh:Internal medicine, lcsh:QH426-470, Cleft Lip, 1q21.1 microdeletion syndrome, Mutation, Missense, Protein Serine-Threonine Kinases, 03 medical and health sciences, TP63, Genetics, medicine, Humans, Abnormalities, Multiple, Amino Acid Sequence, Genetic Testing, lcsh:RC31-1245, business.industry, Tumor Suppressor Proteins, Immunologic Deficiency Syndromes, Eyelids, Genetic Variation, Microarray Analysis, medicine.disease, Megalencephaly, Bartsocas–Papas syndrome, lcsh:Genetics, 030104 developmental biology, Immunoglobulin G, IRF6, business, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d56547dfb8e6b6a1c2cd833f15bd1cbbTest
http://link.springer.com/article/10.1186/s12881-018-0556-2Test -
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المؤلفون: Min-Han Tan, Jun Sugimura, Jonathon A. Ditlev, Annick Vieillefond, Tomoaki Fujioka, Puay Hoon Tan, Ximing J. Yang, Daisuke Matsuda, Delphine Amsellem-Ouazana, Eric J. Kort, Nicolas Thiounn, Chin Fong Wong, Sophie Giraud, Philippe Vielh, Thierry Flam, Bin Tean Teh, Bernard Debré, Stéphane Richard, Sophie Ferlicot, Marc Zerbib, Kyle A. Furge, Sok Kean Khoo, Hwei Ling Tan, Gérard Benoit, Vincent Molinié, Stéphane Droupy
المساهمون: BMC, Ed., Laboratory of Cancer Genetics, Van Andel Institute [Grand Rapids], NCCS-VARI Translational Cancer Research Laboratory, National Cancer Centre Singapore, Department of Medical Oncology, Department of Epidemiology and Public Health, National University of Singapore (NUS), Department of Pathology, Singapore General Hospital, Northwestern University Feinberg School of Medicine, Department of Urology, Iwate Medical University School of Medicine, Laboratory of Computational Biology, Laboratory of Molecular Epidemiology, Laboratoire de Génétique, Hôpital Herriot, Laboratoire d'Anatomie Pathologique, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital de Bicêtre, Pathologie morphologique, Département de biologie et pathologie médicales [Gustave Roussy], Institut Gustave Roussy (IGR)-Institut Gustave Roussy (IGR), Service d'urologie, Hôpital Cochin [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Cytokines et Immunologie des Tumeurs Humaines (U753), Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Institut National de la Santé et de la Recherche Médicale (INSERM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Service d'anatomie pathologique, Hôpital Saint Joseph, Laboratoire d'anatomie pathologique, Consultation d'oncogénétique spécialisée, Hôpital de Bicêtre-Service d'Urologie, We wish to thank the Fischer Family Foundation, the Singapore Cancer Society, the French National Cancer Institute (Kidney PNES, INCa), and the French League against Cancer (Comités du Cher et de l'Indre) for supporting this study. We would also like to thank the Hauenstein Foundation and the Van Andel Foundation for their continued support. We thank the Cooperative Human Tissue Network (CHTN) of the National Cancer Institute for providing samples for analysis. Min-Han Tan is supported by the Singapore Millenium Foundation and the National Kidney Foundation.
المصدر: BMC Cancer, Vol 10, Iss 1, p 196 (2010)
BMC Cancer
BMC Cancer, 2010, 10 (1), pp.196. ⟨10.1186/1471-2407-10-196⟩
BMC Cancer, BioMed Central, 2010, 10 (1), pp.196. ⟨10.1186/1471-2407-10-196⟩مصطلحات موضوعية: Pathology, Cancer Research, Chromophobe Renal Cell Carcinoma, Gene Dosage, Chromophobe cell, urologic and male genital diseases, MESH: Gene Dosage, 0302 clinical medicine, Odds Ratio, Adenoma, Oxyphilic, Oncocytoma, Gene Regulatory Networks, MESH: Nerve Tissue Proteins, Renal oncocytoma, MESH: Gene Regulatory Networks, Oligonucleotide Array Sequence Analysis, Synaptogyrins, 0303 health sciences, MESH: Genetic Testing, MESH: Polymorphism, Single Nucleotide, MESH: Carcinoma, Renal Cell, MESH: Gene Expression Regulation, Neoplastic, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Immunohistochemistry, MESH: Predictive Value of Tests, Kidney Neoplasms, MESH: Reproducibility of Results, Gene Expression Regulation, Neoplastic, Oncology, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, Cytogenetic Analysis, MESH: Membrane Proteins, Research Article, medicine.medical_specialty, MESH: Adenoma, Oxyphilic, MESH: Chromosomes, Human, Pair 1, [SDV.CAN]Life Sciences [q-bio]/Cancer, Nerve Tissue Proteins, Computational biology, Biology, Gene dosage, Polymorphism, Single Nucleotide, lcsh:RC254-282, Diagnosis, Differential, 03 medical and health sciences, MESH: Gene Expression Profiling, [SDV.CAN] Life Sciences [q-bio]/Cancer, MESH: Diagnosis, Differential, Predictive Value of Tests, medicine, Genetics, Biomarkers, Tumor, Humans, MESH: Tumor Suppressor Proteins, Genetic Testing, Carcinoma, Renal Cell, 030304 developmental biology, MESH: Humans, MESH: Cytogenetic Analysis, Gene Expression Profiling, Tumor Suppressor Proteins, MESH: Aquaporin 6, Membrane Proteins, Reproducibility of Results, MESH: Immunohistochemistry, Gene signature, medicine.disease, MESH: Odds Ratio, Aquaporin 6, Gene expression profiling, Clear cell renal cell carcinoma, MESH: Tumor Markers, Biological, MESH: Oligonucleotide Array Sequence Analysis, MESH: Kidney Neoplasms
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51fa544bb98a332f86087d8cf3ff2eddTest
http://www.biomedcentral.com/1471-2407/10/196Test