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101
المؤلفون: Valerie K. Jordan, Tiana M. Scott, Daryl A. Scott, Bum Jun Kim, Peter Kundert, Jenny Carmichael, Hitisha P. Zaveri
المصدر: Human molecular genetics. 30(7)
مصطلحات موضوعية: 0301 basic medicine, Pathology, medicine.medical_specialty, Cleft Lip, Embryonic Development, Chromosome Disorders, Mice, Transgenic, Nerve Tissue Proteins, Wnt1 Protein, Biology, Mesoderm, 03 medical and health sciences, 0302 clinical medicine, Cranial neural crest, Neurodevelopmental disorder, Genetics, medicine, Animals, Humans, Molecular Biology, Genetics (clinical), Cell Proliferation, Mice, Knockout, 1p36 deletion syndrome, Embryogenesis, Chromosome, Gene Expression Regulation, Developmental, Embryo, General Medicine, medicine.disease, Phenotype, Cleft Palate, Mice, Inbred C57BL, Repressor Proteins, Disease Models, Animal, 030104 developmental biology, Chromosomes, Human, Pair 1, Neural Crest, PAX7, Chromosome Deletion, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::082ec83093a17eef82a81252952bc3f2Test
https://pubmed.ncbi.nlm.nih.gov/33772547Test -
102مؤتمر
المؤلفون: Ghoussaini, M, Ahmed, S, Michailidou, K, Gregory, K, Dicks, E, Driver, K, Pharoah, PD, Easton, DF, Dunning, AM
مصطلحات موضوعية: 31 Biological Sciences, 32 Biomedical and Clinical Sciences, 3105 Genetics, 4202 Epidemiology, 4203 Health Services and Systems, 42 Health Sciences, 3211 Oncology and Carcinogenesis, Human Genome, Cancer, Breast Cancer, Women's Health, Genetics, FOS Biological sciences, Cancer Genomics, 2.1 Biological and endogenous factors, 2 Aetiology, Alleles, Breast Neoplasms, Case-Control Studies, Chromosome Mapping, Chromosomes, Human, Pair 1, Computational Biology, Female, Gene Frequency, Genetic Association Studies, Genetic Predisposition to Disease, Genotype, Humans, Linkage Disequilibrium, Neoplasm Grading
الإتاحة: https://doi.org/10.17863/cam.4680Test
https://www.repository.cam.ac.uk/handle/1810/260446Test -
103
المؤلفون: T. Kockmann, A. von Deimling, Tobias Weiss, Ruedi Aebersold, F. Zhang, M. Felix, David E. Reuss, Felix Sahm, Christian Feller, Christel Herold-Mende
المصدر: Acta Neuropathologica. 139:211-213
مصطلحات موضوعية: Proteomics, biology, Brain Neoplasms, Gene Expression Profiling, Oligodendroglioma, Mutant, Astrocytoma, Methylation, DNA Methylation, medicine.disease, Molecular biology, Isocitrate Dehydrogenase, Pathology and Forensic Medicine, Histones, Cellular and Molecular Neuroscience, Histone, Chromosomes, Human, Pair 1, biology.protein, medicine, Humans, Neurology (clinical), Gene Deletion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::745fd7c935c986adc5bd232972b28bdaTest
https://doi.org/10.1007/s00401-019-02096-8Test -
104
المصدر: Congenital Anomalies. 60:128-130
مصطلحات موضوعية: Chromosome Aberrations, Embryology, Tumor Suppressor Proteins, Chromosome Mapping, General Medicine, Computational biology, Biology, Cell division cycle, Chromosomes, Human, Pair 1, Neoplasms, Pediatrics, Perinatology and Child Health, Humans, Genetic Predisposition to Disease, Developmental biology, Developmental Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fae40fffa5e8b94947982977be5a3672Test
https://doi.org/10.1111/cga.12356Test -
105دورية أكاديمية
المصدر: Revista Cubana de Investigaciones Biomédicas, Vol 21, Iss 4, Pp 262-269 (2002)
مصطلحات موضوعية: ENFERMEDAD DE ALZHEIMER, CROMOSOMAS HUMANOS PAR 1, CROMOSOMAS HUMANOS PAR 14, CROMOSOMAS HUMANOS PAR 19, CROMOSOMAS HUMANOS PAR 21, ALZHEIMER DISEASE, CHROMOSOMES, HUMAN, PAIR 1, CHROMOSOMES, HUMAN, PAIR 14, CHROMOSOMES, HUMAN, PAIR 19, CHROMOSOMES, HUMAN, PAIR 21, Medicine (General), R5-920
وصف الملف: electronic resource
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106
المؤلفون: Mohammed Ali Alvi, Victor M. Lu, Mohamad Bydon, Kaisorn L. Chaichana, Alfredo Quinones-Hinojosa
المصدر: Clinical Neurology and Neurosurgery. 182:32-36
مصطلحات موضوعية: Adult, Male, Oncology, medicine.medical_specialty, Multivariate analysis, Population, 1p/19q Codeletion, World Health Organization, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, medicine, Adjuvant therapy, Humans, Registries, education, Aged, education.field_of_study, Brain Neoplasms, Proportional hazards model, business.industry, Cancer, Glioma, General Medicine, Middle Aged, Prognosis, medicine.disease, Combined Modality Therapy, Isocitrate Dehydrogenase, Cancer registry, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, Mutation, Cohort, Female, Surgery, Neurology (clinical), Chromosome Deletion, Neoplasm Grading, business, Chromosomes, Human, Pair 19, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bde731a4eb8f77724b1170b57dffca00Test
https://doi.org/10.1016/j.clineuro.2019.04.027Test -
107
المؤلفون: Carey McDougall, Angela Peron, Lauren B. Carter, Thomas P. Slavin, Lynne M. Bird, Mary Beth Dinulos, Cathy A. Stevens, Ian A. Glass, Mais Hashem, Melanie A. Manning, Aglaia Vignoli, Elaine H. Zackai, Agatino Battaglia, Stephanie E. Vallee, Athena M. Cherry, Beth Keena, Margaret P. Adam, John M. Graham, Maura R.Z. Ruzhnikov, Leah Dowsett, Fowzan S. Alkuraya, Laurie H. Seaver, Anita E. Beck, Louanne Hudgins
المصدر: Am J Med Genet A
American journal of medical genetics. Part A, vol 179, iss 8مصطلحات موضوعية: Male, 0301 basic medicine, Pediatrics, Resuscitation, Chromosome Disorders, Reproductive health and childbirth, Neurodegenerative, 030105 genetics & heredity, Low Birth Weight and Health of the Newborn, Psychological Distress, Hypoxic Ischemic Encephalopathy, Pregnancy, Diagnosis, Infant Mortality, 2.1 Biological and endogenous factors, Medicine, Aetiology, Genetics (clinical), Pediatric, Medical record, Brain, Phenotype, medicine.anatomical_structure, Chromosomes, Human, Pair 1, Neurological, Hypoxia-Ischemia, Brain, Pair 1, Mental health, Female, Chromosome Deletion, Human, medicine.medical_specialty, Physical Injury - Accidents and Adverse Effects, hypoxic ischemic encephalopathy, Intellectual and Developmental Disabilities (IDD), Clinical Sciences, Chromosome Disorder, Chromosomes, Article, Diagnosis, Differential, White matter, 03 medical and health sciences, Neuroimaging, Clinical Research, Preterm, Hypoxia-Ischemia, Genetics, Humans, 1p36, Epilepsy, Periventricular leukomalacia, 1p36 deletion syndrome, business.industry, Neurosciences, Infant, Newborn, Infant, distress, Perinatal Period - Conditions Originating in Perinatal Period, Newborn, medicine.disease, Brain Disorders, Good Health and Well Being, 030104 developmental biology, Differential, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::666822da8ce421ba9792ab05c0ea6ac9Test
https://doi.org/10.1002/ajmg.a.61266Test -
108
المؤلفون: Sebastian Scheinost, Jennifer Hüllein, Benedikt Brors, Markus W. Löffler, Alexander Jethwa, Wolfram Klapper, Hanne Helfrich, Rabea Wagener, Junyan Lu, Stefan Habringer, Ulrich Keller, Kyle Bonneau, Lorenz Trümper, Markus Kreuz, Zhiqin Huang, Stephan Stilgenbauer, Olena Yavorska, Marc Zapatka, Donato Tedesco, Ralf Küppers, Christiane Pott, Maciej Rosolowski, Roma Kurilov, Wolfgang Huber, Thorsten Zenz, René Scholtysik, Mikolaj Slabicki, Michael Hummel, Birgit Burkhardt, Katarzyna Tomska, Marina Lukas, Reiner Siebert
المصدر: Cancer Research. 79:3125-3138
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Cell cycle checkpoint, Medizin, Apoptosis, Cell Cycle Proteins, Biology, Mice, 03 medical and health sciences, 0302 clinical medicine, immune system diseases, RNA interference, Proto-Oncogene Proteins, hemic and lymphatic diseases, Tumor Cells, Cultured, medicine, Animals, Humans, Cell Proliferation, Chromosome Aberrations, Cell growth, Cell Cycle Checkpoints, medicine.disease, Oncogene Addiction, Burkitt Lymphoma, Xenograft Model Antitumor Assays, 3. Good health, Lymphoma, Gene Expression Regulation, Neoplastic, 030104 developmental biology, Oncology, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, FLI1, Mutation, Cancer research, PAX5, CDKN1B, Tumor Suppressor Protein p53
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::846d2b2f9da15470ef0167424f3b0178Test
https://doi.org/10.1158/0008-5472.can-18-3438Test -
109
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 -
110
المؤلفون: Karl H. Plate, Patrick N. Harter, Joachim P. Steinbach, Michael W. Ronellenfitsch, Jenny Zinke, David Capper, Katharina Filipski, Michel Mittelbronn, Marlies Wagner, Peter Baumgarten, Bastian Roller, Gilles Gasparoni, Yannick Braun, Christian Senft, Pia S. Zeiner
المصدر: Acta Neuropathologica
مصطلحات موضوعية: 1p/19q Codeletion, Kaplan-Meier Estimate, Biology, Neoplasm genetics, Pathology and Forensic Medicine, Histones, Cellular and Molecular Neuroscience, chemistry.chemical_compound, Correspondence, Histone code, Humans, Brain Neoplasms, DNA, Neoplasm, Glioma, DNA Methylation, Prognosis, Isocitrate Dehydrogenase, Neoplasm Proteins, Histone Code, chemistry, Chromosomes, Human, Pair 1, DNA methylation, Cancer research, Neurology (clinical), Chromosome Deletion, Chromosomes, Human, Pair 19, DNA
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae861e16234f85f1769d19fdbc1434f5Test
http://europepmc.org/articles/PMC6660498Test