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المؤلفون: Tianqing Ding, Jing Yan, Wencai Li, Li Wang, Xiangxiang Wang, Jingliang Cheng, Dongling Pei, Weiwei Wang, Wenchao Duan, Zhen Liu, Xuanke Hong, Zhicheng Li, Zhen-Yu Zhang, Qiuchang Sun, Xianzhi Liu, Chen Sun, Wenqing Wang, Shenghai Zhang, Yu Guo
المصدر: Laboratory Investigation. 102:154-159
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Validation study, Pathology and Forensic Medicine, Deep Learning, medicine, Humans, Internal validation, Molecular Biology, Lower grade, medicine.diagnostic_test, Receiver operating characteristic, Brain Neoplasms, business.industry, Deep learning, Reproducibility of Results, Magnetic resonance imaging, Glioma, Cell Biology, Middle Aged, Prognosis, Magnetic Resonance Imaging, ROC Curve, Chromosomes, Human, Pair 1, Female, Radiology, Artificial intelligence, Chromosome Deletion, Neoplasm Grading, Adult type, Precision and recall, business, Chromosomes, Human, Pair 19
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1450cbe065207825c175f77be6299487Test
https://doi.org/10.1038/s41374-021-00692-5Test -
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المؤلفون: Claudio Ghimenton, Giampietro Pinna, Michele Simbolo, Francesco Sala, Matteo Brunelli, Serena Ammendola, Maria L. Piredda, Valeria Barresi, Nicolò Caldonazzi, Aldo Scarpa, Pietro Luigi Poliani
المصدر: Virchows Archiv
مصطلحات موضوعية: Male, Pathology, Time Factors, H3K27me3, 1p/19q Codeletion, Histones, 0302 clinical medicine, Recurrence, Medicine, Mutational status, Tumor, Brain Neoplasms, Astrocytoma, General Medicine, Middle Aged, Immunohistochemistry, Phenotype, Isocitrate Dehydrogenase, Progression-Free Survival, Local, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, Pair 1, Original Article, Female, Chromosome Deletion, Human, Adult, X-linked Nuclear Protein, medicine.medical_specialty, Oligodendroglioma, macromolecular substances, Chromosomes, Pathology and Forensic Medicine, 03 medical and health sciences, Predictive Value of Tests, Biomarkers, Tumor, Humans, Molecular Biology, 1p/19q codeletion, Chromosomes, Human, Pair 19, Mutation, Neoplasm Recurrence, Local, ATRX, Pair 19, business.industry, Cell Biology, medicine.disease, Neoplasm Recurrence, business, Biomarkers, 030217 neurology & neurosurgery, Immunostaining
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::004a3d6c08fbad92e19ccd73c786a709Test
https://doi.org/10.1007/s00428-021-03134Test-1 -
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المؤلفون: Hisayuki Matsumoto, Kimikazu Yakushijin, Yu Mizutani, Marika Okuni-Watanabe, Hironobu Minami, Hiroshi Matsuoka, Katsuya Yamamoto, Yoshiharu Miyata, Akihito Kitao, Jun Saegusa, Hideaki Goto, Ako Higashime
المصدر: Cancer Genetics. 254:92-97
مصطلحات موضوعية: Cancer Research, Oncogene Proteins, Fusion, CD33, Bone Marrow Cells, Chromosomal translocation, Translocation, Genetic, Fusion gene, 03 medical and health sciences, Exon, Fatal Outcome, 0302 clinical medicine, Precursor B-Cell Lymphoblastic Leukemia-Lymphoma, hemic and lymphatic diseases, Genetics, Humans, Amino Acid Sequence, RNA, Messenger, B-lymphoblastic leukemia, Cell Shape, Molecular Biology, Aged, KMT2A/EPS15, Base Sequence, biology, Chromosomes, Human, Pair 11, Lymphoblast, Myeloid leukemia, Molecular biology, KMT2A, fms-Like Tyrosine Kinase 3, Fusion transcript, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, Mutation, biology.protein, Female, FLT3 mutation
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd11353279c38566baaa6d569082dbb0Test
http://www.lib.kobe-u.ac.jp/handle_kernel/90008353Test -
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المؤلفون: Saiqun Luo, Tao Su, Xiang Zhou, Wei‐Xin Hu, Jingping Hu
المصدر: The FASEB Journal. 36
مصطلحات موضوعية: Chromosome Aberrations, DNA Copy Number Variations, Chromosomes, Human, Pair 1, Chromosomal Instability, Genetics, Gene Expression, Humans, Multiple Myeloma, Molecular Biology, Biochemistry, Biotechnology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::effaf8ee084f90821cc21b87b7f9918bTest
https://doi.org/10.1096/fj.202200354Test -
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المؤلفون: Qiuyun Yang, Wenjing Tang, Lina Zhou, Xiaodong Zhao, Yanjun Jia, Yunfei An, Zhi-Yong Zhang, Yanping Wang, Xuemei Chen, Xuemei Tang
المصدر: Journal of Clinical Immunology. 40:378-387
مصطلحات موضوعية: 0301 basic medicine, Class I Phosphatidylinositol 3-Kinases, Primary Immunodeficiency Diseases, T-Lymphocytes, Immunology, Loss of Heterozygosity, Activated PI3K-delta syndrome, Biology, Lymphocyte Activation, medicine.disease_cause, Loss of heterozygosity, Mice, 03 medical and health sciences, 0302 clinical medicine, medicine, Animals, Humans, Immunology and Allergy, Copy-number variation, Allele, Cells, Cultured, Mice, Knockout, Mutation, Homozygote, High-Throughput Nucleotide Sequencing, Infant, Chromosome, Cell Differentiation, Uniparental Disomy, medicine.disease, Molecular biology, Uniparental disomy, Pedigree, 030104 developmental biology, Chromosomes, Human, Pair 1, Primary immunodeficiency, Female, 030215 immunology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb0f75665d577b59da0ed781975ddfedTest
https://doi.org/10.1007/s10875-020-00749-yTest -
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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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المؤلفون: Jennifer Kao, K. H. Brian Lam, Ugljesa Djuric, Phedias Diamandis, Michail-Dimitrios Papaioannou, Ihor Batruch, Stefan D Jevtic
المصدر: Mol Cell Proteomics
مصطلحات موضوعية: Proteomics, Biology, Serpin, Biochemistry, Analytical Chemistry, Transcriptome, 03 medical and health sciences, Tandem Mass Spectrometry, Glioma, Tumor Cells, Cultured, medicine, Cluster Analysis, Humans, Protein Interaction Maps, Epithelial–mesenchymal transition, Molecular Biology, 030304 developmental biology, 0303 health sciences, Brain Neoplasms, Sequence Analysis, RNA, Research, 030302 biochemistry & molecular biology, Wild type, medicine.disease, Phenotype, Isocitrate Dehydrogenase, Chromosomes, Human, Pair 1, Tissue Array Analysis, Mutation, RNA splicing, Proteome, Neoplastic Stem Cells, Cancer research, Chromosome Deletion, Chromosomes, Human, Pair 19, Chromatography, Liquid
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d5b21362281d1741a64281ddffd499fTest
https://doi.org/10.1074/mcp.ra119.001521Test -
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المؤلفون: Weiwei Sun, Yajian Wang, Liang Huo, Weiyue Gu, Hua Wang
المصدر: Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)مصطلحات موضوعية: Adult, Male, Models, Molecular, DNA Copy Number Variations, Usher syndrome, Biology, Uniparental Heterodisomy, QH426-470, Glycogen storage disease type III, Clinical Reports, Glycogen Storage Disease Type III, Structure-Activity Relationship, USH2A, Exome Sequencing, medicine, Genetics, GSD3, Humans, Genetic Predisposition to Disease, Copy-number variation, Molecular Biology, Genetics (clinical), Exome sequencing, Genetic Association Studies, Clinical Report, UPiD, Chromosome, Glycogen Debranching Enzyme System, Sequence Analysis, DNA, Middle Aged, Uniparental Disomy, medicine.disease, Uniparental disomy, Pedigree, Uniparental Isodisomy, Chromosomes, Human, Pair 1, Child, Preschool, trio whole exome sequencing, Paternal Inheritance, Female, Usher Syndromes, Biomarkers
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c8e2eeed2dc8a1f023b6a4977c7a267Test
http://europepmc.org/articles/PMC8580083Test -
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المؤلفون: Eva Kriegova, Jakub Savara, Jirina Manakova, Anna Petrackova, Tomas Pika, Regina Fillerova, Michal Vašinek, Martin Dihel, Jiri Minarik, Petr Gajdoš, Marek Behalek, Petra Krhovska, Tomas Papajik, Jana Balcarkova
المصدر: Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Molecular biology, Science, Chromosomal translocation, Bone Marrow Cells, Pilot Projects, Biology, Genome, Article, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Bone Marrow, medicine, Humans, Gene, Multiple myeloma, Aged, Czech Republic, Aged, 80 and over, Chromosome Aberrations, Haematological cancer, Multidisciplinary, Cytogenetics, Chromosome, Middle Aged, medicine.disease, Phenotype, 030104 developmental biology, medicine.anatomical_structure, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, Cytogenetic Analysis, Medicine, Female, Bone marrow, Multiple Myeloma, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a88899195ce7900a8800decec513ce59Test
http://europepmc.org/articles/PMC8289962Test -
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المؤلفون: Yingwei Mao, Joy Yoon
المصدر: International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 5811, p 5811 (2021)مصطلحات موضوعية: 0301 basic medicine, Candidate gene, Microcephaly, Autism Spectrum Disorder, Review, 0302 clinical medicine, Chromosome Duplication, Copy-number variation, Biology (General), Spectroscopy, Genetics, Mental Disorders, copy number variation, neurodegeneration, Neurodegenerative Diseases, General Medicine, Penetrance, Computer Science Applications, Chemistry, Autism spectrum disorder, Schizophrenia, Chromosomes, Human, Pair 1, medicine.symptom, Chromosome Deletion, DNA Copy Number Variations, QH301-705.5, Biology, macrocephaly, Catalysis, Inorganic Chemistry, 03 medical and health sciences, mental disorders, medicine, Humans, Abnormalities, Multiple, Genetic Predisposition to Disease, Physical and Theoretical Chemistry, QD1-999, Molecular Biology, Genetic association, synaptic plasticity, microduplication, Organic Chemistry, Macrocephaly, medicine.disease, Megalencephaly, schizophrenia, 030104 developmental biology, Neurodevelopmental Disorders, microdeletion, 030217 neurology & neurosurgery, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc23b7fe63b728e36af8367eef1a89fcTest
http://europepmc.org/articles/PMC8197994Test