نتائج البحث - "Jiri Hamberg"

المساهمون: Yhteiskuntatieteiden tiedekunta - Faculty of Social Sciences, University of Tampere, Research Programs Unit, Genome-Scale Biology (GSB) Research Program, University of Helsinki, Medicum, Department of Medical and Clinical Genetics, Lauri Antti Aaltonen / Principal Investigator, Department of Pathology, HUSLAB, Gastrointestinal tumorigenesis, Clinicum

المصدر: PLoS Genetics
PLoS Genetics, Vol 14, Iss 3, p e1007200 (2018)

مصطلحات موضوعية: 0301 basic medicine, Male, Cancer Research, MICROSATELLITE INSTABILITY, Colorectal cancer, oncogenes, Receptor, ErbB-2, medicine.disease_cause, COLORECTAL-CANCER, ACTIVATION, Cohort Studies, 0302 clinical medicine, Animal Cells, Adenocarcinomas, Medicine and Health Sciences, Exome, Frameshift Mutation, Genetics (clinical), Exome sequencing, Aged, 80 and over, SMALL-INTESTINE, education.field_of_study, 1184 Genetics, developmental biology, physiology, CELIAC-DISEASE, Nonsense Mutation, Middle Aged, 3. Good health, syöpägeenit, Oncology, 030220 oncology & carcinogenesis, syöpätaudit, Female, SIGNALING PATHWAY, KRAS, Cellular Types, Research Article, Adult, Proto-Oncogene Proteins B-raf, lcsh:QH426-470, SEQUENCING DATA, Immune Cells, Nonsense mutation, Population, Immunology, Antigen-Presenting Cells, Computational biology, suolistosyövät, Biology, Adenocarcinoma, ta3111, Carcinomas, Frameshift mutation, 03 medical and health sciences, Germline mutation, QUALITY-CONTROL, Genetiikka, kehitysbiologia, fysiologia - Genetics, developmental biology, physiology, Syöpätaudit - Cancers, Intestinal Neoplasms, medicine, Genetics, Point Mutation, Humans, education, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Aged, Colorectal Cancer, Biology and Life Sciences, Cancers and Neoplasms, cancerous diseases, Cell Biology, medicine.disease, ta3122, mutations, COMPREHENSIVE MOLECULAR CHARACTERIZATION, lcsh:Genetics, 030104 developmental biology, Mutation, Somatic Mutation, bowel cancer, 3111 Biomedicine, mutaatiot, HIGH-RESOLUTION

وصف الملف: fulltext; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63ac2863de7f9f298a3d54b06c3964bd
http://europepmc.org/articles/PMC5871010

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13

Comprehensive evaluation of coding region point mutations in microsatellite-unstable colorectal cancer

المساهمون: Lauri Antti Aaltonen / Principal Investigator, Genome-Scale Biology (GSB) Research Program, Department of Medical and Clinical Genetics, Institute of Biotechnology, Department of Surgery, Department of Biochemistry and Developmental Biology, Sampsa Hautaniemi / Principal Investigator, Molecular Systems Biology, HUS Abdominal Center, Liu, Xiaonan [0000-0002-9600-0536], Taipale, Jussi [0000-0003-4204-0951], Pitkänen, Esa [0000-0002-9818-6370], Aaltonen, Lauri A [0000-0001-6839-4286], Apollo - University of Cambridge Repository

المصدر: EMBO Molecular Medicine, Vol 10, Iss 9, Pp n/a-n/a (2018)
EMBO Molecular Medicine, Vol. 10, No 9 (2018) P. e8552
EMBO Molecular Medicine

مصطلحات موضوعية: 0301 basic medicine, Medicine (General), Candidate gene, clinical evaluation, genetic identification, genetic analysis, QH426-470, medicine.disease_cause, Chromatin, Epigenetics, Genomics & Functional Genomics, whole exome sequencing, ddc:590, mutator gene, single nucleotide polymorphism, ddc:576.5, Gene Regulatory Networks, Exome, Exome sequencing, Cancer, cancer cell, Genetics, Mutation, 1184 Genetics, developmental biology, physiology, 3. Good health, genetic code, syöpägeenit, priority journal, Molecular Medicine, wild type, point mutation, Systems Medicine, Colorectal Neoplasms, congenital, hereditary, and neonatal diseases and abnormalities, ddc:025.063/570, 3122 Cancers, cancer genetics, Single-nucleotide polymorphism, colorectal cancer, Biology, gene frequency, ta3111, mikrosatelliitit, colony formation, R105W gene, Article, 03 medical and health sciences, R5-920, Gene interaction, Report, medicine, Humans, controlled study, human, neoplasms, paksusuolisyöpä, Point mutation, gene interaction, human cell, tumor-related gene, Microsatellite instability, Molecular Sequence Annotation, Sequence Analysis, DNA, medicine.disease, ta3122, digestive system diseases, human tissue, STK38L gene, 030104 developmental biology, validation process, gene expression, SMARCB1 gene, microsatellite instability, 3111 Biomedicine, gene replication, Reports

وصف الملف: application/pdf; fulltext

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::953f75f6fbc45f190b7b1acf46bc547e
http://hdl.handle.net/10138/299729

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14

Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

المساهمون: Research Programs Unit, Genome-Scale Biology (GSB) Research Program, Department of Medical and Clinical Genetics, Medicum, Lauri Antti Aaltonen / Principal Investigator, Jussi Taipale / Principal Investigator, Clinicum, Department of Surgery, II kirurgian klinikka, Heikki Järvinen / Principal Investigator, HUS Abdominal Center

المصدر: Cancer research. 77(15)