Driver mutations

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Lab affiliation

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University of Vienna, Faculty of Chemistry, Department of Analytical Chemistry (2)
., Department of Laboratory Medicine, Medical University of Vienna, 18-20 Währinger Gürtel, 1090 Vienna, Austria (1)
1.Department of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland. 2.Department for BioMedical Research, University of Bern, 3008 Bern, Switzerland. 3. Conway Institute for Biomolecular and Biomedical Research, University College Dublin, Dublin D04 V1W8, Ireland. (1)
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Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute of Pathology, Berlin, Germany. (1)
Finley and Gygi lab - Cell Biology Department - Harvard Medical School (1)
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Sunnybrook Research Institute, Toronto, ON, Canada / Department of Biochemistry, University of Toronto, Toronto, ON, Canada / Department of Biochemistry and Molecular Biology, Alberta Children’s Hospital Research Institute, Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada / Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada (1)
Max Planck Institute for Metabolism Research Cologne, 50931 Cologne, Germany (1)
PI, Dept. Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg (1)
Max Planck Institute for Multidisciplinary Sciences, Bioanalytical Mass Spectrometry Group, Göttingen, Germany University Medical Center Göttingen, Department of Clinical Chemistry, Bioanalytics Group, Göttingen, Germany (1)
Department of Developmental and Cell Biology, University of California, Irvine, Irvine, CA 92697, USA (1)
Section for Translational Surgical Oncology and Biobanking, Department of Surgery, University of Lübeck and University Hospital Schleswig-Holstein, Campus Lübeck, Ratzeburger Allee 160, 23538 Lübeck Germany (1)
Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA 94158, USA Department of Medicine and Division of Hematology/Oncology, University of California, San Francisco, San Francisco, CA 94158, USA (1)
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BCI Mass spectrometry Facility 1.02 & 1.03 1st floor Barts Cancer Institute Queen Mary, University of London John Vane Science Centre, Charterhouse Square, London EC1M 6BQ (1)
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Emeritus Group Leader Protein Phosphorylation Laboratory The Francis Crick Institute 1 Midland Road London NW1 1AT (1)
Université Paris Cité, CNRS, Institut Jacques Monod, F-75013 Paris, France. (1)
Department of Laboratory Medicine, Wiita Lab, University of California, San Francisco, USA (1)
Protomic Service CIC bioGUNE Bizkaia Tech. Park Build. 800 Derio 48160 Spain (1)

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Keyword

Fruquintinib plus Chemotherapy (1)
RAS mutation (1)

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Frequent driver mutations in histone H3.3 and chromatin remodeling genes in paediatric glioblastoma

Whole exome sequencing identified frequent driver mutations in a series of paediatric glioblastomas We used microarray-based profiling to investigate differences in gene expression according to mutational status of driver genes RNA from 27 primary tumor samples was subject to QC by Agilent BioAnalys...

ORGANISM(S): Homo sapiens

2012-03-01 | E-GEOD-34824 | biostudies-arrayexpress

Targeted DNA sequencing of uveal melanoma driver mutations

PRJNA1258314 | ENA

Targeted DNA sequencing of uveal melanoma driver mutations

PRJNA1258313 | ENA

RNA sequencing of CRC tumor organoids engineered with key driver mutations

PRJNA856659 | ENA

Concurrent DNA copy number alterations and mutations in genes related to maintenance of genome stability in uninvolved glandular tissue from breast cancer patients.

Somatic mosaicism for DNA copy number alterations (SMC-CNA) is defined as gain or loss of chromosomal segments in mitotic cells within a single organism. As cells harboring SMC-CNA have the potential to undergo clonal expansion, SMC-CNA may be present in a substantial portion of cells in differentia...

ORGANISM(S): Homo sapiens

2015-07-31 | E-MTAB-3110 | biostudies-arrayexpress

Clonal biases dictate availability of colonic cancer driver mutations for transformation

PRJNA1372664 | ENA

Deep sequencing of melanoma for driver mutations

EGAS00001000857 | EGA

Accumulating mitochondrial DNA mutations drive premature hematopoietic aging phenotypes molecularly distinct from physiologic stem cell aging

Somatic stem cells mediate tissue maintenance for the lifetime of an organism. Despite the well-established longevity that is a prerequisite for such function, accumulating data argue for compromised stem cell function with age. Identifying the mechanisms underlying age-dependent stem cell dysfuncti...

ORGANISM(S): Mus musculus

2011-05-06 | E-GEOD-27686 | biostudies-arrayexpress

Driver mutations escalating the risk of distant metastasis in Korean breast cancers

Integrative systematic analyses of mutational and transcriptional profiles reveal driver mutations escalating the risk of distant metastasis in Korean breast cancers

PRJEB9083 | ENA

Kin-Driver: a database of driver mutations in protein kinases.

Not available

S-EPMC4237945 | biostudies-literature

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