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Publication date
2018 09 10
Authors
Palin, K Pitkanen, E Turunen, M Sahu, B Pihlajamaa, P Kivioja, T Kaasinen, E Valimaki, N Hanninen, UA Cajuso, T Aavikko, M Tuupanen, S Kilpivaara, O van den Berg, L Kondelin, J Tanskanen, T Katainen, R Grau, M Rauanheimo, H Plaketti, RM Taira, A Sulo, P Hartonen, T Dave, K Schmierer, B Botla, S Sokolova, M Vaharautio, A Gladysz, K Ongen, H Dermitzakis, E Bramsen, JB Orntoft, TF Andersen, CL Ristimaki, A Lepisto, A Renkonen-Sinisalo, L Mecklin, JP Taipale, J Aaltonen, LA
Author KI Usernames
Aaltonen, LA|lauaal Botla, S|sanbot Dave, K|kashda Schmierer, B|beschm Taipale, J|justai
Pubmed ID
30202008
Journal
Nature communications
Doctype
Article
KI Connection
Hög
Mesh SV
Allelisk imbalans CRISPR-Cas system Danmark DNA-kopienummervariationer Fenotyp Genetiska sjukdomsanlag Genomik Genotyp Genuttrycksmönster Helgenomsekvensering Heterozygotförlust Kromosomavvikelser Mikrosatellitupprepningar Människa Människokromosomer, par 8 Proto-onkogenproteiner p21(ras) Punktmutation siRNA Tjock- och ändtarmstumörer Transkriptionsfaktorer Tumörsuppressorprotein p53
Mesh EN
Allelic Imbalance Chromosome Aberrations Chromosomes, Human, Pair 8 Colorectal Neoplasms CRISPR-Cas Systems Denmark DNA Copy Number Variations Gene Expression Profiling Genetic Predisposition to Disease Genomics Genotype Loss of Heterozygosity Microsatellite Repeats Phenotype Point Mutation Proto-Oncogene Proteins p21(ras) RNA, Small Interfering Transcription Factors Tumor Suppressor Protein p53 Whole Genome Sequencing
First date
2018-09-24T14:28:46.334Z