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1 Ergebnisse
1
Low mutation burden and frequent loss of CDKN2A/B and SMARC..:
Pemov, Alexander
;
Hansen, Nancy F
;
Sindiri, Sivasish
...
qt8j58r48q. , 2019
Link:
https://escholarship.org/uc/item/8j58r48q
RT Journal T1
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define pre-malignant neurofibromatosis type 1-associated atypical neurofibromas
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt8j58r48q&Exemplar=1&LAN=DE A1 Pemov, Alexander A1 Hansen, Nancy F A1 Sindiri, Sivasish A1 Patidar, Rajesh A1 Higham, Christine S A1 Dombi, Eva A1 Miettinen, Markku M A1 Fetsch, Patricia A1 Brems, Hilde A1 Chandrasekharappa, Settara A1 Jones, Kristine A1 Zhu, Bin A1 Wei, Jun S A1 Mullikin, James C A1 Wallace, Margaret R A1 Khan, Javed A1 Legius, Eric A1 Widemann, Brigitte C A1 Stewart, Douglas R PB eScholarship, University of California YR 2019 K1 Biomedical and Clinical Sciences K1 Oncology and Carcinogenesis K1 Human Genome K1 Neurofibromatosis K1 Rare Diseases K1 Neurosciences K1 Genetics K1 Pediatric K1 Cancer K1 Cyclin-Dependent Kinase Inhibitor p15 K1 Cyclin-Dependent Kinase Inhibitor p16 K1 Humans K1 Mutation K1 Nerve Sheath Neoplasms K1 Neurofibroma K1 Plexiform K1 Neurofibromatosis 1 K1 Neurofibrosarcoma K1 Transcription Factors K1 atypical neurofibromas K1 benign-to-malignant transformation K1 malignant peripheral nerve sheath tumor K1 neurofibromatosis type 1 K1 plexiform neurofibromas K1 National Intramural Sequencing Center (NISC) Comparative Sequencing Program K1 National Cancer Institute (NCI) Division of Cancer Epidemiology and Genetics (DCEG) Cancer Genomics Research Laboratory K1 Oncology & Carcinogenesis JF qt8j58r48q LK http://dx.doi.org/https://escholarship.org/uc/item/8j58r48q DO https://escholarship.org/uc/item/8j58r48q SF ELIB - SuUB Bremen
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