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Comparative study of IDH1 mutations in gliomas by immunohistochemistry and DNA sequencing
BACKGROUND: Mutations involving isocitrate dehydrogenase 1 (IDH 1) occur in a high proportion of diffuse gliomas, with implications on diagnosis and prognosis. About 90% involve exon 4 at codon 132, replacing amino acid arginine with histidine (R132H). Rarer ones include R132C, R132S, R132G, R132L,...
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| Päätekijät: | , , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3661098/ https://ncbi.nlm.nih.gov/pubmed/23486690 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/not015 |
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