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Infrequent methylation of CDKN2A(MTS1/p16) and rare mutation of both CDKN2A and CDKN2B(MTS2/p15) in primary astrocytic tumours.

In a series of 46 glioblastomas, 16 anaplastic astrocytomas and eight astrocytomas, all tumours retaining one or both alleles of CDKN2A (48 tumours) and CDKN2B (49 tumours) were subjected to sequence analysis (entire coding region and splice acceptor and donor sites). One glioblastoma with hemizygou...

詳細記述

保存先:
書誌詳細
主要な著者: Schmidt, E. E., Ichimura, K., Messerle, K. R., Goike, H. M., Collins, V. P.
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group 1997
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2222701/
https://ncbi.nlm.nih.gov/pubmed/9000591
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