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TSC2 epigenetic defect in primary LAM cells. Evidence of an anchorage-independent survival
Tuberous sclerosis complex (TSC) is caused by mutations in TSC1 or TSC2 genes. Lymphangioleiomyomatosis (LAM) can be sporadic or associated with TSC and is characterized by widespread pulmonary proliferation of abnormal α-smooth muscle (ASM)-like cells. We investigated the features of ASM cells isol...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BlackWell Publishing Ltd
2014
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4119383/ https://ncbi.nlm.nih.gov/pubmed/24606538 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.12237 |
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