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A novel form of ciliopathy underlies hyperphagia and obesity in Ankrd26 knockout mice
Human ciliopathies are genetic disorders caused by mutations in genes responsible for the formation and function of primary cilia. Some are associated with hyperphagia and obesity (e.g., Bardet–Biedl Syndrome, Alström Syndrome), but the mechanisms underlying these problems are not fully understood....
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| 發表在: | Brain Struct Funct |
|---|---|
| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2014
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4601608/ https://ncbi.nlm.nih.gov/pubmed/24633808 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00429-014-0741-9 |
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