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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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Detalhes bibliográficos
Publicado no:Brain Struct Funct
Main Authors: Acs, Peter, Bauer, Peter O., Mayer, Balazs, Bera, Tapan, Macallister, Rhonda, Mezey, Eva, Pastan, Ira
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Acesso em linha: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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