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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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Bibliografske podrobnosti
izdano v:Brain Struct Funct
Main Authors: Acs, Peter, Bauer, Peter O., Mayer, Balazs, Bera, Tapan, Macallister, Rhonda, Mezey, Eva, Pastan, Ira
Format: Artigo
Jezik:Inglês
Izdano: 2014
Teme:
Online dostop: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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