Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader–Willi syndrome

Prader–Willi syndrome (PWS) is a neurodevelopmental disorder caused by deletion or inactivation of paternally expressed imprinted genes on human chromosome 15q11‐q13, the most recognised feature of which is hyperphagia. This is thought to arise as a consequence of abnormalities in both the physiolog...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Eur J Neurosci
Hlavní autoři: Davies, Jennifer R., Humby, Trevor, Dwyer, Dominic M., Garfield, Alastair S., Furby, Hannah, Wilkinson, Lawrence S., Wells, Timothy, Isles, Anthony R.
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2015
Témata:
Behavioural Neuroscience
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4949663/
https://ncbi.nlm.nih.gov/pubmed/26040449
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ejn.12972
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky