PDF) Hypothalamic loss of Snord116 recapitulates the hyperphagia

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SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice

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Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes - Iiro Ilmari Salminen, Bernard J Crespi, Mikael Mokkonen, 2019

JCI Insight - Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production

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Functional link to hyperphagia in PWS

PDF] Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction - ScienceDirect

PDF) A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome

PDF) A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome

Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes - Iiro Ilmari Salminen, Bernard J Crespi, Mikael Mokkonen, 2019

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