Energy homeostasis in Prader-Willi Syndrome: How clinical research informs studies of animal models of genetic obesity

Nutritional phases in Prader-Willi syndrome

(2011) Jennifer L. Miller et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Melanocortin 4 receptor is a transcriptional target of nescient helix-loop-helix-2

(2011) Umesh D. Wankhade et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Necdin Protects Embryonic Motoneurons from Programmed Cell Death

(2011) Julianne Aebischer et al.   PLoS One

Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome

(2010) Brooke Burns et al.   HUMAN MOLECULAR GENETICS

A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene

(2010) Fabienne Schaller et al.   HUMAN MOLECULAR GENETICS

Translational Neuroscience Approaches to Hyperphagia

(2010) M. Perello et al.   JOURNAL OF NEUROSCIENCE

Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader–Willi syndrome

(2010) Michael V. Morabito et al.   NEUROBIOLOGY OF DISEASE

The transition between the phenotypes of Prader-Willi syndrome during infancy and early childhood

(2009) JILL V BUTLER et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Causes and control of excess body fat

(2009) Jeffrey M. Friedman   NATURE

Smith–Magenis syndrome

(2008) Sarah H Elsea et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

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

(2008) Feng Ding et al.   PLoS One