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The Journal of Endocrinology|September 28, 2010
Lipodystrophy: metabolic insights from a rare disorderIsabel Huang-Doran, Alison Sleigh, Justin J Rochford, et al.
Endocrinology|March 3, 2011
Loss of agouti-related peptide does not significantly impact the phenotype of murine POMC deficiencyMarcus P Corander, Debra Rimmington, Benjamin G Challis, et al.
The Journal of Biological Chemistry|July 16, 2011
Human frame shift mutations affecting the carboxyl terminus of perilipin increase lipolysis by failing to sequester the adipose triglyceride lipase (ATGL) coactivator AB-hydrolase-containing 5 (ABHD5)Sheetal Gandotra, Koini Lim, Amandine Girousse, et al.
Endocrinology|September 9, 2006
A comparative study of the central effects of specific proopiomelancortin (POMC)-derived melanocortin peptides on food intake and body weight in pomc null miceY C Loraine Tung, Sarah J Piper, Debra Yeung, et al.
Hormone Research|March 23, 2007
Severe hypoinsulinaemic hypoglycaemia in a premature infant associated with poor weight gain and reduced adipose tissueRaquel Coelho, Jonathan Wells, John Symth, et al.
Science (New York, N.Y.)|August 11, 2007
Leptin regulates striatal regions and human eating behaviorI Sadaf Farooqi, Edward Bullmore, Julia Keogh, et al.
Plos One|December 18, 2009
Genetic variance in the spinocerebellar ataxia type 2 (ATXN2) gene in children with severe early onset obesityKarla P Figueroa, Sadaf Farooqi, Kristopher Harrup, et al.
The American Journal of Clinical Nutrition|May 31, 2002
Early nutrition and leptin concentrations in later lifeAtul Singhal, I Sadaf Farooqi, Stephen O'Rahilly, et al.
The Journal of Clinical Endocrinology and Metabolism|June 28, 2008
Obesity associated genetic variation in FTO is associated with diminished satietyJane Wardle, Susan Carnell, Claire M A Haworth, et al.
Endocrinology|August 16, 2008
Functional characterization of naturally occurring pathogenic mutations in the human leptin receptorWendy Kimber, Frank Peelman, Xavier Prieur, et al.
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