Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Science (New York, N.Y.)|August 11, 2007
Leptin regulates striatal regions and human eating behaviorI Sadaf Farooqi, Edward Bullmore, Julia Keogh, et al.
Human Molecular Genetics|February 18, 2003
Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanismsGiles S H Yeo, Emma J Lank, I Sadaf Farooqi, et al.
Lancet (London, England)|August 28, 2015
Role of melanocortin signalling in the preference for dietary macronutrients in human beingsAgatha van der Klaauw, Julia Keogh, Elana Henning, et al.
The Journal of Endocrinology|November 5, 2004
Studies of the neuromedin U-2 receptor gene in human obesity: evidence for the existence of two ancestral forms of the receptorSumit Bhattacharyya, Jian'an Luan, I Sadaf Farooqi, et al.
The Journal of Clinical Endocrinology and Metabolism|June 28, 2007
Hyperphagia and early-onset obesity due to a novel homozygous missense mutation in prohormone convertase 1/3I Sadaf Farooqi, Karolien Volders, Richard Stanhope, et al.
Nature Neuroscience|October 21, 2004
A de novo mutation affecting human TrkB associated with severe obesity and developmental delayGiles S H Yeo, Chiao-Chien Connie Hung, Justin Rochford, et al.
Obesity Research|May 29, 2004
Melanin-concentrating hormone receptor mutations and human obesity: functional analysisWilliam T Gibson, Pavlos Pissios, Daniel J Trombly, et al.
Journal of Lipid Research|January 27, 2006
Sequence variants in the melatonin-related receptor gene (GPR50) associate with circulating triglyceride and HDL levelsSumit Bhattacharyya, Jian'an Luan, Benjamin Challis, et al.
The Journal of Clinical Endocrinology and Metabolism|August 14, 2008
Mutations in the amino-terminal region of proopiomelanocortin (POMC) in patients with early-onset obesity impair POMC sorting to the regulated secretory pathwayJohn W M Creemers, Yung Seng Lee, Robert L Oliver, et al.
Cell Reports. Medicine|August 16, 2023
Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic diseaseRuth Hanssen, Chiara Auwerx, Maarja Jõeloo, et al.
Pageof 2