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Nature Metabolism|March 1, 2024
Systemic proteome adaptions to 7-day complete caloric restriction in humansMaik Pietzner, Burulça Uluvar, Kristoffer J Kolnes, et al.
The Journal of Clinical Endocrinology and Metabolism|January 24, 2008
Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophyC A Kim, Marc Delépine, Emilie Boutet, et al.
Diabetes|September 28, 2006
Leptin deficiency unmasks the deleterious effects of impaired peroxisome proliferator-activated receptor gamma function (P465L PPARgamma) in miceSarah L Gray, Edoardo Dalla Nora, Johannes Grosse, et al.
Plos Genetics|January 10, 2013
Adult onset global loss of the fto gene alters body composition and metabolism in the mouseFiona McMurray, Chris D Church, Rachel Larder, et al.
Elife|February 1, 2023
A mouse model of human mitofusin-2-related lipodystrophy exhibits adipose-specific mitochondrial stress and reduced leptin secretionJake P Mann, Xiaowen Duan, Satish Patel, et al.
Molecular Metabolism|May 3, 2017
Heterogeneity of hypothalamic pro-opiomelanocortin-expressing neurons revealed by single-cell RNA sequencingBrian Y H Lam, Irene Cimino, Joseph Polex-Wolf, et al.
The New England Journal of Medicine|February 25, 2011
Perilipin deficiency and autosomal dominant partial lipodystrophySheetal Gandotra, Caroline Le Dour, William Bottomley, et al.
The Journal of Clinical Investigation|November 20, 2012
Human SH2B1 mutations are associated with maladaptive behaviors and obesityMichael E Doche, Elena G Bochukova, Hsiao-Wen Su, et al.
Cell Reports. Medicine|September 2, 2023
High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptorSadia Saeed, Roohia Khanam, Qasim M Janjua, et al.
Molecular Metabolism|September 5, 2022
Combined genetic deletion of GDF15 and FGF21 has modest effects on body weight, hepatic steatosis and insulin resistance in high fat fed miceSatish Patel, Afreen Haider, Anna Alvarez-Guaita, et al.
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