Found: 169
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Ovarian Hyperandrogenism and Response to Gonadotropin-releasing Hormone Analogues in Primary Severe Insulin Resistance.
- Published in:
- 2021
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- Publication type:
- journal article
Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome.
- Published in:
- 2018
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- Publication type:
- journal article
Isomer-dependent metabolic effects of conjugated linoleic acid: insights from molecular markers sterol regulatory element-binding protein-1c and LXRalpha.
- Published in:
- 2002
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- Publication type:
- journal article
Regional differences in the response of human pre-adipocytes to PPARgamma and RXRalpha agonists.
- Published in:
- 2002
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- Publication type:
- journal article
A Pharmacogenetic Approach to the Treatment of Patients With Mutations.
- Published in:
- 2018
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- Publication type:
- journal article
OBESITY THERAPY: ALTERING THE ENERGY INTAKE-AND-EXPENDITURE BALANCE SHEET.
- Published in:
- Nature Reviews Drug Discovery, 2002, v. 1, n. 4, p. 276, doi. 10.1038/nrd770
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- Publication type:
- Article
Murine neuronatin deficiency is associated with a hypervariable food intake and bimodal obesity.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-96278-8
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- Publication type:
- Article
Uncoupling protein 2: Adiposity angel and diabetes devil?
- Published in:
- Nature Medicine, 2001, v. 7, n. 7, p. 770, doi. 10.1038/89877
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- Publication type:
- Article
Insights into obesity and insulin resistance from the study of extreme human phenotypes.
- Published in:
- European Journal of Endocrinology, 2002, v. 147, n. 4, p. 435, doi. 10.1530/eje.0.1470435
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- Publication type:
- Article
Leptin-Mediated Changes in the Human Metabolome.
- Published in:
- 2020
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- Publication type:
- journal article
GDF15 Is Elevated in Conditions of Glucocorticoid Deficiency and Is Modulated by Glucocorticoid Replacement.
- Published in:
- 2019
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- Publication type:
- journal article
Genetic architecture of human thinness compared to severe obesity.
- Published in:
- PLoS Genetics, 2019, v. 15, n. 1, p. 1, doi. 10.1371/journal.pgen.1007603
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- Publication type:
- Article
Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance.
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- Journal of Clinical Investigation, 2014, v. 124, n. 9, p. 4028, doi. 10.1172/JCI73264
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- Publication type:
- Article
Rare variants in single-minded 1 (SIM1) are associated with severe obesity.
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- Journal of Clinical Investigation, 2013, v. 123, n. 7, p. 3042, doi. 10.1172/JCI68016
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- Publication type:
- Article
Human SH2B1 mutations are associated with maladaptive behaviors and obesity.
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- Journal of Clinical Investigation, 2012, v. 122, n. 12, p. 4732, doi. 10.1172/JCI62696
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- Publication type:
- Article
Mitochondrial dysfunction in patients with primary congenital insulin resistance.
- Published in:
- 2011
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- Publication type:
- journal article
Postreceptor insulin resistance contributes to human dyslipidemia and hepatic steatosis.
- Published in:
- 2009
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- Publication type:
- journal article
PPAR gamma and human metabolic disease.
- Published in:
- 2006
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- Publication type:
- journal article
PPARγ and human metabolic disease.
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- Journal of Clinical Investigation, 2006, v. 116, n. 3, p. 581, doi. 10.1172/JCI28003
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- Publication type:
- Article
Kinetic analysis of FTO (fat mass and obesity-associated) reveals that it is unlikely to function as a sensor for 2-oxoglutarate.
- Published in:
- Biochemical Journal, 2012, v. 444, n. 2, p. 183, doi. 10.1042/BJ20120065
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- Publication type:
- Article
Shedding pounds after going under the knife: Guts over glory-why diets fail.
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- Nature Medicine, 2012, v. 18, n. 5, p. 666, doi. 10.1038/nm.2747
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- Publication type:
- Article
Breaking the spell of food.
- Published in:
- 2009
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- Publication type:
- Book Review
Is leptin an important physiological regulator of CRP?
- Published in:
- 2007
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- Publication type:
- Letter
Melanocortin receptors weigh in.
- Published in:
- Nature Medicine, 2004, v. 10, n. 4, p. 351, doi. 10.1038/nm0404-351
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- Publication type:
- Article
An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophy.
- Published in:
- Nature Genetics, 2013, v. 45, n. 8, p. 947, doi. 10.1038/ng.2670
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- Publication type:
- Article
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
- Published in:
- Nature Genetics, 2013, v. 45, n. 5, p. 513, doi. 10.1038/ng.2607
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- Publication type:
- Article
TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction.
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- Nature Genetics, 2009, v. 41, n. 3, p. 354, doi. 10.1038/ng.306
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- Publication type:
- Article
Digenic inheritance of severe insulin resistance in a human pedigree.
- Published in:
- Nature Genetics, 2002, v. 31, n. 4, p. 379, doi. 10.1038/ng926
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- Publication type:
- Article
LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 153, doi. 10.1038/72807
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- Publication type:
- Article
Contributions of Function-Altering Variants in Genes Implicated in Pubertal Timing and Body Mass for Self-Limited Delayed Puberty.
- Published in:
- 2017
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- Publication type:
- journal article
Roux-en-Y Gastric Bypass Surgery in the Management of Familial Partial Lipodystrophy Type 1.
- Published in:
- 2017
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- Publication type:
- journal article
Constitutive Activation of AKT2 in Humans Leads to Hypoglycemia Without Fatty Liver or Metabolic Dyslipidemia.
- Published in:
- 2017
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- Publication type:
- journal article
Obesity-associated melanocortin-4 receptor mutations are associated with changes in the brain response to food cues.
- Published in:
- 2014
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- Publication type:
- journal article
Obesity due to melanocortin 4 receptor (MC4R) deficiency is associated with increased linear growth and final height, fasting hyperinsulinemia, and incompletely suppressed growth hormone secretion.
- Published in:
- 2011
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- Publication type:
- journal article
Analysis of naturally occurring mutations in the human lipodystrophy protein seipin reveals multiple potential pathogenic mechanisms.
- Published in:
- Diabetologia, 2013, v. 56, n. 11, p. 2498, doi. 10.1007/s00125-013-3029-3
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- Publication type:
- Article
Effective solutions to the global obesity epidemic -- research future priorities.
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- Biologist, 2010, v. 57, n. 4, p. 211
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- Publication type:
- Article
Hypothalamic-Specific Manipulation of Fto, the Ortholog of the Human Obesity Gene FTO, Affects Food Intake in Rats.
- Published in:
- PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008771
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- Publication type:
- Article
Genetic Variance in the Spinocerebellar Ataxia Type 2 (ATXN2) Gene in Children with Severe Early Onset Obesity.
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- PLoS ONE, 2009, v. 4, n. 12, p. 1, doi. 10.1371/journal.pone.0008280
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- Publication type:
- Article
Treatment with recombinant human insulin-like growth factor (rhIGF)-I/rhIGF binding protein-3 complex improves metabolic control in subjects with severe insulin resistance.
- Published in:
- 2010
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- Publication type:
- journal article
Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor.
- Published in:
- 2009
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- Publication type:
- journal article
Complement abnormalities in acquired lipodystrophy revisited.
- Published in:
- 2009
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- Publication type:
- journal article
Fatty acid metabolism in patients with PPARgamma mutations.
- Published in:
- 2008
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- Publication type:
- journal article
Mutations in the amino-terminal region of proopiomelanocortin (POMC) in patients with early-onset obesity impair POMC sorting to the regulated secretory pathway.
- Published in:
- 2008
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- Publication type:
- journal article
Obesity associated genetic variation in FTO is associated with diminished satiety.
- Published in:
- 2008
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- Publication type:
- journal article
Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 4, p. 1129, doi. 10.1210/jc.2007-1328
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- Publication type:
- Article
Hyperphagia and early-onset obesity due to a novel homozygous missense mutation in prohormone convertase 1/3.
- Published in:
- 2007
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- Publication type:
- journal article
Examining the candidacy of ghrelin as a gene responsible for variation in adult stature in a United Kingdom population with type 2 diabetes.
- Published in:
- 2007
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- Publication type:
- journal article
Energy Expenditure and Adaptive Responses to an Acute Hypercaloric Fat Load in Humans with Lipodystrophy.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 3, p. 1446, doi. 10.1210/jc.2004-1494
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- Publication type:
- Article
Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy.
- Published in:
- 2004
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- Publication type:
- journal article
Proteinuric Nephropathy in Acquired and Congenital Generalized Lipodystrophy: Baseline Characteristics and Course during Recombinant Leptin Therapy.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 7, p. 3199, doi. 10.1210/jc.2003-032140
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- Publication type:
- Article