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Novel therapeutics in rare genetic obesities: A narrative review

Pharmacological research, 2023-05, Vol.191, p.106763-106763, Article 106763

2023

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Rare Genetic Forms of Obesity: Clinical Approach and Current Treatments in 2016

Obesity facts, 2016-06, Vol.9 (3), p.158-173

2016

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Molecular Genetics of Human Obesity-Associated MC4R Mutations

Annals of the New York Academy of Sciences, 2003-06, Vol.994 (1), p.49-57

2003

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Seven Novel Deleterious LEPR Mutations Found in Early-Onset Obesity: a ΔExon6–8 Shared by Subjects From Reunion Island, France, Suggests a Founder Effect

The journal of clinical endocrinology and metabolism, 2015-05, Vol.100 (5), p.E757-E766

2015

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Metabolic and Adipose Tissue Signatures in Adults With Prader-Willi Syndrome: A Model of Extreme Adiposity

The journal of clinical endocrinology and metabolism, 2015-03, Vol.100 (3), p.850-859

2015

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Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

The Journal of clinical investigation, 2017-01, Vol.127 (1), p.293-305

2017

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Novel pharmacological MC4R agonists can efficiently activate mutated MC4R from obese patient with impaired endogenous agonist response

Journal of endocrinology, 2010-11, Vol.207 (2), p.177-183

2010

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Homozygous Null Mutation of the Melanocortin-4 Receptor and Severe Early-Onset Obesity

The Journal of pediatrics, 2007-06, Vol.150 (6), p.613-617.e1

2007

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Melanocortin 4 Receptor Mutations in a Large Cohort of Severely Obese Adults: Prevalence, Functional Classification, Genotype-Phenotype Relationship, and Lack of Association with Binge Eating

The journal of clinical endocrinology and metabolism, 2006-05, Vol.91 (5), p.1811-1818

2006

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Rare melanocortin-3 receptor mutations with in vitro functional consequences are associated with human obesity

Human molecular genetics, 2011-01, Vol.20 (2), p.392-399

2011

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Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations

Human molecular genetics, 2003-01, Vol.12 (2), p.145-153

2003

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Mutational Analysis of the Pro-opiomelanocortin Gene in French Obese Children Led to the Identification of a Novel Deleterious Heterozygous Mutation Located in the α-Melanocyte Stimulating Hormone Domain

Pediatric research, 2008-02, Vol.63 (2), p.211-216

2008

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Genetic aspects of obesity

La Presse médicale (1983), 2007-11, Vol.36 (11 Pt 2), p.1598-1605

2007

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Influence of polymorphisms in candidate genes on early vascular alterations in obese children

Archives of cardiovascular diseases, 2010-01, Vol.103 (1), p.10-18

2010

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Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children

The Journal of pediatrics, 2001-08, Vol.139 (2), p.204-209

2001

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Association between CST3 rs2424577 Polymorphism and Corpulence Related Phenotypes during Lifetime in Populations of European Ancestry

Obesity facts, 2011, Vol.4 (2), p.131-144

2011

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Genetics and epigenetics of obesity: keys to understand

La Revue du praticien, 2019-11, Vol.69 (9), p.1016

Dubern, Béatrice

2019

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Novel therapeutics in rare genetic obesities: A narrative review

Rare Genetic Forms of Obesity: Clinical Approach and Current Treatments in 2016

Molecular Genetics of Human Obesity-Associated MC4R Mutations

Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia

Seven Novel Deleterious LEPR Mutations Found in Early-Onset Obesity: a ΔExon6–8 Shared by Subjects From Reunion Island, France, Suggests a Founder Effect

Metabolic and Adipose Tissue Signatures in Adults With Prader-Willi Syndrome: A Model of Extreme Adiposity

Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

Novel pharmacological MC4R agonists can efficiently activate mutated MC4R from obese patient with impaired endogenous agonist response

Homozygous Null Mutation of the Melanocortin-4 Receptor and Severe Early-Onset Obesity

Melanocortin 4 Receptor Mutations in a Large Cohort of Severely Obese Adults: Prevalence, Functional Classification, Genotype-Phenotype Relationship, and Lack of Association with Binge Eating

Rare melanocortin-3 receptor mutations with in vitro functional consequences are associated with human obesity

Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations

Mutational Analysis of the Pro-opiomelanocortin Gene in French Obese Children Led to the Identification of a Novel Deleterious Heterozygous Mutation Located in the α-Melanocyte Stimulating Hormone Domain

Genetic aspects of obesity

Influence of polymorphisms in candidate genes on early vascular alterations in obese children

Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children

Association between CST3 rs2424577 Polymorphism and Corpulence Related Phenotypes during Lifetime in Populations of European Ancestry

Genetics and epigenetics of obesity: keys to understand

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