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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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Cart Overexpression Is the Only Identifiable Cause of High Bone Mass in Melanocortin 4 Receptor Deficiency

Endocrinology (Philadelphia), 2006-07, Vol.147 (7), p.3196-3202

2006

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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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Follow-up of GK rats during prediabetes highlights increased insulin action and fat deposition despite low insulin secretion

American journal of physiology: endocrinology and metabolism, 2008-01, Vol.294 (1), p.E168-E175

2008

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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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A Homozygous Null Mutation Delineates the Role of the Melanocortin-4 Receptor in Humans

The journal of clinical endocrinology and metabolism, 2004-05, Vol.89 (5), p.2028-2032

2004

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ADD1/SREBP-1c Is Required in the Activation of Hepatic Lipogenic Gene Expression by Glucose

Molecular and Cellular Biology, 1999-05, Vol.19 (5), p.3760-3768

1999

Volltextzugriff (PDF)

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

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

2003

Volltextzugriff (PDF)

Obesity-associated mutations in the melanocortin 4 receptor provide novel insights into its function

Peptides (New York, N.Y. : 1980), 2005-10, Vol.26 (10), p.1909-1919

2005

Volltextzugriff (PDF)

The Human MC4R Promoter

Diabetes (New York, N.Y.), 2003-12, Vol.52 (12), p.2996-3000

2003

Volltextzugriff (PDF)

The human MC4R promoter: Characterization and role in obesity

Diabetes (New York, N.Y.), 2003-12, Vol.52 (12), p.2996-3000

2003

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Obesity-associated mutations in the melanocortin 4 receptor provide novel insights into its function: The melanocortin pathway 2005

Peptides (New York, N.Y. : 1980), 2005, Vol.26 (10), p.1909-1919

2005

Volltextzugriff (PDF)

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

Human molecular genetics, 2003-01, Vol.12 (2), p.145-53

2003

Volltextzugriff (PDF)

Molecular genetics of human obesity-associated MC4R mutations

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

2003

Volltextzugriff (PDF)

Follow-up of GK rats during prediabetes highlights increased insulin action and fat deposition despite low insulin secretion

American journal of physiology: endocrinology and metabolism, 2008, Vol.57 (1)

2008

Volltextzugriff (PDF)

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Molecular Genetics of Human Obesity-Associated MC4R Mutations

Cart Overexpression Is the Only Identifiable Cause of High Bone Mass in Melanocortin 4 Receptor Deficiency

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

Follow-up of GK rats during prediabetes highlights increased insulin action and fat deposition despite low insulin secretion

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

A Homozygous Null Mutation Delineates the Role of the Melanocortin-4 Receptor in Humans

ADD1/SREBP-1c Is Required in the Activation of Hepatic Lipogenic Gene Expression by Glucose

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

Obesity-associated mutations in the melanocortin 4 receptor provide novel insights into its function

The Human MC4R Promoter

The human MC4R promoter: Characterization and role in obesity

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

Obesity-associated mutations in the melanocortin 4 receptor provide novel insights into its function: The melanocortin pathway 2005

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

Molecular genetics of human obesity-associated MC4R mutations

Follow-up of GK rats during prediabetes highlights increased insulin action and fat deposition despite low insulin secretion

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