(Q28117916)

English

A frameshift mutation in MC4R associated with dominantly inherited human obesity

scientific journal article

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scholarly article

1 reference

4 January 2017

A frameshift mutation in MC4R associated with dominantly inherited human obesity (English)

1 reference

4 January 2017

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author name string

G. S. Yeo

1

1 reference

4 January 2017

I. S. Farooqi

2

1 reference

4 January 2017

S. Aminian

3

1 reference

4 January 2017

D. J. Halsall

4

1 reference

4 January 2017

R. G. Stanhope

5

1 reference

4 January 2017

S. O'Rahilly

6

1 reference

4 January 2017

language of work or name

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publication date

1 October 1998

1 reference

4 January 2017

Nature Genetics

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4 January 2017

20

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4 January 2017

111–112

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4 January 2017

2

1 reference

4 January 2017

Obesity, diabetes and functions for proopiomelanocortin-derived peptides

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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Role of melanocortinergic neurons in feeding and the agouti obesity syndrome

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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Targeted disruption of the melanocortin-4 receptor results in obesity in mice

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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Agouti protein is an antagonist of the melanocyte-stimulating-hormone receptor

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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Antagonism of central melanocortin receptors in vitro and in vivo by agouti-related protein

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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G protein-coupled receptor structure and function: the impact of disease-causing mutations

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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Congenital leptin deficiency is associated with severe early-onset obesity in humans

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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A leptin missense mutation associated with hypogonadism and morbid obesity.

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

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A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

1 reference

https://api.crossref.org/works/10.1038%2F2404

7 January 2021

based on heuristic

inferred from DOI database lookup

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4 January 2017

1 reference

4 January 2017

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