(Q24323379)

GOA release 2020-03-11

hair pigmentation

1 reference

inferred from title

adrenal insufficiency

1 reference

H Krude

1

0 references

H Biebermann

2

0 references

W Luck

3

0 references

R Horn

4

0 references

G Brabant

5

0 references

A Grüters

Proopiomelanocortin processing in the pituitary, central nervous system, and peripheral tissues

6

0 references

language of work or name

English

0 references

publication date

June 1998

0 references

published in

Nature Genetics

0 references

volume

19

0 references

page(s)

155-7

0 references

issue

2

0 references

cites work

1 reference

7 January 2021

Isolated congenital ACTH deficiency: a cleavage enzyme defect?

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Role of melanocortinergic neurons in feeding and the agouti obesity syndrome

1 reference

7 January 2021

A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2

1 reference

7 January 2021

Melanocortin receptors in leptin effects.

1 reference

7 January 2021

Complete nucleotide sequence of the human corticotropin-β-lipotropin precursor gene

1 reference

7 January 2021

Isolation and structural organization of the human corticotropin-β-lipotropin precursor gene

1 reference

7 January 2021

The scanning model for translation: an update

1 reference

7 January 2021

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

1 reference

7 January 2021

Mutation creates an open reading frame within the 5' untranslated region of macaque erythrocyte carbonic anhydrase (CA) I mRNA that suppresses CA I expression and supports the scanning model for translation

1 reference

7 January 2021

The agouti gene: turned on to yellow

1 reference

7 January 2021

The role of melanocyte-stimulating hormone (MSH) receptor in bovine coat color determination

1 reference

7 January 2021

Red coat color in Holstein cattle is associated with a deletion in the MSHR gene

1 reference

7 January 2021

Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans

1 reference

7 January 2021

Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair

1 reference

7 January 2021

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

1 reference

7 January 2021

Exocrine gland dysfunction in MC5-R-deficient mice: evidence for coordinated regulation of exocrine gland function by melanocortin peptides

1 reference

7 January 2021

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

1 reference

7 January 2021

A leptin missense mutation associated with hypogonadism and morbid obesity.

1 reference

7 January 2021

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

1 reference

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

7 January 2021

Identifiers

DOI

10.1038/509

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

3809233

1011655085

0 references

3809233

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference