(Q48379426)

11 February 2018

title

Characterization of Mahogunin Ring Finger-1 expression in mice. (English)

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11 February 2018

author

Teresa M. Gunn

5

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11 February 2018

Christina D. Cota

object named as

Christina D Cota

4

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author name string

Pooneh Bagher

1

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11 February 2018

Jian Jiao

2

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11 February 2018

C Owen Smith

3

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11 February 2018

publication date

1 December 2006

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11 February 2018

Pigment Cell & Melanoma Research

published in

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11 February 2018

volume

19

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11 February 2018

issue

6

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11 February 2018

page(s)

635-643

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11 February 2018

The melanocortin-1 receptor is a key regulator of human cutaneous pigmentation.

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Molecular genetics and evolution of melanism in the cat family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

A human beta-actin expression vector system directs high-level accumulation of antisense transcripts

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Spongiform degeneration in mahoganoid mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Characterization of the dog Agouti gene and a nonagoutimutation in German Shepherd Dogs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Effect of alpha- and betamelanocyte stimulating hormones on the skin colour of man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Association of feather colour with constitutively active melanocortin 1 receptors in chicken

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Mechanisms of antiinflammatory action of the neuroimmunomodulatory peptide alpha-MSH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

An agouti mutation lacking the basic domain induces yellow pigmentation but not obesity in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Melanocortin 1 receptor variation in the domestic dog.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

MC1R Studies in Dogs With Melanistic Mask or Brindle Patterns

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

BayGenomics: a resource of insertional mutations in mouse embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Molecular and pharmacological characterization of dominant black coat color in sheep.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

A role for the melanocortin 4 receptor in sexual function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.2006.00340.X

10.1111/J.1600-0749.2006.00340.X

21 January 2018

Identifiers

DOI

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11 February 2018

PubMed ID

17083490

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11 February 2018