(Q40406038)

20 September 2017

title

Altered cell surface expression of human MC1R variant receptor alleles associated with red hair and skin cancer risk (English)

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20 September 2017

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5

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6

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20 September 2017

Kimberley A. Beaumont

object named as

Kimberley A Beaumont

1

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author name string

Richard A Newton

2

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20 September 2017

Darren J Smit

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20 September 2017

J Helen Leonard

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20 September 2017

publication date

22 June 2005

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20 September 2017

published in

Human Molecular Genetics

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20 September 2017

volume

14

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20 September 2017

issue

15

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20 September 2017

page(s)

2145-2154

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Human pigmentation genes: identification, structure and consequences of polymorphic variation

20 September 2017

cites work

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https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

Pharmacological characterization of loss of function mutations of the human melanocortin 1 receptor that are associated with red hair.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

Screening of human primary melanocytes of defined melanocortin-1 receptor genotype: pigmentation marker, ultrastructural and UV-survival studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

Human melanocortin 1 receptor (MC1R) gene variants alter melanoma cell growth and adhesion to extracellular matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

G protein-coupled receptor interacting proteins: emerging roles in localization and signal transduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

RTP family members induce functional expression of mammalian odorant receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

Functional characterization of melanocortin-4 receptor mutations associated with childhood obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

Binding-, intracellular transport-, and biosynthesis-defective mutants of vasopressin type 2 receptor in patients with X-linked nephrogenic diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI219

21 January 2018

Identifiers

DOI

10.1093/HMG/DDI219

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20 September 2017

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