Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
about
Evidence for variable selective pressures at MC1RThe genetics of sun sensitivity in humans.A high-coverage genome sequence from an archaic Denisovan individualMC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2)Melanocortin-1 receptor gene variants in four Chinese ethnic populations.Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma.Melanocortin-1 receptor gene variants determine the risk of nonmelanoma skin cancer independently of fair skin and red hair.Skin as a living coloring book: how epithelial cells create patterns of pigmentation.Melanocortin-1 receptor structure and functional regulation.Genetic counseling in melanoma.MC1R is dispensable for the proteinuria reducing and glomerular protective effect of melanocortin therapy.Growth factors and oncogenes as targets in melanoma: lost in translation?Malignant melanoma in the 21st century: the emerging molecular landscape.A polymorphism in the agouti signaling protein gene is associated with human pigmentation.Melanocortin 1 receptor and risk of cutaneous melanoma: a meta-analysis and estimates of population burden.MC1R, the cAMP pathway, and the response to solar UV: extending the horizon beyond pigmentationRate limiting factors in melanocortin 1 receptor signalling through the cAMP pathway.Loss-of-function variants of the human melanocortin-1 receptor gene in melanoma cells define structural determinants of receptor function.Pharmacological and functional characterization of the guinea-pig B2 bradykinin receptor stably expressed in CHO-K1 cell lineInfluence of oligomerization on the dynamics of G-protein coupled receptors as assessed by normal mode analysis.Effect of Val92Met and Arg163Gln variants of the MC1R gene on freckles and solar lentigines in Japanese.Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma
P2860
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P2860
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
description
1998 nî lūn-bûn
@nan
1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@ast
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@en
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@en-gb
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@nl
type
label
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@ast
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@en
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@en-gb
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@nl
prefLabel
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@ast
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@en
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@en-gb
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@nl
P2093
P3181
P356
P1476
Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor
@en
P2093
M Doufexis
P A Frändberg
V Chhájlani
P3181
P356
10.1006/BBRC.1998.8459
P407
P577
1998-04-17T00:00:00Z