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SLC45A2: a novel malignant melanoma-associated gene
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title
SLC45A2: a novel malignant melanoma-associated gene
(English)
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author
Gloria Ribas Despuig
object named as
G. Ribas
series ordinal
7
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Roger L. Milne
series ordinal
2
object named as
R.L. Milne
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author name string
L.P. Fernandez
series ordinal
1
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G. Pita
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3
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J.A. Avilés
series ordinal
4
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P. Lázaro
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5
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J. Benítez
series ordinal
6
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publication date
September 2008
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published in
Human Mutation
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volume
29
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page(s)
1161-1167
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issue
9
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cites work
The genetics of melanoma
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The genetics of malignant melanoma: lessons from mouse and man.
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Interactive effects of MC1R and OCA2 on melanoma risk phenotypes
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Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression
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Contribution of melanocortin-1 receptor gene variants to sporadic cutaneous melanoma risk in a population in central Italy: a case-control study.
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Re: MC1R, ASIP, and DNA Repair in Sporadic and Familial Melanoma in a Mediterranean Population
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https://api.crossref.org/works/10.1002%2FHUMU.20804
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7 January 2021
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inferred from DOI database lookup
MC1R: three novel variants identified in a malignant melanoma association study in the Spanish population.
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Comprehensive evaluation of allele frequency differences of MC1R variants across populations.
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Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation
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Pigmentary Diversity: Identifying the genes causing human diversity
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Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma
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A polymorphism in the agouti signaling protein gene is associated with human pigmentation
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Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene
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MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population
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Melanocyte biology and skin pigmentation
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Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure
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Melanoma
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7 January 2021
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The genetics of susceptibility to cutaneous melanoma
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The genetics of sun sensitivity in humans
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Evidence for recent positive selection at the human AIM1 locus in a European population.
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Human pigmentation genes: identification, structure and consequences of polymorphic variation
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7 January 2021
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Eye colour: portals into pigmentation genes and ancestry
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A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color
1 reference
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7 January 2021
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The Silver locus product Pmel17/gp100/Silv/ME20: controversial in name and in function
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Melanoma etiology: where are we?
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Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
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Identifiers
DOI
10.1002/HUMU.20804
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PubMed ID
18563784
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