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1  associated with a shift from brown to blond hair color.
2 hIP accrued in hair of subjects with natural hair color.
3 new treatment intervention for lost skin and hair color.
4 sor was evaluated in water, tomato juice and hair color.
5 yme kinetics, which leads to gradual loss of hair color.
6 ated loci previously reported in the GWAS of hair color.
7 D risk increased with decreasing darkness of hair color.
8 ntly inherited defects in either skin and/or hair color.
9  that extend far beyond its determination of hair color.
10 oordinate or independent control of skin and hair color.
11 studied their association with skin type and hair color.
12  was no association between MC1R alleles and hair color.
13  with decreased melanin production and blond hair color.
14 enic association between alopecia areata and hair color.
15 , bleaching (182.3 vs 71.6 ng/mL), permanent hair color (171.9 vs 83.2 ng/mL), and Brazilian blowout/
16 processes produces the diversity of skin and hair color among human populations, and defects in these
17 rs for epidermal thickness, melanin content, hair color and density, and dermal blood content.
18 ccount for substantial variation in skin and hair color and in skin cancer incidence.
19            Four patients with congenital red hair color and nephrotic syndrome caused by idiopathic m
20 ess was shown to be independent from natural hair color and not influenced by the presence of melanin
21                     The associations between hair color and PD were particularly strong for relative
22 gs include associations between MC1R and red hair color and skin color, IL17RA and monocyte count, an
23 gating the causal effects of lipid traits on hair color and skin color; and highlights the causal eff
24 tal nevus count was associated with skin and hair color and tendency to burn, as measured by a sun se
25 lts demonstrate a strong correlation between hair color and the degree of linear polarization.
26 m of the EDNRB gene on 13q22 associated with hair color and the strongest association was the single-
27 c effects: 7% associated to eye color, 6% to hair color, and 1% to reported skin type, which leaves 5
28  of severe sunburns, sunburn susceptibility, hair color, and Fitzpatrick skin types I, II, and III we
29 ed for age, sex, medical history, eye color, hair color, and likeliness of tanning versus burning at
30       All other factors (eg, age, skin type, hair color, and melanoma thickness) showed no significan
31  were nevi, skin type, freckle density, age, hair color, and sunburn history.
32 s meta-analysis with GWAS of nevus count and hair color, and transcriptome association approaches, un
33                      Differences in skin and hair color are principally genetically determined and ar
34 s adaptive (e.g., educational attainment and hair color) are largely attributable to correlated respo
35  1 receptor) gene, which determines skin and hair color, are associated with melanoma.
36        We used a genome-wide association for hair color as a quantitative trait in 151 U. americanus
37 ia areata and the main predictor was natural hair color before graying.
38 election, and multi-allelic traits including hair color, body mass index and blood pressure, showing
39 stantial differences in ancestry for eye and hair color, body mass index, waist/hip circumferences, a
40 ell now shows that Foxn1 also contributes to hair color by marking which cells are to receive pigment
41                                              Hair color change was the commonest adverse event in bar
42 reatment-related adverse events (TRAEs) were hair color changes (76%), elevated creatine phosphokinas
43 relationship between the asp84glu allele and hair color did not achieve statistical significance (chi
44                                              Hair color differences are among the most obvious exampl
45  from Eurasia, describing how skin, eye, and hair color evolved over the past 45,000 y.
46 series of genome-wide association studies on hair color, eye color, number of sunburns, tanning abili
47 riants, especially those associated with red hair color, fair skin, and poor tanning ability (RHC tra
48 association between risk of hearing loss and hair color (for black hair vs. red or blonde hair, multi
49 elle) morphology and quantitatively measured hair colors from 116 extant mammals to reliably reconstr
50 ts: family history of melanoma, blond or red hair colors, higher number of extremity moles, higher su
51                       Information on natural hair color in early adulthood (age 18-21 years) was asse
52 ognized as a Mendelian determinant of yellow hair color in many different mammals, also causes reduce
53 s significantly associated with common blond hair color in northern Europeans.
54 riants that are strongly associated with red hair color increase melanoma risk.
55 s from fetal cat skin reveal that red/yellow hair color is caused by reduced expression of melanogeni
56                  Variation in human skin and hair color is one of the most striking aspects of human
57 e that SERS can be used to detect the dye on hair colored more than two months prior to its spectrosc
58  was also a relation between MC1R status and hair color, most prominently for the b* axis (p<0.001),
59 n adverse events included fatigue, change in hair color, nausea, dysgeusia, and periorbital edema; ad
60           The risk prediction model included hair color, nevus density, first-degree family history o
61                          We examined whether hair color, one of the most important phenotypes of pigm
62 MSC (OR, 1.66 [95% CI, 0.90-3.07]) and light hair color (OR, 1.17 [95% CI, 0.51-2.71]) did not reach
63  suspect or victim, such as their sex, race, hair color, or age.
64 that alopecia areata is modulated by natural hair color, preferentially targeting darker hair.
65 s of the association between KITLG and blond hair color, presenting an intriguing example of how a si
66 96-2002 to test the hypothesis that lifetime hair-coloring product use increases non-Hodgkin's lympho
67 was observed among women who reported use of hair-coloring products before 1980 (odds ratio = 1.3, 95
68 was found only among women who started using hair-coloring products before 1980.
69 : 1.0, 4.0) for those using darker permanent hair-coloring products for more than 25 years and 1.7 (9
70 re and disease among women who started using hair-coloring products in 1980 or later.
71 ning ability-related loci are similar to the hair color-related loci previously reported in the GWAS
72 -1 receptor (MC1R) responsible for human red hair color (RHC) variants are associated with impaired D
73 or (MC1R) variants responsible for human red hair color (RHC-variants) are consequently associated wi
74  hearing loss and skin pigmentation by using hair color, skin tanning ability, and skin reaction to p
75  ancestry, nevus density, freckling density, hair color, tanning ability, adult sunburns, family hist
76 m the baseline survey on phenotypic factors (hair color, tanning ability, nevus density, family histo
77 tability; these sets ranged in size from 28 (hair color) to 3,400 (height) to 2 million (number of ch
78   We report results using direct measures of hair color using objective colorimetric dimensions and H
79  into the polarization properties of various hair colors using several techniques, including polariza
80 dence interval] = 3.39 [1.85-6.20]), and red hair color (vs.
81                                          Red hair color was not significantly different from light br
82 m a genome-wide association study of natural hair color were assessed for associations with the risk
83  1673 cases of alopecia areata with reported hair color were captured and matched by age and sex to 6
84 f nevi, history of severe sunburn, and light hair color were each associated with significantly eleva