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1       The patient developed an intense green skin color.
2 al photoprotection and maintenance of normal skin color.
3 f the epidermis and efficiently restored the skin color.
4  genetic and epigenetic variations determine skin color.
5 t melanin levels in vitro and modulate human skin color.
6 pe distribution across social categories and skin color.
7 ltraviolet-B exposure and tend to have light skin color.
8 hen conditioning the association analyses on skin color.
9 d with traits including scaling patterns and skin color.
10 ereby contributes to the ethnic diversity of skin color.
11  (NSV) is characterized by loss of inherited skin color.
12 t with their known contributions to European skin color.
13 y a mostly progressive loss of the inherited skin color.
14 acterized by a progressive loss of inherited skin color.
15 emplars (N250) were selectively sensitive to skin color.
16 egradation influenced the evolution of human skin color.
17 mic region has a significant effect on human skin color.
18 xillofacial elastomer specimens having human skin colors.
19             It has been suggested that human skin color adapts to balance the need for vitamin D synt
20  characterized by a patchy loss of inherited skin color affecting approximately 0.5% of individuals o
21 xtreme jaundice is present as a phenotype in skin color after 8 h.
22 me is defined as the time required to regain skin color after blanching pressure is applied.
23 d boy with cystic fibrosis reported a bluish skin color after he began ingesting a colloidal silver s
24 n (SpB) levels in multiethnic neonates using skin color analysis.
25 om other aspects of visual appearance (e.g., skin color and facial features).
26  findings suggest that racial differences in skin color and facial structure are detected during the
27 tic architecture and polygenic adaptation of skin color and prioritizes potential causal genes.
28 ent use, body mass index, and for vitamin D, skin color and season, had a larger impact on nutrient c
29      In addition to interviews, constitutive skin color and skin ultraviolet light sensitivity were a
30 ted for income, parental education, maternal skin color and smoking, and breastfeeding duration.
31 re of their surroundings by modulating their skin color and surface morphology simultaneously, for th
32 regimens that achieve objective normality of skin color and texture and are used by compliant patient
33  adjusted to meet a target outcome of normal skin color and texture, with regular long-term follow-up
34 a more complex evolutionary relation between skin color and the vitamin D pathway.
35 uated objective measurements of constitutive skin color and ultraviolet light sensitivity in relation
36 ytes derived from individuals with different skin colors and MC1R genotype and uncovered new informat
37  Reptiles exhibit a spectacular diversity of skin colors and patterns brought about by the interactio
38 is for understanding the origin of different skin colors and responses to UV within different races.
39       Consideration of factors such as diet, skin color, and BMI will be important for selecting stud
40 ging eyelids included age, male sex, lighter skin color, and higher body mass index.
41 es in ascorbic acid, titratable acidity, and skin color, and reduced splitting and decay following 4
42 his association was independent of age, sex, skin color, and sun damage (wrinkling, pigmented spots)
43 al effects of lipid traits on hair color and skin color; and highlights the causal effects of physica
44                 However, persons with darker skin color are often diagnosed at later stages, when ski
45 etic variants and potential causal genes for skin color as well as their polygenic interplay with sun
46 e epidermis determines the wide variation in skin color associated with ethnic skin diversity.
47                                              Skin color at each body site is a strong predictor of re
48                     RS-measured constitutive skin color at the upper volar arm fit a quadratic equati
49          Thus, RS assessment of constitutive skin color at the upper volar arm provides a quick, noni
50 en-site AUIC reproducibility of constitutive skin color at the upper volar arm was 3 and 5% coefficie
51                                 Constitutive skin color at the upper volar arm was equal to the butto
52 ectance study on a population having diverse skin colors at 34 degrees C, the optimal model led to r(
53  DNA sequences have revealed that systems of skin color-based racial and ethnic classification lacked
54 t created classifications and hierarchies of skin-color-based races, which were reinforced by prevail
55 ontrol region, a gene associated with yellow skin color (beta-carotene dioxygenase 2), and a putative
56  the involvement of autophagy in determining skin color by regulating melanosome degradation in kerat
57 mal Hsp70-1A contributes to the diversity of skin color by regulating the amount of melanin synthesiz
58                      Children, stratified by skin color by using Fitzpatrick's definition, were rando
59         We conducted a study to quantify the skin color change using a handheld reflected light color
60 association between self-identified race and skin color changed over the 13-y period and to what exte
61  increased anthocyanin levels and changes in skin color (Chroma).
62 n loci: one for eye color (AHRR) and one for skin color (DDB1).
63  reveal that autophagy has a pivotal role in skin color determination by regulating melanosome degrad
64 nsights into the mechanisms underlying human skin color diversity and adaptive evolution.
65 nhancer contribute to the evolution of human skin color diversity and detect signals of local adaptat
66 broad range of phenotypic values for eye and skin color due to the mix of West African and European a
67 or permanent (e.g., during aging) changes in skin color, environmental factors (e.g., UV), certain dr
68                                     However, skin color evolution and genetics in East Asians are und
69 of dermatologic disease processes across all skin colors, facilitate the monitoring of dermatologic d
70 d with racial identity choice conditional on skin color, finding a weak negative relationship between
71 trol dynamically tunable, driving changes in skin color for camouflage and communication.
72 ened, however, by use of surrogates, such as skin color, for these proxies, the distribution of which
73 ow this association differs by maternal race/skin color, gestational age at birth (term versus preter
74 ned at different stages of ripening based on skin color (green, purple and black).
75                                              Skin color has been proposed to contribute to race-based
76 e genes underpinning population variation in skin color have been identified.
77 factors (male sex, genetic variants, lighter skin color, high body mass index, and possibly current s
78 ciations between MC1R and red hair color and skin color, IL17RA and monocyte count, and IQGAP2 and me
79 es of local adaptation for traits related to skin color, immune response, height, and metabolic proce
80                                We quantified skin color in 48,433 East Asians using image analysis an
81 his polymorphism and quantitatively measured skin color in 59 East Asian humans.
82   This large GWAS for objectively quantified skin color in an East Asian population improves understa
83 111T in SLC24A5, have been linked to lighter skin color in Europeans.
84 uch as head shape in Hawaiian Drosophila and skin color in humans.
85 isms predicted in prior literature to affect skin color in Native Americans caused detectable hypopig
86            It is widely assumed that lighter skin color in populations outside the tropics resulted f
87 ained by changes in interviewer reporting of skin color in the same period.
88 /L] during winter regardless of latitude and skin color.In a longitudinal, double-blind, randomized,
89 ational regulation of factors that determine skin color, including melanin synthesis in epidermal mel
90 sults also suggest that objectively measured skin color is a better predictor of micropore lifetime t
91                                              Skin color is a highly heritable human trait, and global
92                                              Skin color is a key determinant of circulating 25(OH)D c
93                                              Skin color is determined by the amount of eumelanin, a s
94                                              Skin color is determined primarily by melanin, a biopoly
95                                              Skin color is highly variable in Africans, yet little is
96                    Cutaneous pigmentation or skin color is the body's natural protection against sun-
97                  Variation in human hair and skin color is the most striking visible aspect of human
98 evolving under positive selection, including skin color, lactase persistence, and resistance to malar
99 overed in genes controlling potato flesh and skin color, length of plant cycle and tuberization, and
100 , Brown, or Black) are related to respondent skin color (light, medium, or dark).
101 ffects of fruit and vegetable consumption on skin-color longitudinally to determine the magnitude and
102 ayment mode, maternal education, height, and skin color (lower versus middle/higher SEP).
103 and linked to socially relevant cues such as skin color, making ethnic minority status a well-establi
104              Physical examination revealed a skin-colored mass protruding from the right side of her
105 of our social in-group on the basis of their skin color may be a determining factor in our ability to
106 unds is established in groups of grape berry skin color mutant cultivars.
107 ons, forming eleven groups of possible berry skin color mutants, were genotyped with twelve microsate
108 e anthocyanin pigmentation (MYB10) and fruit skin color (MYB1).
109  region that has profound effects on eye and skin color; notably, 50% of variability in eye color is
110 odds ratio 3.47, 95% CI 2.53-4.77), and fair skin color (odds ratio 1.75, 95% CI 1.42-2.15).
111 and TRPS1, which may contribute to the light skin color of Khoesan-speaking populations from Southern
112         This study assesses the influence of skin color on MELD scores calculated using SCr or correc
113 or impaired kidney function across all human skin colors on the Fitzpatrick Skin Scale (FSS).
114                                              Skin color, one of the most diverse human traits, is det
115 sed the odds of an NMSC diagnosis were light skin color (OR, 5.79 [95% CI, 2.79-11.99]), greater numb
116 iation via uni-directional (e.g., lightening skin color) or bi-directional (e.g., modulating immune r
117                                              Skin color patterns are ubiquitous in nature, impact soc
118 d duration of diet change required to change skin-color perceptibly.
119 hite mature skin supports its involvement in skin color regulation.
120  and their contribution to the regulation of skin color, remain unclear.
121 rve a broader range of skin tones, inclusive skin color representation in contemporary educational re
122                      The wide range in human skin color results from varying levels of the pigment me
123 soluble solids (SS), flesh firmness (FF) and skin color (SC).
124 immunosuppression, radiation exposure, light skin color, sex, and T-cell depletion are risk factors f
125                                         Pale skin color showed a protective effect (men: -21.0%Delta;
126                  Photoprotected constitutive skin color sites produced higher AUIC values than photo-
127 r AUIC values than photo-exposed facultative skin color sites.
128  filtering the orange and red bands from the skin color spectrum and by introducing mutations targeti
129 do not account for all variation seen in the skin color spectrum.
130 ed confounding by exercise, fish intake, and skin color suggested some bias away from the null in the
131                                    Age, sex, skin color, tanning ability, hormonal status in women, c
132 cohorts revealed significant associations of skin color, tanning, and sun protection use with various
133 al limb burning pain, swelling, and abnormal skin color, temperature, and sweating.
134                                              Skin color, tendency to burn, and inability to tan were
135 fic sources of information (e.g., affect and skin color) that were successfully reconstructed in ANG.
136  do not know how such changes are related to skin color, the primary marker of race in Brazil.
137             Evidence for adaptation of human skin color to regional ultraviolet radiation suggests sh
138 ateral carpal tunnel syndrome presented with skin-colored to yellow cobblestoned plaques to the neck
139  phenol concentration, antioxidant activity, skin color, total anthocyanin concentration, total solub
140  impaired kidney function and for a range of skin color types.
141 r genes have previously been associated with skin color variation and skin cancer risk, all associati
142         Our interest in the genetic basis of skin color variation between populations led us to seek
143                              Because eye and skin colors vary across European populations, we further
144 95% confidence interval (CI)=4.08-36.94) and skin color (very fair vs. olive OR=11.06, 95% CI=5.90-20
145              A model including age, sex, and skin color was created to most effectively predict the i
146 ries were collected but not analyzed because skin color was more relevant for the purposes of this st
147 the individuals showing dark or intermediate skin colors well into the Bronze and Iron ages.
148 to first summer sun for 1 hour, and hair and skin color were independently associated with BCC.
149                                     Diet and skin-color were recorded at baseline and after three and
150 ratory rate, fresh weight loss, firmness and skin color with delay in the degradation of chlorophyll.
151 n over the range of GFR measured and for all skin colors with a r(2) of 0.90 (95% confidence interval
152          IRF4 is a key locus responsible for skin color, with a vitamin D receptor-binding interval.
153  have been found to be associated with human skin-color (yellowness) in a recent cross-sectional stud

 
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