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1 e of epidermal pigmentation after UV-induced tanning.
2 Ever and past-year exposure to indoor tanning.
3 to melanocyte-stimulating hormone, inducing tanning.
4 , knowledge, and behaviors related to indoor tanning.
5 ps recruited using factors related to indoor tanning.
6 mparably high rates of sunbathing and indoor tanning.
7 fy PGC-1 coactivators as regulators of human tanning.
8 sun-protective behaviors and decrease indoor tanning.
9 tem into the hemolymph and initiates cuticle tanning.
10 -alanine and dopamine used in insect cuticle tanning.
11 NBAD as cross-linking agents during cuticle tanning.
12 tial processes of wing expansion and cuticle tanning.
13 compassing the irradiation period, decreased tanning.
14 he most relevant mechanisms involved in skin tanning.
15 ed in the skin regardless of pigmentation or tanning.
16 t response indistinguishable from UV-induced tanning.
17 on factors, sunbathing vacations, and indoor tanning.
18 g facilities, as well as payment options for tanning.
19 f skin cancer and 12-month history of indoor tanning.
20 llow campus cash cards to be used to pay for tanning.
22 ted with red hair colour, fair skin and poor tanning ability (denoted as RHC variants), are associate
23 confidence interval (CI): 0.90, 1.09), skin tanning ability (for dark tan vs. no tan, multivariable-
24 ligo risk was higher among women with better tanning ability (hazard ratio = 2.59, 95% confidence int
25 ity to sunlight exposure (P = .006) and poor tanning ability (P = .003) were associated with a higher
26 ted with red hair color, fair skin, and poor tanning ability (RHC trait), are more prone to melanoma;
28 n hair color, eye color, number of sunburns, tanning ability and number of non-melanoma skin cancers
29 y history; and sun exposure history, such as tanning ability and number of severe sunburns experience
30 ci in the PGC-1beta gene that correlate with tanning ability and protection from melanoma in humans.
34 evus density, freckling density, hair color, tanning ability, adult sunburns, family history, other c
35 skin pigmentation by using hair color, skin tanning ability, and skin reaction to prolonged sun expo
36 me 1 as a novel locus highly associated with tanning ability, and we confirmed this association in 87
38 ne survey on phenotypic factors (hair color, tanning ability, nevus density, family history), sun exp
41 its tanning response is comparable to human tanning after exposure to ultraviolet radiation (UVR).
42 s for the brown color caused by the "sunless tanning" agent dihydroxyacetone in self-tanning products
45 t radiation from natural sunlight and indoor tanning, although there are several subtypes that are no
48 lleles of MC1R are associated with decreased tanning and increased melanoma risk, which has been attr
50 inal study of the association between indoor tanning and melanoma in a large cohort of Norwegian wome
51 and sex-specific associations between indoor tanning and melanoma to determine if these trends could
52 lpha and burs beta), responsible for cuticle tanning and other developmental processes in insects.
53 ting PKC activity in vivo selectively blocks tanning and reduces basal pigmentation in the epidermis
54 f a dose-response association between indoor tanning and risk of melanoma and supports the hypothesis
57 d to further reduce the prevalence of indoor tanning and sunburn and thus prevent future cases of ski
59 amine the trends in the prevalence of indoor tanning and the association between indoor tanning and s
63 lternatives to ultraviolet radiation induced tanning and whether encouraging these options leads to a
65 bacterial sodium channel NaChBac also blocks tanning and wing expansion and leads to depletion of bur
66 uded here showed that in addition to cuticle tanning and wing expansion reported previously, Tcrk is
67 ut NCCAP, but not in NCCAP-c929, also blocks tanning and wing expansion, we conclude that neurotransm
72 sists of avoiding direct sunlight and indoor tanning, and photoprotection (sunscreen and sun-protecti
73 aled significant associations of skin color, tanning, and sun protection use with various single-nucl
76 e bursicon and its receptor regulate cuticle tanning as well as wing expansion after adult eclosion.
77 women younger than 40 years initiated indoor tanning at a younger age (16 vs 25 years, P < .001) and
78 res, including appearance motivation, indoor tanning attitudes and norms, and intention to tan indoor
79 , the findings highlight that in addition to tanning bed avoidance, it is critical to emphasize sun p
80 for whom next-generation sequencing data and tanning bed exposure history were available were include
81 previous findings on the damaging effects of tanning bed exposure on women, particularly young women.
84 gland county-level melanoma incidence rates, tanning bed facilities location, demographic data, socio
87 certain whether subjects who regularly use a tanning bed have higher 25(OH)D concentrations than do s
91 ns of melanoma in patients with quantifiable tanning bed usage and performed exome sequencing of mela
93 nce for a dose-response relationship between tanning bed use and the risk of skin cancers, especially
96 skin cancer, it is already clear that indoor tanning bed use represents an avoidable risk factor for
98 and the etiology of melanoma associated with tanning bed use, we described the patterns of melanoma i
102 xposed to ultraviolet B (UVB) radiation in a tanning bed wearing a 1-piece bathing suit for 10 minute
105 t compelling evidence that early exposure to tanning beds advances the date of diagnosis of melanoma
106 previous evidence of the negative effects of tanning beds and provides further justification for stro
107 nd sun exposure in childhood and exposure to tanning beds are important preventable risk factors.
108 from the sun and from the widespread use of tanning beds by populations residing in areas of norther
110 cancer for an incremental increase in use of tanning beds of four times per year during both periods
115 ntention to tan indoors, frequency of indoor tanning behavior in the past year, and indoor tanner typ
116 -quality educational interventions to change tanning behavior, particularly among women, people with
119 he roles of UV radiation exposure and indoor tanning behaviors on skin cancer risk are explored here.
120 te whether skin cancer prevalence and indoor tanning behaviors vary by sexual orientation in the gene
122 scale may further advance research on indoor tanning beliefs and can guide health communications to p
123 al outcomes (medication use, sun protection, tanning booth use, and blood glucose testing) estimates
124 ificantly improved when we added ever-indoor tanning, burns from indoor tanning, and MC1R (AUC = 0.77
125 sinase, have been proposed to participate in tanning, but proof of the true identity of the enzyme(s)
129 the United States, the prevalence of indoor tanning decreased from 15.6% (95% CI, 13.7%-17.6%) in 20
130 students, the adjusted prevalence of indoor tanning decreased from 26.4% in 2009 to 20.7% in 2011.
132 at initiation of indoor tanning, duration of tanning-device use, and dose response with melanoma risk
136 associations of age at initiation of indoor tanning, duration of tanning-device use, and dose respon
137 esults suggest that the Comprehensive Indoor Tanning Expectations (CITE) Scale provides a reliable an
138 le), there was no association between indoor tanning exposure and TMB after adjustment for demographi
139 alculated for melanoma in relation to indoor tanning exposure for men and women by diagnosis or refer
142 ediction model incorporating MC1R and indoor tanning extends the work of other skin cancer risk predi
143 e association between average travel time to tanning facilities and county-level melanoma incidence r
145 policy aimed at decreasing access to indoor tanning facilities has the potential to reduce melanoma
149 1-minute increase in average travel time to tanning facilities within 30 minutes travel time thresho
150 nt association between ever-use of an indoor tanning facility and an increased risk of basal cell car
153 yacetone, the browning ingredient in sunless tanning formulations, reacts with amino acids in the out
154 To examine the association between indoor tanning frequency and behaviors related to skin cancer p
155 e: To examine the association between indoor tanning frequency and behaviors related to skin cancer p
157 Despite declines in the prevalence of indoor tanning from 2009 to 2015 among high school students nat
158 Examination of subscales across the 3 indoor tanning groups also revealed significant (P < .001) diff
163 ears or older, with 31.5% engaging in indoor tanning in 2011, and among non-Hispanic white female stu
170 asizes the value of both genotype and indoor tanning in skin cancer risk prediction in young people,
173 upporting the notion that yellowing precedes tanning in the aging process, which is paralleled by fra
175 ion proportional attributable risk of indoor tanning in the United States, Europe, and Australia for
176 anoma cases each year attributable to indoor tanning in the United States, Europe, and Australia.
178 complex belief systems that underlie indoor tanning in young women is a crucial first step in develo
179 d hMC5R, and increases pigmentation (sunless tanning) in a cultured, three-dimensional skin model.
181 complex sets of beliefs that underlie indoor tanning, including positive (motivational) and negative
183 d linear regression to examine age of indoor tanning initiation in relation to age at diagnosis.
199 irradiation from such artificial sources as tanning lamps can result in severe pain and inflammation
202 us WNT16 for physical measures, and the skin tanning locus MC1R and smoking behaviour locus CHRNA3 fo
205 P < .001) and reported more frequent indoor tanning (median number of sessions, 100 vs 40, P < .001)
209 istologically, whereas ultraviolet B-induced tanning of light-skinned swine was inhibited using these
210 ht on the immediate pigmentation and delayed tanning of melanocompetent skin; the results were compar
211 nal molt, coordinates the plasticization and tanning of the initially folded wings with behaviors tha
215 olleges had the highest prevalence of indoor tanning on campus (26.9%), whereas Southern colleges had
221 f industrial applications, including leather tanning, paper production, textile dyeing, and as colora
225 ues about the culture that created it, since tanning processes are often specific to certain indigeno
226 Dihydroxyacetone (DHA), found in sunless tanning products and electronic cigarette aerosol, induc
227 seases) and cosmeceutically (e.g., to design tanning products with potential to reduce skin cancer ri
231 e participants' responses to the burning and tanning questions could not be classified using standard
232 es increased with skin types associated with tanning rather than burning, although trend analysis sho
234 mong high school students nationwide, indoor tanning remains commonplace among certain subgroups, esp
236 tage genome-wide association study (GWAS) of tanning response after exposure to sunlight in over 9,00
237 wide signals identified in a recent GWAS for tanning response indicates that there is a substantial o
238 man pigment induction and modulation, as its tanning response is comparable to human tanning after ex
240 melanocortin 1 receptor (MC1R) mediates the tanning response through induction of cAMP and downstrea
243 role of intercellular MSH signalling in the tanning response, and suggest a clinical strategy for to
244 after ultraviolet irradiation as part of the tanning response, the major recognized photoprotective r
245 to UV irradiation as part of the UV-induced tanning response, we show that while the microphthalmia-
252 radiation dermal insult and subsequent skin tanning, result in a shift in expression from MC1R in fa
253 dicted weakened AHR binding to the risk/poor-tanning rs117132860-A allele, and allele-preferential AH
256 creased with increasing cumulative number of tanning sessions (for highest tertile of use vs. never u
261 of skin cancer cases attributable to indoor tanning, these findings highlight a major public health
262 nce intervals for the relationship of indoor tanning to melanoma risk and linear regression to examin
271 Development of facultative pigmentation (tanning) was important to populations settling between r
272 lvement of these types of enzymes in cuticle tanning, we performed RNA interference experiments to de
274 alence of indoor tanning and frequent indoor tanning were examined as well as their association with
277 ant bursicon induces both wing expansion and tanning, whereas synthetic eclosion hormone induces only
278 and least negative perceptions about indoor tanning, while nontanners had the most negative and leas
279 ne polygenic risk scores (PRSs) for smoking, tanning, white blood cell counts, and educational attain
280 es of bursicon actions in regulating cuticle tanning, wing expansion, and as yet unknown functions.