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1 Ever and past-year exposure to indoor tanning.
2 to melanocyte-stimulating hormone, inducing tanning.
3 , knowledge, and behaviors related to indoor tanning.
4 ps recruited using factors related to indoor tanning.
5 mparably high rates of sunbathing and indoor tanning.
6 fy PGC-1 coactivators as regulators of human tanning.
7 sun-protective behaviors and decrease indoor tanning.
8 tem into the hemolymph and initiates cuticle tanning.
9 -alanine and dopamine used in insect cuticle tanning.
10 NBAD as cross-linking agents during cuticle tanning.
11 tial processes of wing expansion and cuticle tanning.
12 compassing the irradiation period, decreased tanning.
13 he most relevant mechanisms involved in skin tanning.
14 ed in the skin regardless of pigmentation or tanning.
15 t response indistinguishable from UV-induced tanning.
16 g facilities, as well as payment options for tanning.
17 f skin cancer and 12-month history of indoor tanning.
18 llow campus cash cards to be used to pay for tanning.
19 e of epidermal pigmentation after UV-induced tanning.
21 ted with red hair colour, fair skin and poor tanning ability (denoted as RHC variants), are associate
22 confidence interval (CI): 0.90, 1.09), skin tanning ability (for dark tan vs. no tan, multivariable-
23 ligo risk was higher among women with better tanning ability (hazard ratio = 2.59, 95% confidence int
24 ity to sunlight exposure (P = .006) and poor tanning ability (P = .003) were associated with a higher
25 ted with red hair color, fair skin, and poor tanning ability (RHC trait), are more prone to melanoma;
26 n hair color, eye color, number of sunburns, tanning ability and number of non-melanoma skin cancers
27 y history; and sun exposure history, such as tanning ability and number of severe sunburns experience
28 ci in the PGC-1beta gene that correlate with tanning ability and protection from melanoma in humans.
30 skin pigmentation by using hair color, skin tanning ability, and skin reaction to prolonged sun expo
31 me 1 as a novel locus highly associated with tanning ability, and we confirmed this association in 87
35 its tanning response is comparable to human tanning after exposure to ultraviolet radiation (UVR).
36 s for the brown color caused by the "sunless tanning" agent dihydroxyacetone in self-tanning products
41 lleles of MC1R are associated with decreased tanning and increased melanoma risk, which has been attr
43 inal study of the association between indoor tanning and melanoma in a large cohort of Norwegian wome
44 and sex-specific associations between indoor tanning and melanoma to determine if these trends could
45 lpha and burs beta), responsible for cuticle tanning and other developmental processes in insects.
46 ting PKC activity in vivo selectively blocks tanning and reduces basal pigmentation in the epidermis
47 f a dose-response association between indoor tanning and risk of melanoma and supports the hypothesis
50 d to further reduce the prevalence of indoor tanning and sunburn and thus prevent future cases of ski
52 amine the trends in the prevalence of indoor tanning and the association between indoor tanning and s
56 lternatives to ultraviolet radiation induced tanning and whether encouraging these options leads to a
58 bacterial sodium channel NaChBac also blocks tanning and wing expansion and leads to depletion of bur
59 uded here showed that in addition to cuticle tanning and wing expansion reported previously, Tcrk is
60 ut NCCAP, but not in NCCAP-c929, also blocks tanning and wing expansion, we conclude that neurotransm
67 e bursicon and its receptor regulate cuticle tanning as well as wing expansion after adult eclosion.
68 women younger than 40 years initiated indoor tanning at a younger age (16 vs 25 years, P < .001) and
69 res, including appearance motivation, indoor tanning attitudes and norms, and intention to tan indoor
70 , the findings highlight that in addition to tanning bed avoidance, it is critical to emphasize sun p
71 previous findings on the damaging effects of tanning bed exposure on women, particularly young women.
74 certain whether subjects who regularly use a tanning bed have higher 25(OH)D concentrations than do s
78 nce for a dose-response relationship between tanning bed use and the risk of skin cancers, especially
81 skin cancer, it is already clear that indoor tanning bed use represents an avoidable risk factor for
82 xposed to ultraviolet B (UVB) radiation in a tanning bed wearing a 1-piece bathing suit for 10 minute
85 t compelling evidence that early exposure to tanning beds advances the date of diagnosis of melanoma
86 previous evidence of the negative effects of tanning beds and provides further justification for stro
87 nd sun exposure in childhood and exposure to tanning beds are important preventable risk factors.
88 from the sun and from the widespread use of tanning beds by populations residing in areas of norther
90 cancer for an incremental increase in use of tanning beds of four times per year during both periods
94 ntention to tan indoors, frequency of indoor tanning behavior in the past year, and indoor tanner typ
95 -quality educational interventions to change tanning behavior, particularly among women, people with
98 he roles of UV radiation exposure and indoor tanning behaviors on skin cancer risk are explored here.
99 te whether skin cancer prevalence and indoor tanning behaviors vary by sexual orientation in the gene
101 scale may further advance research on indoor tanning beliefs and can guide health communications to p
102 ificantly improved when we added ever-indoor tanning, burns from indoor tanning, and MC1R (AUC = 0.77
103 sinase, have been proposed to participate in tanning, but proof of the true identity of the enzyme(s)
107 the United States, the prevalence of indoor tanning decreased from 15.6% (95% CI, 13.7%-17.6%) in 20
108 students, the adjusted prevalence of indoor tanning decreased from 26.4% in 2009 to 20.7% in 2011.
110 at initiation of indoor tanning, duration of tanning-device use, and dose response with melanoma risk
112 associations of age at initiation of indoor tanning, duration of tanning-device use, and dose respon
113 esults suggest that the Comprehensive Indoor Tanning Expectations (CITE) Scale provides a reliable an
114 alculated for melanoma in relation to indoor tanning exposure for men and women by diagnosis or refer
115 ediction model incorporating MC1R and indoor tanning extends the work of other skin cancer risk predi
120 nt association between ever-use of an indoor tanning facility and an increased risk of basal cell car
123 yacetone, the browning ingredient in sunless tanning formulations, reacts with amino acids in the out
124 To examine the association between indoor tanning frequency and behaviors related to skin cancer p
125 e: To examine the association between indoor tanning frequency and behaviors related to skin cancer p
127 Despite declines in the prevalence of indoor tanning from 2009 to 2015 among high school students nat
128 Examination of subscales across the 3 indoor tanning groups also revealed significant (P < .001) diff
133 ears or older, with 31.5% engaging in indoor tanning in 2011, and among non-Hispanic white female stu
140 asizes the value of both genotype and indoor tanning in skin cancer risk prediction in young people,
144 ion proportional attributable risk of indoor tanning in the United States, Europe, and Australia for
145 anoma cases each year attributable to indoor tanning in the United States, Europe, and Australia.
147 complex belief systems that underlie indoor tanning in young women is a crucial first step in develo
148 complex sets of beliefs that underlie indoor tanning, including positive (motivational) and negative
150 d linear regression to examine age of indoor tanning initiation in relation to age at diagnosis.
166 irradiation from such artificial sources as tanning lamps can result in severe pain and inflammation
171 P < .001) and reported more frequent indoor tanning (median number of sessions, 100 vs 40, P < .001)
174 istologically, whereas ultraviolet B-induced tanning of light-skinned swine was inhibited using these
175 ht on the immediate pigmentation and delayed tanning of melanocompetent skin; the results were compar
176 nal molt, coordinates the plasticization and tanning of the initially folded wings with behaviors tha
180 olleges had the highest prevalence of indoor tanning on campus (26.9%), whereas Southern colleges had
189 ues about the culture that created it, since tanning processes are often specific to certain indigeno
190 seases) and cosmeceutically (e.g., to design tanning products with potential to reduce skin cancer ri
194 e participants' responses to the burning and tanning questions could not be classified using standard
195 es increased with skin types associated with tanning rather than burning, although trend analysis sho
197 mong high school students nationwide, indoor tanning remains commonplace among certain subgroups, esp
199 tage genome-wide association study (GWAS) of tanning response after exposure to sunlight in over 9,00
200 man pigment induction and modulation, as its tanning response is comparable to human tanning after ex
202 melanocortin 1 receptor (MC1R) mediates the tanning response through induction of cAMP and downstrea
204 role of intercellular MSH signalling in the tanning response, and suggest a clinical strategy for to
205 after ultraviolet irradiation as part of the tanning response, the major recognized photoprotective r
206 to UV irradiation as part of the UV-induced tanning response, we show that while the microphthalmia-
211 radiation dermal insult and subsequent skin tanning, result in a shift in expression from MC1R in fa
214 creased with increasing cumulative number of tanning sessions (for highest tertile of use vs. never u
219 of skin cancer cases attributable to indoor tanning, these findings highlight a major public health
220 nce intervals for the relationship of indoor tanning to melanoma risk and linear regression to examin
228 Development of facultative pigmentation (tanning) was important to populations settling between r
229 lvement of these types of enzymes in cuticle tanning, we performed RNA interference experiments to de
231 alence of indoor tanning and frequent indoor tanning were examined as well as their association with
234 ant bursicon induces both wing expansion and tanning, whereas synthetic eclosion hormone induces only
235 and least negative perceptions about indoor tanning, while nontanners had the most negative and leas
236 es of bursicon actions in regulating cuticle tanning, wing expansion, and as yet unknown functions.
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