コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 of exposure, latitude, season, and degree of skin pigmentation.
2 oupled receptor involved in inflammation and skin pigmentation.
3 tor system participates in the regulation of skin pigmentation.
4 tor cells, and the treatment of disorders of skin pigmentation.
5 hort-term PPARgamma antagonization, restored skin pigmentation.
6 ht spectrum, was recently reported to induce skin pigmentation.
7 s of phenotypic differences in hair type and skin pigmentation.
8 finger, as it is the primary determinant of skin pigmentation.
9 ption factor (MITF)-independent mechanism of skin pigmentation.
10 to learn about the evolutionary genetics of skin pigmentation.
11 l validation of adaptive variants related to skin pigmentation.
12 eratinocytes is tightly regulated to warrant skin pigmentation.
13 ; however, there was no evidence of abnormal skin pigmentation.
14 imeter performance difficulties arising from skin pigmentation.
15 ntify a natural acidic formulation to reduce skin pigmentation.
16 opulations to discover new genes influencing skin pigmentation.
17 tion of this analog still led to significant skin pigmentation.
18 HERC2 that are significantly associated with skin pigmentation.
19 n regenerate mature melanocytes for hair and skin pigmentation.
20 as a melanocyte reservoir for both hair and skin pigmentation.
21 l processes including vision, olfaction, and skin pigmentation.
22 mbining different viable mutations affecting skin pigmentation.
23 p53-mediated upregulation of Kitl influences skin pigmentation.
24 nt has pleiotropic effects on eye, hair, and skin pigmentation.
25 attractive and distinct avenue of modulating skin pigmentation.
26 skin represents the key phenotypic event in skin pigmentation.
27 dvanced breast cancer among women with light skin pigmentation.
28 olymorphism associated strongly with lighter skin pigmentation (0.22 [0.21-0.23] s.d.; P = 2.8 x 10(-
29 ammals to respond to UVR by increasing their skin pigmentation, a protective process driven by melani
31 g cells leads to the development of familial skin pigmentation alterations, reminiscent of those in p
33 ta confirm the association of rs1426654 with skin pigmentation among South Asians, consistent with pr
36 that MC1R350 acts as a negative regulator of skin pigmentation and demonstrate for the first time tha
38 the effects of serine protease inhibitors on skin pigmentation and found that the protease-activated
39 ed transcription factor expression can alter skin pigmentation and further confirm the central role o
41 inherited syndrome associated with abnormal skin pigmentation and multiple neoplasias, including PPN
44 a crucial process underlying maintenance of skin pigmentation and photoprotection against UV damage.
45 This disparity contributes to differences in skin pigmentation and photoprotection, but the control o
49 es reflecting cutaneous vitamin D synthesis (skin pigmentation and season) were also strongly associa
52 i et al. explore a direct connection between skin pigmentation and susceptibility to angiogenic disea
55 n identified that are involved in regulating skin pigmentation and these act during development, surv
56 report that PDK1 contributes functionally to skin pigmentation and to the development of melanomas ha
57 intensity, (4) BCVA, (5) VEP asymmetry, (6) skin pigmentation, and (7) hair pigmentation (of head ha
58 SH), and beta-endorphin in the regulation of skin pigmentation, and a role has been put forward for a
59 such as vitamin D supplementation, degree of skin pigmentation, and amount and intensity of sun expos
60 d by the triad of dysplastic nails, abnormal skin pigmentation, and oral leukoplakia; Hoyeraal-Hreida
61 e individual, growth abnormalities, abnormal skin pigmentation, and/or thumb/radius malformations.
63 all of the genetic variation associated with skin pigmentation as opposed to just a small number of l
64 e quantify the impact of hair properties and skin pigmentation, as well as head size, sex and age, on
65 al leukoplakia, nail dystrophy, and abnormal skin pigmentation, as well as high rates of bone marrow
66 e (DDD) is an autosomal-dominant disorder of skin pigmentation associated with mutations in keratin 5
68 l selection in ancient West Eurasians on 170 skin pigmentation-associated variants ascertained in the
70 ctivated receptor 2 (PAR-2) is important for skin pigmentation because activation of keratinocyte PAR
72 confounders [baseline 25(OH)D concentration, skin pigmentation, body mass index, compliance, etc], sp
73 nship between self-reported hearing loss and skin pigmentation by using hair color, skin tanning abil
74 populations, we show how the architecture of skin pigmentation can vary across humans subject to diff
75 e neoplasia syndrome characterized by spotty skin pigmentation, cardiac and other myxomas, endocrine
76 g to extreme sensitivity to sunlight-induced skin pigmentation changes and increased skin cancer risk
77 tivation did not engage the key regulator of skin pigmentation, cyclic AMP, showing a major differenc
78 s, epidermal melanocytes are responsible for skin pigmentation, defence against ultraviolet radiation
80 As safe and effective treatment options for skin pigmentation disorders are limited, these specific
86 ated the association of two previously known skin pigmentation genes, SLC24A5 (minimum p = 2.62 x 10(
87 ividual carries ancestral alleles in several skin pigmentation genes, suggesting that the light skin
91 ritable human trait, and global variation in skin pigmentation has been shaped by natural selection,
95 l role of the IFN-gamma signaling network in skin pigmentation homeostasis, which could have implicat
96 te the genetic factors influencing intrinsic skin pigmentation in a population of South Asian descent
98 so far to characterize the genetic basis of skin pigmentation in admixed populations (N = 2,104).
99 heterozygosity, and correlates with lighter skin pigmentation in admixed populations, suggesting a k
101 screen 1,157 candidate variants influencing skin pigmentation in Africans and identified 165 single-
105 des the SLC24A5 allele associated with light skin pigmentation in Europeans, may represent gene flow
109 als who have ocular features of albinism and skin pigmentation in keeping with their familial backgro
110 ows that the response to selection for light skin pigmentation in West Eurasia was driven by a relati
112 Africa;SLC24A5 and SLC45A2, both involved in skin pigmentation, in Europe; and EDAR and EDA2R, both i
113 ly breastfed infants who have high levels of skin pigmentation, inadequate vitamin D supplementation,
114 rences in genetic factors, sun exposure, and skin pigmentation, iron deficiency may affect vitamin D
120 ese results suggest that clofazimine-induced skin pigmentation is not due to clofazimine precipitatio
121 s involves loss of hair pigmentation whereas skin pigmentation is not reduced, and a predisposition t
126 his, we identify canonical and non-canonical skin pigmentation loci, including near SLC24A5, TYRP1, S
128 keratinocytes and/or fibroblasts that affect skin pigmentation might be regulated differently by UV,
129 t neoplasia syndrome characterized by spotty skin pigmentation, myxomatosis, endocrine tumors, and sc
130 mucocutaneous features that include abnormal skin pigmentation, nail dystrophy, and oral leucoplakia.
131 bone marrow failure and a triad of abnormal skin pigmentation, nail dystrophy, and oral leukoplakia.
132 from 21 to 58 years) with light-to-moderate skin pigmentation, none of whom had current or prior ski
133 t cancer among women with light constitutive skin pigmentation (odds ratio = 0.53, 95% confidence int
137 nresolved limitation of PPG is the effect of skin pigmentation on the signal and its impact on PPG ba
138 ng a reflectometer, we measured constitutive skin pigmentation on the upper underarm (a sun-protected
140 and in adults of all ages who have increased skin pigmentation or who always wear sun protection or l
141 al plasticity, exogenous TH treatment alters skin pigmentation patterns in adult zebrafish after 5 da
143 y assembling a global survey of quantitative skin pigmentation phenotypes, we demonstrate that pigmen
145 toreceptive tasks, such as photic control of skin pigmentation, pupillary aperture, and circadian and
146 presentation and disease burden can vary by skin pigmentation, race and ethnicity, and socioeconomic
148 hromosomal breakage as well as pancytopenia, skin pigmentation, renal hypoplasia, cardiac defects, mi
149 dominant disorder characterized by abnormal skin pigmentation, retinal detachment, anodontia, alopec
151 n in patients with Carney complex was spotty skin pigmentation, similar to that observed in Peutz-Jeg
152 susceptibility to UV radiation (UVR)-induced skin pigmentation, skin cancers, ocular surface disease,
153 n, we examined polymorphisms associated with skin pigmentation (SLC24A5) and with the ability to tast
154 ism and the related ultraviolet response and skin pigmentation standing out as a shared pathway, perh
155 of several physiological functions including skin pigmentation, steroidogenesis, obesity, energy home
156 ortin pathway is an important participant in skin pigmentation, steroidogenesis, obesity, energy home
157 ene, a critical component of the facultative skin pigmentation system, has a highly complex and ineff
158 A5, SNX13, TYRP1, and UVRAG) associated with skin pigmentation, three of which already have been repo
159 protease-activated receptor 2 is involved in skin pigmentation through increased phagocytosis of mela
160 and physiological data, including age, sex, skin pigmentation, tissue thickness, and mean arterial p
161 put to the circuit controlling adaptation of skin pigmentation to background, changes the number of n
162 traits ranging from lactase persistence, to skin pigmentation, to hypoxic response, to arsenic toler
164 dardized erythema responses across different skin pigmentation types and shows strong internal consis
165 rtin 1 receptor polymorphisms correlate with skin pigmentation, UV sensitivity, and skin cancer risk.
167 15 genes have been directly associated with skin pigmentation variation in humans, leading to its ch
169 associations because the trait under study (skin pigmentation) varies with admixture proportions.
170 ur understanding of the mechanism underlying skin pigmentation via a paracrine EV-mediated communicat
171 ic hormone, are important mediators of human skin pigmentation via action at the melanocortin-1 recep
172 ormone are well documented to regulate human skin pigmentation via action at the melanocortin-1 recep
174 complex anthropometric and metabolic traits, skin pigmentation was the only one with significant evid
175 ces and infer possible mechanisms underlying skin pigmentation, we performed a large-scale transcript
176 , arthropathies, arrhythmias, impotence, and skin pigmentation were no more prevalent among the 152 i
177 In our cohort of white women, surrogates for skin pigmentation were not associated with risk of heari
178 haracteristics, receipt of vasopressors, and skin pigmentation were recorded at the time of a clinica
180 se to melanoma as a result of alterations in skin pigmentation (which affords less protection against
182 melanocytes and has a pivotal role in human skin pigmentation, with reduced function in human geneti
185 mma-MSH-NH2 is ideal for inducing short-term skin pigmentation without sun for melanoma prevention.