ライフサイエンスコーパス: pigment

1 the rate of decay of light-activated visual pigment.

2 es with the loss of Muller cells and macular pigment.

3 the ink was used as a drier rather than as a pigment.

4 sterase and perhaps also of activated visual pigment.

5 nd its efficiency in inactivating the visual pigment.

6 ich indicates the use of bitumen as a ground pigment.

7 e to the increase in a large number of brown pigments.

8 bsorption, metabolism and excretion of these pigments.

9 ne, anthraquinone, and diketopyrrolo-pyrrole pigments.

10 rning the fraction of nanoparticles in these pigments.

11 d underlaid with a dark layer of anthocyanin pigments.

12 oduce valuable byproducts such as lipids and pigments.

13 ns a synthetic path to native photosynthetic pigments.

14 ure and energy transfer pathways between LHC pigments.

15 uced by a mixture of these two tetrapyrrolic pigments.

16 re pronounced compared to that of the yellow pigments.

17 anoparticles through the consumption of food pigments.

18 gth-sensitive, and three UV-sensitive visual pigments.

19 addressed, resulting in structurally colored pigments.

20 hromophore of both rod and cone opsin visual pigments.

21 ted by cyanobacteria producing NIR-absorbing pigments.

22 This blue light-illuminated pigmented Abca4(-/-) mouse model presented retinal pigme

23 The pigmented Abca4(-/-) mouse strain only reflects the earl

24 distinct drusen (23.0% versus 2.1%), retinal pigment abnormalities (26.6% versus 7.3%), exudative mac

25 Essential for pigment accumulation is TRANSPARENT TESTA19 (TT19), a gl

26 trand disruption of collagen triple helix in pigmented AKU human cartilage, and in cartilage from pat

27 bunit 18S rRNA gene sequencing and accessory pigment analysis displayed similar trends, indicating ch

28 f long wavelengths through the red screening pigment and by the presence of the blue-absorbing filter

29 Synthetic pigment and pigmented human cartilage tissue both showed

30 e patient presented with rapidly progressing pigmented and hyperautofluorescent drusenoid deposits in

31 Out of 49 targeted minerals, vitamins, pigments and antioxidants, more than 35 parameters were

32 nd are utilized as electron transfer agents, pigments and in defence mechanisms.

33 a thickening, revealing shared regulation of pigments and lamina thickness.

34 f oxygenic organisms by their photosynthetic pigments and light-harvesting complex (Lhc) proteins, th

35 id metabolism, specifically the synthesis of pigments and oxylipins, and the metabolism of carbohydra

36 of glycogen and a decrease in photosynthetic pigments and protein content when nitrogen is available.

37 ion of RPE65 expression, diminishment of RPE pigments, and retraction of microvilli and basal infoldi

38 NADH levels, the release of lipofuscin-like pigments, and the increase in diffuse reflectance of the

39 n and kinetics of spectrally shifted far-red pigments are directly observable and separated from that

40 Both pigments are known porphyrin catabolites and are found i

41 Sorghum derived 3-deoxyanthocyanin (DXA) pigments are stable relative to their anthocyanin analog

42 e pH, which foresees a potential use of this pigment as a broad kind of industries on lipo-soluble fo

43 the synthesis of protein and photosynthetic pigments as well as amino acid pools.

44 either produced photo-protective carotenoid pigments at high irradiance or more chlorophyll, resulti

45 f eyes undergoing SLT, greater IOP and angle pigment before SLT correlated positively with SLT succes

46 However, analysis of pigment binding by plant high-light-inducible protein ho

47 h chlorophylls and carotenoids and show that pigment binding depends on the formation of OHP1/OHP2 he

48 chlorophyll a/b-binding proteins involved in pigment binding have been precisely identified through x

49 ed with light sensing, light absorption, and pigment binding within the thylakoid membrane.

50 ith LIGHT-HARVESTING-LIKE3 proteins, and the pigment-binding ability of cyanobacterial high-light-ind

51 Pigment-binding capacity was completely lost in each of

52 Because of their pigment-binding capacity, we suggest that OHPs function

53 en alga Chlamydomonas reinhardtii, the LHCSR pigment-binding proteins are essential for NPQ.

54 In vitro pigment-binding studies have been performed with LIGHT-H

55 gnin biosynthesis, phenyl propanoid pathway, pigment biosynthesis, and other secondary metabolite pat

56 ore, an automated continuous TSE process for Pigments Black 31 and 32 is demonstrated, with a through

57 search on mutant tobacco plants shows that a pigment called beta-carotene is not necessary for photos

58 reying) is an age-linked loss of the natural pigment called melanin from hair.

59 tructural eye descriptions, but knowledge of pigment cell types beneath the retina and basal matrix (

60 We discovered unique genes expressed by pigment cells and test their expression with double fluo

61 l type, but by extensions of the lateral rim pigment cells that penetrate gaps in the BM.

62 Descriptions of pigment cells within the retina are included in ultrastr

63 As neither pigmented extensions of secondary pigment cells, nor pigment granules in the extensions of

64 putative transporter expressed primarily in pigment cells.

65 Here, we explore the regulation of pigmented cells in the purple sea urchin Strongylocentro

66 diabetic model, were treated with the visual pigment chromophore, 9-cis-retinal.

67 and do not develop significant glaucoma from pigment collecting in the anterior chamber angle.

68 gae extracts, rich in phycocyanin, a protein-pigment complex derived from A. platensis.

69 Here we give key insight on HGA-derived pigment composition and collagen disruption in AKU carti

70 Visual pigment consists of opsin covalently linked to the vitam

71 (2) increased the photosynthetic process and pigment contents, which consequently induced carbohydrat

72 provide the correct anthocyanin profiles of pigmented corns, and emphasise the importance of using a

73 e mitigation of light stress offered by host pigments could facilitate recolonization of bleached tis

74 As kernels continued to mature, pigment coverage across the pericarp progressively incre

75 GBS produce a pigmented, cytotoxic lipid, known as granadaene.

76 mportant details on 2200 emb mutants and 241 pigment-defective embryo (pde) mutants analyzed in my la

77 l and structural factors governing cell-wall pigment deposition in C. neoformans and C. gattii.

78 reased intraocular pressure, bilateral dense pigment deposition of the posterior lens capsule, and a

79 Pigment deposition of the posterior lens capsule, which

80 rare presentation of PG with bilateral dense pigment deposits of the posterior lens capsule.

81 t I(h) is fundamental for the recruitment of pigment dispersing factor (PDF) filled dense core vesicl

82 gap, we examined the effects of mutations of Pigment-dispersing factor (Pdf) and its receptor, Pdfr,

83 e memory in Drosophila requires signaling by Pigment-dispersing factor (PDF), a neuromodulatory signa

84 tation and discoloration of the iris stroma, pigment dispersion, and deposition of pigment in the ang

85 variation in pigment type (i.e., color) and pigment distribution (i.e., color pattern) and highlight

86 ght light did not evoke changes in screening pigment distributions, suggesting a structural inability

87 the lipid composition of whole cells of the pigmented E. gracilis strain Z and two bleached mutants

88 and dilator muscle complex, nonpigmented and pigmented epithelia of the ciliary body, lens epithelium

89 with choroidal vascular atrophy and retinal pigment epithelial (RPE) changes including structural di

90 osphatase PGAM5 leads to accelerated retinal pigment epithelial (RPE) senescence in vitro and in vivo

91 serous retinal detachment (RD) with retinal pigment epithelial (RPE) tear is a rare and severe varia

92 nterphase centrosomes of immortalized retina pigment epithelial (RPE1) cells.

93 cence (NIR-AF) provided evidence for retinal pigment epithelial cell (RPE) involvement.

94 man telomerase reverse transcriptase-retinal pigment epithelial cell line, we show that RanGTP, a sma

95 shepherded within photoreceptors and retinal pigment epithelial cells to facilitate retinoid traffick

96 in wild-type and TP53 knockout human retinal pigment epithelial cells using a focused dual guide RNA

97 Yellow staining of detached pigment epithelial cells were rare.

98 dysbiotic Pg-strains to invade human-retinal pigment epithelial cells(ARPE-19), their survival, intra

99 ber at the population level in human retinal pigment epithelial cells.

100 idal melanoma, and melanocytoma) and retinal pigment epithelial neoplasms showed negative results for

101 tomography (SD-OCT) demonstrated sub-retinal pigment epithelial nodular deposits, some of which were

102 and (4) absence of other signs of a retinal pigment epithelial tear.

103 (ERG), insulin-like growth factor-1 (IGF-1), pigment epithelial-derived factor (PEDF), and serum mono

104 Retinal pigmented epithelial (RPE) cells are essential for maint

105 ing iPSCs to generate photoreceptor, retinal pigmented epithelial (RPE), and-more recently-choroidal

106 OCT was used to evaluate pigmented epithelial detachments, SMH, and subretinal fl

107 nduced pluripotent stem cell-derived retinal pigment epithelium (iPSC-RPE) to test the potential of g

108 n support functions performed by the retinal pigment epithelium (RPE) and on oxygen and nutrients del

109 disruption), components of complete retinal pigment epithelium (RPE) and outer retinal atrophy (e.g.

110 ted Abca4(-/-) mouse model presented retinal pigment epithelium (RPE) and photoreceptor degeneration

111 f cone photopigments may require the retinal pigment epithelium (RPE) and/or retinal Muller glia.

112 ltimodal imaging and ocular history: retinal pigment epithelium (RPE) atrophy with treatment-naive qu

113 Retinal pigment epithelium (RPE) cells are cultured on top of cu

114 culture media was incorporated into retinal pigment epithelium (RPE) cells.

115 spectral-domain OCT with respect to retinal pigment epithelium (RPE) in 836 spectral-domain OCT slic

116 ascular/neural network in DR and the retinal pigment epithelium (RPE) in AMD.

117 The retinal pigment epithelium (RPE) is a highly polarized epithelia

118 The retinal pigment epithelium (RPE) is a particularly vulnerable ti

119 Lipofuscin in the retinal pigment epithelium (RPE) is the major source of fundus a

120 P3 inflammasome activation mainly in retinal pigment epithelium (RPE) or rather in non-RPE cells prom

121 ent genome editing in vivo in murine retinal pigment epithelium (RPE) tissue via subretinal injection

122 onstrated no adverse perturbation of retinal pigment epithelium (RPE) transcriptional programs in any

123 nal hyperreflective material (SHRM), retinal pigment epithelium (RPE), hyperreflective foci (HRF), fi

124 in red cone photoreceptors, while in retinal pigment epithelium (RPE), TH regulates expression of a c

125 photoreceptor layers, despite intact retinal pigment epithelium (RPE), to approximately 70% of baseli

126 ith Ca(V) 1.3 Ca(2+) channels in the retinal pigment epithelium (RPE).

127 ative regulator of the ER-associated retinal pigment epithelium (RPE)65 isomerase necessary for recyc

128 toreceptor zone, ellipsoid zone, and retinal pigment epithelium (RPE, P < 0.001 and P = 0.005-0.045,

129 sign (separation of hyperreflective retinal pigment epithelium [RPE] from Bruch's membrane, with the

130 The 2 biomarkers were RPE65 for retinal pigment epithelium and CD163 for histiocytes, each tagge

131 l time points and from the periphery, fovea, pigment epithelium and choroid of light-responsive adult

132 helium, iris sphincter pupillae muscle, iris pigment epithelium and dilator muscle complex, nonpigmen

133 choriocapillaris, Bruch's membrane, retinal pigment epithelium and occasionally neurosensory retina.

134 ng 2 distinct criteria: (1) complete retinal pigment epithelium and outer retinal atrophy (cRORA) and

135 tagged with different chromogens, yellow for pigment epithelium and purple for CD163-positive (CD163(

136 The normal retinal pigment epithelium and uveal melanocytes did not stain f

137 The presence of histiocytoid pigment epithelium at the Bruch membrane probably also h

138 ge-related macular degeneration, the retinal pigment epithelium can be damaged by light acting on pho

139 erimeter (a measure of the number of retinal pigment epithelium cells exposed at the lesion border).

140 io (3.8%), vessel tortuosity (2.5%), retinal pigment epithelium degeneration (2.5%), myelinated nerve

141 Retinal pigment epithelium degeneration followed by retinal and

142 ), hyperreflective foci (HRF), fibrovascular pigment epithelium detachment (fvPED), and serous PED (s

143 er-reflective intraretinal foci; dome-shaped pigment epithelium detachment (PED); hyper-reflective fl

144 atients with chronic CSCR and flat irregular pigment epithelium detachments (FIPEDs).

145 typical macular cherry-red spot with retinal pigment epithelium dystrophy in the middle periphery, in

146 ed at a variable distance before the retinal pigment epithelium in 56.67% of eyes.

147 showed a hyporeflective band anterior to the pigment epithelium indicating the presence of dysfunctio

148 several treatments available, if the retinal pigment epithelium is damaged, we have to cope with the

149 nsmission of light into the choroid, retinal pigment epithelium loss, and loss of outer retinal layer

150 In normal visual physiology, the pigment epithelium supports photoreceptors and participa

151 (dystrophies primarily involving the retinal pigment epithelium), and H35.50 (unspecified macular deg

152 rtransmission, (2) disruption of the retinal pigment epithelium, (3) photoreceptor degeneration, and

153 ckening of the nerve fiber layer and retinal pigment epithelium-Bruch's membrane, with thinning in ot

154 Pigment epithelium-derived factor (PEDF) is a multifunct

155 We have previously demonstrated that pigment epithelium-derived factor (PEDF) plus docosahexa

156 ifferent retinal layers, such as the retinal pigment epithelium-drusen complex (RPEDC), were assessed

157 with perturbed melanogenesis in the retinal pigment epithelium.

158 nt progressive migration and loss of retinal pigment epithelium.

159 st, but only specifically around the retinal pigment epithelium.

160 nsport between the neural retina and retinal pigment epithelium.

161 , separating photoreceptors from the retinal pigment epithelium.

162 er semiautomatic segmentation of the retinal pigment epithelium/Bruch membrane complex.

163 n visual system (retina, macula, and retinal pigment epithelium/choroid) reveals features of regulato

164 ler cells, endothelial cells, and in retinal pigment epithelium; agonism of PPARalpha with genetic or

165 nt eyes show substantially increased retinal pigmented epithelium (RPE) proliferation in the fissure

166 Retinal pigmented epithelium has plentiful melanosomes, signifyi

167 s therapeutic levels of sunitinib in retinal pigmented epithelium/choroid and retina for more than si

168 toreceptor-specific markers in human retinal pigment epitheliums cells.

169 ccumulation of plastidial isoprenoid-derived pigments, especially carotenoids, and whole-cell focused

170 observed 10-fold symmetry in the segments of pigment expression.

171 As neither pigmented extensions of secondary pigment cells, nor pig

172 On histopathologic evaluation, a pigmented fibrocellular tissue was identified along the

173 of bacteriochlorophyll a (BChl a), the chief pigment for anoxygenic bacterial photosynthesis, include

174 9-cis-retinal administration restored visual pigment formation and decreased oxidative stress and ret

175 lor intensity (up to one unit) and polymeric pigments formation (up to 6.5%) in malvidin-prevalent Me

176 For each fragment, the carbon-black pigment found in the ink is identified as flame carbon (

177 Melanins are a unique class of pigments found throughout the biosphere with a wide vari

178 Cyanidin-3-glucoside (C3G) is a natural pigment, found in many colorful fruits and vegetables.

179 2 and 6 genes during ripening only in orange-pigmented fruits.

180 or expression of several genes important for pigment function, but is only transiently expressed in t

181 us purpuratus, an emerging model for diverse pigment function.

182 Anthocyanin pigments furnish a powerful visual output of the stress

183 M17, TNF and the TNF receptor Grindelwald in pigmented glial cells of the Drosophila retina leads to

184 d extensions of secondary pigment cells, nor pigment granules in the extensions of the cone cell proj

185 of stratified epidermis, fat-rich dermis and pigmented hair follicles that are equipped with sebaceou

186 l pigment remains stable in darkness, a cone pigment has some tendency to dissociate spontaneously in

187 Melanin pigments have various properties that are of technologic

188 Such "photonic pigments" have several key advantages over their crystal

189 ines), and anthocyanins, color and polymeric pigments (higher in wines aged in the new barrels), were

190 Synthetic pigment and pigmented human cartilage tissue both showed hydroquinon

191 de a new role for a commonly found bacterial pigment in controlling herpes simplex virus infection, f

192 troma, pigment dispersion, and deposition of pigment in the angle.

193 Lead white is known as one of the oldest pigments in art and can be used as a dating material.

194 for the anchoring and arrangement of melanin pigments in both C. neoformans and C. gattii species com

195 ally simulate the absorption spectrum of the pigments in Chlorella.

196 , compatible with the arrangement of macular pigments in Henle fibres; (ii) the morphology of MS is d

197 the nondestructive and noninvasive study of pigments in historical artifacts by revealing the charac

198 sources of colors alongside newly introduced pigments in late Edo-period Japan.

199 quantify the lipid molecules associated with pigments in melanin ghosts.

200 degradation mechanisms of inorganic artists' pigments in paintings, including chrome yellows (PbCr(1-

201 ures and molecular identities of the various pigments in photosynthetic systems.

202 ittle is known about the occurrence of these pigments in terrestrial habitats.

203 Spectroscopic analysis of the pigments in two isolated areas confirmed two types of oc

204 on-native product indigoidine, a sustainable pigment, in Pseudomonas putida KT2440, an emerging indus

205 inations, reflecting partitioning of natural pigments into isolates.

206 otably, the spectral range of the Rh6 visual pigment is substantially broadened and its peak sensitiv

207 i(2H-1,4-benzothiazine) scaffold of red hair pigments is disclosed herein.

208 differential absorption of light by macular pigments is perceived as the entoptic phenomena of Maxwe

209 t the diffraction signal of the carbon-based pigment itself can be isolated.

210 By mapping visual pigment kinetics across the central retina, high fidelit

211 to summarise the topography of rod and cone pigment kinetics and descriptive statistics conducted to

212 ented by additional mechanism(s) to maintain pigment levels in the face of high rates of photon captu

213 rescent particles were identified as the age pigment lipofuscin.

214 as a consequence of the accumulation of skin pigment melanin.

215 o-quinones, with formation of brown or black pigments (melanines).

216 ment bleaching, were used to quantify visual pigment metrics.

217 R, pigment, or both than in eyes without any pigment migration (0.33 mm(2) vs. 0.94 mm(2); P = 0.01),

218 used for successful quantitative analysis of pigment mixtures and provide reliable new data for use i

219 m Aspergillus nidulans conidia originates in pigment molecules within the cell wall.

220 n melanocytes reliably produces benign nevi (pigmented 'moles'), yet the same change is the most comm

221 to measure the integrity of locus coeruleus pigmented neurons, and 18F-dihydroxyphenylalanine (FDOPA

222 s within three sub-regions: the parabrachial pigmented nucleus (PBP), parainterfascicular nucleus (PI

223 Cyanidin-based glucosides were the major pigments of purple-pericarp sweetcorn (75.5% of TAC) and

224 idene chromophore associated with the visual pigments of rod and cone photoreceptors.

225 idene chromophore associated with the visual pigments of rod and cone photoreceptors.

226 d ORNV and 13 showed ORHR, of which 5 showed pigment on CFP.

227 6 eyes, and one of them also showed visible pigment on CFP.

228 ion associated with the human remains is red pigment on some of the bones or underlying sediment.

229 lored metabolite of heme degradation (a bile pigment), once believed to be toxic, but recently recogn

230 dose lutein/zeaxanthin supplement on macular pigment optical density (MPOD) and skin carotenoid (SC)

231 e the ability of the technique to map visual pigment optical density and synthesis rates in eyes with

232 e EZ loss area was larger in eyes with ORHR, pigment, or both than in eyes without any pigment migrat

233 Malarial pigment, or hemozoin (Hz), is an undegradable crystallin

234 recapitulate previously observed behavior of pigment organelles in amphibian melanophores.

235 SLT success more often showed greater angle pigment (P = 0.03).

236 Pathogenesis of pigmented paravenous retinochoroidal atrophy may involve

237 The patient was diagnosed with pigmented paravenous retinochoroidal atrophy.

238 LFRS was found to be more sensitive to both pigments, particularly to the presence of vermilion with

239 mental and evolutionary implications of this pigment patterning system.

240 derived and ellagic formulations favored the pigment polymerization, the first in Nebbiolo and Sangio

241 the amino acid residues <6 angstrom from the pigments' porphyrin ring centers.

242 Although treatment of small pigmented posterior choroidal melanoma with PDT effectiv

243 The cellular lineages identified by pigment presence or absence (wild-type or knock-out line

244 Anthocyanins are pigments present in blood oranges which can be enriched

245 d cytolysin ShlA and the biologically active pigment prodigiosin.

246 Melanocytes are the neural crest-derived pigment-producing cells of the skin that possess dendrit

247 autoimmune disease of the skin that targets pigment-producing melanocytes and results in patches of

248 roliferative progeny that differentiate into pigment-producing melanocytes.

249 g the 7 eyes with ORHR and ORNV at baseline, pigment proliferation became visible in 4 eyes.

250 s was recently reported for a photosynthetic pigment-protein complex (Nature Commmun, 9, 2018, 99).

251 Photosystem II (PSII) is a multisubunit pigment-protein complex that uses light-induced charge s

252 report on the intrinsic flexibility of LHCII pigment-protein complexes in a membrane environment, rev

253 nsional electronic spectra of photosynthetic pigment-protein complexes over a decade ago, the origin

254 otective energy dissipation functions within pigment-protein complexes.

255 , chloroplast ultrastructure, and changes in pigment-protein composition.

256 s, and leads to a decrease in photosynthetic pigments, proteins, and free amino acids.

257 ased on histopathologically detected malaria pigment provided the best surrogate measure of adverse b

258 s (PSCs) using a low-cost industrial organic pigment quinacridone (QA) is presented.

259 that without compensation, FAF signals from pigmented rats are lower than that from albinos.

260 FAF images from albino and pigmented rats showed that without compensation, FAF sig

261 locyanines, yellow and red (naphthol AS) azo pigments, red quinacridone, anthraquinone, and diketopyr

262 cal structures present in this heterogeneous pigment remain unknown, limiting understanding of the pr

263 one difference is that, whereas a rod visual pigment remains stable in darkness, a cone pigment has s

264 bolism during the regeneration of the visual pigments required for the detection of light.

265 ted-state vibrational modes of the different pigments, resolving the vibrational relaxation of the ca

266 Cakes from pigmented rice varieties had lower crumb firmness and k

267 (HA) were applied to unpolished and polished pigmented rice varieties.

268 In this study, pigmented rice was characterized in terms of nutraceutic

269 cose homeostasis result in hyperglycemia and pigmented rice, unique combination of high quality starc

270 hanism links elevated HGA to ochronosis; the pigment's chemical identity is still not known, nor how

271 ated on two lettuce cultivars (red and green-pigmented Salanova(R)) grown in a fully controlled Fitot

272 d an AD polygenic risk score or genetic skin pigment score explain the AD disparities in patients wit

273 ld produce white, golden, black or partially pigmented shell.

274 pation of lateral rim cells in a sub-retinal pigment shield in an insect eye.

275 was possible to reveal that the sub-retinal pigment shield of T. evanescens is not formed by a separ

276 (MeV-SIMS) for analysis of synthetic organic pigments (SOPs) that can be usually found in modern and

277 Polyphenols from five pigmented sorghum (PS) flours were in vitro evaluated as

278 athochromic effects in SNs containing all co-pigment sources, except for PRE.

279 Among co-pigment sources, SCSE caused the highest stabilities of

280 determined and dependent on a population of pigment stem cells that are set-aside in a sub-region of

281 Bearing in mind that pigments such as red lead (Pb(3)O(4)) and lead white (hy

282 e more selective to cyanobacteria than other pigments, such as chlorophyll-a, and to present an excel

283 Rod and cone visual pigment synthesis rates in those with AMD (v = 0.043 SD

284 (chl-a), which is the major light harvesting pigment that absorbs light in the blue and red spectrum.

285 ccus neoformans is the production of melanin pigments that are deposited into the cell wall and inter

286 plastics containing a range of additives and pigments that are not generally included in commercial l

287 uring of a kaleidoscopic variety of dyes and pigments that brought about great revolutions in art, co

288 Vincent van Gogh used fugitive red lake pigments that have faded in some paintings.

289 cence measurement of specific cyanobacterial pigments, that is, phycocyanin.

290 Linking the LC-MS analysis of this modified pigment to a naturally purple animal suggested a conserv

291 The results enabled many of the pigments to be identified and their distribution to be s

292 The research of antioxidants and natural pigments to replace synthetic molecules is increasingly

293 uggest that OHPs function in the delivery of pigments to the D1 subunit of PSII.

294 the proximate causes underlying variation in pigment type (i.e., color) and pigment distribution (i.e

295 e (50, 300, 1000 and 2000 mg/kg body weight) pigment was administered to female Wistar rats.

296 During heating, the deterioration of red pigments was more pronounced compared to that of the yel

297 od to different chemical classes of SOPs, 17 pigments were selected for the analyses.

298 pid adaptive diversification of their visual pigments when compared with their terrestrial and amphib

299 te (2PbCO(3).Pb(OH)(2)) and zinc white (ZnO) pigments, which are frequently found in artistic oil pai

300 Betalains are violet-red, natural food grade pigments with health benefits; however, their stability

301 spectrometry, we identify two novel eggshell pigments: yellow-brown tetrapyrrolic bilirubin from the