ライフサイエンスコーパス: pigment

1 tentional content of 5800 mg/kg (Fe as Fe2O3 pigment).

2 techin is the flavanol prone to forming such pigments.

3 relative distance and orientation of the two pigments.

4 relevant molecules, such as antioxidants and pigments.

5 roperties and pump activity of the resulting pigments.

6 th (-)-epicatechin to form xanthylium cation pigments.

7 ue to potential source of phytochemicals and pigments.

8 g of visual chromophore for the opsin visual pigments.

9 nt proteins and 6-decarboxylated betaxanthin pigments.

10 ties for the creation of an abundance of new pigments.

11 roma while promoting the formation of stable pigments.

12 ulatory gene PAP1 (production of anthocyanin pigment 1) from Arabidopsis is reported to increase init

13 Arabidopsis PAP1 (production of anthocyanin pigment 1) was stacked with an onion CHI by crossing.

14 viour, but unusual specialisations of visual pigments [1], mitochondrial tRNAs [2], and postcranial a

15 les, 41.6% were plastic polymers, 23.6% were pigments, 5.50% were amorphous carbon, and 29.1% remaine

16 These pigments accumulate in vacuoles, and their color is infl

17 tematically exhibited fragmented fluorescent pigments adjacent to the disease front as indicated by s

18 erapy (P = 0.01) and greater inherent ocular pigment also were significantly associated with a reduct

19 ocyanin content; it can be used as a natural pigment, also adding potential health benefits.

20 e plastics, and were not identified with the pigments, although the contamination of 4 mg/kg (Fe) was

21 known to exhibit increased levels of melanin pigment and tyrosinase activity.

22 t after extravasation, melanoma cells become pigmented and enact a gene expression program of melanoc

23 monomeric anthocyanin with an increase in co-pigmented and polymeric anthocynins thus affecting the w

24 idation of photoprotective xanthophyll cycle pigments and enhanced emission of volatile monoterpenes.

25 Total acetaldehyde, Mn, Cu/Fe, blue and red pigments and gallic acid seem to be essential to determi

26 nce the product is considered edible and the pigments and volatile changes are not as drastic as obse

27 75 and 90min) were studied for their color, pigments and volatile fraction changes.

28 abic samples, pure and mixed with lead white pigment, and allowed the detection of gum arabic in samp

29 specific metabolites such as fatty acids and pigments, and a full suite of potential critical physico

30 ng impacts on growth fitness, photosynthetic pigments, and total cellular protein and starch concentr

31 pression; (2) indirectly, via suppression of pigment; and (3) Fe/S cluster biosynthesis.

32 lids removed while retaining majority of the pigment ( approximately 98%) in the betalain rich extrac

33 inding modes and conformations of HliD-bound pigments are discussed with respect to the known structu

34 al properties of the eye-colouring screening pigments are discussed within the context of the photoch

35 Carotenoid pigments are responsible for many of the red, orange, an

36 cs, along with exciton transport between the pigments, are included.

37 pes, such as pheomelanin, eumelanin, and non-pigmented areas within the iris.

38 ught of as "programmed solvents", which bind pigments at specific mutual orientations, thus tuning th

39 lorophyll ratios, pools of xanthophyll cycle pigments, beta-carotene and stored monoterpenes.

40 The recent description of the betacyanin pigment betanin in red-violet varieties is here further

41 and Cys303 providing a second, low affinity pigment binding site that is essential for the assembly

42 consistent with the presence of two distinct pigment binding sites in PORB, with Cys276 establishing

43 The sRNAs repress a pigment biosynthesis gene, creating a yellow highlight a

44 ing dysfunctional plastids due to defects in pigment biosynthesis or translation are known to repress

45 er segment photocurrent following equivalent pigment bleaching.

46 ing range of rod phototransduction following pigment bleaching.

47 sensitivity of rod photoresponses following pigment bleaching.

48 Whereas, grater reducing power of pigmented bran was attributed to presence of multiple-OH

49 Hair is also pigmented by melanocytes in the follicle.

50 hers contain red, orange, and yellow polyene pigments called psittacofulvins.

51 erated during regeneration or in response to pigment cell ablation.

52 ts provide insights into mechanisms of adult pigment cell development in the strikingly colorful Plat

53 n3), encoding a peptide factor that promotes pigment cell migration and differentiation in other vert

54 PMEL is a pigment cell protein that forms physiological amyloid in

55 This dome-shaped, melanin-pigmented cell generates enormous turgor and applies phy

56 Many pigment cells acquire unique structural properties and g

57 ers expressed in sequential fashion when new pigment cells are generated during regeneration or in re

58 is known about the developmental origins of pigment cells produced in adult organisms during tissue

59 ping zebrafish larvae, in vivo monitoring of pigment cells suggested that disturbances in melanocyte

60 GPR143, primarily expressed in pigment cells, localizes exclusively to endolysosomal an

61 D in both the mid and far periphery, whereas pigment changes and features of advanced AMD are less fr

62 Nonreticular pigment changes were less frequent in the periphery than

63 First, optical properties of the individual pigment chromophores present in light-harvesting antenna

64 Quality parameters, oxidative stability, pigments, colour and fatty acid profile were assessed, a

65 953mg/100g dw and were more concentrated in pigmented compared to white/yellow-fleshed potatoes.

66 trasonic treatment of bran extracts of seven pigmented (completely) and non pigmented (sparsely) colo

67 e formation of intermolecular anthocyanin:co-pigment complexes.

68 The lead white pigment, composed of two main mineral phases cerussite P

69 yanins, color properties (CIELch, haze), and pigments composition before and after spray drying were

70 Micrographs of kernel showed pigments concentrated in pericarp layer of purple but on

71 brafish Plin6 protein targets the surface of pigment-containing carotenoid droplets (CD).

72 : ripeness influenced saturated fatty acids, pigment content and deacetoxy oleuropein aglycone (DAOA)

73 s provide complementary information on fruit pigments content as a whole and on quali-quantitative pr

74 f photoluminescence properties of lead-white pigments could be used as fingerprints of their origin a

75 Higher DPPH radical scavenging activity of pigmented cultivars was due to higher percentage of phen

76 ents, mislocalization and decrease in visual pigments, decreased expression of retinoic acid-responsi

77 their chlorophyll (Chl) a's, despite a high pigment density.

78 ll understood, the enzyme(s) responsible for pigment dephosphorylation and the functional significanc

79 Elimination of PP2A substantially slows pigment dephosphorylation, visual chromophore recycling,

80 As show cycling expression levels within the pigment dispersing factor (PDF) cell-pacemaker neurons;

81 Light and neuropeptide pigment dispersing factor (PDF) from morning cells (s-LN

82 th running-wheel assays suggested that GABA, pigment-dispersing factor, myoinhibitory peptides (MIPs)

83 Foliar nutrients and photosynthetic pigments displayed little to no elevation trend.

84 enogenic activity, carotenoid stability, and pigment diversity.

85 uvate participate in the formation of stable pigments during fermentation and wine aging.

86 Technological importance of this pigment emerged from various studies demonstrating that

87 ed by maintaining the spatial arrangement of pigments, employing helices as scaffolds.

88 sions, including freckles, nevi, and an iris pigment epithelial (IPE) cyst, were imaged.

89 the immune response, we infected the retinal pigment epithelial (RPE) cell line, ARPE-19, with cell-a

90 id mediators biosynthesized in human retinal pigment epithelial (RPE) cells that are oxygenated deriv

91 to a low glucose condition by using retinal pigment epithelial (RPE) cells, which are a crucial comp

92 present in the apical microvilli of retinal pigment epithelial (RPE) cells.

93 RMS2/HTRA1 locus with subretinal/sub-retinal pigment epithelial (RPE) hemorrhage related to neovascul

94 s examination revealed midperipheral retinal pigment epithelial atrophy and intraretinal pigment migr

95 analysis, visual acuity at referral, retinal pigment epithelial atrophy, and macular scarring were as

96 tubular cell line (TEC) and a human retinal pigment epithelial cell line (ARPE-19).

97 Knockdown of Tgifs in a human retinal pigment epithelial cell line also increased EVI5L expres

98 ds human primary blood leukocytes or retinal pigment epithelial cells at effective concentrations; pr

99 Human retinal pigment epithelial cells were treated with various combi

100 idual cells, such as photoreceptors, retinal pigment epithelial cells, and blood cells in the retinal

101 5 eyes (33.5%) and was observed in drusenoid pigment epithelial detachment (PED) and serous PED with

102 ce tomography angiograhy (OCTA) of drusenoid pigment epithelial detachments (PEDs) in a woman affecte

103 scular membranes as retinal complications of pigment epithelial detachments.

104 and delivery of MPO to lysosomes of retinal pigmented epithelial (RPE) cells acts to clear this harm

105 proangiogenic signaling produced by retinal pigmented epithelial (RPE) cells under different conditi

106 itin in the outer retina in-vivo and retinal-pigment-epithelial (RPE) cells in-vitro.

107 To evaluate the features of acute retinal pigment epitheliitis (ARPE) at onset and in the course o

108 Acute retinal pigment epitheliitis resolved in a sequence of (1) a dec

109 combined hamartoma of the retina and retinal pigment epithelium (CHRRPE) involving the macula.

110 notypes, including the occurrence of retinal pigment epithelium (RPE) abnormalities, choroidal neovas

111 remains elusive, dysfunction of the retinal pigment epithelium (RPE) and dysregulation of complement

112 ents is an important function of the retinal pigment epithelium (RPE) and it is essential for retinal

113 by neighboring epithelial cells, the retinal pigment epithelium (RPE) and podocytes, respectively.

114 etinal disruption and atrophy of the retinal pigment epithelium (RPE) associated with ORT on spectral

115 toreceptor atrophy can occur without retinal pigment epithelium (RPE) atrophy and that atrophy can un

116 s localized to the apical aspects of retinal pigment epithelium (RPE) cells and contributes to a dela

117 lls, mitochondria, Muller cells, and retinal pigment epithelium (RPE) cells and were visualized using

118 te the intraretinal migration of the retinal pigment epithelium (RPE) cells in age-related macular de

119 Cholesterol accumulation beneath the retinal pigment epithelium (RPE) cells is supposed to contribute

120 V4 expression in the endothelium and retinal pigment epithelium (RPE) components of the BRB, and that

121 ar degeneration and atypical central retinal pigment epithelium (RPE) defects not attributable to geo

122 ophy, characterised by extensive sub-retinal pigment epithelium (RPE) deposits, RPE atrophy, choroida

123 d pluripotent stem cells to generate retinal pigment epithelium (RPE) from an individual suffering fr

124 To report on the presence of retinal pigment epithelium (RPE) humps in high myopia, and to de

125 ofiles specifically localized to the retinal pigment epithelium (RPE) in Abca4 (-/-) Stargardt model

126 Daily, the retinal pigment epithelium (RPE) ingests a bolus of lipid and pr

127 While AMD histopathology involves retinal pigment epithelium (RPE) injury associated with immune c

128 ce between the neural retina and the retinal pigment epithelium (RPE) is critical for several process

129 ated from the SD-OCT and the area of retinal pigment epithelium (RPE) loss from the FAF.

130 ase 1/2 (ERK1/2) is increased in the retinal pigment epithelium (RPE) of age-related macular degenera

131 To investigate when retinal pigment epithelium (RPE) tears occur and their associate

132 CT measurement parameters, including retinal pigment epithelium (RPE) thickness, central macular thic

133 transport is a major function of the retinal pigment epithelium (RPE) to support the neural retina.

134 s in regions with normally appearing retinal pigment epithelium (RPE) were the loss of the POS and el

135 cular degeneration (AMD) affects the retinal pigment epithelium (RPE), a cell monolayer essential for

136 ound in the photoreceptor-supporting retinal pigment epithelium (RPE), especially in a zone correspon

137 ordinated terminal maturation of the retinal pigment epithelium (RPE), fenestrated choroid endothelia

138 ontaining lipofuscin pigments in the retinal pigment epithelium (RPE), increased oxidative stress, au

139 eta signaling in the entire eye, the retinal pigment epithelium (RPE), or the vascular endothelium.

140 of ocular and systemic factors with retinal pigment epithelium (RPE)-Bruch's membrane (BM) complex t

141 na, the ciliary margin (CM), and the retinal pigment epithelium (RPE).

142 lial mesenchymal transition (EMT) of retinal pigment epithelium (RPE).

143 ulate the phagocytosis of OSs by the retinal pigment epithelium (RPE).

144 s, especially the involvement of the retinal pigment epithelium (RPE).

145 model of chronic degeneration of the retinal pigment epithelium (RPE).

146 egulated manner in chicken embryonic retinal pigment epithelium (RPE)/choroid in the absence of light

147 cement of the temporal peripapillary retinal pigment epithelium (tRPE) from its position in central g

148 Retinal pigment epithelium abnormalities, AVLs, neovascularizati

149 Quantifying preserved retinal pigment epithelium and EZ areas on FAF and OCT images, r

150 n export the lactate as fuel for the retinal pigment epithelium and for neighboring Muller glial cell

151 adelta T cells in protection against retinal pigment epithelium and retinal injury.

152 Retinal pigment epithelium cells were in the centre, photorecept

153 Finally, in primary human fetal retinal pigment epithelium cells, ligand binding to TLR2 induced

154 olar, horizontal, photoreceptor, and retinal pigment epithelium cells, thus exposing the anatomical s

155 worse vision, presence of atrophy/fibrosis, pigment epithelium detachment, and geographic atrophy/fi

156 ad thickening of Bruchs membrane and retinal pigment epithelium dysfunction.

157 eye, hemorrhage, and absence of sub-retinal pigment epithelium fluid at baseline were associated wit

158 TLR2 was robustly expressed by the retinal pigment epithelium in mouse and human eyes, both normal

159 incidence of atrophic lesions of the retinal pigment epithelium in patients with Stargardt disease as

160 TLR2 signaling, was detected in the retinal pigment epithelium of human eyes, particularly in eyes w

161 Retinal pigment epithelium tears act differently depending on wh

162 e choroidal blood passes through the retinal pigment epithelium to the retina where photoreceptors co

163 Damage of the pigment epithelium was also confirmed.

164 ischemic infarction of the choroid, retinal pigment epithelium, outer part of the retina and the opt

165 Loss of retinal pigment epithelium, the presence of a thin choroid, a pe

166 Retinal pigment epithelium-BM thickness, as measured by SD OCT s

167 tudy, we tested the effect of treatment with pigment epithelium-derived factor (PEDF) in combination

168 a1 transcription factor and are dependent on pigment epithelium-derived factor (PEDF) on the outer su

169 ation of the known neuroprotective molecule, pigment epithelium-derived factor (PEDF) plus docosahexa

170 ppress consumption of glucose by the retinal pigment epithelium.

171 acular degeneration characterized by retinal pigmented epithelium (RPE) death; the RPE also exhibits

172 he major biological functions of the retinal pigmented epithelium (RPE) is the clearance of shed phot

173 we delivered a wild-type Mfrp to the retinal pigmented epithelium (RPE) of Mfrp (rd6) /Mfrp (rd6) mic

174 ocessing enzyme DICER1 in the mature retinal pigmented epithelium (RPE).

175 cative of pathological events in the retinal pigmented epithelium.

176 type of the seed coat regions from yellow to pigmented, even in the presence of the normally dominant

177 d multivariate analyses of fluorescence from pigment extracted in 90% acetone to assess the variabili

178 travitreous injection and (2) in more deeply pigmented eyes.

179 Sixty-one patients with 63 ambiguous pigmented facial macules and 12 control photodamaged fac

180 ectance confocal microscopy (RCM), ambiguous pigmented facial macules and establish a correlation bet

181 Pigmented facial macules on photodamaged skin are a clin

182 onfocal microscopy enhanced the diagnosis of pigmented facial macules with 91.7% sensitivity and 86.8

183 Asymmetric pigmented follicular openings by dermoscopy correlated w

184 The rate of brown pigment formation was shown to be reduced in model Maill

185 neural tube at G16, and differentiated into pigment-forming melanocytes during in vitro culture.

186 Astaxanthin is a carotenoid pigment found in numerous organisms ranging from bacteri

187 emperature for the extraction of anthocyanin pigments from black carrot pomace.

188 What and how pigments function in a fungal species with multiple cell

189 Addition of co-pigments generally increased pKH estimate-values of anth

190 tion tryptophan and its derivatives in black pigmented glutinous and non-glutinous rice grain samples

191 intense autofluorescence from photosynthesis pigments has hindered the investigation.

192 study, we have developed porphyrin-peptoid (pigment-helix) conjugates (PPCs) that can modulate the d

193 taneous sensitivity in darker versus lighter pigmented humans and mouse strains.

194 The best studied pigment in fungi is melanin which coats the surface of s

195 ay when a substantial fraction of the visual pigment in our photoreceptor cells is bleached.

196 n of the excitation energy on a single Chl a pigment in the terminal emitter domain due to very speci

197 he development of truly sustainable photonic pigments in coatings, cosmetics, and security labeling.

198 The area of fragmented fluorescent pigments in diseased coral extended 3.03 mm +/- 1.80 mm

199 irect result of exceptionally densely packed pigments in photosynthetic proteins.

200 allows simultaneous interrogation of various pigments in plants.

201 is work evaluated the formation of polymeric pigments in red musts added with (+)-Catechin, Procyanid

202 otolerans led to larger amounts of polymeric pigments in sequential fermentation.

203 buildup of bisretinoid-containing lipofuscin pigments in the retinal pigment epithelium (RPE), increa

204 holipids.It is currently thought that visual pigments in vertebrate photoreceptors are regenerated ex

205 The color of the pigment, in which the chromate ion acts as a chromophore

206 Although pigment inactivation by phosphorylation is well understo

207 best penetration seen in light to moderately pigmented irides.

208 tyrosine-derived red-violet and yellow plant pigments known for their antioxidant activity, health-pr

209 virus antigen localized to malarial parasite pigment-laden macrophages.

210 To determine the utility of the pigmented lesion assay (PLA) for LINC00518/PRAME express

211 nto their decision as to whether to biopsy a pigmented lesion suggestive of melanoma, dermatologists

212 ed linear, unimodal, or no response to algal pigment levels, depending on the taxonomic group.

213 as both the migratory neural crest cells and pigment localized only to PNA-free areas.

214 arrestin binding and turnover of the visual pigments located in the various photoreceptor types.

215 entation at birth followed by further patchy pigment loss during childhood.

216 een enrichment of carotenoid and xanthophyll pigments may be achieved using higher (16-33%) blue ligh

217 psin (RH1), the temperature-sensitive visual pigment mediating dim-light vision, offers an opportunit

218 Using human primary melanocytes and a highly pigmented melanoma cell line, we demonstrate that reduce

219 1.25-14.13) than those with incident primary pigmented melanomas.

220 In mouse, this local PLR requires the pigment melanopsin [5], originally found in intrinsicall

221 Pigmented mice and albino mice (n = 6 eyes) were used to

222 xA mRNA detection for the first time, in red-pigmented microbial mats within the hot springs of Paoha

223 pigment epithelial atrophy and intraretinal pigment migration.

224 Carotenoids are plant-derived pigment molecules that vertebrates cannot synthesize de

225 lative coupling strength between constituent pigment molecules.

226 acular abnormalities included mild to severe pigment mottling in 27 patients (63%) and lacunar maculo

227 Ocular findings were focal macular pigment mottling, chorioretinal atrophy with a predilect

228 yanin which is an excellent light harvesting pigment needed for the generation of charge carriers for

229 blue-white veil, pseudopods or streaks, and pigment network.

230 Anterior pigmented neuroectodermal disorganization, dysgenesis of

231 50%, and mainly targets the A10 parabrachial pigmented nucleus (PBP) and A8 (retrorubal field, RRF) n

232 expression of rhabdomeric opsin and a visual pigment of the recently described xenopsins in larval ey

233 Porphyrins, called the pigments of life, have been studied for decades.

234 ith zinc oxide, one of the most common white pigments of the 20th century.

235 unsaturated fatty acids may increase macular pigment optical density (MPOD) and thereby protect again

236 A detailed bottom-up model of pigment organization and energy transfer in phycobilisom

237 terminal emitter domain due to very specific pigment orientations.

238 describes a novel mechanical process for the pigmented parts of Gomphrena globosa L.

239 Abruptness of pigment patterns at the periphery of a skin lesion is on

240 d then we examine the collective behavior of pigment-pigment and pigment-protein interactions.

241 ll retained through industrial processing of pigmented potatoes (79-129%).

242 g dw and were mainly present in the flesh of pigmented potatoes.

243 CB hydrolysate-based medium, the highest red pigment production (18.71AU490nm) was achieved under dar

244 ol.m(-2).s(-1) of photon flux density on red pigment production by M. ruber in glucose-based medium w

245 ysate could be an interesting source for red pigment production by Monascus ruber Tieghem IOC 2225.

246 In glucose-based medium, the highest pigment production was achieved in fermentation assisted

247 ay in melanocytes could potentially modulate pigment production.

248 ntiation from neural crest-derived cells and pigment progenitor cells.

249 Photosystem II (PSII), a large pigment protein complex, undergoes rapid turnover under

250 he Fenna-Matthews-Olson (FMO) photosynthetic pigment protein complex.

251 Phycobilisomes are highly organized pigment-protein antenna complexes found in the photosynt

252 correlations among sites in a photosynthetic pigment-protein complex in the Fenna-Matthews-Olson mode

253 s, which include thermal fluctuations of the pigment-protein complexes and changing local environment

254 Photosynthesis begins when a network of pigment-protein complexes captures solar energy and tran

255 oduce multiple types of heterogeneity in the pigment-protein complexes, including structural heteroge

256 s, such as energy transfer in photosynthetic pigment-protein complexes.

257 e collective behavior of pigment-pigment and pigment-protein interactions.

258 tion of natural photovoltaic reaction center pigment proteins in biohybrid architectures for solar en

259 with chlorogenic acid (molar anthocyanin:co-pigment ratios 1:62.5-1:250).

260 ical for several processes, including visual pigment regeneration and retinal attachment to the RPE.

261 Pigment regeneration is critical for the function of con

262 ular mechanisms responsible for this action, pigment regeneration with this locked retinal analogue r

263 enic rods were unable to use cis-retinol for pigment regeneration.

264 ts indicate that light contributes to visual-pigment renewal in mammalian rods and cones through a no

265 th increasing Mnt concentrations, indicating pigment retention by the precipitates.

266 imaging revealed the presence of peripheral pigmented retinal lesions resembling CHRPE lesions in a

267 ide-field retinal imaging, 14 had peripheral pigmented retinal lesions.

268 ies of PROSPECT-MP for spectra modelling and pigment retrieval.

269 These pigments show remarkable signs of degradation after limi

270 ars later, he underwent excision of a raised pigmented skin lesion on his left calf that proved to be

271 xpression in decisions to biopsy a series of pigmented skin lesions.

272 lower and mechanical threshold is higher in pigmented skin.

273 acts of seven pigmented (completely) and non pigmented (sparsely) colored rice cultivars followed by

274 skin aging manifestation, including score of pigment spots on forehead (12.5% more spots per increase

275 e, a genetically determined higher degree of pigmented spots was not associated with higher 25-hydrox

276 in aging features (perceived age, wrinkling, pigmented spots) were assessed either manually or digita

277 Pigment stability was improved with increasing proportio

278 only to repress critical genes involving in pigment synthesis, mitosis, adherent junctions, but also

279 ht represent a more potent source of macular pigments than green leafy vegetables like spinach.

280 low refers to a group of synthetic inorganic pigments that became popular as an artist's material fro

281 nins are a family of heterogeneous polymeric pigments that provide ultraviolet (UV) light protection,

282 ollowing substantial bleaching of the visual pigment, the desensitization of the rod photovoltage is

283 Catechin was found in pigmented tissues whereas epicatechin was restricted to

284 i(k) alleles of the I locus, which restrict pigment to the hilum or saddle region of the seed coat,

285 or potentially within the charge-separating pigments to allow efficient transfer for charge separati

286 and the energetic requirements placed on the pigments to operate in such a regime, that the inverted-

287 values of anthocyanins from 3.28 (without co-pigments) to up to 4.71, thus substantially broadening t

288 Colour, pigments, total phenolic content and antioxidant activit

289 Betalain pigments, uniquely found in the plant order Caryophyllal

290 Ketocarotenoids are high-value pigments used commercially across multiple industrial se

291 mercial processing ranged from 49 to 85% for pigmented varieties and 32-55% for white/yellow.

292 ation of the health potential of anthocyanin-pigmented varieties.

293 vial giant cell tumor (TGCT) or diffuse-type pigmented villonodular synovitis (dtPVNS), and giant cel

294 Release of pigments was negligible within the experimental error fo

295 ion levels of the reactive oxygen-scavenging pigments were observed by Raman microscopic and remote s

296 f 11-cis-retinal, the chromophore for visual pigments, were significantly lower in diabetic retinas c

297 nthocyanins, one of the most important plant pigments, which are responsible of the intense red color

298 zoin, because incubation of purified malaria pigment with DNase abrogated IFN-beta induction.

299 Simply by blending the co-pigments with purple sweet potato anthocyanins at pH-val

300 gh the deposition of diet-derived carotenoid pigments, yet the mechanisms of carotenoid uptake and tr