ライフサイエンスコーパス: pale

1 ers, but in layer 4C, one eye's columns were pale.

2 in-15 and CK 7-positive tonofilaments in the pale acinar cells by myriad mucus granules.

3 ty malts, odorants of commercial products of pale ale (5-9 EBC), Vienna (6-10 EBC), Munich (11-35 EBC

4 ale (30 hL) for 24 h or 72 h and seeded into pale ale beer for bottle conditioning.

5 layer microcapsules, for the production of a Pale Ale beer.

6 To evaluate the method's robustness, Indian Pale Ale-IPA beers and wines from the San Francisco Vall

7 or two beer types: an amber ale and an India pale ale.

8 d sensory of hoppy beer styles such as India Pale Ales (IPAs) has become a major concern for many bre

9 The pale aleurone color1 (pac1) locus, required for anthocya

10 t level was observed in the number of type A pale and centrally located spermatogonia.

11 field is represented, there were alternating pale and dark bands resembling ocular dominance columns.

12 nto regular, alternating pairs (doublets) of pale and dark laminae.

13 c classes of stable derivative alleles, very pale and extremely pale, condition <1% of wild-type acti

14 fetal livers in homozygous ATF4 mutants were pale and hypoplastic.

15 Embryos without placental Fpn1 were pale and runted, and died before birth.

16 Cotyledons were pale and seedling growth was retarded in the mutant.

17 in stripes and interpatch columns project to pale and thick stripes.

18 olstered by injecting different tracers into pale and thick stripes; 10-27% of cells were double labe

19 n of interpatches to common V2 stripe types (pale and thick) merges parvo and magno inputs, making it

20 esolution monochromatic stimuli, we show the pale and yellow subtypes of Dm8s, inheriting retinal mos

21 ely of the branching species, causing tissue paling and decreased photosynthetic efficiency.

22 ina contains two types of ommatidia, called 'pale' and 'yellow', defined by different rhodopsin pairs

23 Mrg15-/- embryos appeared pale, and microarray analysis revealed that alpha-globin

24 in functional organization between the thin, pale, and thick stripes of V2.

25 patches) and three compartments in V2 (thin, pale, and thick stripes).

26 tracts from hypoxic (red), but not normoxic (pale), animals.

27 onocytes are replaced by adult dark (Ad) and pale (Ap) spermatogonia that make up the spermatogonial

28 han one large granule, and the plants have a pale appearance and reduced growth.

29 eatures of atrophic gastritis, which include pale appearance of gastric mucosa, increased visibility

30 ations in C14orf133 encoding VPS16B revealed pale-appearing platelets in blood films and electron mic

31 Phase paling appears to be closely associated with lipid perox

32 litated by our depigmented, white sclera-the pale area around the colored iris-and to underpin human-

33 d phenotype, with leaves that have chlorotic pale areas.

34 orientation selectivity corresponding to CO pale areas.

35 The second pattern consisted of thin pale bands from reduced metabolic activity in both eyes'

36 phenomenon, whereby reef corals turn visibly pale because of the loss of their symbiotic dinoflagella

37 ized samples grafted in methanol resulted in pale blue and light purple colors with lambdamax at appr

38 The resulting cocrystals start out pale blue but turn shiny and copper-colored as the polym

39 rly-stage, loosely compacted lesions such as pale bodies in patient tissue, whereas Lewy bodies, cons

40 assical Parkinson's disease lesions, such as pale bodies or Lewy bodies.

41 two animals with a weak fixation preference, pale border strips were found within the central visual

42 chrome P450 specific to male antennae of the pale-brown chafer, Phyllopertha diversa, has evolved as

43 t terminal bands of human chromosomes appear pale by conventional G-banding techniques.

44 troduction of sulfur-containing substituents pales by comparison.

45 ontributes to a pair oflaminae, one dark one pale, called a doublet, that extends through the mushroo

46 In the right calcarine cortex, the pale CO columns matched the labeled proline columns of t

47 In the left calcarine cortex, the pale CO columns overlapped the unlabeled columns of the

48 The thin dark-wide pale CO pattern was more widespread in the three animals

49 stinct system of alternating thick-pale-thin-pale CO stripes was present.

50 aviest [(3)H]proline labeling was located in pale CO stripes.

51 mma expression patterns define 'yellow' and 'pale' color vision circuits.

52 [11-15] indicates that the fossil snake was pale-colored in ventral regions; dorsal and lateral regi

53 ing mesogenic-units is synthesized, which is pale-colored, non-photoluminescent and non-mesogenic at

54 uality flaw of the muscle characterised by a pale colour and grainy and exudative texture.

55 pfish livers have shown colours ranging from pale (colours 1 and 2), through bright orange (colours 3

56 The wide pale columns resulted from loss of CO activity in the su

57 d of thin dark columns alternating with wide pale columns.

58 n of thin dark columns alternating with wide pale columns.

59 r, remodeling of glucose metabolism pathways pales compared with adaptations in amino acid and lipid

60 f hypoglycemia-blood glucose below 70 mg/dL, pale complexion, profuse perspiration.

61 derivative alleles, very pale and extremely pale, condition <1% of wild-type activity as a result of

62 hiff (PAS) stain identified large cells with pale cytoplasm along the endocardium of PV muscle sleeve

63 th moderately clumped chromatin and a rim of pale cytoplasm infiltrated the sinusoids of the spleen,

64 inal pigment epithelium atrophy and adjacent pale deposits in both eyes.Retinal anatomy was investiga

65 Female heterozygotes (GATA-1+/-) are born pale due to random inactivation of the X chromosome bear

66 23, and two genetically distinct mouse loci, pale ear (ep) and ruby-eye (ru), both with mutant phenot

67 The recessive mutation at the pale ear (ep) locus on mouse chromosome 19 was found to

68 The pale ear (ep) mouse strain is a model for the Hermansky-

69 t phenotypes similar to human HPS, including pale ear (ep), the mouse homolog of HPS1.

70 Euthymic C57BL/L ep/ep (pale ear [PE]) mice halt the visceral replication of int

71 d HPS3/cocoa; and BLOC-3, consisting of HPS1/pale ear and HPS4/light ear.

72 The mouse genes for HPS, pale ear and pearl, orthologous to the human HPS1 and HP

73 in ep but not in ru mice, establishing mouse pale ear as an animal model for human HPS.

74 ified in AMs and BAL from another HPS model, pale ear HPS1 mice.

75 The phenotypes of Hps1-mutant (pale-ear; ep) and Hps4-mutant (light-ear; le) mice and h

76 littermates after day 9.5 in that they were pale, edematous, and growth retarded.

77 During early development, pale ehrlichias with a tight cell wall dominated, but by

78 uire photosynthetic competence by converting pale etioplasts into green chloroplasts.

79 mutants, all R7 and most R8 cells adopt the pale fate, whereas overexpression of spineless is suffic

80 the recombinant molecule developed atypical pale, flat, slightly indurated, and nonulcerative reacti

81 and protein expression in fish with red and pale flesh color.

82 earance of leaf anthocyanin pigmentation and pale flower color as a result of drastic decreases in th

83 les, w4-dp (dilute purple flowers) and w4-p (pale flowers).

84 degrees C under vacuum for 200 h results in pale golden crystals of HBP and amorphous material conta

85 rt-day conditions, eaf1 plants were slightly pale green and had elongated petioles, phenotypes that a

86 However, double mutants are pale green in all photosynthetic tissues and chloroplast

87 ts in the nearly quantitative formation of a pale green intermediate with lambda(max) at 724 nm ( eps

88 reasingly impaired photosynthesis along with pale green leaves and severely stunted growth.

89 e absence of sucrose, noa1 has low fumarate, pale green leaves, slow growth and reduced chlorophyll c

90 y comparing the targeting of APG1 (albino or pale green mutant 1), an example of a stop-transfer subs

91 Here, we isolated and characterized a pale green mutant of the green alga Chlamydomonas reinha

92 CSP41a in mature leaves, correlating with a pale green phenotype and reduced accumulation of the ATP

93 This mutant displays a pale green phenotype, and its transgene contains a parti

94 teins, especially PsbF, lower PSII activity, pale green pigmentation, smaller leaf and plant sizes, a

95 taining media, and have white cotyledons and pale green rosette leaves.

96 Leaves contained pale green sectors and lacked part or all of the leaf la

97 45 degrees C and above, 2-NCMe converts to a pale green species 3 (lambda(max) = 753 nm, epsilon = 28

98 ly seedling development and smaller and more pale green than WT throughout development.

99 the AGH-CuNPs/N@CQDs indicator changed from pale green to yellow and ultimately to brown during bana

100 is thaliana) cpSRP54 null mutant, ffc1-2, is pale green with delayed development.

101 e-silencing lines are albino, variegated, or pale green, confirming that HDR is essential for plants.

102 Seedlings homozygous for elm1 are pale green, show pronounced elongation of the mesocotyl,

103 show that an EMB14 transgene complements the pale green, slow growth phenotype conditioned by mutatio

104 Mutant DeltarbcL plants were heterotrophic, pale-green and contained round plastids with reduced amo

105 nd atHsp93V-DeltaNu failed to complement the pale-green and protein import-defective phenotypes of an

106 AYER1 (AtML1) promoters failed to rescue the pale-green Atglk1 Atglk2 mutant phenotype, confirming th

107 Pale-green coloration of DXO1-deficient plants and our R

108 of the rps14 mRNA; however, the conditional pale-green mutant phenotype contrasts with the normal gr

109 tion of the ClpPRS protease complex led to a pale-green phenotype with delayed shoot development, sma

110 amilies were screened for the segregation of pale-green seedlings in the M(3) generation, and a subse

111 al, whereas a weak allele (rh3-4) results in pale-green seedlings with defects in splicing of several

112 We show that bnq3 mutants have pale-green sepals and carpels and decreased chlorophyll

113 SUFB overexpression and segregated from the pale-green SUFB-deficient phenotype, indicating it is no

114 he YqeH-type GTPase Brassinazole-Insensitive Pale Green2 (BPG2) is a chloroplast nucleoid-associated

115 yet those of the RAS-B grew slowly and even paled; however, once they were fed (RAS-B modified to RA

116 for upstream regulators we identified a LONG PALE HYPOCOTYL (LPH) gene whose activity is indispensabl

117 t GABAergic terminals often encircled large, pale, immunonegative profiles that may be dendritic.

118 s that innovations in proteomic technologies pale in comparison to the advances in NGS, with current

119 vances made in the past quarter century will pale in comparison to those anticipated for the next 25

120 All these accomplishments pale in comparison with the impact that Sig had on a per

121 longer, the economic and social losses will pale in comparison.

122 arlier times, these neurons were swollen and pale in Nissl-stained preparations.

123 Current artificial intelligence systems pale in their understanding of intuitive physics, in com

124 merous populations where imputation accuracy paled in comparison to that of European-ancestry populat

125 ity of all known homogeneous metal catalysts paled in comparison to their heterogeneous and biologica

126 e past 1200 years, we show that this drought pales in comparison to an earlier period of elevated ari

127 hesis have proliferated, their functionality pales in comparison to natural biopolymers-strategies ar

128 ngs, at least in part, because the taste cue pales in comparison to the highly rewarding drug expecte

129 taste cue because the value of the taste cue pales in comparison to the highly rewarding drug of abus

130 contribution of imaging to cancer care costs pales in comparison to those of other key cost component

131 he pentose xylose, the fermentative capacity pales in comparison with glucose, limiting the economic

132 t -1.5 mo of education per generation (which pales in comparison with the increases in EA observed in

133 nfrastructure supporting nephrology research pales in comparison with those for other internal medici

134 c Dgcr8 knockout mice displayed enlarged but pale interscapular brown fat with decreased expression o

135 educed locomotion in the presence of food, a pale intestine, increased intestinal fat storage, and a

136 Pale kidney findings seems to be helpful in diagnosis of

137 ed for as long as 2.5 months, with a diffuse pale/lacy appearance and persistent damage to centrilobu

138 lg(+) and Plg(o) mice had a similar diseased pale/lacy appearance, followed by restoration of normal

139 ol concentrations were determined in diluted pale lager beer and in nonalcoholic beer.

140 been applied to determination of furfural in pale lager beers with different storage times at room te

141 ve, being modulated by odor stimuli, whereas pale laminae are intermittently activated.

142 Axons in pale laminae are sparsely equipped with vesicles.

143 l axons having few vesicles and forming the "pale" laminae.

144 om layers 2/3, only one set of pale stripes (pale lateral) receives significant projections from laye

145 lumns-to-thick stripes, interblob columns-to-pale(lateral) stripes, layer 2/3-4A interblobs-to-pale(m

146 ronounced chloroplast defects exemplified by pale leaves, reduced accumulation of plastid proteins, a

147 rebral hyperplasia and pulmonary hypoplasia, pale livers, hypoplastic spleen, thymus, and bone marrow

148 Myopathic changes include pale M-lines devoid of MURF-1, and gradual sarcomeric di

149 temperature and roasting substrate (barley, pale malt or germinated green malt) on formation of 20 k

150 ondrial morphologic abnormalities (swelling, pale matrix, and disorganized cristae) were found predom

151 jections from layer 4B, while the other set (pale medial) receives few or no layer 4B projections.

152 lateral) stripes, layer 2/3-4A interblobs-to-pale(medial) stripes.

153 rafiltration on the antioxidant potential of pale, melano80 and black malts was evaluated.

154 ath, from lysis as usually judged by a phase pale microscopic appearance.

155 ontaining large, round synaptic vesicles and pale mitochondria, characteristic of retinal terminals (

156 e terminals, identified by their distinctive pale mitochondria, were similar to type II corticothalam

157 including large round synaptic vesicles and pale mitochondria.

158 On the other hand, DKO mice exhibit pale muscles compared to wild-type (WT) littermates.

159 ts (cue3, cue6, and cue8), and (c) uniformly pale mutants (cue4 and cue9).

160 thologic analysis, acute lesions appeared as pale necrotic areas surrounded by hyperemic rims, while

161 are individually induced by hypoxia, lending pale normoxic animals a visible red color when challenge

162 ble chromosomal alterations and that a phase paling observed within 1-2 s of laser exposure is associ

163 e between pale, soft and exudative (PSE) and pale-only muscles.

164 I, the ocular variables (such as strabismus, pale optic disc and visual field defects) were compared.

165 ociated with an absence of macular pigments, pale optic disc, and periphery pigmentation, resulting i

166 causes (N = 80) strabismus (88% versus 64%), pale optic discs (65% versus 27%) and visual field defec

167 igmentation, macular abnormalities, small or pale optic discs, and attenuated vessels with higher pre

168 After pale or thick stripe injection, labeled cells were conce

169 are classified into two subtypes, known as 'pale' or 'yellow', depending on Rhodopsin expression in

170 can exhibit various eye colors ranging from pale orange to intense red, depending on the insertion s

171 The pale-orange, formally divalent trimanganese complex rapi

172 eptors (PRs) are divided into yellow (y) and pale (p) subtypes.

173 Four pale (P1-P4) and four black (B1-B4) BSG extracts were in

174 Disruption of the CEPA1 gene leads to a pale phenotype and retarded plant development but does n

175 thaliana L. Heynh. mutant lcd1-1 exhibits a pale phenotype compared to the wild type.

176 produced in each chloroplast, suppresses the pale phenotype of ss4, and nearly restores normal growth

177 ne rescued both the chloroplast division and pale phenotypes of ftsHi1-1 and the embryo-lethal phenot

178 and easy-to-chew arils); however, arils have pale pink colour and flat sensory profile.

179 ceived colour of the white side changes from pale pink to deep magenta when the perceived shape of th

180 Light microscopy demonstrated pale pink, oval to crescentic intracytoplasmic inclusion

181 Specifically, Punch (Pu) and pale (ple) mutants with reduced dopamine synthesis show

182 nents of the TGFbeta pathway specifically in pale R7.

183 gulator Melted regulates the choice between 'pale' R8 (pR8) fate defined by Rh5 expression and 'yello

184 e edges of ocular dominance columns appeared pale, reflecting a loss of activity in binocular cells f

185 Fundus examination showed pale retina with no cherry red spot.

186 The ap3 bnq3 double mutant displays pale second-whorl organs, supporting the hypothesis that

187 nd replication of chloroplasts 1) mutant has pale seedlings and smaller, more numerous chloroplasts t

188 ction, spleens from IFN-gamma R-/- mice were pale, shrunken, and fibrous.

189 Pale skin color showed a protective effect (men: -21.0%D

190 evated vulnerability, minors and people with pale skin should also be the focus of such interventions

191 People with pale skin, red hair, freckles and an inability to tan--t

192 e genes displayed a lipid-depleted phenotype-pale, skinny, larval-arrested worms that lack fat stores

193 The pale SMI32 columns are those that are dark with CO in la

194 uccessful to completely discriminate between pale, soft and exudative (PSE) and pale-only muscles.

195 le, early protein oxidation and the onset of pale, soft and exudative (PSE) condition in chicken brea

196 d in the development of oxidative changes in pale, soft, exudative (PSE) chicken meat during storage

197 s of high marbling score, rare occurrence of pale, soft, exudative (PSE) meat, but low growth rate an

198 ity problems which are strikingly similar to pale, soft, exudative (PSE) pork.

199 ta at 7 Tesla from nine lightly anesthetized pale spear-nosed bats (Phyllostomus discolor).

200 in the development of abnormally swollen and pale staining mitochondria.

201 y not reported subpopulation of nongranular, pale-staining cells in both dacryoadenotic and normal la

202 a-glutamyl transferase (GGT) cholestasis and pale stool] in 46 cases (37.8%).

203 ncy department with jaundice, dark urine and pale stools.

204 erpatch projections, we injected CTB-Au in a pale stripe and horseradish peroxidase in an adjacent th

205 After pale stripe injection, cells were found in layer 2/3 (87

206 of layer 2/3 cells only project to a single pale stripe type.

207 eover, different tracer injections in nearby pale stripe types revealed that 97-99% of layer 2/3 cell

208 ll retrograde tracer injections in different pale stripe types.

209 nt V1 input from layers 2/3, only one set of pale stripes (pale lateral) receives significant project

210 ection maps, however, were found in V2 thick/pale stripes and avoided thin stripes.

211 s: the middle of the interblob projecting to pale stripes and the blob/interblob border region projec

212 Here we have asked whether the two pale stripes are also anatomically distinct in macaque.

213 results demonstrate that in macaque, the two pale stripes are anatomically distinct compartments, and

214 ive field properties of neurons in thick and pale stripes are generated by local V2 circuits, or by o

215 ulations of cells supplying thin stripes and pale stripes are quite independent.

216 ere we examined the projections to thick and pale stripes in macaques, revealed by retrograde tracer

217 , recent studies have suggested that the two pale stripes may be functionally distinct, and in marmos

218 reas a separate pathway from interpatches to pale stripes mediates form.

219 stinct projection streams from V1 to the two pale stripes of V2.

220 We found that while both pale stripes receive a predominant V1 input from layers

221 e V1 inputs from blob columns, and thick and pale stripes receive common input from interblob columns

222 s in macaque, but both models viewed the two pale stripes within a single stripe cycle as a single co

223 t pathways: magno to thick stripes, parvo to pale stripes, and konio to thin stripes.

224 ate that V1 cells project to either thick or pale stripes, but rarely to both.

225 of their input from layer 4B, compared with pale stripes, consistent with reports that thick stripe

226 Here, we demonstrate that thick and pale stripes, instead, receive spatially segregated V1 i

227 ns outside blob columns project to thick and pale stripes, suggesting functional specialization of V1

228 ck stripes, and no projections to one set of pale stripes.

229 as no clear enrichment of labeling in the CO pale stripes.

230 f CO staining in V2, with strongest input to pale stripes.

231 s different myelination of thin/thick versus pale stripes.

232 er of 1-2%, indicating higher myelination of pale stripes.

233 higher antioxidant activity than those with pale testa, and a positive correlation was found between

234 V2 contains a system of repeating pale-thin-pale- thick stripes of cytochrome oxidase (CO) activity.

235 The repeating pattern of pale-thin-pale-thick stripes of cytochrome oxidase (CO) activity i

236 taining in V2 reveals a repeating pattern of pale-thick-pale-thin stripes.

237 V2 reveals a repeating pattern of pale-thick-pale-thin stripes.

238 n V2, a distinct system of alternating thick-pale-thin-pale CO stripes was present.

239 V2 contains a system of repeating pale-thin-pale- thick stripes of cytochrome oxidase (CO)

240 The repeating pattern of pale-thin-pale-thick stripes of cytochrome oxidase (CO)

241 A mouse model of CMT4J, the Fig4-pale tremor (plt) allele, was dosed with a single-strand

242 f PtdIns(3,5)P2 in cultured fibroblasts from pale tremor mice demonstrates the conserved biochemical

243 The cytoplasm of fibroblasts from pale tremor mice is filled with large vacuoles that are

244 se type-4J (CMT4J) and its animal model, the pale tremor mouse (plt), are caused by mutations of the

245 euronopathy and diluted pigmentation in the 'pale tremor' mouse.

246 The plt (pale tremor) mouse carries a null mutation in the Fig4(S

247 Sdc1-positive stromal cells contrasted with pale tumors developing in the presence of mock-transfect

248 However, rats given LDL-DHA had smaller, pale tumors that were devoid of vascular supply and >80%

249 ysical examination findings of edematous and pale turbinates.

250 ing the Industrial Revolution, of the common pale typica form by a previously unknown black (carbonar

251 A pale ventral coloration distinguishes the light-bellied

252 The choice between pale versus yellow ommatidia is made in R7 cells, which

253 The m1 immunostaining was pale, whereas m3-positive neurons exhibited denser label

254 SU5416 was accompanied by the appearance of pale white tumors that were resected from drug-treated a

255 Day-13.5 K-Ras(-/-) embryos were pale with a marked reduction of mature erythrocytes in t

256 Day-14.5 p85alpha-/- embryos are pale with a marked reduction of mature erythrocytes in t

257 found that Plg(0) livers became enlarged and pale with foci of red nodules as early as 4 weeks after

258 hese were described as the patient "becoming pale with sinking to the floor and staring for approxima

259 sions associated with SpeB- strains appeared pale with surrounding erythema.

260 chx23 mutant leaves were pale yellow and had a much reduced chlorophyll content.

261 However, one site had a pale yellow area of central necrosis surrounded by a fib

262 paint microsamples taken from yellow-orange/pale yellow areas of 12 Van Gogh paintings, demonstratin

263 ney exhibited low antioxidant potential with pale yellow colour.

264 ced by approximately one-third, resulting in pale yellow cotyledons and leaves with reduced chlorophy

265 The colorless or pale yellow crystals are remarkable for the formation of

266 brown seed (br), salmon flower colour (sa), pale yellow flower colour (pa), virescent juvenile leaf

267 The first nectar produced is acidic and pale yellow in color, but slowly becomes alkaline before

268 In this work, seven PYP/XES (Pale Yellow Petal/ Xanthophyll esterase) genes were iden

269 (6)H(6) (S2A) and [L(2)].2DMF.4MeOH (S2B) as pale yellow tablets and blocks, respectively.

270 opper(II) induces a colorimetric change from pale yellow to orange-red and results in imine hydrolysi

271 xidized (2, teal) or fully reduced forms (3, pale yellow), depending on the amount of reducing agent

272 slation and photosynthetic capacity, causing pale-yellow and slow-growth phenotypes.

273 ched Chinese chive (BCC) is renowned for its pale-yellow appearance, delicate flavor, and culinary-me

274 ptical absorption intensity evidenced by the pale-yellow color of In(2)O(3) has prevented the use of

275 nstruct was ineffective at complementing the pale-yellow phenotype of hsp93 Arabidopsis (Arabidopsis

276 reased, leading to a growth phenotype (small pale-yellow plants) that is reminiscent of the pgp1-1 mu

277 el mutant 3735 (wk3735) mutant, which yields pale-yellow seeds characterized by heightened protein bu

278 Characterization of the maize (Zea mays) pale yellow9 (y9) locus has brought to light a new isome