ライフサイエンスコーパス: higher plant

1 t and highest density SNP collection for any higher plant.

2 uncharacterized CIF peptides conserved among higher plants.

3 te ALA synthesis for chlorophyll and heme in higher plants.

4 cellular life, with the notable exception of higher plants.

5 e present as multigene family in most of the higher plants.

6 andidates for long-distance communication in higher plants.

7 c properties to green-type rubiscos found in higher plants.

8 lation in mammals, but via O-fucosylation in higher plants.

9 ulatory component of RBR protein function in higher plants.

10 assessment of the protein import pathway in higher plants.

11 perate in organisms ranging from bacteria to higher plants.

12 a kinase cascade mediating osmoregulation in higher plants.

13 , metabolism, and redox regulation of CEF in higher plants.

14 to the overall photosynthetic performance of higher plants.

15 functional conservation of XyG structure in higher plants.

16 trolled system used to prevent inbreeding in higher plants.

17 etworks that regulate large gene families in higher plants.

18 antenna size twice as large with respect to higher plants.

19 ontrolled mechanism to prevent inbreeding in higher plants.

20 approaches to understanding ABA functions in higher plants.

21 imer or inter-Photosystem II dimer models in higher plants.

22 . mosses and ferns, but interestingly not in higher plants.

23 ss model taxa, including animals, yeasts and higher plants.

24 ee ATP sulfurylases (APS1, APS3 and APS4) in higher plants.

25 r long-lasting variation potentials (VPs) in higher plants.

26 f the evolution of sex chromosome systems in higher plants.

27 us taxonomic groups ranging from protists to higher plants.

28 e development and environmental responses of higher plants.

29 mic spatio-temporal electrical activities in higher plants.

30 rotochlorophyllide a oxygenases (PTC52) from higher plants.

31 ining bacteria and has homologs in algae and higher plants.

32 ion and expansion is a general phenomenon in higher plants.

33 as central to multiple signaling pathways in higher plants.

34 abolism and provide an adaptive advantage to higher plants.

35 h interdependence is not well established in higher plants.

36 ch Cga1 regulates chloroplast development in higher plants.

37 e gametophytes during sexual reproduction of higher plants.

38 l key regulator of growth and development in higher plants.

39 diversity of epigenomic control operating in higher plants.

40 st time in flax and 11 for the first time in higher plants.

41 major component of the primary cell wall of higher plants.

42 n transport and adaptive growth responses in higher plants.

43 hromes are the red/far-red photoreceptors in higher plants.

44 eezing tolerance and are highly conserved in higher plants.

45 orage and environmental stress adaptation in higher plants.

46 ubunits each coded by small gene families in higher plants.

47 L-ascorbic acid (vitamin C) biosynthesis in higher plants.

48 t defenses, and frequently induce disease in higher plants.

49 , directly affecting biomass accumulation in higher plants.

50 ed in the evolution of signaling networks in higher plants.

51 tudied in detail and is well conserved among higher plants.

52 trate phosphorylation site is conserved with higher plants.

53 most eukaryotic genomes, especially those of higher plants.

54 of glucosinolate metabolism and diversity in higher plants.

55 omponent of xyloglucans in the cell walls of higher plants.

56 now represents more than half of all CYPs in higher plants.

57 syB that was previously only associated with higher plants.

58 e problems of multicellularity - animals and higher plants.

59 he modern mono- and sesqui-TPSs found in all higher plants.

60 nd metabolic diversity that characterize the higher plants.

61 gle protein in algae to multiple isoforms in higher plants.

62 n the attenuation of metal(loid) uptake into higher plants.

63 ially conserved in other eukaryotes, such as higher plants.

64 racteristics exist between cyanobacteria and higher plants.

65 trochemical energy at the plasma membrane of higher plants.

66 o be conserved from Physcomitrella patens to higher plants.

67 volved in pivotal physiological functions in higher plants.

68 difference between PSII in cyanobacteria and higher plants.

69 tein in most photosynthesizing organisms and higher plants.

70 (e.g., among grasses, shrubs, and trees) in higher plants.

71 se, is a key enzyme in sucrose metabolism in higher plants.

72 ontrolling leaf wax deltaDn-alkane values in higher plants.

73 transposon- and repeat-derived siRNAs as in higher plants.

74 and critical for the overwhelming success of higher plants.

75 bacterial strains as well as chloroplasts of higher plants.

76 essenger RNA (mRNAs) have been identified in higher plants.

77 Engineering a CCM into higher plants 58 VI.

78 Furthermore, our data show that in higher plants a heterodimeric form of cpSRP is required

79 In higher plants, a cpftsy null mutation inhibits assembly

80 of reproductive strategies and lifestyles of higher plants, a key component of this mobile flowering

81 For thylakoid membranes of higher plants, a long-standing question has been which o

82 All higher plant ABCBs for which auxin transport has been co

83 The life cycle of higher plants alternates between the diploid sporophytic

84 harvesting complex (LHC) gene expression in higher plants and algae.

85 prevent self-fertilization and inbreeding in higher plants and also is known to utilize signaling to

86 es, a soluble class found in the plastids of higher plants and an integral membrane class found in pl

87 across a variety of kingdoms including both higher plants and animals.

88 missive of, and essential to, development of higher plants and animals.

89 The protein is conserved in higher plants and bryophytes but absent in algae and cya

90 low is an ATP-producing pathway essential in higher plants and chlorophytes with a heretofore unappre

91 osynthesis is evolutionarily conserved among higher plants and features a critical 3-hydroxylation re

92 Photosynthetic electron transport rates in higher plants and green algae are light-saturated at app

93 , Archaea, as well as in the chloroplasts of higher plants and green algae, has been implicated in th

94 mportant group of secondary metabolites from higher plants and have been reported to show significant

95 ncing in C. reinhardtii differs from that of higher plants and informs about the evolution and functi

96 ily conserved antiviral defense mechanism in higher plants and invertebrates.

97 n proteins are blue-light receptors found in higher plants and many algae, fungi, and bacteria.

98 helator of Fe, zinc (Zn) and other metals in higher plants and NA-chelated Fe is highly bioavailable

99 1 (CDF1) in Arabidopsis that is conserved in higher plants and Synechocystis.

100 he production of monoenes in the plastids of higher plants and the poorly structurally characterized

101 the biogenesis of the thylakoid membrane in higher plants and to identify auxiliary proteins require

102 tep of triacylglycerol (TAG) biosynthesis in higher plants and yeast.

103 ew outlines 'how' chlorophyll is degraded in higher plants, and gives suggestions as to 'why' the pla

104 canonical targeting signals, particularly in higher plants, and low levels of availability of experim

105 enes are exclusively found in the genomes of higher plants, and the encoded proteins have been found

106 s in diatoms, which is distinct from that of higher plants, animals and other microalgae.

107 tarvation was also compared with that of the higher plant Arabidopsis (Arabidopsis thaliana), the gre

108 Shoot apical meristems of higher plants are dome-like structures, which contain a

109 ive pathways operating in the peroxisomes of higher plants are fairly well characterized, the reactio

110 in controlled expression of the psbA gene in higher plants are highly elusive.

111 Lateral branches in higher plants are often maintained at specific angles wi

112 Many higher plants are polysomatic whereby different cells po

113 te a large family of RNA-binding proteins in higher plants (around 450 genes in Arabidopsis [Arabidop

114 inhardtii differs significantly from that of higher plants as cpSRP43 is not complexed to cpSRP54 in

115 m, flowering time, and photomorphogenesis in higher plants as responses to blue light.

116 Higher plants, as autotrophic organisms, are effective s

117 dyads with ultrastructure closer to that of higher plants, as exemplified by Cooksonia.

118 Soil nutrient contents were mostly lower at higher plant-associated rhizobacterial diversity; among

119 ages of bulk organic carbon and terrestrial higher-plant biomarkers with co-located palaeohydrologic

120 siccation because higher CO(2) also leads to higher plant biomass, and therefore greater transpiratio

121 In higher plants, blue light (BL) phototropism is primarily

122 chloroplast is the site of photosynthesis in higher plants but also functions as the center of synthe

123 is an important factor in gene regulation in higher plants but little is known about its roles in fru

124 reinhardtii is evolutionarily divergent from higher plants, but has a fully functional silencing mach

125 ause reorganization of microtubule arrays in higher plants, but the mechanisms driving these transiti

126 ial step towards enhancing photosynthesis in higher plants by introducing an algal CO(2)-concentratin

127 e loosely associated with PSII in state 1 in higher plants (called "extra" trimers).

128 t cpftsy deletion in green algae, but not in higher plants, can be employed to generate tla mutants.

129 In higher plants, cell cycle activation in the meristems at

130 Many differentiated animal cells, and all higher plant cells, build interphase microtubule arrays

131 In higher plant cells, microtubules (MTs) are nucleated and

132 stigate how cortical arrays are initiated in higher plant cells, we performed live-cell imaging studi

133 In higher plants, cellulose is synthesized by plasma membra

134 In higher plants, cellulose is synthesized by so-called ros

135 ermined and compared with bacterial FtsY and higher plant chloroplast FtsY.

136 The conserved 54-kDa SRP subunit in higher plant chloroplasts (cpSRP54) is not bound to an S

137 carbon concentrating mechanisms (CCMs) into higher plant chloroplasts could increase photosynthetic

138 During the evolution of higher plant chloroplasts from cyanobacteria, the SRP pa

139 aster Rubisco enzyme from cyanobacteria into higher plant chloroplasts may improve photosynthetic per

140 4 and the SRP receptor, FtsY, are present in higher plant chloroplasts.

141 itro and in vivo reconstitution, whereas the higher plant class II photolyase from Arabidopsis thalia

142 st complex IV-deficient mutants described in higher plants, cod1 lines should be instrumental to futu

143 The primary cell wall of higher plants consists of a mixture of polysaccharides w

144 The mTERF family in higher plants consists of roughly 30 members, which loca

145 All higher plants contain an ent-kaurene oxidase (KO), as su

146 Higher plants contain three evolutionarily distinct CA f

147 Higher plants contain two distinct groups of CRTs: CRT1/

148 In higher plants, cortical microtubules help to organize ce

149 rial PSI reaction center and its green algal/higher plant counterpart.

150 oteins that cluster with their corresponding higher plant counterparts.

151 Higher plant cryptochromes (CRYs) control how plants mod

152 represents an important step in the study of higher plant cuticles.

153 g a CPA-accumulating crop, we expressed nine higher plant cyclopropane synthase (CPS) enzymes in the

154 In higher plants, cytb(6) f also acts as a redox-sensing hu

155 Substitution of cyanobacterial D1-Asn87 by higher-plant D1-Ala87 is the principal discriminating fe

156 x through the Calvin-Benson-Bassham cycle in higher plants, dead-end inhibited complexes of Rubisco m

157 Sensitivities are examined including higher planting density at the expense of cattle product

158 cross allocation methodologies, improve with higher planting density, and persist if yield is reduced

159 Chloroplasts of higher plants develop from proplastids, which are undiff

160 erved in peroxisomal processing proteases of higher plants (dicots, monocots) but not present in orth

161 -30 cm) was likewise consistently greater at higher plant diversity and was greater with warming in m

162 Here we show that higher plant diversity increases rhizosphere carbon inpu

163 We show that higher plant diversity leads to more energy stored, grea

164 Our results show that higher plant diversity significantly enhances soil micro

165 Moreover, higher plant diversity was associated with the ameliorat

166 Higher plants encode at least 10 individual AGOs yet the

167 I discovered that higher plants encode more than 10 different TFIIB-like p

168 ubisco is amenable to in vitro assembly, the higher plant enzyme has been refractory to such manipula

169 organic food consumption was associated with higher plant-food and lower animal-food consumption, ove

170 These gene families expanded dramatically in higher plants; for example, there are approximately 339

171 a suitable genetic module was introduced to higher plants from a fungal source and subsequently expl

172 Both vertebrate and higher-plant genomes encode more than one isoform of thi

173 In higher plants, germline differentiation occurs during a

174 uirements of cytokinesis in somatic cells of higher plants gleaned from recent studies using cell bio

175 We report here that, at a higher plant growth temperature (26 degrees C) that perm

176 Shoot apical meristems (SAMs) of higher plants harbor a set of stem cells within the cent

177 The mechanism of green-type Rca found in higher plants has proved elusive, in part because until

178 on particle (SRP) pathway in chloroplasts of higher plants has undergone dramatic evolutionary change

179 Furthermore, our results explain why higher plants have a narrow range of grana diameters sin

180 Higher plants have developed sophisticated mechanisms to

181 Many gene families in higher plants have expanded in number, giving rise to di

182 Recent studies show that in higher plants, HCO3 (-) increases PSII activity by actin

183 The importance of CP12 in vivo in higher plants, however, has not been investigated.

184 e DCL3-dependent miRNAs differ from those of higher plants, however, in that many of them are derived

185 ting that two PsbQ molecules can interact in higher plants in a manner similar to that observed by Li

186 l with Nitrosomonadaceae is critical for the higher plants in pine barrens to reestablish and grow af

187 t strains revealed a further difference from higher plants in that the sRNAs are rarely negative swit

188 Every higher plant, including Arabidopsis and rice, contains a

189 In most species of higher plants, including Arabidopsis thaliana, the megas

190 Flooding is detrimental for nearly all higher plants, including crops.

191 leucine motif responsible for the sorting of higher plant INT1-type transporters to the tonoplast in

192 In primitive and higher plants, intracellular storage lipid droplets (LDs

193 A key feature of the development of a higher plant is the continuous formation of new organs f

194 geochemical cycling and that the uptake into higher plants is an important process.

195 thway of ascorbate biosynthesis described in higher plants is conserved in green algae.

196 Optimal timing of flowering in higher plants is crucial for successful reproduction and

197 ins in the post-ultraviolet (UV) response in higher plants is currently limited.

198 Gene expression in plastids of higher plants is dependent on two different transcriptio

199 The biosynthetic pathway for betaine in higher plants is derived from the oxidation of low-accum

200 thocyanin biosynthesis by TAS4 and miR828 in higher plants is evolutionarily significant and consiste

201 he small M subunit (PetM), whose function in higher plants is unknown.

202 Since ER-ANT1 homologs are restricted to higher plants, it is tempting to speculate that this car

203 In the life cycle of higher plants, it is the fate of meristem cells that det

204 r arguments with radiocarbon ((14)C) data of higher plant leaf-wax n-alkanoic acids.

205 wo surface-exposed alpha-helices of the SSU: higher plant-like helices knock out the pyrenoid, wherea

206 he two clades prior to the divergence of the higher plant lineages.

207 erse taxa of bacteria, fungi, algae and even higher plants metabolize BPA, but anaerobic microbial de

208 However, higher plant mitochondria differ biochemically, morpholo

209 or knockdown of the homologous genes in the higher plant model Arabidopsis thaliana results in mutan

210 In higher plants, molecular responses to exogenous hypoxia

211 nthetic light-harvesting complexes (LHCs) of higher plants, moss, and green algae can undergo dynamic

212 esorption, and fine root biomass, suggesting higher plant N demand.

213 In higher plants, nucleation of microtubules arises from di

214 Pathogen infection of higher plants often induces rapid production of phosphat

215 ities when compared with primary plastids of higher plants or algae.

216 dependently during evolution in yeast and in higher plants, or a suitable genetic module was introduc

217 PCC 6803 (wildtype) with alanine, present in higher plants, or with aspartic acid.

218 ough it is essential at membranes of several higher plant organelles like chloroplasts, peroxisomes,

219 A comparison with the crystal structure of higher plant (pea) PSI-LHCI indicates that Galdieria PSI

220 ue was performed on living single cells of a higher plant, permitting monitoring of the stiffness dis

221 In barley and other higher plants, phosphate homeostasis is maintained by a

222 The light-harvesting antenna of higher plant photosystem II has an intrinsic capability

223 atively modify buried amino acid residues in higher plant Photosystem II membranes.

224 s, which subsequently became integrated with higher plant phototransduction networks.

225 DEFECTIVE KERNEL1 (DEK1) of higher plants plays an essential role in position-depend

226 The presence of these gene families in higher plants points to the existence of an intriguing r

227 All higher plants possess multiple phytochrome photoreceptor

228 Higher plants possess two GluTR isoforms: GluTR1 is pred

229 The specialized root epidermis cells of higher plants produce long, tubular outgrowths called ro

230 All higher plants produce polyphenols, for defence against a

231 offer a route toward transforming algal and higher plant productivity for the future.

232 (CV = 2.5%) increased over the study due to higher plant productivity in the increasingly warm summe

233 at herbivores should benefit from subsequent higher plant protein contents.

234 ociated with increased risks of T2D, whereas higher plant protein intake tended to be associated with

235 In cyanobacteria and higher plants, proteolysis of the precursor D1 protein (

236 tion of these findings within the context of higher plant PS I antenna organization is discussed.

237 Here, we report the structure of the higher plant PSI-LHCI super-complex determined at 2.8 A

238 ide-binding properties of cyanobacterial and higher-plant PSII.

239 ow-temperature-responsive gene expression in higher plants, raising some of the key questions that st

240 Higher plant Rca is a crop improvement target, but its m

241 In higher plants, Rca plays a pivotal role in regulating CO

242 Gs), the most abundant sterol derivatives in higher plants, remains uncertain.

243 Animals and higher plants represent the most complex life-forms that

244 chloroplast organelle in mesophyll cells of higher plants represents a sunlight-driven metabolic fac

245 photosynthetic membranes in the plastids of higher plants requires an extensive supply of lipid prec

246 called non-photochemical quenching which, in higher plants, requires the luminal pH sensor PsbS and o

247 (Psp) systems found in bacteria, archaea and higher plants respond to extracytoplasmic stresses that

248 considered as a tree model for the study of higher plant response to abiotic stresses, survive in th

249 Under saline conditions, higher plants restrict the accumulation of chloride ions

250 In higher plants, roots acquire water and soil nutrients an

251 Recent technological breakthroughs now allow higher plant Rubisco to be engineered and assembled succ

252 oved elusive, in part because until recently higher-plant Rubiscos could not be expressed recombinant

253 ons and exon-intron junctions of present day higher plant's Rca, which is conserved in most species s

254 For example, higher plants sense temperature changes with high respon

255 cts of ptDNA during leaf development in four higher plant species (Arabidopsis thaliana, sugar beet [

256 Higher plant species are known to have additional caffeo

257 to increased plant-derived carbon inputs at higher plant species richness (PSR).

258 Rca alpha and beta isoforms exist in most higher plant species, with the alpha isoform being ident

259 psis, but appears to be conserved in diverse higher plant species.

260 ferences in their architecture from basal to higher plant species.

261 e present in the DGAT1-PTMD9 region of other higher plant species.

262 that SCO4 is a member of an unknown group of higher plant-specific proteinases quite distinct from th

263 arly identify >50 genes, mostly conserved in higher plants, specifically required for cell division b

264 olysaccharide found in the cell wall of most higher plant such as citrus, has drawn much attention du

265 for root tolerance to Fe-toxicity throughout higher plants such as legumes and monocots, which expose

266 ed understanding of the circadian network of higher plants, such as Arabidopsis thaliana, is hampered

267 analogous to the terrestrial C(4) pathway in higher plants, such insights may offer a route toward tr

268 intermediate type between cyanobacteria and higher plants, suggesting that this alga may provide the

269 Long-distance assimilate distribution in higher plants takes place in the enucleate sieve-tube sy

270 LKs) are class of membrane proteins found in higher plants that are involved in diverse functions ran

271 dominantly waxy layer on the aerial parts of higher plants that fulfils a number of essential physiol

272 Unlike higher plants that lack the FDPs and use the Proton Grad

273 otein family found in all eukaryotes (except higher plants) that have roles in membrane remodeling an

274 d in the same transcriptional unit, while in higher plants the plastid atp genes are organized into a

275 In higher plants, the female germline is formed from the me

276 In higher plants, the superfamily of carboxyl-CoA ligases a

277 In higher plants, the thylakoids are segregated into two mo

278 all has many features in common with that of higher plants; therefore, they are useful models to inve

279 In higher plants this is achieved in part by postmeiotic ge

280 Higher-plant thylakoids are differentiated into two inte

281 riven Suc transporters allow phloem cells of higher plants to accumulate Suc to more than 1 M, which

282 cyclase in chlorophototrophic organisms from higher plants to bacteria, and their evolution is discus

283 engineering of functional carboxysomes into higher plants to improve photosynthesis performance and

284 transfer a CO2 -concentrating mechanism into higher plants to increase photosynthetic performance.

285 e have generated ycf4 knockout plants in the higher plant tobacco (Nicotiana tabacum).

286 AtWRKY30 belongs to a higher plant transcription factor superfamily, which res

287 In somatic cells of higher plants, two cytoskeletal arrays, the preprophase

288 in the evolution from bacterial-type SRP to higher plant-type cpSRP system.

289 While higher plants typically do not accumulate high levels of

290 nation of the bioelectrical response mode of higher plants under stress.

291 Higher plants use threonine deaminase (TD) to catalyze t

292 To explore the control of phenotypy in higher plants, we examined the effect of a single plant

293 iously enigmatic breakdown of chlorophyll in higher plants were elucidated.

294 imers, (L2)5, and differs from Rubiscos from higher plants where LSus are glued together by small sub

295 ocots along with their putative orthologs in higher plants with sequenced genomes.

296 are two prominent O-glycosylation enzymes in higher plants, with both overlapped and unique functions

297 ation of LHCII, the major antenna complex of higher plants, with either one of them upon phosphorylat

298 s on the metabolism and functions of NAEs in higher plants, with specific reference to the formation,

299 plast biogenesis has been well documented in higher plants, yet the complex methods used to regulate

300 om the lower plant Physcomitrella patens and higher plant Zea mays.