ライフサイエンスコーパス: alfalfa

1 f leguminous plants such as Medicago sativa (alfalfa).

2 s well as its ortholog from Medicago sativa (alfalfa).

3 a and Arabidopsis) and symbiotic nodules (in alfalfa).

4 rogen-fixing symbiosis with Medicago sativa (alfalfa).

5 its leguminous plant host, Medicago sativa (alfalfa).

6 rts of many agronomically important genes in alfalfa.

7 truncatula genes for genetic improvement of alfalfa.

8 pathogen that causes anthracnose disease of alfalfa.

9 uticular wax loading on leaves of transgenic alfalfa.

10 en-fixing symbiosis between the bacteria and alfalfa.

11 than did the wild type during symbiosis with alfalfa.

12 nal view of random chromosome segregation in alfalfa.

13 12 is targeted and downregulated by SPL13 in alfalfa.

14 ssary for its nitrogen-fixing symbiosis with alfalfa.

15 nal view of random chromosome segregation in alfalfa.

16 infection within the cells of its host-plant alfalfa.

17 t invasion of root nodules on the host plant alfalfa.

18 ting winter hardiness in bivalent tetraploid alfalfa.

19 tion and extension (root nodule invasion) on alfalfa.

20 lgT mutation did not affect its virulence on alfalfa.

21 response mechanisms for grazing tolerance in alfalfa.

22 to flavonoid and other inducers released by alfalfa.

23 in isoflavonoid phytoalexin biosynthesis in alfalfa.

24 wth of S. meliloti near germinating seeds of alfalfa.

25 alyze alpha-tubulin expression in transgenic alfalfa.

26 rts to develop grazing-tolerant cultivars of alfalfa.

27 in plants and regulates MsPRP2 expression in alfalfa.

28 retards growth and development of transgenic alfalfa.

29 invasion by the bacterium of its host plant, alfalfa.

30 genic pea hairy root cultures or regenerated alfalfa.

31 tween R. meliloti Rm1021 and its host plant, alfalfa.

32 us), and the constructs were introduced into alfalfa.

33 esses to Al(3+)-inhibition of root growth in alfalfa.

34 genes and introduced them individually into alfalfa.

35 nd pathways that control grazing response in alfalfa.

36 zium colony-forming units (cfu) than corn or alfalfa.

37 ased linearly with the dietary proportion of alfalfa.

38 etition with alfalfa race aphids on bean and alfalfa.

39 d to the production of stay-green transgenic alfalfa.

40 forage to obtain four dietary proportions of alfalfa (0%, 25%, 50% and 75%) for 98 days on average be

41 romoter-reporter genes when transformed into alfalfa, a heterologous legume, showed significant induc

42 mylase mRNA levels were measured in roots of alfalfa after defoliation, in suspension-cultured cells

43 clover sequence, and 4-year corn-soybean-oat/alfalfa-alfalfa sequence.

44 a 4-yr rotation (maize-soybean-small grain + alfalfa-alfalfa) managed with lower synthetic N fertiliz

45 AR) pea aphids on broad bean, red clover and alfalfa alone.

46 tely required for S. meliloti symbiosis with alfalfa and also for the protection of the bacterium fro

47 ol of the CaMV promoter, both the transgenic alfalfa and Arabidopsis lines exhibited dramatic alterat

48 elated with development of lateral roots (in alfalfa and Arabidopsis) and symbiotic nodules (in alfal

49 te compound leaf development, are present in alfalfa and are still sensitive to KNOX1 regulation.

50 AR suffered fitness loss on both alfalfa and bean in apparent competition with CR on clov

51 n in a more complex agricultural mosaic with alfalfa and broad bean, a second experiment was conducte

52 lays a crucial role in the symbiosis between alfalfa and its symbiont Sinorhizobium meliloti.

53 ally processed Hg) in leaves of both plants (alfalfa and M. vulgare) was similar, in spite of the big

54 nine analog, produced in large quantities by alfalfa and other legumes.

55 rpin in the antifungal defense mechanisms of alfalfa and other legumes.

56 into Arabidopsis to demonstrate that, as in alfalfa and pea, PsUGT1 expression occurs in regions of

57 their capacity to use the legume crops pea, alfalfa and red clover, respectively, were analysed, and

58 ng intracellular symbiont in root nodules of alfalfa and related legumes.

59 i is a nitrogen-fixing bacterial symbiont of alfalfa and related legumes.

60 In response to caterpillar herbivory, alfalfa and related plant species defend themselves thro

61 is required for invasion of root nodules on alfalfa and successful establishment of a nitrogen-fixin

62 methylation step in S lignin biosynthesis in alfalfa and that there is redundancy with respect to the

63 chemical and structural properties of Tulsi, Alfalfa and two varieties of Manuka honey derived from m

64 owed that Hg accumulated at the root apex of alfalfa and was distributed through the vascular system

65 ssella, and Anaerolinea, was associated with alfalfa and zinc removal, and the inverse was found for

66 tutive CaMV 35S promoter in Medicago sativa (alfalfa) and Nicotiana tabacum (tobacco), we show that t

67 tems: Ncotiana benthamiana, Medicago sativa (alfalfa) and Nicotiana tabacum NT1 cells.

68 (alfalfa), and that MYB112 is targeted and downregulated

69 rs to be an over-simplification, at least in alfalfa, and additional enzymes may be needed for the 3-

70 le N consumption, N fixation by soybeans and alfalfa, and N yield by corn, soybeans, and pasture, alt

71 edia and fails to establish a symbiosis with alfalfa, and these defects can be rescued by the additio

72 We demonstrate that the alfalfa antifungal peptide (alfAFP) defensin isolated fr

73 ated leaves of six additional plant species: alfalfa, Arabidopsis, Brassica, cucumber, maize, and ric

74 events demonstrated here in the S. meliloti-alfalfa association may be widely important across many

75 Thus Sinorhizobium-alfalfa associations, which ultimately form symbiotic N(

76 bium meliloti and its leguminous host plant, alfalfa, bacterial nodulation (nod) genes are controlled

77 ation efficacy; and emergence synchrony with alfalfa bloom.

78 sential for developing molecular markers for alfalfa breeding.

79 o terminus, fixes nitrogen in symbiosis with alfalfa, but the plants cannot use this nitrogen for gro

80 CSDX1 was able to form nodules on alfalfa, but these nodules were not able to fix nitrogen

81 C4H), by sense or antisense expression of an alfalfa C4H cDNA.

82 ing of a poly(A)+ library from salt-tolerant alfalfa cells, encodes a novel protein with a Cys4 and H

83 increased by threefold on introduction of an alfalfa chalcone isomerase transgene.

84 ere not increased by expressing both IFS and alfalfa chalcone isomerase, but levels of flavonol conju

85 port here the three-dimensional structure of alfalfa chalcone reductase bound to the NADP+ cofactor a

86 simple laboratory communities of interacting alfalfa, chemical defense, armyworm caterpillars, and pa

87 The three-dimensional structures of alfalfa CHI complexed with different flavanones indicate

88 sed on the recently determined structure for alfalfa CHS, predicts significant effects on protein str

89 oumarins, being predominantly fodder plants (alfalfa, clover and some grasses) considered to be safe.

90 Alfalfa contains multiple IOMT genes, and closely relate

91 , isoflavone O-methyltransferase (IOMT) from alfalfa converts the isoflavone daidzein to 7-O-methyl d

92 el resource to develop anthracnose-resistant alfalfa cultivars and contributes to our understanding o

93 method to reanalyze the same autotetraploid alfalfa data and to conduct a simulation study.

94 gle-dose restriction fragment autotetraploid alfalfa data, and the performance is investigated throug

95 obium meliloti and its host Medicago sativa (alfalfa) depends on several signaling mechanisms, such a

96 t for embryogenesis, are required throughout alfalfa development.

97 ylase enzyme specific activity in transgenic alfalfa did not result in increased root exudation of or

98 in vivo in unchallenged leaves of transgenic alfalfa ectopically expressing IOMT.

99 Alfalfa expressing PsUGT1 antisense mRNA under the contr

100 Transgenic alfalfa expressing red clover PPO should prove an excell

101 Proteolysis in leaf extracts of alfalfa expressing red clover PPO1 was dramatically redu

102 essed red clover PPO proteins were active in alfalfa extracts as evidenced by o-diphenol-dependant ex

103 ule deer selected areas closer to forest and alfalfa for most periods during 2012, but selected areas

104 supplemented with different levels of fresh alfalfa forage to obtain four dietary proportions of alf

105 g Lygus hesperus Knight is a pest of cotton, alfalfa, fruit and vegetable crops, and potentially of s

106 encing of additional clones reveals that the alfalfa genome contains multiple CPSase II gene copies w

107 d much of this ancient gene structure in the alfalfa genome.

108 Twelve alfalfa genotypes that were selected for biomass under s

109 mechanism may lead to superior salt-tolerant alfalfa genotypes.

110 symbiosis between Sinorhizobium meliloti and alfalfa has been studied for over a decade, its function

111 um meliloti, the nitrogen-fixing symbiont of alfalfa, has the ability to catabolize myo-, scyllo-, an

112 the study, rice straw (RS, low-quality) and alfalfa hay (AH, high-quality) diets were fed to lactati

113 ddition of organic amendments in the form of alfalfa hay or alfalfa meal was also helpful in lowering

114 it offers the opportunity to produce premium alfalfa hay with a more greenish appearance.

115 reactor columns containing varying ratios of alfalfa hay, pine woodchips, and sawdust were analyzed o

116 BacA function are impaired in symbiosis with alfalfa host plants and display altered sensitivities to

117 s M. truncatula genes to be used directly in alfalfa improvement.

118 root hairs and forming infection threads in alfalfa in a manner similar to a wild-type strain.

119 l targets for improving drought tolerance in alfalfa in the future.

120 were enough to show disease symptoms in the alfalfa infection.

121 es for understanding the complex S. meliloti-alfalfa interactions which occur during symbiosis.

122 mino acid sequence information from purified alfalfa IOMT, we have isolated three full-length IOMT cD

123 e altered growth phenotype of reduced-lignin alfalfa is a direct result of changes in nodulation or n

124 lic acid 3/5-O-methyltransferase (COMT) from alfalfa is an S-adenosyl-L-Met-dependent O-methyltransfe

125 However, alfalfa is congeneric with the reference legume Medicago

126 iosis between S. meliloti and its plant host alfalfa is dependent on bacterial transcription of nod g

127 le that the Fix+ phenotype of agl mutants on alfalfa is due to these additional functions.

128 Alfalfa is economically the most important forage legume

129 xically, reverse genetic evidence implicates alfalfa isoflavone O-methyltransferase (IOMT) in the bio

130 n that plant by reducing the accumulation of alfalfa isoflavonoids in the bacterial cells.

131 AK631 to establish effective symbiosis with alfalfa, it must be able to synthesize a symbiotically a

132 Alfalfa leaf curl virus, identified here as a third capu

133 The alfalfa leafcutting bee (ALCB), Megachile rotundata F. (

134 sed IOMT-green fluorescent protein fusion in alfalfa leaves show that the operationally soluble IOMT

135 When transiently expressed in alfalfa leaves, green fluorescent protein (GFP) fusions

136 To analyze the functions of putative alfalfa lectin genes, lines of transgenic alfalfa plants

137 activity in root tips of selected transgenic alfalfa led to a 4.2-fold increase in root concentration

138 We grew alfalfa, lentil and soy in a hydroponic system amended w

139 lover, white clover, hairy vetch, mung bean, alfalfa, lentil, snow pea, and lupine, as well as from t

140 The C3H-deficient alfalfa lignins were devoid of beta-1 coupling products,

141 In stems of transgenic alfalfa lines independently downregulated in each of six

142 In addition, most of the transgenic alfalfa lines retained more than 50% of chlorophylls dur

143 SGR gene (MsSGR) was cloned, and transgenic alfalfa lines were produced by RNA interference.

144 nse down-regulation, we generated transgenic alfalfa lines with a range of differences in lignin cont

145 When constitutively expressed in transgenic alfalfa, M. truncatula or white clover, LAP1 induced mas

146 encoding 4-coumarate 3-hydroxylase (C3H) in alfalfa massively but predictably increased the proporti

147 on of cDNAs encoding five different forms of alfalfa MDH, including a plant cytosolic MDH (cMDH) and

148 nic amendments in the form of alfalfa hay or alfalfa meal was also helpful in lowering Se levels.

149 Transgenic alfalfa (Medicago sativa L. cv Regen) roots carrying gen

150 l molecule that enhances root respiration in alfalfa (Medicago sativa L.) and also triggers a compens

151 Tolerance of alfalfa (Medicago sativa L.) to animal grazing varies wi

152 The crystal structure of alfalfa (Medicago sativa L.) vestitone reductase has bee

153 s 1D1609, which was originally isolated from alfalfa (Medicago sativa L.), contains genes that increa

154 the first to the sixth internode in stems of alfalfa (Medicago sativa L.), preceding the deposition o

155 ion factor associated with NaCl tolerance in alfalfa (Medicago sativa L.).

156 dies of calcium spiking in M. truncatula and alfalfa (Medicago sativa) also uncovered the possibility

157 Alfalfa (Medicago sativa) and Arabidopsis were used as m

158 ons of these findings for the development of alfalfa (Medicago sativa) as a dedicated bioenergy crop.

159 uction of lignin levels in the forage legume alfalfa (Medicago sativa) by down-regulation of the mono

160 rs, a critical step during the nodulation of alfalfa (Medicago sativa) by S. meliloti.

161 monocot ryegrass (Lolium perenne) and dicot alfalfa (Medicago sativa) COMTs.

162 n Sinorhizobium meliloti and its legume host alfalfa (Medicago sativa) depends on the timely expressi

163 Its close relative alfalfa (Medicago sativa) is the most widely grown forag

164 Forage crops like alfalfa (Medicago sativa) lack both polyphenol oxidase a

165 T) in thale cress (Arabidopsis thaliana) and alfalfa (Medicago sativa) leads to strongly reduced lign

166 0 nmol g(-1) fresh weight) was engineered in alfalfa (Medicago sativa) leaves by constitutive express

167 ated compositional changes in two low-lignin alfalfa (Medicago sativa) lines with antisense down-regu

168 The behavior of Hg in alfalfa (Medicago sativa) plants grown under controlled

169 In contrast, alfalfa (Medicago sativa) plants, which have limited num

170 Expression of MtPAR in the forage legume alfalfa (Medicago sativa) resulted in detectable levels

171 Alfalfa (Medicago sativa) seed defensin, MsDef1, strongl

172 tubulin gene TubA1 in situ and in transgenic alfalfa (Medicago sativa) to explore its use as a probe

173 rements were used to construct an all-native alfalfa (Medicago sativa) transfer DNA vector that can b

174 pathway were independently downregulated in alfalfa (Medicago sativa) using antisense and/or RNA int

175 isms of uptake and distribution of silver in alfalfa (Medicago sativa) were quantified and visualized

176 Overexpression of a KNOX1 gene in alfalfa (Medicago sativa), a member of the IRLC, resulte

177 M. truncatula is a close relative of alfalfa (Medicago sativa), a widely cultivated crop with

178 thia suspensa), tobacco (Nicotiana tabacum), alfalfa (Medicago sativa), and soybean (Glycine max).

179 guminous plants such as pea (Pisum sativum), alfalfa (Medicago sativa), barrel medic (Medicago trunca

180 xceed efflux rates by 5% to 545% in roots of alfalfa (Medicago sativa), Medicago truncatula, maize (Z

181 dulate, Maackia amurensis Rupr. & Maxim. and alfalfa (Medicago sativa), produced pseudonodules after

182 x production and confer drought tolerance in alfalfa (Medicago sativa), the most important forage leg

183 ecretion and thereby enhance Al tolerance in alfalfa (Medicago sativa), we produced transgenic plants

184 attracted to seed exudates of its host plant alfalfa (Medicago sativa).

185 ene for engineering PAs in the forage legume alfalfa (Medicago sativa).

186 in promoting symbiosis with its host legume, alfalfa (Medicago sativa).

187 rogen-fixing symbiosis with its legume host, alfalfa (Medicago sativa).

188 er the control of a constitutive promoter in alfalfa (Medicago sativa).

189 m of GS (GS1) gene have been introduced into alfalfa (Medicago sativa).

190 of a plant CPSase gene (CPAII) derived from alfalfa (Medicago sativa).

191 cell production in pea had no such effect in alfalfa (Medicago sativa).

192 rassica napus), and somatic embryogenesis in alfalfa (Medicago sativa).

193 n the model legume Medicago truncatula or in alfalfa (Medicago sativa).

194 subgroup of the plant MAPKs, containing the alfalfa MMK3 and tobacco NTF6, are only active in mitoti

195 culation and purified as part of recombinant alfalfa mosaic virions.

196 c plants expressing the coat protein (CP) of alfalfa mosaic virus (AIMV) are resistant to infection b

197 Alfalfa mosaic virus (AlMV) coat protein is involved in

198 ced from the coat protein of trypsin treated alfalfa mosaic virus (AlMV), another bromovirus.

199 e, satellite tobacco necrosis virus RNA, and alfalfa mosaic virus (AMV) 4, were used in wheat germ in

200 s of two members of the Bromoviridae family, alfalfa mosaic virus (AMV) and cucumber mosaic virus (CM

201 Alfalfa mosaic virus (AMV) and ilarvirus RNAs are infect

202 tional switch model describing regulation of alfalfa mosaic virus (AMV) replication have been tested

203 The alfalfa mosaic virus (AMV) RNAs are infectious only in t

204 librium exists for the three genomic RNAs of Alfalfa mosaic virus (AMV).

205 (Pfs25-CP VLP) comprising Pfs25 fused to the Alfalfa mosaic virus coat protein (CP) and produced thes

206 engineered as translational fusions with the alfalfa mosaic virus coat protein and individually expre

207 Alfalfa mosaic virus genomic RNAs are infectious only wh

208 The crystal structure of an alfalfa mosaic virus RNA-peptide complex reveals that co

209 An alfalfa mosaic virus untranslated leader sequence and Ly

210 The alfalfa MsRH2-1 gene encodes a small protein with a RING

211 symbiosis between Sinorhizobium meliloti and alfalfa, mutations in GlnD, the major bacterial nitrogen

212 ear was not affected by refuges of melons or alfalfa near cotton fields.

213 izobial strains produced Nod factor from the alfalfa-nodulating strain, Sinorhizobium meliloti.

214 Alfalfa nodule invasion by S. meliloti can be mediated b

215 te conditions does not allow the invasion of alfalfa nodules.

216 with confirmed food vehicles were related to alfalfa or clover sprouts.

217 and 70 genes were up-regulated in leaves of alfalfa or M. truncatula, respectively, in response to c

218 es between individuals specialized to either alfalfa or red clover in order to perform both a biometr

219 Nitrogen-fixing nodules on plants such as alfalfa, pea and vetch arise from the root inner cortex

220 In forsythia and alfalfa, pith parenchyma cells next to the vascular cyli

221 tablishing a symbiotic relationship with the alfalfa plant (Medicago sativa).

222 Although antisense-expressing alfalfa plants did not show a significantly different ph

223 HCT down-regulated alfalfa plants exhibit a striking reduction in root grow

224 spension cultures derived from the antisense alfalfa plants exhibited a delay in cell cycle from 24-h

225 ve alfalfa lectin genes, lines of transgenic alfalfa plants expressing approximately half of the open

226 levels and growth in a series of transgenic alfalfa plants in which lignin biosynthesis has been per

227 is consistent with the fact that most of the alfalfa plants inoculated with the lsrB1 mutant were sho

228 Transgenic alfalfa plants were generated harboring caffeic acid 3-O

229 Transgenic alfalfa plants with increased cuticular waxes showed enh

230 Leaves of alfalfa plants with the CaMV 35S promoter-GS1 gene showe

231 resistance when transferred into susceptible alfalfa plants.

232 tion using SPL13 overexpression and silenced alfalfa plants.

233 cited a mixture of pink and white nodules on alfalfa plants.

234 d establishing a symbiotic relationship with alfalfa plants.

235 acetate compared with untransformed control alfalfa plants.

236 al both in pea hairy roots and in transgenic alfalfa plants.

237 he belowground organs (roots and nodules) of alfalfa plants.

238 usly showed that transgenic Medicago sativa (alfalfa) plants overexpressing microRNA156 (miR156) show

239 affordable, mass-produced nesting materials; alfalfa pollination efficacy; and emergence synchrony wi

240 based/organic inputs; three perennial crops (alfalfa, poplar, and conifers); and four unmanaged ecosy

241 A recurrent challenge to alfalfa production is the significant yield loss caused

242 the relative fitness on clover race (CR) and alfalfa race (AR) pea aphids on broad bean, red clover a

243 whether or not in apparent competition with alfalfa race aphids on bean and alfalfa.

244 agricultural mosaic on pea aphid clover and alfalfa races.

245 Columns amended with >10% alfalfa removed significantly more sulfate and zinc than

246 hat forms between Sinorhizobium meliloti and alfalfa requires biosynthesis of Nod factor, a beta-1,4-

247 Over-expression of UGT78G1 in transgenic alfalfa resulted in increased anthocyanin accumulation w

248 ined high-pressure frozen/freeze-substituted alfalfa root cap cells with electron microscopy/tomograp

249 Alfalfa root hair cells were impaled with intracellular

250 r example, applying 5 nM lumichrome to young alfalfa roots increased plant growth by 8% (P < 0.05) af

251 found that nodule-like structures formed on alfalfa roots only when the rhizobial strains produced N

252 Moreover, nodulation of transgenic alfalfa roots was delayed and partially inhibited, and s

253 Treating alfalfa roots with 3 nM lumichrome increased root respir

254 Alfin1 mRNA was found predominantly in alfalfa roots.

255 accompanied by their structural changes, in alfalfa roots.

256 provides significant opportunities to expand alfalfa's genomic toolbox.

257 acquisition of such knowledge is hampered by alfalfa's tetrasomic inheritance and outcrossing nature.

258 Our studies of alfalfa seed exudates suggested the presence of multiple

259 g LC-MS, we determined that each germinating alfalfa seed exuded QACs in the nanogram range.

260 ee (GF) cereal-based foods, GF cookies using alfalfa seed flour (ASF), at different substitution leve

261 n seven states having sprouters who received alfalfa seed from a specific lot.

262 urasian nonsocial pollinator transformed the alfalfa seed industry in North America, tripling seed pr

263 e studies also demonstrated that the wounded alfalfa seedling infection model is a useful tool to ide

264 D1, and its isogenic mutants were tested for alfalfa seedling infection.

265 mination and are also released from roots of alfalfa seedlings growing on artificial medium.

266 Alfalfa seedlings with or without apical buds were expos

267 Soaking alfalfa seeds in 5 nM lumichrome before germination incr

268 The SN-contaminated alfalfa seeds were distributed to multiple growers acros

269 Based on the MtSGR sequence, an alfalfa SGR gene (MsSGR) was cloned, and transgenic alfa

270 trated that the M. truncatula sgr mutant and alfalfa SGR-RNAi lines showed hypersensitive-response-li

271 hloem fibers in stems of forsythia, tobacco, alfalfa, soybean, and tomato (Lycopersicon esculentum).

272 Alfalfa sprout and lagoon water samples served as model

273 tios for the association between illness and alfalfa sprout consumption ranged from 5.0 to infinity (

274 A higher proportion of women than men ate alfalfa sprouts (3% versus 2%).

275 nity control subjects to report having eaten alfalfa sprouts in the 5 days preceding illness (41% [17

276 Alfalfa sprouts may be an elusive but important vehicle

277 uenchen infection associated with eating raw alfalfa sprouts was identified in Wisconsin.

278 und that elevated bank strength (provided by alfalfa sprouts) relative to the cohesionless bed materi

279 ever, new food sources such as leaf lettuce, alfalfa sprouts, and goat's milk have been identified, a

280 The SN was grown from seeds and alfalfa sprouts.

281 ade from unpasteurized milk, runny eggs, and alfalfa sprouts.

282 ates in the monolignol pathway in developing alfalfa stem extracts revealed activities in the order:

283 y versus 5-hydroxyferuloyl CoA is present in alfalfa stem internodes, in which relative O-methyltrans

284 re primarily localized to vascular tissue in alfalfa stems.

285 eases of grapevines, citrus, coffee, almond, alfalfa, stone fruits, landscape ornamentals, and native

286 19 cases and no controls recalled eating raw alfalfa-style sprouts in the 5 days before the patient's

287 are unable to form an optimal symbiosis with alfalfa, suggesting that these novel genes may play a gr

288 tant was also found to form pseudonodules on alfalfa that were delayed in appearance relative to thos

289 should facilitate the genetic improvement of alfalfa, the acquisition of such knowledge is hampered b

290 terium Rhizobium meliloti and plants such as alfalfa, the bacteria elicit the formation of nodules on

291 olletotrichum trifolii, a fungal pathogen of alfalfa, the mutationally activated oncogenic fungal Ras

292 In alfalfa, transcripts of seven SQUAMOSA-PROMOTER BINDING

293 In alfalfa, treating roots with 200 microm phenazine, 2,4-d

294 Alfin1 function was tested in transgenic alfalfa under the control of the 35S promoter in the sen

295 Systems analysis of two alfalfa varieties, Wisfal (Medicago sativa ssp. falcata

296 ng that MYB112 may be involved in regulating alfalfa vegetative growth.

297 nificance of the two classes of GS1 genes in alfalfa, we have utilized antisense gene constructs aime

298 Oat, red clover, and alfalfa were not treated with herbicides.

299 In stem extracts from transgenic alfalfa with antisense downregulated caffeoyl CoA O-meth

300 n threads was monitored after inoculation of alfalfa with red- or green-tagged bacteria.

301 tion score of 85.3% comparing lambs that ate alfalfa with those that did not.