ライフサイエンスコーパス: transgenic line

1 s when exposed to light, particularly in the transgenic line.

2 oid in the brain compared with either single transgenic line.

3 inct, brain region-specific profiles in each transgenic line.

4 s are able to generate plasmacytomas in each transgenic line.

5 sRNA appeared to be diverse in the different transgenic lines.

6 e labeling patterns from our newly generated transgenic lines.

7 titative PCR and beta-glucuronidase reporter transgenic lines.

8 -selective (heat-shock) promoters in several transgenic lines.

9 ate compared with the other single or double-transgenic lines.

10 domesticated and wild tomato species and on transgenic lines.

11 ing the interpretation of data from affected transgenic lines.

12 beling experiments were performed in petunia transgenic lines.

13 e mutants, and an inability to create stable transgenic lines.

14 decreasing PME activity as observed in CsF3H transgenic lines.

15 se of internode GA1 to modest levels for the transgenic lines.

16 pulation of diverse GFP-labeled cells across transgenic lines.

17 bidopsis thaliana) using promoter:LUCIFERASE transgenic lines.

18 s vulnerable to degradation in overexpressed transgenic lines.

19 ase activity was reduced by about 30% in the transgenic lines.

20 heir receptor activation mechanism in single transgenic lines.

21 Browser, a cellular resolution atlas of 264 transgenic lines.

22 n seven previously published Cre and CreERT2 transgenic lines.

23 ling and ablating RMs populations in several transgenic lines.

24 We utilized a transgenic LINE-1 mouse model and tracked DNA methylatio

25 From the 4 generated transgenic lines, 2 were selected for further analysis b

26 sis thaliana driven by the CaMV35S promoter (transgenic lines 35S-copC).

27 (QK) and wild-type (Wt) backgrounds to yield transgenic lines A2QK and A2Wt, respectively.

28 Instead, the transgenic lines accumulated a range of hydroxycinnamate

29 Moreover, transgenic lines accumulated the PhCHD substrate cinnamo

30 g rin, nor and Nr, and an ethylene-deficient transgenic line, ACS2-antisense.

31 UV mutagenesis of the psaA transgenic line allowed recovery of 5-FC-resistant, phot

32 We have thus generated a Xenopus laevis transgenic line allowing live imaging and conditional ab

33 ted concurrent generation and phenotyping of transgenic lines, allowing multiple lines to be assessed

34 We analyzed a YFP-COP1-expressing transgenic line and endogenous COP1 after subcellular fr

35 ertaking large-scale generation of mutant or transgenic lines and (v) new GBrowse tracks for transgen

36 ng constitutively expressing PEPR1 and PEPR2 transgenic lines and by analyzing pepr1 and pepr2 mutant

37 The transgenic lines and cis-regulatory constructs reported

38 t drought responses, we generated a range of transgenic lines and exploited the existing mutant plant

39 ete pollen control phenotype was achieved in transgenic lines and expressed stably over multiple year

40 pproaches are limited by the availability of transgenic lines and fluorescent protein combinations th

41 With new developments in transgenic lines and human-rodent chimeras, we anticipat

42 to drive gene expression in stable zebrafish transgenic lines and in mammalian cells.

43 formation from in-depth analysis of specific transgenic lines and independent peak identification val

44 Using specific transgenic lines and inhibitors, we determined that the

45 requirements of several sequences in stable transgenic lines and mutant lines with homozygous deleti

46 sive and time-consuming generation of stable transgenic lines and mutant populations - approaches lim

47 Phloroglucinol was produced in all transgenic lines and the line with the highest PhlD tran

48 in callose deposition between the resistant transgenic lines and the susceptible wild-type plants du

49 Advancing microscopy techniques, transgenic lines and well-characterized molecular marker

50 The converse was true for the hZnT8 WT transgenic line, and dietary Zn(2+) supplementation also

51 ase transcripts were decreased in fruit from transgenic lines, and aconitase activity was reduced by

52 For 880 tagged proteins, we created transgenic lines, and for a total of 207 lines, we asses

53 Using gene ontology, transgenic lines, and in situ hybridization, we found th

54 NtMYC2a increased leaf nicotine levels in T1 transgenic lines approximately 2.3-fold in greenhouse-gr

55 Thus, these subpallial enhancer transgenic lines are data and tool resources to study tr

56 ygen species was remarkably decreased in the transgenic lines as compared with the wild type plants.

57 lso observed in two different inducible AIL6 transgenic lines but not in 35S:ANT, suggesting that AIL

58 s decrease of anthocyanin production in some transgenic lines by down-regulating the expression of an

59 be performed in 1 d; generation of germline-transgenic lines by using this protocol takes approximat

60 rder to drive copC expression to the shoots (transgenic lines cab1-copC).

61 e with a tamoxifen-inducible Cre recombinase transgenic line, CAGGS-Cre-ER.

62 This transgenic line can be used directly to detect deficienc

63 scent protein, and therefore, we generated a transgenic line carrying secreted fluorescent protein an

64 abinosylation was increased by 25% to 30% in transgenic lines carrying either of the transgenes.

65 Analysis of transgenic lines carrying of truncated versions of the A

66 Twenty-seven independent transgenic lines carrying Tnt1 insertions were generated

67 treated milled biomass is nearly 90% for two transgenic lines, compared to only 25% for wild-type pop

68 leading to greater lignin content in the Lc transgenic lines, compared to the wild type.

69 alyses with tonoplast vesicles isolated from transgenic lines confirmed that single-transgenic lines

70 Notably, field tests with near-isogenic and transgenic lines confirmed that the japonica variety car

71 With established transgenic lines, consistent results were observed with

72 ISP2 was not detected in L. donovani, and a transgenic line constitutively expressing ISP2, displaye

73 nable arbuscule development in B. distachyon Transgenic lines constitutively overexpressing BdRAM1 sh

74 2) that influences WUE in Arabidopsis, using transgenic lines contrasting in MPK12 alleles, under fou

75 ne translational fusions and 123 Arabidopsis transgenic lines corresponding to 62 auxin-related genes

76 The PcIMT1-lines or the double transgenic lines (DC1) having PcINO1 and PcIMT1 introgre

77 d on the early stages of infection and using transgenic lines deregulated for the expression of RKS1,

78 pes resulting from AIL6 misexpression in the transgenic lines described here and those previously cha

79 Our analysis shows that one of the transgenic lines, despite overexpressing ThPOK compared

80 icted enhancers analyzed in stable zebrafish transgenic lines directed expression in the larval zebra

81 The transgenic lines displayed a number of changes that rese

82 We have now created barley transgenic lines downregulating the genes encoding the b

83 Lpar1(flox/flox) mice were crossed with cre transgenic lines driven by neural gene promoters for nes

84 ustoria formation was prevented in resistant transgenic lines during both types of powdery mildew inf

85 If explants are prepared from appropriate transgenic lines, dynamic behaviors of epicardial cells

86 The epitope-tagged transgenic line eliminates the need for the self-reporti

87 While transgenic lines emitted dimethyl sulfide from leaves an

88 ificant problem with a widely used Chat(Cre) transgenic line ensures that this map does not contain e

89 For all EGR and MASP1 mutants and transgenic lines examined, enhanced microtubule recovery

90 Metabolite profiling revealed that the transgenic lines exhausted their carbohydrates during th

91 Interestingly, PaSOD and dual transgenic lines exhibit enhanced lignin deposition in t

92 The transgenic lines exhibit unique effects in proteostasis.

93 acid composition was altered; however, these transgenic lines exhibited decreased fertility.

94 sis have been conducted using mutants and/or transgenic lines exhibiting fairly severe meiotic phenot

95 ative rounds of genome-editing we generate a transgenic line expressing P. vivax Duffy binding protei

96 overexpressed Arabidopsis WRI1 in seeds of a transgenic line expressing the castor fatty acid hydroxy

97 human spleen but not lung fibroblasts of the transgenic line expressing the VIR14 protein.

98 Transgenic lines expressing a controllable form of Cre r

99 g fruit citrate levels, we analyzed fruit of transgenic lines expressing an antisense construct again

100 layed flowering were observed in Arabidopsis transgenic lines expressing an artificial miRNA target m

101 method was demonstrated by generating stable transgenic lines expressing beta-glucuronidase plus (GUS

102 isease symptoms of up to 70% was observed in transgenic lines expressing Bs2 with respect to non-tran

103 However, no transgenic lines expressing Cas9 have been developed for

104 Functional analysis of transgenic lines expressing either AtGPA1(S52C) or AtGPA

105 ow its utility by generating multiple stable transgenic lines expressing fluorescent proteins under s

106 Furthermore, analysis of transgenic lines expressing full-length tomato BRI1-Flag

107 Double-transgenic lines expressing Kras(G12V) with one of the t

108 Transgenic lines expressing luciferase in inflammatory c

109 tants exhibited no overt phenotype; however, transgenic lines expressing MYC5 fused to an SRDX (SUPER

110 e generated liver-specific, Tet-on-inducible transgenic lines expressing oncogenic Kras(G12V), RhoA,

111 ed local transcript analysis with the use of transgenic lines expressing tagged NRT1.1 proteins.

112 erase chain reaction, the authors identified transgenic lines expressing transgenes somewhat higher (

113 in cytoadherence, two Plasmodium falciparum transgenic lines expressing two variant proteins pertain

114 More importantly, by generating a WAP-tva transgenic line for expression of ErbB2 selectively in W

115 o function, we made multiple stable reporter transgenic lines for each enhancer in zebrafish.

116 ent species and then screening the resultant transgenic lines for phenotypes of interest.

117 of GFP allows the use of existing GFP-tagged transgenic lines for studies of dynamic processes in liv

118 iation that enabled a global analysis of all transgenic lines from the four independent experiments.

119 Analysis of a DR5 reporter transgenic line further suggested that cytokinin blocks

120 , AtDGAT1, AtLPCAT1 and AtPDAT1 genes in the transgenic lines further supported this conclusion.

121 and genomic data, including genes, alleles, transgenic lines, gene expression, gene function, mutant

122 rafish embryos enabled us to score 67 stable transgenic lines generated from an insertional mutagenes

123 For both transgenic lines, germline transcription of some H chain

124 l astrocytes in three mouse models of AxD, a transgenic line (GFAP(Tg)) in which the normal human GFA

125 These novel transgenic lines greatly expand the ability to monitor a

126 The hZnT8 R325W transgenic line had lower pancreatic [Zn(2+)]i and proin

127 From a single transgenic line harboring five Tnt1 transposon insertion

128 infected with oncogenic A. tumefaciens C58, transgenic lines harbouring the 2S2D::p50 construct indu

129 Transgenic lines harbouring the marker fused to a gene e

130 To date, nine CreER(T2) transgenic lines have been designed using the nestin pro

131 gene expression demonstrate that zmbri1-RNAi transgenic lines have compromised BR signaling.

132 r five photoperiods, three accessions, and a transgenic line, highlighting the plasticity of plant gr

133 similar to mammals, while live imaging using transgenic lines identified the developmental origins of

134 We used this transgenic line in an unbiased multiplex phosphoproteomi

135 They have been extensively studied in a transgenic line in which enhanced green fluorescent prot

136 FR failed to depress PDF1.2 mRNA levels in a transgenic line in which PDF1.2 transcription was up-reg

137 ganglion cells in the mouse retina, using a transgenic line in which these cells, called "W3", are l

138 ation in A. gambiae, resulting in homozygous transgenic lines in approximately 2-3 months.

139 lycine showed significant changes across all transgenic lines in comparison to wild-type plants.

140 of only a tiny fraction of the thousands of transgenic lines in existence have been discovered and r

141 Here, we use new fluorescent transgenic lines in the beetle Tribolium castaneum to sh

142 d lines showed improved growth, whereas only transgenic lines in the wild-type background showed incr

143 dent copy number measurements in independent transgenic lines in these crop species.

144 by establishing two additional sets of mouse transgenic lines in which DNA segments containing these

145 imed at improving our support for mutant and transgenic lines, including (i) enhanced mutant/transgen

146 Numerous homozygous transgenic lines increased biomass productivity by >40%

147 ype tomato fruits and, when overexpressed in transgenic lines, increased plastid number, area, and pi

148 nts, amiRNA lines and 35S:ERF overexpressing transgenic lines indicated that ERF102 to ERF105 have on

149 cytokinin signaling in ARR1 gain-of-function transgenic lines is associated with increased rates of p

150 tion events from a population of independent transgenic lines is desirable.

151 Although several transgenic lines label neural crest subpopulations, few

152 Transcriptomic analysis of transgenic lines misexpressing StCEN identifies early tr

153 ess the basis for such effects in individual transgenic lines, no common mechanism linking lignin mod

154 or Physaria fendleri were overexpressed in a transgenic line of A. thaliana producing C18-HFA, respec

155 these problems, we have adopted the use of a transgenic line of Arabidopsis (Arabidopsis thaliana) wh

156 ll line that was initiated from ovaries of a transgenic line of fish [Tg(gsdf:neo)] that expresses Ne

157 m cell (FGSC) cultures were generated from a transgenic line of fish that expresses Neo and DsRed und

158 By using a newly generated transgenic line of P. falciparum (PfGCaMP3) that express

159 In this work, we generated a transgenic line of zebrafish expressing a photoconvertib

160 In the present study, a transgenic line of zebrafish had been generated using a

161 We developed a transgenic line of zebrafish that expresses a red fluore

162 -system of binary gene expression to develop transgenic lines of Anopheles gambiae in which olfactory

163 n vivo context, we generated multiple stable transgenic lines of Arabidopsis (Arabidopsis thaliana) t

164 erformed genetic complementation analyses of transgenic lines of bacterial artificial chromosomes of

165 For this study, we have developed stable transgenic lines of chilli and tomato expressing CgCOM1-

166 The transgenic lines of F5H-amiRNA and C3H-amiRNA showed a r

167 filin1 in motor neuron disease, we generated transgenic lines of mice expressing human profilin1 with

168 zation of Q-satRNA was completely blocked in transgenic lines of Nicotiana benthamiana (ph5.2nb) that

169 ns to green fluorescent protein expressed in transgenic lines of rice (Oryza sativa).

170 Here, we generated transgenic lines of the chytrid Spizellomyces punctatus,

171 Stable overexpression transgenic lines of TX and TN genes in Arabidopsis produ

172 terning in a range of wild, domesticated and transgenic lines of wheat and Arabidopsis to show that m

173 s in the context of nociception, using novel transgenic lines, optogenetics, and calcium imaging in b

174 of LBD29, either in the dominant repression transgenic lines or in the transfer-DNA (T-DNA) insertio

175 nes (Os07g37920-RNAi) and 10 over-expressing transgenic lines (Os07g37920-OE), but none of them showe

176 ll usually be advantageous when creating new transgenic lines, our method for photoconversion of GFP

177 These transgenic lines outperform control plants when challeng

178 regulated by BZR1 in two independent tomato transgenic lines over-expressing BZR1-1D at four ripenin

179 Plants of four independent wheat transgenic lines overexpressing ca1pase showed up to 30-

180 his study, Arabidopsis wild-type (Col-0) and transgenic lines overexpressing PIP2;7 were used to inve

181 reduced in the rgl3-5 mutant and enhanced in transgenic lines overexpressing RGL3.

182 ith high-chill kiwifruit Actinidia deliciosa transgenic lines overexpressing SVP2 showing suppressed

183 Analysis of the transcriptome of transgenic lines overexpressing the tomato APPR2-Like ge

184 of StCEN accelerates tuber formation whereas transgenic lines overexpressing this gene display delaye

185 The transgenic lines produced flowers 16 months after transf

186 Among the transgenic lines produced, only Tg(RBD2/3*-HA)::RPE-cre:

187 thaliana) seeds 13 d post anthesis of three transgenic lines, producing varying levels of recombinan

188 m2(-/-) (T2(-/-)) mice to the PS19 human tau transgenic line (PS) to investigate whether loss of TREM

189 scently tagged PIP2;7 in TSPO-overexpressing transgenic lines resulted in patchy distribution of the

190 ilencing of MeAPL3 in cassava through stable transgenic lines resulted in plants displaying significa

191 The truncation in both transgenic lines results in deletion of the 3'-most enha

192 RT-qPCR analyses in transgenic lines revealed extremely low abundance of CgC

193 Molecular analysis of transgenic lines revealed stable integration of transgen

194 Molecular analysis of these transgenic lines revealed that Fv SOC1 activates Fv TFL1

195 Transgenic line rNAD-ME1 had 8%, and rPPDK1 had 5% of th

196 s) from B. braunii into wild-type plants and transgenic lines selected for high-level triterpene accu

197 effector in specific neurons; however, most transgenic lines show broad spatiotemporal and cell-type

198 The best peptide transgenic line showed improved agronomic performance re

199 While the PfRh2b deletion transgenic line showed no change in invasion pathway uti

200 Transcriptome profiling of a selected transgenic line showed the induction of genes in differe

201 MtROP9i transgenic lines showed a clear growth-reduced phenotype

202 The doubly transgenic lines showed a three-fold enhancement of isop

203 Transgenic lines showed delayed senescence and enhanced

204 * At the cellular level, all transgenic lines showed increased tolerance to arsenite

205 These transgenic lines showed no biomass penalty despite a 10%

206 pared to wild type plants, whereas RNAi:ERD4 transgenic lines showed reduced leaf number, leaf area,

207 The overexpressing transgenic lines showed significant increase in number o

208 Live imaging of these transgenic lines showed that Cftr is localized to the ap

209 Transgenic lines showed that they are more vulnerable to

210 overexpression of CER1-LIKE1 in Arabidopsis transgenic lines specifically impacted alkane biosynthes

211 leakage exhibited by OsCAF1B overexpression transgenic lines subjected to cold stress indicate that

212 Genome-wide expression analysis using transgenic lines suggested that miR858a targets a number

213 the variety 'Sunset', the progenitor of the transgenic line 'SunUp', and was accidentally carried fo

214 The transgenic lines support negative selection of antigen-s

215 Four homozygous transgenic lines (T4) expressing the mutant 1Ax1 gene (m

216 ons of the gut microbiome in two independent transgenic lines, termed APP(SWE)/PS1(DeltaE9) and APPPS

217 adult heart regeneration in the neural crest transgenic line, Tg(-4.9sox10:eGFP).

218 we show that heat-shock induction of a novel transgenic line, Tg(hsp70l:nkx2.5-EGFP), during the init

219 ere we report the development of a zebrafish transgenic line, Tg(igfbp5a:GFP), which faithfully repor

220 sed nearly 200% more fermentable sugars from transgenic lines than controls, which were not explained

221 o 60% fewer Rubisco active sites in the four transgenic lines than in the wild type.

222 evel of lignin associated pyrolysates in the transgenic lines than the control primarily when the enz

223 more continuous gluten matrix in the mutant transgenic lines than the one line mentioned-above.

224 one or both of the xanthophylls as well as a transgenic line that accumulates lutein via an engineere

225 To visualize memory traces, we created a transgenic line that allows for the comparison between c

226 y crossing myd animals to a recently created transgenic line that expresses LARGE selectively in diff

227 Using a novel transgenic line that labels the endodermal actin cytoske

228 Through the use of a transgenic line that misexpresses cdc25a, we show that t

229 To address these issues we generated transgenic lines that constitutively overexpressed a tru

230 irectly correlates with stress resistance in transgenic lines that ectopically express APT1.

231 pecies and some animal species, and obtained transgenic lines that exhibit phenotypic alterations.

232 n responder transgenes was tested using four transgenic lines that express Cre under tissue-specific

233 Transgenic lines that express forms of a conserved mamma

234 Here, we report the generation of multiple transgenic lines that express Nix under the control of i

235 As such, the Amelx-iCre transgenic lines that we developed may serve as a powerf

236 STATEMENT Due to differences in creation of transgenic lines, the pathological properties of the P30

237 cordings, and neurotransmitter typing in two transgenic lines, the widely used Gal4s1156t and the rec

238 Passage of transgenic lines through two different tissue culture tr

239 To investigate this, we created a transgenic line to ablate the epicardial cell population

240 e then bred these mice with the TNF-alphaglo transgenic line to develop a mouse model with salivary g

241 recombination activating gene (Rag)2:mCherry transgenic line to identify B cell development stages in

242 e and female mice of a doxycycline-inducible transgenic line to induce expression of constitutively a

243 In this study we use an Il-1beta fluorescent transgenic line to show that there is an early innate im

244 c neurons demonstrate the usefulness of this transgenic line to study novel roles of Nav1.8 beyond se

245 Here, we use transgenic lines to define the in vivo relevance of HDAC

246 e Arabidopsis thaliana ecotypes, mutants and transgenic lines to determine how control of VRN2 stabil

247 Here we use stable transgenic lines to evaluate the efficacies of xCas9 and

248 , and overall fertility were analyzed in the transgenic lines to evaluate the requirement of each exo

249 analyses with cytokinin-related mutants and transgenic lines to provide unequivocal evidence that cy

250 99.5% of the progeny following outcrosses of transgenic lines to wild-type mosquitoes.

251 from transgenic lines confirmed that single-transgenic lines TVP1cl19 and TNHXS1cl7 had greater H(+)

252 Growing the transgenic lines under different nitrogen regimes indica

253 such improvement was observed for the SeCspB transgenic lines under field conditions.

254 f the toxic metabolite, methylglyoxal in the transgenic lines under non-stress and stress (drought an

255 Transgenic lines underproducing abscisic acid, with lowe

256 ESSOR1-yellow fluorescent protein (BES1-YFP) transgenic line was developed that showed BR-inducible B

257 th the brown and milled rice grains from the transgenic line was substantially equivalent to that of

258 tritional value and/or energy density of the transgenic lines was increased by ectopic expression of

259 Using a P0-inducible transgenic line, we observed that AGO1 degradation is bl

260 with a Cdh2 tandem fluorescent protein timer transgenic line, we observed that Cdh2-EGFP molecules ap

261 ever we observe phenotypic changes in a TF's transgenic lines, we are always eager to identify its ta

262 In both transgenic lines, we found fewer proprioceptive sensory

263 Utilizing novel transgenic lines, we identified support cell populations

264 By characterizing these transgenic lines, we showed that agrp1-expressing neuron

265 Transgenic lines were analyzed for the production of PG

266 All 4 Amelx-iCre transgenic lines were bred with ROSA26 reporter mice to

267 For each construct, five independent transgenic lines were characterized phenotypically and g

268 elopmental defects in the highest expressing transgenic lines were consistent with the inhibition of

269 0 or 200 mM) treated PDH45 overexpressing T1 transgenic lines were lower as compared to wild type (WT

270 CD79 transgenic lines were made by linking the promoter and u

271 used in the plasmid construction, but seven transgenic lines were obtained with a genetic constructi

272 assays on leaves and fruits showed that the transgenic lines were resistant to anthracnose disease-c

273 nd disulfide groups in gluten of the mut1Ax1 transgenic lines were significantly increased.

274 oter were isolated, and mct8 promoter-driven transgenic lines were used to show that, similar to huma

275 ficantly in the peel of both the control and transgenic lines when exposed to light, particularly in

276 Our results showed that transgenic lines, when exposed to Ag NPs and Ag(+) ions,

277 rvae) without the need to establish germline transgenic lines (which take 12-18 months).

278 MP signaling in HSC ontogeny, we have used a transgenic line, which inducibly expresses an inhibitor

279 was unaffected in the cones of the XOPS-mCFP transgenic line, which lacks rod photoreceptors.

280 quitous and tissue-specific luciferase-based transgenic lines, which we have termed zebraflash, that

281 In transgenic lines, which were generated using the ortholo

282 We generated a transgenic line whose macrophages expressing tumour necr

283 This transgenic line will facilitate high-throughput genetic

284 In this study, we crossed a Pina-expressing transgenic line with a 1Ax1-expressing line of durum whe

285 Here we use a transgenic line with a green fluorescent protein (GFP) e

286 Using CRISPR/Cas9, we created a transgenic line with a homozygous deletion of TpnC41C an

287 Here we utilise a transgenic line with fluorescent oenocytes to purify the

288 onic stem (ES) cells to generate a novel NOD transgenic line with the 77A/G SNP.

289 The gene-edited Dd2 transgenic line with the A578S mutation, which expresses

290 gamma2a genes is at wild type levels for the transgenic line with the larger truncation, but at reduc

291 er truncation, but at reduced levels for the transgenic line with the smaller truncation.

292 ter physiological and biochemical results in transgenic lines with a low level of ROS, MDA and ion ac

293 Transgenic lines with altered PHYB1 and/or PHYB2 express

294 milar to levels in ham1ham2 RNA interference transgenic lines with decreased expression of acetyltran

295 sion analysis following high-light stress in transgenic lines with perturbed AtWRKY40 and AtWRKY63 fu

296 Tobacco (Nicotiana tabacum) transgenic lines with reduced levels of ASR protein show

297 Arabidopsis RNAi transgenic lines with reduced mtPPT expression display t

298 In this study, we generated transgenic lines with simultaneous nfc101 and nfc102 dow

299 d was incorporated to triacylglycerol in the transgenic lines without significant changes in their le

300 The best-performing transgenic line yielded 12.3% higher average grain weigh