ライフサイエンスコーパス: loss-of-function mutant

1 vity, phenotypes not observed with the eIF4G loss of function mutant.

2 activated by NaCl are absent from the Atann1 loss-of-function mutant.

3 tion mutant of PLN, whereas R14del is a mild loss-of-function mutant.

4 truncated rhBARF1 from clone 16 rhLCV was a loss-of-function mutant.

5 (BL)-insensitive phenotype similar to a bri1 loss-of-function mutant.

6 an avirulent bacterial pathogen in the bap1 loss-of-function mutant.

7 utant than to either wild-type I domain or a loss-of-function mutant.

8 to photoperiod in a manner similar to a cdf loss-of-function mutant.

9 l in vivo, as they complemented a yeast GLXI loss-of-function mutant.

10 ity phenotype was similar to that of the AS2 loss-of-function mutant.

11 he striking abnormalities of lin-4 and let-7 loss of function mutants.

12 naling, and this effect is blocked in usp-46 loss-of-function mutants.

13 show an increase in Lys acetylation in srt2 loss-of-function mutants.

14 e Dlx1/2 mutant phenotypes, we made compound loss-of-function mutants.

15 enient and effective approach for generating loss-of-function mutants.

16 altered in MPK6 overexpression lines or mpk6 loss-of-function mutants.

17 ctase were increased in rfd1 and the AUX/IAA loss-of-function mutants.

18 ly predicts root growth, as observed in bri1 loss-of-function mutants.

19 and root apical meristems observed in fbl17 loss-of-function mutants.

20 redundancy was confirmed through analysis of loss-of-function mutants.

21 ted nutations were also eliminated in etr1-7 loss-of-function mutants.

22 s a permissive temperature for wild-type and loss-of-function mutants.

23 ethality that often occurs in both gain- and loss-of-function mutants.

24 what E2F actually does based on analyses of loss-of-function mutants.

25 ina can often complicate the analysis of CBP loss-of-function mutants.

26 f and floral organ production in stm partial loss-of-function mutants.

27 erous breed-specific non-synonymous SNPs and loss-of-function mutants.

28 fect of ethanol, equivalent to that of slo-1 loss-of-function mutants.

29 d trunk mesoderm, and closely resemble nodal loss-of-function mutants.

30 e may be of interest to restore transport in loss-of-function mutants.

31 nted the observation of strong phenotypes in loss-of-function mutants.

32 ns, R205X and E239X, were shown to be Dyrk1a loss-of-function mutants.

33 th pathways was confirmed by the analysis of loss-of-function mutants.

34 creased cell migration beyond canonical PTEN loss-of-function mutants.

35 ark respiration was observed in the eIFiso4G loss of function mutant, a reduction in chlorophyll leve

36 as a promoter, may be mutagenized to isolate loss-of-function mutants able to survive under selection

37 ality of AtCDA in vivo was demonstrated with loss-of-function mutants accumulating high amounts of cy

38 A previously described loss-of-function mutant affecting both isoforms, sr45-1,

39 Arabidopsis (Arabidopsis thaliana) quadruple loss-of-function mutant affecting p24 genes from the del

40 r show that removing MUL1 in PINK1 or parkin loss-of-function mutant aggravates phenotypes caused by

41 istant locomotory behavior, resembling slo-1 loss-of-function mutants, albeit to a lesser extent.

42 We show that the partial loss-of-function mutant alix-1 displays reduced vacuolar

43 entifying EMB genes and characterizing their loss-of-function mutant alleles are needed to understand

44 Biallelic loss-of-function mutant alleles underlie several differe

45 However, the NAD286G loss-of-function mutant also associated with the host fa

46 Through a combination of loss-of-function mutant analyses, genetic mapping, and t

47 A loss-of-function mutant analysis also revealed that sing

48 A combination of loss-of-function mutant analysis and protein interaction

49 of violaxanthin de-epoxidase in the eIFiso4G loss of function mutant and an increase in its xanthophy

50 Experiments using a C5a peptidase loss-of-function mutant and an intranasal infection mode

51 catula development by isolating the lfl/wox3 loss-of-function mutant and performing genetic crosses w

52 Accordingly, cells behave like a rad53 loss-of-function mutant and show reduced NHEJ efficiency

53 ogen insensitivity syndrome (AIS)-associated loss-of-function mutants and 168 prostate cancer-associa

54 Loss-of-function mutants and ectopic expression assays r

55 n of Pm5e was validated by transgenic assay, loss-of-function mutants and haplotype association analy

56 In car-1 loss-of-function mutants and in micu-1 overexpressing an

57 The stabilization of loss-of-function mutants and insensitivity of gain-of-fu

58 GR3, named CGR2, and evaluated the effect of loss-of-function mutants and over-expression lines of CG

59 Analysis of atprx71 loss-of-function mutants and plants overexpressing AtPRX

60 The combined use of cytochrome c (CYTc) loss-of-function mutants and respiratory complex III inh

61 validate genetic experiments performed with loss-of-function mutants and RNA interference (RNAi) lin

62 l fate and polarity, through the analysis of loss-of-function mutants and transgenic plants that ecto

63 riants conferring resistance to malaria are 'loss-of-function' mutants and appear to be recent polymo

64 isolated dominant-negative mutants, unc-108 loss-of-function mutant animals are defective in locomot

65 In Lrrk loss-of-function mutants, anterograde movement of GOPs w

66 n oncogene and neuroprotective protein whose loss-of-function mutants are associated with certain typ

67 propose that the pleiotropic effects of dbf loss-of-function mutants are associated with the require

68 nd phenotypes of blh6, knat7, and blh6 knat7 loss-of-function mutants are consistent with the existen

69 Because BOB1 loss-of-function mutants are embryo lethal, we used a pa

70 r in vitro and, therefore, the corresponding loss-of-function mutants are expected to be lethal.

71 d as having highly branched phenotypes, ccd1 loss-of-function mutants are indistinguishable from wild

72 Atga2ox9 loss-of-function mutants are more sensitive to freezing

73 imb-2 loss-of-function mutants are not viable; however, we ide

74 pment of the trophectoderm lineage and Eomes loss-of-function mutants arrest at implantation.

75 present study, several gain-of-function and loss-of-function mutants as well as engineered mutants o

76 CYTc loss-of-function mutants, as well as the d-LDH mutants,

77 Strong loss-of-function mutants assemble apolar intersecting mi

78 strates accelerated amyloidogenesis in Trem2 loss-of-function mutants at early stages, which progress

79 The method involves generation of partial loss-of-function mutants, at either buried or functional

80 eritability of Cas9 activity in heterozygous loss-of-function mutant backgrounds, to rapidly evaluate

81 er Myc mutants, MycDeltaMBIV is not a simple loss-of-function mutant because it is hyperactive for G2

82 We find that in dfer loss-of-function mutants beta-catenin is hypophosphoryla

83 axotomy, which is absent in ced-4 and ced-3 loss-of-function mutants but present in the ced-4(gf) mu

84 n of an AWC(ON) marker is initiated in nsy-7 loss-of-function mutants, but subsequently lost, so that

85 n wild-type maize and in the isogenic mop1-1 loss-of-function mutant by using Illumina's sequencing-b

86 action, we circumvented the lethality of keg loss-of-function mutants by silencing KEG using an artif

87 In DSAS-6 loss-of-function mutants, centrioles failed to close and

88 We report here characterization of a C-tail loss-of-function mutant, CF327A, and a related suppresso

89 have reduced FLC expression, but, unlike clf loss-of-function mutants, clf-59 mutants do not display

90 , although stomata of the Arabidopsis syp121 loss-of-function mutant close normally in ABA and high C

91 rs1-2 ers2-3 and triple etr2-3 ers2-3 ein4-4 loss-of-function mutants constitutively nutated in air.

92 ucose-fed conditions, the Arabidopsis sr45-1 loss-of-function mutant contains higher amounts of the e

93 Ddok loss-of-function mutant (Ddok(PG155)) germ-line clones p

94 ci appear to be "Myddosomes." The MyD88 S34Y loss-of-function mutant demonstrates how proper cellular

95 Here, we show that single luh loss-of-function mutants develop normal flowers, but lug

96 Zebrafish rad51 loss-of-function mutants developed key features of FA, i

97 We determined that Dh31 loss-of-function mutants (Dh31(#51)) showed normal rhyth

98 dip-2 loss-of-function mutants display a progressive increase

99 Intriguingly, gvs1 loss-of-function mutants display allele- and accession-d

100 We show that partial loss-of-function mutants display temperature-sensitive (

101 A cdf-2 loss-of-function mutant displayed impaired growth and re

102 bt2 loss-of-function mutants displayed a hypersensitive resp

103 jmj17 loss-of-function mutants displayed dehydration stress to

104 mtstmir loss-of-function mutants displayed impaired induction of

105 bhlh121 loss-of-function mutants displayed severe defects in Fe

106 The weak loss-of-function mutant dse1 exhibits pleiotropic phenot

107 activity, but they all appear to manifest as loss-of-function mutants due to defects in solubility, a

108 Here we show that in mef2ca(b1086) loss of function mutant embryos and early larvae, develo

109 Biochemical analysis of single FPGS loss-of-function mutants established that folate polyglu

110 -function ET receptor mutant, etr1-3, or the loss-of-function mutants etr1-7 and ers1-3 and the wild

111 Conversely, wdr-20 and wdr-48 loss-of-function mutants exhibit changes in locomotion b

112 associated with vascular tissues, while vup1 loss-of-function mutants exhibit collapsed morphology of

113 ted deletion of the cmpy locus and find that loss-of-function mutants exhibit excessive NMJ growth.

114 At elevated temperatures, dao loss-of-function mutants exhibit seizures associated wit

115 Frazzled loss of function mutants exhibited similar defects in sy

116 eIFiso4G loss of function mutants exhibited smaller cell, leaf, p

117 sleepless (sss) loss-of-function mutants exhibited altered Shaker locali

118 3 (GH43) family in Arabidopsis thaliana GH43 loss-of-function mutants exhibited root cell expansion d

119 the dominant act-5 mutation, or a recessive loss of function mutant, exhibited normal morphology and

120 similar to glh-1/glh-4(RNAi), the kgb-1(um3) loss-of-function mutant exhibits germline over-prolifera

121 root growth after Al exposure, because alt2 loss-of-function mutants fail to halt root growth after

122 at4, an At4 loss-of-function mutant fails to redistribute Pi to the

123 In a loss of function mutant for genes encoding PHR1 and PHL1

124 Here, the Arabidopsis loss-of-function mutant for annexin1 (Atann1) was found

125 In this study, we used loss-of-function mutants for each receptor isoform to de

126 This method can provide homozygous mammalian loss-of-function mutants for forward genetic application

127 In gain- and loss-of-function mutants for Gsx1 and Olig1/2, we observ

128 planta by feeding [(3)H]serine to the WT and loss-of-function mutants for OAS-TLs in the cytosol, pla

129 onfers increased Al tolerance similar to the loss-of-function mutants for the cell cycle checkpoint g

130 n the North American monarch butterfly using loss-of-function mutants for the circadian activators CL

131 dendrites mimic ALA axon guidance defects in loss-of-function mutants for the extracellular matrix mo

132 te this issue, we produced a complete set of loss-of-function mutants for the three annotated Arabido

133 Ultrastructural analyses of loss of function mutants further show that IFC-2 mutants

134 n297, Ala301, Phe307, and Tyr308 represented loss-of-function mutants; furthermore, the measurable re

135 l(2)tn, along with loss-of-function mutants generated for tn, showed no rel

136 d endoreplicating tissues in Drosophila gatA loss-of-function mutants grow slowly and never achieve w

137 UPR loss-of-function mutants, hac1Delta and ire1Delta, are a

138 Consistently, zat12 loss-of-function mutants had higher Fe content than the

139 The cpr1-2 (cpr30-1) loss-of-function mutant has constitutive defense respons

140 ment from fertilization, the cyp78a8 cyp78a9 loss-of-function mutant has reduced seed set due to oute

141 Chloroplasts prepared from fro7 loss-of-function mutants have 75% less Fe(III) chelate r

142 Loss-of-function mutants have a pleiotropic phenotype in

143 Both NUA and AtMAD2 loss-of-function mutants have a shorter primary root and

144 rte1 loss-of-function mutants have an enhanced ethylene respo

145 tory molecules is wide-ranging, however, few loss-of-function mutants have been identified in miRNA g

146 Because no loss-of-function mutants have been identified, the impor

147 ate earlier than the wild type, whereas etr2 loss-of-function mutants have increased sensitivity to A

148 msca1 loss-of-function mutants have reduced meristem size and

149 Instead, etr1 loss-of-function mutants have reduced sensitivity to abs

150 eproductive and social behaviors, yet rodent loss-of-function mutants have relatively subtle behavior

151 recordings identified the R215H mutant as a loss-of-function mutant in inducing GABAergic synaptogen

152 A loss-of-function mutant in Kif20b, magoo, was found in a

153 By screening for loss-of-function mutants in a Caenorhabditis elegans kil

154 natural ELF3 polyQ variants phenocopied elf3 loss-of-function mutants in a common reference backgroun

155 All three loss-of-function mutants in Arabidopsis (Arabidopsis tha

156 toperiod-dependent flowering in plants, with loss-of-function mutants in barley (Hordeum vulgare), le

157 Loss-of-function mutants in both homeologs of AP2L2 (hen

158 Generation of all major OAS-TL double loss-of-function mutants in combination with radiolabele

159 Loss-of-function mutants in dPIP4K show reduced body wei

160 In particular, pink1 and parkin loss-of-function mutants in Drosophila show similar phen

161 rgan defects and indeterminacy that resemble loss-of-function mutants in E-function floral organ spec

162 ies converge on similar causes for olfactory loss-of-function mutants in evolutionary transitions to

163 te that the phenotypes associated with novel loss-of-function mutants in EXO70, are entirely consiste

164 Here, we report single and higher-order loss-of-function mutants in members of the cation/proton

165 Loss-of-function mutants in one of the genes, designated

166 Loss-of-function mutants in PRC2 subunits initially deve

167 In this study, we isolated loss-of-function mutants in the Arabidopsis MIPS1 gene f

168 dent in the embryonic epidermis of zebrafish loss-of-function mutants in the cognate Matriptase inhib

169 Loss-of-function mutants in the corresponding genes had

170 Here, by generating and analyzing loss-of-function mutants in the liquid facets-Related (l

171 ole of tomosyn in neurosecretion we analysed loss-of-function mutants in the single Caenorhabditis el

172 utant hearts of heartstrings (hst), the tbx5 loss-of-function mutants in zebrafish.

173 rate that the gonadogenesis defects of gon-2 loss-of-function mutants (including a null allele) can b

174 psis resistance to Pst DC3000, whereas ADPG2 loss-of-function mutants increase the resistance to the

175 Importantly, genetic rescue by the loss-of-function mutant indicates that barbed-end bindin

176 tantly, the BIG signature was reduced in Bmp loss-of-function mutants, indicating Bmp-regulated targe

177 sion was drastically reduced in beta-catenin loss-of-function mutants, indicating that Wnt signaling

178 The AtSAP18 loss- of-function mutant is more sensitive to NaCl, and

179 The ABA hypersensitive phenotype of FyPP loss-of-function mutants is ABI5 dependent, and the amou

180 osmotic stress, while the growth of erf5erf6 loss-of-function mutants is less affected by stress.

181 h and show that their derepression in miR164 loss-of-function mutants is likely to account for most o

182 The ability of two loss-of-function mutants, L31A and L31C, of phospholamba

183 n wild-type (WT) STAT1 cells, as well as the loss-of-function mutants L706S and Y701C.

184 While elt-7 loss-of-function mutants lack a discernible phenotype, s

185 phenotype of the etr1-6;etr2-3;ein4-4 triple loss-of-function mutant line was examined.

186 Genomic profiling of H3K27me3 in loss-of-function mutant lines for Maize Enhancer of zest

187 importance of Nisch, here we generated Nisch loss-of-function mutant mice and analyzed their metaboli

188 In contrast to loss-of-function mutants, moderate overexpression of BLF

189 Using a loss-of-function mutant mouse lacking the guanylate kina

190 al prefrontal cortex (n = 21); and 4) a Nrg3 loss-of-function mutant (n = 59) to functionally implica

191 d-type FIT2, whereas FIT1 and a FIT2 partial loss-of-function mutant, N80A, had significantly lower t

192 ll three alleles are similar to those of the loss-of-function mutants obtained by RNA interference or

193 Leaf reticulation in the re and rer3 loss-of-function mutants occurred, along with accumulati

194 etion mutant of FOF2 (FOF2DeltaF), or double loss of function mutant of FOF2 and FOL1 (FOF2-LIKE 1) p

195 Loss of function mutants of BGD2 are acyanogenic in leav

196 Although single loss of function mutants of ELF3 and GI have been well s

197 (GBP) interact with the N terminus of GluTR Loss-of function mutants of ClpR2 and ClpC1 proteins sho

198 ants of AGL15, alone or when combined with a loss-of-function mutant of a closely related family memb

199 We generated a loss-of-function mutant of a coiled-coil domain containi

200 ressing bcl-xL, ced-9, and bcl-xL (G138A), a loss-of-function mutant of bcl-xL.

201 The loss-of-function mutant of BIN2 and its homologs, bin2-3

202 rel map development using barrelless mice, a loss-of-function mutant of calcium/calmodulin-activated

203 R9C is a complete loss-of-function mutant of PLN, whereas R14del is a mild

204 Co-expression of a loss-of-function mutant of polycystin-2 in CHO cells doe

205 We also studied the phenotypes of a loss-of-function mutant of Prosalpha6T generated by targ

206 The loss-of-function mutant of SR1IP1 is more susceptible to

207 We also found that a loss-of-function mutant of the CPD33 homolog in Arabidop

208 expression phenotypes in overexpression and loss-of-function mutants of 15 Arabidopsis A-type heat-s

209 Here we report that loss-of-function mutants of AGL15, alone or when combine

210 We also construct conditional loss-of-function mutants of AGO1 to allow transcript pro

211 , we generated double, triple, and quadruple loss-of-function mutants of all four members of the RWA

212 n content and vein density were increased in loss-of-function mutants of Arabidopsis MYC2, a suppress

213 scriptional machinery during leaf senescence Loss-of-function mutants of Arabidopsis thaliana were us

214 Loss-of-function mutants of AtPTPN were hyposensitive to

215 In midkine-a loss-of-function mutants of both sexes, Muller glia init

216 Because loss-of-function mutants of ftsZ(Bbu) might be lethal, t

217 we investigated the binding of A1 to GOF and loss-of-function mutants of GP Ibalpha with mutations in

218 Here, we generated loss-of-function mutants of Iduna to investigate its phy

219 We found that loss-of-function mutants of LecRKA4.2 and LecRKA4.3 exhi

220 Loss-of-function mutants of LOX6 were more attractive to

221 imilar to the rgi1/2/3/4/5 quintuple mutant, loss-of-function mutants of MPK3 and MPK6, MKK4 and MKK5

222 or P. patens and facilitates the creation of loss-of-function mutants of multiple genes from differen

223 Loss-of-function mutants of PALM1 develop dissected leav

224 Thus, loss-of-function mutants of PptH displayed antimicrobial

225 Loss-of-function mutants of rtp replicate this axonal pr

226 Using gain- and loss-of-function mutants of seven transcription factors

227 wed precocious flowering, whereas the triple loss-of-function mutants of SPL10 and its two homologous

228 cal neurons and impaired root hair growth in loss-of-function mutants of the ATL1 ortholog rhd3 in th

229 The loss-of-function mutants of the BON1 gene family, bon1bo

230 Loss-of-function mutants of the NOP2A candidate gene loc

231 Here, we analyzed loss-of-function mutants of the unicellular cyanobacteri

232 Loss-of-function mutants of these selected differentiall

233 Although loss-of-function mutants of UBP27 do not show obvious ph

234 Here we report the impact of an LCI1 loss-of-function mutant on growth and photosynthesis in

235 ysis of root phenotypes induced by gain- and loss-of-function mutants or in treatments with GLV-deriv

236 In addition to this loss of function, mutant p53 can have a dominant negativ

237 In mrg-1 loss-of-function mutants, pairing is compromised specifi

238 The loss of function mutant phenotype and localization of an

239 comprehensive dataset of 2,400 genes with a loss-of-function mutant phenotype in Arabidopsis.

240 silencing in Drosophila embryos resulted in loss-of-function mutant phenotypes for 43 genes, which i

241 or neurons - where it recapitulates expected loss-of-function mutant phenotypes.

242 GATA17, and GATA17L (GATA17-LIKE), based on loss-of-function mutant phenotypes.

243 tor mutant, myb57-2, closely phenocopied the loss-of-function mutant pin6-2.

244 an phenotypes reported in the literature for loss-of-function mutant plants.

245 In unc-6/netrin and unc-5 loss-of-function mutants, presynaptic components misloca

246 In the loss-of-function mutant pro(DeltaGRAS), all examined GA

247 to freezing temperatures, whereas Atga2ox10 loss-of-function mutants produce considerably more seeds

248 es as either a recessive gain-of-function or loss-of-function mutant protein, depending on signaling

249 NA (mtDNA) in Arabidopsis thaliana Gain- and loss-of-function mutants provided evidence for a role of

250 The RCAR7 loss-of-function mutant revealed no changes in ABA respo

251 Analysis of bhlh loss-of-function mutants revealed that the single bhlh m

252 fted onto PC synthase cad1-3 atpcs2-1 double loss-of-function mutant root tissues.

253 e intestine and interneurons and that ehbp-1 loss-of-function mutants share with rab-10 mutants speci

254 Loss-of-function mutants show an elongated hypocotyl und

255 AtSWEET2 sequesters sugars in root vacuoles; loss-of-function mutants show increased susceptibility t

256 Loss-of-function mutants show irregular, uncoordinated c

257 plants with defective CIA components, grxs17 loss-of-function mutants showed some degree of hypersens

258 scopy of isolated lipid droplets from cgi-58 loss-of-function mutants showed they contain triacylglyc

259 istent enhanced collagen binding whereas the loss-of-function mutants showed variable degrees of func

260 With the help of a mitochondrial SOD2 loss-of-function mutant, Sod2(n283), we measured the sen

261 Similar to unc-43, tir-1 and nsy-1 loss-of-function mutants, specific disruption of microtu

262 In sprouty loss-of-function mutants, splitting of gene expression d

263 on of a phoPR promoter-lacZ fusion in a scoC loss-of-function mutant strain grown in low-phosphate de

264 ant for Pan1p inhibition, and a pan1 partial loss-of-function mutant suppressed the temperature sensi

265 AURKC p.L49Wfs22 is a loss-of-function mutant that perturbs localization of th

266 In a tni partial loss-of-function mutant that was originally isolated bas

267 transferred into etr1-6;etr2-3;ein4-4 triple loss-of-function mutants that have constitutive growth i

268 In unc-89 loss-of-function mutants that lack the SH3 domain, param

269 We identified 18 presumed loss-of-function mutants that reduced the growth of the

270 Moreover, in such loss-of-function mutants the levels of acetylated H4K5,

271 We used the soc1ful loss of function mutant - the woodiest genotype known in

272 fies cytosolic pH and NO(3) (-) In an AtCLCa loss of function mutant, the cytosolic acidification tri

273 In syd-2 loss of function mutants, the normal polarized localizat

274 alt2-1 and atr loss-of-function mutants, the latter of which affects th

275 In SAC gain- and loss-of-function mutants, the levels of PtdIns monophosp

276 Furthermore, we show that in cftr loss-of-function mutants, there is a deficiency of larva

277 ction of secondary roots are impaired in the loss-of-function mutant, thus identifying AtANN1 as a ke

278 as in vivo physiological studies in an LCI1 loss-of-function mutant to reveal the C(i) species prefe

279 Here, we use loss-of-function mutants to show that RNA polymerase II

280 The TPC1-loss-of-function mutant tpc1-2 does not respond to elect

281 BRG1 loss-of-function mutant tumours respond to EZH2 inhibiti

282 ues the late-flowering phenotype of the gi-2 loss-of-function mutant under both short-day and long-da

283 erences in germination between etr1 and etr2 loss-of-function mutants under salt stress could not be

284 By analyzing an rdr2 loss-of-function mutant using two different parallel seq

285 Consistent with these results, a Col-0 rfo1 loss-of-function mutant was more susceptible to f. matth

286 An atfs-1 loss-of-function mutant was partially resistant to the e

287 The enhanced resistance in the loss-of-function mutants was associated with increased i

288 Using the EXORIBONUCLEASE4 (XRN4) loss-of-function mutant, we showed that XRN4 poly(A(+))

289 Using gain- and loss-of-function mutants, we demonstrate that acetylatio

290 Through an extensive analysis of loss-of-function mutants, we demonstrate that the Arabid

291 ting them in the respective four Arabidopsis loss-of-function mutants, we experimentally proved that

292 Using RNA interference (RNAi) to generate loss-of-function mutants, we show dramatic defects in ce

293 pressed AtLTPI-4 Crown galls of the atltpI-4 loss-of-function mutant were much smaller compared with

294 cumulation in wild-type roots, whereas Atao1 loss-of-function mutants were unresponsive to the hormon

295 psis plants expressing HaRxL44 and in med19a loss-of-function mutants, whereas SATI is elevated in pl

296 s found in the arr1-3 arr10-5 arr12-1 triple loss-of-function mutant, which showed almost complete in

297 In contrast to the loss-of-function mutant with large embryo and small endo

298 The isolation of loss-of-function mutants with enhanced disease susceptib

299 this function was only apparent when double loss-of-function mutants with pp2ca-1/ahg3 were generate

300 evelopmental processes in situ by generating loss-of-function mutants within otherwise wildtype tissu