ライフサイエンスコーパス: mutant lacking

1 Most importantly, an RNF126 mutant lacking 11 amino acids that is responsible for th

2 trate that expression of a priming-deficient mutant lacking 17 residues of the domain 3a hinge-loop (

3 chromatic regions, lose DNA methylation in a mutant lacking 22- to 24-nt sRNAs (dicer-like 2, 3, 4 tr

4 NleE mutants lacking (49)GITR(52) were unable to methylate TA

5 ough this result also occurred in a BPV-1 E2 mutant lacking a previously identified phosphorylation s

6 A DeltapstA1 mutant lacking a Pst phosphate uptake system component i

7 grow in co-culture with a G. sulfurreducens mutant lacking a trans-outer membrane porin-cytochrome p

8 In Arabidopsis mutants lacking a functional AtRbohD, the flg22-induced

9 Fungal mutants lacking a functional Fusarium (F)-RALF peptide f

10 own here to be impaired by as much as 35% in mutants lacking ABCB19, an ATP-binding cassette membrane

11 An S6K1 mutant lacking acetylation sites in its CTR shows enhanc

12 A B. bronchiseptica mutant lacking ACT produced more biofilm than the parent

13 In cv Pinot Noir, a red-berried grapevine mutant lacking acylated anthocyanins, Vv3AT contains a n

14 he present studies showed that the S. aureus mutant lacking adenosine production (adsA strain) increa

15 Mutants lacking AHR1 were defective in growth, alkaliniz

16 Cryptococcus HXS1 rendered the S. cerevisiae mutant lacking all 20 hexose transporters a high glucose

17 a phenotype similar to the one observed in a mutant lacking all 6 mce operons suggesting a pleiotropi

18 An APP mutant lacking all C-terminal lysines underwent the most

19 a1Deltalro1Deltaare1Deltaare2Delta quadruple mutant lacking all four triacylglycerol- and steryl este

20 By expression in a mutant lacking all LHCSR isoforms, residues Asp(117), Gl

21 Here, we report on the construction of a mutant lacking all monomeric LHC proteins but retaining

22 on and complementation of a L. monocytogenes mutant lacking all PrfA-regulated genes with PrfA* indic

23 a truncated, constitutively active PKC-zeta mutant lacking all regulatory domain elements and contai

24 cking either one of the TCS components and a mutant lacking all three genes behaved like the wild-typ

25 A Pseudomonas aeruginosa mutant lacking all three known iron acquisition systems

26 Knockout mutants lacking all EBs are viable and fertile and displ

27 In this study, we generated zebrafish mutants lacking all four zebrafish Mesp genes by using T

28 urface expression was rapidly lost, even for mutants lacking all known endocytosis motifs.

29 An alphaS deletion mutant lacking amino-acid residues 71-82 binds to membra

30 Complementation analysis of mutants lacking aminotransferases showed that the SDAP-A

31 A mutant lacking an ATP-binding cassette transporter exhib

32 Among 13 mutants screened, a mutant lacking an extracellular polysaccharide (EPS) loc

33 umbia-0, but is able to do so effectively in mutants lacking at least two of the four Arabidopsis DCL

34 e of rescuing hypomyelination in a zebrafish mutant lacking BACE1.

35 We generated a series of double mutants lacking BAM5 and each of the active plastidic en

36 A Flower mutant lacking binding sites for the endocytic adaptor A

37 stored by expression of GAB2 but not by GAB2 mutants lacking binding sites for its effectors phosphat

38 both catalases, as the survival of a double mutant lacking both CatB and CatP was lower than that of

39 ir spaces; reduced methylesterification in a mutant lacking both CGR-genes 2 and 3 (cgr2/3) resulted

40 In this study, we use a S. aureus mutant lacking both coagulases (Deltacoa/vwb) and dabiga

41 A double mutant lacking both EsxA and EsxB also induced increased

42 Most importantly, we demonstrate that a mutant lacking both of these proton pumps is conditional

43 SpoIIQ shows diffuse localization only in a mutant lacking both pathways.

44 PlcA, PlcB, or ActA grew normally, a double mutant lacking both PlcA and ActA failed to grow in wild

45 ion from the ava4025-vnfDGKEN promoter and a mutant lacking both VnfR1 and VnfR2 made the V-nitrogena

46 itivity is accentuated in a ytpB menA double mutant, lacking both known C35 -PP consuming enzymes, an

47 Remarkably, PLS3 mutants lacking both actin-binding domains were still ab

48 HSV mutants lacking both gE and US9 fail to properly assembl

49 We previously described HSV double mutants lacking both gE and US9 that failed to transport

50 We therefore created conditional mouse mutants lacking both GSK-3alpha and GSK-3beta in newly b

51 ms to be involved, since dpe2-1/phs1a double mutants lacking both PHS1 and the cytosolic DISPROPORTIO

52 t-synaptic currents are eliminated in double mutants lacking both scaffolds.

53 with either wild-type (WT) MV or an isogenic mutant lacking C protein expression (C(ko)) comparably i

54 ession of CYP716A75 in a Medicago truncatula mutant lacking C-28 oxidase activity partially complemen

55 We then constructed two deletion mutants lacking C-terminal regions and mutants with poin

56 Mutants lacking calcineurin, or its client CrzA, display

57 omal H2O2 production in Arabidopsis thaliana mutants lacking CATALASE2 (CAT2) activity (cat2-2).

58 Moreover, mutants lacking cereose germinated faster than the wild

59 ntact mice and changes in gait expression in mutants lacking certain types of commissural interneuron

60 A Chlamydomonas reinhardtii mutant lacking CGL71, a thylakoid membrane protein previ

61 An Arabidopsis ddcc mutant lacking CHH and CHG methylation does not affect s

62 creating Arabidopsis (Arabidopsis thaliana) mutants lacking combinations of starch synthases (SSs) S

63 st investigated whether adjustment occurs in mutants lacking components of the circadian clock or clo

64 e discovered that Corynebacterium glutamicum mutants lacking components of the pupylation machinery s

65 e data from beta2(KO) and beta2(TG) mutants, mutants lacking connexin isoforms, and also the age-depe

66 type yeast and of mss51, pet111, and pet494 mutants lacking Cox1p, Cox2p, and Cox3p, respectively.

67 n of aberrant supercomplexes in CcO assembly mutants lacking Cox2 or Cox4 subunits.

68 Expression of p120 catenin-truncated mutant lacking CRAD also delayed the recovery process af

69 istinct phototransduction systems, we tested mutants lacking CRY and mutants with disrupted opsin-bas

70 ponses to blue light significantly differ in mutants lacking CRY, as well as mutants with disrupted o

71 However, we find that FtsN mutants lacking cysteines give rise to filamentous growt

72 nse to impaired respiration was blocked in a mutant lacking cytochromes caa3 and bc and markedly redu

73 o independent cerk1 null mutants; a deletion mutant lacking D14L, and with D14L complemented as well

74 l B-cell development, whereas an Hdac3 point mutant lacking deacetylase activity failed to complement

75 By systematically imaging mutants lacking defined T4PM proteins or with individual

76 Arabidopsis (Arabidopsis thaliana) xxt1 xxt2 mutants lacking detectable xyloglucan are viable, they d

77 Interestingly, an MHV68 mutant lacking deubiquitinase (DUB) activity, embedded w

78 Furthermore, mutants lacking Dicer in gonadotropes displayed severely

79 Six CHFI mutants lacking different N- and C-terminal portions wer

80 Here we examined mutants lacking each of the major neurotransmitters in C

81 bound by protein VII during infection with a mutant lacking early region E4.

82 g in Chlamydomonas in 1995, the isolation of mutants lacking easily ascertained newly acquired phenot

83 Ribosome profiling of mutants lacking eIF4B or with impaired eIF4A or Ded1 act

84 Cre and Flp recombinase mutants lacking either arginine can be rescued by compen

85 Isogenic H. pylori mutants lacking either GGT or VacA are incapable of prev

86 Purified enzymes inhibit fungal growth and mutants lacking either GH18 grow normally on cellulose a

87 Moreover, Top3beta mutants lacking either its RNA-binding domain or catalyt

88 Interestingly, mutants lacking either one of the TCS components and a m

89 Targeted P. patens knockout mutants lacking either PpSMF1 or PpSCRM1 develop gametop

90 In addition, mutants lacking either SPN or SLO are significantly atte

91 s required the full-length Peg3 as truncated mutants lacking either the N-terminal SCAN domain or the

92 Mutants lacking either the SPR or its central ligand, my

93 Y. enterocolitica mutants lacking either the Ysa or Ysc T3SS were partiall

94 Mutants lacking elements of the stringent response - (p)

95 ression restores cholesterol export to yeast mutants lacking endogenous Pry1 and Pry2.

96 either BLOC-1 or Msb3, but it also occurs in mutants lacking endosome-vacuole fusion machinery such a

97 lost when Kir3.1 subunits were replaced by a mutant lacking essential sites for Gbetagamma-mediated a

98 r overexpressing ESV1 or LESV, and of double mutants lacking ESV1 and another protein necessary for s

99 we determined resection at IR-DSBs in WT and mutants lacking exonuclease1 or Sgs1 helicase.

100 countermeasures and that vaccination with a mutant lacking expression of the protein provides a plat

101 By using isogenic A. baumannii mutants lacking expression of virulence effector protein

102 hese results, together with our finding that mutants lacking fraD or the fra island are not attenuate

103 Plants of T-DNA insertion mutants, lacking FUM2, show marked differences in their

104 abolished by inhibiting DGK and in the rdgA mutant, lacking functional DGK, implicating DGK.

105 Mutants lacking functional Enok exhibited defects in the

106 Analysis of zebrafish mutants lacking functional Pten revealed that HSPCs colo

107 Inhibition of PI3K signaling in mutants lacking functional Pten suppressed hyperprolifer

108 Finally, a mutant lacking Fur and the Isc pathway increased suf exp

109 The mutant lacking galactofuranose exhibited a decreased gro

110 The hypersusceptibility of gshA and gshB mutants lacking gamma-glutamylcysteine and glutathione s

111 Furthermore, a mutant lacking genes encoding both the beta-glucosidase

112 Here we show that, unexpectedly, an Mtb mutant lacking GLPX grows on gluconeogenic carbon source

113 Overexpression of GspA in a mutant lacking gspA and srtA was lethal; conversely, cel

114 re rescued by wild-type FBH1, but not a FBH1 mutant lacking helicase activity.

115 JMJD1A (wild type or mutant lacking histone demethylase activity) bound to HU

116 Isogenic NTHI strain 86-028NP mutants lacking hktE and pdgX had increased susceptibili

117 nt strain efficiently outcompeted the double mutant lacking HMW1 and HMW2.

118 ts confirmed that Synechococcus sp. PCC 7002 mutants lacking hydrocarbons exhibit reduced thylakoid m

119 This prompted the construction of an MCMV mutant lacking ie611 but retaining the coding capacity f

120 scripts prompted the construction of an MCMV mutant lacking ie611 but retaining the coding capacity f

121 rp1 interactions, such that recombinant Drp1 mutants lacking insert B form a stable complex with Mff.

122 ISA1 homomultimer activity existed in mutants lacking ISA2.

123 induced liver fibrosis, we used a PPAR-alpha mutant lacking its DNA-binding-dependent activity on fat

124 nts rescued the replication defect of an HSV mutant lacking its NLS motif.

125 under conditions of oxidative stress and in mutants lacking key antioxidants.

126 hromes caa3 and bc and markedly reduced in a mutant lacking kinase KinB.

127 These results did not occur with 130b mutants lacking lbtU or lbtC, indicating that both endog

128 Mutants lacking LdhA and LdhD showed greatly reduced sur

129 The severest phenotype-observed in a mutant lacking Lhca4 (DeltaLhca4)-displayed a 69% reduct

130 S. aureus mutants lacking LTA are enlarged and show aberrant posit

131 We further show that mutants lacking lysosome-related organelles are defectiv

132 MCMV mutants lacking M45 or expressing C-terminally truncated

133 A CC9605 mutant lacking mccA1, mccA2, and the N-terminal domain o

134 ect can be mimicked with "melanin ghosts"; a mutant lacking melanin showed reduced platelet stimulati

135 nomenon was also observed in a Dictyostelium mutant lacking MidA (C2orf56/PRO1853/Ndufaf7), another C

136 h was mitigated upon co-expression of an Eos mutant lacking miR-17 target sites.

137 e flux, we generated conditional Cox10 mouse mutants lacking mitochondrial respiration in astrocytes,

138 As such, the mkp1 mutant lacking MKP1 displays enhanced PAMP responses and

139 Mutants lacking MltG were also shown to have longer glyc

140 A triple mutant lacking MYC2, MYC3, and MYC4, three basic helix-l

141 Infection of cells with a BTV mutant lacking NS4 results in increased synthesis of IFN

142 ramatic phenotype of the ntrc-trxf1f2 triple mutant, lacking NTRC and f-type Trxs, was also suppresse

143 Arabidopsis mutants lacking NTRC (ntrc) displayed a striking photosy

144 Furthermore, we found that a mutant lacking Nup107, a key NPC-specific component, phe

145 We investigated a deletion mutant lacking only this alpha-helix in stable cell line

146 and two affect virulence in vivo; and (iv) a mutant lacking ORF25 is highly attenuated but induces mo

147 ce of male mice for females is eliminated in mutants lacking oxytocin, a neuropeptide modulating soci

148 Mutants lacking p38 MAPK components pmk-1 or sek-1 resem

149 e overexpression of full-length IL1RAPL1 and mutants lacking part of C-terminal domains leads to simp

150 is effect is abolished when we overexpressed mutants lacking part of N-terminal domains, indicating t

151 tructs encoding PMCA4a, PMCA4b, and a PMCA4b mutant lacking PDZ binding rescued this phenotype of P4K

152 fluctuations are significantly diminished in mutants lacking peroxisome fission factors, leading us t

153 onuclear cells, while its isogenic nonmotile mutant lacking PF resulted in significantly diminished c

154 An RPA32 mutant lacking phosphorylation sites fails to recruit PR

155 A mitofusin (Mfn) 2 mutant lacking PINK1 phosphorylation sites necessary for

156 Mutants lacking plastid-encoded RNA polymerase-associate

157 ession and cell death were observed in clock mutants lacking proper CCA1 and LHY function.

158 nctional complementation of L. monocytogenes mutants lacking prsA2.

159 In comparison with the wild type, growth of mutants lacking Psb28-1 and Psb27, but not Psb28-2, was

160 Phenotypic characterization of mutants lacking PSB33 revealed reduced amounts of PSII-L

161 An S. aureus mutant lacking PSM expression exhibits a transcriptional

162 s Rad51 from undamaged sites on chromosomes; mutants lacking Rad54 accumulate nonrepair-associated co

163 ga and its role in assembly of RNAP, E. coli mutants lacking rpoZ (codes for omega) are viable due to

164 In mutants lacking Schwann cells, regenerating growth cones

165 trajectories, similar to what we observe in mutants lacking Schwann cells.

166 During IFS formation, mutants lacking SEP4 could produce reactive oxygen speci

167 histone H3 and RNA polymerase II (Pol II) in mutants lacking single or multiple cofactors to address

168 cued by adding back wild-type Nap1 but not a mutant lacking sites subject to posttranslational modifi

169 ore, A549 human lung cells infected with GAS mutants lacking SP-PTP displayed increased Ser-/Thr-/Tyr

170 Phenotypic analysis of GAS mutants lacking SP-PTP revealed that the phosphatase act

171 Mutants lacking SPCH do not produce stomata or lineages.

172 ft-right synchronous hopping-like pattern in mutants lacking specific neuron classes, and speed-depen

173 mice and the changes in coordination seen in mutants lacking specific neuron classes.

174 We found that isogenic mutants lacking SPN, SLO, and both toxins are equally im

175 mposition of cardiolipin is modified like in mutants lacking tafazzin.

176 Mutants lacking TAG or impaired of TAG hydrolysis show s

177 We show that pox-neuro (poxn) mutants lacking taste function in the legs and labial pa

178 he progressive neurological deficits seen in mutants lacking TBs; and 2) the insertional mutation in

179 t, an ORF2 nuclear localization mutant, or a mutant lacking the 5 protein kinase A or C phosphorylati

180 rnica multiple nucleopolyhedrovirus (AcMNPV) mutant lacking the antiapoptotic gene p35 (vAc(P35)) and

181 to the level of GAA knock-out mice, as did a mutant lacking the Atg8 family interacting motif (AIM) a

182 icked by the expression of a truncated OPHN1 mutant lacking the BAR domain, demonstrating that the BA

183 An Arg mutant lacking the C-terminal calponin homology actin-bi

184 A mutant lacking the C-terminal half of Hof1 displays miso

185 found that the deletion mutants and a double mutant lacking the C94-C111 and C95-C112 disulfide bonds

186 ITF1 expression and that the JA biosynthetic mutant lacking the CITF1- and SPL7-regulated genes, LOX3

187 ion with AtCBC: many changes observed in the mutant lacking the correct SERRATE activity were common

188 ely impaired when complementing with a TgADF mutant lacking the corresponding residue (Lys-68).

189 Expression of the p120-catenin truncated mutant lacking the CRAD in endothelial cells attenuated

190 on, as DCs expressing a high-mobility ICAM-1 mutant lacking the cytoplasmic domain exhibit diminished

191 in prt6, an Arabidopsis thaliana N-end rule mutant lacking the E3 ligase PROTEOLYSIS6 (PRT6).

192 ation, the full-length receptor (CD21=CR), a mutant lacking the entire cytoplasmic tail (CT), and a c

193 An LRIG1 mutant lacking the ErbB3 interaction motif was insuffici

194 We used this model to analyze a MHV-68 mutant lacking the expression of all miRNAs.

195 the role of GlcNAc metabolism using a triple mutant lacking the genes required to metabolize exogenou

196 An Arabidopsis mutant lacking the glucosyl-transferase, STARCH SYNTHASE

197 Furthermore, overexpression of Mag1 in a mutant lacking the H2A and H3 N-tails rescues base excis

198 relevant structures, because an A. fumigatus mutant lacking the hydrophobin protein induced stronger

199 In a dap160 rescue mutant lacking the interaction between Dap160 and synaps

200 TIS11d, the E220A mutant and the truncation mutant lacking the last two residues (D219/E220) were st

201 A mutant lacking the manganese-dependent superoxide dismut

202 tures of the cleaved form and of an inactive mutant lacking the membrane-spanning region.

203 An M. genitalium mutant lacking the MG491 segment corresponding to the pe

204 The production of small amounts of T4P by a mutant lacking the minor pilin operon was traced to expr

205 Loss of SNPH or expression of an SNPH mutant lacking the mitochondrial localization sequence r

206 KIF17 mutant lacking the motor domain translocated to nuclei a

207 that of the t-LM produced by a C. glutamicum mutant lacking the mptA gene, encoding a membrane alpha1

208 e, we address this issue by studying a HSV-1 mutant lacking the mucin-like domain in gC and the corre

209 A truncation mutant lacking the N terminus (DeltaN) was found to alte

210 Our complementation studies, using a mutant lacking the nitrate/proton symporter NasA from th

211 ith the N terminus of TAP, whereas an HDAg-L mutant lacking the NLS failed to interact with full-leng

212 Unexpectedly, a gp210/Nup210 mutant lacking the NPC-targeting transmembrane and C-ter

213 ve-attenuated herpes simplex virus 1 (HSV-1) mutant lacking the nuclear localization signal (NLS) on

214 A mutant lacking the oligomerization domain (53BP1(oligo))

215 le than that of Src, an effect lost in a Fyn mutant lacking the palmitoylation sites.

216 An R. solanacearum mutant lacking the pathogen's two extracellular nuclease

217 Notch2(DeltaPEST) allele expressing a Notch2 mutant lacking the PEST domain.

218 the sensors expressed in the wild type and a mutant lacking the PHOSPHATE TRANSPORT4;2 plastidic Pi t

219 In previous studies, an M. sedula mutant lacking the primary copper efflux transporter, Co

220 An E.coli mutant lacking the PROSC homolog (DeltaYggS) is pyridoxi

221 he M. mycoides subsp. capri wild type with a mutant lacking the proteolytic phenotype.

222 Infection with an HCMV mutant lacking the pTRS1 PKR binding domain resulted in

223 A MCMV mutant lacking the PVR inhibitor was attenuated in norma

224 ression was only detectable in a Tolypothrix mutant lacking the RcaE photoreceptor required for compl

225 Here, we show that an Arabidopsis mutant lacking the receptor-like kinase FERONIA (FER) sh

226 In this mutant lacking the Snf1-mediated positive feedback loop,

227 rion formation is particularly elevated in a mutant lacking the Sod1 Cu,Zn-superoxide dismutase.

228 the resistant line with the pmr4 disruption mutant lacking the stress-induced callose synthase PMR4

229 An ATRIP mutant lacking the SUMOylation sites fails to localize t

230 is inhibited in a Chlamydomonas reinhardtii mutant lacking the transcription factor Pi Starvation Re

231 both early and late in cells infected with a mutant lacking the UL13 protein kinase, (iv) ICP0 encode

232 nt increase in cAMP, which still occurred in mutants lacking the adenylate cyclases ACG or ACR, or th

233 Notably, PAO1 mutants lacking the alkB2 gene fail to form an elastic l

234 udies of the native translocation domain and mutants lacking the beta-hairpin and/or the alpha-helix.

235 Monarch mutants lacking the BMAL1 C terminus including the TAD e

236 Hypersensitivity of taf1 mutants lacking the C-terminal bromodomain to X-rays and

237 SAP11 mutants lacking the C-terminal domain were impaired in b

238 found to promote cry photoreduction even in mutants lacking the classic Trp triad electron transfer

239 absence of added phage or plasmid and since mutants lacking the CRISPR array or any one of the other

240 uide regenerating axons in vivo, we examined mutants lacking the deleted in colorectal carcinoma (DCC

241 SAP11 mutants lacking the entire N-terminal domain, including

242 HSV-1 but is degraded in cells infected with mutants lacking the genes encoding functional infected c

243 Mutants lacking the GLFG domain of Nup116 displayed decr

244 fective in cellulose synthesis and xxt1 xxt2 mutants lacking the hemicellulose xyloglucan, stomatal a

245 NA repeat with Reb1-binding sites, and using mutants lacking the histone H3K9 methyltransferase Clr4,

246 No strong phenotype of mutants lacking the hydrogenase has been found.

247 by CH25H can inhibit HCV replication, CH25H mutants lacking the hydroxylase activity still carry the

248 p38 MAPK components pmk-1 or sek-1 resemble mutants lacking the hypoxia response component and proly

249 Yeast mutants lacking the intracellular V-ATPase proton pump (

250 LI spheroplasts from mutants lacking the Lpp lipoprotein or PBP6 produced sph

251 However, MinE mutants lacking the MinE membrane-targeting sequence sti

252 inversely correlated to levels of miR398 in mutants lacking the miRNA, or transgenic plants overexpr

253 Mutants lacking the Mld proteins are severely attenuated

254 Truncation mutants lacking the motor region failed to localize to f

255 partially restored target gene regulation to mutants lacking the native p53RE.

256 athogen Candida albicans, deep sequencing of mutants lacking the orthologous protein, Zfs1, revealed

257 te residues, deletion of lpxE or eptA led to mutants lacking the P-Etn group, with consequently incre

258 vivo biofilm infections, we tested isogenic mutants lacking the pel, psl, and alg operons and showed

259 Using Arabidopsis (Arabidopsis thaliana) mutants lacking the peroxisomal CATALASE2 (cat2-2) that

260 We found that yeast mutants lacking the phosphatidylinositol 3-phosphate [PI

261 C was dependent on activation state, and (b) mutants lacking the phosphoregulatory domain could still

262 Disruption of degradosome assembly in mutants lacking the polynucleotide phosphorylase (PNPase

263 While mutants lacking the PrfA-dependent virulence factor PlcA

264 med lineage tracing experiments and analyzed mutants lacking the Prox1 transcription factor, a master

265 but they are not observed in sma-2 and sma-3 mutants lacking the R-Smads functioning downstream of th

266 s LMW PBPs is critical for bacterial growth; mutants lacking the related protein DacA-2 and/or homolo

267 r mutants, or their inability to bind EEs in mutants lacking the RNA-binding protein Rrm4, reduced ri

268 rvations had been made previously with maize mutants lacking the Rubisco biogenesis proteins RAF1 and

269 Arabidopsis thaliana mutants lacking the SS4 isoform of starch synthase have

270 Hence, we could select double mutants lacking the T-DNA already in the first offspring

271 In contrast, mutants lacking the TAD alpha-helix but retaining the mo

272 PSI mutants lacking the U1 snRNP-interacting domain (PSIDelt

273 Pathological Tau mutants lacking the vesicle binding domain still localiz

274 produced single-cell colonies of C. merolae mutants, lacking the PsbQ' subunit in its PSII complex b

275 A BubR1 mutant lacking these motifs is defective in MCC maintena

276 We assessed mutants lacking these glycans for expression and functio

277 l, psl, and alg operons and showed that PA14 mutants lacking these operons can successfully form biof

278 In Escherichia coli, mutants lacking these proteins often have no phenotype,

279 exogenous acids/bases rescue the reaction in mutants lacking these residues, can estimate these catal

280 cell entry between wild-type HCV and a viral mutant lacking this domain.

281 o wild-type Synechocystis PSII and a D1-D61A mutant lacking this hydrogen-bonding interaction demonst

282 A kinesin-5 mutant lacking this N terminus is enzymatically active,

283 gests these polysaccharides extracellularly, mutants lacking this ability are outcompeted.

284 ssible basis for the phenotypes of H. pylori mutants lacking this enzyme.

285 otably, experiments against Candida albicans mutants lacking those genes showed resistance to the com

286 almEFG and the polymyxin B MIC increased in mutants lacking toxRS or leuO Conversely, leuO overexpre

287 Ectopic expression of Oct4 or a mutant lacking transcriptional activity recapitulated de

288 ses included wild type C. elegans but also a mutant lacking two HS sulfotransferases (hst-6 hst-2), a

289 Mutants lacking UL128-131 replicate well on fibroblasts

290 and to function in virion envelopment, since mutants lacking UL37 accumulate capsids in the cytoplasm

291 Blue cone synaptogenesis increases in mutants lacking ultraviolet cones, and when transmitter

292 In C. elegans mutants lacking unc-75 or its targets, regenerating axon

293 Deletion mutants lacking up to five of the six pilin genes displa

294 Mutants lacking V-ATPase activity are avirulent and fail

295 ssion observed in vivo in intact mice and in mutants lacking V0V or all V0 CINs.

296 for IFIT1 restriction of a human coronavirus mutant lacking viral N1 methylation.

297 ab49DeltafbaA was compared to other isogenic mutants lacking virulence genes known to be disproportio

298 Unlike wild-type V. cholerae, mutants lacking wigR fail to recover following exposure

299 idate genes were expressed in an Arabidopsis mutant lacking XyG galactosylation, and two of them resu

300 contributor to carotenoid composition, with mutants lacking ZEP activity showing a remarkable 6-fold