ライフサイエンスコーパス: wild-type level

1 al loci marked with those arrays back to the wild-type level.

2 ral RNA accumulation to ca. 20 to 50% of the wild-type level.

3 activity of the high fidelity mutant to the wild-type level.

4 d the presence of Gap1 for expression at the wild-type level.

5 seed TAG, accumulating only one-third of the wild-type level.

6 normalized most neurochemical alterations to wild-type level.

7 values that equal or exceed the uninhibited wild-type level.

8 he mass of (glyco)sphingolipids persisted at wild type levels.

9 ed surface expression of SERT-R152E/E615K to wild type levels.

10 ore the growth of ethylene-treated eer5-1 to wild-type levels.

11 undant serum proteins to be restored towards wild-type levels.

12 sistance and elevated ROS phenotypes back to wild-type levels.

13 stored the esterification ratio of pectin to wild-type levels.

14 t reestablished Caco-2 invasive phenotype to wild-type levels.

15 inding is required for Ro60 to accumulate to wild-type levels.

16 blocked in vivo, the viral load returned to wild-type levels.

17 type revA gene restored heart infectivity to wild-type levels.

18 s gland size and function can be restored to wild-type levels.

19 roduce biofilms, a DeltaluxS mutant produced wild-type levels.

20 ltures, which restored osteoclastogenesis to wild-type levels.

21 llenge phase restored airway inflammation to wild-type levels.

22 nce to fibronectin, and biofilm formation to wild-type levels.

23 therapeutic agents MYOM3 was restored toward wild-type levels.

24 ic and fibrotic volume and decreased cAMP to wild-type levels.

25 malized the observed adverse effects back to wild-type levels.

26 ue the clotting phenotype in knockin mice to wild-type levels.

27 ficient phenotype of gcbA mutant biofilms to wild-type levels.

28 mutants were reversed; both were restored to wild-type levels.

29 rmination codon restores translation to near wild-type levels.

30 ith inactivation of gcbA in P. aeruginosa to wild-type levels.

31 mbled AChR expressed in HEK cells to 138% of wild-type levels.

32 nitor stages consistently remained less than wild-type levels.

33 e expression signature of the Tg2576 mice to wild-type levels.

34 without restoring single-channel activity to wild-type levels.

35 educed naringenin and increased flavonols to wild-type levels.

36 ophe, but only when RNA recombination was at wild-type levels.

37 of bb0238 expression restored infectivity to wild-type levels.

38 /-) B cell proliferation was reduced to near wild-type levels.

39 found in the mdx mouse was reduced almost to wild-type levels.

40 , and tumor numbers were returned to near to wild-type levels.

41 sult of expressing motor-deficient NMII-B at wild-type levels.

42 tored antimicrobial tolerance of biofilms to wild-type levels.

43 of replication in Atr-deleted cells to near wild-type levels.

44 1 expression and hepatocyte proliferation to wild-type levels.

45 n and, surprisingly, restored P(TSA2)-GFP to wild-type levels.

46 c activity and cytotoxicity levels to nearly wild-type levels.

47 ce to killing by bactericidal antibiotics to wild-type levels.

48 hown to restore CHM mRNA transcripts to near wild-type levels.

49 ODA10p is present on oda8-mutant flagella at wild-type levels.

50 block, and restoration of prozyme protein to wild-type levels.

51 zation levels of the yfiR deletion mutant to wild-type levels.

52 ores the active and repressive marks to near wild-type levels.

53 s of hmp-1(fe4) that revert actin binding to wild-type levels.

54 restored sporulation and solventogenesis to wild-type levels.

55 ckground and restores pathogen resistance to wild-type levels.

56 adherence ability of the strain recovered to wild-type levels.

57 rulence and insect epicuticle germination to wild-type levels.

58 estores DeltaF508 maturation and function to wild-type levels.

59 n vitro cMyBPC reconstitution was similar to wild-type levels.

60 ene expression and genome synthesis occur at wild-type levels.

61 toration of the protein molar ratios to near-wild-type levels.

62 restored body weights of R236H mice to near wild-type levels.

63 197 in bamD restore Bam complex function to wild-type levels.

64 s of several proteins in the bba34 mutant to wild-type levels.

65 replication capacity from <5% to >/= 70% of wild-type levels.

66 f mice expressing GRK1 at 0.3- to 3-fold the wild-type levels.

67 sigV mutant restores lysozyme resistance to wild-type levels.

68 copy of the asd gene, growth was restored to wild-type levels.

69 that restore susceptibility to pathogens to wild-type levels.

70 he checkpoint and returns chromosome loss to wild-type levels.

71 pk3-dependent phosphorylation events to near wild-type levels.

72 ochondrial fusion reduces their lifespans to wild-type levels.

73 e Deltarel DeltarelQ [(p)ppGpp(0)] strain to wild-type levels.

74 ared with CD22(-/-) B cells, although not to wild-type levels.

75 aneuploid gene expression is shifted towards wild-type levels.

76 very of hearing and balance behavior to near wild-type levels.

77 R production and cellular c-di-GMP levels to wild-type levels.

78 ADH dehydrogenase brought ROS levels back to wild-type levels.

79 enic phenotypes are unexpectedly restored to wild-type levels.

80 , motor function and lifespan of the mice to wild-type levels.

81 ically expressed GPC to approximately 20% of wild-type levels.

82 xpression of BLF1 decreases leaf width below wild-type levels.

83 tility, and sperm motility was reimproved to wild-type levels.

84 ransgenic G2019S-LRRK2 mice returned back to wild-type levels.

85 cells restored selectin ligand expression to wild-type levels.

86 -GFP assembles into the dynein 1b complex at wild-type levels.

87 tly assembled and accumulates to only 50% of wild-type levels.

88 C110 restored all phenotypic changes back to wild-type levels.

89 roduce biofilms, whereas CN3685Deltacpb made wild-type levels.

90 red for restoring some phospholipids to near-wild-type levels.

91 double PTAP/PPEY L-domain deletion mutant to wild-type levels.

92 te several lytic cycle mRNAs and proteins at wild-type levels.

93 KII(T286A) mice, but could be established at wild-type level after repeated withdrawals.

94 and reduced shoot Cl(-) and Na(+) content to wild-type levels after growing plants in 50 mm NaCl.

95 stored mitochondrial and cardiac function to wild-type levels after reperfusion.

96 double mutants restored dopamine response to wild-type levels, also suggesting that tight regulation

97 vity, as ibrutinib treatment restored pS6 to wild-type levels, although Btk protein and phosphorylati

98 ne protein P-selectin is expressed at 48% of wild-type levels and externalized upon platelet activati

99 as unexpectedly increased by 40% above basal wild-type levels and inhibitors of apoptosis proteins we

100 rom treated eyes were more than one-third of wild-type levels and OS were well preserved in the injec

101 EN KO cells effectively lowers F2,6P2 to the wild-type levels and reduces their lactate production.

102 reduces Yap1 polypeptide abundance to nearly wild-type levels and, despite the continued Yap hypophos

103 B reduces Notch signaling in FA MPPs to near wild type level, and blocking either NF-kappaB or Notch

104 ants are approximately 2 logs lower than the wild-type level, and plaque diameter was significantly r

105 on in FLG-haploinsufficient keratinocytes to wild-type levels, and counteracted Th2 cytokine-mediated

106 0-null mutant HSV-1 plaque formation to near wild-type levels, and efficiently induced derepression o

107 n latd roots, restores MtRbohC expression to wild-type levels, and promotes an increase in cell lengt

108 Mecp2 KO neurons reduced mEPSC amplitudes to wild-type levels, and restored synaptic scaling down of

109 ead to H protein misincorporation, albeit at wild-type levels, and subsequently affect particle funct

110 henotypes for mutants that bound ephrinB2 at wild-type levels, and the mutant's cell-cell fusion phen

111 ycle arrest were found to proceed at or near wild-type levels, and there was no defect in transitioni

112 Wild-type levels are restored by photoreceptor-specific

113 ogenous mouse Tdp-43 was decreased to 20% of wild type levels as a result of disturbed feedback regul

114 ngly activated at low light, but returned to wild-type levels as irradiance was increased.

115 mutants, SlMYB12 transcripts accumulated to wild-type levels but exhibited the same truncation, whic

116 mice increased hepcidin expression to nearly wild-type levels, but a blunted increase of hepcidin was

117 itonitis between 3 and 24 h that returned to wild type levels by 96 h.

118 xTg-AD mice, mTOR activity can be reduced to wild type levels by genetically preventing Abeta accumul

119 ldup of internal GroPCho that is restored to wild type levels by reintegration of GDE1 into the genom

120 of active protein is stimulated to 61-71% of wild-type level by a feedback mechanism increasing trans

121 Nucleosome density was restored to wild-type level by re-expressing wild-type Lsh but not t

122 e in Flower-deficient CTLs and is rescued to wild-type level by reintroducing Flower or by raising ex

123 esponse in DBP(-/-) mice could be rescued to wild-type levels by administering exogenous DBP.

124 he stationary phase, which increased to near wild-type levels by coexpression of its neighboring gene

125 T-DNA knock-out mutant could be restored to wild-type levels by constructs expressing AtIPMDH1, AtIP

126 the IMP1-null fibroblasts can be restored to wild-type levels by IGF2 in vitro or by re-expression of

127 lin receptor-deficient mice were returned to wild-type levels by selective re-expression of the ghrel

128 the triple mutant in culture is restored to wild-type levels by supplementation with a variety of ir

129 t contains trace zinc; growth is restored to wild-type levels by supplementing medium with zinc but n

130 64A HCA II can be chemically rescued to near wild-type levels by the addition of the exogenous buffer

131 proinflammatory chemokines to approximately wild-type levels, concomitant with reduced IL-12Rbeta2 s

132 n of flavonol glycosides in pollen grains to wild-type levels, corroborating the requirement of FST1

133 adult animal after restoring D2 receptors to wild-type levels, demonstrating a remarkable degree of s

134 By P21, MBP expression was restored to wild-type levels, demonstrating that the loss of ERK2 re

135 nduced morbidity in Mmp10(-/-) recipients to wild-type levels, demonstrating that the protective effe

136 regulation by PfAP2-G is critical for their wild-type level expression.

137 transcriptional regulators are essential for wild-type-level expression of vapA, yet vapA expression

138 iption of the gamma1 and gamma2a genes is at wild type levels for the transgenic line with the larger

139 and synaptic function of gamma2(+/-) mice to wild-type levels for a prolonged period, along with anti

140 monstrated that reduction of SRSF6 to 50% of wild type levels had no effect on incomplete splicing in

141 ine, root growth of epi-lines is restored to wild-type levels, implicating hypermethylation in enhanc

142 f age, but significantly decreased below the wild type level in end-stage 4L;C* brains at 40 days.

143 ICOOH methyl ester was reduced to 12% of the wild-type level in AgNO3-challenged cyp71a12 leaves.

144 Depletion of NatB subunits to 30% of the wild-type level in three Arabidopsis T-DNA insertion mut

145 ses, but protease secretion reverted to near wild-type levels in a Deltavib-1 Deltaime-2 strain.

146 defect in vivo Colonization was restored to wild-type levels in a luxO opaR double mutant and was al

147 stored ATF6 knockout mouse heart function to wild-type levels in a mouse model of I/R, as did adeno-a

148 of ABCC6 was reduced to approximately 38% of wild-type levels in Abcc6+/- mice, no calcium deposits i

149 hich only express approximately 5% of ADAM17 wild-type levels in all tissues and show virtually no sh

150 er iron-limiting conditions, but reversed to wild-type levels in an Deltairr DeltarirA mutant.

151 hin gallate (green tea) was restored back to wild-type levels in ATPase and force measurements.

152 ice restores CFC-associated spine changes to wild-type levels in both the hippocampus and amygdala.

153 utant, but the repression can be restored to wild-type levels in complementation lines expressing pri

154 2A/B/D, CYCS, CAPNI) were normalised towards wild-type levels in Fiona animals.

155 mbers of effector and memory cells closer to wild-type levels in IFN-gamma-deficient mice and reduced

156 vely active MPK4 restored MEKK2 abundance to wild-type levels in mekk1 mutant plants.

157 e severity of joint swelling was restored to wild-type levels in mice infected with an arp mutant clo

158 higher and NK-cell cytotoxicity restored to wild-type levels in mice receiving the SAP vector in com

159 ant does not restore SGK1 phosphorylation to wild-type levels in mSIN1-deficient murine embryo fibrob

160 glucosinolate species down to 32 and 14% of wild-type levels in plant foliage and seeds, respectivel

161 uced the numbers of memory CD8(+) T cells to wild-type levels in Prf-deficient mice.

162 CL can be restored to near wild-type levels in stationary phase in the triple mutan

163 four of the five other duplicated genes over wild-type levels in the brain beginning the second postn

164 complex sphingolipids, were restored to the wild-type levels in the Cers2-rescued Cers1 mutant mouse

165 KDS reductase activity was reduced to 10% of wild-type levels in the loss-of-function tsc10a mutant,

166 ta S. cerevisiae cells can restore growth to wild-type levels in the presence of genotoxic agents tha

167 d lifespan are reduced, but restored to near wild-type levels in the presence of stabilized Acn(S437D

168 The corresponding virus replicated to wild-type levels in three different cancer cell lines bu

169 rsp mutant restored biofilm formation to the wild-type level, indicating that FnbA plays a major role

170 ty phenotype of DeltabrlR mutant biofilms to wild-type levels, indicating that BrlR functions downstr

171 xpression of CD18/beta2 integrin to 2-16% of wild-type levels is associated with progressive loss of

172 l to accumulate several lytic cycle mRNAs at wild-type levels, leading to decreased production of lyt

173 n that genetic restoration of plasma ApoE to wild-type levels normalizes plasma lipids in ApoE KO mic

174 demonstrate that this strategy restores the wild type level of PAS susceptibility in a previously ch

175 ized to the cell periphery, does not support wild type levels of cell edge protrusion.

176 ination is essential and sufficient for near wild type levels of Env7 palmitoylation, membrane locali

177 y Vam7-6A likely contributed to the observed wild type levels of vacuole association, whereas protein

178 ne rNAD-ME1 had 8%, and rPPDK1 had 5% of the wild-type level of activity, and showed dramatic changes

179 the wild-type sequence, hence restoring the wild-type level of CA-CPSF6 interactions.

180 Sa15 is required for a wild-type level of CO formation.

181 The G8 mutant expressed only 0.1% of the wild-type level of full-length TK, considerably lower th

182 utant, but base pairing was retained, a near wild-type level of modification was observed.

183 utation, to reform the base pair, restored a wild-type level of Psi formation.

184 protein, PEROXIREDOXIN Q (PRXQ), to produce wild-type levels of 16:1t.

185 pproximately 2-fold elevated GerB GR levels, wild-type levels of a GerK GR subunit and the GerD prote

186 Young Kcna1(-/-) mice retained wild-type levels of Abeta, tau, and tau phospho-Thr(231)

187 lerant F. succinogenes sufD restored E. coli wild-type levels of acid tolerance, suggesting a possibl

188 entrations of the phosphomimetic mutant p60, wild-type levels of activity could be observed, indicati

189 identified in SPG3A HSP patients, displayed wild-type levels of activity in all assays.

190 thought to be pathogenic were found to have wild-type levels of activity.

191 Because these animals exhibited wild-type levels of acute viremia and immune activation,

192 es carrying bbb22 alone were able to achieve wild-type levels of adenine saturation but not hypoxanth

193 Ygi fimbriae were necessary for wild-type levels of adherence to a human embryonic kidne

194 ntagonizes cadherin endocytosis and restores wild-type levels of adhesion.

195 A cpxR mutant had wild-type levels of antimicrobial peptide resistance; a

196 , which suppresses SA accumulation, restores wild-type levels of aphid susceptibility to spr2.

197 synthesis (acx1) or perception (jai1-1) show wild-type levels of aphid susceptibility, and spr2 retai

198 A complemented strain recovered wild-type levels of both sporulation and CPE production.

199 o confirm that although B capsids containing wild-type levels of capsid proteins were synthesized, th

200 1 that contains only one active site retains wild-type levels of catalytic activity.

201 ver, a Deltavib-1 Deltaime-2 mutant restored wild-type levels of cell death.

202 , the PepN-deficient strain fails to achieve wild-type levels of cells in aggregates, suggesting an e

203 In contrast, sos5-2 seeds have wild-type levels of cellulose but completely lack adhere

204 cells expressed CFTR, they generated nearly wild-type levels of Cl(-) secretion; overexpressing CFTR

205 riplasmic binding proteins were required for wild-type levels of commensal colonization of chicks.

206 corbate-deficient mutant vtc2-1 accumulating wild-type levels of complex I.

207 CMA synthesis, as evidenced by the fact that wild-type levels of coronatine production are restored t

208 esistance were examined, irAOX plants showed wild-type levels of defense-related phytohormones, secon

209 ng and DNA damage repair nevertheless retain wild-type levels of desiccation tolerance, suggesting th

210 articles of HIV-1 strains LAI and NL4.3 lack wild-type levels of Env proteins.

211 ild-type mice treated with DMBA/TPA restored wild-type levels of epidermal proliferation in the mutan

212 S. aureus strain LAC, SSR42 is required for wild-type levels of erythrocyte lysis, resistance to hum

213 The cry1 mutant showed wild-type levels of GPA1 mRNA or GPA1 protein.

214 Furthermore, the apparent wild-type levels of H3K4me3 in the 762-Set1 strain are d

215 deficient in endonuclease activity exhibits wild-type levels of homologous recombination at restrict

216 cells in such mice produce approximately 50% wild-type levels of Igmu (mRNA and protein), and this is

217 ally reduced expression of miR-H2 but showed wild-type levels of infectious virus production and no i

218 elangiectasia mutated (ATM) protein produced wild-type levels of infectious virus.

219 present in group M restored CD4 binding and wild-type levels of infectivity and cell-to-cell fusion.

220 Overall, our results suggest that wild-type levels of insulin signalling reduce female sus

221 Single mutants produce wild-type levels of JA in most tissues, but the double m

222 ype HSV-1, although both viruses established wild-type levels of latency in vivo.

223 rk signaling in the adult hippocampus drives wild-type levels of LTD.

224 pertussis-infected IFNAR1 knockout mice had wild-type levels of lung inflammatory pathology.

225 MntABC was also necessary to maintain wild-type levels of manganese-dependent superoxide dismu

226 ct mechanisms, are important for maintaining wild-type levels of many small RNAs in C. elegans.

227 Expression of wild-type levels of mcm10-4A in mcm5-bob1 mutant cells r

228 Expression of wild-type levels of mcm10-4A resulted in severe growth a

229 When we expressed wild-type levels of mcm10-m2,3,4 in budding yeast cells,

230 ecessary for flagellar biogenesis as well as wild-type levels of motility and transcription of RpoN-d

231 lementation of each fimbrial mutant restored wild-type levels of motility, biofilm formation, adheren

232 destined for amino acid production, restores wild-type levels of NRT2.1 expression, suggesting that m

233 wnstream of OPDA, OPR3-RNAi plants contained wild-type levels of OPDA but failed to accumulate JA or

234 lites and the complete restoration of normal wild-type levels of OS-induced defense metabolites, we c

235 asmid in this mutant only partially restored wild-type levels of persistence in the kidney.

236 In contrast, LtgD was necessary for wild-type levels of PG precursor incorporation and produ

237 alter the PSII repair cycle, as indicated by wild-type levels of phosphorylation of PSII proteins, in

238 t the OspE PDZ-binding motif is required for wild-type levels of PKC activation.

239 Mouse NKT cells expressing wild-type levels of PLZF, but deficient for YY1, had dev

240 PriL lacking the Fe-S cluster domain retains wild-type levels of primer synthesis.

241 P- seeds rebalance the proteome, maintaining wild-type levels of protein and storage triglycerides.

242 and Mtmr13 depend upon each other to achieve wild-type levels of protein expression.

243 rearranged RNAs of recombinant RVs expressed wild-type levels of protein in vivo.

244 se minute (L24+/-) mutant, which resulted in wild-type levels of protein synthesis and attenuation of

245 mice, whereas factor XI-deficient mice show wild-type levels of resistance.

246 or cis-(+)-12-oxo-phytodienoic acid restored wild-type levels of resistance.

247 ent of GINS to Mcm2-7, whereas expression of wild-type levels of sld3-m10 resulted in a severe replic

248 Expression of wild-type levels of sld3-m9 resulted in a severe DNA rep

249 rains recovered from infected humans secrete wild-type levels of SpeB protease activity.

250 x1 subunit of cytochrome oxidase but contain wild-type levels of the bc(1) complex.

251 mutant AAV5 infectious clone generated near-wild-type levels of the double-stranded monomer replicat

252 FliO also appears to be required for wild-type levels of the export apparatus protein FlhA in

253 The phenotypes that emerge in the context of wild-type levels of the HP1 and Mod(mdg4) proteins might

254 nted Arabidopsis rbcs mutants producing near wild-type levels of the hybrid Rubisco were similar to t

255 e G6 mutant expressed approximately 0.01% of wild-type levels of TK polypeptide.

256 n of developing seed AtGPAT9 is required for wild-type levels of triacylglycerol accumulation, and th

257 of Het mice with LM22A-4 for 4 weeks rescued wild-type levels of TrkB phosphorylation in the medulla

258 2Delta mutants grew on glucose and assembled wild-type levels of V-ATPase pumps at the membrane.

259 Finally, mTERT(-)/(-) cells showed wild-type levels of Wnt signaling in vitro.

260 These strains exhibited wild-type levels of Yop secretion in vitro and enabled r

261 ly, elevating D protein concentrations above wild-type levels or compensatory mutations within gene D

262 individual cells with high ratios return to wild-type levels over several hours by developing wide r

263 connectivity, which were fully restored to a wild-type level, particularly when treatment was started

264 is approximately 9-fold elevated relative to wild-type levels, possibly representing molecular compen

265 Restoration of p21 mRNA to wild-type levels rescued the proliferation deficit in ce

266 expression level of one variant to less than wild-type levels restored mismatch repair, suggesting th

267 Genetically restoring Ripk1 to wild-type levels restores peripheral red cell counts as

268 ore SR Ca(2+) transients in I4895T fibres to wild type levels, suggesting that decreased SR Ca(2+) re

269 in animals with striatopallidal knock-out to wild-type levels, suggesting a dependence on adenosine r

270 s both colonization and infection but not to wild-type levels, suggesting an intrinsic role of NanA.

271 , several mutant proteins failed to maintain wild-type levels, suggesting defects in protein stabilit

272 ltaserR mutant background restores growth to wild-type levels, suggesting that both operons have role

273 on of the hns mutation restored virulence to wild-type levels, suggesting that H-NS regulates many ge

274 SERT(-/-) mice normalized bleeding times to wild-type levels, suggesting that loss of SERTs causes a

275 ll alleles (sgb11/esk1-7) of ESK1 restore to wild-type levels the enhanced susceptibility of agb1-2 t

276 and suppressed IFN-inducible transcripts to wild-type levels, thereby linking dysregulation of IFN-g

277 firmed that ATM was not necessary to produce wild-type-level titers in fibroblasts.

278 nts, encompassing a range spanning from near wild type levels to reductions of up to approximately 68

279 ack directed motility but colonize to nearly wild-type levels, trigger less host inflammation.

280 n and transcription is fully restored to the wild-type level upon transfer from glycerol to glucose.

281 during Deltam153 mutant infection reverts to wild-type levels upon exogenous m153 complementation in

282 Threshold is restored to wild-type levels upon reduction of the sulfhydryl modifi

283 Elevating B protein concentrations above wild-type levels via exogenous, cloned-gene expression c

284 of a gcbA mutant strain could be restored to wild-type levels via overexpression of the small regulat

285 ased expression of the validated proteins to wild-type levels was obtained by overexpression of eIFis

286 ed phosphorylated ERK expression relative to wild-type levels was seen for all 6 SOS1 variants, paral

287 d CD18/beta2 integrin expression to 2-16% of wild-type levels, we investigated in this study the infl

288 a 50% drop in Pten expression compared with wild-type levels, we observed enhanced activation of mic

289 t and C1q-hemolytic activity was restored to wild type levels when CD93 was expressed on either hemat

290 A-dependent manner, but could be restored to wild-type levels when grown with lysozyme.

291 ce a greater benefit than expressing CFTR at wild-type levels when targeting small fractions of cells

292 Furthermore, PSI returns to nearly wild-type levels when the O2 concentration in the medium

293 ed Citrobacter virulence and colonization to wild-type levels, whereas complementing with NleH2 reduc

294 s, IL-13, IL-5, and mucous hypersecretion to wild-type levels, whereas eotaxin and airway hyperrespon

295 TN-induced relaxation and GTN denitration to wild-type levels, whereas overexpression in mitochondria

296 ters, although free cholesterol persisted at wild type levels, which might be secondary to the shifts

297 o replicate without Shield-1, but it grew at wild-type levels with Shield-1 or in human foreskin fibr

298 ytokine generation, and airway reactivity to wild-type levels, with contributions from TP receptors l

299 release, cell lysis and biofilm formation to wild-type levels, with phdA overexpression promoting res

300 ffect but also restore protein expression to wild-type levels, yielding a restoration of ABCG2-mediat