ライフサイエンスコーパス: wild-type level

1 97C) had decreased K(+) current (0 to 23% of wild-type levels).

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

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

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

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

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

7 normalized most neurochemical alterations to wild-type level.

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

9 xpression of gamma1 H chains that is <1% the wild-type level.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 1 expression and hepatocyte proliferation to wild-type levels.

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

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

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

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

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

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

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

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

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

40 restored sporulation and solventogenesis to wild-type levels.

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

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

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

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

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

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

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

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

49 197 in bamD restore Bam complex function to wild-type levels.

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

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

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

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

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

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

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

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

58 cleaved concatemeric DNA to ca. 35 to 98% of wild-type levels.

59 Cone opsin levels increased to near wild-type levels.

60 only, cardiac function was also restored to wild-type levels.

61 magnetic resonance imaging, was restored to wild-type levels.

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

63 l, restored both shmooing and cell fusion to wild-type levels.

64 in respective mutants restored adherence to wild-type levels.

65 mised by decreasing cohesin levels to 30% of wild-type levels.

66 f the three antibiotics were reduced to near wild-type levels.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

100 produces receptors that do not accumulate to wild-type levels and are retained mainly in the endoplas

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

102 platelet influx in the TCRdelta(-/-) mice to wild-type levels and increased CXCL1 production by wound

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

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

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

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

107 d-type levels of LIN-56 require LIN-15A, and wild-type levels and/or localization of LIN-15A requires

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

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

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

111 0-null mutant HSV-1 plaque formation to near wild-type levels, and efficiently induced derepression o

112 tation, plasma cholesterol was normalized to wild-type levels, and HDL levels were increased 4-fold.

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

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

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

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

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

118 Wild-type levels are restored by photoreceptor-specific

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

135 64A HCA II can be chemically rescued to near wild-type levels by the addition of the exogenous buffer

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

137 on and restoration of GRP78, CNX, and CRT to wild-type levels, corresponding with mitigated pancreati

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

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

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

141 failed to induce degP expression beyond the wild type level, despite activation of the sigma(E) path

142 le to colonize mice to levels similar to the wild-type level during independent challenge.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

157 like dh siRNAs, dg siRNAs accumulate to near wild-type levels in cells with H3K9 substitutions that c

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

159 2A/B/D, CYCS, CAPNI) were normalised towards wild-type levels in Fiona animals.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

174 inhibition, reverses these abnormalities to wild-type levels in vitro.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

189 k1(T662) is necessary for cells to exhibit a wild-type level of myriocin resistance, a Ypk1(T662A) mu

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

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

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

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

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

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

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

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

198 Yad fimbriae were necessary for wild-type levels of adherence to a bladder epithelial ce

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

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

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

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

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

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

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

206 1 that contains only one active site retains wild-type levels of catalytic activity.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 Wild-type levels of LIN-56 require LIN-15A, and wild-typ

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

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

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

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

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

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

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

237 only uPA expression was sufficient to induce wild-type levels of Mp accumulation, angiogenesis, and n

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

259 QR, we generate strains with 13% and 30% of wild-type levels of the limiting subunit of cohesin, Mcd

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

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

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

263 2Delta mutants grew on glucose and assembled wild-type levels of V-ATPase pumps at the membrane.

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

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

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

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

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

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

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

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

272 y, the levels of Myc are twofold higher than wild-type levels showing that the level of Myc induced b

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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