ライフサイエンスコーパス: retain the ability to

1 e resulted in increased self-acetylation but retained the ability to acetylate histones.

2 ively in protein remodeling with Hsp90Ec but retained the ability to act with DnaK cochaperones.

3 he cord blood of women with preeclampsia and retain the ability to activate AT(1) receptors.

4 enhancer DNA, and as expected these variants retain the ability to activate open complex formation in

5 1 lost the ability to interact with TSC2 but retained the ability to activate mTORC1, although to a l

6 ced TAK1-independent NFkappaB activation and retained the ability to activate substantial gene expres

7 ed mimetic fails to induce "brown" genes but retains the ability to activate "white" genes.

8 genes, including p21, Noxa, and Puma, but it retains the ability to activate a small subset of p53 ta

9 n N-terminally deleted mutant of RalGDS that retains the ability to activate Ral proteins but loses t

10 e, encoding the mutant p53R172P protein that retains the ability to activate the cell-cycle inhibitor

11 se a naturally occurring splice variant that retains the ability to activate the Met receptor.

12 , subsets of DCs in activated DC populations retain the ability to actively phagocytose particulate A

13 In this study we show that diabetic hearts retain the ability to adapt their metabolism in response

14 oites, which had lost the ability to invade, retain the ability to adhere to erythrocytes, and furthe

15 in contrast to IC and ADC synthase, SgcD has retained the ability to aminate chorismate identically t

16 iminished even though NC mutant Gag proteins retained the ability to assemble spherical particles.

17 ndogenous Lsm4, although this mutant protein retained the ability to assemble with Lsm1-7, associate

18 Among the deletion variants that retain the ability to associate with the bud neck, only

19 ant-negative mutant form of myocardin, which retains the ability to associate with SRF but is defecti

20 ive T cells to evade negative selection, yet retain the ability to be activated by self-antigens in t

21 PR/Cas9 and a cytidine deaminase enzyme that retain the ability to be programmed with a guide RNA, do

22 The mutants obtained retain the ability to be targeted to the membrane but fa

23 More importantly, alphaFD retained the ability to be activated by subtilisin to 10

24 DNA retained the ability to be extracted and PCR amplified f

25 no longer induce significant VLP release but retained the ability to be incorporated as a passenger i

26 All six mutants retained the ability to be incorporated into HIV-1 parti

27 Surviving RA-treated cells retained the ability to be replated and this was associa

28 ained highly functional within the liver and retained the ability to become highly activated as evide

29 defective in their ability to bind Krh1p but retain the ability to bind another Gpa2p-interacting pro

30 how that JH-linked RGMc mutant proteins that retain the ability to bind BMPs are also able to functio

31 planation of how highly divergent Ly49s that retain the ability to bind cI molecules might have evolv

32 tants, the NiV G glycosylation stalk mutants retain the ability to bind F, indicating that the fusion

33 , abolishes active transport but the mutants retain the ability to bind galactopyranoside.

34 motility-deficient versions of motors, which retain the ability to bind microtubules and hydrolyze ad

35 he closely related DNA photolyases, but they retain the ability to bind nucleotides such as ATP.

36 151G, although these isolates also appear to retain the ability to bind receptors via HA.

37 though the acyclic cucurbit[n]uril congeners retain the ability to bind to ammonium ions with high af

38 acyclic glycoluril pentamer 5 and hexamer 6 retain the ability to bind to guests typical of CB[6] bu

39 for Plasmodium falciparum virulence and must retain the ability to bind to host receptors while also

40 triguingly, we have found forkhead DBDs that retain the ability to bind very specifically to two comp

41 ted HCR/C that lacked GBP2 binding potential retained the ability to bind and enter Neuro-2A cells.

42 These findings demonstrate that sperm have retained the ability to bind and respond to truncated Cr

43 The mutant F1086A, however, retained the ability to bind ATP and drug substrates.

44 bound Bax, whereas phospho-defective Bcl-xL retained the ability to bind Bax.

45 gated IFIT1/mRNA interaction, whereas IFIT1B retained the ability to bind cap1-mRNA, albeit with redu

46 Cu-NODAGA-PSMA-IgG and (64)Cu-NODAGA-PSMA-Mb retained the ability to bind cell surface PSMA, and both

47 lptA null mutants of strains FA1090 and 273 retained the ability to bind fH when LOS was sialylated.

48 containing deletions in the other nine loops retained the ability to bind Hb.

49 tants that lost the ability to activate Jak2 retained the ability to bind Jak2, thus questioning the

50 s in ATPase activity, though D714E and D714H retained the ability to bind metal ions with high affini

51 Three of the mutants retained the ability to bind the consensus paired domain

52 Each helix mutant retained the ability to bind the mSin3A corepressor.

53 LANA (L1006P) retained the ability to bind to c-Myc and activate ERK1,

54 wn by immunoprecipitation, all CNTF variants retained the ability to bind to CNTFR.

55 Both dimers and trimers of LF(N) retained the ability to bind to PA pores and block ion c

56 howed restricted neutralizing activity, they retained the ability to bind to the E.A244 gp120 HIV-1 e

57 heterotypic binding to claudin-4 while still retaining the ability to bind to claudin-1 and -5.

58 The results showed that although retaining the ability to bind to hPVR, inactivated PV bo

59 substrates relative to the wild-type, while retaining the ability to bind X junctions.

60 employing other sequences, this DNA aptamer retains the ability to bind aminoglycosides, albeit with

61 ing CUL3 mutant (CUL3 Delta403-459) not only retains the ability to bind and ubiquitylate WNK kinases

62 was incapable of bundling microfilaments, it retains the ability to bind F-actin.

63 f TPV-15L revealed no Ig-like domain, but it retains the ability to bind heparin and phosphorylate ne

64 frequencies in myeloproliferative diseases, retains the ability to bind Lnk.

65 In the absence of RepD, PcrA retains the ability to bind to a pre-nicked oriD, but en

66 ility to activate speB expression, Rgg(103P) retains the ability to bind to DNA upstream of norA and

67 in PHD2 within the full-length Msc1 protein retains the ability to bind to Swr1 but eliminates the f

68 ts have revealed that although Fli1 DeltaCTA retains the ability to bind to the collagen promoter in

69 HDAC inhibitors retain the ability to block AR activity in castration-re

70 discovered the functional core of IncA that retains the ability to both inhibit SNARE-mediated fusio

71 ith synthetic luciferyl adenylate because it retains the ability to carry out the oxidative half-reac

72 ne kinase, Ark, and demonstrated that it has retained the ability to catalyze the phosphorylation of

73 d immunosuppressive functional profile, they retain the ability to change their functional profile to

74 nerated and shown to result in proteins that retained the ability to cleave the first strand of the D

75 to assemble into higher-order complexes but retained the ability to co-immunoprecipitate with ROM-1

76 ng adhesion ( approximately 50 mJ m(-2)) and retain the ability to coacervate.

77 These attenuated strains retained the ability to colonize the upper respiratory t

78 As expected, most transposon mutants retained the ability to colonize, but 125 candidate viru

79 hydrated ATPS components for multiplex ELISA retain the ability to compartmentalize antibodies and pr

80 ceptor stem or anticodon stem and loop still retained the ability to complex with PylSn.

81 eans for exposing rare events in SDEs, while retaining the ability to compute bounds on the probabili

82 ents with hippocampal damage and amnesia who retain the ability to construct novel scenes.

83 endocrine lineage regulator Neurogenin3, and retain the ability to contribute to cells within the pan

84 and CD4(-)CD8(-) T cells were functional and retained the ability to control tumor growth without the

85 NS3 mutants lacking the helicase domain retained the ability to control virus signaling initiate

86 ent for forming microcontacts to SAMs) while retaining the ability to deform and flow upon contacting

87 whereas cells with knockdown of HIF1/2alpha retained the ability to degrade plasma membrane Na-K-ATP

88 n of an insulating polydopamine layer, while retaining the ability to detect DA.

89 ferative cells express stem cell markers and retain the ability to differentiate down multiple cell l

90 h cells can self-renew indefinitely but also retain the ability to differentiate into other cell type

91 as differentiated as tissue fibroblasts and retain the ability to differentiate into other cells typ

92 th wild-type controls but the null parasites retain the ability to differentiate to the intracellular

93 Cultured LECs retained the ability to differentiate into gamma-crystal

94 ficient thymocytes had a normal lifespan and retained the ability to differentiate, albeit with reduc

95 ed in vitro for at least five passages while retaining the ability to differentiate into multiprocess

96 The G473A variant retained the ability to dimerize and had steady-state ac

97 ng regardless of whether the mutant proteins retained the ability to dimerize or not.

98 ing simulated data, we also show that alpine retains the ability to discover true positives, similar

99 Interestingly, these mice retained the ability to discriminate both texture and sh

100 To decrease such variability while retaining the ability to distinguish and enumerate trans

101 Meristems retain the ability to divide throughout the life cycle o

102 the mutants, R142A and D148A, were found to retain the ability to down-regulate reporter RNA transla

103 ic defect in Th2-type lung inflammation, yet retain the ability to elicit pulmonary Th1 antiviral res

104 Further this vaccine retains the ability to elicit both antibody and TH1 resp

105 ng CD34 and a 17-fold increase in cells that retain the ability to engraft immunodeficient mice.

106 ZFN-treated HSPCs retained the ability to engraft NOD/SCID/IL2rgamma(null)

107 T cells, B cells and dendritic cells, while retaining the ability to enhance naive T-cell differenti

108 tive in DNA binding (the S335D mutant) still retains the ability to enhance BRLF1 transcriptional eff

109 established that all mutant proteins tested retained the ability to enter the phloem translocation s

110 o decrease variability between animals while retaining the ability to enumerate transmitted/founder v

111 Finally, both individuals retained the ability to evaluate pain despite substantia

112 ghly plastic self-renewing cancer cells that retain the ability to expand ex vivo as tumourspheres, i

113 e with altered molecular characteristics and retain the ability to express c-fos, and Rb is maintaine

114 g following gastrulation, cardiac precursors retain the ability to express markers of the cardiac fie

115 espite these defects, C9orf72 synapses still retain the ability to express presynaptic homeostatic pl

116 specific T cells that proliferate poorly yet retain the ability to express Th1-type cytokines.

117 s than did infected wild-type mice, and they retained the ability to express tumor necrosis factor al

118 aling attenuation in Tfh cells, because they retained the ability to flux calcium and activate NFAT-t

119 cent transmembrane alpha-helices, M1 and M3, retains the ability to flux cations in this uncoupling P

120 espite the expanded backbone, 1 was found to retain the ability to form a tetrameric quaternary struc

121 rface located on the N-terminal domain still retain the ability to form extended nucleoprotein filame

122 of Rta that are unable to form tetramers but retain the ability to form higher-order multimers are re

123 Investigations of model organisms that retain the ability to form new hair cells after embryoge

124 s and propose that the altered AQP5 proteins retain the ability to form open channels in the cell mem

125 eptide bonds in the CNA(2) or CNA(3) domains retain the ability to form pilus bundles.

126 e unable to cleave at recombination hotspots retain the ability to form stable complexes with the hot

127 IL-1R-deficient RAS-expressing keratinocytes retain the ability to form tumors in orthotopic grafts.

128 one lacking all three ectodomain cysteines, retained the ability to form non-covalent dimers, and al

129 nes and arginines are replaced with alanines retains the ability to form amyloid fibrils but is defec

130 elope) is present in the stratum corneum and retains the ability to form covalent inhibitory complexe

131 heir ATPase and transport capabilities still retain the ability to fully use vitamin B12 in vivo.

132 monstrated that, in the absence of AHL, EsaR retains the ability to function as a weak activator of t

133 hylation in recombinant VSV (rVSV) partially retain the ability to G-N-7 methylate a pre-2'-O-methyla

134 oth Mmp14(-/-) and Mmp15(-/-) mammary glands retain the ability to generate intact ductal networks.

135 In contrast, cdh6-positive progenitors retain the ability to generate multiple subtypes of amac

136 t advantage of being expandable in vitro and retaining the ability to give rise to multiple neuronal

137 We further demonstrate that S. enterica LT2 retained the ability to grow on 1,2-propanediol as the s

138 neered to express a foreign gene while still retaining the ability to grow to high titers in cell cul

139 ing all three known iron acquisition systems retains the ability to grow in media containing iron che

140 ve individually been changed to alanine, all retain the ability to hydrolyze the cortex to various de

141 supercomplex with MalE cross-linked to MalG retains the ability to hydrolyze ATP and to transport ma

142 Moreover, this discriminatory MLST scheme retains the ability to identify epidemiologically linked

143 The hybrids also retain the ability to increase their fitness via sexual

144 of several popular processing methods while retaining the ability to incrementally renormalize data

145 terfere with the IFN signaling because cells retain the ability to induce functional but local antivi

146 These results show that recombinant MVs retain the ability to induce MV-specific humoral immunit

147 ss into the CNS of immunodeficient mice, and retained the ability to induce a strong humoral immune r

148 Meanwhile, 19-phenyl-GA retained the ability to induce autophagy and potentially

149 y loss, the 3-O-desulfonated pentasaccharide retained the ability to induce tryptophan fluorescence c

150 lergenicity and increases safety while still retaining the ability to induce effective desensitizatio

151 with plasmid-cured C. muridarum mutants that retain the ability to infect the murine genital tract, b

152 d that plasmid-deficient Chlamydia muridarum retains the ability to infect the murine genital tract b

153 a+ T cells and whether these converted cells retain the ability to inhibit colitis are not clear.

154 ditis elegans mafr-1 that truncate the C-box retain the ability to inhibit the transcription of RNA p

155 In contrast, both CRF-BP mutants retain the ability to inhibit Ucn 1-induced CRFR1 activa

156 Each of the five fluorescent FKBPs retained the ability to inhibit [(3)H]ryanodine binding

157 nous target genes and promote apoptosis, but retained the ability to inhibit cell proliferation when

158 Furthermore, uncontaminated analogs retained the ability to inhibit mTOR, although with dimi

159 taining mutations that abolish dsRNA binding retained the ability to inhibit RIG-I signaling.

160 ed analogs lose all cytotoxic activity while retaining the ability to inhibit protein translation in

161 n is released, the integrin-bound talin head retains the ability to inhibit actin assembly.

162 ing mutant (V26G/P80R) that interacts with Z retains the ability to inhibit Z function, whereas a Pax

163 ctive T cells escape negative selection, yet retain the ability to initiate autoimmunity.

164 Fully mature photoreceptors retain the ability to integrate into the mature retina.

165 mammalian cells confirms that these proteins retain the ability to interact in a heterologous system.

166 ria, and the purified proteins were found to retain the ability to interact in a manner that was depe

167 2 mutants, Munc18-2(R65Q) and Munc18-2(R65W) retain the ability to interact with and stabilize syntax

168 gh mutants do not affect cilia structure and retain the ability to interact with Disheveled, both all

169 main defined by limited proteolysis, did not retain the ability to interact with Rab11, although it w

170 were expressed in mammalian HEK293 cells and retained the ability to interact with a fluorescently la

171 2hc,SLC3A2) and that this stabilised complex retained the ability to interact with a substrate.

172 293T cells, although NC mutant Gag proteins retained the ability to interact with cellular membranes

173 Bound GAGs retained the ability to interact with GAG-binding molecu

174 ucleotide kinase phosphatase (PNKP) not only retained the ability to interact with partner proteins t

175 A subset of PilA point mutants retained the ability to interact with PilS but could no

176 The variant TatC proteins retained the ability to interact with TatB and with a Ta

177 that failed to bind to PIH1D1 in vitro fully retained the ability to interact with the R2TP complex a

178 The mutant capsid retained the ability to interact with the SV40 cellular

179 mino acids (170)EHLKTAVQMAVFIHNFKRKGGI(191)) retaining the ability to interact with TRN-SR2.

180 Here, we show that Lef1DeltaN retains the ability to interact physically and functiona

181 lpha (NT-PGC-1alpha, amino acids 1-270) that retains the ability to interact with and transactivate n

182 ZipA contained in nanodiscs (Nd-ZipA) retains the ability to interact with FtsZ oligomers and

183 ctivity and fails to bind G9a or HDAC1/2 but retains the ability to interact with PRMT5.

184 the primary E3 ligase of RanBP2, whereas IR2 retains the ability to interact with SUMO1 to promote SU

185 This fragment retains the ability to load atypical extender units, unu

186 eriments utilizing FEN1 mutant proteins that retained the ability to localize to telomeric repeats re

187 expressed high levels of functional p53 and retained the ability to lyse transformed versus normal c

188 at have differentiated into stalks really do retain the ability to make new tips, we have removed exi

189 n adapting feedforward control of speech but retain the ability to make online feedback corrections;

190 FliK deletion variants that retain the ability to measure hook length are secreted t

191 with a dual acylated N-terminal epitope tag retained the ability to mediate HR, consistent with this

192 xhibited impaired anticoagulant activity but retained the ability to mediate PAR-1-dependent signalin

193 ced redistribution towards mitochondria, but retains the ability to mitigate toxicity due to mitochon

194 precursor insect viruses; for instance, HAV retains the ability to move from cell-to-cell by transcy

195 e low baseline levels of Ig in the blood but retain the ability to mutate Ig-associated genes that en

196 reduction in lytic activity, but 4 of the 8 retained the ability to oligomerize.

197 69 D5 protein remains stable and soluble and retains the ability to oligomerize and hydrolyze ATP whe

198 Both mutant enzymes retain the ability to oxidize substrate, but the steady-

199 Mast cells retained the ability to phagocytose Escherichia coli par

200 terial cells expressing P1-3C transgenes and retained the ability to process P1 polyproteins from mul

201 esults indicate that animals with strabismus retain the ability to produce conjugate adaptation of sm

202 es (CTLs) fail to degranulate, although they retain the ability to produce cytokines, and cytokine le

203 exhibit features of T-cell exhaustion, they retain the ability to produce cytokines.

204 fully downregulate pluripotency markers and retain the ability to produce ES cell colonies; however,

205 Notably, they retained the ability to produce effector cytokines and c

206 Further, cells that retained the ability to produce IFN-gamma exhibited a de

207 efficient slicing activity, these fish have retained the ability to produce miR-451, a microRNA gene

208 ium-responsive subset of CD4(+) T cells that retained the ability to proliferate and express IL-2.

209 restingly, regardless of age, KLRG1(+) cells retained the ability to proliferate and survive in respo

210 of T cells in vivo, but Uqcrfs1(-/-) T cells retained the ability to proliferate in vivo under lympho

211 xhibited reduced functional properties, they retained the ability to proliferate.

212 This mito-tagged pRB retained the ability to promote apoptosis in response to

213 in tumor-bearing IFN-gamma knockout mice but retained the ability to promote CD8(+)CD44(high) memory

214 also induced comparable immune responses and retained the ability to protect mice against Shigella fl

215 e mesenchymal carcinoma cells within a tumor retained the ability to protect their more epithelial co

216 on transmission in a given environment while retaining the ability to quickly adapt to a new environm

217 intains repetitive character, potentially to retain the ability to rapidly restructure the Ago-bindin

218 icated that transiently primed alphaIIbbeta3 retains the ability to rapidly bind PAC-1 from 2-90 min,

219 onstitutively high sulfate concentration, it retains the ability to re-program its gene expression in

220 We have also established that DCs retain the ability to recognize and kill C. gattii witho

221 icyclic peptides that are cell-permeable and retain the ability to recognize specific intracellular t

222 of highly selective polymeric cavities that retained the ability to recognize PSA post removal of th

223 ils to induce cell surface PS exposure while retaining the ability to recognize carbohydrates and sig

224 x attL and attR x attR recombination whilst retaining the ability to recombine attP x attB.

225 of wild-type DLC1 to focal adhesions, but it retained the ability to reduce the intracellular levels

226 unable to catalyze nitrite reduction despite retaining the ability to reduce a proposed intermediate

227 Furthermore, beta-cells retained the ability to reenter the cell cycle at a far

228 ional stabilization, whereas ICM cells still retain the ability to regenerate TE up to the early blas

229 Some organisms, however, retain the ability to regenerate tissue throughout adult

230 g the formation of a blastema, however, they retained the ability to regenerate partial hindlimb stru

231 pment of Onthophagus horned beetles and have retained the ability to regulate A/P polarity in traditi

232 Notably, p53(3KR) retains the ability to regulate energy metabolism and re

233 ycle arrest, senescence and apoptosis, fully retains the ability to regulate SLC7A11 expression and i

234 eractions indicated that broken helix states retain the ability to relieve membrane-packing stress.

235 agents, a higher hurdle, if the virus is to retain the ability to replicate efficiently.

236 Strikingly, iMac239 retained the ability to replicate in cell lines and prim

237 Surprisingly, the G50pKO mutant retained the ability to replicate in permissive murine f

238 omoters (G50DblKo) revealed that this mutant retained the ability to replicate in the simian kidney e

239 to naive-contact ferrets, while concurrently retaining the ability to replicate within ocular tissue

240 rtually all HCC-associated TR mutants tested retained the ability to repress target genes in the abse

241 spatial resolution from ChIP-Seq data, while retaining the ability to resolve closely spaced events t

242 However, some patients do not retain the ability to respond overtly to command and it

243 icate that neurons of the degenerating brain retain the ability to respond to growth factors with axo

244 Thus, injured neural systems retain the ability to respond to growth signals over the

245 nocytes in patients with active systemic JIA retain the ability to respond to IFNgamma, suggesting th

246 nic Ag stimulation and periodic reactivation retain the ability to respond to local virus challenge.

247 Moreover, cells in the surviving spheres retain the ability to respond to reinduction and thus ma

248 in-knock-out mice and found that these cells retained the ability to respond in a sustained fashion t

249 Additionally, mast cells retained the ability to respond to Ag in vivo as measure

250 Most importantly, PKCtheta-deficient T cells retained the ability to respond to virus infection and t

251 1 may be eliminated, but the truncated genes retain the ability to restore editing site conversion in

252 ation forks blocked by protein-DNA complexes retain the ability to resume replication upon removal of

253 vitro and in vivo, such differentiated cells retain the ability to return to a stem-like state.

254 e discovered that in-vitro-manipulated HSPCs retain the ability to return to latency after transplant

255 nts of incorporated alpha-galactosylceramide retained the ability to robustly activate NKT cells.

256 at bound C. neoformans but did not ingest it retained the ability to ruffle in response to chemoattra

257 indication on whether or not a species/genus retains the ability to salvage deoxyribonucleosides.

258 ordance with primary WM tumors, MWCL-1 cells retain the ability to secrete high amounts of IgM protei

259 n secretion of the motility adhesin RemA but retained the ability to secrete SprB.

260 Some aptamers retain the ability to selectively bind guanine or adenin

261 mutations in the dehydrogenase domain still retain the ability to self-associate and bind target pro

262 Whether MBCs homogeneously retain the ability to self-renew and terminally differen

263 REST-deficient ES cells retained the ability to self-renew and to undergo approp

264 h Bro1 and failed to produce viruses despite retaining the ability to self-assemble.

265 n insertion is abolished, but Yersinia still retains the ability to sense cell contact.

266 (RI-10) of LL-37 as the minimal peptide that retains the ability to signal increased expression of GA

267 PTHrP1-17 retains the ability to signal through PTH1R to induce ca

268 ron microscopy revealed that nhx1Delta cells retain the ability to sort cargo into intralumenal vesic

269 in contact with antigen-specific CD4 T cells retain the ability to stimulate additional naive T cells

270 unable to bind DNA or activate transcription retain the ability to stimulate NER.

271 than native cashew proteins but importantly retained the ability to stimulate cellular proliferation

272 contrast, an inactive catalytic site mutant retained the ability to stimulate the wild-type KD by di

273 actors with little impact on the vasculature retains the ability to stimulate neural precursors and p

274 rmally function in distinct subcomplexes but retain the ability to substitute for one another so as t

275 ind that pre-RCs can be pushed along DNA and retain the ability to support replication.

276 B1 proteins, like wild-type SMARCB1 protein, retain the ability to suppress cyclin D1 activity.

277 However, these mutants retain the ability to suppress noncanonical Wnt signalin

278 Patient-derived mutant PHOX2B constructs retained the ability to suppress cellular proliferation,

279 methyltransferase activity, these mutations retained the ability to suppress the growth defect of th

280 y but did not induce arrest; thus, NKT cells retained the ability to survey antigen presenting cells

281 social insect societies in which individuals retain the ability to switch between reproductive and no

282 Surprisingly, many modern bacteria retain the ability to switch into a wall-free state call

283 The mature thalamus retains the ability to synthesise neurosteroids, thus pr

284 ator complexes containing the mutant protein retain the ability to synthesize siRNAs in vitro.

285 e lung, but surprisingly, we find that cells retain the ability to take up siderophores produced by c

286 Furthermore, truncated Apc appears to retain the ability to target beta-catenin for destructio

287 show that all three PD-linked alphaS mutants retain the ability to transition from the broken helix t

288 ith parasitemia, who may be asymptomatic but retain the ability to transmit disease.

289 The double mutant retained the ability to transport l-glutamate, but its k

290 plasmacytoid dendritic cells, respectively, retaining the ability to trigger Toll-like receptor 7 ex

291 red a synthetic bivalent 37-mer peptide that retains the ability to trigger effector functions.

292 erficial layers of adult mouse visual cortex retain the ability to undergo reversible experience-depe

293 hydrolytically active and inactive subunits retain the ability to unfold protein substrates and/or c

294 Although L97P and K93A/R100A retained the ability to unpair substrates, the cap mutan

295 p53(515C/515C) and Emu-myc::p53(515C/+) mice retain the ability to upregulate p21, resulting in cellu

296 taining the V3 sequences of R5-tropic clones retained the ability to use CXCR4, suggesting that seque

297 did not grow on heme as an iron source, but retained the ability to use ferric chloride.

298 These findings indicate that EIAV(vMA-1c) retains the ability to use ELR1 for entry and suggest th

299 s in the nsP2 gene, but their capsid protein retains the ability to use the nsP1-specific PS of other

300 Progression was slow, and patients retained the ability to walk until the seventh decade.