ライフサイエンスコーパス: mimic of

1 asurements have been made using exchangeable mimics of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholi

2 As a result, the Gh lesion, as a functional mimic of a 1,2-intrastrand crosslink, occupies canonical

3 Here, we present an artificial mimic of a controllable host system that forms via self-

4 We further show, by using both an in vitro mimic of a crowded cellular environment and eukaryotic c

5 inuation of a previous study, a spin-labeled mimic of a glycan acceptor ligand is used to identify ad

6 between this same sterol and an exchangeable mimic of a high-melting phospholipid in liquid-ordered b

7 oteins in a second mechanism by which the WS mimic of a Legionella environmental niche can reverse vi

8 ble mimic of cholesterol and an exchangeable mimic of a low-melting phospholipid in liquid-disordered

9 e that allowed synthesis of a stable peptide mimic of a portion of the RSV fusion protein.

10 We designed mimics of a key alpha-helical domain at the interface of

11 e mechanisms using antisense oligonucleotide mimics of a pause RNA hairpin from the leader region of

12 seagrasses via sediment stabilization, while mimics of aboveground plant structures most facilitate m

13 was applied to histone proteins to install a mimic of acetylated lysine (KAc, an epigenetic marker).

14 COR is a structural mimic of active jasmonic acid (JA) conjugates.

15 emerges at the injury site fashions a close mimic of adult form.

16 an AEf-bound core, we designed a structural mimic of AEf-bound core protein, the V124W mutant.

17 ngenital cataract mutation, and the latter a mimic of age-related oxidative damage.

18 Thus, mutational mimics of allosteric effectors will be useful to confirm

19 emerged as proteolytically stable structural mimics of alpha-helices.

20 out the backbone, are emerging as structural mimics of alpha-helix-forming conventional peptides (com

21 roach to lipophilicity determination using a mimic of an alkyl alcohol with compound partitioning qua

22 s, and biological activity of a megamolecule mimic of an anti-HER2 antibody.

23 e carboxyl-terminal domain of TaiP exposes a mimic of an eukaryotic ATG16L1-binding motif that binds

24 A safe and manufacturable mimic of anabolic bone is the primary goal of bone engin

25 port polyproline as a minimum (bio)synthetic mimic of antifreeze proteins that is accessible by solut

26 field of synthetic macromolecular (polymer) mimics of antifreeze proteins.

27 A new series of aryl-based synthetic mimics of antimicrobial peptides (SMAMPs) with antimicro

28 change model on microplastics in a gut fluid mimic of aquatic biota, and also included food to provid

29 we report that a stable synthetic thioether mimic of AspH substrates can be employed in solid phase

30 ction of acetylcholine (ACh) based on enzyme mimics of Au/Ag nanoparticles (NPs).

31 Mimics of BET bromodomains inhibit aberrant ASM cell pro

32 m natural and synthetic amphiphiles serve as mimics of biological membranes and enable the delivery o

33 the candidacy of glycodendrimersomes as new mimics of biological membranes with programmable glycan

34 Mimics of both miRNAs could deplete endogenous ATRX, and

35 6 lncRNAs were identified as putative target mimics of cassava known miRNAs.

36 alt interactions with butyramide as a simple mimic of cation interactions with protein backbones.

37 protein 1 (LMP1) is an EBV-encoded oncogenic mimic of CD40 that can be re-expressed in PBMCs during S

38 Synthetic mimics of cells, such as liposomes, are typically incapa

39 ipid monolayers were employed as a simple 3D mimic of cellular compartments to reconstitute Min prote

40 introduced decoys that present high-affinity mimics of cellular receptors.

41 YIK-amide, have been coupled to exchangeable mimics of Chol (cholesterol) and Phos (1,2-dipalmitoyl-s

42 pulsive interactions between an exchangeable mimic of cholesterol and an exchangeable mimic of a low-

43 As expected, a simplified artificial mimic of cigarette smoke odor tested at low concentratio

44 +) blockage property, we engineered a set of mimics of CNG channel pores for both structural and func

45 ncluding F229, forms a cage surrounding a Xe mimic of CO.

46 These mimics of core signaling units were assembled to homogen

47 opic investigations on a series of synthetic mimics of cytP450 indicate that a thiolate-bound ferric

48 Specifically, belowground mimics of dense root mats most facilitate seagrasses via

49 odel hydrophobic- and hydrophilic-rich phase mimics of dentin adhesive polymerize similarly and 2) to

50 lvent after a pressure-cooker treatment as a mimic of desorber conditions.

51 2-O-tetradecanoylphorbol-13-acetate (TPA), a mimic of diacylglycerol and PKC activator), hypertonic s

52 As non-interacting size mimics of digestive enzymes, we investigated the diffusi

53 restriction) from bacteriophage T7 acts as a mimic of DNA and inhibits all Type I restriction/modific

54 These dendrimersomes provide mimics of double-bilayer and multibilayer biological mem

55 eered nanostructures could provide effective mimics of ECM for investigation and control of the initi

56 secreted peptides that function as molecular mimics of endogenous plant peptides to promote parasitis

57 Soluble mimics of Env have proven challenging to obtain and have

58 Cys, i-K3Cys) were used to represent minimal mimics of eukaryotic SNARE motifs.

59 ds, which suggests that it might be a useful mimic of ferredoxin cofactors.

60 plex as the fluorescent response core, a DNA mimic of fluorescent proteins was constructed, which suc

61 Nucleic acid mimics of fluorescent proteins can be valuable tools to

62 Nibl is a structural mimic of four-coordinate base-off Cbls, as verified by i

63 xpress them as fusions with Spinach, an 'RNA mimic of GFP'.

64 These sensors are based on Spinach, an RNA mimic of GFP, and they have successfully been used to im

65 These RNA mimics of GFP provide an approach for genetic encoding o

66 Here we identify microbially derived mimics of gliadin epitopes and a parental bacterial prot

67 we show that the P39 peptide is a structural mimic of glyceraldehyde 3-phosphate dehydrogenase (GAPDH

68 have been successfully synthesized as novel mimics of glycoglycerolipids and glycosphingolipids.

69 that residual attractions are present under mimics of good solvent conditions, and for NTL9 they res

70 hosphatidylethanolamine/phosphatidylglycerol mimics of Gram-negative cytoplasmic membranes.

71 magainin 2 (MG2a) and PGLa using lipid-only mimics of Gram-negative cytoplasmic membranes.

72 mportantly, a synthetic exogenous soluble EL mimic of GraS protected the parental MW2 strain against

73 etically encoding fluorescent RNAs using RNA mimics of green fluorescent protein (GFP).

74 of various forms of Ras (loaded with GDP and mimics of GTP or nucleotide-free) at the allosteric and

75 strom cryo-EM structure of Set2 bound to the mimic of H2B ubiquitinated nucleosome.

76 l nucleophiles generated biologically active mimics of H3 with posttranslational modifications includ

77 e hypothesized that a synthetic nanoparticle mimic of HDL (HDL NP) that binds SR-B1 and removes chole

78 m, we tested a library of small, nonpeptidic mimics of HDPs (smHDPs) and identified compounds that ki

79 e functionality as a chemical and structural mimic of histidine.

80 the most promising antigenic and structural mimics of HIV-1 Env is the SOSIP.664-stabilized soluble

81 Finally, we have generated a molecular mimic of HMGB1 plus C1q, which cross-links RAGE and LAIR

82 d residues can serve as effective structural mimics of homologous alpha-amino acid residues within a

83 e (LdTyrRS) namely, aminoacylation, and as a mimic of host CXC chemokine.

84 Sca2, a mimic of host formins [4, 5], was later shown to be requ

85 and programmed cell death are manipulated by mimics of host proteins encoded by pathogenic bacteria.

86 eptides) have been investigated as synthetic mimics of host-defense peptides in recent years.

87 significant step toward a genuine functional mimic of human HDLs.

88 ations for the use of cell lines as faithful mimics of in vivo epigenetic and physiological processes

89 t type 1 IP(3)R (IP(3)R1) revealed that 6, a mimic of Ins(4,5)P(2), is only 4-fold less potent than I

90 l cells were studied in response to in vitro mimics of IRI.

91 singly, we found that K16Q mutation in H4, a mimic of K16 acetylation, leads to a structural disorder

92 Here we test a variety of grommet-like mimics of K30 capsular polysaccharide on wild-type Wza a

93 o generate specific numbers of PM mimics (PM(Mimics)) of known composition for dry, direct deposition

94 of the inhibitors citrate and a phosphinate mimic of l-Ala-d-Asp.

95 ssue engineering substrates, or developed as mimics of living tissue.

96 onstrated to produce a constitutively active mimic of LuxO approximately P.

97 ing that Pto may have evolved as a molecular mimic of LysM-RLK kinase domains.

98 An acetyl-mimic of MEK1 increases inappropriate growth properties,

99 has been applied to the design of structural mimics of membrane active antimicrobial peptides (AMPs)

100 we address this problem in the context of a mimic of microRNA-122 by employing novel nucleobase and

101 Both transfection of mimics of microRNA-192 or -215 and ALCAM knockdown by an

102 However, mimics of microRNA-192 or -215 significantly increased g

103 rovide the first structure of an acetylation mimic of mIDH2 and new insights into the regulatory mech

104 y transfecting cells with an inhibitor and a mimic of miR-146a.

105 reatment of these microglia with a synthetic mimic of miR-155 restored the inflammatory response to a

106 Furthermore, mimics of miR-185 and miR-186 blocked transforming growt

107 as increased in THP-1 cells transfected with mimics of miR-29b, miR-125a-5p, or miR-155.

108 Mimics of miR-30c-2* or miR-497, as well as pharmacologi

109 Transfection studies using mature miR mimics of miR-490 and miR-1192 that target Foxp3 and IL-

110 d whether minimally selective small molecule mimics of missing protein channels might be capable of c

111 Cyanide, a mimic of molecular oxygen, was found to bind to the meta

112 refore, we postulate selenite is a molecular mimic of monocarboxylates which allows selenite to be tr

113 However, acetylation mimics of MORF4L1, including K148L and K148Q, abolished

114 Designing molecular mimics of MoS2 edge sites is an attractive strategy to u

115 Expression of a double acetylation mimic of MPC2 (K19Q/K26Q) in H9c2 cells was sufficient t

116 The feasibility of these novel compounds as mimics of MUC1 antigens has been validated by the X-ray

117 synthesized lipid-tethered glycopolypeptide mimics of mucins and added them to lipid bilayers, allow

118 add another dimension in designing synthetic mimics of mussel adhesive proteins.

119 nt approach for generating glycosulfopeptide mimics of N-terminal PSGL-1 through development of a ste

120 his report, hydrolytically stable structural mimics of N7-guanine-conjugated DPCs were generated by r

121 damers remains a major challenge in creating mimics of native protein structures.

122 Structurally defined mimics of native trimeric Env glycoproteins (e.g., SOSIP

123 of the currently missing technologies is the mimic of natural photosynthesis to convert carbon dioxid

124 ing is an attractive technique for preparing mimics of natural and biological receptors.

125 ical porous columns and serve as fundamental mimics of natural porous helix-forming proteins and supr

126 By in vitro screening of small molecule mimics of naturally occurring host defense peptides (HDP

127 selected for NAE activation can function as mimics of Nedd8 to form thioester conjugates with NAE an

128 rts reveal that a tertiary protein structure mimic of NEMO is necessary for potent inhibition.

129 A metallopeptide-based mimic of nickel-containing superoxide dismutase was used

130 d also exhibits an impressive potential as a mimic of nucleosides, carbohydrates, PNA, amino acids, a

131 ydrolytically stable and accurate structural mimic of O-GlcNAc that can be encoded in mammalian syste

132 Thioglycosides are hydrolase-resistant mimics of O-linked glycosides that can serve as valuable

133 ed enzymes that are supplied with cyanide, a mimic of O2 (-) Studies with CDH and its isolated heme b

134 r of NifEN(M) as a structural and functional mimic of one catalytic alphabeta-half of NifDK while sug

135 constructs as well as oligonucleotide-based mimics of parts of the origin to examine the initiation

136 able reusability, thus making it a promising mimic of peroxidase catalysts.

137 a constitutively active variant (acetylated mimic) of PGAM1 stimulated flux through glycolysis.

138 The resulting selenomelanin is a structural mimic of pheomelanin.

139 atural products containing a C-P bond act as mimics of phosphate esters and carboxylic acids, thereby

140 t, the Hsp27 phospho-mimic is only a partial mimic of phosphorylated Hsp27, both in self-association

141 allographic structure of L-PYK with the S12D mimic of phosphorylation indicates that Cys436 is oxidiz

142 anine (cmF) and carboxyphenylalanine (cF) as mimics of phosphotyrosine (pY).

143 molecular photonic signal transducer and two mimics of photosynthetic photoregulatory processes are d

144 se proteins have been shown to act as ligand mimics of plant CLE peptides and are required for succes

145 ], the unique apolipoprotein of Lp(a), and a mimic of plasminogen.

146 Using genetically engineered mimics of polyubiquitylated PCNA, we have now examined t

147 SV replication were detected upon miR-335-5p mimics of primary PAMs.

148 PRMT1 S297A, a dephosphorylation mimic of PRMT1 had reduced ability to promote gene expre

149 ed azetidine-2-carboxylic acid (Aze), a dual mimic of proline and alanine, is activated by both human

150 hat are 1-2 nm in diameter act as functional mimics of protein channels, and have been used to explor

151 amer backbones have been described as useful mimics of protein secondary structure elements, enabling

152 In the search for synthetic mimics of protein secondary structures relevant to the m

153 chemistry is the identification of effective mimics of protein secondary structures that act as inhib

154 s suggest that rationally designed synthetic mimics of protein subdomains that target the transcripti

155 We also determine that genetic "mimics" of [PSI+] account for up to 80% of all phenotype

156 ings suggest that RaxX serves as a molecular mimic of PSY peptides to facilitate Xoo infection and th

157 ng only a single phosphocysteine (pCys) as a mimic of pThr at 180 was sufficient to switch the kinase

158 Persistent expression of Ag, a mimic of self-antigen, leads to functional inactivation

159 monium ions that were previously designed as mimics of several carbocations are actually better mimic

160 al feeding experiments using synthetic miRNA mimics of Sex-miR-10-1a, Sex-miR-4924, and Sex-miR-9 res

161 pt materials scientists to pursue biopolymer mimics of silk with high performance yet light weight.

162 Of particular interest is the development of mimics of small molecules with important cellular functi

163 y boosting cellular levels of Mn-antioxidant mimics of SOD.

164 The generation of non-natural mimics of SP-B and SP-C has previously been restricted t

165 lity of the 1:1 complex of NCp7 with a 20mer mimic of stem-loop 3 RNA (SL3, also called psi-RNA, in t

166 lts are a promising advance toward synthetic mimics of streptavidin/biotin.

167 al assemblies--potentially as more efficient mimics of structural color as it occurs in nature.

168 We report on a simple mimic of such a system that displays transient, sequence

169 Any artificial mimic of such systems designed for solar fuels productio

170 However, synthetic mimics of such diiron(IV) oxidants are rare.

171 s have shown each to be capable of producing mimics of such marks.

172 h a H2O2-responsive MRI contrast agent and a mimic of superoxide dismutase (SOD).

173 VOT obstruction (LAMPOON) is a transcatheter mimic of surgical chord-sparing leaflet resection.

174 riments, we show that argininamide, a ligand mimic of TAR's cognate protein binding partner Tat, is a

175 action with the ligand argininamide (ARG), a mimic of TAR's cognate protein binding partner, the tran

176 These results suggest that all peptidic mimics of Tat induce the same dynamics in TAR within thi

177 ouse was initially described as a phenotypic mimic of Tetralogy of Fallot with pulmonary atresia; how

178 ere, we report the first Fe-based functional mimic of the active site of [Fe]-hydrogenase, which was

179 the step-by-step construction of a prototype mimic of the AIS that we call an adaptive immune respons

180 ater (WS treatment) prior to infection, as a mimic of the aquatic environment of Legionella.

181 (EBV) protein latent membrane 2a (LMP2a), a mimic of the B cell receptor, provides constitutive surv

182 tify BRMS1 as the first eukaryote structural mimic of the bacterial IpaH E3 ligase family and establi

183 The development of an in-vitro mimic of the BBB requires recapitulating the correct phe

184 We synthesized a macrocyclic peptide mimic of the beta-hairpin from EC869 toxin and solved it

185 coli acyl carrier protein and FabA, a direct mimic of the biological process.

186 Using octatrienoic acid as a mimic of the C(56) polyenoic acid scaffold of ECO-02301,

187 We have constructed a synthetic mimic of the carboxysome, a cyanobacterial carbon-fixing

188 n Cas8f and AcrIF3 suggests that AcrIF3 is a mimic of the Cas8f nuclease recruitment helix.

189 fluorogenic RNA aptamers that bind DFHBI, a mimic of the chromophore in green fluorescent protein, a

190 is noncleavable but is a partial biological mimic of the cleaved form UmuD', has been identified.

191 It is also a stable structural mimic of the damage induced by the nitrofurazone family

192 The biocompatibility of a triazole mimic of the DNA phosphodiester linkage in Escherichia c

193 in the apo state and in complex with GDP, a mimic of the donor substrate, and with a glycopeptide ac

194 -peptide-HLA-B*18:01 complex is a structural mimic of the EBV peptide-HLA-B*18:01 complex, and that t

195 Zinc(II) cyclen, a small molecule mimic of the enzyme carbonic anhydrase, was evaluated un

196 d formation and site-directed mutagenesis, a mimic of the enzyme.substrate complex has been trapped.

197 erol and 10 +/- 2 cm/s in a 100% cholesterol mimic of the experimentally observed noncrystalline chol

198 excited-state electron donor, a dinucleotide mimic of the FADH2 cofactor containing O at the 5'-end a

199 ate ferryl precursor, and a vanadium(IV)-oxo mimic of the ferryl intermediate in the l-arginine 3-hyd

200 Although 1C8 was designed to be a structural mimic of the fused tetracyclic indole compound IDC16 tha

201 This nucleoside was incorporated into a mimic of the glutamate receptor B (GluR B) mRNA R/G edit

202 nt Spinach aptamer, which is a synthetic RNA mimic of the Green Fluorescent Protein, from its split s

203 One of these effectors is IpgB1, a mimic of the human Ras-like Rho guanosine triphosphatase

204 of such exposures, we developed an in vitro mimic of the in vivo event of exposure to PM contaminate

205 blocked by addition of synstatin, a peptide mimic of the integrin activating region present on the s

206 ure to produce a highly populated structural mimic of the intermediate state.

207 roaches: a truncation to generate a fragment mimic of the intermediate, and selective destabilization

208 The TIP peptide, a mimic of the lectin-like domain of TNF, activates ENaC b

209 I)-CO complex of the H103G H-NOX mutant as a mimic of the ligand-free and kinase-inhibitory Fe(II)-NO

210 Further, a neurochemical mimic of the light input pathway evoked larger shifts in

211 y enhanced responsiveness to a neurochemical mimic of the light input pathway to the SCN.

212 n of Cys78 with maleimide creates a solution mimic of the Lys-ligated cyt c that has enhanced peroxid

213 -II, a histidine-containing branched peptide mimic of the malarial biomarker Plasmodium falciparum hi

214 s dipeptidyl-peptidase IVA (DppIVA), a close mimic of the mammalian ectopeptidase CD26, which modulat

215 te peptide (CP20) and ATP to produce a close mimic of the Michaelis complex.

216 Creating an artificial functional mimic of the mitochondrial enzyme cytochrome c oxidase (

217 us expression of MCT12 and MCT12:214Delta, a mimic of the mutant allele, were used to assess protein

218 specific analysis of a recombinant, trimeric mimic of the native HIV-1 viral spike (BG505 SOSIP.664)

219 uence is a faithful antigenic and structural mimic of the native trimer in its prefusion conformation

220 nd acts as a structurally distinct synthetic mimic of the natural ligand, flavin mononucleotide, to r

221 P450cin complexed with nitric oxide, a close mimic of the O(2) complex, shows that Gly238 is likely t

222 N(-) complex is both stable and an excellent mimic of the O(2) complex.

223 ha-d-mannosyl-d-mannose (2alpha-MB), a short mimic of the O9a polymer.

224 oglutarate dioxygenase inhibitor is a better mimic of the overall transcriptional response to hypoxia

225 hem, compounds 2 and 3 appeared to be a good mimic of the parent endogenous thyronamine, T0AM and T1A

226 ntain a sulfamide group as a nonhydrolyzable mimic of the phosphate group in the cognate Ub/Ubl-AMP a

227 A physical mimic of the process using a layered swelling gel captur

228 ily accepted an N-acetylcysteamine thioester mimic of the reduced pentaketide product of Rdc5 to synt

229 and mammalian ribosomes and an RNA stem-loop mimic of the sarcin/ricin loop (SRL) at a higher catalyt

230 Compared with the dephosphorylation mimic of the seven phosphorylation sites, alanine substi

231 presence of the product acetate or a potent mimic of the tetrahedral intermediate were determined by

232 nding to the pre-catalytic state, a vanadate mimic of the transition state, and the product.

233 LMP1 is a constitutively active functional mimic of the tumor necrosis factor receptor superfamily

234 UL144 is a structural mimic of the tumor necrosis factor receptor superfamily

235 posomal nanoparticle loaded with a synthetic mimic of the tumor suppressor miRNA miR-34a as the activ

236 A mimic of the Wacker process for C horizontal lineO bond

237 Here we show a mimic of the Z-scheme with a molecular tetrad.

238 nate interaction through the provision of a "mimic" of the HLA-encoded peptide derived from the immun

239 erent classes of beta-lactam antibiotics, as mimics of the acyl-D-Ala-D-Ala moiety at the allosteric

240 hydrocarbon (PAH) isosteres, which expose BN mimics of the amidic NH functions.

241 on a possible SN1 catalytic mechanism and as mimics of the carbocation in the transition state of hUP

242 of the transmembrane helices is preserved in mimics of the cell bilayer, and that the apparent voids

243 y shown that two of these miRNAs function as mimics of the cellular miRNAs miR-155 and miR-142-3p.

244 We use this strategy to design mimics of the central immune cytokine interleukin-2 (IL-

245 king in S. aureus using fluorescently tagged mimics of the endogenous substrate of penicillin-binding

246 We argue that recombinant mimics of the envelope spike are currently capable of ca

247 Whereas azo-bis-ebselens 7 were poor mimics of the glutathione peroxidase (GPx)-enzymes, nitr

248 In search for better mimics of the glutathione peroxidase enzymes, pyridoxine

249 More generally, mice often provide poor mimics of the human diseases being modeled.

250 Recombinant trimeric mimics of the human immunodeficiency virus type 1 (HIV-1

251 Mimics of the hydrophilic-rich phase were prepared simil

252 trated by experiments that created synthetic mimics of the interior cavity) or if the interior also a

253 We investigated this hypothesis by making mimics of the intermediate that are the ground-state con

254 that synthetic polymers may not be suitable mimics of the intracellular environment.

255 hnology is used to create modular, synthetic mimics of the Large Latent Complex that restrains transf

256 and 2-azadecalins that are close structural mimics of the m/z 202.126 ion, and showed that they are

257 s requires experimental approaches providing mimics of the microenvironment that proteins encounter i

258 Yeast and mouse mimics of the most common variant, P286R, produce mutato

259 involves using recombinant, soluble protein mimics of the native trimer.

260 tion of bNAbs is to design soluble, trimeric mimics of the native viral Env trimer.

261 NAC) fatty acid thioesters have been used as mimics of the natural acyl carrier protein pathway inter

262 Although molecular mimics of the natural catalyst have been proposed, they

263 libraries may be considered to be structural mimics of the natural products pramanicin and epolactaen

264 phylococcus aureus, we show that fluorescent mimics of the natural substrate of PBPs (PG stem peptide

265 use beta-lactams are chemical and structural mimics of the natural substrate, resistance mediated by

266 s of nucleotides are considered to be useful mimics of the natural substrates, but direct structural

267 crystal structures of the Michaelis complex mimics of the PKA catalytic subunit (PKAc) were obtained

268 SIP Env trimers are structural and antigenic mimics of the pre-fusion native, surface-presented Env,

269 Iminoribitol mimics of the ribocation transition state in linkage to

270 rene macrocycles bearing phosphines as crude mimics of the rigid backbones of proteins, we demonstrat

271 Using peptide mimics of the S12 protein bearing deuterium at the 3 pro

272 ity analyses, we designed two cyclic peptide mimics of the TAR-binding beta2-beta3 loop sequences pre

273 Close mimics of the transition state are hypothesized to retai

274 These catalysts were designed as mimics of the two-point hydrogen-bonding interaction pre

275 antibodies by immunization with recombinant mimics of the viral spike.

276 n an anti-HIV screen to identify structural "mimics" of the fused tetracyclic indole compound 1 (IDC1

277 reciprocally compromised the effects of the mimics of their counterparts on M. marinum intracellular

278 elming majority of studies on small-molecule mimics of these enzymes entirely ignores the contributio

279 Importantly, administration of mimics of these miRNAs with sunitinib or axitinib result

280 Mutational mimics of these modifications (glutamine for acetylation

281 etic polymers have recently been explored as mimics of these natural peptides.

282 Synthetic mimics of these natural structures are highly desired to

283 Synthetic mimics of these proteins have been created to function a

284 In this work, we investigate supramolecular mimics of these systems by mixing one-dimensional assemb

285 y of 2,4-difluorotoluene (F), a low-polarity mimic of thymine (T), to form a hydrogen-bonded complex

286 Starting from a noncovalent linear mimic of TMC-95A, a series of dimerized inhibitors using

287 )-L-cysteine, which could be considered as a mimic of Tn antigen.

288 e, while the phosphonyl group is a versatile mimic of transition-states, intermediates, and primary m

289 of several carbocations are actually better mimics of transition state structures for carbocation de

290 e has been probed with a series of synthetic mimics of trehalose dimycolate in binding assays, in str

291 Because these are less than perfect mimics of true biological membranes, the structures are

292 Mimotopes, or peptide mimics of tumor antigens, elicit increased numbers of T

293 Vaccines that incorporate peptide mimics of tumor antigens, or mimotope vaccines, are comm

294 on findings, variant anatomy, artifacts, and mimics of TVAI when evaluating cases of craniocervical t

295 orobenzimidazole, non-hydrogen bonding shape mimics of uracil and hypoxanthine, respectively, is stro

296 de heteroconjugates were generated to act as mimics of UV cross-linked heteroconjugates.

297 t or treatment with cytoplasmic poly(I:C), a mimic of viral dsRNA, activates this pathway to regulate

298 ppaB2 is induced in response to poly(I:C), a mimic of viral dsRNA.

299 Only synthetic TLR7/8 ligand, a mimic of viral ssRNA, induced IL-23 production by LP CD1

300 l for antigen delivery, as adjuvants, and as mimics of viral structures.