ライフサイエンスコーパス: scaffold

1 ical addition of proteins to a ribosomal RNA scaffold.

2 time response through engineered sub-micron scaffold.

3 l marine natural product bromophycoic acid E scaffold.

4 nic semiconductors was assembled using a DNA scaffold.

5 ors, with a specific focus on Gravin, a PLK1 scaffold.

6 ed into a sunflower trypsin inhibitor cyclic scaffold.

7 rapid and modular access to this privileged scaffold.

8 rt2 inhibitors based on the 1,2,4-oxadiazole scaffold.

9 mily) are derived from the C7 epimer of this scaffold.

10 )8 barrel as an inherently evolvable protein scaffold.

11 0 = 0.21 muM, selectivity index (SI) 40) and scaffold.

12 ne, an alkaloid with a structurally distinct scaffold.

13 ary vasculature in a decellularized rat lung scaffold.

14 he 5,7-trans-fused bicyclic pseudolaratriene scaffold.

15 on the hydroxyl groups of the tartaric acid scaffold.

16 radial manner from a minimal flavin-binding scaffold.

17 rmeable membranes that serve as a structural scaffold.

18 residues, despite sharing a common morphinan scaffold.

19 s using N-[3-(2-pyridinyl) phenyl] benzamide scaffold.

20 ne cells, and constructing immune-modulating scaffolds.

21 been limited to cyclopentadienyl (Cp) based scaffolds.

22 lysis of multiple assemblies of the same set scaffolds.

23 assemble 3D crystals to be used as molecular scaffolds.

24 unctional groups inserted within fluorophore scaffolds.

25 ogy has been applied to medicinally relevant scaffolds.

26 en spunbonded poly(l-lactic acid) fiber mesh scaffolds.

27 ructurally and sequentially distinct protein scaffolds.

28 arsenal of synthetic methods to obtain such scaffolds.

29 led from iron and cysteine sulfur on protein scaffolds.

30 ero-vesicle assemblies with complex DNA nano-scaffolds.

31 after the introduction of cadaveric biologic scaffolds.

32 on of saturated bicyclic and tricyclic amine scaffolds.

33 rnished the desired trisubstituted imidazole scaffolds.

34 the inner and outer regions of the biphasic scaffolds.

35 re coumarin- and chomone-3-phenylcarboxamide scaffolds.

36 catalytic use in preparing complex synthetic scaffolds.

37 ration of the peptide assemblies into tissue scaffolds.

38 otentials based on conjugated, light element scaffolds.

39 laps on which a new cell-wall segment can be scaffolded.

40 Rgamma and identification of moieties of the scaffold 1 key to high transcriptional potency.

41 structure-activity relationship (SAR) of the scaffold 1, we synthesized 14 analogs of compound 1 whic

42 this hidden hydrophilicity, thus making this scaffold a good candidate for drug development.

43 ind that ARPP-16 interacts directly with the scaffolding A subunit of the serine/threonine protein ph

44 However, allosteric modulation of their scaffolding abilities and direct targeting of their inte

45 tion (ORR) catalyzed by a cofacial porphyrin scaffold accessed in high yield (overall 53%) using coor

46 nimodipine have the same 1,4-dihydropyridine scaffold and are indicated for hypertension.

47 reparatory period for stem cell seeding on a scaffold and relatively invasive procedures for stem cel

48 (KOP) receptor featuring a diphenethylamine scaffold and showed the promise of these ligands as effe

49 y, HUVEC cells naturally migrated in the ECM scaffold and spontaneously repopulated the lining of dec

50 rovide novel Sirt2 inhibitors with a compact scaffold and structural insights for further inhibitor i

51 applied to a new conformationally controlled scaffold and synthesized to accurately evaluate pairwise

52 third of the kinase-activating Sli15/INCENP scaffold and the catalytic subunit Ipl1/Aurora B.

53 en the patients who received a bioresorbable scaffold and the patients who received a metallic stent.

54 ed in firm integrin-mediated adhesion to the scaffold and well-stratified epithelial constructs, with

55 esults indicate that the respective roles of scaffolding and coat proteins may have been redistribute

56 y bound to phosphorylated M1R, beta-arrestin scaffolds and activates MEK-dependent ERK.

57 e, beta-cell-reactive T cells homed to these scaffolds and became enriched.

58 ising platform for future tissue-engineering scaffolds and biomedical applications.

59 ity ratio of Raman bands associated with the scaffolds and HA with the spatial offset depended on the

60 ule-mediated motility, cytoskeleton-membrane scaffolds and signaling proteins.

61 ning Cla4, a Cdc42-binding effector, Bem1, a scaffold, and Cdc24, a Cdc42 GEF.

62 for virion morphogenesis, release of the D13 scaffold, and the association of EFC proteins with viral

63 id kinase catalytic subunit VPS34, the VPS15 scaffold, and the regulatory BECN1 and ATG14 subunits.

64 fate and anthocyanin were preloaded in CaCO3 scaffold, and then microcapsules were created by coating

65 olds than these of CM/nHA-AL and PLLA/nHA/AL scaffolds, and the mechanical and degradation properties

66 Scaffolds are a core concept in medicinal chemistry, and

67 Non-antibody scaffolds are small proteins that are stable and can be

68 sphorylated protein 1 (Cat-1) is a signaling scaffold as well as an ADP-ribosylation factor-GTPase-ac

69 ing the way to exploiting these new coumarin scaffolds as caging groups that can be removed with visi

70 nes derived from readily available terpenoid scaffolds as efficient multifunctional reagents for the

71 the ascorbic acid units within the hydrogel scaffold; as a consequence, the hydrogel framework colla

72 ods is beneficial both for the developers of scaffold assembly algorithms and for the researchers foc

73 We show that scaffold assembly requires conserved leucine zipper (LZ)

74 re exist numerous methods and techniques for scaffold assembly, identifying similarities and dissimil

75 A microspheres-scaffold-based release system containing AL-encapsulated

76 OPN is the bone glue that acts as a scaffold between bone tissues matrix composition to bind

77 of everolimus-eluting bioresorbable vascular scaffolds (BVS) compared with everolimus-eluting stents

78 cal [AMA]) to Absorb (bioresorbable vascular scaffold [BVS]) using different experimental models.

79 ly increased the complexity of the molecular scaffold by introducing a bicyclic core.

80 Each complex is scaffolded by a specific SMC protein dimer (heterodimer

81 formation in vivo requires an intracellular scaffold called Tight Junction Protein 1b (Tjp1b).

82 To investigate how a different protein scaffold can modulate these energies, we measured DeltaD

83 nce that PSI confinements in synthetic lipid scaffolds can be used for tuning the photoexcitation cha

84 dation site-selectivity, in which the enzyme scaffold causes a specific C-H bond to be functionalized

85 may inhibit immune responses to the antigen-scaffold combination.

86 designed using the 6-OH-benzothiophene (BT) scaffold common to arzoxifene and raloxifene.

87 folds within the equiaxially loaded biphasic scaffolds compared to unstrained samples.

88 rotease inhibitor hydroxyl-ethyl-amine-based scaffold compound 49c.

89 ble nonsteroidal antiandrogens show a common scaffold consisting of two aromatic rings connected by a

90 Cell-scaffold contact measurements are derived from pairs of

91 eds compared to wounds treated with chitosan scaffolds containing control DNA or wounded controls.

92 When scaffolds containing lysates from an insulin-producing b

93 These results suggest that chitosan scaffolds containing plasmid DNA encoding VEGF189 and pe

94 fficient access to unprecedented spirocyclic scaffolds containing up to five stereocenters with high

95 medicinal chemistry on the compounds' basic scaffold could enhance the potency and selectivity for A

96 Contents from infected scaffolds could be transferred to fresh scaffolds to est

97 engineering intestine on vascularized native scaffolds could bridge the gap between cell/tissue-scale

98 G-protein complex (STE4), the pheromone MAPK scaffold (CST5), and the two terminal MAP kinases (CEK1/

99 A second SPB-associated scaffold, Cut12, promotes SPB-associated Cdk1-cyclin B t

100 Phosphorylation abrogates the scaffold-dependent stimulation of GEF activity, renderin

101 critical variable in additively manufactured scaffold design for functional tissue engineering.

102 This combination of RNAi scaffold design with Qbeta VLP packaging is demonstrated

103 inversely regulated by endothelin-1 and CAV1 scaffolding domain after liver injury.

104 blocked CAV1 phosphorylation induced by CAV1 scaffolding domain, indicating that CAV1 interaction wit

105 annulated thiophene/furan-based heterocyclic scaffolds (e.g., 4,5-dihydro-6H-thieno[2,3-c]pyrrol-6-on

106 equence remains highly fragmented, dozens of scaffolds encompassing more than one mapped gene were id

107 te epoxidation on opposite faces of the ring scaffold, evidence of competitive epoxidation pathways,

108 ta from ChEMBL20 to examine the evolution of scaffold features, such as enumerated compounds, biologi

109 ected by the giant protein titin, which is a scaffolding filament, signaling platform, and provider o

110 he inorganic benzene as a versatile aromatic scaffold for engineering of molecular materials with tai

111 to the role of RG cells to provide a stable scaffold for neuronal migration, and suggest that the tr

112 Here we report the engineering of a protein scaffold for preferential binding to K-Ras G12D.

113 odes filamin C-a protein that acts as both a scaffold for the assembly and organization of the centra

114 factors, and implicate Jmjd2c as a molecular scaffold for the assembly of essential enhancer-protein

115 Suramin is thus a promising scaffold for the development of novel therapeutics to in

116 The nucleocapsid acts as a scaffold for virus assembly and as a template for genome

117 thereby providing a potential off-the-shelf scaffold for whole tooth regeneration.

118 onal 3D bioprinting allows fabrication of 3D scaffolds for biomedical applications.

119 otential applicability to the fabrication of scaffolds for cell culture, reconfigurable microfluidic

120 ed the promising application of CM-ALs (10%) scaffolds for drug delivery and bone tissue engineering.

121 ecular-weight gelators (LMWGs) are promising scaffolds for drug-delivery applications.

122 this end, incorporation of suitable protein scaffolds for PSI incorporation is of great scientific a

123 dence from recent studies implicate that the scaffolding function of enzymes could be as important in

124 ost potent sweeteners combines a hydrophobic scaffold functionalized by a limited number of hydrogen

125 Nanobodies, a minimalist scaffold generated from camelid-derived heavy-chain IgGs

126 ce thrombosis occurred in 31 patients in the scaffold group as compared with 8 patients in the stent

127 improvement of the glucose clearance in the scaffold groups compared to diabetic controls.

128 to install and remove halogens from organic scaffolds has evolved in nature.

129 ved great attention, and different molecular scaffolds have been selected to target CB2R subtypes.

130 tight control over pore sizes, inverse opal scaffolds have found widespread use in biomedical applic

131 Although fully bioresorbable scaffolds have the potential to further improve long-ter

132 y model with excitons localized on the arene scaffold, here generalized to Cn symmetry, accurately de

133 In recent years, scaffold hopping calculations are increasingly carried o

134 l investigational agent pretomanid (PA-824), scaffold hopping from delamanid inspired the discovery o

135 tual prevalence of pharmacophore methods for scaffold hopping, a variety of computational approaches

136 -stacks) of stained cells and three types of scaffolds (i.e., spun coat, large microfiber, and medium

137 pared with the Absorb bioresorbable vascular scaffold in an ex vivo porcine arteriovenous shunt model

138 rrounded by other side chains in the protein scaffold in biology, which may alter the apparent DeltaD

139 -pull chromophores based on a novel coumarin scaffold in which the carbonyl of the lactone function o

140 ing soft materials potentially applicable as scaffolds in cardiac tissue engineering (TE).

141 amide analogues relative to a common warhead scaffold, in both noncovalent and covalent binding state

142 correlated, we find that there are apparent scaffold induced changes in DeltaDeltaGsc(o) for more th

143 kinase at DNA lesions; however, the putative scaffold interactions involving the N-terminal BRCT doma

144 ded native de-cellularized rat parotid gland scaffolds into the renal capsule of nude mice led to the

145 tivation in a manner dependent on the ERK1/2 scaffold IQGAP1.

146 Fs to the core SKP1-CUL1-F box protein (SCF) scaffold is facilitated by light signals or PIF3 phospho

147 The xanthine scaffold is known to be the forefather of a class of bio

148 otic genomes; however, at present additional scaffolding is needed to achieve chromosome-level assemb

149 ns and reactions have evolved from ancestral scaffolds is fundamental to understanding chemical and e

150 ent of new antibiotics around proven natural scaffolds is the best short-term solution to the rising

151 yde Probe 573 (FAP573), based on a resorufin scaffold, is the most red-shifted and FA sensitive in th

152 The kinetochore scaffold Knl1, when phosphorylated by Mps1, recruits che

153 e kinases CK2 and p-ERK1/2 and the signaling scaffold KSR1.

154 le of interrogating high quality and diverse scaffold libraries with verifiable folding and stability

155 ion in turning gene expression on or off and scaffold-like properties for protein and small molecule

156 This study demonstrated that scaffolds loaded with PEI-(pBMP-2+pFGF-2) could be an ef

157 ury (SCI), we demonstrated that the tailored scaffolding maintained hMSC stemness, engraftment, and l

158 orescence, where SBB is applied to polymeric scaffold materials before cell seeding.

159 ially problematic, since prior immunity to a scaffold may inhibit immune responses to the antigen-sca

160 nd in vivo experiments revealing how protein scaffolds may cut tubular membranes.

161 nd fidelity, and hCMPs fabricated with these scaffolds may significantly improve recovery from ischem

162 A further scaffold modification to a (4-cyanophenyl)glycinamide (e

163 nding proteins (RBPs) as central active-zone scaffolding molecules.

164 ions by binding to cytoplasmic signaling and scaffolding molecules.

165 bottle gourd inbred line, USVL1VR-Ls, with a scaffold N50 of 8.7 Mb and the longest of 19.0 Mb.

166 ssembly represents >78% of the genome with a scaffold N50 of 88.8 kb that has a high fidelity to the

167 mprovements, and examined the effect of gRNA scaffold, number of gRNAs per gene and number of replica

168 phron portions of renal extracellular matrix scaffolds obtained after decellularization of human rena

169 In vertebrates, the 7SK RNA forms the scaffold of a complex, which regulates transcription pau

170 In addition, the macrolactone scaffold of MTM is smaller than in other macrolides.

171 s share the exact five- to six-bicyclic ring scaffold of the Catharanthus iridoids.

172 s of agarose-derived hydrogels depend on the scaffolding of the polysaccharide network.

173 how orthologs can generate rigid macrocyclic scaffolds of different sizes.

174 sue engineering, autofluorescence of polymer scaffolds often lowers the image contrast, making it dif

175 oDSGCs, but also by interneurons that form a scaffold on which ooDSGC ON dendrites fasciculate.

176 arget binding by (a) truncating the original scaffold or (b) introducing a hydrophilic group to inter

177 These results may reflect a protein scaffold or complex stabilization role of NUWA between E

178 sue devoid of any exogenous material such as scaffolds or growth factors.

179 Removal of the scaffolds or kidney grafts resulted in immediate return

180 ial pi-pi and C-H...pi interactions within a scaffold organized by multiple hydrogen bonds dictate st

181 residing at the plasma membrane in neurons, scaffolds PKA to target proteins to mediate downstream s

182 Three-dimensional porous scaffolds play a pivotal role in tissue engineering and

183 designed with 3D printing, and indicate that scaffold pore architecture is a critical variable in add

184 lates (GPs) drive elongation by generating a scaffold progressively replaced by bone.

185 In summary, trend analyses of scaffold properties could support scaffold selection and

186 , and by spatially patterning cell types and scaffold properties in three dimensions.

187 espectively, of the AMPA-receptor regulatory scaffold protein A-kinase anchoring protein (AKAP) 79/15

188 ctor receptor-associated factor 2 (TRAF2), a scaffold protein and E3 ubiquitin ligase important for i

189 1 to double-strand breaks (DSBs) through the scaffold protein CCDC98 (Abraxas) and facilitates DNA da

190 ransmembrane protein A17 and the capsid-like scaffold protein D13 was sufficient to form similar ER-a

191 esolution the distribution of the inhibitory scaffold protein gephyrin in response to protocols induc

192 Anillin is a conserved scaffold protein involved in organizing the structural c

193 yndrome (HGPS), a mutant form of the nuclear scaffold protein lamin A distorts nuclei and sequesters

194 The abnormal particles retained the D13 scaffold protein of immature virions, were severely defi

195 XRCC1 is a molecular scaffold protein that assembles multi-protein complexes

196 The scaffold protein X-ray repair cross-complementing 1 (XRC

197 nstructed truncated versions of the membrane scaffold protein, allowing the preparation of a range of

198 IGF-I receptor signals through an alternate scaffold protein, SHPS-1, resulting in pathophysiologic

199 rane beta-barrel Escherichia coli OmpLA as a scaffold protein.

200 transmembrane beta-barrel E. coli PagP as a scaffold protein.

201 bstitutions ranged from inefficient internal scaffolding protein B binding to faulty procapsid elonga

202 id elongation reactions mediated by external scaffolding protein D.

203 Keratin 16 (K16) is a cytoskeletal scaffolding protein highly expressed at pressure-bearing

204 The scaffolding protein Homer assembles SOC complexes, but i

205 rtant new insights into the role of FAK as a scaffolding protein in molecular complexes that regulate

206 omplementation group A (XPA) is an essential scaffolding protein in the multiprotein nucleotide excis

207 RLTPR encodes a recently described scaffolding protein in the T-cell receptor signaling pat

208 also called AKAP450/CG-NAP/AKAP9) is a large scaffolding protein located at both the centrosome and G

209 sis of human metastatic genes identified the scaffolding protein metastasis suppressor 1 (MTSS1) as a

210 Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2, are causal of gray platelet

211 The Cas family scaffolding protein p130Cas is a Src substrate localized

212 where it associates with and stabilizes the scaffolding protein PSD95, promoting dendritic spine mat

213 We have previously shown that the scaffolding protein Ran-binding protein 9 (RanBP9), whic

214 The chromatin scaffolding protein SMCHD1 (structural maintenance of ch

215 We examined whether the scaffolding protein sodium-hydrogen exchanger regulatory

216 cells by knocking down ANLN, a cytoskeletal scaffolding protein that regulates cytokinesis and might

217 9 (AC9) is found tightly associated with the scaffolding protein Yotiao and the IKs ion channel in he

218 multiple ankyrin repeat domains 3 (SHANK3B) scaffolding protein, defective expression of which has b

219 nhibitor, pointed to a mechanism involving a scaffolding protein, Wag31, involved in polar elongation

220 interaction with Ajuba, an actin binding and scaffolding protein.

221 redistributed during the evolution of a two-scaffolding-protein system.

222 It currently contains 273 scaffold proteins and 1118 associated signaling pathways

223 Mice deficient for either of these scaffold proteins exhibit distinct maturation patterns o

224 a lipid bilayer surrounded by a boundary of scaffold proteins have emerged as a powerful tool for me

225 Scaffold proteins modulate signalling pathway activity s

226 aptic density (PSD) contains a collection of scaffold proteins used for assembling synaptic signaling

227 ion, we observed marked loss of postsynaptic scaffolding proteins and reduced complexity of the sub-s

228 as associated with reduced recruitment of TZ scaffolding proteins and reduced Smoothened levels at ci

229 eodomain finger-containing (BRPF) family are scaffolding proteins important for the recruitment of hi

230 ) exchanger regulatory factor (NHERF) family scaffolding proteins that are required for many aspects

231 depend on interactions between claudins, ZO scaffolding proteins, and the cytoskeleton.

232 ignal through Gi/o-coupled G-proteins and/or scaffolding proteins, such as beta-arrestin, we find tha

233 n of G protein-coupled receptor signaling by scaffolding proteins.

234 rmediates are converted to a known genotoxic scaffold, providing metabolic support of our mechanistic

235 evel of scaffolds rather than compounds, and scaffold queries increasingly abstract from chemical str

236 are increasingly carried out at the level of scaffolds rather than compounds, and scaffold queries in

237 NS cells seem to be a good tool for scaffold repopulation, paving the way for experimental i

238 as is the case for other alternative binding scaffolds, represent complementary affinity reagents to

239 set of high-fidelity contigs and a sequence scaffold, representing a mean 98% of the target region.

240 e, the 5-membered chiral biaryl heterocyclic scaffold represents a departure from 6-membered P,N-liga

241 structure-activity relationship of these two scaffolds, resulting in nanomolar potencies in an ATP sy

242 The scaffold's core design combines (ortho-tolyl)amide and o

243 Moreover, acellular liver scaffolds seeded with hepatocytes produced functional bi

244 nalyses of scaffold properties could support scaffold selection and prioritization in small molecule

245 reated with FHs alone or in the absence of a scaffold showed disorganized collagen formation and poor

246 tly far more candidate antigens than antigen scaffolding strategies.

247 Despite a similar scaffold strut thickness, the Magmaris sirolimus-eluting

248 in vivo monitoring the mineralization in 3D scaffolds subcutaneously implanted in small animals.

249 that SMAPs act by binding to the PP2A Aalpha scaffold subunit to drive conformational changes in PP2A

250 NF-kappaB essential modulator (NEMO) is the scaffolding subunit of the inhibitor of kappaB kinase (I

251 erstood neddylation targets are the cullins, scaffold subunits of E3 ubiquitin ligases, where neddyla

252 Further, biologically relevant scaffolds, such as alpha-quaternary beta-homo prolines a

253 Furthermore, these PA scaffolds support myogenic progenitor cell survival and

254 Furthermore, recellularization of the scaffold supported the proliferation of SCAP throughout

255 r integration with complementary phasing and scaffolding techniques.

256 e sustained drug release of CM-AL-containing scaffolds than these of CM/nHA-AL and PLLA/nHA/AL scaffo

257 We show that FER acts as a RALF-regulated scaffold that modulates receptor kinase complex assembly

258 data reveal intersectin as an autoinhibited scaffold that serves as a molecular linker between the s

259 ed by conformational dynamics of the protein scaffold that surrounds the active site, yet the exact n

260 Cell junctions are scaffolds that integrate mechanical and chemical signali

261 ivity of functional gene groups by acting as scaffolds that promote the local assembly of tissue-spec

262 Scaffolding the calcium/calmodulin-dependent phosphatase

263 ing two sulfur atoms to a single carboxylate scaffold, the molecular solid reaches a reversible capac

264 n the current CE-mark approved bioresorbable scaffolds, their basic characteristics, and clinical res

265 hromophores and establish the use of the DNA scaffold to arrange carbon layers in homogeneous, rapidl

266 The annealing of the scaffold to form functional RNAs is intramolecular and i

267 ast stem cells (TSCs) in a three-dimensional scaffold to generate structures whose morphogenesis is m

268 on laser lithography is employed for LC cell scaffolding to accurately verify theoretical predictions

269 nd high levels of interferons can be used as scaffolds to carry therapeutic oligonucleotides, while p

270 g cells are seeded within porous biomaterial scaffolds to create functional cardiac patches.

271 adaptive immune system, providing versatile scaffolds to display diverse antigen-binding surfaces.

272 cted scaffolds could be transferred to fresh scaffolds to establish new infections for at least three

273 A variety of assembly and scaffolding tools are available, but it is not always ob

274 tify selective degradation of the signalling scaffold TRAF3.

275 The tricarbocyclic scaffold was assembled starting from an easily accessibl

276 The bioresorbable scaffold was associated with a higher incidence of devic

277 The resulting maleimide scaffold was optimized to subnanomolar potency while ret

278 METHODS AND The scaffold was seeded with approximately 50 000 human-indu

279 is sirolimus-eluting bioabsorbable magnesium scaffold was significantly less thrombogenic compared wi

280 stimulating nerve repair in a nerve-guidance scaffold was used to explore the regenerative effect of

281 logues, novelized with high-valued bioactive scaffolds was synthesized by means of click-chemistry un

282 Using scaffolds, we tested the capacity of different stromal c

283 l and degradation properties of CM-ALs (10%) scaffolds were comparable to that of PLLA/nHA control.

284 Several novel potentiator scaffolds were identified with efficacy comparable with

285 In this study, chitosan scaffolds were prepared via freeze drying and loaded wit

286 pulp stem cells, encapsulated in a hydrogel scaffold, were injected into half the experimental teeth

287 based on the 1,4,5-trisubstituted imidazole scaffold which are appended with aliphatic linkers that

288 ed dihydropyridopyrimidine pan-BET inhibitor scaffold, which was uncovered via a virtual screen follo

289 ed us to obtain a completely acellular renal scaffold while maintaining the extracellular matrix stru

290 we report the first synthetic, ceramic-based scaffold whose architecture closely mimics that of cuttl

291 lthiazoles were reported previously as a new scaffold with antibacterial activity against an array of

292 ted the proliferation of SCAP throughout the scaffold with differentiation into odontoblast-like cell

293 e class of NIR dyes via modifying the rhodol scaffold with fused tetrahydroquinoxaline rings is descr

294 Extending this scaffold with suitable residues resulted in an interfere

295 d assembly of the American alligator genome, scaffolded with in vitro proximity ligation (Chicago) da

296 possibility to repopulate naturally obtained scaffolds with cells of different sources is advancing.

297 array of medicinally important heterocyclic scaffolds with diverse functional group tolerance.

298 echnique produces extracellular matrix-based scaffolds with exceptional resolution and fidelity, and

299 o Tra1, hence it does not act as a molecular scaffold within SAGA.

300 e identification of new Cruzipain inhibitory scaffolds within the GlaxoSmithKline HAT (Human African

301 tives of Cl-amidine, hypothesizing that this scaffold would allow access to a series of PAD2-selectiv