ライフサイエンスコーパス: attachment of @2 to

1 The successful covalent attachment of up to 11 tetraphenyl porphyrins in a row o

2 oupling methodology was developed for direct attachment of butyl acrylate to 5-iodoracil, 5-iodocytos

3 F]-radiotracers were generated by the direct attachment of (18)F to a carbon in the organic backbone

4 ing enzymes, (iii) enzymes that catalyze the attachment of a probe to a target sequence, and (iv) bia

5 The attachment of a sugar to a hydrophobic polyisoprenyl car

6 stinct case studies, we demonstrate that the attachment of ACT to a ligand does not significantly alt

7 rt a general approach for the regioselective attachment of antibodies to a surface using truncated fo

8 Attachment of azobenzene leads to a distortion of the DN

9 nding in an engineered site and the covalent attachment of benzocaine-methanethiosulfonate to a cyste

10 Here, we show that the attachment of butterfly wings to a solar cell increases

11 c (Young's) modulus of cells using AFM, good attachment of cells to a substrate is paramount.

12 es form in a sequential process initiated by attachment of cells to a surface, followed by the format

13 vealed that OxyR plays a role in the primary attachment of cells to a surface.

14 idence of regiospecific decompositions after attachment of fluoride anion to a specific hydroxyl grou

15 c-type cytochromes, defined by the covalent attachment of heme to a CXXCH motif, are key electron ca

16 tochromes, which are defined by the covalent attachment of heme to a CXXCH motif.

17 Attachment of ligature to a second maxillary molar induc

18 natural hydrolytic mode of action, allow the attachment of N-glycans to a wide variety of substrates

19 n OvCa primary cells and cell lines, reduced attachment of OvCa cells to a 3D organotypic model of me

20 The azide functionalization allows for attachment of the ligand to a surface by conventional cl

21 as the substrates of PPTase for the covalent attachment of the probes to a specific Ser residue in th

22 The attachment of ubiquitin to a protein substrate is accomp

23 Covalent attachment of ubiquitin to a substrate is catalysed by t

24 mophilic interaction is not required for the attachment of bacteria to abiotic surfaces.

25 demonstrates a direct link between disrupted attachment of myosin molecules to actin monomers and mus

26 eckpoint (SAC) arrests mitosis until bipolar attachment of spindle microtubules to all chromosomes is

27 g that CpcS-I and CpcU are also required for attachment of PCB to allophycocyanin subunits in vivo, a

28 step in Pneumocystis infection involves the attachment of organisms to alveolar epithelial cells (AE

29 protein modification that involves enzymatic attachment of sugars to amino acid residues.

30 The covalent attachment of PARP-1 to AP site-containing DNA appears t

31 Our data suggest a bivalent attachment of WASp to Arp3 (within peptides 162-191 and

32 a chemical tagging approach that enables the attachment of multiple modifications to bacterially expr

33 , but the mechanisms underlying the covalent attachment of FAD remain to be fully elucidated.

34 f-assembly of nanoelectronic devices and the attachment of nanoparticles to biomolecules for single-m

35 ins are emerging as important factors in the attachment of bacteria to biotic and abiotic surfaces.

36 Tendons and ligaments mediate the attachment of muscle to bone and of bone to bone to prov

37 cDNA molecule is uniquely labeled by random attachment of barcode sequences to both ends.

38 on of Notch signaling, and they also control attachment of GSCs to cap cells and E-cadherin levels at

39 al aspect of the biology of nematodes is the attachment of phosphorylcholine (PC) to carbohydrate.

40 mber, milk, and lettuce) even after covalent attachment of BREs to carboxy groups of CBMAA.

41 In vitro, attachment of MBCD4 to CD4+ T cells was significantly gr

42 by binding to gp120 and interfering with the attachment of virus to CD4+ T-cells.

43 sin networks, which generates force, and the attachment of actin networks to cell-cell junctions, whi

44 sociated HN and F glycoproteins directed the attachment of VLPs to cell surfaces and fusion of VLP me

45 l surface molecules that are involved in the attachment of poxviruses to cells.

46 ot alter cell surface expression of JAM-A or attachment of reovirus to cells.

47 While LSTc is involved in the initial attachment of virus to cells via interactions with VP1,

48 er development and is partly achieved by the attachment of viral DNA to cellular chromatin during cel

49 Because the attachment of xyloglucan to cellulose hampers depolymeri

50 o the dynein heavy chain and may mediate the attachment of dynein to centrosomes and other cargoes.

51 Chromosome congression requires the stable attachment of microtubules to chromosomes mediated by th

52 ing cell internalization by active pathways, attachment of cargo molecules to CPPs invariably reduces

53 re, CpcSU is the bilin lyase-responsible for attachment of PCB to Cys-82 of CpcB and Cys-81 of ApcA a

54 th CpcS-I and CpcU are required for covalent attachment of PCB to Cys-82 of the PC beta subunit in th

55 s through S-nitrosylation, that is, covalent attachment of NO to cysteine residues to form S-nitrosot

56 ge multimeric glycoprotein that mediates the attachment of platelets to damaged endothelium and also

57 rCypA inhibited the attachment of Hc to DC, but not to Mphi.

58 ing the structure or surface to minimize the attachment of microbes or to delay the development of bi

59 ing NMDA receptors, consistent with observed attachment of ADDLs to dendritic spines.

60 esents a new direction for the site-specific attachment of biomolecules to device platforms.

61 After attachment of LCAT to discoidal HDL, the helix 5/5 domai

62 se a model whereby B. anthracis LCPs promote attachment of SCWP precursors to discrete locations in t

63 anism that cumulatively involved both direct attachment of ubiquitin chains to DMalpha and a function

64 cs) have been modulated by direct peripheral attachment of up to eight ferrocenes.

65 ssays, which showed a strong decrease in the attachment of BCs to endothelial cells when MUC1 and CD4

66 SPON-1 maintains strong attachments of muscles to epidermis; in the absence of S

67 is organisms, plays an important role in the attachment of this organism to epithelial cells and macr

68 polyclonal anti-PfRH5 Abs inhibit the tight attachment of merozoites to erythrocytes and are capable

69 transpeptidation to facilitate site-specific attachment of PEG to extend cytokine half-life with full

70 nit, indicating either partial or disordered attachment of cofilin to F-actin and/or competition betw

71 n FA-BRCA pathway activation is the covalent attachment of monoubiquitin to FANCD2 and FANCI.

72 The attachment of tumor cells to fetuin-A was accompanied by

73 sin SdrG is necessary and sufficient for the attachment of this pathogen to Fg-coated materials.

74 Herein we report that attachment of oligodendrocytes (OLs) to fibronectin via

75 y a longer duration consistent with covalent attachment of the ligand to functionally important targe

76 des identifies parameters that influence the attachment of oligonucleotide probes to GAPSII slides, s

77 The attachment of thiolated DNA to gold nanoparticles (AuNPs

78 The L protein mediates attachment of virions to heparan sulfate proteoglycans o

79 The attachment of bacteria to host cells and tissues, and th

80 y, bacterial surface components that mediate attachment of GBS to host cells or the extracellular mat

81 Here, we characterized the attachment of influenza virus to host cell receptors usi

82 Among these, the sigma1 protein mediates attachment of reovirus particles to host cells via inter

83 Attachment of reovirus to host cells is mediated by the

84 he pathogenesis of infective endocarditis is attachment of the organisms to host platelets.S. sanguin

85 sis was completely blocked when we prevented attachment of the parasites to host cells while allowing

86 The attachment of UPEC to host cells is mediated by FimH, a

87 However, LDLR-independent attachment of VSV to HPAF-II cells was dramatically impr

88 Our data show a dramatically weaker attachment of VSV to HPAF-II cells, the most resistant h

89 Our findings support a model in which attachment of HBV to HSPGs is mediated by the AGL HS bin

90 Here, we show that upon attachment of L. pneumophila to human monocyte-derived m

91 array analysis was used to determine whether attachment of M. catarrhalis to human bronchial epitheli

92 iae in the rosE mutant resulted in increased attachment of S. typhimurium to human colonic epithelial

93 kinetics of cell spreading and the level of attachment of cells to hydrophobic surfaces.

94 ariety of bacteria and viruses, and mediates attachment of S. mutans to hydroxyapatite on the surface

95 n O-linked glycosylation, which involves the attachment of glycans to hydroxyl groups of serine or th

96 on-defective receptors demonstrated that the attachment of ubiquitins to Ig beta is required for endo

97 ry, we have previously demonstrated specific attachment of acyl chains to individual acylation sites.

98 and light chains (LC) which result from the attachment of drug conjugates to interchain cysteine res

99 Attachment of SUMO moieties to internal lysines in Ubc9

100 tion of cellulose fibrils is involved in the attachment of Agrobacterium tumefaciens to its plant hos

101 We found that the attachment of LCMV to its cellular receptor alpha-dystro

102 Therefore, attachment of Cpa to K173 of a T3 subunit would block fu

103 ins fibronectin and vitronectin and mediates attachment of H. ducreyi to keratinocytes.

104 chment of HIV to T cells and macrophages and attachment of HSV-1 to keratinocytes but can also inhibi

105 One favoured route for attachment of APP to kinesin-1 involves the scaffolding

106 e segregation through monitoring the bipolar attachment of microtubules to kinetochores.

107 f chromosomes in mitosis requires the stable attachment of microtubules to kinetochores.

108 indle assembly checkpoint, that monitors the attachment of spindle microtubules to kinetochores as a

109 In fission yeast, erroneous attachments of spindle microtubules to kinetochores are

110 romosome segregation requires stable bipolar attachments of spindle microtubules to kinetochores.

111 observed in situ at low temperature, and the attachment of monomer to ligand was confirmed by GC/MS a

112 he roles of pmrHFIJK in the biosynthesis and attachment of L-Ara4N to lipid A and renamed these genes

113 One hypothesis is that a tight noncovalent attachment of TM proteins to lipids that have a strong a

114 8-MAPK, JNK, ERK5, and NF-kappaB promote the attachment of human neutrophils to lung microvascular EC

115 ng chemistry which controls the differential attachment of 18C6 to lysine by using ubiquitin as a mod

116 s varied by multiples of 324, indicating the attachment of lactose to lysine residues in the proteins

117 In this case, attachment of ubiquitin to lysine 123 (K123) of H2B is i

118 n the host cell plasma membrane and promotes attachment of bacteria to mammalian cells by binding to

119 rcalated disc formation and a failure in the attachment of myofibrils to membrane complexes.

120 ellization can promote temperature triggered attachment of the micelles to membranes, thus rescuing b

121 The controlled attachment of chromophores to metal or semiconducting su

122 This method not only improves the attachment of DNA to metal surfaces but also represents

123 Proper attachment of chromosomes to microtubules is crucial for

124 e assembly checkpoint (SAC) monitors correct attachment of chromosomes to microtubules, an important

125 The mitotic checkpoint monitors the attachment of kinetochores to microtubules and delays an

126 C is thought to monitor two distinct events: attachment of kinetochores to microtubules and the stret

127 By improving the attachment of molecular motors to microtubules, huntingt

128 Attachment of kinesin-1 to mitochondria involves the out

129 actor (MBR; nominal pore size 0.04 mum): (i) attachment of virus to mixed liquor solids; (ii) virus r

130 r SERS sensor can be utilized to investigate attachment of targeting ligands to nanocarriers (attachm

131 ylation illustrates an alternative means for attachment of carbohydrates to natural products.

132 n a reactive electrophile, enabling covalent attachment of the photoswitch to naturally occurring nuc

133 For the first time, attachment of small anions to neutral molecules in laser

134 active alkylating group that facilitates the attachment of the fluorochrome to nucleophilic moieties

135 ed the effects of solution conditions on the attachment of capture antibodies, to optimize the assay

136 Attachment of OvCa cells to peritoneum and omentum repre

137 pblA and pblB mediate the attachment of S. mitis to platelets and play a significa

138 In this study, we report the reversible attachment of lysozyme to poly(ethylene glycol) (PEG) by

139 The reversible attachment of proteins to polymers is one potential stra

140 chemoenzymatic method for the site-specific attachment of lipids to protein substrates is described.

141 critical factor may be the lack of covalent attachment of PS to protein in intact Pn, highlighting t

142 The reversible covalent attachment of chemical probes to proteins has long been

143 ne is an extremely useful site for selective attachment of labels to proteins for many applications,

144 sylation is a stepwise procedure of covalent attachment of oligosaccharide chains to proteins or lipi

145 The controlled attachment of synthetic groups to proteins is important

146 Ubiquitination, the covalent attachment of ubiquitin molecules to proteins, is emergi

147 Subsequently, it was discovered that the attachment of ubiquitin to proteins can modify their fun

148 ng end-grafted GAG chains that mimic the end attachment of these chains to proteoglycans.

149 nges in the photocurrent denote irreversible attachment of NPs to Pt UMEs (<30 mum diameter).

150 Post-translational attachment of geranylgeranyl isoprenoids to Rab GTPases,

151 glycosylated proteins that involves chemical attachment of aminooxy glycans to recombinantly produced

152 S, suggesting a link between OPN and reduced attachment of COM crystals to renal epithelium.

153 dicts the formation of HbS polymer fibers by attachment of monomers to rough fiber ends and the growt

154 and and midgut peptide 1 (SM1), which blocks attachment of sporozoites to salivary glands; a single-c

155 N-glycosylation involves the attachment of an oligosaccharide to selected asparagine

156 propose that high-specificity, low-affinity attachment of MERS-CoV to sialoglycans during the preatt

157 , we demonstrate that these proteins mediate attachment of bacterial cells to sialylated gangliosides

158 Attachment of oocysts to silica surface in a radial stag

159 Chromosome biorientation, the attachment of sister kinetochores to sister spindle pole

160 These results suggest that initial attachment of S. aureus to smooth titanium is mostly med

161 al tendon-to-bone surgical repairs is direct attachment of tendon to smooth bone.

162 nalized SNPs in plasma demonstrated that the attachment of polyP to SNPs to form polyP-SNPs creates a

163 ssential family of enzymes that catalyze the attachment of amino acids to specific tRNAs during trans

164 n revealed the existence of two steps in the attachment of elongating muscles to specific tendon cell

165 ING E3 ligase that functions in the covalent attachment of ubiquitin to specific substrates, and muta

166 8 activity is required for the timely stable attachment of all kinetochores to spindle microtubules,

167 ul chromosome segregation is accomplished by attachment of chromosomes to spindle microtubules using

168 -the multiprotein structure that facilitates attachment of chromosomes to spindle microtubules.

169 omosome segregation is dependent upon stable attachment of kinetochores to spindle microtubules durin

170 ation during cell division depends on stable attachment of kinetochores to spindle microtubules.

171 egation through the formation of bi-oriented attachments of kinetochores to spindle microtubules.

172 may shed new light upon the mechanism of the attachment of heme to substrate apocytochrome within the

173 Attachment of ubiquitin to substrate is typically though

174 The attachment of bacteria to surfaces provides advantages s

175 The attachment of single cells to surfaces involves an initi

176 Glycoprotein C (gC) mediates the attachment of HSV-1 to susceptible host cells by interac

177 Attachment of MB(D) to SVR cells (mean, 0.74 MBs per cel

178 ractions; for example, galectins can promote attachment of HIV to T cells and macrophages and attachm

179 required both for T3 polymerization and for attachment of Cpa to T3.

180 CpaN dimer provides a model for the covalent attachment of Cpa to target receptors and thus the strep

181 a novel method that integrates the covalent attachment of DNA handles to target proteins with a sele

182 Attachment of SUMO to target proteins is catalyzed by SU

183 E3 ligases mediate the covalent attachment of ubiquitin to target proteins thereby enabl

184 cy virus (HIV) infectivity by increasing the attachment of virions to target cells.

185 f Met-tRNA(Met)(i) to 40S/mRNA complexes, if attachment of 40S subunits to the mRNA places the initia

186 yphosphonate group to a linker moiety and an attachment of a nucleobase to the other end of the linke

187 d to nonuniform charge arising from covalent attachment of ampholytes to the benzophenone-functionali

188 ical impedance spectroscopy (EIS) and direct attachment of antibodies to the gold electrode the assay

189 g the hydrophobic interaction determines the attachment of aqu-nC60 to the collector surface.

190 We previously reported that attachment of atrial myocytes to the extracellular matri

191 inding of E. coli to mucin and increased the attachment of bacteria to the epithelial surface via int

192 mediated loss of hemidesmosomes could weaken attachment of basal keratinocytes to the basement membra

193 Ligation results in covalent attachment of biotin to the microplate and provides a co

194 opose that the C4b.MASP-2 interaction favors attachment of C4b near to the activating MBL.MASP comple

195 The attachment of carbohydrates to the surface using biotin-

196 ration of HCECs toward a magnetic source and attachment of cells to the corneal stroma without affect

197 Attachment of charged groups to the nicotinic acid of NA

198 n by delaying anaphase until correct bipolar attachment of chromatids to the mitotic spindle is achie

199 Both the biosynthesis and the attachment of chromophores to the apophycobiliprotein ha

200 c spindle checkpoint monitors proper bipolar attachment of chromosomes to the mitotic spindle.

201 Attachment of CL1 to the cytosolic protein Ura3p destabi

202 y, SEM imaging of the extracted wires showed attachment of cocci aggregations to the wire metal surfa

203 ntibody aimed for dengue detection: physical attachment of dengue antibodies to the surface and coval

204 ce of commonly used chemical methods for the attachment of effector-molecules to the antibody of inte

205 f each structure differ through the order of attachment of Fab peptides to the sequential hinge cyste

206 ybridization efficiency was evaluated by the attachment of fluorescent oligonucleotides to the fluore

207 ding in EF-hand 4 has no role in the primary attachment of GCAP1 to the cyclase, and it only triggers

208 We have previously shown that attachment of genes to the NaCl-isolated nuclear matrix

209 Covalent attachment of GlcNAc to the HAT domain of long OGA drama

210 dels propose that CcmFH facilitates covalent attachment of haem to the apocytochrome; namely, that it

211 SPMs facilitated the attachment of HCECs to the corneal stroma in the human a

212 This movement occurs through the attachment of heart cells to the overlying ectoderm whic

213 es required for S motility and show that the attachment of heptose to the lipopolysaccharide inner co

214 ned, thereby demonstrating a robust covalent attachment of intact clusters to the graphene surface.

215 Beauveria bassiana, initiates infection via attachment of its spores to the epicuticle or waxy layer

216 indle assembly checkpoint (SAC) monitors the attachment of kinetochores (KTs) to the plus ends of spi

217 t (SAC) is essential for ensuring the proper attachment of kinetochores to the spindle and, thus, the

218 id peptide endomorphin-1 (1) was modified by attachment of lactose to the N-terminus via a succinamic

219 iated cytotoxicity either via regulating the attachment of lytic granules to the actin-based cytoskel

220 Attachment of M. genitalium to the host cell's apical su

221 Cleavage resulted in covalent attachment of MBP-VirD2 to the 5'-cleaved end, consisten

222 ngression and segregation require the proper attachment of microtubules to the two sister kinetochore

223 emperature and ionic strength through simple attachment of modified DNA to the QD surface remains a c

224 integrins function in concert to promote the attachment of muscles to the basement membrane.

225 A26 also has roles in the attachment of MVs to the cell surface and incorporation

226 N-myristoylation is the covalent attachment of myristic acid to the N terminus of protein

227 N-myristoylation refers to the attachment of myristic acid to the N-terminal glycine of

228 It involves the chemical attachment of NAD(+) to the silica matrix using glycidox

229 ormation of primary heteroaggregates via the attachment of nanoparticles to the clay.

230 -index-matched porous medium followed by the attachment of nanoparticles to the photoswitched region

231 action to netrin-1, we found that mechanical attachment of netrin-1 to the substrate was required for

232 ranspeptidase activity, thereby facilitating attachment of new PG to the sacculus.

233 on of sublattice domains to the preferential attachment of nitrogen to the edge sites of graphene dur

234 The free energy profile for the chemical attachment of O2 to the enzyme active site was investiga

235 Covalent attachment of palmitate to the N-terminal cysteine of Sh

236 olecule 1 (ICAM-1), a molecule important for attachment of parasitized RBCs to the endothelial cell.

237 nsitivity, and electron microscopy confirmed attachment of phage particles to the surface of each of

238 The covalent attachment of polysaccharide antigens to the carrier pro

239 Stable attachment of progerin to the nuclear membrane disrupts

240 y(ethylene glycol)-carboxyl allowed covalent attachment of proteins to the particles using standard c

241 e microvilli meshwork and ensures the proper attachment of RCs to the PM, thereby counteracting the i

242 Proper bipolar attachment of sister kinetochores to the mitotic spindle

243 -free chromosome segregation requires stable attachment of sister kinetochores to the opposite spindl

244 The SAC monitors proper attachment of spindle microtubules to the kinetochore fo

245 The spindle checkpoint monitors the attachment of spindles to the kinetochore or spindle ten

246 We demonstrate here that the attachment of spores to the intestine is essential in th

247 ed glycosylation often involves the covalent attachment of sugar moieties to the hydroxyl group of se

248 The attachment of tailed bacteriophages to the host cell wal

249 ibution of Sun1, a protein essential for the attachment of telomeres to the nuclear envelope.

250 used by topo II or Stu2 impairment depend on attachment of telomeres to the nuclear envelope.

251 ameters in green microalgae without physical attachment of the bacteria to the microalgae.

252 e in the output signal with time, due to the attachment of the bacteria to the POF probe and conseque

253 einaceous kinetochore and is responsible for attachment of the chromosome to the spindle at mitosis a

254 dination of Mn(III) with ligands allowed the attachment of the complexes to the UO2 surface to facili

255 polysaccharides by influencing CpsA-mediated attachment of the CPS to the bacterial cell surface.

256 COL7A1 secures the attachment of the epidermis to the dermis, and its mutat

257 es are moderate and do not impose a complete attachment of the filaments to the lipid bilayer.

258 Trypanosoma brucei cell shape is the lateral attachment of the flagellum to the cell body, mediated b

259 Covalent attachment of the hydrogel to the substrate was essentia

260 a kinetoplastid-specific kinesin facilitates attachment of the junction to the microtubules in the ma

261 tributes to establishment of correct bipolar attachment of the kinetochore to the spindle microtubule

262 he two proteins and (ii) different points of attachment of the linker to the protein (either near the

263 These data also suggest that attachment of the MC to the ILM provides important polar

264 The attachment of the oligonucleotide to the Co(III) complex

265 s the genomic RNA (gRNA) and is required for attachment of the phage to the host pilus.

266 esting a direct role for fibulin 2 in the re-attachment of the retina to the retinal pigment epitheli

267 is a thiol-cyanine adduct in which covalent attachment of the thiol to the polymethine bridge disrup

268 ng protein that concentrates at the point of attachment of the TM to the stereocilia and, when mutate

269 ism.IMPORTANCE Herpesviruses enter cells via attachment of the virion to the cellular surface and fus

270 degrees C, we demonstrate that EGCG prevents attachment of the virus to the cell surface, probably by

271 The diverse nature of the attachment of the virus to the cell surface, the initial

272 egrees C, we showed that FQ does not prevent attachment of the virus to the cell surface.

273 The tail mediates attachment of the virus to the host surface receptor, as

274 The attachment of these proteins to the peptidoglycan is ach

275 Moraxella catarrhalis is presumed to involve attachment of this bacterium to the mucosa.

276 ique role within the gamma-TuC components in attachment of this complex to the major MTOC site.

277 omosome and spindle behaviors to prevent the attachment of unpartnered chromosomes to the meiotic spi

278 is that SecA and Sortase A, required for the attachment of virulence factors to the cell wall, locali

279 Attachment of VPg to the genome occurs in at least two s

280 Our data show very inefficient attachment of VSV to the most resistant human PDAC cell

281 Initial attachments of chromosomes to the spindle involve random

282 anner to the correction of erroneous initial attachments of chromosomes to the spindle.

283 Creating stable yet flexible attachments of spindle microtubules to the kinetochore i

284 tidomain proteins that catalyze the covalent attachment of amino acids to their cognate transfer RNA.

285 Aminoacyl-tRNA synthetases catalyze the attachment of amino acids to their cognate tRNAs for pro

286 Aminoacyl-tRNA synthetases catalyze the attachment of amino acids to their cognate tRNAs.

287 Protein synthesis involves the accurate attachment of amino acids to their matching transfer RNA

288 L51 complex is important for maintaining the attachment of infected cells to their surroundings throu

289 over long distances and couples cytoskeleton attachment of integrins to their high-affinity state.

290 tions are weaker in reticulocytes, as is the attachment of transmembrane proteins to these structures

291 Therefore attachment of carbohydrate moieties to this class of mol

292 t network geometry coupled with preferential attachment of nodes to this geometry fills this gap.

293 , has also been prepared and employed in the attachment of the complex to TiO2 nanoparticles.

294 It mediates attachment of S. mutans to tooth surfaces and has been a

295 Protein C-mannosylation is the attachment of alpha-mannopyranose to tryptophan via a C-

296 ase catalyzed the site-specific and covalent attachment of resorufin to various cellular proteins gen

297 The covalent attachment of ubiquitin (Ub) to various intracellular pr

298 Rap1b/talin interaction becomes strong upon attachment of activated Rap1b to vesicular membranes tha

299 The frequency of attachment of X. fastidiosa to xylem vessels was 20-fold

300 d surface activation by alkanethiols for the attachment of antibodies to yield gold nanorod molecular