ライフサイエンスコーパス: formation of @3 by

1 The formation of phenO2 was confirmed by (1)H NMR and ESI-MS

2 e insulin containing formulation resulted in formation of granulomas, which resolved by 28 weeks.

3 otein degradation within 2 weeks that led to formation of AAA by 4 weeks.

4 Vacuum frying reduced the formation of acrylamide by 98% and also other Maillard r

5 n/detergent/water number ratios revealed the formation of a proteomicelle characterized by a constant

6 hanism, consisting of the pseudoequilibrated formation of a zwitterion followed by a rate controlling

7 Controlled formation of alkylzinc halides by a combination of CrCl2

8 Our results indicate the formation of alpha-terpineol by a nucleophilic attack of

9 Bacteria have a role in the formation of colonies by a species of single-celled orga

10 agent-induced base excision repair (BER) and formation of DPCs is enhanced by a PARP inhibitor.

11 This typically involves the formation of founder cells, followed by a number of cell

12 ed intracellular accumulation of ATZ and the formation of globular inclusions by a pathway that requi

13 as formation of hairpin 1 by a hydrophobic collapse mechani

14 e studied the role of the yeast GPATs in the formation of LPs induced by a surplus of oleic acid.

15 ir triacylglycerol composition, with a quick formation of metastable crystals, followed by a polymorp

16 functional theory computations explores the formation of mixed aggregates by a dilithium salt of a C

17 variable environmental conditions during the formation of nitrate, and (III) by a minor impact of den

18 mal genesis of photoreceptors, including the formation of cilia, followed by abnormal elaboration of

19 ical by tens of kilojoules, or, analogously, formation of a stable radical (by abstraction or homolyt

20 sing spin traps show that l-Trp quenches the formation of azidyl radicals, probably by acting as an e

21 Furthermore, PLZF causes the formation of barrier-type boundaries by acting on insert

22 Here we show that 5-LO regulates the formation of Abeta by activating the cAMP-response eleme

23 , particle growth proceeds after the initial formation of stable clusters by addition of silver monom

24 Rush also causes formation of endosome clusters, possibly by affecting fu

25 Furthermore, origin ssDNA may stimulate the formation of the CMG complex by alleviating inhibitory i

26 Here, we report the formation of 100S ribosomes by an HPF homolog in Listeri

27 The formation of relativistic jets by an accreting compact o

28 nergy availability might also facilitate the formation of internal storage polymers by anaerobic micr

29 impact of individual genetic factors on the formation of the adaptive immunity by analyzing the T-ce

30 by retinal vascular responses, including the formation of new vessels by angiogenesis (neovasculariza

31 GAC activation requires the formation of homotetramers, promoted by anionic alloster

32 ddition of stromal supporting cells enhances formation of vessel-like structures by approximately 10-

33 Formation of the RMP metabolites by APRT was negligible,

34 a for fractures in the layered rocks suggest formation of Al-rich smectites by aqueous leaching.

35 Arg stimulates formation of actin filament branches by Arp2/3 complex a

36 When using H(2)(18)O, the formation of isoAsp and Asp by Asn deamidation during sa

37 nstrate that the particle model predicts the formation of HbS polymer fibers by attachment of monomer

38 leased from descending projections modulates formation of motor neurons by attenuating the response o

39 Mossbauer spectroscopy confirmed the formation of transition carbides by auto-tempering as we

40 The formation of biofilms is initiated by bacteria transitio

41 gp2 inhibits formation of open promoter complex by binding to the bet

42 ded with the surface wind, implying that the formation of O3 was impacted by both exports of plumes u

43 ation of C4aOOH is only 1.4 kcal/mol and the formation of C4aOOH by C2 is fast ( approximately 10(6)

44 The formation of anserine is catalyzed by carnosine N-methyl

45 xchange rates can also be used to detect the formation of a covalent bond by catalyCEST MRI.

46 We report formation of holocytochromes c by CcmFH and CcmG, a peri

47 Formation of 3D structures facilitated by cell death may

48 Proper formation of ceramides by CerS has been shown previously

49 miR-126 in mice inhibited neointimal lesion formation of carotid arteries induced by cessation of bl

50 The in situ formation of nanoparticles is controlled by changing the

51 n, which resulted in cytokinesis failure and formation of binucleate cells, or by chemical inhibition

52 Formation of dimers was shown by chemical cross-linking

53 The formation of NDMA by chloramination of less reactive mod

54 ts are of great importance to understand the formation of NDMA by chloramination of tertiary amines.

55 hough all recombinant proteins catalyzed the formation of anserine, as confirmed by chromatographic a

56 egiospecific second-order rate constants for formation of each product by Cl(2), Cl(2)O, and HOCl.

57 ry ammonium groups efficiently inhibited the formation of biofilms by clinically important Gram-posit

58 In this study, the formation of diastereomeric complexes by coadsorbed meth

59 S-TL A, OAS-TL B, and OAS-TL C, catalyze the formation of Cys by combining O-acetylserine and sulfide

60 y to benefit from AOs in two ways, namely by formation of abscisic acid and by concomitant formation

61 oups in oleylamine are not necessary for the formation of CuInSe(2) nanocrystals by conducting succes

62 ne) has B cell-intrinsic roles in regulating formation of Ab-secreting cells by controlling the activ

63 h signals dictate the initial aspects of the formation of each villus by controlling mesenchymal clus

64 and geospatial behavior, documenting how the formation of cores is preceded by coordination behavior

65 Vertical concentration profiles revealed formation of Fe(II) by corrosion of Fe(0) with O2 and in

66 ney tubules, where they are required for the formation of a concentrated urine by countercurrent mult

67 in nuclear envelope protein Man1 ensures the formation of identical daughter nuclei by coupling nucle

68 could bind O2 are consistent with concerted formation of the alkylperoxo followed by Criegee rearran

69 Formation of the "mating plug" by cross-linking Plugin i

70 For the first time, we report the formation of a PROTAC by Cu(I)-catalyzed cycloaddition o

71 e and suitable densities are crucial for the formation of pentamers, driven by cyclic hydrogen bondin

72 e that beta-catenin signaling is involved in formation of contractile membranes by dedifferentiated R

73 It also inhibited formation of contractile membranes by dedifferentiated R

74 CH3Hg to such reactive sites facilitates the formation of (CH3)2Hg by degradation of the adsorbed CH3

75 ical samples aim to minimize the deleterious formation of ice by dehydrating cells and promoting the

76 combinatorial signaling context, preventing formation of doubly phosphorylated STAT3 by depleting GS

77 The formation of ketene is predicted by detailed DFT calcula

78 ut it moved to the tip of filopodia upon the formation of dimer induced by dimer-inducing reagent.

79 Here we report a method for the formation of C-C bonds by directed cleavage of tradition

80 mersome in a plastic bag, as well as through formation of a hydrogel by disintegrating an assembled p

81 alization of the SMN protein, preventing the formation of nuclear 'gems' by disrupting the recruitmen

82 ure induced the development of browning, the formation of large protein aggregates by disulfide excha

83 iological network can be used to control the formation of a synthetic material by diverse classes of

84 5' polarity of editing is determined by the formation of upstream mRNA anchors by downstream editing

85 ancestral gymnosperm MYB gene and subsequent formation of TAS4 by duplication of the miR828* arm.

86 sm distinct from the "zinc zipper." Finally, formation of two domains by each repeat (as in SasG) mig

87 Formation of ELS is preceded by ectopic expression of ly

88 This method relies on in situ formation of hydroxide ions by electro mediated water re

89 Selective formation of radicals was achieved by electron beam irra

90 ole, phenoxazine, and phenazine suggests the formation of these species by electrophilic substitution

91 ic silencing of miR-200c, which promotes the formation of breast CSCs defined by elevated cell surfac

92 als that a class I HDAC inhibitor alters the formation of auditory memory by enabling more acoustic i

93 MAPK signaling promotes formation of PanINs by enabling dedifferentiation of aci

94 lated odontoblast-like cells (OD21), and the formation of endothelial monolayers by endothelial colon

95 ty to induce the secretion of VEGF-A and the formation of tubes by endothelial cells.

96 recruitment of cPLA(2)alpha to the Golgi and formation of tubules by endothelial cells.

97 diacy of hydrogen peroxide (H(2)O(2)) in the formation of .OH was supported by enhancement of .OH for

98 es oxidative modifications of WP, as well as formation of amyloid-like structures by enhancement of M

99 repeated ethanol experience may promote the formation of drug-associated memories by enhancing synap

100 immune cells to the plaque and impaired the formation of foam cells by enhancing cholesterol efflux

101 Formation of heterodimers by ERAP1 and ERAP2 has been pr

102 ternary complex, the concentration-dependent formation of which was quantified by experimental-based

103 The formation of anastomoses is mediated by extension of cyt

104 re and are commonly thought to stabilize the formation of tertiary contacts by favorably interacting

105 The bioelectrode reactions involved the formation of H2O2 by FcAOx biocatalysis of substrate alc

106 Formation of plaque by fibrils of beta-amyloid (Abeta) p

107 s surface pressure drops coincident with the formation of PIP2 clusters visualized by fluorescence, a

108 evelopmental functions, including the proper formation of dendritic arbors by forebrain neurons.

109 e absence of tetrahydrofolate and subsequent formation of formate by formaldehyde dehydrogenase.

110 simulations were utilized to first show the formation of a tetramer unit by four separate Abeta42 pe

111 Herein, we study the formation of indazolones by Friedel-Crafts cyclization o

112 in the regulation of orthologous genes, the formation of new genes by gene duplications, and the rec

113 assumption is that the leading edge prevents formation of additional fronts by generating long-range

114 Indeed, ACT inhibits formation of NETs by generating cAMP and consequently in

115 rate a recombinase architecture that reduces formation of these undesirable homodimers by >500-fold.

116 affinity peptide:MHC complexes prevented the formation of KIR microclusters by high-affinity peptide:

117 The kinetics of the formation of radicals in meat by high pressure processin

118 y activation with ADP promoted migration and formation of capillary structures by human umbilical vei

119 that sPLA2-X plays a significant role in the formation of CysLTs by human eosinophils.

120 mutations, especially when combined, enabled formation of extensive syncytia by human cancer cell lin

121 lites by APRT was negligible, and so was the formation of the ribosylated metabolites by human purine

122 ecific oxidation of 18:2n-6 and 18:3n-3 with formation of 13S-hydroperoxides by hydrogen abstraction

123 nantiotropic nematic phase attributed to the formation of supramolecular complexes by hydrogen bondin

124 We propose that formation of this species occurs by hydrogen-transfer fr

125 rmore, [kappa(3)-Tptm]ZnH also catalyzes the formation of triethoxysilyl formate by hydrosilylation o

126 er, whether increased aPKC function triggers formation of excess neuroblasts by inactivating Numb rem

127 thout sequence specificity, facilitating the formation of compact nucleoprotein structures by increas

128 We find that the formation of distributed memories, embodied by increased

129 on-phosphorylatable forms of Numb suppressed formation of excess neuroblasts triggered by increased c

130 alpha-synuclein inclusions after the initial formation of alpha-synuclein pathology by increasing a p

131 tivation of 5-HT2A receptors may lead to the formation of visual hallucinations by increasing cortica

132 e findings demonstrate that Nfil3 drives the formation of mature NK cells by inducing Eomes expressio

133 ased the stability of TRiC and decreased the formation of HttQ103-GFP aggregates by inhibiting VRK2.

134 her extending the concept that Msx2 controls formation of mineralized tissues by inhibition of the Wn

135 of wild-type G to mediate fusion, either by formation of mixed trimers or by inhibition of trimer fu

136 Thus, ARNO-ARF1 regulates formation of podosomes by inhibition of RhoA/myosin-II a

137 daily limit of 50 mug/kg/day, may block the formation of new memories by interfering with neural pla

138 The formation of a supramolecule linked by intermolecular hy

139 The formation of fibrous minerals by intertwining filaments

140 Here we attempt to illuminate the formation of an amorphous precursor by investigating the

141 This method operates via the in situ formation of aminobenzylfuran, followed by its recycliza

142 te ions indicated that GRP-78 can induce the formation of calcium phosphate polymorphs by itself, whe

143 ty, anchorage-independent proliferation, and formation of xenograft tumors by KRAS-dependent PDAC cel

144 The formation of tubular organoids by KSP+ cells induced the

145 The formation of dA* was followed by laser flash photolysis,

146 the change in SWCNT photoluminescence to the formation of oxygen-containing defects by lipid hydroper

147 We quantitatively explain the formation of this gradient by local exchange between con

148 ions, we propose a minimal model for initial formation of integrin clusters, facilitated by localized

149 ed by chromatin state; and cohesin-dependent formation of TADs, possibly by loop extrusion, which hel

150 method was also successfully applied to the formation of cyclic peptides by macrocyclization.

151 Rac1, and Cdc42 have been implicated in the formation of actin-rich protrusions by macrophages, but

152 Interestingly, formation of extracellular traps by macrophages during M

153 The mechanism for the formation of 3 was rationalized by means of DFT calculat

154 The reaction occurs through the formation of pyrazolines by means of a formal dipolar cy

155 We report controlling the formation of single-molecule junctions by means of elect

156 ctron microscopy (TEM) is used to assess the formation of the fibrils, predominantly by measuring fib

157 ur data suggests that RARgamma initiates the formation of death signaling complexes by mediating RIP1

158 ICP8 scaffolds could facilitate the formation of replication compartments by mediating inter

159 sition of the HED meteorites, confirming the formation of Vesta's crust by melting of a chondritic pa

160 Biomethanation involves the formation of methane by microbes that live in oxygen-fre

161 Herein we show the formation of a polymer stereocomplex by mixing isotactic

162 Formation of native PulD-multimers by mixing protomers t

163 This is a remarkable finding, because the formation of extended beta-strands by monomeric Abeta pr

164 , may be evolutionarily adapted to avoid the formation of traffic jams by moving only with moderate p

165 than 1 and 5%, respectively, of the rates of formation of PGH(2) by native PGHS-2.

166 stase activity, previously shown to regulate formation of extracellular traps by neutrophils.

167 reoisomeric 2,5-dideoxy-2,5-iminohexitols by formation of the pyrrolidine ring by nitrogen substituti

168 eally positioned to explain the preferential formation of turanose by NpAS.

169 al studies show that N17 and C38 promote the formation of ordered fibrils by NTFs.

170 efects), and this may eventually lead to the formation of disordered structures, characterised by nuc

171 es are a simple class of foldamers, with the formation of helices driven by offset aromatic stacking

172 tron microscopy, reminiscent of the reported formation of amorphous deposits by other crystallin muta

173 tivating enzyme E1 by PYR-41 or blocking the formation of ubiquitin chains by over-expressing the lys

174 The oxidation process occurs during formation of the SAM by oxidation of the -C identical wi

175 ) in the mitochondria efficiently allows the formation of ATP by oxidative phosphorylation.

176 -keto acids as intermediate compounds in the formation of Strecker aldehydes by oxidised lipids.

177 Laccase catalyzed the formation of covalent bonds by oxidizing unreactive hydr

178 we elucidate the mechanisms underpinning the formation of crystalline biofilms by P. mirabilis.

179 plant's own pathway for trehalose synthesis, formation of T6P or trehalose by pathogens can result in

180 is compatible with nucleophiles to allow for formation of formal AAA products by Pd-catalyzed additio

181 e, we provide spectroscopic evidence for the formation of diamondene by performing Raman spectroscopy

182 = 359 ng . h/mL) at 10 mg/kg was due to the formation of O-glucuronide conjugate by phase 2 metaboli

183 es through intramolecular oxidative S-N bond formation of imidoyl thioureas by phenyliodine(III) bis(

184 Furthermore, the exclusive formation of oxaloacetate by phosphoenolpyruvate (PEP) c

185 However, the formation of RNA by plausible prebiotic reactions remain

186 The detailed work also supports the formation of cis-isomer by preferential addition of o-ha

187 h show that EGCG efficiently inhibits fibril formation of hCT by preventing the initial association o

188 fold and improves data quality by minimizing formation of a deleterious by-product, reducing ligation

189 Formation of a volatile flavour by-product, 1-butanethio

190 NaClO dosing had no adverse impact on the formation of currently regulated disinfection by-product

191 olving S-adenosyl-l-methionine result in the formation of the toxic by-product, 5'-methylthioadenosin

192 th organic matter in wash water promotes the formation of chlorine by-products.

193 on course at various temperatures reveal the formation of tetrachloro addition by-products and thus s

194 ion catalysts were modulated to minimize the formation of undesired by-products.

195 ecise and concise fashion while avoiding the formation of unwanted kinetic by-products.

196 autophagy protein ATG5 is essential for the formation of autophagosomes by promoting the lipidation

197 ve renin inhibitor BILA 2157, which excludes formation of angiotensin I by proteases other than renin

198 Gaining insight into the formation of such sites by protonation and/or electronat

199 mitochondrial intermembrane space, allowing formation of PE by Psd1 in the inner membrane.

200 di-GMP effector PelD that is critical to the formation of pellicles by Pseudomonas aeruginosa.

201 ight results in a 50-fold enhancement in the formation of furfuryl alcohol by Pt supported on TiO(2),

202 ince their oxidation leads to the reversible formation of bispyrylium species by radical dimerization

203 reaction was found to proceed through rapid formation of azidohydrin intermediates followed by rate-

204 Formation of such channels by RBC-PAs may help rescue is

205 The formation of silylium ion 20 by reaction of silyliumylid

206 Lipofuscin, the formation of which is driven by reactive oxygen species

207 ALP-labeled antibody can be detected through formation of CdS QDs, monitored by recording emission sp

208 Astrocyte-secreted glypican 4 induces formation of active excitatory synapses by recruiting AM

209 ascorbate prevented actin polymerization and formation of stress fibers by reducing the activation of

210 The reaction sequence involves the initial formation of thiourea followed by regioselective nucleop

211 4-dependent transcription directs the proper formation of prefrontal cortical minicolumns by regulati

212 FOXF1 is required for the formation of embryonic vasculature by regulating endothe

213 ical type I cadherin that contributes to the formation of neural circuits by regulating growth cone m

214 S. cerevisiae Wee1 homolog Swe1 prevents the formation of multinucleate cells by restraining M phase

215 reports that the kinesin Kif24 controls the formation of primary cilia by restricting the nucleation

216 ding redistributes these motions, inhibiting formation of the DNA complex by restricting coupled fast

217 mg kg(-1) day(-1) per os, Pz-1 abrogated the formation of tumors induced by RET-mutant fibroblasts an

218 identification of the rules that control the formation of synaptic laminae by RGC axons.

219 ulating systems, and cytoskeletal changes in formation of axonal spheroids triggered by ROS.

220 The formation of myelin by Schwann cells (SCs) occurs via a

221 nfirmed that the selectivity arises from the formation of chiral helical polymers by self-association

222 lso show that the compound inhibits in vitro formation of peptidoglycan chains by several different P

223 presence of phenylalanine is consistent with formation of a side-by-side ACT dimer.

224 Formation of multinucleate myotubes by SMN-deficient mus

225 These data demonstrate the formation of functional synapses by Sox11-stimulated CST

226 espread evolutionary strategy to prevent the formation of nonphysiological complexes by specializing

227 Formation of polarons is supported by spectroscopy and e

228 The formation of new blood vessels by sprouting angiogenesis

229 GCase substrate, directly influenced amyloid formation of purified alpha-syn by stabilizing soluble o

230 ions (pH = 11.5) metatorbernite dissolves by formation of etch pits bounded by steps parallel to [100

231 In the present work, we show that formation of MDTB is accompanied by stoichiometric gener

232 de produced by B. subtilis that inhibits the formation of aerial hyphae by streptomycetes.

233 unneling on the excited state surface in the formation of naphthalene is suggested by studies of part

234 Prior exposure to L-703606 prevented the formation of DVs by Sub P, implicating the neurokinin-1

235 q type of G protein coupled receptor, in the formation of DVs by Sub P.

236 cortex but that SAD kinases are required for formation of central axonal arbors by subsets of sensory

237 ion, aneuploidy, chromosome breakage and the formation of micronuclei by targeting cellular ligases t

238 Details of the mechanism of formation of supramolecular polymer nanowires by templat

239 The reaction occurs by sensitized formation of (1)O(2) by the lowest metal-to-ligand charg

240 he presence of pentaarylboroles leads to the formation of 1,2-phosphaborines by the formal insertion

241 een CI dimers bound to OR and OL through the formation of a loop by the intervening DNA segment.

242 paper is used as the understructure for the formation of a membrane substrate by the classical phase

243 The formation of a zygote by the fusion of egg and sperm inv

244 itionally we used CPE to observe the in situ formation of Ag-NPs produced by the reduction of Ag(+) w

245 The two-step synthesis begins with the formation of alpha-chloro ketones by the coupling of a W

246 The formation of amyloid fibrils by the intrinsically disord

247 r a methyl radical to IB, thus launching the formation of b-PIB by the radical mechanism while leavin

248 other diguanylate cyclase is related to the formation of biofilm governed by the Gac/Rsm pathway fur

249 In contrast, the formation of biphenyl is facilitated by the coordination

250 r the anthocyanins quantification based on a formation of blue-colored complexes by the known reactio

251 first direct evidence for the effects of the formation of dust and aerosols by the impact and their i

252 e complexes also significantly influence the formation of edema, caused by the intraplantar applicati

253 ess the molecular determinants governing the formation of functional amyloids by the class I fungal h

254 At the same time, the potential-dependent formation of gamma-NiOOH characterized by the Raman doub

255 Herein we report the formation of H2S by the action of NO on synthetic [2Fe-2

256 Computer simulations revealed that the formation of helices is determined by the interplay of v

257 Our results suggest that the formation of integrin clusters by the proposed mechanism

258 triggered by the activation of H(2) and the formation of iridium hydride, accompanied by the breakin

259 ng Lewis acid and induces simultaneously the formation of l-PIB by the cationic mechanism.

260 The presence of either ATP or ADP induces formation of larger complexes formed by the stacking of

261 Inactivation of atlS resulted in formation of long chains by the cells, markedly decrease

262 The first step in methanol oxidation is formation of methoxy by the thermal dissociation of the

263 Formation of milk gels produced by the extracts and chym

264 ata provide a framework for the simultaneous formation of multiple cell types by the same transcripti

265 Because endolysin function requires the formation of mum-scale holes by the phage holin, the lys

266 rimentally and theoretically investigate the formation of nanodroplets by the solvent exchange proces

267 The formation of olefins by the eliminative dimerization and

268 Formation of smHSSs is initiated by the hydrolysis of te

269 biotic interactions are characterized by the formation of specialized membrane compartments, by the h

270 iary epithelial cells by siRNA disrupted the formation of the microfibril meshwork by the cells.

271 The formation of the SNARE complex by the vesicle SNARE syna

272 ment in some oleaginous plant species is the formation of triacylglycerol (TAG) by the acyl-CoA-depen

273 composite nanospheres which facilitates the formation of ultrathin nanosheets by the oxidation of th

274 iltration and decreased stenosis but blocked formation of vascular neotissue, evidenced by the absenc

275 el of S. flexneri dissemination in which the formation of VLPs is mediated by the PIK3C2A-dependent p

276 ia a particle-mediated process involving the formation of primary nanoparticles, followed by their co

277 Increased formation of (Z)-isomers by thermal processing has not b

278 CRAF, and recent studies have shown that the formation of complexes by these different isoforms has a

279 larene) undergoes partial desilylation, with formation of a vinylarene, by three different routes: (a

280 We probed the formation of a refolding intermediate by time-resolved f

281 elated cancers through the inhibition of the formation of tumors induced by tobacco carcinogens.

282 In contrast, silylated allenes favor the formation of propargylic cation intermediates by transfe

283 The formation of AuNPs was confirmed by transmission electro

284 remains a great concern, as reflected in the formation of teratomas by transplanted pluripotent cells

285 secondary sites show that extravasation and formation of micrometastases by TRCs are more efficient

286 machinery at least two ways: by inducing the formation of SGs by triggering PKR phosphorylation, ther

287 which it functions to spatially restrict the formation of repressive chromatin marked by trimethylate

288 EGF10 and MEGF11, have critical roles in the formation of mosaics by two retinal interneuron subtypes

289 The formation of toroids is dominated by two competing free

290 ETS transcription factor (SPDEF) suppresses formation of colon tumors by unclear mechanisms.

291 ligomeric DOPAL adducts potently inhibit the formation of mature amyloid fibrils by unmodified aS.

292 rate that Shp2 is required for RANKL-induced formation of giant multinucleated OCs by up-regulating t

293 try to overcome that problem and investigate formation of the smallest fullerene by use of a pulsed l

294 ch and light microscopy techniques to follow formation of NR by using pulse-chase experiments to exam

295 We examine the physical basis for the formation of symmetric shells, and by using a minimal mo

296 This study explored the formation of BPs by UV irradiation of polybrominated dip

297 t these do have the potential to mediate the formation of protons by various mechanisms, and the thus

298 The formation of worm-stars by Verde1 occurred only when wor

299 A knockdown of ZO-1 completely inhibited the formation of gap junctions by wild-type Cx50 in HeLa cel

300 Unexpectedly, we find that the formation of Ub chains by WWP1 occurs in two distinct ph

301 rI dif site before CTXvarphi, depends on the formation of a HJ by XerD catalysis, which is then resol