ライフサイエンスコーパス: formation of @3 by

1 The formation of ester was confirmed by (1)HNMR, FTIR and UV

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

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

4 induced neurogenesis after SE can reduce the formation of spontaneous recurrent seizures by 65%.

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

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

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

8 Controlled formation of alkylzinc halides by a combination of CrCl2

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

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

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

12 as formation of hairpin 1 by a hydrophobic collapse mechani

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

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

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

16 red biological functions may have driven the formation of these lymphoid structures by a process of c

17 ls, while it weakened, but did not abrogate, formation of tumors induced by a control oncogene (HRAS/

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

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

20 n the presence of TGFbeta, SHCA promotes the formation of small, dynamic adhesions by acting as a nuc

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

22 The formation of amyloid plaques by aggregated amyloid beta

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

24 The formation of relativistic jets by an accreting compact o

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

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

27 of coopted vessels, resulting in hypoxia and formation of new vessels by angiogenesis.

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

29 Formation of the RMP metabolites by APRT was negligible,

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

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

32 nucleation-promoting factor SPIN90 promotes formation of unbranched filaments by Arp2/3, a process t

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

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

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

36 The formation of biofilms is initiated by bacteria transitio

37 This reaction proceeds via in situ formation of Schiff-base followed by base mediated alkyl

38 of the gamma(1)34.5 protein, which prevents formation of the autophagophore by binding to Beclin 1,

39 evealed that pyridine binding slows down the formation of the tetrazido complex by blocking azide coo

40 -cis constrained dienes lead to preferential formation of (4 + 2) products by both stepwise and conce

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

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

43 es in real-time collective migration and the formation of cell-cell junctions by C6 glioma cells seed

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 e PBI with seeds of another PBI leads to the formation of supramolecular block copolymers by chain-gr

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

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

53 Formation of dimers was shown by chemical cross-linking

54 se two different groups led to the selective formation of gamma-(ACB)-d4TTPs by chemical hydrolysis a

55 a much higher reactivity than Cr(III) in the formation of Cr(VI) by chlorine.

56 AT locus on chromosome III and monitored the formation of gamma-H2AX by chromatin immunoprecipitation

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

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

59 Our results suggest that the formation of ordered linear assemblies by clustered prot

60 (13)CO(2) experiments confirmed the formation of H(13)COO(-) by CO(2) reduction with the for

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

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

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

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

65 We propose that the PCDHGs contribute to the formation of balanced inhibitory networks by controlling

66 e results reveal that the selectivity in the formation of products was obtained by controlling the fu

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

68 les for the organic additive, including: the formation of cube-like nanostructures by corrosion of th

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

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

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

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

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

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

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

76 This study reports the heat-induced formation of furan by decarboxylation of 2-furoic acid,

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

78 It also inhibited formation of contractile membranes by dedifferentiated R

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

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

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

82 The formation of ketene is predicted by detailed DFT calcula

83 uorescent sensors, which directly report the formation of active receptor conformations by detecting

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

85 tion of beta-parvalbumin is initiated by the formation of dimers stabilized by disulfide bonds and th

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

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

88 otubular structures, is actively involved in formation of protective envelope, followed by dynamic sc

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

90 Selective formation of radicals was achieved by electron beam irra

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

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

93 brid sensor SagS plays a central role in the formation of Pseudomonas aeruginosa biofilms, by enablin

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

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

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

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

100 In pluripotent cells, TDP-43 represses the formation of paraspeckles by enhancing the polyadenylate

101 Formation of heterodimers by ERAP1 and ERAP2 has been pr

102 e architectural constraints that dictate the formation of polyMOFs were assessed by examining poly(1,

103 Here, we study the formation of fibrils and oligomers by exon 1 of huntingt

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

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

106 r H(2)O(2)-induced oxidative stress, and the formation of graviquinone was confirmed by Fenton's reac

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

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

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

115 roach concluded that the free CTD blocks the formation of ParB networks by heterodimerisation with fu

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

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

120 to the developing human brain; however, the formation of OH-PCBs by human cytochrome P450 (P450) iso

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

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

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

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

125 Formation of AAA was driven by increased smooth muscle c

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

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

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

129 This promotes the formation of fibronectin fibrils by indolent cells that

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

131 ly phenotype of the disease, upregulates the formation of these transient DRMs by inducing the intern

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

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

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

135 The data are suggestive of the formation of these loops by interactions between repress

136 The formation of a supramolecule linked by intermolecular hy

137 The formation of fibrous minerals by intertwining filaments

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

139 The formation of 3 was confirmed by its independent synthesi

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

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

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

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

144 reater than those in Cu, implying the easier formation of vacancies by lattice structure relaxation o

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

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

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

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

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

150 Interestingly, formation of extracellular traps by macrophages during M

151 While regulation of the formation of this structure by major signaling pathways

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

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

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

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

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

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

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

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

160 Formation of native PulD-multimers by mixing protomers t

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

162 ng a polarity-optimized protocol reduced the formation of amyloid plaques by more than 70%.

163 f atherosclerosis, from lesion initiation to formation of advanced lesions characterized by necrotic

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

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

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

167 ng AgSO(4)-induced toluene deprotonation and formation of benzyl carbocation, followed by nucleophili

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

169 deamination of adenosine to inosine and the formation of tRNAValIACin vitro by ON-MS.

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

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

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

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

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

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

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

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

178 ncy in secondary transplants and reduced the formation of spontaneous lung micrometastases by PDX tum

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

180 = 359 ng . h/mL) at 10 mg/kg was due to the formation of O-glucuronide conjugate by phase 2 metaboli

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

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

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

184 The formation of organophosphate molecules by prebiotic proc

185 disability by assisting actions such as the formation of hand aperture, or by preventing others incl

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

187 ization of a bioproduct while minimizing the formation of a given by-product, two common requirements

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

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

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

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

192 ater disinfection inadvertently leads to the formation of numerous disinfection by-products (DBPs), s

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

194 The formation of toxic disinfection by-products (DBPs) is am

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

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

197 nced signaling by the T cell receptor in the formation of functional immune synapses by promoting the

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

199 Our data suggest that CTCF enables the formation of chromatin loops by protecting cohesin again

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

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

202 cellular matrix protein, is required for the formation of GABAergic, perisomatic synapses by PV(+) ce

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

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

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 ow that photogenerated superoxide can induce formation of AgNPs by reducing Ag(I) ions.

210 t Hoxa13 acts hierarchically to initiate the formation of digit 1 by reducing Gli3 transcription and

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

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

213 4-dependent transcription directs the proper formation of prefrontal cortical minicolumns by regulati

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

215 sed (pMHCII-based) nanomedicines trigger the formation of multicellular regulatory networks by reprog

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

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

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

219 NPA101.3 (10 mg/kg/day) completely prevented formation of tumors induced by RET/C634Y-transformed cel

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

221 ort chain fatty acids may be useful to limit formation of a biofilm by S. epidermidis.

222 The methodology involves the formation of DNA/RNA heterohybrids by sandwich hybridiza

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

224 These data indicate that ZIKV disrupts the formation of stress granules by sequestering stress gran

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

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

227 Formation of multinucleate myotubes by SMN-deficient mus

228 lecular buta-1,3-diyne cyclizations with the formation of iodoethynylheterocycles, followed by Sonoga

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

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

231 Formation of polarons is supported by spectroscopy and e

232 The formation of S1P is catalyzed by sphingosine kinase 1 or

233 The formation of new blood vessels by sprouting angiogenesis

234 ut checkpoint delays abscission and prevents formation of binucleated cells by stabilizing the cytoki

235 s to show that a kink in helices affects the formation of membrane pores by stabilizing toroidal pore

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

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

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

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

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

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

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

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

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

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

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

247 The formation of amyloid fibrils by the intrinsically disord

248 e set out an unprecedented procedure for the formation of benzothiophenes by the twofold vicinal C-H

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

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

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

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

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

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

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

256 These observations explain how reversible formation of labile polymers by the Pbp1 LC domain enabl

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

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

259 Formation of milk gels produced by the extracts and chym

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

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

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

263 The formation of olefins by the eliminative dimerization and

264 Formation of smHSSs is initiated by the hydrolysis of te

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

266 ry calculations to rationalize the competing formation of tetrahydropyridones and enaminones by the d

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

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

269 onversion of ethanol to 1,3-butadiene or the formation of this product by the reaction of ethanol and

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

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

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

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

274 lithiated hemiaminal carbenoids leads to the formation of singlet carbenes followed by their trapping

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

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

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

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

279 ursue a molecular-level understanding of the formation of Al nanocrystals by titanium(IV) isopropoxid

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

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

282 The formation of AuNPs was confirmed by transmission electro

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

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

285 ls, the Us11 protein drastically reduces the formation of autophagosomes mediated by TRIM23 or TBK1.

286 Here we report the formation of supramolecular block copolymers by two-comp

287 The formation of toroids is dominated by two competing free

288 high amounts of reactive radicals enable the formation of polymer/gel by ultrasound activation.

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

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

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

292 s following bile duct injury and promote the formation of ductular scars by upregulating pro-fibrogen

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

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

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

296 We hypothesize that the formation of reactive species initiated by UV-A light ma

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

298 e in apple juice, its oxidation leads to the formation of newly formed molecules by which dehydrodime

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

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