ライフサイエンスコーパス: rearrangement

1 ally significant catalytic process (Beckmann rearrangement).

2 se of the difficulty of inducing the initial rearrangement.

3 intermediate generated during [3,3]-acyloxy rearrangement.

4 ate group participation during [3,3]-acyloxy rearrangement.

5 ydropiperidines in a highly stereocontrolled rearrangement.

6 ha genes, and its deletion impaired the Tcra rearrangement.

7 trectinib, regardless of tumour type or gene rearrangement.

8 ufficient to predict the onset of rapid cell rearrangement.

9 its occupation by competing Ca(2+) slows the rearrangement.

10 te myelination depends on actin cytoskeleton rearrangement.

11 uently developed based on a key Wittig-Still rearrangement.

12 evel copy-number gains and frequent inverted rearrangements.

13 host interactions such as water-induced bond rearrangements.

14 to deformations, and fast internal molecular rearrangements.

15 ukemias, notably those with KMT2A (MLL) gene rearrangements.

16 transient or persistent mutations and genome rearrangements.

17 extraordinary carbon backbone and side-chain rearrangements.

18 ice using acquired mutations and chromosomal rearrangements.

19 R3 promoter and elicits occlusive nucleosome rearrangements.

20 lterations that co-occurred with ERG genomic rearrangements.

21 EJ and ATM kinase inhibition influence these rearrangements.

22 (including prophages) combined with genomic rearrangements.

23 ocarcinoma with and without FGFR2 fusions or rearrangements.

24 e stable length or collapse to initiate cell rearrangements.

25 hion and shows typical TRGV9- and TRDV2-like rearrangements.

26 ns within a polypeptide chain and/or subunit rearrangements.

27 des in surface TCRs and carry Trbv31-DJbeta2 rearrangements.

28 , a breakage-fusion-bridge and other complex rearrangements.

29 72 adults with AML and recurrent 11q23/KMT2A rearrangements, 141 of whom had outcome data available.

30 through a three-step cascade involving Cope rearrangement, 6-exo-trig cyclization, and a final elect

31 I 26.5-45.4]) patients with FGFR2 fusions or rearrangements achieved an objective response (three com

32 or the characterization of the transcriptome rearrangements affecting disease progression independent

33 tion and subsequently catalyze covalent bond rearrangement, affording selective assembly of the oligo

34 ions, 57% of which are cryptic adjacent gene rearrangements (AGRs).

35 HsZnT8 subunit undergoes a large structural rearrangement, allowing for alternating access to the pr

36 chromatin interaction datasets, we identify rearrangements altering the regulatory landscape of gene

37 While the reconstructed sequence of genome rearrangements among the protein-coding and ribosomal RN

38 of the central problems presented in genome rearrangement analysis since finding the most likely tru

39 ccurs through a BvnE-controlled semi-pinacol rearrangement and a subsequent spontaneous intramolecula

40 imary mechanism that accelerates genomic DNA rearrangement and amplification into ecDNA and enables r

41 argeted therapy for AML patients with an MLL rearrangement and an FLT3-ITD.

42 ents; however, these can promote local lipid rearrangement and can cause fluctuations in the oligomer

43 ustering by Gal-9 may influence cytoskeleton rearrangement and coclustering of CD3, which likely impa

44 dynamically favored through an electrophilic rearrangement and concomitant 1,9-aryl migration without

45 anscription, these complexes undergo dynamic rearrangement and disassembly as Pol II moves away from

46 HSV induces host organelle rearrangement and forms multiple, dispersed assembly com

47 on Pten-NOLC1 originated from a chr10 genome rearrangement and identified through a transcriptome seq

48 oximal V(H)s, where additional CBEs activate rearrangement and impede scanning any further upstream(5

49 , the cascade continues with a Dowd-Beckwith rearrangement and leads to the formation of the 13(14 ->

50 natural specificities and a repertoire, VDJ rearrangements and CDRH3 characteristics similar to thos

51 nation signal sequences limiting synchronous rearrangements and essential for allelic exclusion.

52 by G(s)-coupled GPCRs, inducing cytoskeletal rearrangements and formation of filopodia-like structure

53 has led to identification of recurrent gene rearrangements and fusions in a variety of tumors.

54 embedded between receptor-G protein complex rearrangements and G protein activation.

55 Chromosomal rearrangements and gene copy number variation (CNV) are

56 Immunoglobulin (Ig) gene rearrangements and oncogenic translocations are routinel

57 esponse that involves dynamic receptor dimer rearrangements and that is kinetically embedded between

58 trifurcating organic reaction, a carbocation rearrangement, and solvent-dependent Pummerer-like react

59 on transfer (SET) to this system initiates a rearrangement, and the catalytic cycle is completed by r

60 including lipid-protein interactions, domain rearrangement, and water-mediated diffusion mechanisms.

61 orchestrated nuclear cleavages, cytoskeletal rearrangements, and directed membrane growth lead to the

62 Sigmatropic rearrangements are an important fundamental toolbox in o

63 Such structural rearrangements are infrequent in ferrocenyl mixed-valent

64 However, these rearrangements are less pronounced in the KPC-4 than the

65 t for molecular electronics but because such rearrangements are low energy, measuring their rapid dyn

66 nd prognostic impact of specific 11q23/KMT2A rearrangements are not fully understood.

67 Conversely, 71 derived rearrangements are shared between at least two species,

68 Rearrangements at lower temperatures typically provided

69 it revealed previously unrecognized complex rearrangements at the breakpoints.

70 ation, accompanied by substantial structural rearrangements at the cytoplasmic intersubunit interface

71 ich combines the advantages of homology- and rearrangements-based methods.

72 osed as minimization of the number of genome rearrangements between extant and ancestral genomes.

73 r, have provided a picture of how structural rearrangements between transmembrane helices control lig

74 nes and malononitrile, not only initiate the rearrangement but also are responsible for the nature of

75 on ancestor and share the same initial V(D)J rearrangement, but their B cell receptor (BCR) sequence

76 gle nucleotide variants to large chromosomal rearrangements, but the extent of structural variation i

77 enzyme and promotes CSR and aberrant genomic rearrangements by suppressing the insertional DNA repair

78 enium hydride-mediated isomerization/Claisen rearrangement cascade and a ring-closing metathesis that

79 mes of 1,097 patients without an 11q23/KMT2A rearrangement categorized according to the 2017 European

80 ic and non-allelic mutations and chromosomal rearrangements characteristic of nuclease-dependent proc

81 tes whose electrophile-induced 1,2-metallate rearrangement chemistry enables a broad range of C-C bon

82 ith certain specific oxidation patterns, are rearrangement-competent.

83 The reversible solid-state rearrangement, confirmed in situ using powder X-ray diff

84 are an unanticipated major source of somatic rearrangements, contributing to oncogenic remodeling thr

85 and have to break extensive contacts before rearrangement, corresponding to slower fusion.

86 hylogeny, direct inference of phylogeny from rearrangement data in MLGO resulted in a highly discorda

87 T cells using Vdelta1(+) and Vdelta3(+) TRD rearrangements did not significantly expand after birth.

88 Rearrangement-driven tumors were diagnosed at a younger

89 ial genomes are marked by high rates of gene rearrangement, duplications of the control region and tR

90 Here, we focus on a conformational rearrangement during translocation, known as P/E hybrid-

91 d whether the cofactor undergoes significant rearrangement during turnover; resolution of these issue

92 morphogen signaling and large-scale cellular rearrangements during morphogenesis and growth.

93 at undergoes multiple large-scale structural rearrangements during protein elongation.

94 sight about both strain rate and constituent rearrangement dynamics in the sample at earlier times.

95 und that it also carried multiple unselected rearrangements elsewhere in its genome.

96 A vinyl cyclopropane rearrangement embedded in an iridium-catalyzed hydrogen

97 ects cells away from the niche, while random rearrangements enable cells away from the niche to be fa

98 that form an aromatic pathway whose dynamic rearrangements enable H(+) movement outside the Cl(-) po

99 lineage, although frequent recombination and rearrangement events between them have led to a complex

100 n of U2 to the spliceosome, and identify RNP rearrangements facilitated by PRP5 that are required for

101 Additionally, we unravel a unique ligand rearrangement for these classes of anionic mesoionic car

102 the entire cleavage module undergo extensive rearrangements for activation, triggered through the rec

103 an anion that undergoes a polar Truce-Smiles rearrangement, forming a C-C bond.

104 The rearrangement found in our cases, presumably causing a s

105 with a higher quality target elevates Vbeta rearrangement frequency before feedback inhibition, dram

106 d interpreting clinically relevant rare gene rearrangements from next-generation sequencing data.

107 etic system that generates gross chromosomal rearrangements (GCRs) mediated by foldback inversions co

108 Replication-based mechanisms of rearrangement generate varied chromosomal structures wit

109 ytotoxic lesions that can lead to chromosome rearrangements, genomic instability and cell death.

110 Patients with 11q23/KMT2A rearrangements had a low number of additional gene mutat

111 tudy shows that patients with an 11q23/KMT2A rearrangement have distinct mutational patterns and outc

112 th 1,3-diketones, easily undergo the Curtius rearrangement in boiling tBuOH to give Boc-protected alp

113 ila germband predict the onset of rapid cell rearrangement in both wild-type and snail twist mutant e

114 ays for melanoidin formation via the Amadori rearrangement in contrast to the reaction from Glc/Ala.

115 MPRSS2-ERG fusion is the most common genomic rearrangement in human prostate cancer.

116 ic dynamical modes facilitate compaction and rearrangement in the cell nucleus.

117 ubstituent X on the extent of the structural rearrangement in the process XS -> XS(-) cannot be expla

118 xtrusion, at least partly, by inducing actin rearrangement in the surrounding cells.

119 These analyses identified conformational rearrangements in beta2R-Y199(5.38)A that propagated fro

120 mouse spermatocytes and spontaneous genomic rearrangements in C. elegans.

121 the wide-ranging consequences of structural rearrangements in cancer genomes.

122 from T-cell receptor and immunoglobulin gene rearrangements in context of lymphoproliferative disorde

123 powerful tool for investigating large-scale rearrangements in genome structure upon cell differentia

124 that XLF-dependent C-NHEJ promotes deletion rearrangements in human cells and that cell type-specifi

125 lisation could not anticipate the effects of rearrangements in plant-frugivore communities following

126 Although AUX1 is necessary for full actin rearrangements in response to auxin, cytoplasmic auxin (

127 lix 6 and ultimately inducing conformational rearrangements in the GB2 transmembrane domain via a lev

128 ein correlation profiling to map IFN-induced rearrangements in the human protein-protein interaction

129 te activation of DcuS, indicating structural rearrangements in the linker.

130 NFKBIZ and TOB1, focal deletions in BRD4 and rearrangements in the loci of AKR1C genes.

131 We also show that structural rearrangements in the N-terminal segment (NTS) can stabi

132 a6 linker that likely mediate conformational rearrangements in the protein and cognate rRNA upon inte

133 orm non-B-form DNA induced gross chromosomal rearrangements in yeast and displayed high indel frequen

134 identified, and a myriapod-specific genomic rearrangement including Hox3 is also observed.

135 ussed, such as "motif extensions" and "motif rearrangements", including with concomitant extension of

136 Clastogen exposure can result in chromosomal rearrangements, including large deletions and inversions

137 ree RNA highlight the significant structural rearrangements induced by capsid proteins and invite the

138 ubtelomeric tandem repeats; and a variety of rearrangements initiated through breaks in interstitial

139 anoparticles which, in turn, allow for their rearrangement into crystalline domains via solid-state t

140 ative analysis revealed extensive structural rearrangements, introgressions from wild relatives and d

141 old catalyzes an unprecedented benzilic acid rearrangement involving migration of a carboxylate group

142 Balanced rearrangements involving the KMT2A gene, located at 11q2

143 This rearrangement is accompanied by drastic changes in the (

144 L) with mixed lineage leukemia 1 (MLL1) gene rearrangement is characterized by increased expression o

145 The possible mechanism of rearrangement is discussed.

146 The mechanism of the organocatalytic Cope rearrangement is elucidated through a combined computati

147 r evolves predominantly via the Stevens type rearrangement leading to an [n + 1] ring expansion of th

148 GAPDH and CD4 genes, that caused a deletion rearrangement leading to CD4 expression from the GAPDH p

149 uncover potential risk factors for germline rearrangements leading to 22q11.2DS offspring.

150 rs form, grow, fuse, and evolve via internal rearrangement, leading to overall hydrogelation.

151 or fast desensitization and that substantial rearrangements likely correspond to stable desensitized

152 oncurrently, p53 loss instigated chromosomal rearrangements linked to LINE sequences and also provoke

153 through different processes, including gene rearrangements, local nucleotide changes, and the transp

154 s and if left unrepaired can lead to genomic rearrangement, loss of genetic information, and eventual

155 to the fusion of discrete TADs, and complex rearrangements markedly change chromatin folding maps in

156 rrelating energetics data with the molecular rearrangements measured during confinement, we find that

157 hese data suggest that sigma1 conformational rearrangements mediate the efficiency of reovirus host c

158 s accomplished efficiently by employing ring-rearrangement metathesis and ring-closing metathesis as

159 ides, [3 + 2]-cycloaddition, 1,3-sigmatropic rearrangement, Michael addition, and Pictet-Spengler rea

160 This technique not only integrates a naive rearrangement model with a phylogenetic model for BCR se

161 These outcomes indicate that conformational rearrangements must occur in the N terminus of FepA duri

162 A novel fusion gene, generated by genomic rearrangement, MYB-NHSL1, was also noted.

163 ailing a gold(I)-catalyzed propargyl Claisen rearrangement/Nazarov cyclization, a [4+2] cycloaddition

164 In contrast, reactions in which aryl rearrangement occurs proceed through an enantiodetermini

165 The rearrangement occurs readily under physiological conditi

166 They demonstrate that Vbeta-to-DbetaJbeta rearrangement occurs stochastically on two competing Tcr

167 ron oxidation, ring-contractive 1,2-metalate rearrangement occurs to give a cyclobutyl boronic ester.

168 As a result, unusual rearrangement of 1,3-oxazinoquinolines to form either 2-

169 his mode of binding induces allosterically a rearrangement of a noncanonical toggle switch and the op

170 ne A that likely originates from a 1,2-alkyl rearrangement of a protonated 3,3'-spiroindolenine was i

171 sized through controlled Lewis acid promoted rearrangement of a spiroketal trimer.

172 yclic carbenes (NHCs) catalyzing aza-Claisen rearrangement of alpha,beta-unsaturated enals with cycli

173 sotope effects (KIEs) for the di-pai-methane rearrangement of benzobarrelene fit with statistical exp

174 findings support a hypothesis of an overall rearrangement of brain connections during human evolutio

175 The rearrangement of carbon-carbon (C-C) single bonds in rea

176 repolarization of root hairs, including the rearrangement of cytoskeletal filaments.

177 leading to the discovery of an Amadori-type rearrangement of dopegal in the reaction with several am

178 and TM6b more broadly, help trigger the bulk rearrangement of DraNramp to the inward-open state upon

179 on proceeds via a reductive iodonium Claisen rearrangement of in situ-generated beta-pyridinium silyl

180 approach involves the Fe(II)/Au(I)-catalyzed rearrangement of key 4-propargylisoxazole building block

181 The thermally induced rearrangement of Mes*P=C=C(H)R' (R' = tBu, Ad) afforded

182 osynthetic routes can now be designed by the rearrangement of nature's unlimited number of enzymes an

183 e the phenomenon does not rely on a physical rearrangement of nuclear positions, material constraints

184 whether the mechanism of the degenerate Cope rearrangement of semibullvalene can be affected by the p

185 fluxes can be inferred from a characteristic rearrangement of stable isotope tracers (e.g., 13C or 15

186 on of ultrasound and chilling contributed to rearrangement of starch molecules, causing a decrease in

187 in, we describe a gold-catalyzed sigmatropic rearrangement of sulfonium and selenium ylides (39 examp

188 , a system of inducible in vivo deletion and rearrangement of synthetic yeast chromosomes, diversifyi

189 slation initiation, AUG recognition triggers rearrangement of the 48S preinitiation complex (PIC) fro

190 The dynamic rearrangement of the actin cytoskeleton is an essential

191 bond of isocyanate, generated by the Curtius rearrangement of the azidocarbonyl group.

192 location pathway via the XIP, resulting in a rearrangement of the Ca(2+)-binding transport site in th

193 e boronate complexes undergo the desired 1,2-rearrangement of the carbon-based group with complete re

194 t His175 stabilizes the binuclear complex by rearrangement of the CcP heme-coordinating helix.

195 agment subsequently mediates a stepwise Cope rearrangement of the doubly dearomatized intermediate to

196 The rearrangement of the ECD-TMD interface is characterized

197 is molecularly characterized by chromosomal rearrangement of the NUT gene to another gene, most comm

198 that monoubiquitination triggers a complete rearrangement of the open, trough-like ID structure thro

199 is monometallic and proceeds via dearomative rearrangement of the phenethylcopper nucleophile to a Cp

200 Dynamic changes and rearrangement of the plant cell wall is an important res

201 Promoter rearrangement of the TERT gene juxtaposes the coding seq

202 lly impact the secondary/tertiary structural rearrangement of this region.

203 tants show that ceftazidime acylation causes rearrangement of three loops; the Omega, 240, and 270 lo

204 Lewis acid-catalyzed rearrangements of 4,5-dihydro-1,3-dioxepines have been i

205 nstead, assemble terpenes via intramolecular rearrangements of a single substrate.

206 Asymmetric Wagner-Meerwein rearrangements of beta-substituted styrenes are catalyze

207 odel of the genome, we study the large-scale rearrangements of chromatin that happen at different sta

208 Changes in growth cone morphology require rearrangements of cytoskeletal networks, and changes in

209 Changes in growth cone morphology require rearrangements of cytoskeletal networks, but the roles o

210 Reported here are novel formic-acid-mediated rearrangements of dearomatized acylphloroglucinols to ac

211 ructures of tetrameric PfISN1 reveal complex rearrangements of domain organization tightly associated

212 EpiGraph can objectively compare the rearrangements of epithelial cells during development an

213 ody mutation trajectories mediate long-range rearrangements of framework (FW) and complementarity det

214 ll lymphoma, high-grade B-cell lymphoma with rearrangements of MYC and either BCL2, BCL6, or both (do

215 of density functional theory calculations on rearrangements of potential biosynthetic precursors to t

216 -box helicase proteins perform ATP-dependent rearrangements of structured RNAs throughout RNA biology

217 Studies have shown genomic rearrangements of the AR gene underlie expression of div

218 The light-triggered rearrangements of the cofactor configuration and eventua

219 Divergent genomic rearrangements of the MHC II pathway among fully pregnan

220 That rearrangements of the molecular starch structure depend

221 y dynamic structural and functional seasonal rearrangements of the photosynthetic apparatus occur.

222 al analyses, we have explored the structural rearrangements of the respiratory chain in human cell li

223 Finally, we analysed brain-wide rearrangements of the vasculature in animal models of co

224 arily public clones, characterized by simple rearrangements of Vgamma9 and Vdelta2 chains with low ju

225 M kinase inhibitor increased C-NHEJ-mediated rearrangements only in U2OS cells.

226 main disruptions can result from chromosomal rearrangements or perturbation of architectural factors.

227 blood expressing a characteristic Vgamma9JP rearrangement paired with Vdelta2.

228 hree cohorts: patients with FGFR2 fusions or rearrangements, patients with other FGF/FGFR alterations

229 d an aryne to access these unusual transient rearrangement precursors.

230 ng identified the same T-cell receptor gamma rearrangement present in the gastric biopsies.

231 go robust D-to-J(H) but little V(H)-to-DJ(H) rearrangements, presumably owing to lack of locus contra

232 enation using a novel tandem acylation/[3,3]-rearrangement process and the reductive 1,2-oxazine ring

233 ith B cell diversification such as the V(D)J rearrangement process.

234 fructosylalanine - the corresponding Amadori rearrangement product - were compared.

235 akage-fusion-bridge cycles and simple genome rearrangements rather than chromothripsis.

236 The base-induced (t-BuOK) rearrangement reactions of 3,4-dihydro-2H-1,2,3-benzothi

237 we report on the limitations of sigmatropic rearrangement reactions of aryl allyl anilines, which de

238 different mechanisms are operative in these rearrangement reactions, with the pathway depending on t

239 We showed this HC rearrangement, redefined as two processes named Rock and

240 the influence of the mode of microstructure rearrangements remains evident.

241 It is highly probable that circle-derived rearrangements represent an ongoing mutagenic process.

242 le conformations revealed the intramolecular rearrangements required for alternating access of the me

243 dimer together, likely preventing structural rearrangements required for fusion.

244 systems could facilitate the conformational rearrangements required to create hierarchical structure

245 nd CD4 genes induced an LPCAT3-CD4 inversion rearrangement resulting in CD4 expression.

246 resulting from relaxed selection, or neutral rearrangements resulting from genetic drift.

247 RET gene rearrangements retaining the kinase domain are oncogenic

248 A novel rearrangement sequence of 3-hydroxyazetidines via a Ritt

249 ular plants is limited, suggesting extensive rearrangements since divergence.

250 s group because of their tendency to undergo rearrangement, sometimes forming bridged ions, as well a

251 effect experiments demonstrate that the Cope rearrangement step, rather than iminium formation, is ra

252 ly of targets based on an abiotic annulation/rearrangement strategy resulting in a 10-step total synt

253 s), loss of heterozygosity (LOH) and complex rearrangements, such as in chromothripsis.

254 the spiral seam undergo nucleotide-specific rearrangements, supporting substrate translocation.

255 t, a new variation of the anionic Fries-type rearrangement, takes place when nitriles, imines, or alk

256 nd when bound to IP6 revealed an active-site rearrangement that allows for ATP binding and catalysis.

257 A dearomative [3,3']-sigmatropic rearrangement that converts N-alkenylbenzisoxazolines in

258 uiv of an isocyanide followed by a molecular rearrangement that installs four new bonds.

259 t control mechanism for NK cell cytoskeletal rearrangement that is differentially regulated by glucoc

260 a of individual oligomers suggest structural rearrangement that is necessary for oligomers with an an

261 ytic mechanism, including a major structural rearrangement that primes the Cys-122-Cys-66 disulfide f

262 chanical communication is sufficient for the rearrangements that implement epithelial morphogenesis.

263 et of recurrent gliomas carries MGMT genomic rearrangements that lead to MGMT overexpression, indepen

264 characterized by massive, clustered genomic rearrangements that occurs in cancer and other diseases.

265 actions, and allowing us to infer structural rearrangements that permit certain sequence variants to

266 onal changes, including high-energy backbone rearrangements, that cooperatively organized the catalyt

267 n genomic architectures are caused by genome rearrangements, this problem is often posed as minimizat

268 ation and chromothripsis, complex chromosome rearrangements thought to be a major driving force in ca

269 ng catalytic, enantioselective carbocationic rearrangements through the intermediacy of alkyl iodanes

270 structures reveals concerted conformational rearrangements through which the HA mediates membrane fu

271 zenylcycloheptatetraene, or a new, potential rearrangement to cyanoazepine.

272 trile imine 38 is predicted to undergo a new rearrangement to cyanopyridine N-imide 40 with an activa

273 d subsequently undergoes complete structural rearrangement to drive fusion of viral and cellular memb

274 ddition product with Rh(2) (OAc)(4) caused a rearrangement to occur to give a 2-(1H-indol-3-yl)-2-eno

275 equence include a DMAP-mediated O- to C-acyl rearrangement to unite the side chains with the tetramic

276 ent carbocycles and enables abiotic skeletal rearrangements to additional underlying architectures.

277 equent in patients with specific 11q23/KMT2A rearrangements to assess their associations with outcome

278 from cycloaddition reactions and sigmatropic rearrangements to C-H functionalizations, thus allowing

279 complex, Set1 undergoes multiple structural rearrangements to cement interactions with the nucleosom

280 Molecular motors drive cytoskeletal rearrangements to change cell shape.

281 al viral capsids must undergo conformational rearrangements to coordinate essential processes during

282 is therefore not competitive with the known rearrangements to phenyldiazirines, ring expansion to di

283 dergo reversible solid-state inter-molecular rearrangements to produce dinuclear [Cu-Br.(alkene)](2)

284 Caller identifies both heavy and light chain rearrangements to provide additional information on thei

285 and the PDEgamma subunits, driving extensive rearrangements to relieve all inhibitory constraints on

286 , azo coupling resulted in a ring-degenerate rearrangement toward a 2-aryl-4-azotriazapentalene, whic

287 ociation kinetics, undergoing conformational rearrangement upon initial binding.

288 t lowers the free-energy barrier of the Cope rearrangement via an associative transition state that i

289 The number of somatic mutations per rearrangement was also higher in the graft than in the b

290 No interchromosomal rearrangement was identified in any species.

291 This conformational rearrangement was observed both in detergent-solubilized

292 methylation reactions: a cyclopropylcarbinyl rearrangement was used to trap the substrate radical and

293 Additionally, the rearrangement was utilized in the synthesis of a stereoc

294 responsible for a lumirubin-like structural rearrangement, was thoroughly investigated by liquid chr

295 These gene rearrangements were absent from all 126 control pancreat

296 Chromothripsis-related rearrangements were linked with univocal mutational sign

297 No inter-chromosomal structural rearrangements were observed on any of the 19 chromosome

298 re B-cell neoplasm initially driven by CCND1 rearrangement with 2 molecular subtypes, conventional MC

299 gh-throughput sequencing techniques, complex rearrangements with multiple breakpoints are often diffi

300 l binding induces wide-spread conformational rearrangements within the transmembrane domains.