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1 urements over times long enough for cells to rearrange.
2 en when underlying cancer genomes are highly rearranged.
3 ; adult, DDX41 mutated; and pediatric, NUP98 rearranged.
4 de chains become disordered and which become rearranged.
5 grated vectors were partially deleted and/or rearranged.
6                         None are degraded or rearranged.
7 cipal discriminating feature: it drastically rearranges a network of proximal hydrogen bonds, modifyi
8 advanced our assay to investigate effects of rearranging actin filaments on the lateral membrane orga
9 , delivering the scissile phosphate into the rearranged active site.
10 elapsed acute lymphoblastic leukemia and MLL-rearranged acute leukemia.
11                                          MLL-rearranged acute myeloid leukemia (AML) remains a fatal
12 reas eight- and twelve-membered rings are un-rearranged adducts.
13 t, TP53 mutated; NPM1 mutated; KMT2A mutated/rearranged; adult, DDX41 mutated; and pediatric, NUP98 r
14 possess a visible tail structure, one vertex rearranges after interacting with host lipopolysaccharid
15 ression was also variable in a pediatric MLL-rearranged ALL patient dataset, highlighting the existen
16 e acetyltransferases EP300 and CREBBP ZNF384-rearranged ALL showed significant up-regulation of CLCF1
17  pediatric mixed-lineage leukemia gene (MLL)-rearranged ALL were established in NOD.Cg-Prkdc(scid) Il
18 escence in situ hybridization, we mapped the rearranged alleles in these subjects.
19 dels in vitro, as well as in the in vivo MLL-rearranged AML BMT model coupled with treatment of "5 +
20 ate that AMPK maintains the epigenome of MLL-rearranged AML by linking acetyl-coenzyme A (CoA) homeos
21 EVI1 expression are required to recognize 3q-rearranged AML cases.
22 as further confirmed in human and murine MLL-rearranged AML cell models in vitro, as well as in the i
23 B) in human and mouse mixed lineage leukemia-rearranged AML cells, which were further increased after
24 d induces apoptosis of primary LSCs from MLL-rearranged AML patients in vitro and in vivo in xenograf
25 ncy granulopoiesis in a murine model of MLL1-rearranged AML, associated with accelerated leukemogenes
26 d postchemotherapy relapse in mice with MLL1-rearranged AML, but remission was sustained by ongoing R
27 at ALOX5 is especially down-regulated in MLL-rearranged AML, via transcription repression mediated by
28 induces leukemia stem cell expansion in MLL1-rearranged AML.
29 rget for selectively eliminating LSCs in MLL-rearranged AML.
30 itizer, with a therapeutic potential, in MLL-rearranged AML.
31 sis and leukemia suppressor function in MLL1-rearranged AML.
32  bone marrow progenitors from mice with MLL1-rearranged AML.
33  an EC enriched with patients with MLL/KMT2A-rearranged AML.
34 cence, and promoting LSC self-renewal in MLL-rearranged AML.
35 can be classified as a single entity of 3q26-rearranged AMLs.
36 tin binding did the catalytic triad in OTUB2 rearrange and bring the active site into a catalytically
37 ynthetic pathway, an isomerocyclase that can rearrange and cyclize geranylated indolenine (2) to a pr
38 ence of larger size aggregates that possibly rearrange and/or dissociate upon dilution.
39 entified CCI-006 as a novel inhibitor of MLL-rearranged and CALM-AF10 translocated leukemias that sha
40                                          MYC rearranged and double-hit groups were strongly over-repr
41 by duplication and translocation, frequently rearranged and lost in most Mycena species, but conserve
42 of Streptomyces sp.QL37, elucidated 24 other rearranged and non-rearranged angucyclines, 11 of which
43  the transcription factor ERG is recurrently rearranged and plays a critical role in prostate oncogen
44 1, triggering a series of transitions, first rearranging and bringing the two transmembrane domains i
45 QL37, elucidated 24 other rearranged and non-rearranged angucyclines, 11 of which were previously und
46  amount of information encoded by all of the rearranged antibody and T cell receptor genes in one per
47 linearity, whereas the remaining were highly rearranged as a result of inversions and inter- and intr
48 class of systems that the time delays can be rearranged as long as the total time delay over the cons
49 egments dock onto each other and continue to rearrange at the vicinity of the ribosome.
50  a palladium(II) complex, but this gradually rearranged at higher temperatures to afford a C-methyl c
51 the less thermodynamically stable isotopomer rearranges at cryogenic temperatures in the dark to the
52 h the BH3-mimetic ABT-199 in eradicating MLL-rearranged B-ALL cells.
53 nsitivity to vincristine chemotherapy in MLL-rearranged B-ALL patient samples.
54 Highlighting the central role of BCL6 in MLL-rearranged B-ALL, conditional deletion and pharmacologic
55 6 as a novel target for the treatment of MLL-rearranged B-ALL.
56               These Mphi precursors have non-rearranged B-cell receptor genes and coexpress myeloid (
57 ed in mixed lineage leukemia-rearranged (MLL-rearranged) B-acute lymphoblastic leukemia (B-ALL), whic
58 om polymers) to a macrocyclic product with a rearranged basic skeleton.
59 ndomized phase 2-like PDX trial using 13 MLL-rearranged BCP-ALL samples.
60 ent option for infants and children with MLL-rearranged BCP-ALL who have a poor outcome when treated
61 ib has been tested for the treatment of FGFR-rearranged bladder cancer.
62 his is followed by 1,5-boron shift to give a rearranged boranorcaradiene.
63                      However, the latter can rearrange by an unusual 1,3-chlorine shift, resulting in
64 me direction but at different velocities, to rearrange by differential migration.
65 annealing reveal that on Ag(111), structures rearrange by rotation and elongation of bonds in order t
66 eleton of a young adult male in a bear nest, rearranged by postdecomposition inundation, and the vari
67 nfected with a DFMO output strain containing rearranged cagY or the parental strain in which the wild
68 ovel methodological framework for recovering rearranged cancer chromosomes from karyotype graphs.
69 nding a collection of linear and/or circular rearranged cancer chromosomes that are determined by the
70  and/or circular structure of the underlying rearranged cancer chromosomes, thus limiting possible an
71                              CCR can recover rearranged cancer contigs from karyotype graphs thereby
72 ation in inferring chromosomal structures of rearranged cancer genomes and advancing our understandin
73 haplotype-specific karyotypes of one or more rearranged cancer genomes from DNA sequencing data from
74 into a karyotype graph representation of the rearranged cancer genomes.
75 6051b is effective in treating ROS1- or NTRK-rearranged cancer in preclinical models, including crizo
76 2032R mutant ROS1-rearranged cancers or NTRK-rearranged cancers in vitro and in vivo.
77 ion of both wild type and G2032R mutant ROS1-rearranged cancers or NTRK-rearranged cancers in vitro a
78 051b, in preclinical models of ROS1- or NTRK-rearranged cancers.
79 o a solid-like dorsal region with larger non-rearranging cells, and a more fluid-like ventral region
80 dhesion at apical vertices is compromised in rearranging cells, with apical tears in the cortex formi
81 esponse to external cues, molecular machines rearrange/change their structures to perform certain fun
82        In TB, lack of sexual transmission of rearranged chromosomes associates with low gamete viabil
83 ealed that radio-sensitivity of structurally rearranged chromosomes is dependent on radiation dose.
84 f ATP hydrolysis and conformational flipping rearranges client-binding sites, providing a paradigm of
85  (2n = 80), while falcon (2n = 50) is highly rearranged compared to the avian ancestor.
86 cell clones, characterized by their uniquely rearranged complementarity-determining region 3, were de
87  most common cytokine receptor-like factor 2-rearranged (CRLF2-rearranged) Ph-like ALL subset.
88 -, eight-, and twelve-membered rings, the un-rearranged dibenzothiophene Diels-Alder adduct is isolat
89 al work reveals that TFIID's conversion to a rearranged DNA binding conformation is enhanced in the p
90 y, we confirmed that the cytoplasmic domains rearrange during VRAC opening.
91 naptic connections in the nervous system are rearranged during development and in adulthood as a feat
92        However, the tree has been profoundly rearranged during this time.
93 inase (ALK), ROS proto-oncogene 1 (ROS1) and rearranged during transfection (RET)) has established an
94 Asp act as an integral until which minimally rearranges even as the bulk undergoes extensive reorgani
95 ary gene copies are commonly found on highly rearranged, extrachromosomal circular DNA (ecDNA).
96  timescale of a few minutes, these complexes rearrange, folding and compacting the DNA.
97           First, the aryls are lithiated and rearranged, followed by Fc and N-heterocycles.
98 taining, we investigate how dendritic spines rearrange following contextual fear conditioning (CFC) i
99 e., the variety of ways the analyte ions can rearrange following electrospray into kinetically stable
100 and M4 helices of agonist-activated receptor rearrange, forming a tighter interaction with the GluN1
101 ndomness of the order and orientation of the rearranged fragments, are all consistent with a chromoth
102 t jointly exert nuclear lamina- and membrane-rearranging functions (multicomponent NEC).
103 Igs ABCs express, we sequenced VH and Vkappa rearranged genes from unimmunized 22-mo-old C57BL/6 mice
104  rearrangements that delete self-reactive VJ rearranged genes.
105 tenance of heterozygosity by mechanisms that rearrange genomes and reduce recombination.
106 rocolinearity, except for a few species with rearranged genomes.
107 e and complex, consisting of deletion(s) and rearranged genomic fragments, which sometimes originated
108 stitutively activate GPHR, (b) can by itself rearrange GPHR into a fully active conformation, (c) sta
109 ecific complete sequences for mRNAs encoding rearranged heavy and light chain immunoglobulins in B ce
110 odent cardiac phospholipidome is extensively rearranged; however, whether specific acyl chains impair
111 ) technology, involving inserting functional rearranged human variable exons into the mouse IgH and I
112 rules for Watson-Crick base pairing but have rearranged hydrogen bonding donor and acceptor groups.
113 m paired heavy- and light-chain sequences of rearranged Ig genes from multiple descendants of the sam
114 S(-) PC in H. pylori infection, we sequenced rearranged Ig genes from single cell-sorted PC from biop
115 ly genes previously shown to be also used in rearranged Ig loci of MALT B cell lymphomas.
116 C), where the IgHC encoded by a productively rearranged Igh allele assembles into a PreB cell recepto
117 ger RNA (mRNA) (IgHR) from a nonproductively rearranged Igh allele is degraded by nonsense-mediated d
118                In contrast to a productively rearranged Igh allele, the Igh messenger RNA (mRNA) (IgH
119 s to improve the reconstruction of their VDJ-rearranged immune receptor mRNAs.
120 of particles are thermodynamically driven to rearrange in regions of low density and bond orientation
121 enes and intron regions of 28 genes that are rearranged in cancer cells.
122 er replication stress conditions recurrently rearranged in cancer.
123 m di-n-butylboron triflate and triethylamine rearranged in good yields and high selectivities with ex
124 for 4 kinase genes previously reported to be rearranged in Ph-like ALL.
125 egulate the cell secretory pathway and to be rearranged in thyroid and lung cancers, was strongly enr
126  which bears an unsaturated phosphanyl ring, rearranges in solution to yield a spirocyclic compound (
127          While RslO9 can further convert the rearranged intermediate to rishirilide D and lupinacidin
128  much slower second step, the kinase domains rearrange internally.
129 to overcome a barrier of 9.1 kcal mol(-1) to rearrange into cyclohexyne (with DeltaE for ring expansi
130 to surmount a barrier of 1.6 kcal mol(-1) to rearrange into cyclopentyne (with DeltaE for ring expans
131                Water films on this scale can rearrange into one or two layers with strongly suppresse
132             The catalytic GGQ loop of RF2 is rearranged into a long beta-hairpin that plugs the pepti
133 e loss of infectivity; virion associated mu1 rearranged into an altered conformation.
134 H(4)(+)C o-Me(2)-2.1.1], which spontaneously rearranged into the larger and thermodynamically more st
135                      Second, the mu1 protein rearranges into a protease-sensitive conformation to gen
136 ormation of a semicarbazone conjugate, which rearranges into a stable diazaborine.
137 ucleic-acid sequence being transcribed, RNAP rearranges into an elemental, catalytically inactive con
138 ve hairpin intermediate (H1) that eventually rearranges into the native fold.
139 whereas transcription inhibition stalled and rearranged it.
140    This was because it lacked the ability to rearrange itself upon binding.
141                        Archetype rather than rearranged JCPyV seems to drive the pathogenesis of JCPy
142      The total synthesis of principinol D, a rearranged kaurane diterpenoid, is reported.
143 r, we find that ribavirin treatment of KMT2A-rearranged (KMT2A-R) infant ALL cells and the KMT2A-AFF1
144                    Structural variants (SVs) rearrange large segments of DNA(1) and can have profound
145 dels, we found that cancer cells dynamically rearrange leader and follower positions during collectiv
146 lence subbands of the AlN/GaN DA is properly rearranged leading to the heavy-hole (HH) miniband being
147 n or polymer chains pack loosely and readily rearrange, leading to fast fusion.
148  histone demethylases in AML, especially MLL-rearranged leukaemia.
149 he basis for a new therapeutic target in MLL-rearranged leukemia and act as further validation of a b
150 he relevance of MLL2 as a drug target in MLL-rearranged leukemia and suggest its broader significance
151 and apoptosis in a subset (7/11, 64%) of MLL-rearranged leukemia cell lines within a few hours of tre
152 sensitized an intrinsically unresponsive MLL-rearranged leukemia cell to CCI-006, indicating that thi
153 o observe an unexpected role for MLL2 in MLL-rearranged leukemia cells and identify potential therape
154  novel small molecule that rapidly kills MLL-rearranged leukemia cells by targeting a metabolic vulne
155                         The unresponsive MLL-rearranged leukemia cells did not undergo mitochondrial
156                In addition, unresponsive MLL-rearranged leukemia cells expressed increased levels of
157 to the sensitive cells, the unresponsive MLL-rearranged leukemia cells were characterized by a more g
158 et of low HIF1alpha/low MEIS1-expressing MLL-rearranged leukemia cells.
159 scover cytotoxic compounds selective for MLL-rearranged leukemia identified CCI-006 as a novel inhibi
160  impairs propagation of murine and human MLL-rearranged leukemia in vitro and in vivo.
161  suffering from mixed lineage leukemia (MLL)-rearranged leukemia remain below 50% and more targeted,
162 sly undescribed metabolic variability in MLL-rearranged leukemia that may contribute to the heterogen
163 ness of the biologic features underlying MLL-rearranged leukemia, targeted therapies for this leukemi
164 on the requirement for wild-type MLL1 in MLL-rearranged leukemia.
165 ion as novel target for the treatment of MLL-rearranged leukemia.
166 nd DOT1L for more effective treatment of MLL-rearranged leukemia.
167  that endogenous MLL1 is dispensable for MLL-rearranged leukemia.
168 lead to improved clinical outcomes for NUP98-rearranged leukemia.
169 licing, is consistently overexpressed in MLL-rearranged leukemias.
170 hibitors as a targeted approach to treat MLL-rearranged leukemias.
171 eral genes including those essential for MLL-rearranged leukemogenesis, such as DOT1L and SETD1A.
172 nation of the unique features of the sirtuin rearranging ligands (SirReals) as highly potent and isot
173 lament in which the molecules adopt a vastly rearranged, lower energy fold compared to wild-type fibr
174 12, and April 30, 2016, 26 patients with RET-rearranged lung adenocarcinomas were enrolled and given
175  inhibitor, is highly effective against ROS1-rearranged lung cancer and is used in clinic.
176             The accrual of patients with RET-rearranged lung cancer to this protocol has been complet
177 1 have nonredundant roles in controlling ALK-rearranged lymphoma survival and morphology but are redu
178 rently dire outcomes for patients with NUP98-rearranged malignancies, therapeutic strategies have bee
179                        Furthermore, germline rearrange-ments in intron 1 of TP53 are associated with
180 thylation in the egg cell depends on DOMAINS REARRANGED METHYLASE 2 (DRM2) and RNA polymerase V (Pol
181  including RNA POLYMERASE V (POL V), DOMAINS REARRANGED METHYLTRANSFERASE 2 (DRM2) and SAWADEE HOMEOD
182                Precise regulation of DOMAINS REARRANGED METHYLTRANSFERASE 2 (DRM2), the de novo Arabi
183 clude the de novo methyltransferase, DOMAINS REARRANGED METHYLTRANSFERASE 2 (DRM2), which methylates
184 hark Igs are encoded by 100-200 autonomously rearranging miniloci.
185 aused them to expand their apical cytoplasm, rearrange mitochondrial/lysosome trafficking, and genera
186        Relapse remains the main cause of MLL-rearranged (MLL-r) acute lymphoblastic leukemia (ALL) tr
187  is a potential therapeutic strategy for MLL-rearranged (MLL-r) leukemia.
188 r treatment of NPM1-mutant (NPM1mut) and MLL-rearranged (MLL-r) leukemias.
189 ally overexpressed in mixed lineage leukemia-rearranged (MLL-rearranged) B-acute lymphoblastic leukem
190 therapeutic vulnerabilities at play in NUP98-rearranged models.
191                    Our analyses suggest that rearranged mtDNAs appeared early during unionid radiatio
192 ith PML had a single neurotropic strain with rearranged NCCR, and 1 patient had a single strain with
193    The natural history of PDGFRA- and PDGFRB-rearranged neoplasms has been dramatically altered by im
194 eukoencephalopathy of the brain is caused by rearranged neurotropic JCPyV, little is known about vira
195 f clinical response are unpredictable in ALK-rearranged non-small cell lung cancer (NSCLC) patients t
196 ddress this, we evolved resistance in an ALK rearranged non-small cell lung cancer line (H3122) to a
197 K)-rearranged or ROS proto-oncogene 1 (ROS1)-rearranged non-small-cell lung cancer (NSCLC) are sensit
198 h untreated anaplastic lymphoma kinase (ALK)-rearranged non-small-cell lung cancer (NSCLC) is not kno
199 t chemotherapy in patients with advanced ALK-rearranged non-small-cell lung cancer who had previously
200  intracranial activity, in patients with ALK-rearranged non-small-cell lung cancer.
201 in untreated patients with stage IIIB/IV ALK-rearranged non-squamous NSCLC was done in 134 centres ac
202                              Thirty-nine ALK-rearranged NSCLC patients treated with crizotinib as fir
203 ive biomarker for crizotinib efficacy in ALK-rearranged NSCLC patients.
204      Patients with brain metastases from ALK-rearranged NSCLC treated with radiotherapy (SRS and/or W
205 s chemotherapy in patients with advanced ALK-rearranged NSCLC.
206  crizotinib-treated and crizotinib-naive ALK-rearranged NSCLC.
207                        Since NuRD physically rearranges nucleosomes, the dynamic mobility of this com
208 io)cyanates and arylcarbodiimides led to non-rearranged o-functionalized O-arylcarbamates.
209         The textbook view is upstream Vbetas rearrange only by deletion and TRBV31 rearranges only by
210 recede those in IgL loci, 2) IgLlambda genes rearrange only when IgLkappa genes are consumed, and 3)
211 Vbetas rearrange only by deletion and TRBV31 rearranges only by inversion to create VbetaDJCbeta gene
212 enient and robust method to site-selectively rearrange or cleave bonds with submolecular precision in
213  association between baseline numbers of ALK-rearranged or ALK-CNG CTCs and PFS was observed.
214 gression of leukemia in mouse models of MLL1-rearranged or NPM1-mutated leukemia, including patient-d
215 tients with anaplastic lymphoma kinase (ALK)-rearranged or ROS proto-oncogene 1 (ROS1)-rearranged non
216                Mutations that add, subtract, rearrange, or otherwise refashion genome structure often
217 ssion-free survival (PFS) in a cohort of ALK-rearranged patients.
218 , however, binding was retained against both rearranged peptides and no peptide (r = 0.85 and r = 0.7
219 be an adaptive signaling plasticity of CRLF2-rearranged Ph-like ALL following selective TKI pressure,
220 lly pragmatic therapeutic strategy for CRLF2-rearranged Ph-like ALL.
221 ine receptor-like factor 2-rearranged (CRLF2-rearranged) Ph-like ALL subset.
222           The (R)-BINOL Fc phosphate gave Fc-rearranged phosphonate in 91% de.
223   Nature often creates complex structures by rearranging pre-existing units.
224 s transition state TS8, directly forming the rearranged product 23.
225 d in a continuous flow process to afford the rearranged product in 22 min of residence time.
226 ide chains of residues coordinating the zinc rearrange quickly to promote the nucleophilic attack of
227 contrast, our results demonstrate the use of rearranged receptors to mediate diverse modes of recogni
228 mmune system relies on germline-encoded, non-rearranging receptors expressed by innate immune cells r
229 g of Pm1a and its identification in a highly rearranged region of chromosome 7A provides insight into
230 , we demonstrate that targeting structurally rearranged regions, in particular tandem or interspersed
231                            For instance, ALK-rearranged renal cell carcinomas have shown responses to
232 g of the ArfA N-terminus in the second state rearranges RF2 into an extended conformation that docks
233  solution of 3a or 3b at reflux afforded the rearranged species ArSn(3-tricyclo[2.2.1.0(2,6)]heptane)
234  The enantioselective total synthesis of the rearranged spongian diterpenoid (-)-macfarlandin C is re
235             This is the first synthesis of a rearranged spongian diterpenoid in which the bulky hydro
236 lution of a strategy to access the family of rearranged spongian diterpenoids harboring a concave-sub
237 ted patients aged at least 18 years with ALK-rearranged stage IIIB or IV non-small-cell lung cancer (
238 played a role in the emergence of the highly rearranged structure of the gibbon genome by disrupting
239 le repetitions of the same conspecific song, rearranging syllable order reinstated strong responses.
240 s, resulting in death if the affinity of the rearranged TCR is below the threshold for positive selec
241 -associated TCRbeta paired with endogenously rearranged TCRalpha endowed unprimed T cells with autoan
242  and the intrinsic properties of somatically rearranged TCRs.
243 nd leukemic cells with functional ability to rearrange the actin cytoskeleton and engraft successfull
244  ORF52 play critical roles in its ability to rearrange the architecture of the MT cytoskeleton.
245 -cellular ciliary and contractile activities rearrange the cell's underlying helical cytoskeleton to
246 on levels due to a repeated measurement will rearrange the grouping of data points such that these cl
247                                  Plants must rearrange the network of complex carbohydrates in their
248 of samples, and insertions and deletions can rearrange the spatial distribution of CpGs.
249 e above W583 might act as flexible linker to rearrange the tryptophan gate.
250 des B cell development and proliferation and rearranged the IgH gene locus.
251 meable 2-aminoquinoline inhibitors and later rearranged the scaffold to decrease off-target binding.
252                      A provocative new study rearranges the base of the dinosaur evolutionary tree, u
253  Flavin monooxygenase RslO9 then oxidatively rearranges the carbon backbone, presumably via lactone-f
254                                        CB[7] rearranges the substrate in a highly reactive conformati
255             Its C-terminal cupin domain then rearranges the triply modified arginine to N(delta)-hydr
256 of guide RNA fastens the subdomains, thereby rearranging the active-site residues and increasing the
257 d then resolves the structure by iteratively rearranging the local genome structure, in a randomized
258 rget network, is constructed by sampling and rearranging the original temporal network.
259                                              Rearranging the regression equation, we determined the p
260 is believed to underlie adaptive behavior by rearranging the way neuronal circuits process informatio
261 sion to mark pre-T cells that have failed to rearrange their beta-chain.
262 gy from the electromagnetic field by rapidly rearranging their positions.
263  to a lesser extent, the entropic benefit of rearranging those networks during binding.
264 n time and temperature, the obtained allenes rearrange to 1,3-biaryl-1-trifluoromethyl-1H-indenes.
265 erate nitrile imines (13, 19, and 38), which rearrange to 1H-diazirines, imidoylnitrenes, and carbodi
266 e latent regime, the adsorbed polymer chains rearrange to anchor their ends onto the surface and cont
267 rbenes or of heteroarylcarbenes, which again rearrange to arylnitrenes.
268 re precursors of imidoylnitrenes, which also rearrange to carbodiimides or add intramolecularly to ar
269  the cyclization to 1 H-diazirines and hence rearrange to carbodiimides.
270 ses (e.g., aryl- and silylnitrile imines) or rearrange to carbodiimides.
271 *)) to produce a phenolic compound or it can rearrange to form a bicyclic peroxy intermediate that su
272  remaining four helices and connecting loops rearrange to form the interface with actin.
273 ing group, such as C(4)-Cl or C(5)-NO2, they rearrange to products 4 in the presence of aqueous ammon
274 2,5)]pent-3-ylidene is a carbene foreseen to rearrange to pyramidane (c-C(4)H(4))C, a highly strained
275 methylazines and azinylcarbenes, which often rearrange to the energetically more stable arylnitrenes.
276 h, in the presence of protic or Lewis acids, rearranged to dienes or lupanes bearing a bicyclo[3.3.1]
277 hannel, whereas T. maritima sigma1.1 must be rearranged to fit therein.
278 nt, while the tRNA cluster trnW-trnC-trnY is rearranged to trnY-trnW-trnC in J. hyalinus, the first r
279 rt a mechanism whereby the borepin initially rearranges to a boranorcaradiene by a thermal 6pai-elect
280 tions are released and a single 14-3-3 dimer rearranges to bridge the C-terminal pS729 binding sites
281  intersystem crosses to its ground state and rearranges to form the (6-4) photoadduct.
282 ] induces formal oxidation, and the compound rearranges to incorporate the Si atom into the carbocycl
283 ns among S14, H73, G74, N111, R177, and G158 rearranges to open the phosphate release site.
284 ular processes involve proteins structurally rearranging to accommodate molecular partners.
285 way and must dissociate to monomers prior to rearranging to amyloid fibrils.
286  and produce cytoplasmic protrusions, before rearranging to form two continuous epithelial layers.
287 roviding sufficient free volume for atoms to rearrange, to form the melt.
288 ntly, Matsuda et al. (Pioneer factor NeuroD1 rearranges transcriptional and epigenetic profiles to ex
289 ngton's disease model, that integration of a rearranged transgene with coincident deletion of 5,444 b
290 sily obtained but showed to be unreactive or rearranged under these cyclization conditions.
291 nd the active states and (ii) a network that rearranges upon activation.
292                           Introgression of a rearranged Valpha14-Jalpha18 TCR-alpha chain gene into t
293 g strategies using targeted amplification of rearranged variable regions comprised of V(D)J gene segm
294 al regioisomeric species, which subsequently rearrange via stepwise [1,3]- or concerted [3,3]-sigmatr
295 ghly labile and by visible or IR irradiation rearranges via a 1,2-fluorine migration from boron to ca
296                                    The ester rearranges via a tetrahedral hemiorthoamide to yield an
297 ks mediating the interactions are constantly rearranged with a characteristic timescale and, possibly
298          Many cancer genomes are extensively rearranged with aberrant chromosomal karyotypes.
299          Many cancer genomes are extensively rearranged with highly aberrant chromosomal karyotypes.
300 complex concatenated mtDNA-derived sequences rearranged within the nuclear genome.

 
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