ライフサイエンスコーパス: be disrupted by

1 These states are disrupted by a brief repression and reset upon a sec

2 vealed that tertiary contacts within the PDZ are disrupted by a partial unfolding transition that ena

3 We hypothesize that RGTA2 function might be disrupted by a 12-amino acid insertion in a conserved

4 interacts with BBS-5 and the interaction can be disrupted by a conserved mutation identified in human

5 s - the function of a gene is less likely to be disrupted by a mutation close to the distal ends.

6 r contextual threat-conditioned memories can be disrupted by a reminder-extinction procedure that put

7 Clusters of functionally related genes can be disrupted by a single copy number variant (CNV).

8 unctional unit required for activity and can be disrupted by a single point mutation.

9 Vascular barrier integrity can be disrupted by a variety of soluble permeability factor

10 rom the first ATG and the open reading frame is disrupted by a 1-bp insertion, expresses very small a

11 Intriguingly, binding of each PIP is disrupted by a different subset of mutations.

12 When vimentin organization is disrupted by a dominant-negative mutant or by silenci

13 Nine Mile reference isolate, where the gene is disrupted by a frameshift mutation, resulting in a ps

14 required for optimal iron homeostasis, which is disrupted by a mechanism not yet determined in the ye

15 To determine if NK cell function is disrupted by a model of human shift-work and jet-lag,

16 aptic termini, and this function of dynactin is disrupted by a mutation that causes motor neuron dise

17 inding is cooperative, but the cooperativity is disrupted by a phospho-mimic mutation S249D in the 4.

18 cal neuron subtype fate specification, which is disrupted by a psychiatric-disorder-associated geneti

19 , the intron is crippled and the target gene is disrupted by a series of stop codons.

20 ative geotaxis in flies, scored as climbing, is disrupted by a static EMF, and this is mediated by cr

21 ranslation, and eIF3-mediated FTL repression is disrupted by a subset of SNPs in FTL that cause hyper

22 the major flowering-time repressor gene FLC is disrupted by a TE insertion specifically in the rapid

23 The resultant unstable chromophore is disrupted by a unique cycloisomerization promoted at

24 This delicate balance in the liver is disrupted by a variety of pathological states includi

25 alcium-binding aspartate residue, Asp307Ala, was disrupted by a c.920A>C change in one family that pr

26 A 200-km large asteroid was disrupted by a collision in the Main Asteroid Belt,

27 d both nucleotide binding domains (NBDs) and was disrupted by a cystic fibrosis mutation in NBD1 (G55

28 virus (ADinUL79(stop)) in which the UL79 ORF was disrupted by a stop codon mutation and found that AD

29 In 1 case, CUX1 was disrupted by a translocation, resulting in a loss-of

30 associations with foot shock or food reward were disrupted by a highly-specific actin cycling inhibi

31 No organ recoveries or transplantations were disrupted by a lack of SARS-CoV-2 testing.

32 Moreover, these various forms of plasticity were disrupted by Abeta exposure.

33 on via a lysine-phosphate salt bridge, which was disrupted by acetyl-Lys resulting in backbone flexib

34 involves glutamate residues at distal NT and is disrupted by acidosis.

35 Interaction between AR and SLIRP was disrupted by Ack1 kinase activity as well as androge

36 everal alternative nucleosomal arrays, which are disrupted by activation.

37 ated with the I(Ks)-Yotiao complex and could be disrupted by addition of the AC9 N terminus.

38 the functions of these circadian oscillators are disrupted by age, environment, or genetic mutation,

39 Ca(2+) homeostasis is disrupted by alpha-synuclein (alpha-syn), a small lip

40 Interestingly, this interaction was disrupted by AMPylation.

41 point to a gephyrin-dependent mechanism that is disrupted by an autism-associated mutation at R705 an

42 ant recipients in whom tolerance maintenance is disrupted by an episode of acute CMV infection.

43 Although HIV latency is disrupted by an initial VOR dose, the effect of subse

44 mouse model in which IL-1R1 gene expression is disrupted by an intronic insertion of a loxP flanked

45 inant virus SMin92, in which pM92 expression was disrupted by an insertional/frameshift mutation.

46 along traditional routes, many of which have been disrupted by anthropogenic disturbances.

47 nd inhibition of calcium currents by galanin were disrupted by anti-G(o)2alpha antibodies.

48 blishes in the colon when the gut microbiota are disrupted by antibiotics or disease.

49 ssion of B1R and CPM-E264Q in the same cell, was disrupted by antibody that dissociates CPM from B1R,

50 nstrate how MAG-ganglioside interactions can be disrupted by antiganglioside antibodies that override

51 present forces; this organization can easily be disrupted by any small external stimuli.

52 Organization of F-actin in appressoria is disrupted by application of antioxidants, whereas lat

53 is an important ecological process that can be disrupted by artificial lighting.

54 ider how this mutator-nonmutator balance can be disrupted by beneficial mutations and analyze the cir

55 he physical interaction between TAP2 and TPN is disrupted by benzene, a compound known to interfere w

56 les form stable complexes with HLA-DM, which are disrupted by binding of high-affinity peptide.

57 e cGMP-induced enhancement of LTP and memory was disrupted by blockade of Abeta, suggesting that the

58 Galphaq/11 interactions in endothelial cells are disrupted by both competitive inhibition and HS degr

59 of the AP-2 complex (AP2M) was confirmed to be disrupted by both acute and repeated fluoxetine treat

60 ive, suggesting neural connections to the PV were disrupted by both PV isolation and GP ablation.

61 repair pathway, translesion synthesis (TLS), is disrupted by BPLF1, which deubiquitinates the DNA pro

62 y of the Golgi and trans-Golgi network (TGN) is disrupted by brefeldin A (BFA), which inhibits the Go

63 interaction between TRIP8b and the HCN1 CNBD was disrupted by cAMP and that TRIP8b binding to the CNB

64 d conscious awareness and have been shown to be disrupted by cannabinoids in animal studies.

65 and active regulatory mechanisms, which may be disrupted by cardiopulmonary disease, but this is not

66 stribution of pulmonary perfusion, which may be disrupted by cardiopulmonary disease, but this is not

67 When these interactions are disrupted by cationic antimicrobial peptides, or by

68 ed to catalyze these events when replication is disrupted by certain impediments in vivo.

69 vels and targets of methylation are known to be disrupted by chemicals and are therefore of great int

70 After DNA damage, the MDMX-CK1alpha complex is disrupted by Chk2-mediated phosphorylation of MDMX at

71 d a functional bile canaliculi system, which was disrupted by cholestasis-inducing drugs such as trog

72 on of JNK by TGF-beta in the absence of Dab2 is disrupted by cholesterol depletion.

73 g-related shift in novel environments should be disrupted by cholinergic antagonism; and (3) in famil

74 t role in nicotine reward and their function is disrupted by chronic nicotine exposure, suggesting ni

75 ta signaling and inflammatory response genes were disrupted by CIE treatment in microglia gene networ

76 regulated and evolves; and how splicing can be disrupted by cis- and trans-acting mutations leading

77 coevolved plant-pollinator relationships to be disrupted by climatic warming.

78 was shifted to weaning foods and appeared to be disrupted by complementary feeding.

79 re of motor representations is that they can be disrupted by constraints on an observed agent's actio

80 inding protein as protein.heme complexes can be disrupted by contact with an apoprotein (e.g. apomyog

81 e consolidated memory for the experience can be disrupted; by contrast, protein synthesis inhibition

82 RNA isoform transitions and are predicted to be disrupted by CUG(exp)-associated mechanisms in utero.

83 on microscopy shows that the Abeta42 fibrils are disrupted by curcumin.

84 This interaction can be disrupted by CXCR4 antagonists.

85 mplex, TMC1 and TMC2, and these interactions are disrupted by deafness-causing Cib2 mutations.

86 in injectoporated hair cells, a pattern that is disrupted by deafness-associated PJVK mutations.

87 regulates tip-link assembly, a process that is disrupted by deafness-causing Tmhs mutations.

88 The clustering can be disrupted by deletion of various proteins in mice, in

89 r of the two Cdc42 apical recycling pathways was disrupted by deletion of Rdi1, a guanine nucleotide

90 These effects of inflammatory stimuli were disrupted by deletion of inhibitor of NF-kappaB kin

91 Normal epigenetic states could be disrupted by detrimental mutations and expression alt

92 he molecular properties of alpha-crystallins are disrupted by diabetes and contribute to the loss of

93 th and homeostasis; however, these processes are disrupted by diabetes.

94 her these data suggest that nuclear position is disrupted by distinct mechanisms in EDMD and CNM.

95 are present in each NS1 monomer, and tubules are disrupted by divalent cation chelation and restored

96 safeguard epigenetic integrity at loci that are disrupted by DNA breakage.

97 Here we report that D loops can also be disrupted by DNA topoisomerase 3 (Top3), and this dis

98 tion delocalization and Coulomb gap collapse are disrupted by doping-induced disorder, suppressing th

99 Inhibitory signals via KIR3DL1 are disrupted by downregulation of HLA class I ligands o

100 In summary, the BBB is disrupted by downregulation of the Shh pathway and br

101 Because the sphingolipid domains are disrupted by drugs that depolymerize the cells actin

102 hat localization of both nNOSmu and nNOSbeta is disrupted by dystrophin deficiency.

103 ells on adjacent epithelial cancer cells can be disrupted by either inhibiting VEGF-C in EMT cells or

104 en this differential proliferation mechanism is disrupted by either ectopic overexpression or mutatio

105 The reasoning system would be disrupted by emotion, especially for traumatic events

106 But willpower can be disrupted by emotions and depleted over time.

107 ues in CytR and CRP (cAMP receptor protein), is disrupted by exogenous cytidine.

108 target promoters and VirR : promoter binding was disrupted by exogenous addition of the signalling mo

109 get tissue after the blood brain barrier has been disrupted by exposure to a hyperosmolar mannitol so

110 This is disrupted by expression of K-Ras V12 or B-Raf V600E b

111 Repression required both proteins and was disrupted by FBF-2 alleles that failed to bind CPB-1

112 complementation assay, and this association is disrupted by flagellin treatment.

113 h the skin occurs when skin barrier function is disrupted by, for example, genetic predisposition, me

114 e in TMP metabolism, mitochondrial membranes were disrupted by freezing and thawing.

115 he brain parenchyma in regions where the BBB is disrupted by FUS and MBs.

116 Physcomitrella patens when both HY2 and PUBS were disrupted by gene targeting.

117 Here, we discuss how transcriptional control is disrupted by genetic alterations in cancer cells, why

118 ZIKV infection was disrupted by genetic targeting of ITGAV or its bindi

119 e line (Gad1(-/-)) in which GAD67 expression is disrupted by genomic insertion of the green fluoresce

120 This complex is disrupted by genotoxic stress, resulting in the displ

121 n the blood-rich marginal zone and follicles is disrupted by GRK2 deficiency and by mutation of an S1

122 ure native quaternary structure, which could be disrupted by heterochiral associations.

123 Acquisition of left/right identity is disrupted by heterozygous mutations in mosaic eyes an

124 Theory suggests these cycles can be disrupted by high amplitude seasonal fluctuations in

125 in with H3K4 unmethylated histone tails that is disrupted by histone H3K4 methylation and histone ace

126 nscription factor coexpression profiles that is disrupted by HIV infection and suggest a role for HIV

127 C2) complex components, and this interaction was disrupted by HIV Tat, suggesting that LINC00313 may

128 l barriers between species are continuing to be disrupted by human activities.

129 ration governed terminal differentiation and were disrupted by human skin barrier disease-associated

130 a highly complex collection of proteins that is disrupted by hundreds of gene mutations causing over

131 Bindings of both HDAC and PcG to Arf are disrupted by inactivation of p53 and can be restored

132 trandings suggests that their navigation may be disrupted by increased radio frequency noise generate

133 mer dilution, where WT receptor dimerization is disrupted by increasing expression of nonfunctional C

134 Maternal behavior in postpartum rats is disrupted by increasing norepinephrine release in the

135 stin assembly during the saccular stage that is disrupted by inflammatory signaling and could be amen

136 tions via protein-protein interaction, which is disrupted by inherited disease mutations.

137 The emergence of these correlated networks was disrupted by inhibiting vCA1 shock responses during

138 ed reinstatement and synaptic depotentiation were disrupted by inhibiting AMPAR internalization via i

139 n 10 nm of one another and that the clusters are disrupted by inhibition of Src and Syk family kinase

140 thogenesis, and suggest that T4P systems may be disrupted by inhibitors that do not preclude componen

141 s, which revealed that vimentin localization is disrupted by inhibitors of signaling that belong to a

142 Furthermore, degradation can be disrupted by insertion of two N-terminal myc tags, im

143 monstrate that cellular actions of metformin are disrupted by interference with its metal-binding pro

144 cts with the N-terminal domain of AR and can be disrupted by JQ1.

145 some phospholipid bilayer, the bilayer would be disrupted by laser irradiation so that drug release w

146 failed to reseal a plasma membrane that had been disrupted by laser irradiation.

147 ap, and NIH 3T3 cells in which the actin cap is disrupted by latrunculin A.

148 othalamic E2 were observed, thermoregulation was disrupted by letrozole in females only, indicating s

149 precisely at this positionally cued line and are disrupted by Lgn.

150 slow fluctuations and neuronal synchronicity is disrupted by light general anesthesia.

151 ioning required extracellular prosaposin and was disrupted by lipid raft perturbation using methyl-be

152 In some individuals, mineral homeostasis can be disrupted by long-term therapy with certain antiepile

153 The transition to coordinated activity was disrupted by long-term optical inhibition of sporadi

154 n mechanisms that regulate osmotic stability are disrupted by loop diuretics in rats.

155 Cholinergic input to the cortex was disrupted by making bilateral injections of the immu

156 We also find that these activity patterns are disrupted by manipulating cadherin or gap junction e

157 eration and subsequent fetal stages can also be disrupted by maternal immune activation in the 1st tr

158 elopment of event-related neuronal responses was disrupted by MeCP2 mutation, suggesting that impaire

159 prediction error and incentive value signals were disrupted by methamphetamine in the left nucleus ac

160 ed increased co-localisation with LDs, which was disrupted by microtubule depolymerising agent nocoda

161 growth is a highly ordered process that can be disrupted by misalignment of individual amino acids a

162 The interaction between WT1 and TET2 is disrupted by multiple AML-derived TET2 mutations.

163 When droplet sequestration is disrupted by mutating Jabba, embryos display an eleva

164 lar, mostly electrostatic, interactions that were disrupted by mutating a positively charged (Lys-ric

165 54-465 as the main binding site, which could be disrupted by mutation.

166 elements whose normal cellular functions can be disrupted by mutation.

167 This intramolecular interaction is disrupted by mutation of Tyr633 within the Mint1 auto

168 st if the structure of Lys(48)-linked chains is disrupted by mutation of ubiquitin or if chains are l

169 Moreover, if this normal folding nucleus is disrupted by mutation, the interdomain interface is s

170 588) of ATDC and the RING domain of RNF8 and was disrupted by mutation of ATDC Ser-550 to alanine.

171 cells that nucleolar localization of RPL23aA was disrupted by mutation of various combinations of fiv

172 Importantly, this action of PDZ-GEF1 was disrupted by mutation within its putative cyclic nuc

173 physiological actions by 1,25(OH)(2)D, which are disrupted by mutations in the VDR.

174 hat is largely not understood, but which can be disrupted by mutations.

175 a compact platform-like architecture, which is disrupted by mutations implicated in developmental di

176 norhabditis elegans muscle, but this pattern is disrupted by mutations in the mitochondrial fission c

177 level of Ribosomal Protein L27a (RPL27a) and is disrupted by mutations in the two paralogs RPL27aC an

178 membrane homeostasis, and that this function is disrupted by mutations that cause CMT4J and YVS.

179 ion in the human thymic epithelial cell line was disrupted by mutations in the homogenously staining

180 In contrast, axonal targeting of the VMAT2 was disrupted by neither dominant-negative SEC24C nor do

181 tion, is conserved in human development, and is disrupted by neurodegeneration.

182 ing respiration, posture and locomotion that are disrupted by neurodegenerative diseases such as amyo

183 e normal visual input during development and are disrupted by NMDAR blockade.

184 quire an intact optic nerve, its fine-tuning is disrupted by ONS.

185 Protection in females was disrupted by ovariectomy and restored by short-term

186 the normal asymmetric localization of Vangl2 was disrupted by overexpressing Vangl2 in clusters of ce

187 r Tks5 but decreased when XB130/Tks5 binding was disrupted by overexpression of XB130 N-terminal dele

188 d that this wild-type/pathogenic heterodimer is disrupted by oxidative stress, leading to DJ-1/E163K

189 restore barrier integrity and function that are disrupted by PAO1 and 3O-C12-HSL.

190 ng had major depression or the adoptive home was disrupted by parental death or divorce.

191 anguage disorders, and that this interaction is disrupted by pathogenic mutations affecting either pr

192 resence of the distal coiled-coil domain and was disrupted by pathogenic missense mutations.

193 c pathways in addition to BDNF signaling may be disrupted by Pb(2+) exposure.

194 and ALX/FPR2 receptor-dependent manner that was disrupted by PDP1-specific antibodies.

195 plete picture of how hERG surface expression is disrupted by pentamidine at the cellular and molecula

196 ntrinsically active interface that could not be disrupted by peptides derived from the Nox4 C-terminu

197 yme required for normal lung development can be disrupted by perinatal inflammation in preterm infant

198 more, this match is activity-dependent as it is disrupted by perturbing pyramidal cell activity.

199 genome, representing a unified node that can be disrupted by pharmacologic inhibition.

200 clones and activated ex vivo CD8(+) T cells was disrupted by pharmacological inhibition, knockdown o

201 -1A-5RK/A mutant complex with SUR1 could not be disrupted by PIP2, consequently reducing PIP2 activat

202 The long-range order is disrupted by polycrystalline disorder and the variati

203 (LO) circuits: extracting targets from noise is disrupted by PPC stimulation, in contrast to judging

204 that the efficiency of A(H3N2)v transmission is disrupted by preexisting immunity induced by seasonal

205 he radial symmetry of spherulitic growth can be disrupted by preferentially selecting the molecular o

206 dolescence and furthermore that this process is disrupted by prenatal stress.

207 phology and microstructure at term, and this was disrupted by preterm birth.

208 nnection was very strong at river sites, but was disrupted by processes occurring in rivermouths (the

209 These interactions are disrupted by proteolysis of the CA-SP1 junction duri

210 stablishment of a tolerant B cell repertoire is disrupted by PTPN22-R620W action during immature B ce

211 3 when its nuclear localization signal (NLS) was disrupted by R101S and R105S substitutions.

212 In HCM, this ring was disrupted by reduced FA, consistent with published h

213 omal RNAs and assembly of ribosomal subunits were disrupted by reduced expression of RPL15.

214 lexes, and demonstrate that this association is disrupted by S21 phosphorylation.

215 The SigT-clpPp interaction could be disrupted by secondary metabolites, giving rise to th

216 nt DNA methylation-driven gene silencing can be disrupted by selectively targeting this coiled-coil c

217 that oligomeric forms of defensin, which may be disrupted by serum, contribute to the anti-HIV-1 acti

218 The Sgo1-cohesin binding can be disrupted by SET in a dose-dependent manner in vitro

219 ow that the interaction and SETX sumoylation are disrupted by SETX mutations associated with AOA2 but

220 This novel interaction is disrupted by several cardiomyopathy-linked mutations

221 zed to anterior cell edges and this polarity was disrupted by several Wnt antagonists.

222 etained over the course of evolution and can be disrupted by simple amino acid substitutions.

223 This binding is disrupted by single mutations of non-cysteine amino a

224 TFBS were disrupted by site-directed mutagenesis (SDM) to eva

225 drug discovery, and in a number of cases can be disrupted by small molecules.

226 This process was disrupted by small interfering RNA (siRNA)-based dow

227 h, the normal development of this region may be disrupted by social deprivation.

228 The intramolecular H-bonding is disrupted by solvents that support intermolecular H-b

229 lts suggest that mGluR1a signaling in cancer is disrupted by somatic mutations with multiple downstre

230 ities shift across pregnancy, a process that is disrupted by stress.

231 ween the ACC and the fusiform face area that was disrupted by stress odors under PLC.

232 osure dissociate extremely slowly and cannot be disrupted by strictly competitive inhibitors.

233 ly after training is so unstable that it can be disrupted by subsequent new learning until after pass

234 Gating in these K(+) channels can be disrupted by substitution of residues for the hinge g

235 This association is disrupted by substitution of a conserved arginine (R1

236 g gene, SHANK2, located on Chromosome 11q13, was disrupted by SVs in 14% of MYCN nonamplified high-ri

237 ins conserved despite the fact that it would be disrupted by synonymous mutations, which raises the p

238 acute illnesses where clock gene expression is disrupted by systemic inflammation.

239 ly related members of the DUF579 family have been disrupted by T-DNA insertions contain less xylose i

240 6/Eto2 is a transcriptional corepressor that is disrupted by t(16;21) in acute myeloid leukemia.

241 transmission of B. burgdorferi to humans can be disrupted by targeting 2 key elements in its enzootic

242 ion, and actin and microtubule assembly have been disrupted by targeting integrins.

243 e altered when early and recycling endosomes are disrupted by the expression of dominant-negative mut

244 tinoblastoma (pRb) tumor suppressor pathways are disrupted by the human papilloma virus (HPV) E6 and

245 ut it suggests that interdomain interactions are disrupted by the mutation.

246 re, we demonstrate that this interaction can be disrupted by the addition of an NCL binding aptamer (

247 delocalization in redox-active polymers may be disrupted by the heterogeneity of the environment tha

248 ydrolysis of plasma triglycerides by LPL can be disrupted by the protein angiopoietin-like 4 (ANGPTL4

249 Notably, this functional circuitry can be disrupted by the small-molecule kinase inhibitor pacr

250 This connectivity is increasingly being disrupted by the construction of dams, mining, lan

251 9 Kb downstream of TAL1 and this interaction is disrupted by the -31CBS inversion in T-ALL cells.

252 n haplotype variant however this interaction is disrupted by the A allele of rs3219175.

253 cal polarity complexes at the tight junction is disrupted by the adaptor protein Amot.

254 We previously reported that this association is disrupted by the binding of the second messenger Ap4A

255 This behavior is disrupted by the disconnection of amygdala pathways t

256 ion is conferred by the LRRK2 Roc domain and is disrupted by the familial R1441G mutation and artific

257 c, requires the ZnF-UBP domain of USP22, and is disrupted by the inactivating H363Y mutation within S

258 ere it directly binds KLF11 in a manner that is disrupted by the MODY7 A347S variant.

259 ysosomal positioning, and that this function is disrupted by the most common PD-causing LRRK2 mutatio

260 N terminus of Na(v)1.6, and this interaction is disrupted by the mutation p.VAVP(77-80)AAAA.

261 inely tuned allosteric PKA signaling network is disrupted by the oncogenic J-C subunit, ultimately le

262 y interaction with the ARP2/3 complex, which is disrupted by the phosphorylation of Coro1B.

263 whereas at dusk EMF1 binding to FT chromatin is disrupted by the photoperiod pathway, leading to prop

264 The interaction is disrupted by the pol30-113 mutation that results in a

265 reversed by reassociation with PKAc, and it is disrupted by the presence of AKAP peptides, mutations

266 is the first to show that sodium regulation is disrupted by the presence of citrate-capped Ag NPs, a

267 This finding suggests that BBSome assembly is disrupted by the R632P substitution, providing molecu

268 ory intramolecular interaction within DIAPH1 is disrupted by the sequential binding of RhoA and IQGAP

269 lved xenon in an aqueous liquid crystal that is disrupted by the shear forces of bubbling, and we obs

270 ia Nef's SMR motif and that this interaction is disrupted by the SMRwt peptide.

271 When the IHB is disrupted by the solvent or by substitution of the hy

272 lamellar order present in new packing boxes is disrupted by the weathering process.

273 Phosphorylation of Ser(16) was disrupted by the cardiomyopathy-associated DeltaArg(

274 ffected by the infusion of cycloheximide but was disrupted by the DNA methyltransferase inhibitor, 5-

275 g that surface trafficking of CaValpha2delta was disrupted by the double mutation.

276 ular responses induced when gBcyt regulation was disrupted by the gB[Y881F] substitution.

277 ed on the extent to which normal social life was disrupted by the illness and depended on the age and

278 ly identified site between adjacent subunits was disrupted by the M3 G329I substitution, both propofo

279 The acquired motor learning was disrupted by the optical shrinkage of the potentiate

280 The interactions were disrupted by the Cys694Arg mutation, which resulted

281 y fatty acid synthesis and lipolysis), which were disrupted by the FFD, were found to be modulated by

282 tein reveals that a common molecular process is disrupted by these mutations, implying an active role

283 ving the hypothalamus-pituitary-thyroid axis is disrupted by these stimulating autoantibodies.

284 he enzyme catalytic cycle (SAM regeneration) is disrupted by this single mutation.

285 to motoneurons (MNs) and Renshaw cells (RCs) is disrupted by thoracic spinal cord transection at post

286 globalized economy, production of goods can be disrupted by trade disputes.

287 with VDACs when the function of mitochondria is disrupted by treating cells with the proton uncoupler

288 ontaining PyVmT, p85 (PI3K), and ErbB3, that is disrupted by treatment with lapatinib.

289 A mutant protein in which the NLS motif was disrupted by triple mutation (RRR to AAA) was able t

290 The majority of nascent D-loops are disrupted by two pathways: one supported by the Srs2

291 r flowered, possibly because Tre6P signaling was disrupted by two unidentified disaccharide-monophosp

292 requires U1:pre-mRNA base-pairing, which can be disrupted by U1 antisense oligonucleotide (U1 AMO), t

293 ion experiments, PAR4 formed homodimers that were disrupted by unlabeled PAR4 in a concentration-depe

294 IL-10 and IFN-gamma signaling were disrupted by using blocking antibodies.

295 The effects of Zn(2+) are disrupted by V228L, Y529A, and Y232A.

296 Rb in the DREAM complex and how the complex is disrupted by viral oncoproteins.

297 r genes, including cytokine regulators, that are disrupted by virus integration, and we determined me

298 regimes during early development that could be disrupted by warming.

299 ween the substrate- and product-side ligands are disrupted by water in nonprocessive cellulase clefts

300 The interaction of PACT with RIG-I is disrupted by wild-type VP35, but not by VP35 mutants