ライフサイエンスコーパス: be disrupted in

1 Tolerance is disrupted in 2-12H/MRL/lpr mice where IL-6 and sCD40L

2 Sdhc was disrupted in 2 different strains of mice via cre rec

3 aphy and in 45 eyes (83%) on FA; this arcade was disrupted in 48 eyes (92%) and 39 eyes (72%) on OCT

4 Genes of interest were disrupted in 5 to 15% of preselected clones ( appro

5 vides the first evidence that these networks are disrupted in a dissociable fashion with regard to th

6 mph nodes and the subsequent T-cell response are disrupted in a mouse we recently described lacking t

7 AQP2 was also shown to be disrupted in a laboratory-selected MPXR strain.

8 CTCF binding to CTCF clusters in HSV-1 would be disrupted in a reactivation event.

9 oxin, Cyclosporine A, the epithelial barrier is disrupted in a dose-dependent manner.

10 The most extreme mutant is disrupted in a hydroxyproline O-arabinosyltransferase

11 We show that WRM-1 cortical release is disrupted in a hypomorphic cyclin-dependent protein k

12 after injury is vital to human survival and is disrupted in a spectrum of disorders.

13 Cerebellar function is disrupted in a variety of psychiatric disorders, incl

14 fundamental cellular/molecular process that is disrupted in a variety of psychiatric, neurological,

15 ptic strength, even when Na(V)1.2 expression was disrupted in a cell-autonomous fashion late in devel

16 The threshold maximum BRET signal was disrupted in a concentration-dependent manner by unl

17 ortantly, the midcell localization of YFP-p1 was disrupted in a strain that does not express FtsZ, an

18 The frequency and temporal structure of SWRs was disrupted in a transgenic mouse model of tauopathy (

19 NPC structure and function are disrupted in aged nondividing metazoan cells, althou

20 rhythmicity of oxygen consumption rate (Vo2) was disrupted in aged obese CT-1-deficient (CT-1(-/-)) m

21 at is normally maintained through autophagy, is disrupted in alcoholic liver disease (ALD).

22 The U2 snRNP-intron interaction is disrupted in all complexes by Prp43_Ntr1GP, and in th

23 performing a critical cellular function that is disrupted in ALS.

24 It is believed that the BBB is disrupted in Alzheimer's disease (AD), potentially in

25 e removal of amyloid beta from the brain and is disrupted in Alzheimer's disease and aging.

26 r membranes and its subcellular localization is disrupted in Alzheimer's disease, but many of its bio

27 food intake and that this neural circuit may be disrupted in an anorexic-like condition.

28 ic metabolism in the acr2 hac1 double mutant is disrupted in an identical manner to that described fo

29 the individual's response to threat and may be disrupted in anxiety and post-trauma psychopathology.

30 The tumor suppressor NF2 is disrupted in approximately half of all meningiomas, b

31 pk mutant line, aimless, myosin polarization is disrupted in approximately one third of the cells, in

32 tolic SR [Ca(2+)] are influenced by CSQ2 and are disrupted in arrhythmic conditions.

33 put before sensory feedback can be processed are disrupted in ASD.

34 rm that visual-motor functional connectivity is disrupted in ASD.

35 (LS), contributes to social behavior, which is disrupted in ASD.

36 integration of social contextual information are disrupted in association with atrophy in key fronto-

37 al retardation protein (FMRP), some of which are disrupted in autism, as well as in many known autism

38 ral circuits involved with social processing are disrupted in autism, but to date no neuroimaging stu

39 er for inundating sensory information, which is disrupted in autism, schizophrenia, and other psychia

40 earning and represents a sensory filter that is disrupted in autism, schizophrenia, and several other

41 This miR-19:miR-92 antagonism is disrupted in B-lymphoma cells that favor a greater in

42 showed that the development of this circuit is disrupted in BDNF Met carriers due to insufficient BD

43 tennae, while rhythmic clock gene expression is disrupted in black-painted antennae.

44 ystrophy was fully developed only when ClC-2 was disrupted in both astrocytes and oligodendrocytes.

45 This effect was disrupted in both valproic acid-exposed and Fmr1 kno

46 ich one, two, or all three of these pathways were disrupted in both pure line and hybrid contexts.

47 a large-scale network of emotion processing is disrupted in BPD.

48 hesized by TK2 over medium TMP and that this is disrupted in broken mitochondria.

49 3) and ring finger protein 43 (RNF43), which are disrupted in cancer.

50 atic balance to control normal growth, which is disrupted in cancer cells.

51 Many selective pressures are disrupted in captivity, including social behavioral

52 CICR is disrupted in cardiac hypertrophy and heart failure, w

53 architecture of CCM2 and how the CCM complex is disrupted in CCM disease.

54 st and viral chromatin is highly dynamic and is disrupted in cells undergoing an extensive lytic reac

55 Synchrony is disrupted in cells with increased interspindle distan

56 Polar localization of TnaA, GroES and YqjD was disrupted in cells lacking the MinCDE proteins, sugg

57 ncoupling protein 3 (UCP3), but this complex was disrupted in cells treated with DOX.

58 rom CFTR to Ezrin to PI3K/AKT signaling that is disrupted in CF, and thus promotes hyper-inflammation

59 live imaging we found that KV morphogenesis is disrupted in cftr mutants.

60 r findings show that high-gamma oscillations are disrupted in children after treatment for a brain tu

61 Evidence is accumulating that this program is disrupted in children with severe acute malnutrition

62 aberrantly down-regulated and BA homeostasis is disrupted in cholestatic mice, but the underlying mec

63 indicates that frontal-striatal connectivity is disrupted in chronic cocaine users in a baseline (res

64 or proper ciliary function, and this process is disrupted in ciliopathies.

65 ogether, renal FGF23-Klotho signaling, which is disrupted in CKD, is essential for homeostatic contro

66 transcription, splicing, and nuclear export are disrupted in clbn, either through intron retention o

67 Oscillation of p75(NTR) is disrupted in Clock-deficient and mutant mice, is E-bo

68 fected by addition of one water molecule but are disrupted in clusters with one less water molecule.

69 e ezrin phosphomimetic Y353E or Y145 mutants were disrupted in colonic Caco-2 cells, similar to ezrin

70 When either RIP3 or Casp8 is disrupted in combination with RIP1, the resulting dou

71 ith their biological functions and how these are disrupted in common visual disorders.

72 rcuitry during postnatal development and may be disrupted in conditions that cause intellectual disab

73 thermore, we demonstrate that this mechanism is disrupted in congenital muscular dystrophy patient my

74 IGF-1 rhythms are disrupted in Cry-deficient mice, and IGF-1 level is

75 which hippocampal information processing may be disrupted in dementia, which may provide targets for

76 intain emotional equilibrium, a process that is disrupted in depression.

77 a is a highly choreographed process that can be disrupted in developing neurons by overexpressing neu

78 e that subserves critical functions that can be disrupted in developmental and degenerative disorders

79 intenance of immune tolerance, and this role is disrupted in diabetes-prone NOD mice.

80 splicing modulates myriad cell functions and is disrupted in disease.

81 ilable data suggest that this phenomenon may be disrupted in diseases where cytoplasmic calcium ion l

82 Gamma oscillations are disrupted in disorders for which cognitive deficits

83 ster regulators of oxygen homeostasis, which is disrupted in disorders affecting the circulatory syst

84 doplasmic reticulum (ER) calcium homeostasis is disrupted in diverse pathologies, including neurodege

85 However A/B polarity, which is disrupted in Drosophila Scrib mutants, is largely una

86 persists under constant light conditions and is disrupted in dysfunctional clock mutants, demonstrati

87 activation in response to motion perception is disrupted in DYT1 dystonia.

88 regulating gene expression in the liver that is disrupted in early metabolic liver disease and may co

89 ng to the tip of HGF-induced cell extensions is disrupted in EB1-depleted cells.

90 al residues, and this membrane sequestration is disrupted in EHEC that expresses constitutively activ

91 scovered that this mechanically quiet period is disrupted in embryos with high levels of dNTPs, which

92 Both actin and tubulin cytoskeletons were disrupted in Erg-deficient ECs, with a dramatic inc

93 The Atad3-Tufm complex is disrupted in Fancd2-/- mice and those deficient for t

94 on microscopy reveals that cell organisation is disrupted in Fat4 mutants.

95 n and R current in hippocampal neurons which is disrupted in FMRP KO mice.

96 inhibitor balance regulating cusp patterning was disrupted in Foxi3 cKO.

97 Parental nucleosomes are disrupted in front of the replication fork.

98 Neurogenesis was disrupted in Gabrd(-/-) mice as the migration, matur

99 aberrantly activated and stem cell functions are disrupted in gastric cancer and other disorders.

100 between received and expected reinforcement) is disrupted in generalized anxiety disorder.

101 These are disrupted in Gli-deficient embryos.

102 e an interaction with the spacer domain that is disrupted in GoF ADAMTS13.

103 tudies have shown that bile acid homeostasis is disrupted in HCC patients with elevated serum bile ac

104 We discovered that this surveillance pathway is disrupted in HCV-infected cells, causing potentially

105 molecule glycosylphosphatidylinositol (GPI) is disrupted in hematopoietic stem and progenitor cells

106 ake, a result that is not seen when the gene is disrupted in hepatocytes or pancreatic islets.

107 Glycolysis and lactate production were disrupted in HSCs to determine if metabolism influe

108 on, tissue development, and homeostasis, and are disrupted in human cancers.

109 3-kinase (PI3K)/AKT signalling cascade that are disrupted in human overgrowth conditions.

110 nd evidence suggests that CREB signaling may be disrupted in human AD brains as well.

111 tudy, we provide evidence that HA catabolism is disrupted in human intestinal microvascular endotheli

112 of the core clock transcription factor BMAL1 is disrupted in human OA cartilage and in aged mouse car

113 demonstrate that the EphB1-ephrin-B1 pathway is disrupted in human stem cell derived astrocyte and mo

114 Diurnal triglyceride patterns were disrupted in human placentas from pregnancies with

115 control as well as other cellular processes, is disrupted in Huntington's disease (HD).

116 wed the nuclear/cytoplasmic Ran distribution is disrupted in Hutchinson-Gilford Progeria syndrome (HG

117 FT25 (HSPB11), the binding partner of IFT27, was disrupted in Ift27 mutant cells, and Ift25-null mice

118 It remains unclear whether BBB is disrupted in INCL and if so, what might be the molecu

119 hat the normal processes of brain maturation are disrupted in individuals whose mothers drank heavily

120 Corticotropin releasing hormone (CRH) is disrupted in individuals with PTSD and early-life str

121 ion of SARS-CoV-2 antigen-specific responses was disrupted in individuals >= 65 years old.

122 y are normally correlated, this relationship is disrupted in infants with high levels of physiologica

123 transamidating activity and O-GlcNAcylation is disrupted in infected cells because host hexosamine b

124 ring monomer observed in the absence of drug are disrupted in its presence.

125 the regulation of the SCFA-MCT1-HMGCS2 axis is disrupted in K8(-/-) colonocytes, suggesting a role f

126 s in maintaining APP regulation of Fe, which is disrupted in late stages of AD.

127 mation of translation-competent 60S subunits is disrupted in leukaemia-associated ribosomopathies.

128 in cholesterol and lipid metabolism in liver were disrupted in LIRKO mice.

129 crossed with AhCre mice; in offspring, Axin1 was disrupted in liver following injection of beta-napht

130 milar response was observed when HS function was disrupted in long bone anlagen explants by genetic,

131 roresolving signaling and metabolic pathways are disrupted in lung tissue from patients with chronic

132 nd DTI measures reported in healthy controls were disrupted in MA and MAP groups; these involved area

133 ting data indicate that the glutamate system is disrupted in major depressive disorder (MDD), and rec

134 First, we found that neurogenesis was disrupted in male and female mice chronically defici

135 luation, and effort-related processes, which are disrupted in many mental and emotional disorders.

136 Eye movements are disrupted in many neurodegenerative diseases and are

137 , and sleep-wake homeostasis, behaviors that are disrupted in many psychiatric disorders such as atte

138 n important role in defining cell types, and is disrupted in many diseases.

139 mic reticulum (ER) and the secretory pathway is disrupted in many protein misfolding disorders.

140 While proton-pumping activity was disrupted in many of the spectrally shifted variants

141 ing risk-taking decisions-a process shown to be disrupted in MD-is able to predict susceptibility for

142 DNA-bending proteins; one conserved AT-hook is disrupted in MeCP2-R270X, lending further support to

143 yed in adult mice, and that this correlation was disrupted in MIA offspring.

144 The expression of most of these genes is disrupted in mice lacking CTIP2, and these alteration

145 However, S1-SC topography is disrupted in mice lacking ephrin-As, which we find ar

146 locus shows circadian oscillations, but this is disrupted in mice with bronchiole-specific ablation o

147 lation calcium activity of dorsomedial iMSNs was disrupted in mice lacking D2Rs on iMSNs, suggesting

148 chemical chaperone 4-phenylbutyric acid, but was disrupted in mice lacking the transcription factor N

149 OPC migration in vivo was disrupted in mice with defective vascular architectu

150 Muc1 and RAG1 were disrupted in mice (Muc/RAG double knockout mice); T

151 When Abcb1 and Abcg2 were disrupted in mice, brain uptake of (11)C-erlotinib

152 Pacemaker firing regularity was disrupted in MitoPark mice and ion channel conductan

153 activation of Gwl, its association with PP1 is disrupted in mitotic cells and egg extracts.

154 rms a functional complex with filamin A that is disrupted in MKS and causes defects in neuronal migra

155 These properties are disrupted in models of Parkinsonism.

156 its strong presence in the axonal shaft, MPS is disrupted in most presynaptic boutons but is present

157 Gap junction coupling is known to be disrupted in mouse models of pre-diabetes.

158 Thalamic RSN is disrupted in MS, and decreased performance in cogniti

159 y, mitochondria and myelin form a triad that is disrupted in MS.

160 Mobilization of Cu out of senescing leaves was disrupted in MT-deficient plants.

161 ronal encoding and information transfer, and are disrupted in multiple brain disorders.

162 These behaviors are disrupted in multiple human neurodevelopmental and n

163 e-6-phosphate receptors (CI-MPR) in the soma is disrupted in mutant hAPP neurons, causing defects in

164 ession studies showed that chromatin binding was disrupted in mutant compared with wild-type IKZF5, a

165 Phospholipid and bile acid metabolism is disrupted in NASH, likely due to enhanced hepatic inf

166 r characterizing brain networks and how they are disrupted in neural disorders.

167 Neuronal activity patterns are disrupted in neurodegenerative disorders, including

168 nal cortex (EC) is one of the first areas to be disrupted in neurodegenerative diseases such as Alzhe

169 cortical critical period, features that may be disrupted in neurodevelopmental disorders.

170 ity and critical periods, is hypothesized to be disrupted in neurodevelopmental disorders.

171 diate muscle development, how these pathways are disrupted in neuromuscular disorders, and advances i

172 epresentations to guide appropriate behavior is disrupted in neuropsychiatric and neurological disord

173 wn that communication between cortical areas is disrupted in non-REM sleep and anesthesia.

174 An Sw-5b SD mutant that is disrupted in NSm recognition failed to enhance the ab

175 anisms play a role and that these mechanisms are disrupted in obesity.

176 nk between inflammation and autophagy, which is disrupted in obesity and diabetes.

177 ed in controls, but this correlation pattern was disrupted in OPMD.

178 The Prkd1 gene was disrupted in Panc1 cells using CRISPR-Cas9 or knocke

179 Secretory autophagy was disrupted in Paneth cells of mice harboring a mutati

180 This balance is disrupted in Parkinson's disease and in l-3,4-dihydro

181 originates from the brainstem raphe nuclei, is disrupted in Parkinson's disease.

182 s, the nuclear clustering of CP190 complexes is disrupted in Parp mutant cells.

183 key roles in many cognitive functions and to be disrupted in pathological conditions, such as schizop

184 apically with the actomyosin network, which was disrupted in patient cells, causing impaired nucleok

185 es both frontal and cerebellar networks that are disrupted in patients with schizophrenia.

186 lving mechanisms for lung responses that can be disrupted in patients with disease.

187 The maintenance of normal body weight is disrupted in patients with anorexia nervosa (AN) for

188 en the hypothalamus and the subgenual cortex is disrupted in patients with major depression with psyc

189 Multisensory integration is disrupted in patients with schizophrenia, but little

190 Kamin blocking is disrupted in people with schizophrenia, their relativ

191 Our results suggest transcription is disrupted in peripheral cells in HD through mechanism

192 second heart field-derived progenitor cells were disrupted in Pitx2 mutants.

193 on, during which positional identities could be disrupted in pola2 mutants, leading to regeneration o

194 Here, we report that the BBB is disrupted in Ppt1-KO mice and that T(H)17 lymphocytes

195 We sought to determine: (i) whether the BBB is disrupted in Ppt1-KO mice, (ii) if so, do T(H)17-lymp

196 nt of their proteome and how these processes are disrupted in pre-malignant and malignant states.

197 their regulation of Schwann cell development is disrupted in primary human schwannoma cells.

198 ive plasticity in stable MS patients, and it is disrupted in progressing MS patients.

199 Neural innervation to the outer HCs is disrupted in Prox1DTA mice and auditory brainstem res

200 Specific nodes of this tripartite network are disrupted in psychiatric diseases, divorcing areas t

201 memory in rhinal cortices, in processes that are disrupted in psychiatric diseases.

202 tive functions and emotional regulation that are disrupted in psychiatric disorders.

203 he view that cortical information processing is disrupted in psychosis and provides new evidence that

204 y of dorsal corticostriatal circuitry, which is disrupted in psychosis patients and individuals at hi

205 P-binding site and adenylate kinase activity were disrupted in Q1291F CFTR.

206 cortical entrainment of STN neural activity is disrupted in R6/2 mice and may be one of the mechanis

207 l immunoreactivity in the hippocampus, which was disrupted in Rev-erbalpha(-/-) mice.

208 olic calcium ([Ca(2)(+)](cyt) ) oscillations were disrupted in root hairs of agd1.

209 frame (ORF) encoding the KSHV ORFK15 homolog was disrupted in RRV26-95.

210 Elastin organization was disrupted in saccular stage lungs of preterm infants

211 gamma (30-80 Hz) and theta (4-7 Hz) ranges, are disrupted in schizophrenia and are involved in vario

212 receptors and the dopaminergic pathways that are disrupted in schizophrenia and the histologic eviden

213 cortex and its regulation by afferent inputs are disrupted in schizophrenia.

214 and they characterize neural events that may be disrupted in schizophrenia.

215 auditory function and are often reported to be disrupted in schizophrenia.

216 central executive and default mode networks is disrupted in schizophrenia and associated with cognit

217 at function and connectivity of the striatum is disrupted in schizophrenia(1-5).

218 ociated with glutamatergic neurotransmission is disrupted in schizophrenia, but it was unknown if the

219 d that predictive coding during vocalization is disrupted in schizophrenia.

220 excitation and inhibition (EI) is thought to be disrupted in several neuropsychiatric conditions, yet

221 clear envelope transmembrane proteins (NETs) is disrupted in several human diseases.

222 try of solutes from blood into the brain and is disrupted in several neurological diseases.

223 nt is essential in a dynamic environment and is disrupted in several neuropsychiatric disorders.

224 tium shapes chemical signaling processes and is disrupted in several pathologies.

225 computations underlying cognition and might be disrupted in severe neuropsychiatric illnesses such a

226 on that the global pattern of nest predation is disrupted in shorebirds.

227 FB neurons, but this homeostatic adjustment is disrupted in short-sleeping cv-c mutants.

228 ing in murine models of cancer cachexia that is disrupted in skeletal muscle of patients with cancer

229 We hypothesized that astrocyte functions are disrupted in SMA, exacerbating disease progression.

230 ation of axo-glial interactions at paranodes was disrupted in SMA mice.

231 leus pacemaker, daily TSH secretion profiles are disrupted in some patients with hypothyroidism and h

232 also present evidence that this process may be disrupted in some cases of Weaver syndrome.

233 differences in dopamine (DA) function, which is disrupted in some forms of psychopathology.

234 ial for efficient and proper myelination and is disrupted in some types of congenital muscular dystro

235 ic growth and the sucrose-Tre6P relationship were disrupted in some complementation lines.

236 ssion programs during normal development and are disrupted in specific disease states, particularly i

237 pathogenic familial ALS genetic variants and were disrupted in sporadic ALS spMNs.

238 anule neurons, a pathway previously shown to be disrupted in Src(-/-) mice.

239 between 5-HT2CR editing and gene expression is disrupted in suicide victims.

240 To test the pore model, these linkages were disrupted in SULT2A1 via mutagenesis, and the effec

241 uggest that ACC glutamate control mechanisms are disrupted in T1D, which affects glutamatergic neurot

242 This regulation was disrupted in T2D subjects, implying a role for the i

243 Although both GLI2 and GLI3 processing were disrupted in talpid(2) mutants, only GLI3 activator

244 We confirmed that primary cilia were disrupted in talpid(2) mutants.

245 memory is a crucial cognitive function that is disrupted in temporal lobe epilepsy.

246 ophages form contacts with each other, which are disrupted in the absence of microbiome, monocyte rec

247 Because these dynamics are disrupted in the early stages of type 2 diabetes, dy

248 Adherens junctions between RGCs are disrupted in the mutants, progenitor cells are widel

249 ur normally in one-half of the AAA ring, but are disrupted in the other half.

250 don progenitors and cells, only long tendons are disrupted in the Scx (-/-) mutant; short tendons app

251 the robust circadian clock in N. crassa can be disrupted in the dark when maintained in a consistent

252 The mutant was found to be disrupted in the P4-ATPase AMINOPHOSPHOLIPID ATPASE 3

253 results indicate that the cpTAT pathway may be disrupted in the plsp1-null mutant, and that there ar

254 robe-graphene oxide sensor elements that can be disrupted in the presence of breast cells to give flu

255 ergoes movement, codon-anticodon interaction is disrupted in the absence of EF-G, resulting in slippa

256 aper, forms a dense-core-like structure that is disrupted in the absence of Fam65b.

257 experience with histone acetylation dynamics is disrupted in the aged hippocampus.

258 ependent, and we report that this plasticity is disrupted in the aged hippocampus.

259 ent active site cleft present in PCD enzymes is disrupted in the alpha-carboxysome PCD-like protein.

260 sease aetiology is Zn(2+) homeostasis, which is disrupted in the brains of Alzheimer's disease suffer

261 ortholog is bound to introns whose splicing is disrupted in the cfm1 mutant.

262 the OSR1/SPAK/M025alpha signaling apparatus is disrupted in the DCT.

263 lation of genes for iron-containing proteins is disrupted in the DeltaprrF1-prrF2 mutant during infec

264 RBX1-CUL1-containing SCF(FBW7) complex, and is disrupted in the disease Glomuvenous Malformation.

265 known about the extent to which methylation is disrupted in the earliest stages of CRC development.

266 restores a JNK-docking site within MKK7 that is disrupted in the larger isoform.

267 lular variability in wild-type sepals, which is disrupted in the less-variable cells of ftsh4 mutants

268 This intercortical communication is disrupted in the neural networks of patients with foc

269 K14-Cre mice, and WNT-beta-catenin signaling is disrupted in the palatal mesenchyme.

270 en surface-adsorbed CO and interfacial water is disrupted in the presence of the two larger cations.

271 nt to the ATP site in the propeller form and is disrupted in the quatrefoil form.

272 nt on tectorin alpha (tecta) function, which is disrupted in the rolling stones (rst) mutant.

273 ha helix containing the ATM recognition site is disrupted in the serine isoform of RASSF1A (RASSF1A-p

274 buffer, and the normal localization of Nhe1 was disrupted in the htt(-) mutant.

275 angiotensin-II receptor, type 1, with Cav-3 was disrupted in the hypertrophic ventricular myocytes.

276 n indicated that odontoblast differentiation was disrupted in the mutant mice likely contributing to

277 findings indicated that BDNF/TrkB signalling was disrupted in the OC of Nhe6 KO mice, probably due to

278 TgPI1 function, the endogenous genomic locus was disrupted in the RH strain background.

279 Residual B cell subtype distribution was disrupted in the spleen, but adoptive transfer studi

280 The RANKL/OPG ratio was disrupted in the synovial fluid of RRV patients, and

281 When SynAas was disrupted in the tocopherol-deficient, alpha-linolen

282 d ErbB2 receptor expression after PNS injury were disrupted in the absence of alphaBC.

283 tion [vegetative incompatibility (vic)] loci were disrupted in the chestnut blight fungus Cryphonectr

284 Several clock genes were disrupted in the early stages of cartilage degenera

285 cluding the splicing of small introns, which were disrupted in the mutant cerebellum.

286 or eliminated, suggesting that gap junctions were disrupted in the Netrin mutants.

287 infected with herpes simplex virus 2 (HSV-2) are disrupted in their ability to form stress granules (

288 er immune defects, natural killer (NK) cells are disrupted in these mice, permitting efficient engraf

289 olae, and that the caveolae structure should be disrupted in these vessels.

290 The TRIF gene was disrupted in these lines by CRISPR/Cas9, before reco

291 the oriented movements of these progenitors are disrupted in this context.

292 y compromised when the SA, JA, or ET pathway was disrupted in this mutant.

293 known transcriptional pair in healthy cells, was disrupted in tumors.

294 d and spatially restricted branching process is disrupted in turnout mutants we identified in a forwa

295 This interaction is disrupted in vitro and in vivo by structure-based, lo

296 dshake" that conjoins the four molecules can be disrupted in vivo by intense stimulation and in vitro

297 when active transport, NBCe1, or CA activity was disrupted in vivo, corneal edema ensued and was asso

298 r by other factors, candidate repair factors were disrupted in XLF- or XRCC4-deficient cells.

299 yte specification, migration and myelination are disrupted in znf16l mutants.

300 eability and the localization of TJ proteins are disrupted in ZO-1/-2-depleted cells.