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 Saturn's slow seasonal evolution was disrupted in 2010-2011 by the eruption of a bright s

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

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

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 The reeler cortex is disrupted in a more complex fashion, with some region

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

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

15 P-body formation is disrupted in A. nidulans strains deleted for Edc3, an

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

17 Specifically, the threaded loop structure was disrupted in a nonamer containing alternating N-(S)-

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

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

20 at behaviors requiring the perirhinal cortex are disrupted in advanced age, and suggest that at least

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

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

23 n of substrates involved in calcium handling were disrupted in AKAP5 knockout cardiomyocytes.

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

25 ned activities of both of these proteins may be disrupted in ALS and FTD.

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

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

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

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

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 ulin 3/human augmin-like complex, subunit 3, was disrupted in Arabidopsis thaliana, gametogenesis fre

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

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

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

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

37 ird of protein-coding genes are predicted to be disrupted in at least one accession.

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

39 Neural communication is disrupted in autism by unknown mechanisms.

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

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

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

43 Orthologs of these genes were disrupted in B. pseudomallei, and nearly all mutant

44 proteins and polarized intercalary behavior is disrupted in baz mutants.

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

46 Furthermore, the silencing of genes on Xi is disrupted in both Orc2- and HP1alpha-depleted cells.

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

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

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

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

51 Lipid rafts/caveolae were disrupted in C6 cells by either short-term choleste

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

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

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

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

56 Among these, PARD3 is disrupted in cell lines and primary tumors from squam

57 p and its nuclear shape-determining function are disrupted in cells from mouse models of accelerated

58 o the Rab11-positive recycling endosome that is disrupted in cells expressing the Eps15S mutant, lead

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

60 Synchrony is disrupted in cells with increased interspindle distan

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

78 emotional and neurovegetative functions that are disrupted in core features of bipolar disorder.

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

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

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

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

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

84 Sleep continuity is disrupted in different neurological and psychiatric c

85 uggest a mechanism by which this ability may be disrupted in disease.

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

87 Gamma oscillations are disrupted in disorders for which cognitive deficits

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

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

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

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

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

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

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

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

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

97 participating in epistatic interactions that are disrupted in flies with HMS.

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

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

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

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

102 response to the odor used for conditioning, was disrupted in gish mutants.

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

104 ions are maintained in gentle detergents but are disrupted in harsh detergents such as Triton X-100.

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

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

107 ulator of protein homeostasis and longevity, is disrupted in HD.

108 tion of proteins that regulate contractility are disrupted in heart failure.

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

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

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

112 3-kinase (PI3K)/AKT signalling cascade that are disrupted in human overgrowth conditions.

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

114 Development of both structures is disrupted in human chromosomal microdeletion of 22q11

115 anistic studies revealed that Spry2 function is disrupted in human HCC via multiple mechanisms at bot

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

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

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

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

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

121 lleles that are functional within one genome are disrupted in hybrid genomes.

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

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

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

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

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

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

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

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

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

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

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

133 Interestingly, many of the identified genes were disrupted in LVS and SchuS4 but not in their corres

134 ugh the lymphoid architecture of milky spots was disrupted in lymphotoxin-deficient mice, normal arch

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

136 enes after ET exposure was observed when APC was disrupted in macrophages using siRNA or in bone marr

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

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

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

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

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

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

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

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

145 cadian regulation of C/EBPbeta and autophagy is disrupted in mice lacking a functional liver clock.

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

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

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

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

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

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

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

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

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

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

156 tnatal growth of collagen fibrils in tendons was disrupted in Mkx(-/-) mice.

157 These properties are disrupted in models of Parkinsonism.

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

159 Furthermore, myelination was disrupted in motor nerves of zebrafish lacking alpha

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

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

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

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

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

165 m-like cells surrounding chondrocyte nodules is disrupted in mutant micromass cultures.

166 ephalic sensory neurons, cilium architecture is disrupted in mutants lacking specific ciliary tubulin

167 plasticity in response to visual deprivation is disrupted in mutants.

168 ion of col10a1, indian hedgehog, and patched was disrupted in mutants, reflecting improper chondrocyt

169 ironment that is dependent on myosin-XVa and is disrupted in Myo15(sh2/sh2) inner hair cells, but not

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

171 parallel axon fibers and neuronal migration is disrupted in Nav2 mutants.

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

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

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

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

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

177 lear, catecholamine signalling is thought to be disrupted in obesity, leading to the development of i

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

179 transgenic mice in which microRNA processing was disrupted in OL precursor cells (OPCs) and OLs by ta

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

181 Such functions may be disrupted in oxidative stress seen in a variety of ca

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

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

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

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

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

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

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

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

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

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

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

193 However, these interactions were disrupted in pol30 mutants with defects linked to A

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

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

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

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

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

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

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

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

204 Chemotaxis to volatile odorants was disrupted in RGEF-1b-deficient (rgef-1(-)/(-)) anima

205 ed genes belonging to the same pathways that are disrupted in RNA profiles of DBA patient cells.

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

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

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

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

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

211 ror, or reversing decisions, mechanisms that are disrupted in schizophrenia.

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

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

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

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

216 iring is crucial for cortical processing and is disrupted in schizophrenia.

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

218 One such gene is disrupted-in-schizophrenia 1 (DISC1).

219 These functions may be disrupted in several diseases, and for most of them t

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

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

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

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

226 EM) showed that the myofilament architecture was disrupted in skeletal muscle of Clock(Delta19), Bmal

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

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

229 ta-activated kinase 1 (TAK1)/ATF-2 signaling was disrupted in Smad3(-/-) mouse chondrocytes at the le

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

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

232 ntial for sperm head and flagellar formation was disrupted in spermatids of MEIG1-deficient mice.

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

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

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

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

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

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

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

240 gnaling component localization to the cilium are disrupted in the absence of Arl13b.

241 it is possible that 11-cis-retinol supplies are disrupted in the absence of IRBP.

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

243 Both angiogenesis and vasculogenesis are disrupted in the hyperoxia-induced vaso-obliteration

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

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

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

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

248 oli, rpoE is an essential gene that can only be disrupted in the presence of additional suppressor mu

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

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

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

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

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

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

255 nce have suggested that the GABAergic system is disrupted in the brains of individuals with autism an

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

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

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

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

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

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

262 eta consensus sequence surrounding LKB1 S307 is disrupted in the LKB1 SL26 mutant, thus providing a l

263 Fragile X mental retardation protein (FMRP) is disrupted in the most common inherited form of cognit

264 monstrated that the myoepithelial cell layer is disrupted in the p190A deficient glands, which may re

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

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

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

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

269 One of the mutants isolated was disrupted in the 3' untranslated region (3'UTR) of a

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

271 y the precursor of cysteine, O-acetylserine, was disrupted in the hy5 mutant.

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

273 o increased proliferation and survival, Pten was disrupted in the KrasG12D mutant mice.

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

275 Fiber cell differentiation was disrupted in the PDGF-A and DN-Spry2 lenses, whereas

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

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

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

279 ich is involved in the salt stress response, was disrupted in the tno1 mutant.

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

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

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

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

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

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

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

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

288 required for normal lip formation and fusion is disrupted in these mutants.

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

290 otubule polymerization and cortical rotation are disrupted in trim36-depleted embryos, in a manner de

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

292 larger than 500 kDa, the formation of which is disrupted in two mutant alleles, indicative of the bi

293 AV channels are disrupted in type 2 diabetes, even before the onset

294 The p53 pathway is disrupted in virtually every human tumor.

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

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

297 The E2 gene was significantly more likely to be disrupted in women who tested positive for HPV18 in t

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.