ライフサイエンスコーパス: basolateral

1 owever, modelling showed that a reduction in basolateral AE2 activity by approximately 80% was essent

2 PEA (basolateral) also reversed increased permeability when a

3 ortex (mPFC), ventral hippocampus (vHIP) and basolateral amygdala (AMY).

4 The basolateral amygdala (BL) is involved in fear and anxiet

5 We recorded basolateral amygdala (BL) neurons in a seminaturalistic

6 valbumin-expressing (PV) interneurons in the basolateral amygdala (BLA) a dedicated role in the selec

7 he dorsomedial prefrontal cortex (dmPFC) and basolateral amygdala (BLA) and altered synaptic transmis

8 ing the intrinsic functional connectivity of basolateral amygdala (BLA) and centromedial amygdala (CM

9 aversive unconditioned stimuli (USs) in the basolateral amygdala (BLA) and have examined their role

10 that NgR1 expression is required in both the basolateral amygdala (BLA) and infralimbic (IL) cortex t

11 The effects of inactivation of the basolateral amygdala (BLA) and ketamine administration o

12 ation of specific brain regions, such as the basolateral amygdala (BLA) and nucleus accumbens (NAc),

13 , we investigate causal contributions of the basolateral amygdala (BLA) and orbitofrontal cortex (OFC

14 ered activity in brain systems including the basolateral amygdala (BLA) and orbitofrontal cortex (OFC

15 The basolateral amygdala (BLA) and orbitofrontal cortex (OFC

16 gion of the dorsal hippocampus (CA1) and the basolateral amygdala (BLA) and that of dopaminergic, nor

17 in the higher-order auditory cortex Te2 and basolateral amygdala (BLA) and their crosstalk during th

18 The neuronal circuits of the basolateral amygdala (BLA) are crucial for acquisition,

19 (vHPC), medial prefrontal cortex (mPFC), and basolateral amygdala (BLA) are each required for the exp

20 eir synaptic connections with neurons in the basolateral amygdala (BLA) at neonatal to adult developm

21 The basolateral amygdala (BLA) contributes to emotion-relate

22 Given the basolateral amygdala (BLA) contributes to these behavior

23 a dampening of neuronal excitability in the basolateral amygdala (BLA) ex vivo and in vivo, and were

24 We provide a cellular mechanism in the basolateral amygdala (BLA) for the rapid stress regulati

25 By contrast, inhibitory Gi-DREADDs in the basolateral amygdala (BLA) impaired the acquisition of b

26 udies implicate cholinergic signaling in the basolateral amygdala (BLA) in behaviors related to stres

27 n between the roles of the central (CeA) and basolateral amygdala (BLA) in regulating social behavior

28 The basolateral amygdala (BLA) integrates sensory input from

29 The prefrontal cortex (PFC) and basolateral amygdala (BLA) interact to control emotional

30 Previous work showed that the basolateral amygdala (BLA) is a critical substrate for d

31 s of E2 signaling.SIGNIFICANCE STATEMENT The basolateral amygdala (BLA) is a key structure of the fea

32 The basolateral amygdala (BLA) is a site of convergence of n

33 The basolateral amygdala (BLA) is critical for encoding the

34 Basolateral amygdala (BLA) is critical for fear learning

35 dator) induces long-lasting sensitization of basolateral amygdala (BLA) noradrenergic (NE) receptors

36 either central nucleus of amygdala (CeA) or basolateral amygdala (BLA) of female rats with one parti

37 by specifically overexpressing FKBP51 in the basolateral amygdala (BLA) or central amygdala resulted

38 divergent downstream structures such as the basolateral amygdala (BLA) or nucleus accumbens (NAc).

39 memory but was ineffective when given in the basolateral amygdala (BLA) or the ventral medial prefron

40 ow that neuropeptide-receptor systems in the basolateral amygdala (BLA) play an important role in the

41 The basolateral amygdala (BLA) plays a central role in such

42 Basolateral amygdala (BLA) principal cells are capable o

43 The lateral orbitofrontal cortex (lOFC) and basolateral amygdala (BLA) promote cocaine-seeking behav

44 as negatively related to both aggression and basolateral amygdala (BLA) reactivity to angry faces, wh

45 The basolateral amygdala (BLA) receives input from subcortic

46 ions between the prefrontal cortex (PFC) and basolateral amygdala (BLA) regulate emotional behaviors.

47 Western blot analysis of the basolateral amygdala (BLA) revealed an increase in the G

48 The basolateral amygdala (BLA) sends excitatory projections

49 f the medial prefrontal cortex (mPFC) or the basolateral amygdala (BLA) to examine the effects of bet

50 AMPAR)-silent excitatory synapses within the basolateral amygdala (BLA) to nucleus accumbens (NAc) pr

51 t involve activation of projections from the basolateral amygdala (BLA) to the medial prefrontal cort

52 cannabinoid 1 receptor (Cnr1) and CCK in the basolateral amygdala (BLA), a brain region critical for

53 the BLA evokes norepinephrine release in the basolateral amygdala (BLA), alters BLA neuronal activity

54 ginate from medial prefrontal cortex (mPFC), basolateral amygdala (BLA), and ventral subiculum of the

55 ommunication between the hippocampus and the basolateral amygdala (BLA), but the mechanisms of this p

56 Within the basolateral amygdala (BLA), LAC did not reduce, but slig

57 excitatory input from pyramidal cells of the basolateral amygdala (BLA), neurons that are activated b

58 ue-guided alcohol seeking is mediated by the basolateral amygdala (BLA), nucleus accumbens (NAc), and

59 omous receptor of neuregulin 1 (NRG1) in the basolateral amygdala (BLA), was expressed in GABAergic n

60 we visualized robust c-fos expression in the basolateral amygdala (BLA), which was reduced in mice pr

61 ronal activity in one key limbic region, the basolateral amygdala (BLA), whose activity fluctuates ac

62 Here, we identify a basolateral amygdala (BLA)-ventral striatum (NAc) pathwa

63 apid mobilization of endocannabinoids in the basolateral amygdala (BLA).

64 he nucleus (DRN) neurons that project to the basolateral amygdala (BLA).

65 ntext and require glutamate signaling in the basolateral amygdala (BLA).

66 educed fear-evoked theta oscillations in the basolateral amygdala (BLA).

67 endent electrophysiological responses in the basolateral amygdala (BLA).

68 e, selectively control PCs projecting to the basolateral amygdala (BLAPC) compared to those projectin

69 norepinephrine (NE) administration into the basolateral amygdala after training on an inhibitory avo

70 In addition, basolateral amygdala AMPA, but not NMDA glutamate recept

71 As in other species, the OFC projects to the basolateral amygdala and dorsal striatum in mice.

72 et, PTEN, colocalized with miR-144-3p in the basolateral amygdala and showed functional downregulatio

73 ted decreases were also observed between the basolateral amygdala and the rACC.

74 revealed that functional Hcn channels in the basolateral amygdala are necessary for conditioned fear

75 macology, revealing that Hcn channels in the basolateral amygdala are required for fear acquisition a

76 negative and positive representations in the basolateral amygdala are unknown.

77 Synaptic plasticity in the basolateral amygdala complex (BLA) mediates the acquisit

78 disruption by actin depolymerization in the basolateral amygdala complex (BLC).

79 , including the lateral nucleus (LAT) of the basolateral amygdala complex, is sensitive to stress.

80 on how distinct interneuron subtypes in the basolateral amygdala contribute to the acquisition and e

81 intracellular signaling pathways within the basolateral amygdala during stress-induced reinstatement

82 -2 in the mThal, prefrontal cortex (PFC), or basolateral amygdala from acute brain slices.

83 ctify this, we monitored, in near-real time, basolateral amygdala glutamate concentration changes dur

84 e we combined chemogenetic excitation of rat basolateral amygdala glutamatergic neurons with a variet

85 ndamide and CRF1 signaling exhibited blunted basolateral amygdala habituation, which further mediated

86 that activation of Galphas signaling in the basolateral amygdala has a role in anxiety.

87 Intra-basolateral amygdala inhibition of CaMKII promoted memor

88 nduction of beta-adrenergic signaling in the basolateral amygdala is sufficient to induce acute and s

89 The basolateral amygdala is the main entry site for sensory

90 Activation of noradrenergic circuitry in the basolateral amygdala is thought to have a role in stress

91 Compound 6c was not efficacious in the basolateral amygdala kindling rat model of temporal lobe

92 The findings also suggest that the basolateral amygdala modulates memory consolidation via

93 nsic excitability and synaptic plasticity in basolateral amygdala neurons that give rise to temporall

94 itioning, which does not involve infralimbic-basolateral amygdala neurons.

95 re) produces a long-lasting sensitization of basolateral amygdala noradrenergic substrates [via a cor

96 was also seen in the infralimbic cortex and basolateral amygdala of stress-susceptible male mice aft

97 There was no increase in IL-1beta in the basolateral amygdala or the perirhinal cortex.

98 The basolateral amygdala participates in this process, but p

99 complex, and local plasticity in excitatory basolateral amygdala principal neurons is considered to

100 nstrate that C1ql3-expressing neurons in the basolateral amygdala project to the medial prefrontal co

101 underling the sAHP or excitability of CA1 or basolateral amygdala pyramidal neurons.

102 miR-144-3p overexpression in the basolateral amygdala rescued impaired fear extinction in

103 RNA sequencing of the basolateral amygdala revealed transcriptional divergence

104 Here we show that basolateral amygdala to orbitofrontal cortex projections

105 ogical investigation of projections from the basolateral amygdala to the medial prefrontal cortex and

106 , we report that transient inhibition of the basolateral amygdala triggered a profound increase in so

107 strocytes depressed excitatory synapses from basolateral amygdala via A1 adenosine receptor activatio

108 Intra-CeA (but not intra-basolateral amygdala) PACAP dose-dependently induced ano

109 olateral prefrontal cortex, hippocampus, and basolateral amygdala) to identify imaging predictors of

110 chronized theta oscillations between V2L and basolateral amygdala, a physiological correlate of succe

111 dal neurons such as hippocampal area CA1 and basolateral amygdala, a slow afterhyperpolarization (sAH

112 anyl induced similar oxygen decreases in the basolateral amygdala, indicating that brain hypoxia coul

113 tral amygdala, but MJN110 infusions into the basolateral amygdala, interfered with the naloxone-preci

114 e found in the dorsal striatum, hippocampus, basolateral amygdala, or prefrontal cortex.

115 umber of Fos-positive neurons in central and basolateral amygdala, orbitofrontal cortex, ventral and

116 s (NAc) shell from ventral subiculum (vSub), basolateral amygdala, paraventricular thalamus, and vent

117 idate, miR-144-3p, robustly expressed in the basolateral amygdala, showed specific extinction-induced

118 malian brain, such as the hippocampus or the basolateral amygdala, the clustering of the scaffolding

119 became silent with time, engram cells in the basolateral amygdala, which were necessary for fear memo

120 cortex via the paraventricular thalamus and basolateral amygdala.

121 ippocampal-entorhinal cortex network and the basolateral amygdala.

122 INs, and principal excitatory neurons in the basolateral amygdala.

123 y transmission in the PFC at inputs from the basolateral amygdala.

124 exclusively within excitatory neurons of the basolateral amygdala.

125 mbens, the medial prefrontal cortex, and the basolateral amygdala.

126 gulation of AMPA-receptor endocytosis in the basolateral amygdala.

127 in emotion-related circuits anchored in the basolateral amygdala.

128 contralateral cortex, nucleus accumbens, and basolateral amygdala.

129 mmunofluorescence, and RNA sequencing of the basolateral amygdala.

130 Within the basolateral amygdaloid complex (BLA), neuropeptide Y (NP

131 ojections, and innervate interneurons in the basolateral amygdaloid complex.

132 greater level in naked mole-rats include the basolateral amygdaloid nucleus and dentate gyrus, but th

133 s exceeds that in Cape mole-rats include the basolateral amygdaloid nucleus, hippocampal CA3 subfield

134 clei, the fasciculus retroflexus of Meynert, basolateral and basomedial amygdaloid nuclei, anterior p

135 erior cingulate cortex innervated mostly the basolateral and CeM amygdalar nuclei, poised to activate

136 tric changes in the anterior hippocampus and basolateral and centromedial amygdala.

137 teractions between the systemic circulation (basolateral) and the retina (apical).

138 1) of the deep pallial nuclei, the lateral, basolateral, and basomedial nuclei contained a very dens

139 pharmacological inactivation of the central, basolateral, and lateral nuclei of the amygdala nonethel

140 ry gating, because inactivating the central, basolateral, and lateral nuclei of the amygdala selectiv

141 We propose that reduced basolateral anion-exchange activity in A-ICs inhibits tr

142 by luminal H(+) secretion is removed by the basolateral anion-exchanger AE1.

143 is required for efficient neutralization by basolateral antibodies.

144 restricting the accumulation of AJCs to the basolateral-apical boundary.

145 Basolateral application of JZL184 decreased permeability

146 an inhibitory effect on the channel, whereas basolateral ATP and [Ca(2+)]i have a stimulatory effect.

147 scence analysis demonstrated near absence of basolateral bile salt uptake transporters OATP1B2, OATP1

148 subregions of basal amygdala nuclei- rostral basolateral (BLA) and basal posterior (BAP)- as they pro

149 The most well characterized of these being basolateral (BLA) and central nucleus (CeA).

150 of apical amiloride and strongly reduced by basolateral bumetanide as well as by depletion of basola

151 Finally, basolateral but not apical EHV1 infection of EREC was de

152 ry bronchial epithelial cells, we found that basolateral, but not apical, application of SMase leads

153 Stx3 present at the basolateral-but not the apical-plasma membrane is rapidl

154 which is believed to provide a key route for basolateral Ca(2+) efflux in the renal epithelia, thus c

155 t N28 and N80, resulting in retention of the basolateral CA12 in the ER.

156 n of ENaC-dependent Isc was also produced by basolateral carbachol in all preparations except rabbit

157 However, recent reports of apical and basolateral cargoes traversing post-Golgi compartments a

158 later quantifying virus in fluid bathing the basolateral cell surface (maintained at pH 7.4).

159 preferentially bound to and entered EREC at basolateral cell surfaces.

160 (KO) mice suggested that ClC-K2 is the main basolateral chloride channel in the thick ascending limb

161 xpression systems fully explains the reduced basolateral chloride conductance in affected kidneys and

162 ated by various apical transporters, whereas basolateral chloride exit is thought to be mediated by C

163 ies (CFTR), and reducing the activity of the basolateral Cl(-) /HCO3(-) exchanger (anion exchanger 2;

164 ateral bumetanide as well as by depletion of basolateral Cl(-), suggesting that Na(+)/K(+)/2Cl(-) (NK

165 a sentinel carbon sensor, all located in the basolateral compartment (BC) of a cell culture plate.

166 , paving the way for H. pylori to access the basolateral compartment and trigger pathogenesis.

167 docytosed virus was released into apical and basolateral compartments.

168 c and task related communication between the basolateral complex of the amygdala (BLA) and the medial

169 on of the information processing between the basolateral complex of the amygdala and central nuclei o

170 e downregulation of A2ARs selectively in the basolateral complex of the amygdala, using a lentivirus

171 have established a new role for AP-1 in the basolateral constitutive secretion of VWF.

172 e polarity loss was associated with abnormal basolateral contractile actomyosin and Enabled (Ena) acc

173 orylation triggers Lgl dissociation from the basolateral cortex to facilitate planar orientation of t

174 and TbetaRII, respectively) localize to the basolateral domain in polarized epithelia.

175 and anion exchanger 1 kAE1 colocalize in the basolateral domain of alpha-intercalated cells in the di

176 us chloride channel usually localized to the basolateral domain of epithelia that regulates cell volu

177 h microvilli substantially extended into the basolateral domain of LKB1(-/-) livers.

178 ller extent (59)Fe-Tf from the apical to the basolateral domain.

179 nd SLC39A14 localized to the canalicular and basolateral domains of polarized hepatic cells, respecti

180 K-ATPase and E-cadherin are localized to the basolateral domains of the plasma membrane.

181 ll surface by cell junctions into apical and basolateral domains.

182 ecause hepcidin reduces iron efflux from the basolateral enterocyte, it is uncertain whether luminal

183 our data indicate that MCT12 functions as a basolateral exit pathway for creatine in the proximal tu

184 This reduced basolateral exocytosis in part explained the less severe

185 acini exhibited a reduction in pathological basolateral exocytosis of ZGs resulting from a decrease

186 hat the size and concentration of apical and basolateral exosomes remained relatively stable across 3

187 ining the targeting motif was able to direct basolateral expression of the apically sorted nerve grow

188 pical membrane CO2 permeability and vigorous basolateral HCO3 (-)uptake, which was sensitive to Na(+)

189 , with apical increases being inhibitory and basolateral increases stimulating channel activity.

190 man enterocyte-models and mouse organoids by basolateral incubation with a high concentration (1 mM)

191 both at adherens junctions as well as along basolateral interfaces.

192 amily 26 member A6; SLC26A6), increasing the basolateral K(+) permeability and apical Cl(-) and HCO3(

193 Basolateral ligand delivery nonetheless remains entirely

194 his was confirmed by comparison with a known basolateral localized protein, the alpha subunit of Na(+

195 water permeation barrier as the endothelial basolateral membrane and show that the apical membrane i

196 derived iPSC-RPE, BEST1 was expressed at the basolateral membrane and the apical membrane.

197 Type I hair cells are characterized by their basolateral membrane being enveloped in a single large a

198 brake in their development, such that their basolateral membrane currents and synaptic machinery ret

199 brake in their development, such that their basolateral membrane currents and synaptic machinery ret

200 3 overexpression depletes uPAR from distinct basolateral membrane domains in breast cancer cells, res

201 f this newly delivered protein traverses the basolateral membrane en route to the apical membrane.

202 EGFP-EAAT2a or EGFP-EAAT2b and found robust basolateral membrane expression of the EAAT2b isoform.

203 Whereas TfR recycles to the basolateral membrane from CRE, Megalin, like pIgR, traff

204 ude that Munc18c's role in mediating ectopic basolateral membrane fusion of ZGs contributes to the in

205 Core regulators of epithelial basolateral membrane identity localize to T-tubules, and

206 also acquired an extensive brush border and basolateral membrane invaginations resembling those obse

207 nal domain is targeted constitutively to the basolateral membrane irrespective of dietary copper conc

208 naesthetic MS-222, which reduces the size of basolateral membrane K(+) currents.

209 ATP11C is essential for basolateral membrane localization of multiple bile salt

210 ATP11C localized to the basolateral membrane of central hepatocytes in the liver

211 al glucose transporter GLUT1 appeared at the basolateral membrane of enterocytes.

212 gene confirmed that ATP7 is expressed at the basolateral membrane of larval midgut copper cells and t

213 dhesion molecule (EpCAM) is expressed at the basolateral membrane of most normal epithelial cells but

214 started the infection preferentially at the basolateral membrane of polarized MDCK II cells; however

215 reduced accumulation of NBCe1 protein in the basolateral membrane of proximal-tubule epithelia is the

216 thought to function as an ion channel in the basolateral membrane of retinal pigment epithelial (RPE)

217 PrP(C) is expressed on the basolateral membrane of retinal-pigment-epithelial (RPE)

218 tributed to a residual calyx attached to the basolateral membrane of the hair cells.

219 uitination of Stx3 leads to removal from the basolateral membrane to achieve apical polarity, that St

220 ced a significant retrieval of Ntcp from the basolateral membrane, which was accompanied by an activa

221 e by the Na(+),K(+)-ATPase located along the basolateral membrane.

222 ng that Fyn mediates Ntcp retrieval from the basolateral membrane.

223 pithelial cells along the apical but not the basolateral membrane.

224 ents through patch pipette electrodes at the basolateral membrane.

225 ency results in a redistribution of CUA-1 to basolateral membranes for copper efflux to peripheral ti

226 ocalize in bands just beneath the apical and basolateral membranes in two different cortical collecti

227 Basolateral membranes of DCT cells were depolarized, nea

228 .Glu143Lys missense variant localized to the basolateral membranes of polarized Madin-Darby canine ki

229 2 in the kidney and found that it resides on basolateral membranes of proximal tubules.

230 abundance of AQP1 in brush border apical and basolateral membranes was augmented >2-fold by increasin

231 tip of the growing canal and the dynamics of basolateral microtubules.

232 plicated by increasing the activities of the basolateral Na(+) -HCO3(-) cotransporter (NBC1) and apic

233 The addition of a basolateral Na(+) -K(+) -2Cl(-) cotransporter (NKCC1), a

234 a coordinated stimulation of apical ENaC and basolateral Na(+),K(+)-ATPase.

235 is expressed in the BLA, particularly in the basolateral nucleus (BL), in male and female rodents.

236 es excitatory and inhibitory inputs from the basolateral nucleus (BLA) and serotonin receptor subtype

237 carinic receptors (M2Rs) in the rat anterior basolateral nucleus (BLa) is critical for the consolidat

238 The basolateral nucleus of the amygdala (BL) receives LA inp

239 The basolateral nucleus of the amygdala (BLA) and prelimbic

240 nal-regulated kinase (ERK) activation in the basolateral nucleus of the amygdala (BLA) and was necess

241 tween the orbitofrontal cortex (OFC) and the basolateral nucleus of the amygdala (BLA) provide a crit

242 Projections from the basolateral nucleus of the amygdala (BLA) to the cortex

243 ry cortex (GC) receives projections from the basolateral nucleus of the amygdala (BLA).

244 (BFc) neurons send a dense projection to the basolateral nucleus of the amygdala (BLA).

245 ntity of the protein(s) participating in the basolateral Pi efflux remains unknown.

246 lockade and redirection of exocytosis to the basolateral plasma membrane at supramaximal doses.

247 plasma membrane-derived exosomes, but not in basolateral plasma membrane exosomes from mouse cortical

248 n the apical plasma membrane compared to the basolateral plasma membrane exosomes.

249 derived from the apical plasma membrane and basolateral plasma membrane of polarized murine cortical

250 ,K(+)-ATPase, which is normally found at the basolateral plasma membrane of renal epithelial cells, i

251 rom the trans Golgi network to the apical or basolateral plasma membrane.

252 Loss of AJs or basolateral polarity components promotes tumor formation

253 d by Lats2 that is activated by the Scribble basolateral polarity protein.

254 Basolateral polymerization of cellular fibronectin (FN)

255 Surprisingly, disruption of AJs and loss of basolateral proteins produced very different effects on

256 lting from failure of the exocyst to deliver basolateral proteins to the cortex.

257 e secretory pathway required for delivery of basolateral proteins to the plasma membranes of epitheli

258 ing of apical junctions and the formation of basolateral protrusions in distinct subsets of hypoderma

259 that regulates epithelial intercalation via basolateral protrusive activity.

260 The basolateral recycling and transcytotic pathways of epith

261 revealed distinct effects on the apical and basolateral recycling and transcytotic pathways, demonst

262 and such endosomes accumulate high levels of basolateral recycling cargo.

263 DPN-1 is a resident protein of the early and basolateral recycling endosomes in the C. elegans intest

264 nts display phenotypes indicating a block in basolateral recycling transport.

265 ong dependence on PARD6B for apical, but not basolateral, recycling, implicating this cell polarity g

266 structural plasticity within the medial and basolateral regions of the amygdala in response to prolo

267 isolated from media bathing either apical or basolateral RPE surfaces, and two subpopulations of smal

268 and 4) can accumulate HCO3 (-)ions from the basolateral side and secrete them at the apical membrane

269 t that IL-22 signals exclusively through the basolateral side of polarized Caco-2 cell monolayers.

270 ndothelial cells, Muller glia cells, and the basolateral side of the retinal pigment epithelium.

271 The CC are deposited on the basolateral side, and compromise endothelial function.

272 VWF secretion can occur from both apical and basolateral sides of endothelial cells, and from constit

273 o in which ESMI(623)LL acts as the authentic basolateral signal of ClC-2.

274 Hepatic transporters, located along basolateral (sinusoidal) and apical (canalicular) membra

275 cells display highly coordinated apical and basolateral sodium transport rates.

276 are dispensable for repression of Yki, while basolateral Spectrins (alpha/beta dimers) are essential.

277 Our findings identify both apical and basolateral Spectrins as regulators of Hippo signalling

278 eveloped a method of applied pressure to the basolateral surface of alveolar epithelia.

279 Imaging and analysis of the basolateral surface of cells expressing some 50 molecule

280 ntrast, infected MDMs and DCs applied to the basolateral surface of HAE grown on large-pore (3.0-mum)

281 ikewise, infected MDMs or DCs applied to the basolateral surface of HAE grown on small-pore (0.4-mum)

282 d nectin-4 to efficiently deliver MeV to the basolateral surface of HAE.

283 urrent study we found that DCs docked to the basolateral surface of lymphatic vessels and transited t

284 s engagement with receptors expressed on the basolateral surface of the epithelium.

285 ocalizes with complement deposited along the basolateral surface of the proximal renal tubule in asso

286 eate a more efficient budding process at the basolateral surface.

287 uptake from the apical surface than from the basolateral surface.

288 Particles are released from the apical and basolateral surfaces and are indistinguishable, indicati

289 nt mice expressed far less Ae1 in A-ICs, but basolateral targeting of the mutant protein was preserve

290 n residues 158 and 163 (VxxEED) required for basolateral TbetaRI expression.

291 liver, and has been implicated in regulating basolateral to apical transcytosis.

292 provide evidence for a regulated, vectorial, basolateral-to-apical bicarbonate transport in polarized

293 Thus, loss of MYO5B disturbs both apical and basolateral trafficking of proteins and causes MVID in m

294 YO5B is involved not only in apical but also basolateral trafficking of proteins.

295 es, and knockdown of AP-1gamma, required for basolateral trafficking, redirects FGF from T-tubules to

296 tein-sorting station for distinct apical and basolateral transport carriers that reach their respecti

297 with rapid efflux by functionally associated basolateral transporters.

298 hesis that ATP11C deficiency interferes with basolateral uptake of unconjugated bile salts, a process

299 glucose transporter GLUT2 is located at the basolateral, vascular side, while SGLT1 is exposed to lu

300 de the first evidence that apical NTRp75 and basolateral VSVG in Madin-Darby canine kidney cells stil