ライフサイエンスコーパス: basolateral

1 nhanced manganese transport in the apical-to-basolateral (absorptive) direction.

2 PEA (basolateral) also reversed increased permeability when a

3 ated with distinct oscillatory states in the basolateral amygdala (BLA) and medial prefrontal cortex

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

5 ions directly stimulate GIRK currents in the basolateral amygdala (BLA) and potentiate baclofen-induc

6 c properties of ventral hippocampus (vHipp), basolateral amygdala (BLA) and prefrontal cortex (PFC) i

7 ctions from the ventral hippocampus (vHipp,) basolateral amygdala (BLA) and prefrontal cortex (PFC) o

8 mbic (IL) cortex neurons that project to the basolateral amygdala (BLA) and reduced CD response compa

9 epend on functional interactions between the basolateral amygdala (BLA) and the nucleus accumbens cor

10 e of the medial prefrontal cortex (mPFC) and basolateral amygdala (BLA) and their reciprocal inhibito

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

12 deling of relative excitatory drive from the basolateral amygdala (BLA) away from corticotropin relea

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

14 lcohol consumption, whereas knockdown in the basolateral amygdala (BLA) decreased alcohol consumption

15 glutamatergic terminals from the PeF to the basolateral amygdala (BLA) enhanced the acquisition, del

16 We first show that the rat basolateral amygdala (BLA) exhibits prominent gamma osci

17 pharmacological manipulations, we found that basolateral amygdala (BLA) glutamatergic activity tracks

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

19 young and aged rats to test the role of the basolateral amygdala (BLA) in intertemporal decision mak

20 nd (3) excitatory synaptic physiology in the basolateral amygdala (BLA) in male Sprague Dawley rats.

21 r insular cortex (aIC) that project into the basolateral amygdala (BLA) in response to conditioned ta

22 earch has established a crucial role for the basolateral amygdala (BLA) in social experiential learni

23 neurons of mice integrate auditory cues and basolateral amygdala (BLA) inputs non-linearly in a NMDA

24 The basolateral amygdala (BLA) integrates sensory input from

25 Extensive evidence indicates that the basolateral amygdala (BLA) interacts with other brain re

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

27 The basolateral amygdala (BLA) is integral in mood and emoti

28 The basolateral amygdala (BLA) modulates the consolidation o

29 formed and stored in a genetically distinct basolateral amygdala (BLA) neuronal population that driv

30 e behavior and increase spine-density in the basolateral amygdala (BLA) of rats 10 days later.

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

32 and associated with anatomical variation in basolateral amygdala (BLA) perineuronal nets, which are

33 The basolateral amygdala (BLA) plays a critical role in fear

34 The basolateral amygdala (BLA) plays a vital role in associa

35 Basolateral amygdala (BLA) principal cells are capable o

36 version of diazepam (CD) that was tested on basolateral amygdala (BLa) pyramidal cells in mouse brai

37 The basolateral amygdala (BLA) regulates conditioned respons

38 The basolateral amygdala (BLA) sends excitatory projections

39 Whole-cell recordings in basolateral amygdala (BLA) slices from rats revealed hig

40 Here, we show that stress increases basolateral amygdala (BLA) spike firing.

41 Y1R+ neurons projecting from the mPFC to the basolateral amygdala (BLA) this efferent population was

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

43 were analyzed with anterograde tracing from basolateral amygdala (BLA) to PFC to identify sex-specif

44 g factor (CRF) modulate the responses of the basolateral amygdala (BLA) to stress and are associated

45 s coeruleus (LC) neurons that project to the basolateral amygdala (BLA) using a DREADD (designer rece

46 r learning, disengaged mesolimbic circuitry, basolateral amygdala (BLA), and plasticity-related AMPA

47 ess effects on the dorsal hippocampus (HPC), basolateral amygdala (BLA), and somatosensory cortex (SS

48 This avoidance requires prelimbic (PL) PFC, basolateral amygdala (BLA), and ventral striatum (VS).

49 onmuscle myosin II inhibition (NMIIi) in the basolateral amygdala (BLA), but not dorsal hippocampus (

50 ties in the medial prefrontal cortex (mPFC), basolateral amygdala (BLA), dorsomedial striatum (DMS) a

51 and alteration of synaptic plasticity in the basolateral amygdala (BLA), in male rats.

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

53 ess in BLA.SIGNIFICANCE STATEMENT Within the basolateral amygdala (BLA), neuropeptide Y (NPY) is asso

54 ctivation in the prefrontal cortex (PFC) and basolateral amygdala (BLA), we examined electron microsc

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

56 In the present study, a basolateral amygdala (BLA)-prefrontal cortex (PFC)-peria

57 Here, we show that the mouse basolateral amygdala (BLA)-prelimbic prefrontal cortex (

58 A strong candidate is the basolateral amygdala (BLA).

59 tory synaptic proteins and physiology in the basolateral amygdala (BLA).

60 sity on parvalbumin (PV) interneurons in the basolateral amygdala (BLA).

61 s-induced norepinephrine (NE) release in the basolateral amygdala (BLA).

62 ity within the anterior insula (aIC) and the basolateral amygdala (BLA).

63 hat appears to project downstream to CA1 and basolateral amygdala (BLA).

64 ion, the medial prefrontal cortex (mPFC) and basolateral amygdala (BLA).

65 A particularly strong candidate is the basolateral amygdala (BLA).

66 solateral prefrontal cortex (dlPFC), and the basolateral amygdala (BLA).

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

68 The prelimbic (PL) area and basolateral amygdala (lateral [LA] and basolateral [BL]

69 d overlapping brain circuits and depended on basolateral amygdala activity for expression.

70 hancement was associated with an increase in basolateral amygdala activity.

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

72 cortical nucleus, whereas in the lateral and basolateral amygdala alpha1, alpha2, alpha5, beta1, beta

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

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

75 to the OFC, but not in projections from the basolateral amygdala and thalamus.

76 scillatory neuronal interactions between the basolateral amygdala and the rostral anterior cingulate

77 to the NAc shell and strengthens input from basolateral amygdala and ventral hippocampus.

78 Intra-basolateral amygdala antagonism of dopamine D1-receptors

79 n at inputs from the ventral hippocampus and basolateral amygdala but not from the mediodorsal nucleu

80 ex and increased immunoreactive cells in the basolateral amygdala compared with WT littermates.

81 xpression in the infralimbic cortex (IL) and basolateral amygdala complex (BLA) that were associated

82 The basolateral amygdala complex (BLA), extensively connecte

83 ck requires de novo protein synthesis in the basolateral amygdala complex (BLA), whereas consolidatio

84 lidation of conditioned fear memories in the basolateral amygdala complex (BLA).

85 y enhanced memory and heightened cFos in the basolateral amygdala complex (BLC) with retrieval of the

86 entromedial prefrontal cortex or hippocampal-basolateral amygdala connectivity-differentiated between

87 show that increasing neural activity in the basolateral amygdala enhances both conditioned anticipat

88 without affecting anxiety-like behaviors and basolateral amygdala firing.

89 sory cortex, and increased activation of the basolateral amygdala in response to repeated whisker sti

90 and medial prefrontal cortices as well as at basolateral amygdala inputs and striatal cholinergic int

91 ation were specific to MD inputs; activating basolateral amygdala inputs produced opposite effects.

92 The basolateral amygdala is the main entry site for sensory

93 unction of the ventral striatum, whereas the basolateral amygdala mediates processing of the threat c

94 revealed that these arrests are effected by basolateral amygdala neurons projecting to the central a

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

96 ), with little AT(2)R-eGFP expression in the basolateral amygdala or lateral division of the central

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

98 The basolateral amygdala projection (BLAp) innervates broad

99 is a form of one-trial learning dependent on basolateral amygdala projection neurons (BLApn).

100 entation of anandamide hydrolysis within the basolateral amygdala reduces behavioral indices of stres

101 identified a distinct neural ensemble in the basolateral amygdala that encodes the negative affective

102 projection-defined neuronal ensemble in the basolateral amygdala that is active during self-paced be

103 The basolateral amygdala therefore facilitates cue-induced c

104 Here we show that basolateral amygdala to orbitofrontal cortex projections

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

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

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

108 e thalamus, bed nucleus of stria terminalis, basolateral amygdala, and medial prefrontal cortex as pr

109 uding the locus coeruleus, and much later in basolateral amygdala, dorsal raphe nucleus, and the subs

110 egions, namely the medial prefrontal cortex, basolateral amygdala, hippocampus, anterior cingulate co

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

112 lly into the ventromedial prefrontal cortex, basolateral amygdala, or hippocampal CA1 region.

113 mPFC projections to the NAcS, but not to the basolateral amygdala, partially reversed suppression of

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

115 sory cortex, and increased activation of the basolateral amygdala, suggesting that impaired somatosen

116 projections to NAcS, or vmPFC projections to basolateral amygdala, to punished EtOH-SA.

117 cortex, but not to the infralimbic cortex or basolateral amygdala, were more active to safety and com

118 trengthened the coupling between the cmA and basolateral amygdala, whereas LZP increased the interpla

119 ch as the nucleus accumbens shell (NAcS) and basolateral amygdala, which encode positive and negative

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

121 d that in vivo optogenetic activation of the basolateral amygdala-nucleus accumbens (BLA-NAc) glutama

122 h a marker of synaptic plasticity within the basolateral amygdala.

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

124 in GABA- and glutamate-positive cells in the basolateral amygdala.

125 l hippocampus, and projection neurons in the basolateral amygdala.

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

127 contralateral cortex, nucleus accumbens, and basolateral amygdala.

128 pus but did not prevent hyperactivity in the basolateral amygdala.

129 l, and lateral shell; anterior and posterior basolateral amygdala; ventral pallidum; and periaqueduct

130 n the serum of patients with anxiety and the basolateral amygdaloid nucleus (BLA) in chronic stress m

131 both proteins and bile concomitantly at its basolateral and apical domains, respectively.

132 columnar polarized HLCs with clearly defined basolateral and apical membranes separated by tight junc

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

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

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

136 proteins, of which 38% were apical, 51% were basolateral, and 11% were nonpolar.

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

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

139 g MAlk by opposing HCO(3) (-) efflux via the basolateral anion exchanger AE2; and (3) inhibits NaCl r

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

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

142 a and basolateral amygdala (lateral [LA] and basolateral [BL] nuclei) have closely related functions

143 om the apical side of polarized cells, while basolateral BMP-SMAD signaling is unaffected.

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

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

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

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

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

149 ole of liprin-alpha1 in secretion toward the basolateral compartment and identify a subset of ECM com

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

151 yme fatty acid amide hydrolase (FAAH) in the basolateral complex of amygdala (BLA) is thought to buff

152 hemisphere p = 0.032, r(2) = 0.32) and right basolateral complexes (p = 0.05, r(2) = 0.24) also displ

153 cell properties based on molecular markers, basolateral conductances and synaptic properties yet ste

154 r high- nor low-potassium diets affected the basolateral DCT's potassium conductance and membrane pot

155 tion of the apical dendrite without altering basolateral dendrite dynamics.

156 onfocal microscopy, we found that apical and basolateral dendrites are coordinately sculpted during d

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

158 stood, how Scrib module proteins specify the basolateral domain remains unknown.

159 r and mediated MHCI internalization from the basolateral domain, while myosin IIB localized at the ba

160 o mediate communication via their apical and basolateral domains and suggest that defective ESCRT fun

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

162 itioned at the future boundary of apical and basolateral domains.

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

164 This reduced basolateral exocytosis in part explained the less severe

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

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

167 f hnRNPA2B1 had no significant impact on the basolateral export of HSV-1 from infected to uninfected

168 nd bacterial growth, following apical versus basolateral exposure.

169 under conditions of static fluid, apical and basolateral flow, and flow plus repetitive stretch.

170 recovered BCG from the apical, membrane and basolateral fractions over time.

171 1) promotes NH(4) (+) shunting by increasing basolateral HCO(3) (-) uptake to neutralize apical NH(4)

172 ain is essential for supporting the membrane basolateral identity and binding to Llgl.

173 ibble/Dlg module is well-known for promoting basolateral identity during polarity maintenance.

174 In the absence of basolateral IFN-gamma, the compartmentalization of the I

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

176 rk of cholinergic axons terminate within the basolateral infoldings of the lamellate cells.

177 Whether the basolateral, inwardly rectifying potassium channel Kir4.

178 stereociliary bundles for mechanosensation, basolateral ion channels that shape receptor potential,

179 Further, Kir4.1 deletion not only abolished basolateral K(+) conductance and depolarized the DCT mem

180 ting effects induced by low sodium intake on basolateral K(+) conductance and hyperpolarization.

181 asolateral Kir4.1/Kir5.1 activity, increased basolateral K(+) conductance, and hyperpolarized the mem

182 e inhibited the potassium channel, decreased basolateral K(+) currents, and depolarized the membrane.

183 Basolateral Kir4.1/Kir5.1 activity in the DCT partially

184 Low sodium intake stimulated basolateral Kir4.1/Kir5.1 activity, increased basolatera

185 As the pH of ASL increases towards that of basolateral liquid, paracellular HCO(3) (-) flux becomes

186 f several apical (Par6, aPKC, and Pals1) and basolateral (Llgl1 and Llgl2) identity proteins.

187 arly mouse embryo depends on the restricted, basolateral localization of BMP receptors.

188 of ZIP14 as the major transporter mediating basolateral manganese uptake in enterocytes.

189 The presence of alpha-Gal in the basolateral medium was investigated by immunoblotting, t

190 containing peptides were not detected in the basolateral medium.

191 ted from beef, alpha-Gal was detected in the basolateral medium.

192 The basolateral membrane (BLM) Na/K-ATPase provides the favo

193 These basolateral membrane changes were most severe for C57BL/

194 in the IHCs from most mouse strains, but the basolateral membrane current profile remains unchanged.

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

196 mal developmental acquisition of mature-like basolateral membrane currents in low-frequency (apical)

197 vive normally but they fail to acquire adult basolateral membrane currents, retain pre-hearing curren

198 3 overexpression depletes uPAR from distinct basolateral membrane domains in breast cancer cells, res

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

200 ly increased CFTR's co-localization with the basolateral membrane in cystic mice.

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

202 are known to localize to only the apical or basolateral membrane of polarized cell lines in vitro.

203 anion transporter 1 (OAT1), expressed at the basolateral membrane of renal proximal tubule epithelial

204 d a 40-pS and 20-pS potassium channel in the basolateral membrane of the DCT in wild-type and knockou

205 orms the Kir4.1/Kir5.1 heterotetramer in the basolateral membrane of the distal convoluted tubule (DC

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

207 Although the ageing OHCs retained a normal basolateral membrane protein profile, they showed a redu

208 epithelial migration of neutrophils from the basolateral membrane surface to the apical airway surfac

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

210 d role in polarized sorting of cargos to the basolateral membrane.

211 f megalin, causing its redistribution to the basolateral membrane.

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

213 sterolemia protein (ARH), for sorting to the basolateral membrane.

214 for luminal acidification in apical, but not basolateral, membrane protein sorting and transport.

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

216 Basolateral membranes of DCT cells were depolarized, nea

217 within the cells and also at the apical and basolateral membranes.

218 ed medium from vaccinated cattle upon apical-basolateral migration of BCG was examined by quantifying

219 NBCn1 and NBCn2 are present in the basolateral mTAL, where NBCn1 promotes NH(4) (+) shuntin

220 These effects required the basolateral Na(+), K(+)-ATPase, indicating that apical a

221 We propose that upregulation of basolateral NBCn1 and NBCn2 plus the IRBITs in the mTAL:

222 Nonpyramidal GABAergic interneurons in the basolateral nuclear complex (BNC) of the amygdala are cr

223 tions of interneurons (INs) in the amygdalar basolateral nuclear complex (BNC) of the rat can be reco

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

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

226 One of the main subcortical inputs to the basolateral nucleus of the amygdala (BL) originates from

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

228 y portion of the insular cortex (GC) and the basolateral nucleus of the amygdala (BLA) however, its s

229 s from both polyps and turbinates maintained basolateral PAR-2 polarization, suggesting that the calc

230 mary nasal epithelial ALIs responded only to basolateral PAR-2 stimulation, indicated by calcium elev

231 rimary cultures responded to both apical and basolateral PAR-2 stimulation.

232 while remaining fully responsive to invasive basolateral pathogens.

233 tion in the apical pathway compared with the basolateral pathway.

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

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

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

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

238 meter of podosomes in close proximity to the basolateral plasma membrane, and phosphoinositide-bindin

239 ntrols the localisation and levels of Lgl, a basolateral polarity regulator, in a layer autonomous as

240 While AP-1B silencing mainly affected basolateral polarity, AP-1A silencing seemed to cause co

241 eemed to cause comparable loss of apical and basolateral polarity.

242 ating far from their normal positions at the basolateral pole, and auditory-nerve terminals extend to

243 ation treatment with apical PC945 and either basolateral posaconazole or voriconazole resulted in a s

244 rgistic interaction observed when apical and basolateral posaconazole or voriconazole were combined.

245 At later stages, EGFR localized to basolateral positions of the FCs.

246 The basolateral potassium channel in the distal convoluted t

247 mice fed a normal potassium diet had higher basolateral potassium conductance, a more negative DCT m

248 ium channel alpha-subunit, largely abolished basolateral potassium ion conductance (to a degree simil

249 The basolateral protein Scribble (Scrib), a member of the LA

250 AP-1 in polarized distribution of apical and basolateral proteins and introduce surface proteomics as

251 -1A, AP-1B, or both caused redistribution of basolateral proteins as expected but also, of a large po

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

253 the polarized trafficking of fast recycling basolateral receptors.

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

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

256 sport in the absorptive direction via direct basolateral reuptake of freshly absorbed manganese.

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

258 beta-Intercalated cells express basolateral secretin receptors and apical CFTR and pendr

259 T under flow conditions increased apical and basolateral secretion of cGMP relative to the level unde

260 reased epithelial cell height and apical and basolateral secretion of cyclic GMP (cGMP) under baselin

261 Epithelial cell basolateral secretions (1, 2 and 3 days post-loading), b

262 However, differences in apical and basolateral sEV composition and numbers were observed.

263 terocytes, where bile acids are delivered to basolateral side by ileal bile acid binding protein (IBA

264 the apical side and, additionally, from the basolateral side in the case of high valency NCs which a

265 Cleavage of the receptor at the basolateral side of endothelial cells facilitated NC tra

266 red that viral infections emanating from the basolateral side of IECs elicit a stronger intrinsic imm

267 g of Toll-like receptor 3 (TLR3) towards the basolateral side of IECs.

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

269 of free amino acids (176 nM) arriving on the basolateral side of the co-culture with notable levels o

270 VLY permeabilized cells on the basolateral side of the tissues but failed to permeabili

271 The cholangiocyte basolateral side was more vulnerable than the apical sid

272 or clusters remain stable exclusively at the basolateral side, suggesting that endocytosis of non-can

273 ree-dimensional and have distinct apical and basolateral sides, enabling comparison of the effects of

274 apical secretion of IL-6 in response to the basolateral stimulation with IFN-gamma.

275 d cell vacuolation when interacting with the basolateral surface compared to the apical surface.

276 rsely, we find that protein secretion at the basolateral surface is focused on components of the extr

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

278 anic anion transport proteins (OATPs) on the basolateral surface of hepatocytes mediate uptake of a n

279 th forms of VacA bound preferentially to the basolateral surface of organoid monolayers and caused in

280 ively define large populations of apical and basolateral surface proteins in Madin-Darby canine kidne

281 Invasion via the basolateral surface was at least 2-log(10) units more ef

282 arized HIE monolayers preferentially via the basolateral surface.

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

284 irectionally released on the apical, but not basolateral, surface.

285 enabled independent access to the apical and basolateral surfaces of the cholangiocyte channel, allow

286 te distinct signaling agendas via apical and basolateral surfaces to communicate with different cell

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

288 the so-called LAPSDb domain is essential for basolateral targeting of these proteins, while the LAPSD

289 tion in the endoplasmic reticulum, vesicular basolateral targeting, and ciliogenesis in the kidney.

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

291 in rodents the glutamatergic connection from basolateral to central amygdala (BLA-CeA) develops rapid

292 r (pIgR) transports immunoglobulins from the basolateral to the apical surface of epithelial cells.

293 Lack of ZIP14 severely impaired basolateral-to-apical (secretory) manganese transport an

294 able to reduce the 32-mer peptide apical-to-basolateral translocation in in vitro simulated intestin

295 They expressed all apical and basolateral transporters that are important for drug met

296 a layer of epithelial cells, with apical and basolateral transporters that vary according to cell typ

297 drugs via proximal tubule-specific apical or basolateral transporters, and displayed increased cell d

298 nalysis of lipid droplets, by measurement of basolateral triglyceride concentration and by analysing

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

300 ins are asymmetrically distributed along the basolateral wall of cochlear-supporting cells, and are r