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1 ne specific (Caco-2, not Hep-G2, HeLa-S3, or Madin-Darby canine kidney cells).
2 al and apical surfaces of stably transfected Madin Darby canine kidney cells.
3 ane proteins in fully polarized filter-grown Madin-Darby canine kidney cells.
4 iosynthetic traffic, on polarized traffic in Madin-Darby canine kidney cells.
5 and colon epithelial cells and in polarized Madin-Darby canine kidney cells.
6 osition-independent basolateral targeting in Madin-Darby canine kidney cells.
7 SEP levels in the apical domain of polarized Madin-Darby canine kidney cells.
8 f hepatocytes and polarized WifB, HepG2, and Madin-Darby canine kidney cells.
9 injected into live Chinese hamster ovary and Madin-Darby canine kidney cells.
10 ro studies of epithelial cell colonies using Madin-Darby canine kidney cells.
11 K, in kidney glomeruli and when expressed in Madin-Darby canine kidney cells.
12 ctivity and expression of the Na,K-ATPase in Madin-Darby canine kidney cells.
13 e viruses in African green monkey kidney and Madin-Darby canine kidney cells.
14 lly to the basolateral membrane of polarized Madin-Darby canine kidney cells.
15 -Ostbeta were analyzed in stably transfected Madin-Darby canine kidney cells.
16 alpha are accelerated in NKD2-overexpressing Madin-Darby canine kidney cells.
17 bserved at the surface of stably transfected Madin-Darby canine kidney cells.
18 s and poorly stimulates the proliferation of Madin-Darby canine kidney cells.
19 tin organization during cell-cell contact in Madin-Darby canine kidney cells.
20 mily interacting protein 1, was expressed in Madin-Darby canine kidney cells.
21 of ARE-mediated protein sorting in polarized Madin-Darby canine kidney cells.
22 rane region of human submandibular gland and Madin-Darby canine kidney cells.
23 th a unique trafficking pattern in polarized Madin-Darby canine kidney cells.
24 essed TRPC1 in human submandibular gland and Madin-Darby canine kidney cells.
25 97 in lysates from rat brain and transfected Madin-Darby canine kidney cells.
26 ruits Dock1 to initial cell-cell contacts in Madin-Darby canine kidney cells.
27 ments in HeLa cells and enhanced motility in Madin-Darby canine kidney cells.
28 h endogenous MAGI-1 at the tight junction of Madin-Darby canine kidney cells.
29 e alpha(2A)-AR to the basolateral surface of Madin-Darby canine kidney cells.
30 nd Pals2 localize to the lateral membrane in Madin-Darby canine kidney cells.
31 both non-polarized HeLa cells and polarized Madin-Darby canine kidney cells.
32 ic cells but pronounced in CXCR7-transfected Madin-Darby canine kidney cells.
33 n Caco-2 cells and activated the promoter in Madin-Darby canine kidney cells.
34 the Neu5Ac(alpha2-3)Gal-binding variants in Madin-Darby canine kidney cells.
35 with the use of the calcium switch model in Madin-Darby canine kidney cells.
36 enin reporter gene in Pa-4 cells, but not in Madin-Darby canine kidney cells.
37 lts are obtained using HEp2 and nonpolarized Madin-Darby canine kidney cells.
38 tween SCs in ears from chickens and mice and Madin-Darby canine kidney cells.
39 endoplasmic reticulum of stably transfected Madin-Darby canine kidney cells.
40 sociated with the apical recycling system of Madin-Darby canine kidney cells.
41 hetic and postendocytic traffic in polarized Madin-Darby canine kidney cells.
42 tivates progelatinase A when co-expressed in Madin-Darby canine kidney cells.
43 directly to the apical surface of polarized Madin-Darby canine kidney cells.
44 ic transposon mutants for internalization by Madin-Darby canine kidney cells.
45 es are localized on the lateral subdomain of Madin-Darby canine kidney cells.
46 nd was found predominantly in the nucleus of Madin-Darby canine kidney cells.
47 ible for its direct basolateral targeting in Madin-Darby canine kidney cells.
48 aces, respectively, when expressed stably in Madin-Darby canine kidney cells.
49 f mRNAs for HSP70 and betaine transporter in Madin-Darby canine kidney cells.
50 actomyosin network at the apical surface of Madin-Darby canine kidney cells.
51 also found in Chinese hamster ovary, but not Madin-Darby canine kidney cells.
52 in of the human transferrin receptor (TR) in Madin-Darby canine kidney cells.
53 of two members of this transporter family in Madin-Darby canine kidney cells.
54 merizing agent), on postendocytic traffic in Madin-Darby canine kidney cells.
55 ateral domain upon expression in transfected Madin-Darby canine kidney cells.
56 ed efficiently to the basolateral surface of Madin-Darby canine kidney cells.
57 d and their surface distribution analyzed in Madin-Darby canine kidney cells.
58 d 4 were found to be endogenously present in Madin-Darby canine kidney cells.
59 lized, metabolically labeled pIgR-expressing Madin-Darby canine kidney cells.
60 < or = 0.001) higher infection rates than in Madin-Darby canine kidney cells.
61 sult in partial mis-sorting of E-cadherin in Madin-Darby canine kidney cells.
62 ered to the basolateral surface of polarized Madin-Darby canine kidney cells.
63 the circumferential junctional actin ring in Madin-Darby canine kidney cells.
64 e 6-fluoro atom) was lost in HGPRT-deficient Madin-Darby canine kidney cells.
65 ursor in the GPI lipid remodeling process in Madin-Darby canine kidney cells.
66 SVPs at the apical surface of live polarized Madin-Darby canine kidney cells.
67 erimental system to an epithelial monolayer, Madin-Darby canine kidney cells.
68 vation during cell-cell contact formation in Madin-Darby canine kidney cells.
69 over direct lysosomal delivery in polarized Madin-Darby canine kidney cells.
70 urified membranes and at apical junctions in Madin-Darby canine kidney cells.
71 A also improved maturation of ABCB4-I541F in Madin-Darby canine kidney cells.
72 ide exchange factor, inhibit ciliogenesis in Madin-Darby canine kidney cells.
73 otor, at the distal tips of primary cilia in Madin-Darby canine kidney cells.
74 that occludin localizes with centrosomes in Madin-Darby canine kidney cells.
75 ntrol of the beta(1) and beta(2) subunits in Madin-Darby canine kidney cells.
76 ts cleavage forms) with endogenous IP(3)R in Madin-Darby canine kidney cells.
77 nt routes to the apical surface of polarized Madin-Darby canine kidney cells.
78 icking of apical and basolateral proteins in Madin-Darby canine kidney cells.
79 ress measurements within monolayers of MDCK (Madin Darby canine kidney) cells.
80 rapid protein tyrosine dephosphorylation in Madin-Darby canine kidney cells, a nontransformed epithe
81 igated the role of GRHL2 in tubulogenesis of Madin-Darby canine kidney cells, a process requiring tra
82 and protein expression were also observed in Madin-Darby canine kidney cells, a tubular cell line, tr
83 geting, we examined the sorting of mAChRs in Madin-Darby canine kidney cells, a widely used model sys
84 upon calcium-induced junction biogenesis in Madin-Darby canine kidney cells, ABalphaC, a major prote
85 NF-kappaB and protection of DU-145 and MDCK (Madin-Darby canine kidney) cells against the topoisomera
90 ceramide, N-acetylsphingosine, was found in Madin-Darby canine kidney cell and mouse tissue homogena
91 ys after transfection of cocultured COS7 and Madin-Darby canine kidney cells and achieved levels of 1
92 a C2 (PKCalphaC2) domains were identified in Madin-Darby canine kidney cells and compared with that o
93 se (PI5K) increased actin comet frequency in Madin-Darby canine kidney cells and concomitantly stimul
95 ntaining protein complexes from membranes of Madin-Darby canine kidney cells and identified three maj
96 o pGL3 vector induced luciferase activity in Madin-Darby canine kidney cells and in mouse inner medul
97 olateral localization of hCTR1 also in renal Madin-Darby canine kidney cells and opossum kidney cells
98 protein regulated tight junction function in Madin-Darby canine kidney cells and pathways that direct
99 mbrane trafficking, to the primary cilium of Madin-Darby canine kidney cells and showed that it was i
100 nesis and nephrogenesis using Tuba knockdown Madin-Darby canine kidney cells and tuba knockdown in ze
102 tion of PA103 by polarized epithelial cells (Madin-Darby canine kidney cells) and J774.1 macrophage-l
103 proliferation and damage to distal tubular (Madin-Darby canine kidney cells) and proximal (LLC-PK1 c
104 nsity in primary canine kidney tubule cells, Madin-Darby canine kidney cells, and human umbilical vei
105 stably transfected normal rat kidney cells, Madin-Darby canine kidney cells, and Rat1 fibroblasts, a
106 kyrin (AnkR, a product of the ANK1 gene) and Madin-Darby canine kidney cell ankyrin (AnkG, a product
107 PE on Transwell cultures of CaCo-2 cells and Madin-Darby canine kidney cells, another polarized cell
109 etains the capacity to enhance the growth of Madin-Darby canine kidney cells as cysts in three-dimens
110 nsporter 1 (hCNT1), when stably expressed in Madin-Darby canine kidney cells as yellow fluorescent fu
112 stream of tyrosine kinases, was decreased in Madin-Darby canine kidney cells but increased in some of
113 are both expressed at the apical membrane of Madin-Darby canine kidney cells, but the locations of th
114 lity of human CFTR in the plasma membrane of Madin-Darby canine kidney cells by photobleaching of gre
115 ferent laminin isoforms, in the migration of Madin-Darby canine kidney cells by suppressing expressio
116 lcohols; also, inhibition of PA formation in Madin-Darby canine kidney cells by treatment with 1% eth
117 ion in LB significantly enhances invasion of Madin-Darby canine kidney cells by wild-type S. typhimur
118 lthough the mouse ENT1 (mENT1), expressed in Madin-Darby canine kidney cells, can transport FIAU, con
119 airway epithelia, as well as in transfected Madin-Darby canine kidney cells, CAR is expressed exclus
120 Stronger R-Ras phosphorylation was seen in Madin-Darby canine kidney cells cells transformed with t
121 ateral recycling of transferrin in polarized Madin-Darby canine kidney cells cells, consistent with r
122 cal microscopy experiments were conducted in Madin-Darby canine kidney cells co-expressing alpha- and
123 pithelial cell types (neural progenitors and Madin-Darby canine kidney cells) co-distributed with cer
125 rofluorimetric measurements in fura-2 loaded Madin-Darby canine kidney cells confirmed the occurrence
130 ctor-induced tubulogenesis in Tuba knockdown Madin-Darby canine kidney cell cysts cultured in a colla
131 ctional component of mTORC2, was silenced in Madin-Darby canine kidney cell cysts grown in 3D culture
133 xpression of FLAG-tagged mAChRs in polarized Madin-Darby canine kidney cells demonstrated that the M(
134 localization and activity of DbpA and YAP in Madin-Darby canine kidney cells depleted either of ZO-1,
138 ive or dominant-negative alleles of Rab13 in Madin-Darby canine kidney cells disrupts TGN38/46 locali
139 showed that at least half of the proteins in Madin-Darby canine kidney cell DRMs (other than cytoskel
142 ble expression of wild type PIPKIgamma661 in Madin-Darby canine kidney cells enhanced transferrin upt
144 s seen in both S256L-AQP2 mutant mice and in Madin-Darby canine kidney cells expressing an S256A muta
147 tibility of epithelial cells to viral entry, Madin-Darby canine kidney cells expressing endogenous ne
149 s ectopically expressing the receptor and in Madin-Darby canine kidney cells expressing the native re
150 Y8 was applied to the basolateral surface of Madin-Darby canine kidney cells expressing the rat neona
151 ties of pendrin were determined in polarized Madin-Darby canine kidney cells expressing the sodium io
154 ve for seasonal A(H1N1) were inoculated onto Madin-Darby canine kidney cells for virus isolation.
155 drogen peroxide scavenger pyruvate protected Madin-Darby canine kidney cells from loss of transepithe
157 ide could be added to the apical membrane of Madin-Darby canine kidney cells growing as a polarized e
159 ing duct epithelia, we also expressed PGT in Madin-Darby canine kidney cells grown on filters, where
160 depletion of multiple galectins expressed in Madin-Darby canine kidney cells had no effect on p75 sor
163 the basolateral plasma membrane of polarized Madin-Darby canine kidney cells; however, membrane stain
164 cycling endosomes en route to the surface of Madin-Darby canine kidney cells; however, the routes use
165 kinase activated branching morphogenesis of Madin-Darby canine kidney cells in collagen gels even in
167 ound beta subunits were expressed in 293 and Madin-Darby canine kidney cells in the absence of the li
168 ssage of A/Turkey/Minnesota/833/80 (H4N2) in Madin-Darby canine kidney cells in the presence of incre
169 find that mutant Met induces the motility of Madin-Darby canine kidney cells in vitro and experimenta
171 ct of pp66 in cultured parietal cells and in Madin-Darby canine kidney cells indicate that pp66 prefe
172 lusively into the apical medium of polarized Madin-Darby canine kidney cells, indicating that no spec
173 d HepG2, but inactive in NIH3T3, Caco-2, and Madin-Darby canine kidney cells, indicating that the det
174 crease in cell proliferation in both 293 and Madin-Darby canine kidney cells, indicating that this gr
176 for influenza detection for a case study of Madin-Darby canine kidney cells infected with influenza
179 try, we determined the lipidomes of the host Madin-Darby canine kidney cell, its apical membrane, and
181 demonstrated that the knockdown of PALS1 in Madin Darby canine kidney cells leads to tight junction
182 ression of mislocalized mutant syntaxin 3 in Madin-Darby canine kidney cells leads to basolateral mis
183 ha12 or constitutively active (QL)alpha12 in Madin-Darby canine kidney cells led to increased apoptos
184 ized the subcellular localization in MDCKII (Madin-Darby canine kidney (cell line)) cells and in mous
185 duction of BGT1 mRNA in the renal epithelial Madin-Darby canine kidney cell line is inhibited by SB20
186 ric-thiol conjugates were characterized in a Madin-Darby canine kidney cell line stably transfected w
187 amatically up-regulated in a Src-transformed Madin-Darby canine kidney cell line, indicating that the
188 address this hypothesis, we generated stable Madin-Darby canine kidney cell lines depleted of both ZO
191 ls stably expressing wild-type (WT) UT-A1 to Madin-Darby canine kidney cell lines stably expressing m
192 ns 1A, 1B, 2, 3, and 4 in stably transfected Madin-Darby canine kidney cell lines was studied with co
193 parallel, inhibition of NCX1 by KB-R7943 in Madin-Darby canine kidney cells, LLC-PK1, and human prim
194 redistribute to intracellular locations when Madin-Darby canine kidney cells lose their cellular pola
195 bind specifically to phosphorylated c-Src in Madin-Darby canine kidney cell lysates, suggesting that
196 ession of a luciferase reporter gene in both Madin Darby canine kidney cells (MDCK) and primary rat c
197 ain-derived endothelial cells (bEND.3), (ii) Madin Darby Canine Kidney Cells (MDCK-2), and mouse myob
198 renergic receptor (AR) subtypes in polarized Madin-Darby canine kidney cells (MDCK II) and the mechan
199 ed TRPC3 was localized apically in polarized Madin-Darby canine kidney cells (MDCK) and salivary glan
201 ypically E-cadherin dominant epithelial line Madin-Darby canine kidney cells (MDCK) to analyze cell a
207 crease in tight junction permeability across Madin-Darby canine kidney cell monolayers, as evidenced
212 found in detergent-resistant raft domains of Madin-Darby canine kidney cells or baby hamster kidney c
213 nt mutants grew as well as parental virus in Madin-Darby canine kidney cells or in embryonated chicke
214 A protein doublet of approximately 30 kDa in Madin-Darby canine kidney cells or pig brain cytosol (al
217 ion of exogenous Crumbs3 in Snail-expressing Madin-Darby Canine Kidney cells partially restores cell-
218 bound to cadherins at adherens junctions of Madin-Darby canine kidney cells recruited ABP from the c
219 of Akt/PKB protein were observed in detached Madin-Darby canine kidney cells relative to cells attach
220 eptor determinant, sialic acid, by selecting Madin-Darby canine kidney cells resistant to a lectin sp
221 to the apical and basolateral compartment of Madin-Darby canine kidney cells, respectively, consisten
222 clude that RGD-induced [Ca2+]i transients in Madin-Darby canine kidney cells result primarily from th
223 nocytogenes-infected, EGFP-actin-transfected Madin-Darby canine kidney cells results in a 3-fold leng
225 ng an extracellular hemagglutinin epitope in Madin-Darby canine kidney cells results in co-localizati
227 ey band 3 in both nonpolarized and polarized Madin-Darby canine kidney cells showed that most of the
229 d the interaction between pIgR and CaM using Madin-Darby canine kidney cells stably expressing cloned
232 epithelial cells has been investigated using Madin-Darby canine kidney cells stably expressing variou
233 ary (MCF-7) cancer cell lines, as well as in Madin-Darby canine kidney cells stably expressing variou
236 e that apical NTRp75 and basolateral VSVG in Madin-Darby canine kidney cells still undergo progressiv
237 tively activated Galpha(12) (QLalpha(12)) in Madin Darby canine kidney cells stimulated PP2A activity
238 d to the cilia of retinal photoreceptors and Madin-Darby canine kidney cells, suggesting a broader ph
239 om the plasma membrane in stably transfected Madin-Darby canine kidney cells, suggesting that methyla
240 ed selective accumulation in the basolateral Madin Darby canine kidney cell surface, whereas c-myc ep
244 conserved intracellular segment (S4) of the Madin-Darby canine kidney cell taurine transporter enhan
245 injections with cRNA from and expressing the Madin-Darby canine kidney cell taurine transporter pNCT.
246 cells, which endogenously express villin and Madin-Darby canine kidney cells that ectopically express
248 l Ebola virus proteins were transfected into Madin Darby canine kidney cells, the Ebola virus VP35 pr
249 ec10 was exogenously expressed in epithelial Madin-Darby canine kidney cells, there was a selective i
250 nternalized from opposite poles of polarized Madin-Darby canine kidney cells, they accumulate in dist
251 are cointernalized from the apical poles of Madin-Darby canine kidney cells, they enter a shared api
252 regulates morphogenic growth of benign MDCK (Madin Darby Canine Kidney) cells through effects on the
253 hosphate-stimulated protein kinase (AMPK) in Madin-Darby canine kidney cells through treatment with C
260 ompound, we conducted transport studies with Madin-Darby canine kidney cells transfected with human M
261 rred in vitro with a Km of 1.3 microm and in Madin-Darby canine kidney cells transfected with meprin
265 DNA methylomes at single-base resolution of Madin-Darby canine kidney cells undergoing EMT and trans
266 ant conditional aggregation domains, in live Madin-Darby canine kidney cells using spinning disk conf
268 genin promoter in rat parotid Pa-4 cells and Madin-Darby canine kidney cells was minimal, ranging fro
269 reassembly of Y398D/Y402D mutant occludin in Madin-Darby canine kidney cells was significantly delaye
270 ous YFP-linked beta(1) subunits expressed in Madin-Darby canine kidney cells was used to assess beta(
272 of endogenous proteins in stably transfected Madin-Darby canine kidney cells, we found that MRK-beta
273 FP (yellow fluorescent protein) expressed in Madin-Darby canine kidney cells, we identified amino aci
274 utants of Tamm-Horsfall protein in polarized Madin-Darby canine kidney cells, we show here that a cys
275 ged dopamine transporter stably expressed in Madin-Darby canine kidney cells, we show in live cells t
276 re, using three-dimensional cell cultures of Madin-Darby canine kidney cells, we show that the ARF6 G
277 n mediates the polarized expression of CFTR, Madin-Darby canine kidney cells were stably transfected
282 targeted exclusively to the apical milieu in Madin-Darby canine kidney cells, were packaged into reco
283 s concentrated at cell-cell contact sites of Madin-Darby canine kidney cells, where it colocalized wi
284 e apical or basolateral surface in polarized Madin-Darby canine kidney cells, whereas in double tyros
286 x (M) proteins M1 and M2, we doubly infected Madin-Darby canine kidney cells with amantadine (1-amino
288 train A/Brisbane/59/2007 (H1N1) was grown in Madin-Darby canine kidney cells with or without escalati
290 n mutant (ARTL27) is not sorted in polarized Madin-Darby canine kidney cells, with approximately 65%
291 n (3-NC), selectively inhibited PLC-gamma in Madin-Darby canine kidney cells without affecting the ac
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