ライフサイエンスコーパス: transferrin receptor

1 tinol-binding protein (vitamin A), and iron (transferrin receptor).

2 screened, including CD54 (ICAM-1) and CD71 (transferrin receptor).

3 curium-transferrin complexes by the cognate transferrin receptor.

4 d with clathrin and the IR, but not with the transferrin receptor.

5 cycling endosomes positive for Rab11 and the transferrin receptor.

6 cling endosomes, where it interacts with the transferrin receptor.

7 calization of CD44 with the nonraft protein, transferrin receptor.

8 mal markers, but showed coincidence with the transferrin receptor.

9 a non-ER resident type II protein, the human transferrin receptor.

10 eceptor, while New World arenaviruses hijack transferrin receptor.

11 ed for hemoglobin, serum ferritin, and serum transferrin receptor.

12 nds on transferrin-bound iron uptake via the transferrin receptor.

13 were observed for serum ferritin and soluble transferrin receptor.

14 r (CIMPR) without affecting that of TGN46 or transferrin receptor.

15 ermined from hemoglobin, serum ferritin, and transferrin receptor.

16 t up unless first transfected with the mouse transferrin receptor.

17 ind to the extracellular domain of the mouse transferrin receptor.

18 beyond changes to expression of ESAG6/7, the transferrin receptor.

19 ar compartment which also contained Rab5 and transferrin receptor.

20 s apoptosis through its interaction with the transferrin receptor.

21 ue and change in plasma ferritin and soluble transferrin receptor.

22 nsferrin uptake and lysosomal degradation of transferrin receptors.

23 stitution impairs the endocytic recycling of transferrin receptors.

24 lex class I-like protein that interacts with transferrin receptors.

25 gested that circulating levels of shed human transferrin receptor 1 (hTfR1) are regulated by PC7.

26 ly regulate iron metabolism genes, including transferrin receptor 1 (TfR1) and ferritin H and L subun

27 Each uses human transferrin receptor 1 (TfR1) as its obligate receptor.

28 ates entry into grivet and bat cells through transferrin receptor 1 (TfR1) binding but that OCEV glyc

29 alpha-dystroglycan by Lassa fever virus and transferrin receptor 1 (TfR1) by certain New World clade

30 g activity but did not affect ferritin H and transferrin receptor 1 (TfR1) expression, whereas knockd

31 Transferrin receptor 1 (Tfr1) facilitates cellular iron

32 Interactions between HFE and transferrin receptor 1 (TfR1) have been mapped to the al

33 Upregulation of transferrin receptor 1 (TfR1) in brain microvasculature

34 Transferrin receptor 1 (TfR1) is a cellular receptor for

35 Transferrin receptor 1 (TfR1) is a ubiquitous type II me

36 thogenic arenaviruses of the same clade, use transferrin receptor 1 (TfR1) of their host species to e

37 ty of these viruses to use various mammalian transferrin receptor 1 (TfR1) orthologs, including those

38 receptors, alpha-dystroglycan (alpha-DG) and transferrin receptor 1 (TfR1), are expressed in polarize

39 rophic receptors and cognate ligands such as transferrin receptor 1 (TfR1), but not TfR2.

40 had a homozygous p.Tyr20His substitution in transferrin receptor 1 (TfR1), encoded by TFRC.

41 ransferrin receptor 2 (TfR2) is a homolog of transferrin receptor 1 (TfR1), the receptor responsible

42 The antibody engages the GP1 site that binds transferrin receptor 1 (TfR1)-the host cell surface rece

43 ated with decreased ferritin H and increased transferrin receptor 1 (TfR1).

44 lters expression of the iron uptake receptor transferrin receptor 1 (TfR1).

45 GPC architecture and share a host receptor, transferrin receptor 1 (TfR1).

46 iated with the placental nonheme Fe importer transferrin receptor 1 (TfR1).

47 he metabolite stearic acid (C18:0) and human transferrin receptor 1 (TFR1; also known as TFRC) as mit

48 tomography (PET) radiotracer that binds the transferrin receptor 1 (TFRC, CD71) with high avidity.

49 restricted to reticulocytes expressing both transferrin receptor 1 (Trf1 or CD71) and the Duffy anti

50 l iron pools and increased the expression of transferrin receptor 1 and iron regulatory protein 2 con

51 were decreased in the epithelial cells, and transferrin receptor 1 distribution was shifted from the

52 k has demonstrated the requirement for human transferrin receptor 1 for virus entry, and the absence

53 IRP2 RNA binding is correlated with reduced transferrin receptor 1 mRNA abundance.

54 this, we found that IOP1 knockdown increases transferrin receptor 1 mRNA levels and decreases ferriti

55 Iron-loaded transferrin binds to transferrin receptor 1 on the surface of most body cells

56 rom transferrin without increasing levels of transferrin receptor 1 or the uptake of transferrin.

57 cellular iron was associated with increased transferrin receptor 1 protein and mRNA levels and incre

58 Western blot analysis revealed a decline in transferrin receptor 1 protein levels following inductio

59 pathogenic New World arenaviruses use human transferrin receptor 1 to enter cells.

60 ession of the mesangial IgA1 receptor, TfR1 (transferrin receptor 1).

61 volved in iron metabolism (e.g. ferritin and transferrin receptor 1).

62 We demonstrate that loss of transferrin receptor 1, but not loss of ferroportin, can

63 However, loss of transferrin receptor 1, involved in iron uptake, caused

64 rived cell lines through a low-pH-dependent, transferrin receptor 1-independent mechanism, suggesting

65 ed for iron homeostasis such as ferritin and transferrin receptor 1.

66 Hepatic levels of transferrin receptors 1 and 2 and ZRT/IRT-like protein 1

67 sing expression cloning, we identified human transferrin receptor-1 (TfR1) as an important receptor f

68 rristatin (NSC30611) acts by down-regulating transferrin receptor-1 (TfR1) via receptor degradation.

69 sion of hepcidin and increased expression of transferrin receptor-1 and erythroferrone, suggesting th

70 egulates iron homeostasis components such as transferrin receptor-1 and ferritin-H in hepatic and ske

71 n-responsive elements present in the UTRs of transferrin receptor-1 and ferritin-H transcripts.

72 iron-responsive elements present in UTRs of transferrin receptor-1 and ferritin-H.

73 , divalent metal transporter-1, ferritin and transferrin receptor-1 and greater accumulation of iron.

74 fectively depleted cellular Fe, resulting in transferrin receptor-1 up-regulation, ferritin down-regu

75 Increased transferrin receptor-1, decreased ferritin-H, and increa

76 specifically with its cell-surface receptor transferrin receptor-1.

77 Mutations in the transmembrane glycoproteins transferrin receptor 2 (TfR2) and HFE are associated wit

78 HFE and transferrin receptor 2 (TFR2) are each necessary for the

79 Mutations in transferrin receptor 2 (TfR2) cause a rare form of the h

80 utations in hemochromatosis protein (HFE) or transferrin receptor 2 (TFR2) cause hereditary hemochrom

81 Transferrin receptor 2 (TFR2) contributes to hepcidin re

82 Embryos with transferrin-a or transferrin receptor 2 (TfR2) deficiency exhibited low l

83 Transplanting TM1 into transferrin receptor 2 (TfR2) induces Golgi accumulation

84 Transferrin receptor 2 (TfR2) is a homolog of transferri

85 Mutations in HFE, transferrin receptor 2 (Tfr2), hemojuvelin (HJV), or bon

86 regulatory genes, hemochromatosis (Hfe) and transferrin receptor 2 (Tfr2).

87 hereditary hemochromatosis proteins HFE and transferrin receptor 2 may intersect with the BMP pathwa

88 n), HFE (hemochromatosis protein), and TfR2 (transferrin receptor 2), these proteins do not control t

89 atosis-related proteins hemojuvelin, HFE and transferrin receptor 2, also regulates hepcidin expressi

90 Expression of human TfR1, but not human transferrin receptor 2, in hamster cell lines markedly e

91 (BMP6), hereditary hemochromatosis protein, transferrin receptor 2, matriptase-2, neogenin, BMP rece

92 he hereditary hemochromatosis protein (HFE), transferrin-receptor 2 (TfR2), hemojuvelin, hepcidin, or

93 iron, including HFE and, in rarer instances, transferrin-receptor 2 and hemojuvelin, or make its rece

94 Hemojuvelin (HJV), HFE, and transferrin receptor-2 (TfR2) facilitate this process pr

95 s been associated with mutations in the HFE, transferrin receptor-2 (TfR2), and hemojuvelin (HJV) gen

96 nclude newly identified interactions between transferrin receptor-2 and the erythropoietin receptor.

97 tes cellular iron uptake by interacting with transferrin receptor, a crucial protein during erythropo

98 ovary cells with a GFP-tagged transmembrane transferrin receptor, a well-known benchmark of membrane

99 Expression of transferrin receptor and 24p3R were reduced in tubules f

100 issorting of AP-1B-dependent cargos, such as transferrin receptor and a truncated low-density lipopro

101 nt receptors in T cell progenitors: CD71 the transferrin receptor and CD98 a subunit of L-amino acid

102 M images identified < or =200 nm clusters of transferrin receptor and clathrin light chain at < or =2

103 nin virus (JUNV) failed to down-regulate the transferrin receptor and did not induce superinfection e

104 uryi, has been recently demonstrated to bind transferrin receptor and exhibit potential anticancer ef

105 determined that CSCs preferentially require transferrin receptor and ferritin, two core iron regulat

106 tamate, and stabilizes surface expression of transferrin receptor and GLAST transporter.

107 lass I partially localized together with the transferrin receptor and internalized transferrin in end

108 many types of cancer cell lines by targeting transferrin receptor and modulating nuclear factor-kappa

109 th factor type-I receptor localized with the transferrin receptor and Rab11-positive endosomes in a l

110 brogates the somatodendritic polarity of the transferrin receptor and several glutamate receptor type

111 lathrin-mediated internalization of both the transferrin receptor and the beta2 adrenergic receptor.

112 We further found that the cell surface transferrin receptor and the glutamine-fueled intracellu

113 teractions between the basolateral signal of transferrin receptor and the medium subunits of both AP-

114 eceptors and plasma membrane lipids, such as transferrin receptors and sphingomyelin, are delivered t

115 host cell iron (e.g. up-regulation of Tfrc (transferrin receptor) and Lcn2 (lipocalin 2)), facilitat

116 l recycling endosomes positive for Rab11 and transferrin receptor, and CvpA membrane interactions wer

117 alysis was used to determine the presence of transferrin receptor, and ELISA was used to determine to

118 n the aged RPE/choroid, whereas transferrin, transferrin receptor, and ferroportin mRNAs did not chan

119 Serum ferritin, serum transferrin receptor, and hemoglobin concentrations were

120 coexpressing Dendra2-hemagglutinin, PAmKate-transferrin receptor, and PAmCherry1-beta-actin fusion c

121 on and vitamin A biomarkers (ferritin, serum transferrin receptor, and retinol binding protein) in se

122 e binding partners of these deposits (sCD89, transferrin receptor, and transglutaminase 2) decreased

123 ritin, transferrin saturation, serum soluble transferrin receptors, and the serum soluble transferrin

124 ndosomes co-localized with subsets of Rab5-, transferrin receptor-, and Lamp1/Lysotracker-marked comp

125 i-intracellular adhesion molecule 1 and anti-transferrin receptor antibodies.

126 = 200 nm, height (h) = 200 nm) labeled with transferrin receptor antibody (NP-OKT9) or human transfe

127 nhibit receptor activity simultaneously; and transferrin receptor antibody, to target the tumor vascu

128 leaves unchanged the rate by which MC4R and transferrin receptor are constitutively excluded from th

129 constitutively recycled, HSP90-independent, transferrin receptor are found within modified endosomes

130 We found that transferrin receptors are delivered selectively from cla

131 The effect of GA mediated through transferrin receptor as down-regulation of the receptor

132 rin uptake is due to a decrease in available transferrin receptor at the cell surface, and not to a s

133 in uptake in mitosis occurs despite abundant transferrin receptor at the surface of HeLa cells.

134 approach using expression of a biotinylated transferrin receptor (bTfnR) and controlling its local c

135 ith the endosomal markers including EEA1 and transferrin receptors but also with the TGN marker synta

136 ers and found that the TM motifs of CD40 and transferrin receptor, but not that of CD45, could functi

137 rine brain endothelioma cells overexpressing transferrin receptors, by about 1.4-fold and 2.3-fold co

138 (Tf) and evaluate the ability of the natural transferrin receptor CD71 to modulate immunity.

139 l precursors that can be graded by levels of transferrin receptor (CD71) expression.

140 The transferrin receptor (CD71) is up-regulated in duodenal

141 /proerythroblast stage, a point at which the transferrin receptor (CD71) is upregulated, iron is impo

142 owever, the selective tropism of P vivax for transferrin receptor (CD71)-positive reticulocytes remai

143 he mTOR-dependent cell surface expression of transferrin receptor (CD71).

144 surface of HeLa cells and inhibited LDLR and transferrin receptor clustering.

145 anism to induce transport of the transferrin/transferrin receptor complex across the BBB.

146 n calculated from serum ferritin and soluble transferrin receptor concentrations allows for the evalu

147 e calculated from serum ferritin and soluble transferrin receptor concentrations, can be used to asse

148 cality of current biomarkers such as soluble transferrin-receptor concentrations and others, and caus

149 ing spreading, but endoplasmic reticulum and transferrin receptor-containing vesicles are not.

150 creased early in flight, and transferrin and transferrin receptors decreased later, which indicated t

151 which stalled transit of a1 and transferrin-transferrin receptor, decreased proton efflux, and reduc

152 For iron, this regulation is achieved by transferrin receptor, DMT1, and ferroportin, whereas mam

153 pe SH3TC2, but not mutant SH3TC2, influences transferrin receptor dynamics, consistent with a functio

154 CD4, the asialoglycoprotein receptor, or the transferrin receptor eliminates intramembrane proteolysi

155 equence into the proteins sonic hedgehog and transferrin receptor enabled good in vitro and in vivo P

156 erfering dynamin mutant (Dyn/K44A) inhibited transferrin receptor endocytosis, it had no effect on ph

157 tively correlated with the levels of soluble transferrin receptor, erythropoietin and ferritin.

158 rformed PALM imaging using PAmCherry1-tagged transferrin receptor expressed alone or with photoactiva

159 This was reflected in increased transferrin receptor expression and increased splenic ir

160 ginase-1 and YM1 transcription and increased transferrin receptor expression by phagocytic cells.

161 Furthermore, the decrease in transferrin receptor expression in the microvasculature

162 oehner et al. (2014) describe a modular anti-transferrin receptor Fab approach for shuttling therapeu

163 d levels of ferritin and increased levels of transferrin receptor, features characteristic of cellula

164 transferrin receptors, and the serum soluble transferrin receptors-ferritin index are more accurate t

165 ron can effectively reach the brain by using transferrin receptors for crossing the blood-brain barri

166 tures, known mediators of rapid recycling of transferrin receptor from endosomes.

167 normal values: ferritin < or = 8.7 microg/L, transferrin receptors > or = 8.4 microg/mL, and transfer

168 Blood concentrations of ferritin, transferrin receptor, hemoglobin, and red cell indexes w

169 that mislocalize the dendritic marker human transferrin receptor (hTfR), we found that kinesin heavy

170 nt glycoprotein, GP1, and cell surface human transferrin receptor (hTfR1).

171 Consistent with this, there was stronger transferrin receptor immunoreactivity in the light-expos

172 tially colocalizes with TGN38 at the TGN and transferrin receptors in RE.

173 the protein level, decreased transferrin and transferrin receptor, increased ferritin and ceruloplasm

174 ical early endosomal recycling receptor, the transferrin receptor, indicating that this viral protein

175 pid stress disrupted later steps of MC4R and transferrin receptor internalization to endosomes as wel

176 ugh integrin beta1 endocytosis was impaired, transferrin receptor internalization was unaffected.

177 rrin receptor recycling but has no effect on transferrin receptor internalization.

178 e for Rabenosyn-5 in determining the fate of transferrin receptors internalized by clathrin-mediated

179 e for the first time that endocytosis of the transferrin receptor is a regulated process that require

180 ereas the CME of constitutively internalized transferrin receptors is mainly dependent on the ubiquit

181 es detecting activated complement factor C3, transferrin receptor, L-ferritin, and macrophages.

182 tus (ferritin level, transferrin saturation, transferrin receptor level, reticulocyte hemoglobin leve

183 iron availability, as noted by a decrease in transferrin receptor levels and iron uptake from transfe

184 ) and negatively correlated with the soluble transferrin receptor/log(ferritin) ratio but not correla

185 c characterization, these studies prove that transferrin receptor-mediated endocytosis is a viable me

186 f zinc finger nucleases (ZFN) proteins using transferrin receptor-mediated endocytosis.

187 ize, low cellular toxicity and the efficient transferrin receptor-mediated uptake render the AspA tag

188 Transferrin receptor mRNA (Tfrc), an indicator of iron l

189 Moreover, quantification of transferrin receptor mRNA in single cells agrees well wi

190 Type 1 transferrin receptor mRNA was unexpectedly decreased in

191 Transferrin receptor mRNA, which contains two highly con

192 posomal preparation was also targeted to the transferrin receptor of cancer cells by modifying the su

193 >/=1 biomarker of iron [ferritin or soluble transferrin receptor or vitamin A status (retinol-bindin

194 on hemoglobin, serum ferritin (SF), soluble transferrin receptor, or body iron was conducted.

195 r iron uptake by endocytosis of Fe(3+)-bound transferrin receptors, or after lysosomal degradation of

196 stricted to this membrane cargo, however, as transferrin receptors packaged in the same population of

197 ized by J774.2 cells and accumulates in CD71 transferrin receptor-positive endosomes.

198 ically isolated labeled RBCs and in isolated transferrin receptor-positivereticulocytes was used to d

199 NA 2.7-fold after 11 days and also increased transferrin receptor protein.

200 0.22; beta = -0.17 (95% CI: -0.25, -0.09)], transferrin receptor [R(2) = 0.23; beta = 2.79 (95% CI:

201 activating protein for Rab4A that regulates transferrin receptor recycling and EGFR trafficking and

202 , but not the inactive R494A mutant, reduces transferrin receptor recycling but has no effect on tran

203 ation of Bves function specifically inhibits transferrin receptor recycling, and results in gastrulat

204 the modified CLC reduces beta1-integrin and transferrin receptor recycling, as well as cell migratio

205 ing complex pathway, its knockdown arresting transferrin receptor recycling.

206 nd AP2-dependent cargoes, integrin beta1 and transferrin receptor, respectively.

207 cysteines 556 and 558 on the surface of the transferrin receptor resulting in subsequent endocytic u

208 ed concentrations of erythropoietin, soluble transferrin receptor (sCD71), and thrombopoietin.

209 that is calculated from ferritin and soluble transferrin receptor (sTfR) allows for the evaluation of

210 < or = 0.05), and concentrations of soluble transferrin receptor (sTfR) and hemoglobin and the red c

211 ons.We assessed the relation between soluble transferrin receptor (sTfR) concentrations and inflammat

212 serum ferritin decreased (P < 0.0001), serum transferrin receptor (sTfR) increased (P < 0.0001), and

213 Soluble transferrin receptor (sTfR) is thought to be unaffected

214 n, ferritin, C-reactive protein, and soluble transferrin receptor (sTfR) strongly predicted incorpora

215 wich assay (SA) for the detection of soluble transferrin receptor (sTfR), a biomarker of IDA, on a ph

216 time, measured by sFer, hemoglobin, soluble transferrin receptor (sTfR), and estimated total body ir

217 ir relations with serum ferritin (SF), serum transferrin receptor (sTfR), and hemoglobin.

218 rically to include plasma ferritin), soluble transferrin receptor (sTfR), and total body iron (TBI) w

219 line hemoglobin, ferritin, hepcidin, soluble transferrin receptor (sTfR), and transferrin were measur

220 in (SF), transferrin saturation, and soluble transferrin receptor (sTfR), as well as erythrocyte prot

221 timated on the basis of plasma iron, soluble transferrin receptor (sTfR), ferritin, transferrin, tran

222 ess hemoglobin, serum ferritin (SF), soluble transferrin receptor (sTfR), hepcidin, serum iron, eryth

223 iciency, defined by raised levels of soluble transferrin receptor (sTfR), was investigated in 98 pati

224 Similar results are found for transferrin receptor, suggesting a general mechanism of

225 r trafficking of the endogenously expressing transferrin receptor, suggesting ethanol does not have a

226 followed an innovative approach of combining transferrin receptor targeting with enhanced cell penetr

227 T-cells and induced large vacuoles marked by transferrin receptor, TCR, and SNAREs implicated in TCR-

228 o specifically adsorb His-tagged transferrin-transferrin receptor (Tf-TfR) complexes from insect and

229 epidermal growth factor receptor (EGFR) and transferrin receptor (TfnR) exhibited changes in steady-

230 e found that Arf6 colocalized with AP-1B and transferrin receptor (TfnR) in REs.

231 duodenal cytochrome b (Dcytb) 1.8-fold, and transferrin receptor (TfR) 1.8-fold.

232 t external cues induced up-regulation of the transferrin receptor (TfR) and down-regulation of ferrit

233 ealed differences in the dynamic behavior of Transferrin Receptor (TfR) and Langerin proteins.

234 on depletion, using iron chelators targeting transferrin receptor (TfR) and ribonucleotide reductase

235 aracterized basolateral protein markers, the transferrin receptor (TfR) and the vesicular stomatitis

236 tosis, plasma membrane receptors such as the transferrin receptor (TfR) are internalized by a caveola

237 ch iron loaded transferrin (Tf) binds to the transferrin receptor (TfR) at the cell surface.

238 The P2Ns manifest transferrin receptor (TfR) colocalization in ex vivo int

239 res and impairs recycling of the transferrin-transferrin receptor (TfR) complex to the plasma membran

240 Antibodies to transferrin receptor (TfR) have potential use for therap

241 characterize the organization of pIgA-R and transferrin receptor (TFR) in endocytic membranes of pol

242 Our results identify a role for PICALM in transferrin receptor (TfR) internalization and demonstra

243 Increased surface expression of transferrin receptor (TfR) is a downstream event of MYC

244 Transferrin receptor (TFR) is an important iron transpor

245 te of iron acquisition in vertebrates is the transferrin receptor (TfR) mediated endocytotic pathway,

246 iron ions which are delivered to cells in a transferrin receptor (TFR) mediated process.

247 (hTF) molecules to the specific homodimeric transferrin receptor (TFR) on the cell surface.

248 rom raccoons do not efficiently bind the dog transferrin receptor (TfR) or infect dog cells, a single

249 We have investigated the transferrin receptor (TfR) pathway, which is not only es

250 Transferrin receptor (TfR) represents a unique target fo

251 target a protein complex of transferrin and transferrin receptor (TfR) through a non-canonical allos

252 n alone (BI-ferritin) or the ratio of plasma transferrin receptor (TfR) to ferritin (BI-TfR/ferritin)

253 in the form of tunable nanosystems (NS) for transferrin receptor (TfR) utilizing gambogic acid (GA),

254 monoclonal antibody (MAb) against the mouse transferrin receptor (TfR), and these fusion proteins ar

255 monoclonal antibody (MAb) against the mouse transferrin receptor (TfR), and this fusion protein is d

256 Both viruses bind their host transferrin receptor (TfR), enter cells by clathrin-medi

257 Similar to the constitutive endocytosis of transferrin receptor (TfR), ligand- triggered endocytosi

258 g because of the active participation of the transferrin receptor (TFR), salt, a chelator, lobe-lobe

259 t epithelia to relocate AP-1B cargo, such as transferrin receptor (TfR), to the apical PM.

260 monoclonal antibody (MAb) against the mouse transferrin receptor (TfR), which is designated as the c

261 monoclonal antibody (MAb) against the mouse transferrin receptor (TfR), which is designated the cTfR

262 NHE5 is associated with transferrin receptor (TfR)- and Rab11-positive recycling

263 fect on the clathrin-mediated endocytosis of transferrin receptor (TfR).

264 conditions, as well as their ability to bind transferrin receptor (TfR).

265 Transferrin receptor (TfR, CD71) has long been a therape

266 of 3 abnormal ferritin (< 12 mug/L), soluble transferrin receptor (TfR; > 8.3 mg/L), or zinc protopor

267 anine parvovirus (CPV) capsids with cellular transferrin receptors (TfR) on the surfaces of live feli

268 ptake of systemically dosed antibodies (anti-transferrin receptor [TfR] bispecific versus control ant

269 Ti2HsTf (2 equiv) binds the transferrin receptor TfR1 with Kd1 = 6.3 +/- 0.4 nM and

270 nd significance of positive selection on the transferrin receptor TfR1, a housekeeping protein requir

271 Transferrin Receptor (TfR1) is the cell-surface receptor

272 consequence, IRP1 target genes, such as the transferrin receptor (TfR1), a membrane-associated glyco

273 PN), the iron efflux pump, is decreased, and transferrin receptor (TFR1), the iron importer, is incre

274 ily via receptor-mediated endocytosis of the transferrin receptor (Tfr1).

275 transmembrane protease, serine 6 (TMPRSS6), transferrin receptor (TFR2), N-acetyltransferase 2 (aryl

276 biquitin C (UBC) in head and neck cancer and Transferrin receptor (TFRC) and beta-Glucuronidase (GUSB

277 y recognized CPV host-to different carnivore transferrin receptors (TfRs) using single-particle track

278 ed in dynamin-dependent endosomes labeled by transferrin receptors (TfRs).

279 icroscopy and biochemical analyses show that transferrin receptor, the cellular receptor for canine p

280 ot other cell surface receptors, such as the transferrin receptor, the receptor tyrosine kinase TrkA,

281 0 mg/kg and calculated from the log ratio of transferrin receptor to ferritin (the body iron model) t

282 ressed in vivo and has been coexpressed with transferrin receptor to increase iron loading in cells.

283 carnivores due to its interactions with the transferrin receptor to mediate infection.

284 both Rab11 and the constitutively recycling transferrin receptor to the periphery of cells.

285 d an increased dependence of Cd1 GP on human transferrin receptor type 1 (hTfR-1) for entry, which ma

286 ized by different abilities to use the human transferrin receptor type 1 (hTfR1) protein as a recepto

287 ve feline panleukopenia virus (FPV) bind the transferrin receptor type 1 (TfR) to infect their host c

288 300Lys) altered the binding of the capsid to transferrin receptor type 1 (TfR), particularly during v

289 mutations that allowed binding to the canine transferrin receptor type 1 (TfR).

290 ization of beta1 integrins without affecting transferrin receptor uptake.

291 ytosis and coincided with the recruitment of transferrin receptor, VAMP3, and dynamin-2.

292 umours respect to surrounding liver, whereas transferrin receptor was up-regulated.

293 For example, the transferrin receptor was upregulated in both light-expos

294 rtantly, the constitutive internalization of transferrin receptors was unaffected by either treatment

295 ed blood cell distribution width and soluble transferrin receptor were elevated (P < 0.05), and serum

296 status biomarkers (ie, ferritin and soluble transferrin receptor) were significantly associated with

297 points, internalized GPR17 co-localized with transferrin receptor, whereas at later times it partiall

298 interfering RNA changed the localization of transferrin receptor, which is a marker of the recycling

299 DNA damage, p53 induced FTH1 and suppressed transferrin receptor, which regulates iron entry into ce

300 tress, including a failure to upregulate the transferrin receptor, which we show is a novel stress ta