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1 ive product shows homology to the glycerol-3-phosphate transporter.
2 al, and structural studies of the glycerol-3-phosphate transporter.
3 onse, a marked increase in mRNA levels for a phosphate transporter.
4 creases in cells that are defective in other phosphate transporters.
5 se (P46), and putative glucose and inorganic phosphate transporters.
6 nd OsSPX-MFS2, these genes encoding vacuolar phosphate transporters.
7 rs it easily incorporated into cells via the phosphate transporters.
8 er from the unrelated lactose and glycerol 3-phosphate transporters.
9 f H(+)-coupled phosphate transporters of the PHOSPHATE TRANSPORTER 1 (PHT1) family(2) at the plasma m
10 atalysing Pi uptake in chlorophytes, whereas PHOSPHATE TRANSPORTER 1 (PHT1) proteins are the H(+) /Pi
11 ch is a phosphate analog and a substrate for Phosphate transporter 1 (Pht1) transporters.
12     Whereas KoRV-A uses the sodium-dependent phosphate transporter 1 (PiT1) as a receptor, KoRV-B emp
13     We tested this hypothesis using Vacuolar Phosphate Transporter 1 (VPT1), a SPX domain-containing
14 the transmembrane multipass sodium-dependent phosphate transporter 1 PiT1/SLC20A1 as the receptor for
15 nucleotides (ASOs) specific to the glucose 6-phosphate transporter-1 (G6PT1) enabled reduction of hep
16 ith structural similarity to a type 1 sodium phosphate transporter, 12 novel histone genes, and a gen
17 the binding affinity to the sodium-dependent phosphate transporter 2a (Npt2a) as compared with WT PDZ
18 iants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter 2a and 2c are rare causes of phosp
19 argets including the Npt2a (sodium-dependent phosphate transporter 2a).
20 , namely RAM2, STUNTED ARBUSCULES (STR), and PHOSPHATE TRANSPORTER 4 (PT4), in Nicotiana benthamiana
21 e homeostasis through effects on alternative phosphate transporter activity and alveolar osteoprotege
22 ntified NaSIPP, a mitochondrial protein with phosphate transporter activity, as a novel NaStEP-intera
23                     RPTECs express the NPT2A phosphate transporter, alphaKlotho, FGFR1, FGFR3, FGFR4,
24        Ram-1 acts as both a sodium-dependent phosphate transporter and a receptor for amphotropic ret
25 sive disease caused by mutation of glucose-6-phosphate transporter and characterized by altered glyco
26 t mutant revealed that MtPT1 is a functional phosphate transporter and Northern analyses revealed tha
27 l stores via the production of high-affinity phosphate transporters and the synthesis of intracellula
28  mutants indicated that MtPT4 functions as a phosphate transporter, and estimates of the K(m) suggest
29                PHO84 encodes a high-affinity phosphate transporter, and mutations in PHO86 cause many
30 ding the PHOX alkaline phosphatase, the PTB2 phosphate transporter, and the regulatory element PSR1.
31 PHO84 gene encodes a high affinity inorganic phosphate transporter, and we find that its disruption r
32 enes encoding glycogen biosynthetic enzymes, phosphate transporters, and the RNA polymerase sigma-38
33 (A-MuLV) utilizes the Pit-2 sodium-dependent phosphate transporter as a cell surface receptor to infe
34 el that used the Escherichia coli glycerol 3-phosphate transporter as a template has been described.
35  (A-MuLV) utilizes the PiT2 sodium-dependent phosphate transporter as its cell surface receptor to in
36 ter structures (lactose permease, glycerol-3-phosphate transporter) as well as to a low resolution pr
37 of SOMBRERO is associated with expression of phosphate transporters at the root tip.
38                                              PHOSPHATE TRANSPORTER B (PTB) proteins are hypothesized
39       Hence, the data support the glycerol 3-phosphate transporter-based homology model of PCFT and t
40 brate brain-specific Na+-dependent inorganic phosphate transporter (BNPI).
41  significantly different from the plant root phosphate transporters cloned to date.
42 nces from phoA, senX3, and the high-affinity phosphate transporter component pstS, demonstrating dire
43       Deletion of pstA1, which encodes a Pst phosphate transporter component, causes constitutive act
44 dy of neutrophils deficient in the glucose-6-phosphate transporter, describe a novel role for the per
45 as a plasma membrane Na+-dependent inorganic phosphate transporter (differentiation-associated Na+/P(
46 s with short sequence motifs shared by known phosphate transporters enabled the identification of a n
47 regulate expression of 3 members of the PHT1 phosphate transporter family SiPHT1;2 SiPHT1;3 and SiPHT
48 orters enabled the identification of a novel phosphate transporter from M. truncatula, MtPT4.
49 e demonstrate in a eukaryotic, high-affinity phosphate transporter from Piriformospora indica (PiPT)
50 ion was accompanied by delocalization of the phosphate transporter from the plasma membrane.
51 ucose homeostasis, is comprised of glucose 6-phosphate transporter (G6PT) and G6Pase.
52  1b is caused by a deficiency in a glucose 6-phosphate transporter (G6PT) that translocates glucose 6
53 ) is caused by a deficiency in the glucose-6-phosphate transporter (G6PT), a 10 transmembrane domain
54 type-Ib (GSD-Ib), deficient in the glucose-6-phosphate transporter (G6PT), is characterized by impair
55 ciency in a ubiquitously expressed glucose-6-phosphate transporter (G6PT).
56 ) is caused by a deficiency in the glucose-6-phosphate transporter (G6PT).
57  transcription factor that mediates arsenate/phosphate transporter gene expression and restricts arse
58                                  Recently, a phosphate transporter gene in potato was shown to be ind
59               Mutations of Fgf23, Klotho and phosphate transporter genes have been identified to caus
60                    Previously, we cloned two phosphate transporter genes, MtPT1 and MtPT2 from Medica
61 e, several phosphate-starvation response and phosphate-transporter genes displayed reduced induction
62 ve phosphate sensor), and the uhpT (a hexose phosphate transporter) genes.
63 lease correlated with the level of glucose 6-phosphate transporter (Glc-6-PT) mRNA, which was found t
64 ency in the ubiquitously expressed glucose 6-phosphate transporter (Glc-6-PT).
65  to that of the distantly related glycerol 3-phosphate transporter GlpT.
66 ures of the related transporters, glycerol-3-phosphate transporter (GlpT) and lactose permease (LacY)
67                         In the sn-glycerol-3-phosphate transporter (GlpT) from Escherichia coli, the
68 n to the crystal structure of the glycerol 3-phosphate transporter (GlpT) from Escherichia coli.
69                                   Glycerol 3-phosphate transporter (GlpT) mediates the import of glyc
70  glycerol metabolism, including a glycerol-3-phosphate transporter (GlpT), a glycerol-3-phosphate deh
71 ster phosphodiesterase (GlpQ) and glycerol-3-phosphate transporter (GlpT), respectively.
72  Using the x-ray structure of the glycerol 3-phosphate transporter (GlpT), we devised a model for the
73 e one hand, and up-regulation of a GLUCOSE-6-PHOSPHATE TRANSPORTER (GPT2), on the other hand.
74 enes encode proteins that comprise inorganic phosphate transporters, growth factor and its receptor,
75                            The bidirectional phosphate transporter has an intrinsic dissociation cons
76                       Similar proton-coupled phosphate transporters have been found in different prot
77   Two cDNAs (AtPT1 and AtPT2) encoding plant phosphate transporters have been isolated from a library
78                         The sodium-dependent phosphate transporter (HOST5/SLC34A2) expression was ass
79            We further characterized putative phosphate transporters, identifying two new phosphate tr
80 traints drive the evolution of high-affinity phosphate transporters; (ii) Charge-, hydrogen- and magn
81 m that controls expression of the UhpT sugar phosphate transporter in Escherichia coli in response to
82 es of omics data to identify XPR1 as a major phosphate transporter in platelets.
83    The similarity of Pho84p, a high-affinity phosphate transporter in Saccharomyces cerevisiae, to th
84 the wild type, implying an important role of phosphate transporters in PFOS sensing.
85 began these studies to determine the role of phosphate transporters in signaling phosphate starvation
86  as well as that of PiT1 and PiT2 (inorganic phosphate transporters), in blood and airway neutrophils
87                  In addition, the glycerol-3-phosphate transporter is monomeric and stable over a wid
88  this approach, we find that the affinity of phosphate transporters is related to the concentration o
89 coli uhpT gene, encoding the inducible sugar phosphate transporter, is dependent on the response regu
90 s of root symbioses, it is apparent that the phosphate transporters known to operate at the root-soil
91                                  White lupin phosphate transporter (LaPT1) and secreted acid phosphat
92  operon, encoding homologues of an inorganic phosphate transporter, leads to constitutive expression
93 y we identified MtPT4, a Medicago truncatula phosphate transporter located in the periarbuscular memb
94 ate uptake through solute carrier family 20 (phosphate transporter), member 1 (SLC20a1) supports oste
95 domain" that contains the symbiosis-specific phosphate transporter, MtPT4, and an "arbuscule trunk do
96                     In addition, analysis of phosphate transporter mutants implicates the trans-Golgi
97 ion, we investigated the effect of glucose-6-phosphate transporter mutation on immune cell homeostasi
98  activity and protein of the principal renal phosphate transporter NaPi-2a.
99 by the action of the apical sodium-dependent phosphate transporters, NaPi-IIa/NaPi-IIc/Pit2.
100 , reduced expression of the sodium-dependent phosphate transporter NPT2a in the proximal tubules, and
101 A2 and a subpopulation of germ cells express phosphate transporter NPT2a, Osteocalcin, and RUNX2 high
102 nd increased protein expression of the renal phosphate transporter Npt2a.
103  kidney by retrieval of the sodium-dependent phosphate transporters (Npt2a and Npt2c) from the apical
104  (PTH)-responsive sequestration of the renal phosphate transporter, Npt2a, with ensuing urinary phosp
105 nternalization of the major sodium-dependent phosphate transporter, Npt2a.
106                              UhpT, the sugar phosphate transporter of Escherichia coli, acts to excha
107 h genetic deficiency in either the glucose-6-phosphate transporter of the endoplasmic reticulum (G6PT
108 from the soil and is distinct from the other phosphate transporter of this class described to date.
109  acid sequence similarity with high-affinity phosphate transporters of Saccharomyces cerevisiae, Neur
110 te by adapting the abundance of H(+)-coupled phosphate transporters of the PHOSPHATE TRANSPORTER 1 (P
111 thin the plant in part through the action of phosphate transporters of the PHT1 family.
112                  Overexpression of unrelated phosphate transporters or a glycerophosphoinositol trans
113 d rice genome at hand, only the Oryza sativa phosphate transporter (OsPT) gene OsPT11 was specificall
114    The double mutants of PGK3 and the triose-phosphate transporter (pgk3.2 tpt3) displayed a drastic
115 ession of Arabidopsis (Arabidopsis thaliana) phosphate transporter PHO1;H3 comprising MYB15, MYB84, b
116 1 signaling in C. albicans revealed that the phosphate transporter Pho84 is required for normal TORC1
117  coding-region polymorphism in the inorganic phosphate transporter PHO84 underlies sensitivity to two
118 y of S. cerevisiae transporters, including a phosphate transporter (Pho84p), and both inositol transp
119  phosphate transporters, identifying two new phosphate transporters, PHO90 and PHO91.
120 -affinity phosphate-binding component of the phosphate transporter, phoA, an alkaline phosphatase, an
121 rol 3-phosphate dehydrogenase and glycerol 3-phosphate transporter/phosphodiesterase, respectively.
122 nt, which requires the precise regulation of phosphate transporter (PHT) trafficking from the endopla
123 disrupting phosphorus metabolism to increase phosphate transporter (PHT) transcript.
124 all subunit RBCS2B [RBCS]) or heterotrophic (phosphate transporter PHT1.2 [PHT]) cell-specific promot
125    We showed that arsenate repression of the phosphate transporter PHT1;1 is associated with the degr
126 d was dependent on the activity of the major phosphate transporter PHT1;4.
127        MVB-mediated sorting of high-affinity phosphate transporters (PHT1) to the vacuole limits thei
128                              The Arabidopsis phosphate transporter PHT4;1 was previously localized to
129 ransmembrane monomeric Piriformospora indica phosphate transporter (PiPT), a member of the major faci
130 fungal (Piriformospora indica) high-affinity phosphate transporter, PiPT, in an inward-facing occlude
131 ormal cellular functions as sodium-dependent phosphate transporters (Pit-1 and Pit-2, respectively).
132    We demonstrated that knockdown of XPR1, a phosphate transporter present in MIN6m9 cells and pancre
133 ns bind specifically to cells expressing the phosphate transporter protein Pit1, demonstrating for th
134 ls expressing either of two widely expressed phosphate transporter proteins, Pit1 or Pit2.
135                   Expression of an inorganic phosphate transporter (PTA3) was enriched approximately
136 rice OsPT8 protein, which is a member of the phosphate transporters (PTs) Pht1 family and also plays
137 red to phosphate, modifies the expression of phosphate transporters (PTs).
138 etitive index assays, mutation of a putative phosphate transporter reduced in vivo competitiveness by
139 rst in plants, in coordination with arsenate/phosphate transporter repression, which immediately rest
140 ndent inorganic phosphate (Pi) cotransporter phosphate transporter/retrovirus receptor 1 (PiT-1).
141 utants implicates the trans-Golgi network in phosphate transporter secretion.
142 t SPX domains--which are found in eukaryotic phosphate transporters, signaling proteins, and inorgani
143 ple osteogenic differentiation genes and the phosphate transporter Slc20a1 in cerebral microvessels.
144 he human type III sodium-dependent inorganic phosphate transporter, SLC20A1, formerly known as PiT1.
145 ns specifically maintained expression of the phosphate transporter SLC20A2 at higher levels relative
146  knocked into the sodium-dependent inorganic phosphate transporter SLC34a1 locus, which is expressed
147 ses such as loss-of-function variants in the phosphate transporter SLC34A2.
148 d HOST5 codes for a type II sodium-dependent phosphate transporter (SLC34A2).
149 quisition (the Pho1 acid phosphatase and the phosphate transporter SPBC8E4.01c), without affecting th
150 FT, based upon theEscherichia coliglycerol 3-phosphate transporter structure, predicted that PCFT tra
151  B cell clones, are directed against the Mtb phosphate transporter subunit PstS1.
152  contains a unique set of proteins including phosphate transporters such as Medicago truncatula MtPT4
153  to utilize urea and possesses high-affinity phosphate transporter systems (phnCDE) for surviving pho
154                         We have identified a phosphate transporter (TcPho91) localized to the bladder
155 high-yielding rice cultivar modulates mainly phosphate transporters, TFs, auxin-responsive proteins,
156 seq analysis revealed the important roles of phosphate transporters, TFs, auxin-responsive proteins,
157 by Pi deficiency and arsenate, and encodes a phosphate transporter that has a high affinity for arsen
158 s in the SLC34A3 gene for a sodium-dependent phosphate transporter that were present in 5% cases comp
159 he lumen, and putative glucose and inorganic phosphate transporters that allow exit of the products o
160 rieved genome does not contain all inorganic phosphate transporters that are characteristic of PAOs (
161  as well as the eukaryotic organellar triose phosphate transporter (TPT) and nucleotide-sugar transpo
162 anscription-factor gene is flanked by triose-phosphate transporter (TPT) and RNA helicase genes [9].
163  in phosphate transporter1 (PHT1) family and phosphate transporter traffic facilitator1 (PHF1) in pho
164 hypothesis that the bacterium-derived hexose-phosphate transporter UhpC might have been the primordia
165 tein is required for expression of the sugar phosphate transporter UhpT in Escherichia coli and is re
166 the Escherichia coli uhpT gene for the sugar phosphate transporter UhpT in response to extracellular
167     Expression of the Escherichia coli sugar phosphate transporter UhpT is induced by extracellular g
168                                 In the sugar phosphate transporter UhpT, gain-of-function derivatives
169 otein which controls production of the sugar phosphate transporter UhpT.
170 that tightly regulate expression of a hexose phosphate transporter (UhpT).
171 ative feedback loops leads to bistability in phosphate transporter usage--individual cells express pr
172 on of transcripts encoding plant PHT1 family phosphate transporters varied among lines.
173                            Although vacuolar phosphate transporters (VPTs) are essential for plant ph
174         The uhpT gene, which encoded a sugar phosphate transporter, was the most frequently isolated
175 etic lethal phenotype was observed when five phosphate transporters were inactivated, and the contrib
176 exposed to As(V), transcript levels of As(V)/phosphate-transporters were similar or even higher than
177           We evaluated the expression of two phosphate transporters which we have found to be associa
178        Expression and activity of intestinal phosphate transporter, which did not change after nephre
179 te (apparently by both passive diffusion and phosphate transporters), with bulk root tissue Se concen
180                               Proton-coupled phosphate transporters within the major facilitator fami

 
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