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1 og of the Escherichia coli FadLEc long-chain fatty acid transporter.
2 l approaches to assess the role of NPC1 as a fatty acid transporter.
3 re independent of the role of any particular fatty acid transporter.
4 AMPs and PAMPs, as well as a long chain free fatty acid transporter.
5 ransport with TgFLP12 validates TgFLP12 as a fatty acid transporter.
6 pressed member of a family of six long chain fatty acid transporters.
7 but overexpressing acyl-CoA synthetase 1 and fatty acid transporter 1.
8                              Upregulation of fatty acid transporters 1 and 4 on MM cells mediated the
9 idney proximal tubules express transmembrane fatty acid transporter-2 (FATP2), encoded by Slc27a2, bu
10 , producing mutations in the very long chain fatty acid transporter, ALD protein.
11              mRNA levels of genes regulating fatty acid transporter and metabolic enzymes are suppres
12        Identification of several proteins as fatty acid transporters, and emerging evidence from gene
13 XR, PXR, and PPARgamma establishes this free fatty acid transporter as a common target of orphan nucl
14 identification of a putative plasma membrane fatty acid transporter as mitochondrial aspartate aminot
15    To this end, stable cell lines expressing fatty acid transporters as well as primary hepatocytes f
16  inactivation required the expression of the fatty-acid transporter carnitine palmitoyl transferase 1
17 ease in expression of Parkin (Park2) and the fatty acid transporter CD36 along with an increase in fa
18 PA-induced prometastatic memory requires the fatty acid transporter CD36 and is associated with the s
19 ted with an increased expression of the free fatty acid transporter CD36 and several accessory lipoge
20 we identified increased translocation of the fatty acid transporter CD36 from its endosomal storage c
21 epletion of KC2 or targeted silencing of the fatty acid transporter Cd36 highlighted a crucial contri
22  significantly upregulated the levels of the fatty acid transporter CD36 molecule (CD36) and adipose
23 ncrease in the uptake of (14)C-palmitate and fatty acid transporter CD36 that was further exacerbated
24                            Expression of the fatty acid transporter CD36 was dramatically increased i
25                            We found that the fatty acid transporter CD36 was upregulated in the S508A
26  translocation, plasmalemmal presence of the fatty acid transporter CD36, and myocellular lipid accum
27 ia and actively imported linoleic acid via a fatty acid transporter CD36.
28 adipogenesis regulators Pparg and Cebpa, and fatty acid transporter Cd36.
29 cially within a subpopulation expressing the fatty acid transporter CD36.
30 A or acetyl-CoA in the absence of changes in fatty acid transporters CD36 and CPT1 or beta-hydroxyacy
31 gnaling-related genes, such as Akt2, and the fatty-acid transporter CD36.
32                   mRNA levels of sarcolemmal fatty acid transporters (CD36, FATP6), acylation enzymes
33                   mRNA levels of sarcolemmal fatty acid transporters (CD36, FATP6), acylation enzymes
34 GAT1, a triglyceride synthesis gene, and the fatty acid transporter, CD36.
35 rt, which are rescued by deletion of CD36, a fatty acid transporter, despite persistent activation of
36 CL accompanied by the over-expression of the fatty acid transporter-encoding gene SLC27A1 as well as
37                            Of three membrane fatty acid transporters expressed in adipocytes, plasma
38 ity, but similar muscle glycolytic capacity, fatty acid transporter expression, and PPAR expression.
39 s of acyl-CoA synthesis), Slc27a2 (encodes a fatty acid transporter), Fabp2 (encodes fatty acid bindi
40                            The OM long-chain fatty acid transporter FadL from E. coli is a unique par
41  report crystal structures of the long-chain fatty acid transporter FadL from Escherichia coli at 2.6
42 olar) substrate binding to the OM long-chain fatty acid transporter FadL from Escherichia coli causes
43                  Sey1 and the L. pneumophila fatty acid transporter FadL were implicated in palmitate
44 e Escherichia coli outer membrane long-chain fatty acid transporter FadL.
45 dentification of this evolutionary conserved fatty acid transporter family will allow us to gain a be
46 port and are part of a subfamily of the FadL fatty acid transporter family.
47 Kazal-type trypsin inhibitor type 1; and the fatty acid transporter fatty acid transport protein 4 ha
48                An elevation in the levels of fatty acid transporter gene expression was also observed
49 nd adipocytes with a concomitant decrease in fatty acid transporter gene expression.
50 pecifically investigate the role of the Cd36 fatty acid transporter gene in the insulin-sensitizing a
51 ments clearly establish FATP1 as a regulated fatty acid transporter in both adipose tissue and muscle
52 expression of LRH1 metabolic sensor and CD36 fatty acid transporter in conjunction with changes in gl
53 ckout mouse model, the inhibition of CD36, a fatty acid transporter in ECs, led to a compensatory inc
54    This suggests that FATP4 is the principal fatty acid transporter in enterocytes and may constitute
55 We also demonstrate that Mce1 functions as a fatty acid transporter in Mtb and determine that facilit
56                Hepatic expression of Cd36, a fatty acid transporter, is enhanced in obese and diabeti
57 g with the basal higher expression levels of fatty acid transporters, led accumulation of long-chain
58 yond their main biological role as cytosolic fatty acid transporters, many aspects regarding their bi
59 CD36 by PXR and PPARgamma suggests that this fatty acid transporter may function as a common target o
60 ity of free fatty acids and the abundance of fatty acid transporters, may influence the rate of muscl
61 ing protein 1; and solute carrier family 27 (fatty acid transporter), member 2; and demonstrated that
62 er these proteins function as membrane-bound fatty acid transporters or as acyl-CoA synthetases, whic
63 nalysis of immunoprecipitated proteins, that fatty acid transporter protein 2 (FATP2) (also known as
64 ng also up-regulated placental expression of fatty acid transporter protein, metabolic signaling path
65 723/LucA and putative components of the Mce1 fatty acid transporter (Rv0200/OmamB, Rv0172/Mce1D, and
66 s levels of cluster of differentiation 36, a fatty acid transporter, through an intracellular signali
67 nd 1.4-fold up-regulation of plasma membrane fatty acid transporter/translocase proteins (glutamic-ox
68                           Gene expression of fatty acid transporters was greater in abdominal than fe
69  CD36, aspartate aminotransferase, caveolin) fatty acid transporters was measured.
70                                 If NPC1 is a fatty acid transporter, we expect to find fatty acid acc