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1 ich include ATP citrate lyase, ACC, FAS, and stearoyl-CoA desaturase.
2 ine motif required for catalytic activity in stearoyl-CoA desaturase.
3 oenzyme A synthase, fatty acid synthase, and stearoyl-CoA desaturase.
4 atory element binding protein (SREBP1c), and stearoyl-CoA desaturase.
5 se 1 (ACC1), fatty acid synthase (FASN), and stearoyl CoA desaturase 1 (SCD1)] to AML and eBL cell li
7 P-2 (vesicle-associated membrane protein 2), stearoyl CoA desaturase 1, and cAMP-specific phosphodies
9 Herein, we demonstrate that inhibition of stearoyl-CoA desaturase 1 (SCD-1) halts the biosynthesis
11 f the mice with a disruption in the gene for stearoyl-CoA desaturase 1 (SCD1) (SCD1-/-) is deficient
12 e model, here we show that expression of the stearoyl-CoA desaturase 1 (Scd1) gene is downregulated i
13 r strategies to combat this growing problem, stearoyl-CoA desaturase 1 (SCD1) inhibition has been pro
16 SREBPs (1a and 2) led to elevated mRNAs for stearoyl-CoA desaturase 1 (SCD1), an isoform that is det
17 r Xenopus kinesin-like protein 2 (TPX2), and stearoyl-CoA desaturase 1 (SCD1), significantly reduced
18 ChREBP overexpression induced expression of stearoyl-CoA desaturase 1 (Scd1), the enzyme responsible
20 oupling of fatty acid synthase activity from stearoyl-CoA desaturase 1 (SCD1)-mediated desaturation.
21 n as well as reduction in mRNA expression of stearoyl-CoA desaturase 1 and genes associated with fatt
22 that mice with a targeted disruption in the stearoyl-CoA desaturase 1 gene (SCD1-/-) have increased
25 seen with genetic deletion or inhibition of stearoyl-CoA desaturase 1 promotes inflammation, TLR4 hy
26 ohydrate response element-binding protein or stearoyl-CoA desaturase 1 resulted in lethality on high
27 ary cell line that overexpressed transfected stearoyl-CoA desaturase 1, a rate-limiting enzyme in the
28 pression, most notably reduced expression of stearoyl-CoA desaturase 1, a rate-limiting enzyme in the
29 n of SFA in the body is tightly regulated by stearoyl-CoA desaturase 1, an enzyme that converts endog
30 crophage LXR/RXR target genes, we identified stearoyl-CoA desaturases 1 and 2 (Scd1 and Scd2), and su
33 was also a significant downregulation of the stearoyl CoA desaturase-1 gene, which has been associate
34 ed hyperleptinemia without downregulation of stearoyl CoA desaturase-1 or fatty acid synthase and by
36 several accessory lipogenic enzymes, such as stearoyl-CoA desaturase-1 (SCD-1) and long chain free fa
38 sed the mRNA levels for fatty acid synthase, stearoyl-CoA desaturase-1 (SCD-1), and epidermal fatty a
39 ting a high activity of the lipogenic enzyme stearoyl-CoA desaturase-1 (SCD-1), has been shown to be
40 RNA levels and enzymatic activity of hepatic stearoyl-CoA desaturase-1 (SCD-1), which catalyzes the b
44 cell death effect ORCTL3 targets the enzyme stearoyl-CoA desaturase-1 (SCD1) in fatty acid metabolis
46 Genetic or pharmacological inhibition of stearoyl-CoA desaturase-1 (SCD1), the enzyme that conver
50 activate transcription of the genes encoding stearoyl-CoA desaturase-1 and -2, thereby markedly enhan
51 erides or in the exercise-suppressed hepatic stearoyl-CoA desaturase-1 and peroxisome proliferator-ac
52 r-activated receptor gamma2 (PPARgamma2) and stearoyl-CoA desaturase-1 and up-regulated PPARalpha ind
54 n in wild-type mice increased PPARgamma2 and stearoyl-CoA desaturase-1 mRNA and hepatic triglyceride
55 yl-CoA carboxylase, fatty acid synthase, and stearoyl-CoA desaturase-1 were all elevated markedly, as
56 yl-CoA carboxylase, fatty-acid synthase, and stearoyl-CoA desaturase-1 were increased in apoB/BATless
57 d-type mice, with the induction of the Scd1 (stearoyl-CoA desaturase-1) gene preceding that of other
58 e, glycerol-3-phosphate acyltransferase, and stearoyl-CoA desaturase-1) showed a complete failure of
59 y acid synthase, acetyl-CoA carboxylase, and stearoyl-CoA desaturase-1, were reduced in ob/ob-PPARgam
65 secondary analysis, each SD increase of log-stearoyl-coA desaturase activity (16:1n-7/16:0 ratio) wa
68 -binding cassette transporter A1 (ABCA1) and stearoyl CoA desaturase, and expression of these genes i
69 Lipocalin 2, haptoglobin, serum amyloid A3, stearoyl-CoA desaturase, and 11beta-hydroxysteroid dehyd
70 the molecular mechanism for the induction of stearoyl-CoA desaturase by peroxisome proliferators.
75 ) and other fatty acids on the expression of stearoyl-CoA desaturase gene 1 were investigated in full
76 ouse model with a targeted disruption of the stearoyl-CoA desaturase gene-1 (SCD1-/-) have revealed t
77 ce was identified at the N-terminus of mouse stearoyl-CoA desaturase I (SCD I) comprised of (30)KVKTV
78 tin in the cytoplasm of basal sebocytes, and stearoyl CoA desaturase in the cytoplasm of basal and lu
80 onse-element-binding protein-1 (SREBP-1) and stearoyl-CoA desaturase in the immortalized sebaceous gl
84 Analysis revealed that four of the genes [stearoyl-CoA desaturase; NADH-ubiquinone oxidoreductase
85 erilipin-5, adipose triglyceride lipase, and stearoyl-CoA desaturase protein was higher in the NWA gr
87 saturase (D5D), Delta6 desaturase (D6D), and stearoyl-CoA desaturase (SCD) activity and T2D risk.
89 h arachidonic acid resulted in a decrease in stearoyl-CoA desaturase (Scd) enzyme activity and scd1 m
92 T3-L1 preadipocyte cells are correlated with stearoyl-CoA desaturase (SCD) expression (mRNA and prote
93 f fatty acid uptake and synthesis and higher stearoyl-CoA desaturase (SCD) expression, Ncb5or(-/-) li
105 esis: four desaturases were induced, and one stearoyl-CoA desaturase (SCD) was strongly repressed.
108 atty acid metabolism, including induction of stearoyl-CoA desaturase (SCD)-1, which converts saturate
114 or depletion of the lipid metabolism enzymes stearoyl-CoA-desaturases (SCD) and S-adenosyl methionine
115 sion, its expression was compared to that of stearoyl CoA desaturase (Scd1) in B6 mice exposed to die
116 scle carnitine palmitoyl-transferase (MCPT), stearoyl CoA desaturase (SCD1), and fatty acid transloca
117 fatty-acid synthase, acetyl-CoA carboxylase, stearoyl-CoA desaturase, squalene synthase, farnesyl-pyr
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