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1 ich include ATP citrate lyase, ACC, FAS, and stearoyl-CoA desaturase.
2 id desaturation pathway that is dependent on stearoyl-CoA desaturase.
3 ine motif required for catalytic activity in stearoyl-CoA desaturase.
4 clusions that can be prevented by inhibiting stearoyl-CoA desaturase.
5 tively reversed by Aramchol, an inhibitor of stearoyl-CoA desaturase.
6 oenzyme A synthase, fatty acid synthase, and stearoyl-CoA desaturase.
7 atory element binding protein (SREBP1c), and stearoyl-CoA desaturase.
10 se 1 (ACC1), fatty acid synthase (FASN), and stearoyl CoA desaturase 1 (SCD1)] to AML and eBL cell li
12 P-2 (vesicle-associated membrane protein 2), stearoyl CoA desaturase 1, and cAMP-specific phosphodies
14 e obesity-derived adipokine leptin (LEP) and stearoyl-CoA desaturase 1 (SCD), a critical enzyme in fa
15 Herein, we demonstrate that inhibition of stearoyl-CoA desaturase 1 (SCD-1) halts the biosynthesis
17 f the mice with a disruption in the gene for stearoyl-CoA desaturase 1 (SCD1) (SCD1-/-) is deficient
18 e model, here we show that expression of the stearoyl-CoA desaturase 1 (Scd1) gene is downregulated i
19 r strategies to combat this growing problem, stearoyl-CoA desaturase 1 (SCD1) inhibition has been pro
23 ing exercise expressed increased endothelial stearoyl-CoA desaturase 1 (SCD1) that catalyzes anti-inf
24 SREBPs (1a and 2) led to elevated mRNAs for stearoyl-CoA desaturase 1 (SCD1), an isoform that is det
25 wed increased fatty acid synthase (FASN) and stearoyl-CoA desaturase 1 (SCD1), both associated with N
26 r Xenopus kinesin-like protein 2 (TPX2), and stearoyl-CoA desaturase 1 (SCD1), significantly reduced
27 ChREBP overexpression induced expression of stearoyl-CoA desaturase 1 (Scd1), the enzyme responsible
28 the in vitro expression and activity of the Stearoyl-CoA Desaturase 1 (SCD1), the hepatic Delta9-des
30 oupling of fatty acid synthase activity from stearoyl-CoA desaturase 1 (SCD1)-mediated desaturation.
32 n as well as reduction in mRNA expression of stearoyl-CoA desaturase 1 and genes associated with fatt
34 that mice with a targeted disruption in the stearoyl-CoA desaturase 1 gene (SCD1-/-) have increased
35 terize SC lipidome alteration in response to stearoyl-CoA desaturase 1 inhibition and, additionally,
36 ntify the antifibrotic effect of Aramchol, a stearoyl-CoA desaturase 1 inhibitor in development for m
39 seen with genetic deletion or inhibition of stearoyl-CoA desaturase 1 promotes inflammation, TLR4 hy
40 ohydrate response element-binding protein or stearoyl-CoA desaturase 1 resulted in lethality on high
41 pression, most notably reduced expression of stearoyl-CoA desaturase 1, a rate-limiting enzyme in the
42 ary cell line that overexpressed transfected stearoyl-CoA desaturase 1, a rate-limiting enzyme in the
43 n of SFA in the body is tightly regulated by stearoyl-CoA desaturase 1, an enzyme that converts endog
44 , acetyl-CoA carboxylase, ATP citrate lyase, stearoyl-CoA desaturase 1, cluster of differentiation 36
45 crophage LXR/RXR target genes, we identified stearoyl-CoA desaturases 1 and 2 (Scd1 and Scd2), and su
49 0.37, 95% CI: 0.04, 0.70), 6 desaturase, and stearoyl CoA desaturase-1 (SCD-1) index were directly as
51 was also a significant downregulation of the stearoyl CoA desaturase-1 gene, which has been associate
52 ed hyperleptinemia without downregulation of stearoyl CoA desaturase-1 or fatty acid synthase and by
54 several accessory lipogenic enzymes, such as stearoyl-CoA desaturase-1 (SCD-1) and long chain free fa
56 sed the mRNA levels for fatty acid synthase, stearoyl-CoA desaturase-1 (SCD-1), and epidermal fatty a
57 ting a high activity of the lipogenic enzyme stearoyl-CoA desaturase-1 (SCD-1), has been shown to be
58 RNA levels and enzymatic activity of hepatic stearoyl-CoA desaturase-1 (SCD-1), which catalyzes the b
63 cell death effect ORCTL3 targets the enzyme stearoyl-CoA desaturase-1 (SCD1) in fatty acid metabolis
69 Genetic or pharmacological inhibition of stearoyl-CoA desaturase-1 (SCD1), the enzyme that conver
73 activate transcription of the genes encoding stearoyl-CoA desaturase-1 and -2, thereby markedly enhan
74 erides or in the exercise-suppressed hepatic stearoyl-CoA desaturase-1 and peroxisome proliferator-ac
75 r-activated receptor gamma2 (PPARgamma2) and stearoyl-CoA desaturase-1 and up-regulated PPARalpha ind
77 n in wild-type mice increased PPARgamma2 and stearoyl-CoA desaturase-1 mRNA and hepatic triglyceride
78 yl-CoA carboxylase, fatty acid synthase, and stearoyl-CoA desaturase-1 were all elevated markedly, as
79 yl-CoA carboxylase, fatty-acid synthase, and stearoyl-CoA desaturase-1 were increased in apoB/BATless
80 d-type mice, with the induction of the Scd1 (stearoyl-CoA desaturase-1) gene preceding that of other
81 e, glycerol-3-phosphate acyltransferase, and stearoyl-CoA desaturase-1) showed a complete failure of
82 y acid synthase, acetyl-CoA carboxylase, and stearoyl-CoA desaturase-1, were reduced in ob/ob-PPARgam
87 Here we report that selective ablation of stearoyl CoA desaturase-2 (Scd2) in aHSC globally suppre
89 secondary analysis, each SD increase of log-stearoyl-coA desaturase activity (16:1n-7/16:0 ratio) wa
92 aturated fatty acid (MUFA) biosynthetic gene stearoyl-CoA desaturase, altering the ratio of MUFA-PLs
93 -binding cassette transporter A1 (ABCA1) and stearoyl CoA desaturase, and expression of these genes i
94 Lipocalin 2, haptoglobin, serum amyloid A3, stearoyl-CoA desaturase, and 11beta-hydroxysteroid dehyd
95 the molecular mechanism for the induction of stearoyl-CoA desaturase by peroxisome proliferators.
98 abolism by maintaining the expression of the stearoyl-CoA desaturase FAT-7, an oxygen consuming, rate
99 mutant, acdh-11, in which expression of the stearoyl-CoA desaturase FAT-7/SCD1 is constitutively inc
103 ) and other fatty acids on the expression of stearoyl-CoA desaturase gene 1 were investigated in full
104 ouse model with a targeted disruption of the stearoyl-CoA desaturase gene-1 (SCD1-/-) have revealed t
105 ce was identified at the N-terminus of mouse stearoyl-CoA desaturase I (SCD I) comprised of (30)KVKTV
106 tin in the cytoplasm of basal sebocytes, and stearoyl CoA desaturase in the cytoplasm of basal and lu
108 onse-element-binding protein-1 (SREBP-1) and stearoyl-CoA desaturase in the immortalized sebaceous gl
113 From the crystal structure of the mouse stearoyl-CoA desaturase (mSCD1) it was proposed that Tyr
114 Analysis revealed that four of the genes [stearoyl-CoA desaturase; NADH-ubiquinone oxidoreductase
115 ameliorated by pharmacologically inhibiting stearoyl-CoA desaturase or by conditioning the cells in
116 is toxicity can be ameliorated by inhibiting stearoyl-CoA desaturase or by saturated fatty acid condi
117 erilipin-5, adipose triglyceride lipase, and stearoyl-CoA desaturase protein was higher in the NWA gr
119 that YTX-7739, a clinical-stage inhibitor of stearoyl CoA desaturase (SCD), triggers lipotoxicity in
122 saturase (D5D), Delta6 desaturase (D6D), and stearoyl-CoA desaturase (SCD) activity and T2D risk.
123 ricted activator of the key lipogenic enzyme stearoyl-CoA desaturase (SCD) and that SCD is required f
125 h arachidonic acid resulted in a decrease in stearoyl-CoA desaturase (Scd) enzyme activity and scd1 m
127 ted fatty acids, a reaction catalyzed by the stearoyl-CoA desaturase (SCD) enzyme, resulting in apopt
129 T3-L1 preadipocyte cells are correlated with stearoyl-CoA desaturase (SCD) expression (mRNA and prote
130 f fatty acid uptake and synthesis and higher stearoyl-CoA desaturase (SCD) expression, Ncb5or(-/-) li
131 rationally designed combination therapy of a stearoyl-CoA desaturase (SCD) inhibitor with an isocalor
143 3K cellular screen identified inhibitors of stearoyl-CoA desaturase (SCD) that robustly prevent the
144 esis: four desaturases were induced, and one stearoyl-CoA desaturase (SCD) was strongly repressed.
146 in many cellular functions, is regulated by stearoyl-CoA desaturase (SCD), a rate-limiting enzyme in
147 ayers involved in metabolic reprogramming is stearoyl-CoA desaturase (SCD), which converts saturated
150 atty acid metabolism, including induction of stearoyl-CoA desaturase (SCD)-1, which converts saturate
158 or depletion of the lipid metabolism enzymes stearoyl-CoA-desaturases (SCD) and S-adenosyl methionine
159 sion, its expression was compared to that of stearoyl CoA desaturase (Scd1) in B6 mice exposed to die
160 er Research, Tesfay and colleagues show that stearoyl CoA desaturase (SCD1) is expressed at high leve
161 scle carnitine palmitoyl-transferase (MCPT), stearoyl CoA desaturase (SCD1), and fatty acid transloca
162 Aramchol, a partial inhibitor of hepatic stearoyl-CoA desaturase (SCD1) improved steatohepatitis
163 y, ADAR1-mediated A-to-I editing on 3'UTR of stearoyl-CoA desaturase (SCD1) increases binding of KH d
164 ation by inducing proteasomal degradation of stearoyl-CoA desaturase (SCD1), LXRalpha activation can
165 examined the contribution to ferroptosis of stearoyl-CoA desaturase (SCD1, SCD), an enzyme that cata
166 fatty-acid synthase, acetyl-CoA carboxylase, stearoyl-CoA desaturase, squalene synthase, farnesyl-pyr