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1 a coactivator 1alpha (PGC-1alpha, encoded by Ppargc1a).
2 and transcription regulation (INSIG1, PPARG, PPARGC1A).
3 ogenesis and known to interact with PPARs or PPARGC1A.
4 vity and combinatorial binding patterns with PPARGC1A.
5 and had a parallel pattern of expression to PPARGC1A.
6 PARG G allele (rs1801282) and noncarriers of PPARGC1A A allele (rs8192678) had 21 and 13% lower hepat
7 ceptor gamma-coactivator 1alpha; also called PPARGC1A) a coactivator of the Kdm5a target genes, is su
8 ctivated receptor gamma coactivator 1-alpha (PPARGC1A), a coactivator of the transcription factor PPA
9 in PPAR gamma (PPARG) co-activator 1 alpha (PPARGC1A), a gene encoding a co-activator of the LCPUFA-
10 ctivated receptor-gamma coactivator-1 alpha (PPARGC1A), a master transcriptional regulator of mitocho
12 ARGC1a (also known as PGC-1alpha; encoded by Ppargc1a), a transcriptional coactivator that regulates
17 ap of targets including a novel link between PPARGC1A and HSF1, a TF regulating the conserved heat sh
18 tudies have focused on the interplay between PPARGC1A and individual TFs, but little is known about h
19 to 8-br-cAMP with a 200% greater increase in Ppargc1a and Pck1 expression, and a 30% increase in G6pc
20 eta (PGC-1alpha and PGC-1beta, also known as Ppargc1a and Ppargc1b, respectively) and the downstream
21 inhibits, whereas Notch inhibition induces, Ppargc1a and Prdm16 transcription in white adipocytes.
22 epG2 cells were transfected with variants of PPARGC1A and protein and messenger RNA levels were measu
24 tor (MC2R), MC3R, PPARG coactivator 1 alpha (PPARGC1A), and tumor necrosis factor (TNF), was changed
26 50 directly targets and represses Prdm16 and Ppargc1a, and that forced expression of miR-150 attenuat
27 iptional regulators of metabolism, PPARG and PPARGC1A, as well as SCD1, the rate-limiting enzyme for
28 a coactivator-1alpha (PGC-1alpha, encoded by Ppargc1a) by SIRT1 activators, our results illustrate ho
29 their co-activators Pgc1alpha (also known as Ppargc1a), CBP/p300 (Crebbp) and Src1 (Ncoa1) to the PPR
31 ndividual TFs, but little is known about how PPARGC1A combines with all of its partners across the ge
32 ficient hearts, suggesting that up-regulated Ppargc1a confers increased mitochondrial metabolism and
33 s of down-regulated genes (e.g. AMPK, TORC2, PPARGC1A) correspond to a single common pathway importan
35 atment did not affect the heart size of Flcn/Ppargc1a doubly inactivated hearts, further supporting t
37 d is required for the transcription of Ucp1, Ppargc1a (encoding PGC-1alpha), and oxidative phosphoryl
38 nhibition of HNF-1beta significantly reduced PPARGC1A expression and altered mitochondrial morphology
39 We also demonstrated downregulation of renal PPARGC1A expression in a patient with an HNF1B germinal
42 Increasing physical activity, which induces PPARGC1A expression, is a potential strategy to slow DNA
43 zygous or homozygous disruption of Ppargc1a (Ppargc1a(f/+)Alb-cre(+/0) and Ppargc1a(f/f) Alb-cre(+/0)
44 Oxidative damage was observed in livers from Ppargc1a(f/+)Alb-cre(+/0) mice of each sex, in a cell-au
45 he increased liver damage observed in female Ppargc1a(f/+)Alb-cre(+/0) mice; while, compensatory incr
46 n of Ppargc1a (Ppargc1a(f/+)Alb-cre(+/0) and Ppargc1a(f/f) Alb-cre(+/0) mice, respectively) were fed
48 ne distributions of DNA sequence variants in PPARGC1A for association with NV AMD and interaction of
49 a Tug1-binding element (TBE) upstream of the Ppargc1a gene and showed that Tug1 binds with the TBE to
54 n and examined the relationship between nine PPARGC1A genetic variants, DNA damage, type 2 diabetes,
55 variants showed significant association, and PPARGC1A haplotypes exhibited significant association af
57 deficient hearts and indeed, inactivation of Ppargc1a in Flcn-deficient hearts significantly reduced
60 activated receptor-gamma coactivator-1alpha (PPARGC1A) in skeletal muscle and subcutaneous adipose ti
66 induced early and transient inflammation and PPARGC1A inhibition, which overlapped with downregulatio
70 ted hearts, further supporting the idea that Ppargc1a is the critical element leading to deregulation
71 a) coactivator alpha (PGC-1alpha, encoded by Ppargc1a) is functionally regulated by the lncRNA taurin
73 nal ischaemia, Pgc1alpha(-/-) (also known as Ppargc1a(-/-)) mice develop local deficiency of the NAD
74 of starved mice also had increased levels of Ppargc1a mRNA and Creb3l3 mRNA, which encode a transcrip
77 d receptor-gamma (PPARG) coactivator 1alpha (PPARGC1A or PGC1A) is inversely correlated with liver fa
79 transcription factor MITF drives PGC1alpha (PPARGC1A) overexpression in a subset of human melanomas
81 with liver-specific hemizygous disruption of Ppargc1a placed on an obesogenic diet expressed increase
83 cific hemizygous or homozygous disruption of Ppargc1a (Ppargc1a(f/+)Alb-cre(+/0) and Ppargc1a(f/f) Al
88 ligo patients, whereas its predicted targets PPARGC1A, RRM2, and TAOK1 were reciprocally up-regulated
91 e evaluated the independent influence of the PPARGC1A rs8192678 risk A allele on pediatric NAFLD afte
92 , sex, and PNPLA3 rs738409 polymorphism, the PPARGC1A rs8192678 risk A allele was an independent risk
93 We aimed to test the hypothesis that the PPARGC1A rs8192678 risk A allele would influence the ris
95 mong 9 genes (ADRB3, ENPP1, FTO, LEP, PPARG, PPARGC1A, SLC2A2, TCF7L2, and UCP2) associated with type
96 ed that seven genes (CDKN1A, ESR1, MAX, MYC, PPARGC1A, SP1, and STK11) and one novel MYC-centered pat
97 cription factor (PPARG co-activator 1 alpha, PPARGC1A) to age-related macular degeneration (AMD) and
98 r demonstrate that SCF/Kit directly promotes Ppargc1a transcription and mitochondrial biogenesis.
100 ic genes, such as PPAR-gamma coactivator 1a (Ppargc1a), uncoupling protein 1 (Ucp1) and acyl-CoA synt
101 irst mapped the genome-wide binding sites of PPARGC1A using chromatin-IP followed by high-throughput
106 erator-activated receptor gamma cofactor 1A (PPARGC1A) was 1.75-fold reduced with insulin resistance
107 eceptor-gamma coactivator (PGC)-1alpha gene (PPARGC1A) was identified to be associated with nonalcoho
109 R-resident regulatory variant (rs3774923) in PPARGC1A were independently associated with NV AMD (exac
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