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Keywords: gene expression
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Biochem J (2019) 476 (19): 2927–2938.
Published: 11 October 2019
... genes incorporated into the host genome in a stable cell line or the global gene expression of host genome. This ability is not associated with PKR/RNase L system, as PKR inhibitors does not block MCPIP1-mediated mRNA degradation of exogenously transfected genes. Lastly, expression of MCPIP1 suppressed...
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Biochem J (2018) 475 (9): 1643–1667.
Published: 15 May 2018
...Nicoletta Bianchi; Simone Beninati; Carlo M. Bergamini The type 2 isoenzyme is the most widely expressed transglutaminase in mammals displaying several intra- and extracellular activities depending on its location (protein modification, modulation of gene expression, membrane signalling...
Includes: Supplementary data
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Biochem J (2015) 472 (2): 147–156.
Published: 13 November 2015
... muscle biopsies as described [ 11 ]. Cell cultures were maintained at 37°C under 7.5% CO 2 as myoblast cells and myoblast cells were used to transfect promoter plasmids. To measure gene expression of human skeletal muscle cells, myoblast cells were differentiated into myotubes. To initiate...
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Biochem J (2015) 467 (3): 453–460.
Published: 17 April 2015
... Igfbp-2 and PPARα expression levels were increased. Wy14643, a selective PPARα agonist, significantly induced Igfbp-2 gene expression in primary cultured hepatocytes. However, Igfbp-2 gene expression in Pparα null mice was not affected by fasting or Wy14643. In addition, through transient...
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Biochem J (2015) 466 (1): 29–36.
Published: 06 February 2015
...). calcium homoeostasis excitation–contraction coupling gene expression Extraocular muscles (EOMs) are among the fastest and most fatigue-resistant skeletal muscles [ 1 ]. More than 20 years ago, they were categorized as a separate group of muscles or ‘allotype’ since they represent a unique group...
Includes: Supplementary data
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Biochem J (2014) 461 (3): 383–390.
Published: 10 July 2014
... by the lipid PtdIns5 P produced by PIKfyve and MTMR3 and that the activities of these druggable enzymes are important for cancer cell migration and invasion. analysis software cell migration gene expression myotubularin-related protein 3 (MTMR3) PIKfyve PtdIns5 P We have shown previously...
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Biochem J (2013) 455 (1): 67–73.
Published: 13 September 2013
...Michael Aregger; Victoria H. Cowling Gene expression in eukaryotes is dependent on the mRNA methyl cap which mediates mRNA processing and translation initiation. Synthesis of the methyl cap initiates with the addition of 7-methylguanosine to the initiating nucleotide of RNA pol II (polymerase II...
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Biochem J (2013) 451 (3): 439–451.
Published: 12 April 2013
...Marta Magdalena Gabryelska; Eliza Wyszko; Maciej Szymański; Mariusz Popenda; Jan Barciszewski Hammerhead ribozyme is a versatile tool for down-regulation of gene expression in vivo . Owing to its small size and high activity, it is used as a model for RNA structure–function relationship studies...
Includes: Supplementary data
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Biochem J (2012) 446 (2): 203–212.
Published: 14 August 2012
... Journal compilation © 2012 Biochemical Society 2012 cis- acting regulatory element cystic fibrosis transmembrane conductance regulator ( CFTR ) enhancer gene expression transcriptional network The recruitment of TFs (transcription factors) and chromatin remodellers to cis- regulatory...
Includes: Supplementary data
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Biochem J (2012) 444 (1): 39–49.
Published: 26 April 2012
... was assessed by denaturing 0.8% agarose gel electrophoresis, and RNA quantification was performed by measuring A 260 in a BioPhotometer (Eppendorf). gene expression glucose starvation Snf1 stress tolerance yeast Fermentation of sugars, preferably glucose, is the favoured energy source...
Includes: Supplementary data
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Biochem J (2011) 440 (1): 73–84.
Published: 27 October 2011
... to the manufacturer's instructions. CpG gene expression methylation nuclear factor Y (NF-Y) sodium–vitamin C co-transporter 2 (SVCT2) upstream stimulating factor (USF) Human cell lines HeLa (cervical cancer), U2OS (osteosarcoma), HepG2 (liver carcinoma), SHS-Y5Y (neuroblastoma), HT1080...
Includes: Supplementary data
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Biochem J (2011) 438 (3): 523–533.
Published: 26 August 2011
... and that change in the activity of the PKA pathway alters tolerance to alkaline pH. The results of the present paper also indicate that the adaptive response to high pH involves PKA-regulated Msn2/Msn4-mediated gene remodelling. Activation of PKA has a major impact on gene expression. Consequently, several...
Includes: Supplementary data
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Biochem J (2011) 437 (3): 477–482.
Published: 13 July 2011
... macrophages, enterocytes and hepatocytes towards plasma. Abnormal levels of hepcidin expression alter plasma iron parameters and lead to iron metabolism disorders. Understanding the mechanisms controlling hepcidin ( HAMP encodes hepcidin) gene expression is therefore an important goal. We identified...
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Biochem J (2011) 435 (2): 313–325.
Published: 29 March 2011
... on the transcriptional regulation of the recently identified NHE8 isoform is also highlighted. Therefore the present review bridges a gap in our knowledge of the transcriptional mechanisms underlying the alterations in the gene expression of intestinal epithelial luminal membrane Na + and Cl − transporters involved...
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Biochem J (2011) 434 (3): 549–558.
Published: 24 February 2011
.... Surprisingly, most tumour suppressor mechanisms co-ordinated by p38α have been reported to occur at the post-translational level. This contrasts with the important role of p38α in the regulation of transcription and the profound changes in gene expression that normally occur during tumorigenesis. We have...
Includes: Supplementary data
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Biochem J (2011) 434 (2): 253–263.
Published: 11 February 2011
... 8 2010 5 11 2010 16 12 2010 16 12 2010 © The Authors Journal compilation © 2011 Biochemical Society 2011 cellular localization gene expression inhibitory κB β (IκBβ) nuclear factor κB (NF-κB) tumour necrosis factor α (TNFα) NF-κB (nuclear factor κB) is a homo...
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Biochem J (2010) 432 (3): 473–486.
Published: 25 November 2010
... tissue axis. In the present study, we show that PGC-1α [PPARγ (peroxisome-proliferator-activated receptor γ) co-activator 1α] interacts with and co-activates SF-1 to induce LH β (luteinizing hormone β) and α GSU (α-glycoprotein subunit) gene expression, subsequently leading to the increased secretion...
Includes: Supplementary data
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Biochem J (2010) 431 (2): 169–178.
Published: 28 September 2010
.... Moreover, GSH recruitment and sequestration in the nucleus during the G 1 - and S-phases of the cell cycle has a profound impact on cellular redox homoeostasis and on gene expression. For example, the abundance of transcripts encoding stress and defence proteins is decreased when GSH is sequestered...
Includes: Multimedia, Supplementary data
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Biochem J (2010) 427 (2): 255–264.
Published: 29 March 2010
...Francesca Aguiló; Nuria Camarero; Joana Relat; Pedro F. Marrero; Diego Haro In the cytosol of lipogenic tissue, ketone bodies are activated by AACS (acetoacetyl-CoA synthetase) and incorporated into cholesterol and fatty acids. AACS gene expression is particularly abundant in white adipose tissue...
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Biochem J (2009) 422 (3): 443–453.
Published: 27 August 2009
... 26 6 2009 26 6 2009 © The Authors Journal compilation © 2009 Biochemical Society 2009 Ccr4–Not complex gene expression mRNA deadenylation proteomics transcription regulation The evolutionarily conserved Ccr4–Not complex is important for multiple cellular functions...
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Biochem J (2009) 420 (3): 403–411.
Published: 27 May 2009
... © The Authors Journal compilation © 2009 Biochemical Society 2009 gastrointestinal tissue gene expression ghrelin Krüppel-like factor 4 (KLF4) promoter The gastrointestinal tract plays a crucial role in homoeostasis through its effects on the digestion, absorption and assimilation...
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Biochem J (2009) 420 (1): 57–65.
Published: 28 April 2009
..., ON, Canada, M5S 1A8. Arabidopsis gene expression P i starvation mass spectrometry phosphoenolpyruvate carboxylase kinase (PPCK) protein phosphorylation PEPC [PEP (phosphoenolpyruvate) carboxylase] (EC 4.1.1.31) is a ubiquitous cytosolic enzyme in vascular plants that is also distributed...
Includes: Supplementary data
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Biochem J (2009) 417 (2): 561–571.
Published: 23 December 2008
... differential mechanisms in the Cic gene regulation by different PUFA. citrate carrier gene expression lipogenesis polyunsaturated fatty acids (PUFA) rat liver sterol regulatory element-binding protein-1 (SREBP-1) CiC (citrate carrier), also known as tricarboxylate carrier, is a mitochondrial...
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Biochem J (2008) 415 (3): 467–475.
Published: 15 October 2008
... the importance of the TTAATAA core element and pin-point nucleotides that flank this element as crucial for Yap8p binding and in vivo activation of ACR3 expression. A genome-wide search for this element combined with global gene expression analysis indicates that the principal function of Yap8p is to control...
Includes: Supplementary data
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Biochem J (2008) 414 (3): 327–341.
Published: 27 August 2008
... in the mature nervous system to maintain appropriate gene-expression patterns in differentiated cells. Underpinning the function of the nervous system is its plasticity in response to external stimuli, and many transcription factors are involved in regulating gene expression in response to neuronal activity...
Includes: Multimedia, Supplementary data
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Biochem J (2008) 413 (3): 369–387.
Published: 15 July 2008
.... 3 Correspondence can be addressed to either of these authors (email [email protected] or [email protected] ). 7 4 2008 7 5 2008 7 5 2008 © The Authors Journal compilation © 2008 Biochemical Society 2008 acetyl-CoA biotin gene expression...
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Biochem J (2008) 413 (1): 151–161.
Published: 12 June 2008
... correspondence should be addressed (email [email protected] ). 30 1 2008 13 3 2008 28 3 2008 28 3 2008 © The Authors Journal compilation © 2008 Biochemical Society 2008 gene expression liver microarray selenocysteine (Sec) tRNA Trsp knockout xenobiotic...
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Biochem J (2007) 405 (1): 191–198.
Published: 13 June 2007
... differentiation [TTG1 (TRANSPARENT TESTA GLABRA1), GL3 (GLABRA3) and EGL3 (ENHANCER OF GL3)] positively regulate PPCK gene expression in response to P i starvation. BHLH32 can physically interact with TTG1 and GL3. We propose that BHLH32 interferes with the function of TTG1-containing complexes and thereby...
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Biochem J (2006) 396 (1): 163–172.
Published: 26 April 2006
... be addressed (email [email protected] ). 12 9 2005 1 2 2006 21 2 2006 21 2 2006 The Biochemical Society, London 2006 cardiomyocyte collagen extracellular matrix (ECM) gene expression p38 MAPK transcription factor The p38 MAPK (mitogen-activated protein kinase...
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Biochem J (2005) 389 (2): 413–421.
Published: 05 July 2005
..., we conducted gene expression analysis using microarrays containing probes for most of the known mouse genes. Throughout, verification of the specificity of PPARα in mediating effects resulting from WY 14,634 was achieved by carrying out identical experiments in PPARα-knockout mice. PPARα...
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Biochem J (2005) 389 (2): 279–287.
Published: 05 July 2005
... ]. Accordingly, the antioxidant enzymes may play a key role in the prevention of oxidative damage at an inflammation site. gene expression growth-regulated oncogene inflammation peroxide tone phospholipid hydroperoxide glutathione peroxidase polymorphonuclear leucocyte On the other hand...
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Biochem J (2005) 387 (3): 561–571.
Published: 26 April 2005
..., London 2005 Dicer gene expression gene silencing PAZ Piwi domain protein (PPD protein) RNA-induced silencing complex (RISC) RNA interference (RNAi) 1 These authors contributed equally to this work. In vertebrates, PPD proteins appear to be important for regulating...
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