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Keywords: redox
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Biochem J (2015) 472 (3): 309–318.
Published: 27 November 2015
...-containing redox regulatory protein, is a novel secreted protein with potent anti-inflammatory properties. PAMM is secreted from mature human adipocytes but not preadipocytes. Overexpression of PAMM significantly attenuated lipopolysaccharide (LPS)-induced macrophage inflammation. Incubation of macrophages...
Biochem J (2015) 468 (3): 385–400.
Published: 15 June 2015
...Jehad Shaikhali; Céline Davoine; Kristoffer Brännström; Nicolas Rouhier; Joakim Bygdell; Stefan Björklund; Gunnar Wingsle The eukaryotic mediator integrates regulatory signals from promoter-bound transcription factors (TFs) and transmits them to RNA polymerase II (Pol II) machinery. Although redox...
Includes: Supplementary data
Biochem J (2014) 462 (1): 67–75.
Published: 24 July 2014
... selenoprotein expression. These findings may offer an explanation for the movement phenotype of selenoprotein P-deficient mice and the movement disorder and mental retardation described in a patient carrying SECISBP2 mutations. cholinergic glutathione peroxidase neurodegeneration parvalbumin redox...
Includes: Multimedia, Supplementary data
Biochem J (2011) 437 (1): 109–115.
Published: 14 June 2011
...Xudong Wang; Gail J. Mick; Edmund Maser; Kenneth McCormick With the exception of the oxidation of G6P (glucose 6-phosphate) by H6PDH (hexose-6-phosphate dehydrogenase), scant information is available about other endogenous substrates affecting the redox state or the regulation of key enzymes which...
Biochem J (2011) 436 (3): 641–650.
Published: 27 May 2011
... pentose phosphate pathway 6-phosphogluconolactonase Plasmodium malaria redox 1 These authors contributed equally to this work. 2 To whom correspondence should be addressed (email katja.becker@ernaehrung.uni-giessen.de ). G6PD (glucose-6-phosphate dehydrogenase) deficiency...
Includes: Supplementary data
Biochem J (2009) 424 (3): 491–500.
Published: 10 December 2009
...Barry R. Imhoff; Jason M. Hansen The redox status of the extracellular compartment has only just been elucidated as a mechanism controlling intracellular signal transduction and correlates with aging, diabetes, heart disease and lung fibrosis. In the present paper, we describe a mechanism by which...
Biochem J (2006) 400 (1): 13–22.
Published: 27 October 2006
... contains the FAD cofactor covalently bound to His 121 . It was previously demonstrated that the H121A substitution results in a ≈100 mV decrease in the midpoint redox potential and a ≈40-fold decrease in turnover number compared to wild-type enzyme [Motteran, Pilone, Molla, Ghisla and Pollegioni (2001...
Biochem J (2004) 381 (3): 675–683.
Published: 27 July 2004
... model whereby the redox environment within the cell selectively regulates stress signalling through MEKK1 versus ASK1, and may thereby participate in the induction of apoptosis by oxidative stress. 1 To whom correspondence should be addressed (e-mail templeton@virginia.edu ). 9 4 2004...
Biochem J (2000) 351 (1): 87–93.
Published: 26 September 2000
... present study may be used to determine the oxidation status of specific proteins in cells. PDTC methoxy-polyethylene glycol-maleimide redox tumour suppressor nuclear accumulation 1 To whom correspondence should be addressed (e-mail jmomand@calstatela.edu ). 25 4 2000 30 6...
Biochem J (2000) 350 (3): 609–629.
Published: 08 September 2000
... are functionally distinct, as discussed in the present review. In energy metabolism, H 4 MPT permits redox-flux features that are distinct from the pathway on H 4 folate. In the reductive direction, ATP is consumed in the entry of carbon from CO 2 into the H 4 folate pathway, but not in entry into the...