School of Life and Health Sciences
Aston University
Birmingham B4 7ET
UK
Tel : +44 (0)121 204 4005
Email : s.t.russell1@aston.ac.uk
Career history
I completed my PhD in Pharmacy in 2002 from Aston University having previously gained my
BSc (Hons) in Pharmacology (93) and MSC in Human and Animal Physiology (95) at Aberdeen University.
I am currently a Research Fellow under Professor Tisdale, my main interest being Cachexia.
Modules:
I am module coordinator for PH3 CM1 and BI4009 Chemotherapy and selective toxicity.
Publications
Russell ST, Tisdale MJ, Role of b-adrenergic receptors in the anti-obesity and anti-diabetic effects of zinc-a2-glycoprotein (ZAG). Biochem et Biophys Acta 2012 1821:590-599
Russell ST, Tisdale MJ, Studies on the anti-obesity activity of zinc-α2-glycoprotein in the rat. Int J Obes (Lond). 2011 35(5):658-65.
Russell ST, Tisdale MJ, Studies on the antiobesity effect of zinc-α2-glycoprotein in the ob/ob mouse. Int J Obes (Lond). 2011 Mar;35(3):345-54
Russell ST, Tisdale MJ,Mechanism of attenuation of skeletal muscle atrophy by zinc-alpha2-glycoprotein. Endocrinology. 2010 Oct;151 (10):4696-704.
Russell ST, Siren PM, Siren MJ, Tisdale MJ. The role of zinc in the anti-tumour and anti-cachectic activity of D-myo-inositol 1,2,6-triphosphate. Br J Cancer. 2010 Mar 2;102 (5):833-6.
Eley HL, Russell ST, Tisdale MJ, Mechanism of activation of dsRNA-dependent protein kinase (PKR) in muscle atrophy. Cell Signal. 2010 May; 22(5):783-90.
Russell ST, Tisdale MJ,Antidiabetic properties of zinc-alpha2-glycoprotein in ob/ob mice. Endocrinology. 2010 Mar;151 (3):948-57
Russell ST, Siren PM, Siren MJ, Tisdale MJ, Mechanism of attenuation of protein loss in murine C2C12 myotubes by D-myo-inositol 1,2,6-triphosphate. Exp Cell Res. 2010 Jan 15;316(2):286-95.
Russell ST, Tisdale MJ, Mechanism of attenuation by beta-hydroxy-beta-methylbutyrate of muscle protein degradation induced by lipopolysaccharide. Mol Cell Biochem. 2009 Oct;330(1-2):171-9.
Russell ST, Siren PM, Siren MJ, Tisdale MJ, Attenuation of skeletal muscle atrophy in cancer cachexia by D-myo-inositol 1,2,6-triphosphate. Cancer Chemother Pharmacol. 2009 Aug;64(3):517-27
Russell ST, Rajani S, Dhadda RS, Tisdale MJ, Mechanism of induction of muscle protein loss by hyperglycaemia.Exp Cell Res. 2009 Jan 1;315(1):16-25.
Eley HL, Russell ST, Tisdale MJ, Attenuation of depression of muscle protein synthesis induced by lipopolysaccharide, tumor necrosis factor, and angiotensin II by beta-hydroxy-beta-methylbutyrate. Am J Physiol Endocrinol Metab. 2008 Dec;295(6):E1409-16.
Eley HL, Russell ST, Tisdale MJ. Mechanism of attenuation of muscle protein degradation induced by tumor necrosis factor-alpha and angiotensin II by beta-hydroxy-beta-methylbutyrate.Am J Physiol Endocrinol Metab. 2008 Dec;295(6):E1417-26.
Eley HL, McDonald PS, Russell ST, Tisdale MJ,Inhibition of activation of dsRNA-dependent protein kinase and tumour growth inhibition.Cancer Chemother Pharmacol. 2009 Mar;63(4):651-9.
Eley HL, Russell ST, Tisdale MJ, Role of the dsRNA-dependent protein kinase (PKR) in the attenuation of protein loss from muscle by insulin and insulin-like growth factor-I (IGF-I). Mol Cell Biochem. 2008 Jun; 313(1-2):63-9.
Russell ST, Eley HL, Wyke SM, Tisdale MJ.Involvement of phosphoinositide 3-kinase and Akt in the induction of muscle protein degradation by proteolysis-inducing factor.Biochem J. 2008 Feb 1;409(3):751-9.
Eley HL, Russell ST, Tisdale MJ, Effect of branched-chain amino acids on muscle atrophy in cancer cachexia. Biochem J. 2007 Oct 1;407(1):113-20.
Eley HL, Russell ST, Baxter JH, Mukerji P, Tisdale MJ,Signaling pathways initiated by beta-hydroxy-beta-methylbutyrate to attenuate the depression of protein synthesis in skeletal muscle in response to cachectic stimuli.Am J Physiol Endocrinol Metab. 2007 Oct;293(4):E923-31.
Editoral
Russell ST, Adipokines have a role to play in the treatment of metabolic disease. Future Medicinal Chemistry. 2010 Dec 2(12): p17211724
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