2022 - DSc honoris causa, University of Bath
2022 - Honorary Fellowship of the British Pharmacological Society
2009 - Member of Academia Europaea
2008 - Fellow of the Royal Society of Biology (FRSB), United Kingdom
2008 - Fellow of The Academy of Medical Sciences, United Kingdom
1990 - Fellow of the Royal Society of Chemistry (FRSC)
Barry V. L. Potter mainly investigates Biochemistry, Stereochemistry, Steroid sulfatase, Internal medicine and Endocrinology. His research on Biochemistry frequently links to adjacent areas such as Cell biology. In his study, Nuclear magnetic resonance spectroscopy is strongly linked to Cyclitol, which falls under the umbrella field of Stereochemistry.
His Steroid sulfatase study combines topics from a wide range of disciplines, such as Estrone, Aromatase, Enzyme inhibitor and In vivo. His research integrates issues of Cell culture, Cell growth and Tricyclic in his study of Internal medicine. His Inositol study integrates concerns from other disciplines, such as Stereospecificity and Intracellular.
Barry V. L. Potter mostly deals with Stereochemistry, Biochemistry, Inositol, Steroid sulfatase and Enzyme. His study looks at the intersection of Stereochemistry and topics like Ring with Group. His Biochemistry study frequently involves adjacent topics like Calcium.
Inositol is a subfield of Receptor that Barry V. L. Potter investigates. He has included themes like Estrone and In vivo in his Steroid sulfatase study. Within one scientific family, he focuses on topics pertaining to Cancer research under Internal medicine, and may sometimes address concerns connected to 2-Methoxyestradiol.
His primary areas of study are Stereochemistry, Biochemistry, Inositol, Structure–activity relationship and Enzyme. The concepts of his Stereochemistry study are interwoven with issues in Tubulin, Microtubule, Steroid sulfatase and Stereoisomerism. His research in Adenosine, Second messenger system, Agonist, Active site and Binding site are components of Biochemistry.
Inositol is a primary field of his research addressed under Receptor. His Structure–activity relationship research includes elements of Microsome, Substituent, 11β-hydroxysteroid dehydrogenase type 1 and In vivo. His Enzyme research includes themes of Inositol pentakisphosphate, Phosphorylation and Metabolism.
Barry V. L. Potter mainly focuses on Stereochemistry, Biochemistry, Structure–activity relationship, Steroid sulfatase and Inositol. His Stereochemistry research integrates issues from In vivo and Active site. His is doing research in Adenosine, Binding site, Agonist, Enzyme and Second messenger system, both of which are found in Biochemistry.
The Structure–activity relationship study combines topics in areas such as Microtubule, Ring and Stereoisomerism. His study in Steroid sulfatase is interdisciplinary in nature, drawing from both Aryl, Aromatase, Sulfatase and Pharmacology. The subject of his Inositol research is within the realm of Receptor.
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Steroid sulfatase: molecular biology, regulation, and inhibition.
M. J. Reed;A. Purohit;L. W. Lawrence Woo;Stephen P. Newman.
Endocrine Reviews (2005)
Chemistry of Inositol Lipid Mediated Cellular Signaling
Barry V. L. Potter;Dethard Lampe.
Angewandte Chemie (1995)
Pulsatile intracellular calcium release does not depend on fluctuations in inositol trisphosphate concentration
Makoto Wakui;Barry V. L. Potter;Ole H. Petersen.
cGMP mobilizes intracellular Ca2+ in sea urchin eggs by stimulating cyclic ADP-ribose synthesis.
Antony Galione;Alison White;Nicholas Willmott;Michelle Turner.
Regulation of calcium signalling in T lymphocytes by the second messenger cyclic ADP-ribose
A. H. Guse;C. P. Da Silva;I. Berg;A. L. Skapenko.
Characterisation of the binding of [3H]methyllycaconitine: a new radioligand for labelling α7-type neuronal nicotinic acetylcholine receptors
Andrew R.L Davies;David J Hardick;Ian S Blagbrough;Barry V.L Potter.
Estrone sulfamates: potent inhibitors of estrone sulfatase with therapeutic potential.
Nicola M. Howarth;Atul Purohit;Michael J. Reed;Barry V. L. Potter.
Journal of Medicinal Chemistry (1994)
Phase I Study of STX 64 (667 Coumate) in Breast Cancer Patients: The First Study of a Steroid Sulfatase Inhibitor
Susannah J Stanway;Atul Purohit;L W Lawrence Woo;Saulat Sufi.
Clinical Cancer Research (2006)
Structure of the PH domain from Bruton's tyrosine kinase in complex with inositol 1,3,4,5-tetrakisphosphate.
Elena Baraldi;Kristina Djinovic Carugo;Marko Hyvönen;Paola Lo Surdo.
Nicotinic Acid Adenine Dinucleotide Phosphate (Naadp+) Is an Essential Regulator of T-Lymphocyte Ca2+-Signaling
Ingeborg Berg;Barry V.L. Potter;Georg W. Mayr;Andreas H. Guse.
Journal of Cell Biology (2000)
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