Shamshad Cockcroft focuses on Biochemistry, Phosphatidylinositol, Cell biology, G protein and Phospholipase D. His study in GTP', Secretion, Phosphatidylinositol transfer protein, Phospholipase C and Inositol is carried out as part of his Biochemistry studies. As a part of the same scientific family, Shamshad Cockcroft mostly works in the field of Phosphatidylinositol transfer protein, focusing on Kinase and, on occasion, Signal transducing adaptor protein.
His study looks at the relationship between Phosphatidylinositol and fields such as Diacylglycerol kinase, as well as how they intersect with chemical problems. His Cell biology study integrates concerns from other disciplines, such as Exocytosis, Membrane, Cell membrane and Actin cytoskeleton. His Phospholipase D research incorporates themes from Phosphatidic acid, Phosphatidate, Receptor tyrosine kinase and ADP ribosylation factor.
His primary areas of investigation include Cell biology, Biochemistry, Phosphatidylinositol, Phosphatidylinositol transfer protein and Phospholipase C. His research integrates issues of Exocytosis and Phosphatidic acid in his study of Cell biology. His Biochemistry research focuses on Inositol, G protein, Secretion, Diacylglycerol kinase and GTP'.
His studies in Phosphatidylinositol integrate themes in fields like Golgi apparatus and Phosphatidylcholine. The concepts of his Phosphatidylinositol transfer protein study are interwoven with issues in Plant lipid transfer proteins, Plasma protein binding, Sphingomyelin, Pleckstrin homology domain and Saccharomyces cerevisiae. His Phospholipase C research includes elements of Phospholipase, Phospholipase A2, Arachidonic acid and Lipid signaling.
The scientist’s investigation covers issues in Phosphatidylinositol, Cell biology, Phospholipase C, Endoplasmic reticulum and Phosphatidylinositol transfer protein. Phosphatidylinositol is a subfield of Biochemistry that Shamshad Cockcroft investigates. His Cell biology research is multidisciplinary, incorporating perspectives in Membrane, Caenorhabditis elegans and Ion channel.
His work deals with themes such as Diacylglycerol kinase, Actin cytoskeleton, Phosphatidic acid, Phosphorylation and Membrane lipids, which intersect with Phospholipase C. He interconnects Membrane contact site, Drosophila Protein, G protein, Protein structure and Membrane protein in the investigation of issues within Endoplasmic reticulum. His research in Phosphatidylinositol transfer protein intersects with topics in Plasma protein binding, Mutant, Signal transduction, Phosphatidylethanolamine and Phosphatidylinositol binding.
His main research concerns Cell biology, Endoplasmic reticulum, Phosphatidylinositol, Phospholipase C and Phosphatidylinositol transfer protein. His Cell biology research integrates issues from Membrane, Biochemistry, Membrane contact site and Phosphatidic acid. His studies in Phosphatidic acid integrate themes in fields like Drosophila Protein, Membrane protein, G protein and Membrane lipids.
Shamshad Cockcroft has included themes like Phospholipid transport, Biochemical Activity and Organelle in his Endoplasmic reticulum study. His Phosphatidylinositol transfer protein study combines topics in areas such as Cell membrane, Caenorhabditis elegans, Sphingomyelin and Intracellular parasite. His Diacylglycerol kinase research incorporates elements of Phospholipase D, Lipid Transport, Phosphatidylglycerol and Plasma protein binding.
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Role of guanine nucleotide binding protein in the activation of polyphosphoinositide phosphodiesterase.
Shamshad Cockcroft;Bastien D. Gomperts.
Nature (1985)
Phospholipase D: a downstream effector of ARF in granulocytes
Shamshad Cockcroft;Geraint M. H. Thomas;Amanda Fensome;Blandine Geny.
Science (1994)
Inositol-lipid-specific phospholipase C isoenzymes and their differential regulation by receptors.
S Cockcroft;G M H Thomas.
Biochemical Journal (1992)
Polyphosphoinositide phosphodiesterase: regulation by a novel guanine nucleotide binding protein, Gp
Shamshad Cockcroft.
Trends in Biochemical Sciences (1987)
Two roles for guanine nucleotides in the stimulus-secretion sequence of neutrophils.
M. M. Barrowman;S. Cockcroft;B. D. Gomperts.
Nature (1986)
Stimulated neutrophils from patients with autosomal recessive chronic granulomatous disease fail to phosphorylate a Mr-44,000 protein.
Anthony W. Segal;Paul G. Heyworth;Shamshad Cockcroft;Margaret M. Barrowman.
Nature (1985)
Characterization of p150, an Adaptor Protein for the Human Phosphatidylinositol (PtdIns) 3-Kinase: SUBSTRATE PRESENTATION BY PHOSPHATIDYLINOSITOL TRANSFER PROTEIN TO THE p150·;PtdIns 3-KINASE COMPLEX *
Christina Panaretou;Jan Domin;Shamshad Cockcroft;Michael D. Waterfield.
Journal of Biological Chemistry (1997)
THE ATP4- RECEPTOR OF RAT MAST-CELLS
S Cockcroft;B D Gomperts.
Biochemical Journal (1980)
ATP induces nucleotide permeability in rat mast cells
S Cockcroft;B D Gomperts.
Nature (1979)
Two G-proteins act in series to control stimulus-secretion coupling in mast cells: use of neomycin to distinguish between G-proteins controlling polyphosphoinositide phosphodiesterase and exocytosis.
Shamshad Cockcroft;Tim W. Howell;Bastien D. Gomperts.
Journal of Cell Biology (1987)
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