Titlebook: Biochemistry, Molecular Biology, and Physiology of Phospholipase A2 and Its Regulatory Factors; Anil B. Mukherjee Book 1990 The Editor(s)

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IRS

FRET

Soluble Phospholipase A2 in Human Pathology: Clinical-Laboratory Interface, membrane bound and as cytosolic enzymes (2). Whereas the former acts intracellularly, the latter has the potential to be released from the cell upon a variety of stimuli (3). In humans, such soluble extracellular enzyme of pancreatic origin has indeed been found in the blood (4).

PATHY

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Book 1990g endogenous and synthetic inhibitors and activators of this enzyme. To review these important areas in PLA2 research we invited scientists who made significant contributions in this field. The papers in this volume are organized to emphasize the recent advances in several areas of investigation, in

Fortuitous

A Novel Bifunctional Mechanism of Surface Recognition by Phospholipase A2,holipids lend themselves ideally to such studies in that they form a variety of stable and structurally well-defined surfaces in micelles, reverse micelles, monolayers, planar bilayers, and curved vesicles with which to study catalysis at the boundary between two phases.

hemoglobin

Stimulation of Phospholipases A2 by Transglutaminases, of inter or intramolecular covalent crosslinks. These enzymes have been detected both intra and extracellularly in higher animals including man. The best characterized extracellular TG is variously known as fibrin-stabilizing factor, Laki-Lorand factor or coagulation Factor XIII.

Ophthalmologist

Functional Consequences of Phospholipase A2 Activation in Human Monocytes,e agents..Release of arachidonic acid by the action of PLA. or other phospholipid hydrolyzing enzymes leads directly to the formation of cyclooxygenase products. In the presence of markedly elevated calcium concentrations, 5-lipoxygenase (LO) is activated as well, leading to the formation and releas

騙子

absorbed