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Jeremy E. Turnbull

Researcher at University of Liverpool

Publications -  163
Citations -  10405

Jeremy E. Turnbull is an academic researcher from University of Liverpool. The author has contributed to research in topics: Heparan sulfate & Fibroblast growth factor. The author has an hindex of 52, co-authored 154 publications receiving 9565 citations. Previous affiliations of Jeremy E. Turnbull include Liverpool School of Tropical Medicine & University of Manchester.

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Extracellular matrix and cell signalling: the dynamic cooperation of integrin, proteoglycan and growth factor receptor

TL;DR: This review focuses on the current understanding of integrins and heparan sulphate proteoglycans as the essential cellular machineries that sense, integrate and respond to the physical and chemical environmental information either by directly connecting with the local adhesion sites or by regulating global cellular processes through growth factor receptor signalling pathways, leading to the integration of both external and internal signals in space and time.
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Identification of the basic fibroblast growth factor binding sequence in fibroblast heparan sulfate.

TL;DR: The data indicate a primary role for contiguous sequences of IdoA(2-OSO3)alpha 1,4GlcNSO3 in mediating the high affinity binding between fibroblast HS and bFGF.
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Heparan sulfate: decoding a dynamic multifunctional cell regulator.

TL;DR: This review discusses recent developments and surveys emerging experimental strategies that hold promise for revealing the functional specificity and mechanisms of action of heparan sulfates as multifunctional cell regulators.
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Examination of the substrate specificity of heparin and heparan sulfate lyases.

TL;DR: These enzymes showed activity against solitary glucuronate-containing disaccharides in otherwise highly sulfated domains including the saccharide sequence that contains the antithrombin binding region in heparin, and are powerful reagents for the structural/sequence analysis of hepar in and heparan sulfate.
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Heparan Sulfate Oligosaccharides Require 6-O-Sulfation for Promotion of Basic Fibroblast Growth Factor Mitogenic Activity

TL;DR: Analysis of the structure-activity relationships in the dodecasaccharide fractions in particular, suggests that a minimum bFGF activation sequence exists which is dependent on the positioning of at least one 6-O-sulfate group.