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Martin R Turner

Researcher at University of Oxford

Publications -  519
Citations -  40655

Martin R Turner is an academic researcher from University of Oxford. The author has contributed to research in topics: Amyotrophic lateral sclerosis & RNA-binding protein. The author has an hindex of 98, co-authored 503 publications receiving 34965 citations. Previous affiliations of Martin R Turner include University College London & Drexel University.

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Defective antigen receptor-mediated proliferation of B and T cells in the absence of Vav

TL;DR: It is reported that antigen receptor-mediated proliferative responses of B and T cells in vitro are severely reduced in the absence of Vav, and a direct link between the low proliferative response of VAV-deficient B andT cells and the reduced number of these cells in peripheral lymphoid organs of chimaeric mice is suggested.
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Biomarkers in amyotrophic lateral sclerosis.

TL;DR: Potential biomarkers that are sensitive to the progression of disease, which might enhance the diagnostic algorithm and provide new drug targets, are now being identified from analysis of the blood and cerebrospinal fluid, as well as from neuroimaging and neurophysiology studies.
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Tyrosine kinase SYK: essential functions for immunoreceptor signalling

TL;DR: Gene-targeting studies have identified the cell types that require SYK for development and function, and the receptors that use SYK as well as their downstream signalling effectors.
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Neurofilament light chain: A prognostic biomarker in amyotrophic lateral sclerosis.

TL;DR: This report provides Class III evidence that the NfL electrochemiluminescence immunoassay accurately distinguishes patients with sporadic ALS from healthy controls and offers potential for N fL as a pharmacodynamic biomarker in future therapeutic trials.
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Cutting Edge: The Foxp3 Target miR-155 Contributes to the Development of Regulatory T Cells

TL;DR: It is reported that miR-155-deficient mice have reduced numbers of Tregs, both in the thymus and periphery, due to impaired development, and that additional miRNAs control Treg function.