TREM-like transcript 1: a more sensitive marker of platelet activation than P-selectin in humans and mice

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TREM-like transcript 1: a more sensitive marker of platelet activation than P-selectin in humans and mice

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scientific article published on 01 August 2018

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wetenschappelijk artikel

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наукова стаття, опублікована в серпні 2018

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TREM-like transcript 1: a more ...... P-selectin in humans and mice

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TREM-like transcript 1: a more ...... P-selectin in humans and mice

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TREM-like transcript 1: a more ...... P-selectin in humans and mice

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TREM-like transcript 1: a more ...... P-selectin in humans and mice

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TREM-like transcript 1: a more ...... P-selectin in humans and mice

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TREM-like transcript 1: a more ...... P-selectin in humans and mice

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TREM-like transcript 1: a more ...... P-selectin in humans and mice

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Christopher W Smith

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Lola Parfitt

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Cutting edge: TREM-like transcript-1, a platelet immunoreceptor tyrosine-based inhibition motif encoding costimulatory immunoreceptor that enhances, rather than inhibits, calcium signaling via SHP-2

A TREM family member, TLT-1, is found exclusively in the alpha-granules of megakaryocytes and platelets

Hierarchical organization in the hemostatic response and its relationship to the platelet-signaling network.

Par4 is required for platelet thrombus propagation but not fibrin generation in a mouse model of thrombosis.

The platelet interior revisited: electron tomography reveals tubular alpha-granule subtypes.

Proteinase-activated receptors 1 and 4 counter-regulate endostatin and VEGF release from human platelets.

Icy: an open bioimage informatics platform for extended reproducible research.

The first comprehensive and quantitative analysis of human platelet protein composition allows the comparative analysis of structural and functional pathways.

Selective sorting of alpha-granule proteins.

Angiogenesis is regulated by a novel mechanism: pro- and antiangiogenic proteins are organized into separate platelet alpha granules and differentially released.

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2072-2078

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scholarly article

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10.1182/BLOODADVANCES.2018017756

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English

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2018-08-01T00:00:00Z

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30120105

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6113608

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