Eleyna Martin

University of Birmingham

United Kingdom

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Articles (10)

Year:

2024

Year:

2024

Year:

2023

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Collaborators (17)

Mark Thomas

University of Birmingham

UNITED KINGDOM

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Natalie J. Jooss

University of Oxford

UNITED KINGDOM

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Samantha Montague

University of Birmingham

UNITED KINGDOM

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Ángel García

Associate Professor - Head of the Platelet Proteomics Group

Universidade de Santiago de Compostela

SPAIN

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David Stegner

GERMANY

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Steve P. Watson

UNITED KINGDOM

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Caroline Kardeby

Aston University

UNITED KINGDOM

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Deirdre Kavanagh

University of Oxford

UNITED KINGDOM

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Luis Arturo Moran Lara

University of Bristol

UNITED KINGDOM

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Cedric Duval

Lecturer

University of Leeds

UNITED KINGDOM

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Joanne Clark

University of Birmingham

UNITED KINGDOM

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Alexandre Slater

Dr at University of Birmingham

University of Birmingham

UNITED KINGDOM

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Todd Mize

University of Birmingham

UNITED KINGDOM

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Barrie Kellam

Professor of Medicinal Chemistry

University of Nottingham

UNITED KINGDOM

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Magdolna Nagy

University of Maastricht

UNITED STATES

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Jonas Emsley

professor of macromolecular crystallography

University of Nottingham

UNITED KINGDOM

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Natalie Poulter

University of Birmingham

UNITED KINGDOM

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Eleyna Martin

Research Interests

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Articles (10)

PF4 activates the c-Mpl–Jak2 pathway in platelets

Trivalent nanobody-based ligands mediate powerful activation of GPVI, CLEC-2 and PEAR1 in human platelets whereas FcγRIIA requires a tetravalent ligand

Characterizing the binding of glycoprotein VI with nanobody 35 reveals a novel monomeric structure of glycoprotein VI where the conformation of D1+D2 is independent of dimerization

Experimental validation of computerised models of clustering of platelet glycoprotein receptors that signal via tandem SH2 domain proteins

Katacine Is a New Ligand of CLEC-2 that Acts as a Platelet Agonist

Platelet activation by charged ligands and nanoparticles: platelet glycoprotein receptors as pattern recognition receptors.

GPVI (Glycoprotein VI) Interaction With Fibrinogen Is Mediated by Avidity and the Fibrinogen αC-Region

Structural characterization of a novel GPVI-nanobody complex reveals a biologically active domain-swapped GPVI dimer

Evidence that GPVI is Expressed as a Mixture of Monomers and Dimers, and that the D2 Domain is not Essential for GPVI Activation

The structure of CLEC-2: mechanisms of dimerization and higher-order clustering.

Collaborators (17)

Mark Thomas

Natalie J. Jooss

Samantha Montague

Ángel García

David Stegner

Steve P. Watson

Caroline Kardeby

Deirdre Kavanagh

Luis Arturo Moran Lara

Cedric Duval

Joanne Clark

Alexandre Slater

Todd Mize

Barrie Kellam

Magdolna Nagy

Jonas Emsley

Natalie Poulter

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