Maguelonne Roux

Institut Pasteur

France

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Articles (6)

Year:

2023

Year:

2022

Year:

2021

Year:

2020

Year:

2020

Year:

2020

Collaborators (8)

Taija Makinen

Professor

Uppsala University

SWEDEN

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Marie-christine ALESSI

Professor / Director

Aix-Marseille University

FRANCE

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Paul Gray

Joint Head of Department

AUSTRALIA

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Qian Zhang

INSERM

FRANCE

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Sebastian Havervall

Karolinska Institutet

SWEDEN

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Maria Jesus Iglesias Mareque

KTH Royal Institute of Technology

SWEDEN

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Beatrice Jaspard-Vinassa

University of Bordeaux

FRANCE

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Lynn M. Butler

UiT The Arctic University of Norway

NORWAY

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Maguelonne Roux

Research Interests

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Articles (6)

APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis.

A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism

A novel rare c.-39C>T mutation in the PROS1 5′UTR causing PS deficiency by creating a new upstream translation initiation codon

Anti-integrin αv therapy improves cardiac fibrosis after myocardial infarction by blunting cardiac PW1+ stromal cells

Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis

Collaborators (8)

Taija Makinen

Marie-christine ALESSI

Paul Gray

Qian Zhang

Sebastian Havervall

Maria Jesus Iglesias Mareque

Beatrice Jaspard-Vinassa

Lynn M. Butler

Make your next move.

Maguelonne Roux

Research Interests

Explore related searches

Contact this professor

Articles (6)

APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis.

A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism

A novel rare c.-39C&gt;T mutation in the PROS1 5′UTR causing PS deficiency by creating a new upstream translation initiation codon

Anti-integrin αv therapy improves cardiac fibrosis after myocardial infarction by blunting cardiac PW1+ stromal cells

Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis

Collaborators (8)

Taija Makinen

Marie-christine ALESSI

Paul Gray

Qian Zhang

Sebastian Havervall

Maria Jesus Iglesias Mareque

Beatrice Jaspard-Vinassa

Lynn M. Butler

Make your next move.

A novel rare c.-39C>T mutation in the PROS1 5′UTR causing PS deficiency by creating a new upstream translation initiation codon