Remi Favier
6PUBLICATIONS
34CO-AUTHORS
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Publications (6)
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|Sep 11, 2019
Correction of Severe Myelofibrosis, Impaired Platelet Functions and Abnormalities in a Patient with Gray Platelet Syndrome Successfully Treated by Stem Cell Transplantation.Rémi Favier, Xavier Roussel, Sylvain Audia
|Mar 28, 2019
MYH9-related disease mutations cause abnormal red blood cell morphology through increased myosin-actin binding at the membrane.Alyson S Smith, Kasturi Pal, Roberta B Nowak
|Jan 04, 2019
Disrupted filamin A/αIIbβ3 interaction induces macrothrombocytopenia by increasing RhoA activity.Alessandro Donada, Nathalie Balayn, Dominika Sliwa
|Jun 15, 2018
Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice.Inga Hofmann, Mitchell J Geer, Timo Vögtle
|Nov 02, 2017
Mutations of the integrin αIIb/β3 intracytoplasmic salt bridge cause macrothrombocytopenia and enlarged platelet α-granules.Marie Favier, Jean-Claude Bordet, Remi Favier
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Frequent Collaborators
2 joint publications
Jean-Claude Bordet
1 joint publications
Inga Hofmann
1 joint publications
Mitchell J Geer
1 joint publications
Alastair Barr
1 joint publications
Marijke J E Kuijpers
1 joint publications
Kathleen Freson
1 joint publications
Gavin E Jarvis
1 joint publications
Kyriacos Markianos
1 joint publications
Ernest Turro
1 joint publications
Willem H Ouwehand
