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Gaël Nicolas
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Journal Articles

Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders

Romain Duval, Gaël Nicolas, Alexandra Willemetz, Yoshiko Murakami, Mahmoud Mikdar, Cedric Vrignaud, Hisham Megahed, Jean-Pierre Cartron, Cecile Masson, Samer Wehbi, Bérengere Koehl, Marie Hully, Karine Siquier, Nicole Chemlay, Agnes Rotig, Stanislas Lyonnet, Yves Colin, Giulia Barcia, Vincent Cantagrel, Caroline Le Van Kim, Olivier Hermine, Taroh Kinoshita, Thierry Peyrard, Slim Azouzi
Journal: Blood
Blood (2021) 137 (26): 3660–3669.
https://doi.org/10.1182/blood.2020009810
Published: 2021
Includes: Supplemental data
Journal Articles

Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregation

Slim Azouzi, Mahmoud Mikdar, Patricia Hermand, Emilie-Fleur Gautier, Virginie Salnot, Alexandra Willemetz, Gaël Nicolas, Cédric Vrignaud, Alexandre Raneri, Patrick Mayeux, Christine Bole‐Feysot, Patrick Nitschké, Jean-Pierre Cartron, Yves Colin, Olivier Hermine, Gabriele Jedlitschky, Marc Cloutier, Jessica Constanzo-Yanez, Carole Ethier, Nancy Robitaille, Maryse St-Louis, Caroline Le Van Kim, Thierry Peyrard
Journal: Blood
Blood (2020) 135 (6): 441–448.
https://doi.org/10.1182/blood.2019002320
Published: 2020
Includes: Supplemental data
Journal Articles

The Multidrug Transporter MRP4/ABCC4 Involved in the Leukemia Clinical Course Specifies the Novel PEL Human Blood Group System

Slim Azouzi, PhD, Mahmoud Mikdar, MSc, Patricia Hermand-Tournamille, PhD, Emilie-Fleur Gautier, PhD, Virginie Salnot, PhD, Alexandra Willemetz, MSc, Gaël Nicolas, PhD, Cedric Vrignaud, MSc, Alexandre Raneri, Patrick Mayeux, PhD, Christine Bole-Feysot, PhD, Patrick Nitschke, PhD, Jean-Pierre Cartron, PhD, Yves Colin Aronovicz, PhD, Olivier Hermine, Gabriele Jedlitschky, PhD, Marc Cloutier, PhD, Jessica Constanzo-Yanez, Carole Ethier, Nancy Robitaille, MD, Maryse St-Louis, Caroline Le Van Kim, PhD, Thierry Peyrard, PharmD/PhD
Journal: Blood
Blood (2019) 134 (Supplement_1): 715.
https://doi.org/10.1182/blood-2019-124082
Published: 2019
Journal Articles

A Dominant Mutation in Mitochondrial Unfoldase CLPX Results in Erythropoietic Protoporphyria

Yvette Y Yien, PhD, Gael Nicolas, PhD, Lisa van der Vorm, Laurent Gouya, MD PhD, Hector Begonia, Martin Kafina, Jean-Charles Deybach, MD PhD, Tania Baker, PhD, Julia Kardon, PhD, John D. Phillips, PhD, Hervé Puy, MD PhD, Barry H. Paw, MD, PhD
Journal: Blood
Blood (2016) 128 (22): 77.
https://doi.org/10.1182/blood.V128.22.77.77
Published: 2016
Journal Articles

Matriptase-2 is essential for hepcidin repression during fetal life and postnatal development in mice to maintain iron homeostasis

Brief Report
Alexandra Willemetz, Anne Lenoir, Jean-Christophe Deschemin, Carlos Lopez-Otin, Andrew J. Ramsay, Sophie Vaulont, Gaël Nicolas
Journal: Blood
Blood (2014) 124 (3): 441–444.
https://doi.org/10.1182/blood-2014-01-551150
Published: 2014
Includes: Supplemental data
Journal Articles

Iron-deficiency anemia from matriptase-2 inactivation is dependent on the presence of functional Bmp6

Brief Report
Anne Lenoir, Jean-Christophe Deschemin, Léon Kautz, Andrew J. Ramsay, Marie-Paule Roth, Carlos Lopez-Otin, Sophie Vaulont, Gaël Nicolas
Journal: Blood
Blood (2011) 117 (2): 647–650.
https://doi.org/10.1182/blood-2010-07-295147
Published: 2011