A. Lenoir

发表

Inactive matriptase‐2 mutants found in IRIDA patients still repress hepcidin in a transfection assay despite having lost their serine protease activity

C. Beaumont, C. Oudin, B. Grandchamp, 2012, Human mutation.

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

C. López-Otín, S. Vaulont, A. Ramsay, 2011, Blood.

Iron-deficiency anemia from matriptase-2 inactivation is dependent on the presence of functional Bmp 6 *

C. López-Otín, S. Vaulont, A. Ramsay, 2011 .

Iron deficiency anemia due to matriptase-2 inactivation is dependent upon the presence of functional Bmp 6 Short title : Matriptase-2 and Bmp 6 deficiency in mice

C. López-Otín, S. Vaulont, A. Ramsay, 2010 .

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

C. López-Otín, S. Vaulont, A. Ramsay, 2014, Blood.

Spontaneous hair cell regeneration in the neonatal mouse cochlea in vivo

R. Chai, J. Zuo, Zhiyong Liu, 2014, Development.

Amodiaquine-lnduced Hepatitis: A Report of Seven Cases

D. Pessayre, G. Feldmann, J. Benhamou, 1986 .

Amodiaquine-induced hepatitis. A report of seven cases.

G. Feldmann, J. Benhamou, A. Castot, 1986, Annals of internal medicine.