Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease

Autor: Tutois, S, Montagutelli, X., da Silva, V, Jouault, H, Rouyer-Fessard, P, Leroy-Viard, K, Guénet, J, Nordmann, Y, Beuzard, Y, Deybach, J, Jouault, J

Publikováno v: Journal of Clinical Investigation
Journal of Clinical Investigation, 1991, 88 (5), pp.1730-1736. ⟨10.1172/jci115491⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 1991, 88 (5), pp.1730-1736. ⟨10.1172/jci115491⟩

International audience; A viable autosomal recessive mutation (named fch, or ferrochelatase deficiency) causing jaundice and anemia in mice arose in a mutagenesis experiment using ethylnitrosourea. Homozygotes (fch/fch) display a hemolytic anemia, ph

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fa60c7c72043579430aba54a61cbcb3
https://hal.uca.fr/hal-01920370

Identification of a novel cDNA, encoding a cytoskeletal associated protein, differentially expressed in diffuse large B cell lymphomas.

Autor: Maouche-Chrétien, L, Deleu, N, Badoual, C, Fraissignes, P, Berger, R, Gaulard, P, Roméo, P H, Leroy-Viard, K

Publikováno v: Oncogene; 9/10/98, Vol. 17 Issue 10, p1245, 7p, 1 Black and White Photograph, 4 Diagrams

Improvement of Mouse β-Thalassemia by Recombinant Human Erythropoietin

Autor: Leroy-Viard, K., Rouyer-Fessard, P., Beuzard, Y.

Publikováno v: Blood; September 1991, Vol. 78 Issue: 6 p1596-1602, 7p

Expression of TAL-1 proteins in human tissues

Autor: Pulford, K, Lecointe, N, Leroy-Viard, K, Jones, M, Mathieu-Mahul, D, Mason, DY

Publikováno v: Blood; February 1995, Vol. 85 Issue: 3 p675-684, 10p

Mouse beta thalassemia, a model for the membrane defects of erythrocytes in the human disease

Autor: Rouyer-Fessard, P, Leroy-Viard, K, Domenget, C, Mrad, A, Beuzard, Y

Publikováno v: Journal of Biological Chemistry; November 1990, Vol. 265 Issue: 33 p20247-20251, 5p