Anti-spectrin in sera containing smooth muscle autoantibodies from patients with chronic active hepatitis.

Por Garbarz, M, Dhermy, D, Bournier, O, Bezeaud, A, Boivin, P
Publicado em 1981

Fast screening methods to detect mutations of spectrin in subjects with hereditary elliptocytosis.

Por Boulanger, L, LeCompte, M C, Dhermy, D, Garbarz, M
Publicado em 1992

Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a...

Por Garbarz, M, Tse, W T, Gallagher, P G, Picat, C, Lecomte, M C, Galibert, F, Dhermy, D, Forget, B G
Publicado em 1991

Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.

Por Tse, W T, Lecomte, M C, Costa, F F, Garbarz, M, Feo, C, Boivin, P, Dhermy, D, Forget, B G
Publicado em 1990

Spectrin beta-chain variant associated with hereditary elliptocytosis.

Por Dhermy, D, Lecomte, M C, Garbarz, M, Bournier, O, Galand, C, Gautero, H, Feo, C, Alloisio, N, Delaunay, J, Boivin, P
Publicado em 1982

A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic c...

Por Gallagher, P G, Tse, W T, Coetzer, T, Lecomte, M C, Garbarz, M, Zarkowsky, H S, Baruchel, A, Ballas, S K, Dhermy, D, Palek, J
Publicado em 1992

A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.

Por Jenkins, P B, Abou-Alfa, G K, Dhermy, D, Bursaux, E, Féo, C, Scarpa, A L, Lux, S E, Garbarz, M, Forget, B G, Gallagher, P G
Publicado em 1996