αII-Spectrin interacts with Tes and EVL, two actin-binding proteins located at cell contacts von ROTTER, Björn, BOURNIER, Odile, NICOLAS, Gael, DHERMY, Didier, LECOMTE, Marie-Christine

Volltext

Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosis von Dhermy, D, Galand, C, Bournier, O, King, M J, Cynober, T, Roberts, I, Kanyike, F, Adekile, A

Volltext

Tyrosine Phosphorylation Regulates Alpha II Spectrin Cleavage by Calpain von Nicolas, Gaël, Fournier, Catherine M., Galand, Colette, Malbert-Colas, Laurence, Bournier, Odile, Kroviarski, Yolande, Bourgeois, Monique, Camonis, Jacques H., Dhermy, Didier, Grandchamp, Bernard, Lecomte, Marie-Christine

Volltext

Coinheritance of two α-spectrin gene defects in a recessive spherocytosis family von Dhermy, D., Steen-Johnsen, J., Bournier, O., Hetet, G., Cynober, T., Tchernia, G., Grandchamp, B.

Volltext

A natural variant with a point mutation resulting in a homozygous Arg to His substitution at position 388 in prothrombin von D'AUDIGIER, Clément, PASMANT, Eric, BOURNIER, Odile, LAURIAN, Yves, GUILLIN, Marie Claude, BEZEAUD, Annie

Volltext

Protein 4.1 Lille, a novel mutation in the downstream initiation codon of protein 4.1 gene associated with heterozygous 4,1(−) hereditary elliptocytosis von Garbarz, M., Devaux, I., Bournier, O., Grandchamp, B., Dhermy, D.

Volltext

Spectrin beta-chain variant associated with hereditary elliptocytosis von Dhermy, D, Lecomte, M C, Garbarz, M, Bournier, O, Galand, C, Gautero, H, Feo, C, Alloisio, N, Delaunay, J, Boivin, P

Volltext

Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects von Dhermy, Didier, Galand, Colette, Bournier, Odile, Boulanger, Laurent, Cynober, Thérèse, Schismanoff, Pierre Olivier, Bursaux, Elisabeth, Tchernia Boivin, Gil, Pierre, Garbarz, Michel

Volltext

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis von Lecomte, MC, Dhermy, D, Solis, C, Ester, A, Feo, C, Gautero, H, Bournier, O, Boivin, P

Volltext

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis von Garbarz, M, Lecomte, MC, Dhermy, D, Feo, C, Chaveroche, I, Gautero, H, Bournier, O, Picat, C, Goepp, A, Boivin, P

Volltext

Anti-spectrin in sera containing smooth muscle autoantibodies from patients with chronic active hepatitis von Garbarz, M, Dhermy, D, Bournier, O, Bezeaud, A, Boivin, P

Volltext

A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis von Garbarz, M, Dhermy, D, Lecomte, MC, Feo, C, Chaveroche, I, Galand, C, Bournier, O, Bertrand, O, Boivin, P

Volltext

Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family: transmission of the same molecular defect in spectrin through three generations with different clinical expr... von LECOMTE, M. C, DHERMY, D, GARBARZ, M, FEO, C, GAUTERO, H, BOURNIER, O, PICAT, C, CHAVEROCHE, I, GALAND, C, BOIVIN, P

Volltext

Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin von Dhermy, D., Feo, C., Garbarz, M., Lecomte, M. C., Bournier, O., Chaveroche, I., Gautero, H., Boivin, P., Daffos, F., Forestier, F.

Volltext

Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemia von DHERMY, D, LECOMTE, M. C, GARBARZ, M, FEO, C, GAUTERO, H, BOURNIER, O, GALAND, C, HERRERA, A, GRETILLAT, F, BOIVIN, P

Volltext

A 5′ splice region G → C mutation in exon 3 of the human β‐spectrin gene leads to decreased levels of β‐spectrin mRNA and is responsible for dominant hereditary spherocytosis (spec... von Garbarz, Michel, Galand, Colette, Bibas, Dominique, Bournier, Odile, Devaux, Isabelle, Harousseau, Jean‐Luc, Grandchamp, Bernard, Dhermy, Didier

Volltext

Hereditary Spherocytosis with Spectrin Deficiency Related to Null Mutations of the β-Spectrin Gene von Dhermy, Didier, Galand, Colette, Bournier, Odile, Cynober, Thérèse, Méchinaud, Françoise, Tchemia, Gil, Garbarz, Michel

Volltext

Coinheritance of two α-spectrin gene defects in a recessive spherocytosis family: α-spectrin haplotypes in hereditary spherocytosis von Dhermy, D., Steen-Johnsen, J., Bournier, O., Hetet, G., Cynober, T., Tchernia, G., Grandchamp, B.

Volltext

Hereditary pyropoikilocytosis and elliptocytosis in a white french family with the spectrin αI/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the sp... von GARBARZ, M, LECOMTE, M.-C, FORGET, B. G, BOIVIN, P, DHERMY, D, FEO, C, DEVAUX, I, PICAT, C, LEFEBVRE, C, GALIBERT, F, GAUTERO, H, BOURNIER, O, GALAND, C

Volltext

Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis von GARBARZ, M, BIBAS, D, CYNOBER, T, GALAND, C, BOURNIER, O, DEVAUX, I, TCHERNIA, G, DHERMY, D

Volltext