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C Galand

Showing results (81-90 of 87) with videos related to

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Blood|April 15, 1990
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domainM Garbarz, M C Lecomte, C Féo, et al.
Human Genetics|January 1, 1985
Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosisM C Lecomte, D Dhermy, M Garbarz, et al.
Pediatric Research|October 1, 1984
Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemiaD Dhermy, M C Lecomte, M Garbarz, et al.
Transgenic Research|November 1, 1992
Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin geneG Grimber, C Galand, M Garbarz, et al.
British Journal of Haematology|February 1, 1992
Elliptocytosis-associated spectrin Rouen (beta 220/218) has a truncated but still phosphorylatable beta chainM C Lecomte, H Gautero, O Bournier, et al.
British Journal of Haematology|October 1, 1996
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in BeninC Glele-Kakai, M Garbarz, M C Lecomte, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 9, 1999
Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPID Moatti, P Seknadji, C Galand, et al.
Pageof 9

Showing results (81-90 of 87) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 87 results.
Blood|April 15, 1990
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domainM Garbarz, M C Lecomte, C Féo, et al.
Human Genetics|January 1, 1985
Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosisM C Lecomte, D Dhermy, M Garbarz, et al.
Pediatric Research|October 1, 1984
Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemiaD Dhermy, M C Lecomte, M Garbarz, et al.
Transgenic Research|November 1, 1992
Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin geneG Grimber, C Galand, M Garbarz, et al.
British Journal of Haematology|February 1, 1992
Elliptocytosis-associated spectrin Rouen (beta 220/218) has a truncated but still phosphorylatable beta chainM C Lecomte, H Gautero, O Bournier, et al.
British Journal of Haematology|October 1, 1996
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in BeninC Glele-Kakai, M Garbarz, M C Lecomte, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 9, 1999
Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPID Moatti, P Seknadji, C Galand, et al.
Pageof 9