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C Galand

Showing results (61-70 of 87) with videos related to

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Blood Cells, Molecules & Diseases|August 26, 1998
Hereditary spherocytosis with spectrin deficiency related to null mutations of the beta-spectrin geneD Dhermy, C Galand, O Bournier, et al.
Acta Haematologica|January 1, 1984
Hereditary elliptocytosis with a spectrin molecular defect in a white patientM C Lecomte, D Dhermy, M Garbarz, et al.
British Journal of Haematology|November 1, 1993
Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variantsM C Lecomte, M Garbarz, H Gautero, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|October 1, 1996
Search for the candidate genes in dominant hereditary spherocytosis using linkage analysisM Garbarz, D Bibas, T Cynober, et al.
Clinical and Experimental Immunology|June 15, 2011
Immune adaptive microenvironment profiles in intracerebral and intrasplenic lymphomas share common characteristicsS Donnou, C Galand, C Daussy, et al.
British Journal of Haematology|October 1, 1994
Location and PCR-based detection of three polymorphisms of the human erythrocyte beta-spectrin gene (SPTB)P G Gallagher, M C Lecomte, C Galand, et al.
British Journal of Haematology|April 1, 1990
Severe recessive poikilocytic anaemia with a new spectrin alpha chain variantM C Lecomte, C Feo, H Gautero, et al.
Blood|January 9, 1999
Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosisD Dhermy, C Galand, O Bournier, et al.
Journal of the Canadian Association of Radiologists|December 1, 1982
Narrowband teleradiologyG Pagé, J Sylvestre, F A Roberge, et al.
British Journal of Haematology|February 5, 1998
A 5' splice region G-->C mutation in exon 3 of the human beta-spectrin gene leads to decreased levels of beta-spectrin mRNA and is responsible for dominant hereditary spherocytosis (spectrin Guemene-Penfao)M Garbarz, C Galand, D Bibas, et al.
Pageof 9

Showing results (61-70 of 87) with videos related to

Sort By:
Pageof 9
Blood Cells, Molecules & Diseases|August 26, 1998
Hereditary spherocytosis with spectrin deficiency related to null mutations of the beta-spectrin geneD Dhermy, C Galand, O Bournier, et al.
Acta Haematologica|January 1, 1984
Hereditary elliptocytosis with a spectrin molecular defect in a white patientM C Lecomte, D Dhermy, M Garbarz, et al.
British Journal of Haematology|November 1, 1993
Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variantsM C Lecomte, M Garbarz, H Gautero, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|October 1, 1996
Search for the candidate genes in dominant hereditary spherocytosis using linkage analysisM Garbarz, D Bibas, T Cynober, et al.
Clinical and Experimental Immunology|June 15, 2011
Immune adaptive microenvironment profiles in intracerebral and intrasplenic lymphomas share common characteristicsS Donnou, C Galand, C Daussy, et al.
British Journal of Haematology|October 1, 1994
Location and PCR-based detection of three polymorphisms of the human erythrocyte beta-spectrin gene (SPTB)P G Gallagher, M C Lecomte, C Galand, et al.
British Journal of Haematology|April 1, 1990
Severe recessive poikilocytic anaemia with a new spectrin alpha chain variantM C Lecomte, C Feo, H Gautero, et al.
Blood|January 9, 1999
Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosisD Dhermy, C Galand, O Bournier, et al.
Journal of the Canadian Association of Radiologists|December 1, 1982
Narrowband teleradiologyG Pagé, J Sylvestre, F A Roberge, et al.
British Journal of Haematology|February 5, 1998
A 5' splice region G-->C mutation in exon 3 of the human beta-spectrin gene leads to decreased levels of beta-spectrin mRNA and is responsible for dominant hereditary spherocytosis (spectrin Guemene-Penfao)M Garbarz, C Galand, D Bibas, et al.
Pageof 9