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C Galand

Showing results (71-80 of 87) with videos related to

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Blood|July 1, 1994
Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact siteN Parquet, I Devaux, L Boulanger, et al.
British Journal of Haematology|July 1, 1995
Ethnic distribution of allele alpha LELY, a low-expression allele of red-cell spectrin alpha-geneJ Maréchal, R Wilmotte, A Kanzaki, et al.
Blood|August 15, 1992
Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin geneM Garbarz, L Boulanger, S Pedroni, et al.
Radiology|August 1, 1981
Teleradiology in northern QuebecG Pagé, A Grégoire, C Galand, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 casesD Dhermy, M Garbarz, M C Lecomte, et al.
Blood|November 1, 1984
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosisM Garbarz, D Dhermy, M C Lecomte, et al.
The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.
British Journal of Haematology|July 1, 1997
Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defectsD Dhermy, C Galand, O Bournier, et al.
Blood|August 15, 1989
Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypesM C Lecomte, M Garbarz, B Grandchamp, et al.
Human Genetics|December 1, 1987
Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expressionM C Lecomte, D Dhermy, M Garbarz, et al.
Pageof 9

Showing results (71-80 of 87) with videos related to

Sort By:
Pageof 9
Blood|July 1, 1994
Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact siteN Parquet, I Devaux, L Boulanger, et al.
British Journal of Haematology|July 1, 1995
Ethnic distribution of allele alpha LELY, a low-expression allele of red-cell spectrin alpha-geneJ Maréchal, R Wilmotte, A Kanzaki, et al.
Blood|August 15, 1992
Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin geneM Garbarz, L Boulanger, S Pedroni, et al.
Radiology|August 1, 1981
Teleradiology in northern QuebecG Pagé, A Grégoire, C Galand, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 casesD Dhermy, M Garbarz, M C Lecomte, et al.
Blood|November 1, 1984
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosisM Garbarz, D Dhermy, M C Lecomte, et al.
The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.
British Journal of Haematology|July 1, 1997
Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defectsD Dhermy, C Galand, O Bournier, et al.
Blood|August 15, 1989
Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypesM C Lecomte, M Garbarz, B Grandchamp, et al.
Human Genetics|December 1, 1987
Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expressionM C Lecomte, D Dhermy, M Garbarz, et al.
Pageof 9