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M Garbarz

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Clinical and Experimental Immunology|January 1, 1981
Anti-spectrin in sera containing smooth muscle autoantibodies from patients with chronic active hepatitisM Garbarz, D Dhermy, O Bournier, et al.
European Journal of Cell Biology|November 1, 1985
Characterization of rat hepatocyte plasma membrane domains by monoclonal antibodiesM Maurice, A M Durand-Schneider, M Garbarz, et al.
Human Mutation|January 1, 1995
Protein 4.1 Lille, a novel mutation in the downstream initiation codon of protein 4.1 gene associated with heterozygous 4,1(-) hereditary elliptocytosisM Garbarz, I Devaux, O Bournier, et al.
British Journal of Haematology|November 1, 1990
Abnormal tryptic peptide from the spectrin alpha-chain resulting from alpha- or beta-chain mutations: two genetically distinct forms of the Sp alpha I/74 variantM C Lecomte, H Gautero, M Garbarz, et al.
Human Genetics|September 1, 1993
Spectrin alpha IIa variant in dominant and non-dominant spherocytosisP Boivin, C Galand, I Devaux, et al.
Journal of Oncology Pharmacy Practice : Official Publication of the International Society of Oncology Pharmacy Practitioners|September 26, 2017
Pharmacy workload benchmarking: Establishing a health-system outpatient infusion productivity metricJeffrey S Reichard, David M Garbarz, Amanda L Teachey, et al.
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.
Blood|June 1, 1985
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1L Morlé, M Garbarz, N Alloisio, et al.
Blood|September 15, 1994
A second allele of spectrin alpha-gene associated with the alpha I/65 phenotype (allele alpha Ponte de Sôr)L Boulanger, D Dhermy, M Garbarz, 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.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Clinical and Experimental Immunology|January 1, 1981
Anti-spectrin in sera containing smooth muscle autoantibodies from patients with chronic active hepatitisM Garbarz, D Dhermy, O Bournier, et al.
European Journal of Cell Biology|November 1, 1985
Characterization of rat hepatocyte plasma membrane domains by monoclonal antibodiesM Maurice, A M Durand-Schneider, M Garbarz, et al.
Human Mutation|January 1, 1995
Protein 4.1 Lille, a novel mutation in the downstream initiation codon of protein 4.1 gene associated with heterozygous 4,1(-) hereditary elliptocytosisM Garbarz, I Devaux, O Bournier, et al.
British Journal of Haematology|November 1, 1990
Abnormal tryptic peptide from the spectrin alpha-chain resulting from alpha- or beta-chain mutations: two genetically distinct forms of the Sp alpha I/74 variantM C Lecomte, H Gautero, M Garbarz, et al.
Human Genetics|September 1, 1993
Spectrin alpha IIa variant in dominant and non-dominant spherocytosisP Boivin, C Galand, I Devaux, et al.
Journal of Oncology Pharmacy Practice : Official Publication of the International Society of Oncology Pharmacy Practitioners|September 26, 2017
Pharmacy workload benchmarking: Establishing a health-system outpatient infusion productivity metricJeffrey S Reichard, David M Garbarz, Amanda L Teachey, et al.
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.
Blood|June 1, 1985
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1L Morlé, M Garbarz, N Alloisio, et al.
Blood|September 15, 1994
A second allele of spectrin alpha-gene associated with the alpha I/65 phenotype (allele alpha Ponte de Sôr)L Boulanger, D Dhermy, M Garbarz, 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.
Pageof 6