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J Palek

Showing results (51-60 of 118) with videos related to

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Progress in Clinical and Biological Research|January 1, 1978
Crosslinking of the nearest membrane protein neighbors in ATP depleted, calcium enriched and irreversibly sickled red cellsJ Palek, S C Liu, P A Liu
Bailliere'S Clinical Haematology|January 1, 1992
The elliptocytoses, ovalocytosis and related disordersG T Nurse, T L Coetzer, J Palek
The American Journal of Physiology|January 1, 1971
Effects of calcium and adenosine triphosphate on volume of human red cell ghostsJ Palek, W A Curby, F J Lionetti
Blood|June 1, 1995
Comparison of the ankyrin (AC)n microsatellites in genomic DNA and mRNA reveals absence of one ankyrin mRNA allele in 20% of patients with hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
The Journal of Biological Chemistry|October 5, 1985
Hemin-mediated dissociation of erythrocyte membrane skeletal proteinsS C Liu, S Zhai, J Lawler, et al.
Blood|September 1, 1987
Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosisT Coetzer, J Lawler, J T Prchal, et al.
The Journal of Clinical Investigation|March 1, 1995
A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
The Journal of Clinical Investigation|November 1, 1982
Molecular defect of spectrin in hereditary pyropoikilocytosis. Alterations in the trypsin-resistant domain involved in spectrin self-associationJ Lawler, S C Liu, J Palek, et al.
The Journal of Clinical Investigation|June 1, 1984
A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-associationJ Lawler, S C Liu, J Palek, et al.
Blood|November 15, 1990
Effect of hemoglobin oxidation products on the stability of red cell membrane skeletons and the associations of skeletal proteins: correlation with a release of heminP Jarolim, M Lahav, S C Liu, et al.
Pageof 12

Showing results (51-60 of 118) with videos related to

Sort By:
Pageof 12
Progress in Clinical and Biological Research|January 1, 1978
Crosslinking of the nearest membrane protein neighbors in ATP depleted, calcium enriched and irreversibly sickled red cellsJ Palek, S C Liu, P A Liu
Bailliere'S Clinical Haematology|January 1, 1992
The elliptocytoses, ovalocytosis and related disordersG T Nurse, T L Coetzer, J Palek
The American Journal of Physiology|January 1, 1971
Effects of calcium and adenosine triphosphate on volume of human red cell ghostsJ Palek, W A Curby, F J Lionetti
Blood|June 1, 1995
Comparison of the ankyrin (AC)n microsatellites in genomic DNA and mRNA reveals absence of one ankyrin mRNA allele in 20% of patients with hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
The Journal of Biological Chemistry|October 5, 1985
Hemin-mediated dissociation of erythrocyte membrane skeletal proteinsS C Liu, S Zhai, J Lawler, et al.
Blood|September 1, 1987
Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosisT Coetzer, J Lawler, J T Prchal, et al.
The Journal of Clinical Investigation|March 1, 1995
A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
The Journal of Clinical Investigation|November 1, 1982
Molecular defect of spectrin in hereditary pyropoikilocytosis. Alterations in the trypsin-resistant domain involved in spectrin self-associationJ Lawler, S C Liu, J Palek, et al.
The Journal of Clinical Investigation|June 1, 1984
A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-associationJ Lawler, S C Liu, J Palek, et al.
Blood|November 15, 1990
Effect of hemoglobin oxidation products on the stability of red cell membrane skeletons and the associations of skeletal proteins: correlation with a release of heminP Jarolim, M Lahav, S C Liu, et al.
Pageof 12