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J Palek

Showing results (111-120 of 118) with videos related to

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The New England Journal of Medicine|November 29, 1990
Molecular defect of the band 3 protein in southeast Asian ovalocytosisS C Liu, S Zhai, J Palek, et al.
The Journal of Clinical Investigation|January 1, 1996
Red cell membrane remodeling in sickle cell anemia. Sequestration of membrane lipids and proteins in Heinz bodiesS C Liu, S J Yi, J R Mehta, et al.
The Journal of Clinical Investigation|December 1, 1995
Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosisH Hassoun, J N Vassiliadis, J Murray, et al.
Blood|July 1, 1997
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiencyH Hassoun, J N Vassiliadis, J Murray, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosisP Jarolim, J Palek, D Amato, et al.
The Journal of Clinical Investigation|March 1, 1992
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrinP G Gallagher, W T Tse, T Coetzer, et al.
Blood|July 1, 1995
Molecular basis of altered red blood cell membrane properties in Southeast Asian ovalocytosis: role of the mutant band 3 protein in band 3 oligomerization and retention by the membrane skeletonS C Liu, J Palek, S J Yi, et al.
Blood|December 1, 1996
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiencyP Jarolim, J L Murray, H L Rubin, et al.
Pageof 12

Showing results (111-120 of 118) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 118 results.
The New England Journal of Medicine|November 29, 1990
Molecular defect of the band 3 protein in southeast Asian ovalocytosisS C Liu, S Zhai, J Palek, et al.
The Journal of Clinical Investigation|January 1, 1996
Red cell membrane remodeling in sickle cell anemia. Sequestration of membrane lipids and proteins in Heinz bodiesS C Liu, S J Yi, J R Mehta, et al.
The Journal of Clinical Investigation|December 1, 1995
Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosisH Hassoun, J N Vassiliadis, J Murray, et al.
Blood|July 1, 1997
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiencyH Hassoun, J N Vassiliadis, J Murray, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosisP Jarolim, J Palek, D Amato, et al.
The Journal of Clinical Investigation|March 1, 1992
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrinP G Gallagher, W T Tse, T Coetzer, et al.
Blood|July 1, 1995
Molecular basis of altered red blood cell membrane properties in Southeast Asian ovalocytosis: role of the mutant band 3 protein in band 3 oligomerization and retention by the membrane skeletonS C Liu, J Palek, S J Yi, et al.
Blood|December 1, 1996
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiencyP Jarolim, J L Murray, H L Rubin, et al.
Pageof 12