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J Palek

Showing results (101-110 of 118) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Isolation and characterization of cDNA clones for human erythrocyte beta-spectrinJ T Prchal, B J Morley, S H Yoon, et al.
Blood|July 1, 1977
Effect of procaine HCLl on ATP: calcium-dependent alterations in red cell shape and deformabilityJ Palek, A Liu, D Liu, et al.
The Journal of Clinical Investigation|August 1, 1994
A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosisH Hassoun, T L Coetzer, J N Vassiliadis, et al.
Blood|February 1, 1995
Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
Blood|August 26, 1998
Targeted inactivation of murine band 3 (AE1) gene produces a hypercoagulable state causing widespread thrombosis in vivoH Hassoun, Y Wang, J Vassiliadis, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
cDNA sequence for human erythrocyte ankyrinS Lambert, H Yu, J T Prchal, et al.
The New England Journal of Medicine|January 28, 1988
Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosisT L Coetzer, J Lawler, S C Liu, et al.
Biochemistry|August 5, 1997
Red cell membranes of ankyrin-deficient nb/nb mice lack band 3 tetramers but contain normal membrane skeletonsS J Yi, S C Liu, L H Derick, et al.
American Journal of Hematology|September 1, 1989
Severe hemolysis and red cell fragmentation caused by the combination of a spectrin mutation with a thrombotic microangiopathyP Jarolim, J Palek, T L Coetzer, et al.
Blood|June 1, 1990
Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosisT Coetzer, J Palek, J Lawler, et al.
Pageof 12

Showing results (101-110 of 118) with videos related to

Sort By:
Pageof 12
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Isolation and characterization of cDNA clones for human erythrocyte beta-spectrinJ T Prchal, B J Morley, S H Yoon, et al.
Blood|July 1, 1977
Effect of procaine HCLl on ATP: calcium-dependent alterations in red cell shape and deformabilityJ Palek, A Liu, D Liu, et al.
The Journal of Clinical Investigation|August 1, 1994
A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosisH Hassoun, T L Coetzer, J N Vassiliadis, et al.
Blood|February 1, 1995
Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
Blood|August 26, 1998
Targeted inactivation of murine band 3 (AE1) gene produces a hypercoagulable state causing widespread thrombosis in vivoH Hassoun, Y Wang, J Vassiliadis, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
cDNA sequence for human erythrocyte ankyrinS Lambert, H Yu, J T Prchal, et al.
The New England Journal of Medicine|January 28, 1988
Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosisT L Coetzer, J Lawler, S C Liu, et al.
Biochemistry|August 5, 1997
Red cell membranes of ankyrin-deficient nb/nb mice lack band 3 tetramers but contain normal membrane skeletonsS J Yi, S C Liu, L H Derick, et al.
American Journal of Hematology|September 1, 1989
Severe hemolysis and red cell fragmentation caused by the combination of a spectrin mutation with a thrombotic microangiopathyP Jarolim, J Palek, T L Coetzer, et al.
Blood|June 1, 1990
Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosisT Coetzer, J Palek, J Lawler, et al.
Pageof 12