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J Palek

Showing results (91-100 of 118) with videos related to

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Blood|June 1, 1994
Phosphorylation of protein 4.1 in Plasmodium falciparum-infected human red blood cellsA H Chishti, G J Maalouf, S Marfatia, et al.
Blood|July 15, 1992
Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblastsM Hanspal, J S Hanspal, R Kalraiya, et al.
Blood|March 15, 1996
Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrinH Hassoun, J N Vassiliadis, J Murray, et al.
Blood|January 1, 1991
Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrinM Hanspal, S H Yoon, H Yu, et al.
Blood|February 1, 1989
Viscoelastic properties of red cell membrane in hereditary elliptocytosisA Chabanel, K L Sung, J Rapiejko, et al.
Biochimica Et Biophysica Acta|October 17, 1977
Partition of catalase and its peroxidase activities in human red cell membrane: effect of ATP depletionL M Snyder, S C Liu, J Palek, et al.
Blood|September 15, 1992
Band 3 Memphis: a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG----GAG (Lys----Glu) in codon 56P Jarolim, H L Rubin, S Zhai, et al.
Blood|November 15, 1994
The homozygous state for the band 3 protein mutation in Southeast Asian Ovalocytosis may be lethalS C Liu, P Jarolim, H L Rubin, et al.
Blood|June 25, 1998
Temporal synthesis of band 3 oligomers during terminal maturation of mouse erythroblasts. Dimers and tetramers exist in the membrane as preformed stable speciesM Hanspal, D E Golan, Y Smockova, et al.
The Journal of Clinical Investigation|September 1, 1991
Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosisT L Coetzer, K Sahr, J Prchal, et al.
Pageof 12

Showing results (91-100 of 118) with videos related to

Sort By:
Pageof 12
Blood|June 1, 1994
Phosphorylation of protein 4.1 in Plasmodium falciparum-infected human red blood cellsA H Chishti, G J Maalouf, S Marfatia, et al.
Blood|July 15, 1992
Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblastsM Hanspal, J S Hanspal, R Kalraiya, et al.
Blood|March 15, 1996
Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrinH Hassoun, J N Vassiliadis, J Murray, et al.
Blood|January 1, 1991
Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrinM Hanspal, S H Yoon, H Yu, et al.
Blood|February 1, 1989
Viscoelastic properties of red cell membrane in hereditary elliptocytosisA Chabanel, K L Sung, J Rapiejko, et al.
Biochimica Et Biophysica Acta|October 17, 1977
Partition of catalase and its peroxidase activities in human red cell membrane: effect of ATP depletionL M Snyder, S C Liu, J Palek, et al.
Blood|September 15, 1992
Band 3 Memphis: a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG----GAG (Lys----Glu) in codon 56P Jarolim, H L Rubin, S Zhai, et al.
Blood|November 15, 1994
The homozygous state for the band 3 protein mutation in Southeast Asian Ovalocytosis may be lethalS C Liu, P Jarolim, H L Rubin, et al.
Blood|June 25, 1998
Temporal synthesis of band 3 oligomers during terminal maturation of mouse erythroblasts. Dimers and tetramers exist in the membrane as preformed stable speciesM Hanspal, D E Golan, Y Smockova, et al.
The Journal of Clinical Investigation|September 1, 1991
Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosisT L Coetzer, K Sahr, J Prchal, et al.
Pageof 12