J. Palek

发表

Visualization of the hexagonal lattice in the erythrocyte membrane skeleton

L. Derick, S. Liu, J. Palek, 1987, The Journal of cell biology.

Spectrin tetramer–dimer equilibrium and the stability of erythrocyte membrane skeletons

Shih-Chun Liu, J. Palek, 1980, Nature.

Partial spectrin deficiency in hereditary pyropoikilocytosis.

T. Coetzer, J. Palek, 1986, Blood.

Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis.

P. Jarolim, Shih-Chun Liu, K. Sahr, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency.

J. Prchal, P. Jarolim, L. Snyder, 1996, Blood.

Band 3 Memphis: a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG---- GAG (Lys----Glu) in codon 56

P. Jarolim, Shih-Chun Liu, K. Sahr, 1992 .

The homozygous state for the band 3 protein mutation in Southeast Asian Ovalocytosis may be lethal.

P. Jarolim, S. Liu, J. Palek, 1994, Blood.

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 spherocytosis.

H. Wichterle, C. Brugnara, P. Jarolim, 1995, Blood.

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 skeleton.

D. Golan, J. D. Corbett, M. Cho, 1995, Blood.

Red cell membrane skeletal defects in hereditary and acquired hemolytic anemias.

S. Lux, J. Palek, 1983, Seminars in hematology.

Ultrastructural studies of the interaction of spectrin with phosphatidylserine liposomes

Shih-Chun Liu, L. Derick, J. Palek, 1986 .

Ultrastructural studies of the interaction of spectrin with phosphatidylserine liposomes.

L. Derick, S. Liu, J. Palek, 1986, Blood.

Protein kinases and membrane protein phosphorylation in normal and abnormal human erythrocytes: variation related to mean cell age.

J. Palek, G. Fairbanks, J. Dino, 1983, Blood.

correlation with a release of hemin membrane skeletons and the associations of skeletal proteins: Effect of hemoglobin oxidation products on the stability of red cell

P. Jarolim, Shih-Chun Liu, J. Palek, 2011 .

Effect of hemoglobin oxidation products on the stability of red cell membrane skeletons and the associations of skeletal proteins: correlation with a release of hemin.

P. Jarolim, Shih-Chun Liu, S. Liu, 1990, Blood.

Effect of hemoglobin oxidation products on the stability of red cell membrane skeletons and the associations of skeletal proteins: correlation with a release of hemin.

P. Jarolim, Shih-Chun Liu, J. Palek, 1990 .

RELEASE OF SPECTRIN-FREE VESICLES FROM HUMAN

H. Lutz, Shih-Chun Liu, J. Palek, 1977 .

Release of spectrin-free vesicles from human erythrocytes during ATP depletion: 1. characterization of spectrin-free vesicles

J. Palek, H. Lutz, Sc Liu, 1977, The Journal of cell biology.

Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.

J. Prchal, K. Sahr, J. Palek, 1991, The Journal of clinical investigation.

Differential control of band 3 lateral and rotational mobility in intact red cells.

D. Golan, P. Agre, J. D. Corbett, 1994, The Journal of clinical investigation.

Red cell membranes of ankyrin-deficient nb/nb mice lack band 3 tetramers but contain normal membrane skeletons.

D. Golan, M. Cho, Shih-Chun Liu, 1997, Biochemistry.

Hereditary spherocytosis: a review of the clinical and molecular aspects of the disease.

J. Palek, H. Hassoun, Hani Hassoun, 1996, Blood reviews.

Hemoglobin enhances the self-association of spectrin heterodimers in human erythrocytes.

S. Liu, J. Palek, 1984, The Journal of biological chemistry.

Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis.

E. Fibach, J. Nachman, K. Sahr, 1993, Blood.

Does a patient with hereditary spherocytosis qualify for preoperative autologous blood donation?

R. Weinstein, J. Palek, H. Hassoun, 1997, Transfusion.

Metabolic dependence of protein arrangement in human erythrocyte membranes. II. Crosslinking of major proteins in ghosts from fresh and ATP-depleted red cells.

S. Liu, J. Palek, S. C. Liu, 1979, Blood.

Membrane protein organization in ATP-depleted and irreversibly sickled red cells.

Shih-Chun Liu, S. Liu, J. Palek, 1979, Journal of supramolecular structure.

Effect of procaine HCLl on ATP: calcium-dependent alterations in red cell shape and deformability.

L. Snyder, N. Fortier, J. Palek, 1977, Blood.

Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin.

J. Prchal, J. Palek, Huilan Yu, 1991, Blood.

Spontaneous, reversible protein cross-linking in the human erythrocyte membrane. Temperature and pH dependence.

S. Liu, J. Palek, G. Fairbanks, 1977, Biochemistry.

Protein immunolocalization in the spread erythrocyte membrane skeleton.

A. Chishti, Shih-Chun Liu, L. Derick, 1992, European journal of cell biology.

Isolation and characterization of cDNA clones for human erythrocyte beta-spectrin.

J. Conboy, Y. Kan, J. Prchal, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Hereditary elliptocytosis, spherocytosis and related disorders: consequences of a deficiency or a mutation of membrane skeletal proteins.

J. Palek, Jiri Palek, 1987, Blood reviews.

Oligomeric states of spectrin in normal erythrocyte membranes: Biochemical and electron microscopic studies

Shih-Chun Liu, J. Palek, P. Windisch, 1984, Cell.

Complete Deficiency of Glycophorin A in Red Blood Cells From Mice With Targeted Inactivation of the Band 3 (AE1) Gene

A. Chishti, T. Hanada, K. Sahr, 1998 .

Molecular defect of the band 3 protein in southeast Asian ovalocytosis.

D. Golan, P. Jarolim, Shih-Chun Liu, 1990, The New England journal of medicine.

Synthesis and assembly of membrane skeletal proteins in mammalian red cell precursors

J. Palek, M. Hanspal, 1987, The Journal of cell biology.

The State of Actin Polymerization in Tetracaine-Treated Platelets

J. Palek, G. Davies, Gregg E. Davies, 1982, Thrombosis and Haemostasis.

Platelet protein organization: analysis by treatment with membrane-permeable cross-linking reagents.

J. Palek, G. Davies, G. E. Davies, 1982, Blood.

Red cell membrane remodeling in sickle cell anemia. Sequestration of membrane lipids and proteins in Heinz bodies.

D. Golan, P. Yacono, Shih-Chun Liu, 1996, The Journal of clinical investigation.

Spinal cord compression secondary to extramedullary hematopoiesis: A noninvasive management based on MRI

E. Lathi, J. Palek, H. Hassoun, 1991, American journal of hematology.

A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.

J. Lawler, J. Prchal, S. Liu, 1984, The Journal of clinical investigation.

Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit.

J. Lawler, J. Prchal, S. Liu, 1983, Blood.

Molecular defect of spectrin in hereditary pyropoikilocytosis. Alterations in the trypsin-resistant domain involved in spectrin self-association.

J. Lawler, J. Prchal, Shih-Chun Liu, 1982, The Journal of clinical investigation.

125I-Labeling of platelet proteins with Bolton-Hunter reagent.

J. Palek, G. Davies, G. E. Davies, 1981, Analytical biochemistry.

β spectrinPRAGUE: a truncated β spectrin producing spectrin deficiency, defective spectrin heterodimer self‐association and a phenotype of spherocytic elliptocytosis

H. Wichterle, P. Jarolim, J. Palek, 1995 .

Beta spectrin PRAGUE: a truncated beta spectrin producing spectrin deficiency, defective spectrin heterodimer self-association and a phenotype of spherocytic elliptocytosis.

H. Wichterle, P. Jarolim, J. Palek, 1995, British journal of haematology.

cDNA sequence for human erythrocyte ankyrin.

Y. Kan, D. Speicher, J. Lawler, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Molecular Basis of Spectrin Deficiency in Hereditary Pyropoikilocytosis

E. Fibach, J. Nachman, K. Sahr, 1993 .

Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis.

J. Lawler, J. Prchal, T. Coetzer, 1987, Blood.

Sp alpha I/65: a new variant of the alpha subunit of spectrin in hereditary elliptocytosis.

J. Lawler, H. Jacob, J. Palek, 1985, Blood.

Changes in the Structure and Function of the Red Cell Membrane Skeleton and Hemolytic Anemias

P. Jarolim, Shih-Chun Liu, T. Coetzer, 1989 .

Selective erythroid and magakaryocytic aplasia after sulfasalazine administration.

J. Palek, G. Davies, 1980, Archives of internal medicine.

Hereditary spherocytosis, elliptocytosis, and related disorders

J. Palek, 1995 .

Polymerisation of red cell membrane protein contributes to spheroechinocyte shape irreversibility

S. Liu, J. Palek, P. Liu, 1978, Nature.

Size dependence of ghosts from stored erythrocytes on calcium and adenosine-triphosphate. Evidence for two ghost populations.

J. Palek, F. Lionetti, W. A. Curby, 1972, Vox sanguinis.

Dependence of the permanent deformation of red blood cell membranes on spectrin dimer-tetramer equilibrium: implication for permanent membrane deformation of irreversibly sickled cells.

Shih-Chun Liu, L. Derick, S. Liu, 1993, Blood.

Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblasts.

K. Sahr, S. Liu, J. Palek, 1992, Blood.

Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.

P. Agre, L. Derick, S. Liu, 1990, Blood.

Identification of the protein 4.1 binding site to phosphatidylserine vesicles.

J. Lawler, L. Derick, S. Liu, 1988, Biochemistry.

Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton

A. Chishti, J. Palek, C. Southgate, 1996, Nature Genetics.

Red Cell Membrane Alterations Associated with the Sickling Phenomenon

J. Palek, P. Tsung, Zaven Boornazian, 1981 .

SPECTRIN ASSEMBLY IN IRREVERSIBLY SICKLED CELL MEMBRANES: ROLE OF CALCIUM AND ATP

S. Liu, J. Palek, P. Liu, 1978 .

Red cell calcium content and transmembrane calcium movements in sickle cell anemia.

J. Palek, M. Thomae, D. Ozog, 1977, The Journal of laboratory and clinical medicine.

RED CELL MEMBRANE INJURY IN SICKLE CELL ANAEMIA

J. Palek, 1977, British journal of haematology.

Phosphorylation of protein 4.1 in Plasmodium falciparum-infected human red blood cells.

A. Chishti, Shih-Chun Liu, S. Liu, 1994, Blood.

Relation of Ca plus plus-activated ATPase to Ca plus plus-linked shrinkage of human red cell ghosts.

J. Palek, F. Lionetti, W. A. Curby, 1971, The American journal of physiology.

Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosis.

J. Prchal, S. Liu, J. Palek, 1981, The Journal of clinical investigation.

Genetics of the red cell membrane skeleton.

J. Palek, S. Lambert, 1990, Seminars in hematology.

Red cell membrane protein phosphorylation in hemolytic anemias and muscular dystrophies

J. Palek, P. Tsung, 1980, Muscle & nerve.

Modulation of lateral mobility of band 3 in the red cell membrane by oxidative cross-linking of spectrin

J. Palek, Deborah K. Smith, 1982, Nature.

Metabolic dependence of protein arrangement in human erythrocyte membranes. I. Analysis of spectrin-rich complexes in ATP-depleted red cells

L. Snyder, S. Liu, J. Palek, 1978 .

2,3‐Diphosphoglycerate Metabolism in Hereditary Spherocytosis

V. Brabec, J. Palek, L. Mirčevová, 1969 .

The dependence of shape of human erythrocyte ghosts on calcium, magnesium, and adenosine triphosphate.

J. Palek, F. Lionetti, G. Stewart, 1974, Blood.

Detection of hemin release during hemoglobin S denaturation.

S. Liu, J. Palek, S. Zhai, 1988, Blood.

The expression and synthesis of the band 3 protein initiates the formation of a stable membrane skeleton in murine Rauscher-transformed erythroid cells.

J. Palek, J. Hanspal, M. Hanspal, 1992, European journal of cell biology.

A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis.

S. Saad, K. Sahr, J. Palek, 1994, The Journal of clinical investigation.

Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrin.

C. Johnson, J. Palek, J. Murray, 1996, Blood.

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 spherocytosis.

S. Winter, R. Ware, J. Palek, 1995, The Journal of clinical investigation.

Mutations of the red blood cell membrane proteins: from clinical evaluation to detection of the underlying genetic defect.

K. Sahr, J. Palek, 1992, Blood.

Combination of two mutant alpha spectrin alleles underlies a severe spherocytic hemolytic anemia.

H. Wichterle, P. Jarolim, J. Palek, 1996, The Journal of clinical investigation.

Biogenesis of normal and abnormal red blood cell membrane skeleton.

J. Palek, M. Hanspal, 1992, Seminars in hematology.

Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2.

J. Prchal, P. Jarolim, C. M. Cohen, 1992, Blood.

Hematologic abnormalities simulating anorexia nervosa in an obligatory athlete.

J. Palek, R. Liberman, 1984, The American journal of medicine.

Partition of catalase and its peroxidase activities in human red cell membrane: effect of ATP depletion.

S. Srivastava, L. Snyder, N. Fortier, 1977, Biochimica et biophysica acta.

Temporal synthesis of band 3 oligomers during terminal maturation of mouse erythroblasts. Dimers and tetramers exist in the membrane as preformed stable species.

D. Golan, M. Cho, S. Liu, 1998, Blood.

The composition of red cell lipids and the activity of two enzymes of the erythrocyte membrane (ATPase and acetylcholinesterase) in primary refractory anemias.

V. Brabec, J. Palek, C. Michalec, 1969, Clinica chimica acta; international journal of clinical chemistry.

Effects of calcium and adenosine triphosphate on volume of human red cell ghosts.

J. Palek, F. Lionetti, W. A. Curby, 1971, The American journal of physiology.

Adenosine Triphosphatase Activity of the Red Cell Membrane in Paroxysmal Nocturnal Haemoglobinuria

V. Brabec, J. Palek, L. Mirčevová, 1969, British journal of haematology.

The effect of anti A antibody on red cell organic phosphates and adenosine triphosphatase activity in vitro.

V. Brabec, J. Palek, A. Májský, 2009, Scandinavian journal of haematology.

Adenosintriphosphatase activity in hereditary spherocytosis

V. Brabec, J. Palek, L. Mirčevová, 1967, Blut.

Size Dependence of Ghosts from Stored Erythrocytes on Calcium and Adenosine‐Triphosphate

J. Palek, F. Lionetti, W. A. Curby, 1971, Blood.

Dependence of spectrin organization in red blood cell membranes on cell metabolism: implications for control of red cell shape, deformability, and surface area.

S. Liu, J. Palek, 1979, Seminars in hematology.

Hereditary elliptocytosis and related disorders.

J. Palek, 1985, Clinics in haematology.

The elliptocytoses, ovalocytosis and related disorders.

T. Coetzer, J. Palek, G. Nurse, 1992, Bailliere's clinical haematology.

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 pyropoikilocytosis.

J. Lawler, B. Alter, J. Prchal, 1990, Blood.

Severe hemolysis and red cell fragmentation caused by the combination of a spectrin mutation with a thrombotic microangiopathy

J. Moake, J. Lawler, H. Jacob, 1989, American journal of hematology.

Viscoelastic properties of red cell membrane in hereditary elliptocytosis.

K. Sung, S. Chien, J. Prchal, 1989, Blood.

Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis.

J. Lawler, J. Prchal, R. Moore, 1988, Blood.

Partial spectrin deficiency in hereditary pyropoikilocytosis.

T. Coetzer, J. Palek, 1986, Blood.

Sp all65: A New Variant of the a Subunit of Spectrin in Hereditary Elliptocytosis

J. Lawler, T. Coetzer, H. Jacob, 1985 .

Clinical expression and laboratory detection of red blood cell membrane protein mutations.

J. Palek, P. Jarolím, 1993, Seminars in hematology.

Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit

J. Lawler, J. Prchal, Shih-Chun Liu, 1983 .

Sulfhydryl reagents induce altered spectrin self-association, skeletal instability, and increased thermal sensitivity of red cells.

J. Palek, D. Smith, 1983, Blood.

Defective spectrin dimer-dimer association with hereditary elliptocytosis.

J. Prchal, Shih-Chun Liu, S. Liu, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis.

J. Prchal, S. Liu, J. Palek, 1981, Blood.

Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.

J. Lawler, J. Prchal, S. Liu, 1988, The New England journal of medicine.

Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.

P. Njølstad, J. Rogus, J. Palek, 1997, Blood.

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 spherocytosis.

J. Palek, H. L. Rubin, V. Brabec, 1995, The Journal of clinical investigation.

Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene.

A. Chishti, T. Hanada, K. Sahr, 1998, Blood.

Alterations of spectrin assembly in the red cell membrane: functional consequences.

Shih-Chun Liu, S. Liu, J. Palek, 1981, Scandinavian journal of clinical and laboratory investigation. Supplementum.

Metabolic dependence of protein arrangement in human erythrocyte membranes. I. Analysis of spectrin-rich complexes in ATP-depleted red cells.

L. Snyder, S. Liu, J. Palek, 1978, Blood.

Altered red cell cytoskeletal protein associations leading to membrane instability.

S. Liu, J. Palek, 1981, Progress in clinical and biological research.

Metabolic dependence of protein arrangement in human erythrocyte membranes. II. Crosslinking of major proteins in ghosts from fresh and ATP-depleted red cells

J. Palek, Sc Liu, 1979 .

Cross-linkings between spectrin and band 3 in human erythroycte membranes.

S. Liu, J. Palek, S. C. Liu, 1979, Journal of supramolecular structure.

Reduced invasion and growth of Plasmodium falciparum into elliptocytic red blood cells with a combined deficiency of protein 4.1, glycophorin C, and p55.

A. Chishti, Shih-Chun Liu, S. Liu, 1996, Blood.

Effect of propranolol on normal human erythrocytes.

L. Snyder, N. Fortier, J. Palek, 1977, The Journal of laboratory and clinical medicine.

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 spherocytosis.

J. Palek, H. L. Rubin, V. Brabec, 1995, Blood.

Targeted inactivation of murine band 3 (AE1) gene produces a hypercoagulable state causing widespread thrombosis in vivo.

A. Chishti, S. Liu, J. Palek, 1998, Blood.

Glutathione instability in stored blood

J. Palek, V. Volek, 1964, Experientia.

Uncoupling of the spectrin-based skeleton from the lipid bilayer in sickled red cells.

Shih-Chun Liu, L. Derick, S. Liu, 1991, Science.

Band 3 Memphis: a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG----GAG (Lys----Glu) in codon 56.

K. Sahr, S. Liu, J. Palek, 1992, Blood.

Separation of the lipid bilayer from the membrane skeleton during discocyte-echinocyte transformation of human erythrocyte ghosts.

Shih-Chun Liu, L. Derick, S. Liu, 1989, European journal of cell biology.

Isolation of skeleton-associated knobs from human red blood cells infected with malaria parasite Plasmodium falciparum.

A. Chishti, K. Andrabi, L. Derick, 1992, Molecular and biochemical parasitology.

Defective spectrin dimer-dimer association in hereditary elliptocytosis ( spectrin transformation / membrane skeleton )

Shih-Chun Liu, J. Palek, Joseph T. PRCHALt, 2022 .

Biogenesis of erythrocyte membrane skeleton in health and disease

J. Prchal, J. Palek, M. Hanspal, 1993, Stem cells.

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 spectrin.

A. Baruchel, B. Forget, S. Ballas, 1992, The Journal of clinical investigation.

Erythrocyte membrane alterations in Plasmodium falciparum malaria sequestration

Steven S. Oh, A. Chishti, Shih-Chun Liu, 1997, Current opinion in hematology.

Clinical and laboratory study of two Caucasian families with hereditary pyropoikilocytosis and hereditary elliptocytosis.

L. Peterson, J. Lawler, J. Palek, 1987, American Journal of Clinical Pathology.

Defective membrane skeleton assembly in hereditary elliptocytosis.

J. Prchal, J. Palek, S. C. Liu, 1981, Progress in clinical and biological research.

Overexpression of AE1 Prague, but not of AE1 SAO, inhibits wild-type AE1 trafficking in Xenopus oocytes

S. Alper, J. Palek, M. Chernova, 1995, The Journal of Membrane Biology.

Hereditary spherocytosis: a review of the clinical and molecular aspects of the disease.

J. Palek, Hani Hassoun, 1996, Blood reviews.

Hemin-mediated dissociation of erythrocyte membrane skeletal proteins.

J. Lawler, J. Palek, S. Zhai, 1985, The Journal of biological chemistry.

Red cell carbohydrate metabolism in primary refractory anemias.

V. Brabec, J. Palek, B. Friedmann, 1967, Clinica chimica acta; international journal of clinical chemistry.

The changes of the pentose phosphate pathway in red cells during their ageingin vitro

J. Palek, 1963, Experientia.

Red cell lipids in autoimmune hemolytic anemia.

V. Brabec, J. Palek, C. Michalec, 1969, Blood.