FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

J Palek

Research Profile

Chemicals & Drugs

Anatomy

Disorders

Co-author Network

Publications

TOP 3
Hani Hassoun; Y Wang; J Vassiliadis; Mohini Lutchman; J Palek; LEO S AISH; I S Aish; Shih-Chun Liu; Athar H Chishti
Targeted inactivation of murine band 3 (AE1) gene produces a hypercoagulable state causing widespread thrombosis in vivo.
Manjit Hanspal; David E Golan; Y Smockova; SJ Yi; Michael R Cho; Shih-Chun Liu; J Palek
Temporal synthesis of band 3 oligomers during terminal maturation of mouse erythroblasts. Dimers and tetramers exist in the membrane as preformed stable species.
Hani Hassoun; T Hanada; Mohini Lutchman; Kenneth E Sahr; J Palek; Manjit Hanspal; Athar H Chishti
Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of J Palek (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

1998: Hani Hassoun; Y Wang; J Vassiliadis; Mohini Lutchman; J Palek; LEO S AISH; I S Aish; Shih-Chun Liu; Athar H Chishti
Targeted inactivation of murine band 3 (AE1) gene produces a hypercoagulable state causing widespread thrombosis in vivo.
Blood 1998;92(5):1785-92.
1998: Manjit Hanspal; David E Golan; Y Smockova; SJ Yi; Michael R Cho; Shih-Chun Liu; J Palek
Temporal synthesis of band 3 oligomers during terminal maturation of mouse erythroblasts. Dimers and tetramers exist in the membrane as preformed stable species.
Blood 1998;92(1):329-38.
1998: Hani Hassoun; T Hanada; Mohini Lutchman; Kenneth E Sahr; J Palek; Manjit Hanspal; Athar H Chishti
Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene.
Blood 1998;91(6):2146-51.
1997: R Weinstein; R Martinez; Hani Hassoun; J Palek
Does a patient with hereditary spherocytosis qualify for preoperative autologous blood donation?
Transfusion 1997;37(11-12):1179-83.
1997: SJ Yi; Shih-Chun Liu; L H Derick; J Murray; J E Barker; Michael R Cho; J Palek; David E Golan
Red cell membranes of ankyrin-deficient nb/nb mice lack band 3 tetramers but contain normal membrane skeletons.
Biochemistry 1997;36(31):9596-604.
1997: Hani Hassoun; J N Vassiliadis; J Murray; P R Njolstad; J J Rogus; S K Ballas; F Schaffer; P Jarolim; V Brabec; J Palek
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.
Blood 1997;90(1):398-406.
1997: Steven S Oh; Athar H Chishti; J Palek; Shih-Chun Liu
Erythrocyte membrane alterations in Plasmodium falciparum malaria sequestration.
Current opinion in hematology 1997;4(2):148-54.
1997: V Brabec; J Palek; K Petrtýlová; Jaroslav Cermák; P Jarolím
[Relation between types of erythrocyte membrane defects and the clinical picture in hereditary spherocytosis].
Vnitr̆ní lékar̆ství 1997;43(2):91-4.
1996: Petr Jarolim; J L Murray; HL Rubin; W M Taylor; Josef T Prchal; S K Ballas; L M Snyder; L Chrobak; W D Melrose; V Brabec; J Palek
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency.
Blood 1996;88(11):4366-74.
1996: H Wichterle; Manjit Hanspal; J Palek; Petr Jarolim
Combination of two mutant alpha spectrin alleles underlies a severe spherocytic hemolytic anemia.
The Journal of clinical investigation 1996;98(10):2300-7.
1996: C D Southgate; Athar H Chishti; B Mitchell; S J Yi; J Palek
Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton.
Nature genetics 1996;14(2):227-30.
1996: Hani Hassoun; J Palek
Hereditary spherocytosis: a review of the clinical and molecular aspects of the disease.
Blood reviews 1996;10(3):129-47.
1996: Athar H Chishti; J Palek; D Fisher; G J Maalouf; Shih-Chun Liu
Reduced invasion and growth of Plasmodium falciparum into elliptocytic red blood cells with a combined deficiency of protein 4.1, glycophorin C, and p55.
Blood 1996;87(8):3462-9.
1996: Hani Hassoun; J N Vassiliadis; J Murray; S J Yi; Manjit Hanspal; C A Johnson; J Palek
Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrin.
Blood 1996;87(6):2538-45.
1996: Shih-Chun Liu; S J Yi; J R Mehta; P E Nichols; S K Ballas; P W Yacono; David E Golan; J Palek
Red cell membrane remodeling in sickle cell anemia. Sequestration of membrane lipids and proteins in Heinz bodies.
The Journal of clinical investigation 1996;97(1):29-36.
1995: Hani Hassoun; J N Vassiliadis; J Murray; S J Yi; Manjit Hanspal; Russell E Ware; Stuart S Winter; S S Chiou; J Palek
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.
The Journal of clinical investigation 1995;96(6):2623-9.
1995: Marina N Chernova; Petr Jarolim; J Palek; Seth L Alper
Overexpression of AE1 Prague, but not of AE1 SAO, inhibits wild-type AE1 trafficking in Xenopus oocytes.
The Journal of membrane biology 1995;148(2):203-10.
1995: Petr Jarolim; H Wichterle; Manjit Hanspal; J Murray; HL Rubin; J Palek
Beta spectrin PRAGUE: a truncated beta spectrin producing spectrin deficiency, defective spectrin heterodimer self-association and a phenotype of spherocytic elliptocytosis.
British journal of haematology 1995;91(2):502-10.
1995: Shih-Chun Liu; J Palek; S J Yi; P E Nichols; L H Derick; S S Chiou; D Amato; J D Corbett; Michael R Cho; David E Golan
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.
Blood 1995;86(1):349-58.
1995: Petr Jarolim; HL Rubin; V Brabec; J Palek
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.
Blood 1995;85(11):3278-82.
1995: Petr Jarolim; HL Rubin; V Brabec; J Palek
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.
The Journal of clinical investigation 1995;95(3):941-7.
1995: Petr Jarolim; HL Rubin; V Brabec; L Chrobak; A S Zolotarev; Seth L Alper; Carlo Brugnara; H Wichterle; J Palek
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.
Blood 1995;85(3):634-40.
1994: Shih-Chun Liu; Petr Jarolim; HL Rubin; J Palek; D Amato; K Hassan; M Zaik; P Sapak
The homozygous state for the band 3 protein mutation in Southeast Asian Ovalocytosis may be lethal.
Blood 1994;84(10):3590-1.
1994: J D Corbett; Peter Agre; J Palek; David E Golan
Differential control of band 3 lateral and rotational mobility in intact red cells.
The Journal of clinical investigation 1994;94(2):683-8.
1994: Hani Hassoun; T L Coetzer; J N Vassiliadis; Kenneth E Sahr; G J Maalouf; Sara T O Saad; L Catanzariti; J Palek
A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis.
The Journal of clinical investigation 1994;94(2):643-8.
1994: Athar H Chishti; G J Maalouf; Shirin Marfatia; J Palek; W Wang; D Fisher; Shih-Chun Liu
Phosphorylation of protein 4.1 in Plasmodium falciparum-infected human red blood cells.
Blood 1994;83(11):3339-45.
1993: J Palek; Petr Jarolim
Clinical expression and laboratory detection of red blood cell membrane protein mutations.
Seminars in hematology 1993;30(4):249-83.
1993: Manjit Hanspal; J S Hanspal; Kenneth E Sahr; E Fibach; J Nachman; J Palek
Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis.
Blood 1993;82(5):1652-60.
1993: Manjit Hanspal; Josef T Prchal; J Palek
Biogenesis of erythrocyte membrane skeleton in health and disease.
Stem cells (Dayton, Ohio) 1993;11 Suppl 1():8-12.
1993: Shih-Chun Liu; L H Derick; J Palek
Dependence of the permanent deformation of red blood cell membranes on spectrin dimer-tetramer equilibrium: implication for permanent membrane deformation of irreversibly sickled cells.
Blood 1993;81(2):522-8.
1992: Manjit Hanspal; J Palek
Biogenesis of normal and abnormal red blood cell membrane skeleton.
Seminars in hematology 1992;29(4):305-19.
1992: Petr Jarolim; HL Rubin; S Zhai; Kenneth E Sahr; Shih-Chun Liu; T J Mueller; J Palek
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.
Blood 1992;80(6):1592-8.
1992: Manjit Hanspal; J S Hanspal; R Kalraiya; J Palek
The expression and synthesis of the band 3 protein initiates the formation of a stable membrane skeleton in murine Rauscher-transformed erythroid cells.
European journal of cell biology 1992;58(2):313-8.
1992: J Palek; Kenneth E Sahr
Mutations of the red blood cell membrane proteins: from clinical evaluation to detection of the underlying genetic defect.
Blood 1992;80(2):308-30.
1992: Manjit Hanspal; J S Hanspal; R Kalraiya; Shih-Chun Liu; Kenneth E Sahr; D Howard; J Palek
Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblasts.
Blood 1992;80(2):530-9.
1992: Petr Jarolim; J Palek; HL Rubin; Josef T Prchal; C Korsgren; C M Cohen
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.
Blood 1992;80(2):523-9.
1992: Athar H Chishti; K I Andrabi; L H Derick; J Palek; Shih-Chun Liu
Isolation of skeleton-associated knobs from human red blood cells infected with malaria parasite Plasmodium falciparum.
Molecular and biochemical parasitology 1992;52(2):283-7.
1992: L H Derick; Shih-Chun Liu; Athar H Chishti; J Palek
Protein immunolocalization in the spread erythrocyte membrane skeleton.
European journal of cell biology 1992;57(2):317-20.
1992: G T Nurse; T L Coetzer; J Palek
The elliptocytoses, ovalocytosis and related disorders.
Baillière's clinical haematology 1992;5(1):187-207.
1991: Petr Jarolim; J Palek; D Amato; K Hassan; P Sapak; G T Nurse; HL Rubin; S Zhai; Kenneth E Sahr; Shih-Chun Liu
Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(24):11022-6.
1991: T L Coetzer; Kenneth E Sahr; Josef T Prchal; H Blacklock; L Peterson; R Koler; J Doyle; J Manaster; J Palek
Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.
The Journal of clinical investigation 1991;88(3):743-9.
1991: Manjit Hanspal; R Kalraiya; J Hanspal; Kenneth E Sahr; J Palek
Erythropoietin enhances the assembly of alpha,beta spectrin heterodimers on the murine erythroblast membranes by increasing beta spectrin synthesis.
The Journal of biological chemistry 1991;266(24):15626-30.
1991: Hani Hassoun; L Lawn-Tsao; E R Langevin; E S Lathi; J Palek
Spinal cord compression secondary to extramedullary hematopoiesis: a noninvasive management based on MRI.
American journal of hematology 1991;37(3):201-3.
1991: Shih-Chun Liu; L H Derick; S Zhai; J Palek
Uncoupling of the spectrin-based skeleton from the lipid bilayer in sickled red cells.
Science (New York, N.Y.) 1991;252(5005):574-6.
1991: Manjit Hanspal; S H Yoon; H Yu; J S Hanspal; S Lambert; J Palek; Josef T Prchal
Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin.
Blood 1991;77(1):165-73.
1990: Shih-Chun Liu; S Zhai; J Palek; D E Golan; D Amato; K Hassan; G T Nurse; D Babona; T Coetzer; Petr Jarolim
Molecular defect of the band 3 protein in southeast Asian ovalocytosis.
The New England journal of medicine 1990;323(22):1530-8.
1990: Petr Jarolim; M Lahav; Shih-Chun Liu; J Palek
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.
Blood 1990;76(10):2125-31.
1990: J Palek; S Lambert
Genetics of the red cell membrane skeleton.
Seminars in hematology 1990;27(4):290-332.
1990: Shih-Chun Liu; L H Derick; Peter Agre; J Palek
Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.
Blood 1990;76(1):198-205.
1990: T Coetzer; J Palek; J Lawler; Shih-Chun Liu; Petr Jarolim; M Lahav; Josef T Prchal; W Wang; BLANCHE ALTER; G Schewitz
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.
Blood 1990;75(11):2235-44.
1990: S Lambert; H Yu; Josef T Prchal; J Lawler; P Ruff; D Speicher; M C Cheung; Y W Kan; J Palek
cDNA sequence for human erythrocyte ankyrin.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(5):1730-4.
1989: Petr Jarolim; J Palek; T L Coetzer; J Lawler; E Velez-Garcia; J Fradera; A Charles; H S Jacob; J L Moake
Severe hemolysis and red cell fragmentation caused by the combination of a spectrin mutation with a thrombotic microangiopathy.
American journal of hematology 1989;32(1):50-6.
1989: Shih-Chun Liu; L H Derick; M A Duquette; J Palek
Separation of the lipid bilayer from the membrane skeleton during discocyte-echinocyte transformation of human erythrocyte ghosts.
European journal of cell biology 1989;49(2):358-65.
1988: J Lawler; T L Coetzer; Vipul N Mankad; R B Moore; Josef T Prchal; J Palek
Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis.
Blood 1988;72(4):1412-5.
1988: Shih-Chun Liu; S Zhai; J Palek
Detection of hemin release during hemoglobin S denaturation.
Blood 1988;71(6):1755-8.
1988: T L Coetzer; J Lawler; Shih-Chun Liu; Josef T Prchal; R J Gualtieri; M C Brain; J V Dacie; J Palek
Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.
The New England journal of medicine 1988;318(4):230-4.
1988: A M Cohen; Shih-Chun Liu; J Lawler; L Derick; J Palek
Identification of the protein 4.1 binding site to phosphatidylserine vesicles.
Biochemistry 1988;27(2):614-9.
1987: M Hanspal; J Palek
Synthesis and assembly of membrane skeletal proteins in mammalian red cell precursors.
The Journal of cell biology 1987;105(3):1417-24.
1987: J Palek
Hereditary elliptocytosis, spherocytosis and related disorders: consequences of a deficiency or a mutation of membrane skeletal proteins.
Blood reviews 1987;1(3):147-68.
1987: Shih-Chun Liu; L H Derick; J Palek
Visualization of the hexagonal lattice in the erythrocyte membrane skeleton.
The Journal of cell biology 1987;104(3):527-36.
1987: J Palek; T Coetzer
Clinical expression of alpha spectrin mutants in hereditary elliptocytosis.
Blood cells 1987;13(1-2):237-50.
1986: A M Cohen; Shih-Chun Liu; L H Derick; J Palek
Ultrastructural studies of the interaction of spectrin with phosphatidylserine liposomes.
Blood 1986;68(4):920-6.
1984: J Lawler; S C Liu; J Palek; Josef T Prchal
A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.
The Journal of clinical investigation 1984;73(6):1688-95.
1983: J Lawler; J Palek; S C Liu; Josef T Prchal; William M Butler
Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit.
Blood 1983;62(6):1182-9.
1982: J Lawler; S C Liu; J Palek; Josef T Prchal
Molecular defect of spectrin in hereditary pyropoikilocytosis. Alterations in the trypsin-resistant domain involved in spectrin self-association.
The Journal of clinical investigation 1982;70(5):1019-30.
1981: S C Liu; J Palek; Josef T Prchal; R P Castleberry
Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosis.
The Journal of clinical investigation 1981;68(3):597-605.
1981: J Palek; S C Liu; P Y Liu; Josef T Prchal; R P Castleberry
Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis.
Blood 1981;57(1):130-9.
1981: S C Liu; J Palek; Josef T Prchal
Defective membrane skeleton assembly in hereditary elliptocytosis.
Progress in clinical and biological research 1981;56():157-69.