Zobrazeno 1 - 10 of 423 pro vyhledávání: '"J. Palek"'
1
Phosphorylation of protein 4.1 in Plasmodium falciparum-infected human red blood cells
Autor: AH Chishti, GJ Maalouf, S Marfatia, J Palek, W Wang, D Fisher, SC Liu
Publikováno v: Blood. 83:3339-3345
The composition of the erythrocyte plasma membrane is extensively modified during the intracellular growth of the malaria parasite Plasmodium falciparum. It has been previously shown that an 80-kD phosphoprotein is associated with the plasma membrane
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e1581e65adc1ea2b7e100b72d674e284
https://doi.org/10.1182/blood.v83.11.3339.bloodjournal83113339
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2
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
Autor: P Jarolim, HL Rubin, S Zhai, KE Sahr, SC Liu, TJ Mueller, J Palek
Publikováno v: Blood. 80:1592-1598
Band 3 Memphis (b3M) is a variant of the erythrocyte band 3 protein detected in individuals of virtually all ethnic groups and characterized by a reduced mobility of proteolytic fragments derived from the N-terminus of the cytoplasmic domain of band
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6ccac5b57617c0bc8d9b3bbdd689fe11
https://doi.org/10.1182/blood.v80.6.1592.bloodjournal8061592
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3
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
Autor: P Jarolim, J Palek, HL Rubin, JT Prchal, C Korsgren, CM Cohen
Publikováno v: Blood. 80:523-529
Protein 4.2 is a major red blood cell (RBC) protein that interacts with the band 3 protein and with ankyrin. Inherited deficiencies of this protein are associated with spherocytic hemolytic anemia, but the molecular basis of this defect is unknown. W
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6b92ca4470eb49ec92d5da2fadecd788
https://doi.org/10.1182/blood.v80.2.523.523
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5
Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis
Autor: SC Liu, LH Derick, P Agre, J Palek
Publikováno v: Blood. 76:198-205
The membrane skeleton of normal erythrocytes is largely organized into a hexagonal lattice of junctional complexes (JC) crosslinked by spectrin tetramers, and occasional double tetramers and hexamers. To explore possible skeletal alterations in hered
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::94e5c34403cf598fcbab6e41fee9babb
https://doi.org/10.1182/blood.v76.1.198.bloodjournal761198
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7
Temporal synthesis of band 3 oligomers during terminal maturation of mouse erythroblasts. Dimers and tetramers exist in the membrane as preformed stable species
Autor: M, Hanspal, D E, Golan, Y, Smockova, S J, Yi, M R, Cho, S C, Liu, J, Palek
Publikováno v: Blood. 92(1)
Band 3, the anion transport protein of the erythrocyte membrane, exists in the membrane as a mixture of dimers (B3D) and tetramers (B3T). The dimers are not linked to the skeleton and constitute the free mobile band 3 fraction. The tetramers are link
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::72cfa84374b6711b9b41d9f94016fd72
https://pubmed.ncbi.nlm.nih.gov/9639533
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8
[Relation between types of erythrocyte membrane defects and the clinical picture in hereditary spherocytosis]
Autor: V, Brabec, J, Palek, K, Petrtýlová, J, Cermák, P, Jarolím
Publikováno v: Vnitrni lekarstvi. 43(2)
From total number of 130 patients with hereditary spherocytosis from 75 families in 119 patients from 69 families a defect of membrane proteins was detected. In 23 families (33.3%) a spectrin defect was involved, in 32 families (46.3%) a combined def
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7348d3e55889deb643930cacbe376c7e
https://pubmed.ncbi.nlm.nih.gov/9245075
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9
Reduced invasion and growth of Plasmodium falciparum into elliptocytic red blood cells with a combined deficiency of protein 4.1, glycophorin C, and p55
Autor: A H, Chishti, J, Palek, D, Fisher, G J, Maalouf, S C, Liu
Publikováno v: Blood. 87(8)
In this investigation, we have measured the invasion and growth of the malaria parasite Plasmodium falciparum into elliptocytic red blood cells (RBCs) obtained from subjects with homozygous hereditary elliptocytosis. These elliptocytic RBCs have been
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4ce3931f673c4a6b491500f776a3c02e
https://pubmed.ncbi.nlm.nih.gov/8605365
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10
Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrin
Autor: H, Hassoun, J N, Vassiliadis, J, Murray, S J, Yi, M, Hanspal, C A, Johnson, J, Palek
Publikováno v: Blood. 87(6)
Red cell membrane protein analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and direct quantitation by radioimmunoassay or cytofluorometry defines four distinct subsets of patients with hereditary spherocytosis: Patient
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::71504752ca9bcb3c97070465194cbf0b
https://pubmed.ncbi.nlm.nih.gov/8630421
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