Palek J - Search Results

1

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.

Jarolim P, Rubin HL, Brabec V, Chrobak L, Zolotarev AS, Alper SL, Brugnara C, Wichterle H, Palek J. Jarolim P, et al. Among authors: palek j. Blood. 1995 Feb 1;85(3):634-40. Blood. 1995. PMID: 7530501 Free article. Clinical Trial.

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.

Jarolim P, Rubin HL, Zhai S, Sahr KE, Liu SC, Mueller TJ, Palek J. Jarolim P, et al. Among authors: palek j. Blood. 1992 Sep 15;80(6):1592-8. Blood. 1992. PMID: 1520883 Free article.

3

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

Jarolim P, Palek J, Amato D, Hassan K, Sapak P, Nurse GT, Rubin HL, Zhai S, Sahr KE, Liu SC. Jarolim P, et al. Among authors: palek j. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11022-6. doi: 10.1073/pnas.88.24.11022. Proc Natl Acad Sci U S A. 1991. PMID: 1722314 Free PMC article.

4

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.

Coetzer T, Palek J, Lawler J, Liu SC, Jarolim P, Lahav M, Prchal JT, Wang W, Alter BP, Schewitz G, et al. Coetzer T, et al. Among authors: palek j. Blood. 1990 Jun 1;75(11):2235-44. Blood. 1990. PMID: 2346784 Free article.

5

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.

Jarolim P, Rubin HL, Brabec V, Palek J. Jarolim P, et al. Among authors: palek j. Blood. 1995 Jun 1;85(11):3278-82. Blood. 1995. PMID: 7756660 Free article.

6

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.

Jarolim P, Rubin HL, Brabec V, Palek J. Jarolim P, et al. Among authors: palek j. J Clin Invest. 1995 Mar;95(3):941-7. doi: 10.1172/JCI117802. J Clin Invest. 1995. PMID: 7883994 Free PMC article.

7

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

Palek J, Jarolim P. Palek J, et al. Semin Hematol. 1993 Oct;30(4):249-83. Semin Hematol. 1993. PMID: 8266114 Review. No abstract available.

8

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

Jarolim P, Wichterle H, Hanspal M, Murray J, Rubin HL, Palek J. Jarolim P, et al. Among authors: palek j. Br J Haematol. 1995 Oct;91(2):502-10. doi: 10.1111/j.1365-2141.1995.tb05330.x. Br J Haematol. 1995. PMID: 8547102

9

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

Chernova MN, Jarolim P, Palek J, Alper SL. Chernova MN, et al. Among authors: palek j. J Membr Biol. 1995 Nov;148(2):203-10. doi: 10.1007/BF00207276. J Membr Biol. 1995. PMID: 8606369

10

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

Wichterle H, Hanspal M, Palek J, Jarolim P. Wichterle H, et al. Among authors: palek j. J Clin Invest. 1996 Nov 15;98(10):2300-7. doi: 10.1172/JCI119041. J Clin Invest. 1996. PMID: 8941647 Free PMC article.

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