Palek J - Search Results

1

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.

Jarolim P, Palek J, Rubin HL, Prchal JT, Korsgren C, Cohen CM. Jarolim P, et al. Among authors: palek j. Blood. 1992 Jul 15;80(2):523-9. Blood. 1992. PMID: 1378323 Free article.

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

cDNA sequence for human erythrocyte ankyrin.

Lambert S, Yu H, Prchal JT, Lawler J, Ruff P, Speicher D, Cheung MC, Kan YW, Palek J. Lambert S, et al. Among authors: palek j. Proc Natl Acad Sci U S A. 1990 Mar;87(5):1730-4. doi: 10.1073/pnas.87.5.1730. Proc Natl Acad Sci U S A. 1990. PMID: 1689849 Free PMC article.

4

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

Hanspal M, Yoon SH, Yu H, Hanspal JS, Lambert S, Palek J, Prchal JT. Hanspal M, et al. Among authors: palek j. Blood. 1991 Jan 1;77(1):165-73. Blood. 1991. PMID: 1702027 Free article.

5

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.

6

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.

Jarolim P, Lahav M, Liu SC, Palek J. Jarolim P, et al. Among authors: palek j. Blood. 1990 Nov 15;76(10):2125-31. Blood. 1990. PMID: 2242431 Free article.

7

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.

8

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

Lawler J, Coetzer TL, Mankad VN, Moore RB, Prchal JT, Palek J. Lawler J, et al. Among authors: palek j. Blood. 1988 Oct;72(4):1412-5. Blood. 1988. PMID: 3167214 Free article.

9

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.

10

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.

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