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Journal Articles

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

P Jarolim, JL Murray, HL Rubin, WM Taylor, JT Prchal, SK Ballas, LM Snyder, L Chrobak, WD Melrose, V Brabec, J Palek

Blood (1996) 88 (11): 4366–4374.

https://doi.org/10.1182/blood.V88.11.4366.4366

Published: 1996

Journal Articles

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

P Jarolim, HL Rubin, V Brabec, J Palek

Blood (1995) 85 (11): 3278–3282.

https://doi.org/10.1182/blood.V85.11.3278.bloodjournal85113278

Published: 1995

Journal Articles

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

P Jarolim, HL Rubin, V Brabec, L Chrobak, AS Zolotarev, SL Alper, C Brugnara, H Wichterle, J Palek

Blood (1995) 85 (3): 634–640.

https://doi.org/10.1182/blood.V85.3.634.bloodjournal853634

Published: 1995

Journal Articles

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

SC Liu, P Jarolim, HL Rubin, J Palek, D Amato, K Hassan, M Zaik, P Sapak

Blood (1994) 84 (10): 3590–3591.

https://doi.org/10.1182/blood.V84.10.3590.3590

Published: 1994

Journal Articles

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, HL Rubin, S Zhai, KE Sahr, SC Liu, TJ Mueller, J Palek

Blood (1992) 80 (6): 1592–1598.

https://doi.org/10.1182/blood.V80.6.1592.1592

Published: 1992

Journal Articles

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

P Jarolim, J Palek, HL Rubin, JT Prchal, C Korsgren, CM Cohen

Blood (1992) 80 (2): 523–529.

https://doi.org/10.1182/blood.V80.2.523.523

Published: 1992

NARROW

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

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

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

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

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

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

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ASH Publications

American Society of Hematology

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

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

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

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

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

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

Email alerts

ASH Publications

American Society of Hematology

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