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H L Rubin

Showing results (11-20 of 20) with videos related to

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Genomics|December 1, 1994
The structure and organization of the human erythroid anion exchanger (AE1) geneK E Sahr, W M Taylor, B P Daniels, et al.
Blood|July 15, 1992
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 4.2P Jarolim, J Palek, H L Rubin, et al.
Blood|September 15, 1992
Band 3 Memphis: a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG----GAG (Lys----Glu) in codon 56P Jarolim, H L Rubin, S Zhai, et al.
Blood|November 15, 1994
The homozygous state for the band 3 protein mutation in Southeast Asian Ovalocytosis may be lethalS C Liu, P Jarolim, H L Rubin, et al.
Blood|February 1, 1995
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 spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosisP Jarolim, J Palek, D Amato, et al.
The Journal of Clinical Investigation|January 1, 1994
Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE)P Jarolim, H L Rubin, S C Liu, et al.
Blood|December 1, 1996
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiencyP Jarolim, J L Murray, H L Rubin, et al.
Human Gene Therapy|February 18, 1999
Bone marrow stromal cell-mediated gene therapy for hemophilia A: in vitro expression of human factor VIII with high biological activity requires the inclusion of the proteolytic site at amino acid 1648G G Chiang, H L Rubin, V Cherington, et al.
The Journal of Biological Chemistry|April 16, 1998
Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchangerP Jarolim, C Shayakul, D Prabakaran, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Genomics|December 1, 1994
The structure and organization of the human erythroid anion exchanger (AE1) geneK E Sahr, W M Taylor, B P Daniels, et al.
Blood|July 15, 1992
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 4.2P Jarolim, J Palek, H L Rubin, et al.
Blood|September 15, 1992
Band 3 Memphis: a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG----GAG (Lys----Glu) in codon 56P Jarolim, H L Rubin, S Zhai, et al.
Blood|November 15, 1994
The homozygous state for the band 3 protein mutation in Southeast Asian Ovalocytosis may be lethalS C Liu, P Jarolim, H L Rubin, et al.
Blood|February 1, 1995
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 spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosisP Jarolim, J Palek, D Amato, et al.
The Journal of Clinical Investigation|January 1, 1994
Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE)P Jarolim, H L Rubin, S C Liu, et al.
Blood|December 1, 1996
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiencyP Jarolim, J L Murray, H L Rubin, et al.
Human Gene Therapy|February 18, 1999
Bone marrow stromal cell-mediated gene therapy for hemophilia A: in vitro expression of human factor VIII with high biological activity requires the inclusion of the proteolytic site at amino acid 1648G G Chiang, H L Rubin, V Cherington, et al.
The Journal of Biological Chemistry|April 16, 1998
Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchangerP Jarolim, C Shayakul, D Prabakaran, et al.
Pageof 2