H. L. Rubin

发表

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

P. Jarolim, Shih-Chun Liu, K. Sahr, 1991, Proceedings of the National Academy of Sciences of the United States of America.

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

J. Prchal, P. Jarolim, L. Snyder, 1996, Blood.

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, Shih-Chun Liu, K. Sahr, 1992 .

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

P. Jarolim, S. Liu, J. Palek, 1994, Blood.

Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE).

C. Brugnara, P. Jarolim, M. Cho, 1994, The Journal of clinical investigation.

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.

H. Wichterle, C. Brugnara, P. Jarolim, 1995, Blood.

Characterization of Seven Low Incidence Blood Group Antigens Carried by Erythrocyte Band 3 Protein

P. Jarolim, M. Reid, J. Storry, 1998 .

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 1648.

J. Greenberger, J. Sobolewski, G. Chiang, 1999, Human gene therapy.

Laboratory diagnosis of leptospirosis of domestic animals.

J. R. Cole, H. L. Rubin, H. Ellinghausen, 1979, Proceedings, annual meeting of the United States Animal Health Association.

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

H. Wichterle, P. Jarolim, J. Palek, 1995, British journal of haematology.

Characterization of seven low incidence blood group antigens carried by erythrocyte band 3 protein.

P. Jarolim, M. Reid, J. Storry, 1999, Blood.

Characterization of Seven Low Incidence Blood Group Antigens Carried by Erythrocyte Band 3 Protein: Presented in part at the 49th Annual Meeting of the American Association of Blood Banks, Orlando, FL, October 6-10, 1996.

P. Jarolim, M. Reid, J. Storry, 1998 .

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.

J. Prchal, P. Jarolim, C. M. Cohen, 1992, Blood.

SEROLOGICAL STUDIES ON LEPTOSPIROSIS IN GUATEMALA.

H. L. Rubin, A. Alexander, P. Acha, 1963, The American journal of tropical medicine and hygiene.

A survey of eastern equine encephalomyelitis in Florida horses: Prevalence, economic impact, and management practices, 1982–1983

H. L. Rubin, E. Gibbs, T. Lane, 1986 .

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.

J. Palek, H. L. Rubin, V. Brabec, 1995, The Journal of clinical investigation.

A Thr552—>Ile substitution in erythroid band 3 gives rise to the Warrior blood group antigen

H. L. Rubin, T. Zelinski, G. Coghlan, 1997, Transfusion.

Blood group antigens Rb(a), Tr(a), and Wd(a) are located in the third ectoplasmic loop of erythroid band 3

J. Murray, E. Smart, H. L. Rubin, 1997, Transfusion.

The structure and organization of the human erythroid anion exchanger (AE1) gene.

K. Sahr, B. Daniels, H. L. Rubin, 1994, Genomics.

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.

J. Palek, H. L. Rubin, V. Brabec, 1995, Blood.

The Occurrence of Salmonella in the Lymph Glands of Normal Hogs.

H. L. Rubin, R. Weaver, M. Scherago, 1942 .

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.

K. Sahr, S. Liu, J. Palek, 1992, Blood.

Melioidosis--a military medical problem?

H. L. Rubin, R. Yager, A. Alexander, 1963, Military medicine.

Equine infection with Micronema deletrix.

H. L. Rubin, J. C. Woodard, 1974, Journal of the American Veterinary Medical Association.

A New Salmonella Type Isolated from Apparently Normal Hogs.∗

H. L. Rubin, P. R. Edwards, D. W. Bruner, 1940 .