HL Rubin - Concepedia

Author

HL Rubin

St. Elizabeth's Medical Center

Also Known As

HL Rubin

Publications

615

Citations

H-Index

Concepts

All Affiliations

St. Elizabeth's Medical Center St. Elizabeth's Hospital

About

HL Rubin is an author at St. Elizabeth's Medical Center specializing in pathology, cytogenetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	123
2	Biology	2	2	123
3	Molecular Genetics	2	2	123
4	Pathology	2	2	123
5	Genetics	2	2	123

HL Rubin

Publications

612

Citations

H-Index

Page 1

	Year	Citations
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency J. G. Murray, HL Rubin, WM Taylor, Blood	1996	130
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 HL Rubin, V Brabec, L Chrobák, Blood	1995	97
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 Palek, HL Rubin, JT Prchal, Blood	1992	84
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 Palek, HL Rubin, JT Prchal, Blood	1992	72
The homozygous state for the band 3 protein mutation in Southeast Asian Ovalocytosis may be lethal [letter] SC Liu, P Jarolim, HL Rubin, Blood BiologySoutheast Asian OvalocytosisCytogeneticsGenetic DisorderGenetics	1994	66
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 HL Rubin, S Zhai, KE Sahr, Blood	1992	66
The homozygous state for the band 3 protein mutation in Southeast Asian Ovalocytosis may be lethal [letter] SC Liu, HL Rubin, J Palek, Blood BiologySoutheast Asian OvalocytosisCytogeneticsGenetic DisorderGenetics	1994	57
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, Blood	1995	28
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency J. G. Murray, HL Rubin, WM Taylor, Blood	1996	12

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