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Blood Cells, Molecules & Diseases|August 1, 1997
A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern EnglandG Willis, B A Jennings, E Goodman, et al.
Blood Cells, Molecules & Diseases|August 1, 1997
Cloning of the murine platelet glycoprotein Ibalpha gene highlighting species-specific platelet adhesionJ Ware, S Russell, Z M Ruggeri
Blood Cells, Molecules & Diseases|August 1, 1997
Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 casesR L Sham, C Y Ou, J Cappuccio, et al.
Blood Cells, Molecules & Diseases|March 28, 1998
Expression of alpha IIb beta 3 integrin (GPIIb-IIIa) in myeloid cell lines and normal CD34+/CD33+ bone marrow cellsC D Wall, P B Conley, J Armendariz-Borunda, et al.
Blood Cells, Molecules & Diseases|March 26, 1998
Articles in Blood Cells, Molecules, & Diseases Are Posted on the World Wide Web Every Two Weeks. The Current Issue Is Not Complete. Please See the Abstract for More Information
Blood Cells, Molecules & Diseases|June 6, 1998
Molecular identification and expression of erythroid K:Cl cotransporter in human and mouse erythroleukemic cellsC M Pellegrino, A C Rybicki, S Musto, et al.
Blood Cells, Molecules & Diseases|November 26, 2003
Ferroportin 1 (SCL40A1) variant associated with iron overload in African-AmericansErnest Beutler, James C Barton, Vincent J Felitti, et al.
Blood Cells, Molecules & Diseases|November 26, 2003
Genotypic and phenotypic heterogeneity of African Americans with primary iron overloadJames C Barton, Ronald T Acton, Charles A Rivers, et al.
Blood Cells, Molecules & Diseases|November 26, 2003
Blood group does not correlate with disease severity in patients with Fabry disease (alpha-galactosidase A deficiency)Gabor E Linthorst, Claudia C Folman, Johannes M F G Aerts, et al.
Blood Cells, Molecules & Diseases|May 7, 2003
Intranuclear organization of RUNX transcriptional regulatory machinery in biological control of skeletogenesis and cancerGary S Stein, Jane B Lian, Janet L Stein, et al.
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