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Interference with hemoglobin A(1C) determination by the hemoglobin variant Shelby.
Am J Clin Pathol
September 2007
The Department of Pathology, University of California San Diego, La Jolla, CA, USA.
Hemoglobin variant carrier status was found in a 46-year-old African American man following detection of a falsely elevated hemoglobin A1c (HbA1c) by ionexchange high-performance liquid chromatography (HPLC, VARIANT A1c, Bio-Rad Laboratories, Hercules, CA). Additional analysis of the hemoglobin variant using the Beta Thal Short program (Bio-Rad) revealed an unknown peak with a retention time of 4.84 minutes and a proportion of 26.
View Article and Find Full Text PDFWe, herein, report the first observation of compound heterozygosity for hemoglobin Shelby and hemoglobin S identified in the south of Brazil. The variant hemoglobin was identified by isoelectric focusing (IEF), high performance liquid chromatography (HPLC) and DNA sequence analysis.
View Article and Find Full Text PDFHb Shelby [beta 131(H9)Gln-->Lys] in association with Hb S [beta 6(A3)Glu-->Val]: characterization, stability, and effects on Hb S polymerization.
Hemoglobin
August 1993
Division of Hematology, Children's Hospital of Philadelphia, PA.
When first tested for abnormal hemoglobins, a 2-year-old boy, appeared to have Hb F, Hb S and Hb A2. Confirmatory testing revealed a beta chain variant inherited from his father and beta S from his mother. Analysis of tryptic peptides in conjunction with automated DNA sequence analysis showed that the variant hemoglobin was Hb Shelby [beta 131(H9)Gln-->Lys (CAG-->AAG)].
View Article and Find Full Text PDFHb Shelby [alpha 2 beta 2(131)(H9)Gln----Lys]-beta zero-thalassemia [codon 15 (TGG----TGA)] identified by DNA sequencing.
Hemoglobin
December 1992
Department of Biochemistry, Medical College of Georgia, Augusta.
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