Human HKR Isozyme: Organization of the Hexokinase I Gene, the Erythroid-Specific Promoter, and Transcription Initiation Site
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference36 articles.
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4. Hereditary nonsherocytic hemolytic anemia due to a new hexokinase variant with reduced stability;Magnani;Blood,1985
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1. Energy Metabolism | Hexokinase/Glucokinase;Encyclopedia of Biological Chemistry III;2021
2. A Dominant Mutation in Hexokinase 1 (HK1) Causes Retinitis Pigmentosa;Investigative Opthalmology & Visual Science;2014-11-07
3. Enzymes of the Red Blood Cell;Tietz Textbook of Clinical Chemistry and Molecular Diagnostics;2012
4. Unique expression pattern of human nicotinamide mononucleotide adenylyltransferase isozymes in red blood cells;Blood Cells, Molecules, and Diseases;2010-06
5. First mutation in the red blood cell-specific promoter of hexokinase combined with a novel missense mutation causes hexokinase deficiency and mild chronic hemolysis;Haematologica;2009-07-16
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