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Characterization of the 5' end of the gene for human glucose phosphate isomerase .
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Cloning of a glucose phosphate isomerase/neuroleukin-like sperm antigen involved in sperm agglutination.
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Expression and enzymatic characterization of human glucose phosphate isomerase variants accounting for GPI deficiency.
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Fine mapping of a polymorphic CA repeat marker on human chromosome 19 and its use in population studies.
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Glucosephosphate isomerase deficiency mutations associated with hereditary nonspherocytic hemolytic anemia .
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Human glucose phosphate isomerase: exon mapping and gene structure.
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Identification of a novel tandemly repeated sequence present in an intron of the glucose phosphate isomerase gene in mouse and man.
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Isolation of single-copy human genes from a library of yeast artificial chromosome clones.
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Molecular basis of neurological dysfunction coupled with haemolytic anaemia in human glucose-6-phosphate isomerase deficiency.
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Mouse glucose-6-phosphate isomerase and neuroleukin have identical 3' sequences.
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Neuroleukin: a lymphokine product of lectin-stimulated T cells.
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Neurotrophic activity of monomeric glucophosphoisomerase was blocked by human immunodeficiency virus and peptides from HIV-1 envelope glycoprotein.
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Phosphohexose isomerase/autocrine motility factor/neuroleukin/maturation factor is a multifunctional phosphoprotein.
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Study of the molecular defects in glucose phosphate isomerase-deficient patients affected by chronic hemolytic anemia
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The characterization of gene mutations for human glucose phosphate isomerase deficiency associated with chronic hemolytic anemia.
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The first stable variant of erythrocyte glucose-phosphate isomerase associated with severe hemolytic anemia.
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