Loss of transferase enzyme activity of transfused erythrocytes in galactosemia.

Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical disease.

Glucosyl transferase activity of bovine galactosyl transferase.

Labeling of creatine phosphokinase without loss of enzyme activity.

Implication of lysine residues in the loss of 6-phosphogluconate dehydrogenase activity in aging human erythrocytes.

Enzyme loading of nucleated chicken erythrocytes.

Genetic basis of galactosemia.

Galactose-1-phosphate uridyltransferase activities in erythrocytes from a patient with galactosemia: discrepancy between two methods.

Molecular characterization of two galactosemia mutations: correlation of mutations with highly conserved domains in galactose-1-phosphate uridyl transferase.

Masking of peptidyl transferase activity in polyribosomes.

Gamma-glutamyl transferase: a secretory enzyme.

The vitamin B6 requirement in oral contraceptive users. I. Assessment by pyridoxal level and transferase activity in erythrocytes.

Terminal deoxynucleotidyl transferase in AKR leukemic cells and lack of relation of enzyme activity to cell cycle phase.

Selective deficiency of 3-beta-d-galactosyltransferase (T-transferase) in Tn-polyagglutinable erythrocytes.

Mannitol excretion in galactosemia patients.

Letter: Unconjugated hyperbilirubinemia in galactosemia.

The photochemical inactivation of peptidyl transferase activity.

Activity Assay of Glutathione S-Transferase (GSTs) Enzyme as a Diagnostic Biomarker for Liver Hydatid Cyst in Vitro.

Terminal deoxynucleotidyl transferase activity in lymphoma.

Toad carbonic anhydrase: purification of the enzyme from erythrocytes of Bufo marinus and comparison with the enzyme activity in the urinary bladder.

Terminal deoxynucleotidyl transferase activity in malignant lymphomas.

The genetic defect in galactosemia.

Gastrointestinal Health in Classic Galactosemia.

Vertically-Oriented and Shape-Tailored Electrocatalytic Metal Nanowire Arrays for Enzyme-Free Galactosemia Rapid Diagnosis.

Relative extents of activity loss between enzyme-substrate interactions and combined environmental mechanisms.

Suggest Documents

Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical disease.

Glucosyl transferase activity of bovine galactosyl transferase.

Labeling of creatine phosphokinase without loss of enzyme activity.

Implication of lysine residues in the loss of 6-phosphogluconate dehydrogenase activity in aging human erythrocytes.

Enzyme loading of nucleated chicken erythrocytes.

Genetic basis of galactosemia.

Galactose-1-phosphate uridyltransferase activities in erythrocytes from a patient with galactosemia: discrepancy between two methods.

Molecular characterization of two galactosemia mutations: correlation of mutations with highly conserved domains in galactose-1-phosphate uridyl transferase.

Masking of peptidyl transferase activity in polyribosomes.

Gamma-glutamyl transferase: a secretory enzyme.

The vitamin B6 requirement in oral contraceptive users. I. Assessment by pyridoxal level and transferase activity in erythrocytes.

Terminal deoxynucleotidyl transferase in AKR leukemic cells and lack of relation of enzyme activity to cell cycle phase.

Selective deficiency of 3-beta-d-galactosyltransferase (T-transferase) in Tn-polyagglutinable erythrocytes.

Mannitol excretion in galactosemia patients.

Letter: Unconjugated hyperbilirubinemia in galactosemia.

The photochemical inactivation of peptidyl transferase activity.

Activity Assay of Glutathione S-Transferase (GSTs) Enzyme as a Diagnostic Biomarker for Liver Hydatid Cyst in Vitro.

Terminal deoxynucleotidyl transferase activity in lymphoma.

Toad carbonic anhydrase: purification of the enzyme from erythrocytes of Bufo marinus and comparison with the enzyme activity in the urinary bladder.

Terminal deoxynucleotidyl transferase activity in malignant lymphomas.

The genetic defect in galactosemia.

Gastrointestinal Health in Classic Galactosemia.

Vertically-Oriented and Shape-Tailored Electrocatalytic Metal Nanowire Arrays for Enzyme-Free Galactosemia Rapid Diagnosis.

Relative extents of activity loss between enzyme-substrate interactions and combined environmental mechanisms.

Loss of transferase enzyme activity of transfused erythrocytes in galactosemia.

Recommend Documents

Follow Us