Dihydroxyacetone metabolism by human erythrocytes: demonstration of triokinase activity and its characterization

Triosephosphate isomerase deficiency: repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated families.

American journal of hematology·1995

Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemia.

The Journal of clinical investigation·1995

Erythrocyte fragility and chronic intermittent pigmenturia in a dog.

Journal of the American Veterinary Medical Association·1995

2-Chlorodeoxyadenosine activity in patients with untreated chronic lymphocytic leukemia.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology·1995

Three new exon 10 glucose-6-phosphate dehydrogenase mutations.

Blood cells, molecules & diseases·1995

Molecular heterogeneity of G-6-PD deficiency in Mexico.

Archives of medical research·1995

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Modular in vivo engineering of the reductive methylaspartate cycles for synthetic CO2 fixation.

Trends in biotechnology·2026

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Multi-scale characterization of calcium hydroxide mediated cell wall deconstruction during mild pretreatment.

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Dihydroxyacetone metabolism by human erythrocytes: demonstration of triokinase activity and its characterization

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Triosephosphate isomerase deficiency: repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated families.

Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemia.

Erythrocyte fragility and chronic intermittent pigmenturia in a dog.

2-Chlorodeoxyadenosine activity in patients with untreated chronic lymphocytic leukemia.

Three new exon 10 glucose-6-phosphate dehydrogenase mutations.

Molecular heterogeneity of G-6-PD deficiency in Mexico.

A new reporter strategy reveals a subset of nonmigratory hematopoietic stem cells located in a dynamic bone marrow niche.

A randomized phase 2 study combining midostaurin, low-dose cytarabine and venetoclax in newly diagnosed AML ≥60 years.

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