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Early mitochondrial dysfunction leads to altered redox chemistry underlying pathogenesis of TPI deficiency

Neurobiology of disease, 2013-06, Vol.54, p.289-296

2013

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Real-time PCR genotyping assay for feline erythrocyte pyruvate kinase deficiency and mutant allele frequency in purebred cats in Japan

Journal of Veterinary Medical Science, 2015, Vol.77(6), pp.743-746

2015

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Erythrocyte pyruvate kinase deficiency mutation identified in multiple breeds of domestic cats

BMC veterinary research, 2012-10, Vol.8 (1), p.207-207

2012

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HEREDITARY ANAEMIAS IN LABORATORY ANIMALS

British journal of haematology, 1976-03, Vol.32 (3), p.299-308

1976

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Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family

BMC medical genomics, 2021-07, Vol.14 (1), p.191-191, Article 191

2021

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Triosephosphate isomerase deficiency: New insights into an enigmatic disease

Biochimica et biophysica acta, 2009-12, Vol.1792 (12), p.1168-1174

2009

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Metabolic-Flux Profiling of the Yeasts Saccharomyces cerevisiae and Pichia stipitis

Eukaryotic Cell, 2003-02, Vol.2 (1), p.170-180

2003

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Sequence characterization of alleles Gpi1-Sa and Gpi1-Sb at the glucose phosphate isomerase structural locus

Mammalian genome, 1995-08, Vol.6 (8), p.537-539

1995

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Molecular characterization of glucose-6-phosphate isomerase deficiency in a mammalian cell mutant

Biochemical Society transactions, 1990-04, Vol.18 (2), p.259

1990

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Characteristics of Methylobacillus flagellatum KT mutants, deficient for phosphoglucoisomerase, an enzyme of the ribulose monophosphate cycle of obligate methylotrophic bacteria

Molekulârnaâ genetika, mikrobiologiâ i virusologiâ, 1987-08 (8), p.26

1987

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The pentose phosphate pathway: evidence for the indispensable role of glucose-phosphate isomerase

FEBS letters, 1981-07, Vol.130 (1), p.124-126

Morgan, Michael J.

1981

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Enzymatic anomaly of erythrocytes in congenital nonspherocytic hemolytic anemia. 2

Tohoku journal of experimental medicine, 1961-12, Vol.75, p.263-269

TADA, K

1961

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CLINICAL AND LABORATORY OBSERVATIONS ON FOUR CASES OF NONSPHEROCYTIC HEMOLYTIC ANEMIA

Naika hokan. Japanese archives of internal medicine, 1964-11, Vol.11, p.429

1964

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Early mitochondrial dysfunction leads to altered redox chemistry underlying pathogenesis of TPI deficiency

Real-time PCR genotyping assay for feline erythrocyte pyruvate kinase deficiency and mutant allele frequency in purebred cats in Japan

Erythrocyte pyruvate kinase deficiency mutation identified in multiple breeds of domestic cats

HEREDITARY ANAEMIAS IN LABORATORY ANIMALS

Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family

Triosephosphate isomerase deficiency: New insights into an enigmatic disease

Metabolic-Flux Profiling of the Yeasts Saccharomyces cerevisiae and Pichia stipitis

Sequence characterization of alleles Gpi1-Sa and Gpi1-Sb at the glucose phosphate isomerase structural locus

Molecular characterization of glucose-6-phosphate isomerase deficiency in a mammalian cell mutant

Characteristics of Methylobacillus flagellatum KT mutants, deficient for phosphoglucoisomerase, an enzyme of the ribulose monophosphate cycle of obligate methylotrophic bacteria

The pentose phosphate pathway: evidence for the indispensable role of glucose-phosphate isomerase

Enzymatic anomaly of erythrocytes in congenital nonspherocytic hemolytic anemia. 2

CLINICAL AND LABORATORY OBSERVATIONS ON FOUR CASES OF NONSPHEROCYTIC HEMOLYTIC ANEMIA

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