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Mechanism for increased hepatic glycerol synthesis in the citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mouse: Urine glycerol and glycerol 3-phosphate as potential diagnostic markers of human citrin deficiency

Biochimica et biophysica acta. Molecular basis of disease, 2015-09, Vol.1852 (9), p.1787-1795

2015

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Failure of the feeding response to fasting in carnitine-deficient juvenile visceral steatosis (JVS) mice: Involvement of defective acyl-ghrelin secretion and enhanced corticotropin-releasing factor signaling in the hypothalamus

Biochimica et biophysica acta, 2009-11, Vol.1792 (11), p.1087-1093

2009

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Secondary abnormality of carnitine biosynthesis results from carnitine reabsorptional system defect in juvenile visceral steatosis mice

Biochimica et biophysica acta, 1997-12, Vol.1362 (2), p.263-268

1997

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Prolonged effect of single carnitine administration on fasted carnitine-deficient JVS mice regarding their locomotor activity and energy expenditure

Biochimica et biophysica acta, 2006-10, Vol.1761 (10), p.1191-1199

2006

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Expression of three mitochondrial solute carriers, citrin, aralar1 and ornithine transporter, in relation to urea cycle in mice

Biochimica et biophysica acta. Gene structure and expression, 2002-04, Vol.1574 (3), p.283-292

2002

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Primary defect of juvenile visceral steatosis (jvs) mouse with systemic carnitine deficiency is probably in renal carnitine transport system

Biochimica et biophysica acta, 1994-04, Vol.1226 (1), p.25-30

1994

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Aberrations of ammonia metabolism in ornithine carbamoyltransferase-deficient spf-ash mice and their prevention by treatment with urea cycle intermediate amino acids and an ornithine aminotransferase inactivator

Biochimica et biophysica acta, 1999-09, Vol.1455 (1), p.1-11

1999

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Purification and immunochemical studies of pyruvate dehydrogenase complex from rat heart, and cell-free synthesis of lipoamide dehydrogenase, a component of the complex

Biochimica et biophysica acta, 1983-10, Vol.741 (1), p.86-93

1983

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Abnormal expression of urea cycle enzyme genes in juvenile visceral steatosis (jvs) mice

Biochimica et biophysica acta, 1992-02, Vol.1138 (2), p.167-171

1992

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Novel mRNA molecules are induced in hypertrophied ventricles of carnitine-deficient mice and belong to a family of up-regulated gene in cells overexpressing c-erbB-2

Biochimica et biophysica acta, 2002-09, Vol.1577 (3), p.437-444

2002

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Altered expression of carnitine palmitoyltransferase II in liver, muscle, and heart of mouse strain with juvenile visceral steatosis

Biochimica et biophysica acta, 1996-02, Vol.1289 (1), p.131-135

1996

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Expression of three mitochondrial solute carriers, citrin, aralar1 and ornithine transporter, in relation to urea cycle in mice

Biochimica et biophysica acta, 2002-04, Vol.1574 (3), p.283

2002

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Immunological identification of a new component of Ascaris pyruvate dehydrogenase complex

Biochimica et biophysica acta, 1987-10, Vol.926 (1), p.54-60

1987

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Biochemical analysis of decreased ornithine transport activity in the liver mitochondria from patients with hyperornithinemia, hyperammonemia and homocitrullinuria

Biochimica et biophysica acta, 1988-01, Vol.964 (1), p.90-95

1988

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Proteolytic activities in yeast

BBA - Enzymology, 1975-03, Vol.384 (1), p.203-214

1975

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The α-ketoacid dehydrogenase complexes. Sequence similarity of rat pyruvate dehydrogenase with Escherichia coli and Azotobacter vinelandii α-ketoglutarate dehydrogenase

Biochimica et biophysica acta, 1991-05, Vol.1089 (1), p.1-7

1991

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Mechanism for increased hepatic glycerol synthesis in the citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mouse: Urine glycerol and glycerol 3-phosphate as potential diagnostic markers of human citrin deficiency

Failure of the feeding response to fasting in carnitine-deficient juvenile visceral steatosis (JVS) mice: Involvement of defective acyl-ghrelin secretion and enhanced corticotropin-releasing factor signaling in the hypothalamus

Secondary abnormality of carnitine biosynthesis results from carnitine reabsorptional system defect in juvenile visceral steatosis mice

Prolonged effect of single carnitine administration on fasted carnitine-deficient JVS mice regarding their locomotor activity and energy expenditure

Expression of three mitochondrial solute carriers, citrin, aralar1 and ornithine transporter, in relation to urea cycle in mice

Primary defect of juvenile visceral steatosis (jvs) mouse with systemic carnitine deficiency is probably in renal carnitine transport system

Aberrations of ammonia metabolism in ornithine carbamoyltransferase-deficient spf-ash mice and their prevention by treatment with urea cycle intermediate amino acids and an ornithine aminotransferase inactivator

Purification and immunochemical studies of pyruvate dehydrogenase complex from rat heart, and cell-free synthesis of lipoamide dehydrogenase, a component of the complex

Abnormal expression of urea cycle enzyme genes in juvenile visceral steatosis (jvs) mice

Novel mRNA molecules are induced in hypertrophied ventricles of carnitine-deficient mice and belong to a family of up-regulated gene in cells overexpressing c-erbB-2

Altered expression of carnitine palmitoyltransferase II in liver, muscle, and heart of mouse strain with juvenile visceral steatosis

Expression of three mitochondrial solute carriers, citrin, aralar1 and ornithine transporter, in relation to urea cycle in mice

Immunological identification of a new component of Ascaris pyruvate dehydrogenase complex

Biochemical analysis of decreased ornithine transport activity in the liver mitochondria from patients with hyperornithinemia, hyperammonemia and homocitrullinuria

Proteolytic activities in yeast

The α-ketoacid dehydrogenase complexes. Sequence similarity of rat pyruvate dehydrogenase with Escherichia coli and Azotobacter vinelandii α-ketoglutarate dehydrogenase

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