R. Slee

发表

McArdle's disease: a study on the molecular basis of two different etiologies of myophosphorylase deficiency.

T. V. van Berkel, A. Wintzen, F. Jennekens, 1979, Clinica chimica acta; international journal of clinical chemistry.

Comparison of the inactivation of microsomal glucose-6-phosphatase by in situ lipid peroxidation-derived 4-hydroxynonenal and exogenous 4-hydroxynonenal.

H. Esterbauer, J. Koster, J. Lang, 1986, Free radical research communications.

The involvement of iron and lipid peroxidation in the pathogenesis of HCB induced porphyria.

J. Wilson, J. Koster, A. Edixhoven-Bosdijk, 1985, Biochemical pharmacology.

Ferritin, a physiological iron donor for microsomal lipid peroxidation

J. Koster, R. Slee, R.G. Slee, 1986, FEBS letters.

Canine glycogen storage disease type II. A biochemical study of an acid alpha-glucosidase-deficient Lapland dog.

J. Koster, H. C. Walvoort, R. Slee, 1982, Biochimica et biophysica acta.

Physico-chemical and immunological properties of acid α-glucosidase from various human tissues in relation to glycogenosis type II (pompe's disease)

J. Koster, J. V. Moorsel, R. Slee, 1976 .

Lipid peroxidation of rat liver microsomes.

J. Koster, R. Slee, 1980, Biochimica et biophysica acta.

A family with different clinical forms of acid maltase deficiency (glycogenosis type 11)

J. Martín, J. Tager, M. Niermeijer, 1981, Neurology.

On the lipid peroxidation of rat liver hepatocytes, the formation of fluorescent chromolipids and high molecular weight protein.

T. V. van Berkel, J. Koster, R. Slee, 1982, Biochimica et biophysica acta.

Identity and activities of superoxide dismutase in parenchymal and nonparenchymal cells from rat liver.

T. V. van Berkel, J. K. Kruijt, J. Koster, 1977, Archives of biochemistry and biophysics.

Lipid peroxidation of human erythrocyte ghosts induced by organic hydroperoxides.

J. Koster, R. Slee, 1983, Biochimica et biophysica acta.

Biochemical genetics of the Lapland dog model of glycogen storage disease type II (acid alpha-glucosidase deficiency).

A. Reuser, J. Koster, H. C. Walvoort, 1984, American journal of medical genetics.

The influence of glucose I,6-diphosphate on the enzymatic activity of pyruvate kinase.

T. V. van Berkel, G. Staal, J. Koster, 1972, Biochimica et biophysica acta.

On the biochemical basis of hereditary fructose intolerance.

J. Fernandes, J. Koster, R. Slee, 1975, Biochemical and biophysical research communications.

Identification of heterozygotes for glycogenosis 2 (Acid maltase deficiency)

J. Martín, J. Tager, M. Niermeijer, 1981, Clinical genetics.

The electrophoretic pattern and activities of acid and neutral maltase of cultivated fibroblasts and amniotic fluid cells from controls and patients with the variant of glycogen storage disease type II (Pompe's disease).

W. C. Hülsmann, M. Niermeijer, J. Koster, 1972, Clinica chimica acta; international journal of clinical chemistry.

Studies on cumene hydroperoxide-induced lipid peroxidation in the isolated perfused rat heart.

H. Stam, C. Essed, J. Koster, 1985, Journal of molecular and cellular cardiology.

Possible involvement of the lipid-peroxidation product 4-hydroxynonenal in the formation of fluorescent chromolipids.

H. Esterbauer, E. Koller, J. Koster, 1986, The Biochemical journal.

Isoenzyme pattern of phosphorylase in white blood cells and fibroblasts from patients with liver phosphorylase deficiency.

J. Fernandes, J. Koster, J. Dreyfus, 1976, Clinica chimica acta; international journal of clinical chemistry.

Hepatic phosphorylase deficiency: a biochemical study.

T. V. van Berkel, J. Fernandes, W. C. Hülsmann, 1973, Biochemical and biophysical research communications.

The Development of Lightweight, Ambient Air Breathing, Tubular PEM Fuel Cell

J. Lakeman, Kevin John Green, Ranulf Slee, 2002 .

Glycogenosis type II: the infantile- and late-onset acid maltase deficiency observed in one family.

T. V. van Weerden, H. Busch, J. Koster, 1978, Clinica chimica acta; international journal of clinical chemistry.

An appraisal of human trials in enzyme replacement therapy of genetic diseases.

J. Tager, J. Koster, A. Schram, 1980, Birth defects original article series.

The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease).

W. C. Hülsmann, J. Koster, R. Slee, 1974, Clinica chimica acta; international journal of clinical chemistry.

Isoenzymes of human phosphofructokinase.

T. V. van Berkel, J. Koster, R. Slee, 1980, Clinica chimica acta; international journal of clinical chemistry.

Some properties of human liver acid α-glucosidase

J. Koster, R. Slee, 1977 .