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Humangenetik|October 7, 1975
Molecular mechanism of erythrocyte pyruvate kinase deficiencyA Kahn, J Marie, C Galand, et al.
Scandinavian Journal of Haematology|April 1, 1976
Chronic haemolytic anaemia in two patients heterozygous for erythrocyte pyruvate kinase deficiency. Electrofocusing and immunological studies of erythrocyte and liver pyruvate kinaseA Kahn, J Marie, C Galand, et al.
Acta Haematologica|January 1, 1976
Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) typeA Kahn, J Marie, J C Desbois, et al.
Biochimica Et Biophysica Acta|December 6, 1982
Molecular organization of human L' and L pyruvate kinasesM P Simon, J Marie, O Bertrand, et al.
European Journal of Biochemistry|January 1, 1980
Phosphorylation of human erythrocyte pyruvate kinase by soluble cyclic-AMP-dependent protein kinases. Comparison with human liver L-type enzymeJ Marie, H Buc, M P Simon, et al.
Biochimica Et Biophysica Acta|March 14, 1978
The genetic system of the L-type pyruvate kinase forms in man. Subunit structure, interrelation and kinetic characteristics of the pyruvate kinase enzymes from erythrocytes and liverA Kahn, J Marie, H Garreau, et al.
Annals of Human Genetics|May 1, 1981
Research on molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). Use of new protein mapping and immunological techniquesD Daegelen-Proux, A Kahn, J Marie, et al.
The Journal of Biological Chemistry|February 5, 1986
Sequences complementary to the brain-specific "identifier" sequences exist in L-type pyruvate kinase mRNA (a liver-specific messenger) and in transcripts especially abundant in muscleY C Lone, M P Simon, A Kahn, et al.
FEBS Letters|January 20, 1986
Complete nucleotide and deduced amino acid sequences of rat L-type pyruvate kinaseY C Lone, M P Simon, A Kahn, et al.
Isozymes|January 1, 1983
Genetic and epigenetic control of the pyruvate kinase isozymes in mammalsJ Marie, M J Levin, M P Simon, et al.
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