Molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency): RNA and DNA analysis von GAUTRON, S, DAEGELEN, D, MENNECIER, F, DUBOCQ, D, KAHN, A, DREYFUS, J.-C

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Molecular cloning of cDNA for rat L-type pyruvate kinase and aldolase B von Simon, M P, Besmond, C, Cottreau, D, Weber, A, Chaumet-Riffaud, P, Dreyfus, J C, Trépat, J S, Marie, J, Kahn, A

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Dietary and hormonal regulation of aldolase B gene expression von MUNNICH, A, BESMOND, C, DARQUY, S, REACH, G, VAULONT, S, DREYFUS, J.-C, KAHN, A

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Evaluation of possible first trimester prenatal diagnosis in lysosomal diseases by trophoblast biopsy von POENARU, L, KAPLAN, L, DUMEZ, J, DREYFUS, J. C

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Dietary control of aldolase B and L-type pyruvate kinase mRNAs in rat. Study of translational activity and hybridization with cloned cDNA probes von Weber, A, Marie, J, Cottreau, D, Simon, M P, Besmond, C, Dreyfus, J C, Kahn, A

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Immunological screening of standard cDNA libraries in pBR322 vectors: Detection of human fibrinogen and prothrombin cDNA clones von Plaisancié, Henri, Alexandre, Yvonne, Uzan, Georges, Besmond, Claude, Benarous, Richard, Frain, Monique, Trepat, JoséSala, Dreyfus, Jean-Claude, Kahn, Axel

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Nucleotide sequence of a cDNA clone for human aldolase B von Besmond, Claude, Dreyfus, Jean-Claude, Gregori, Claudine, Frain, Monique, Zakin, Mario M., Trepat, JoséSala, Kahn, Axel

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Electrophoretic study of hexosaminidases. Hexosaminidase C von Poenaru, L., Dreyfus, J.C.

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Molecular heterogeneity of McArdle disease von Daegelen, D., Gautron, S., Mennecier, F., Dreyfus, J. ‐C., Kahn, A.

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Red cell enzymopathies: Molecular mechanisms von Dreyfus, Jean-Claude, Kahn, Axel

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White blood cells and the diagnosis of alpha-glucosidase deficiency von Dreyfus, J C, Poenaru, L

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Purification of human liver uridylyl transferase and comparison with the erythrocyte enzyme von Banroques, J., Gregori, C., Dreyfus, J.C.

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Transient transcriptional inhibition of the transferrin gene by cyclic AMP von Tuil, David, Vaulont, Sophie, Levin, Mariano J., Munnich, Arnold, Moguilewsky, Martine, Bouton, Marie M., Brissot, Pierre, Dreyfus, Jean-Claude, Kahn, Axel

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Expression of the transferrin gene during development of non-hepatic tissues: High level of transferrin mRNA in fetal muscle and adult brain von Levin, Mariano J., Tuil, David, Uzan, George, Dreyfus, Jean-Claude, Kahn, Axel

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Modifications of Purified Glucose-6-phosphate Dehydrogenase and other Enzymes by a Factor of Low Molecular Weight Abundant in Some Leukemic Cells von Kahn, Axel, Boivin, Pierre, Rubinson, Henriette, Cottreau, Dominique, Marie, Joelle, Dreyfus, Jean-Claude

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Induction of glycolytic enzyme synthesis in proliferating fibroblasts. Study of phosphofructokinase, glucose phosphate isomerase and pyruvate kinase von Meienhofer, M C, Dreyfus, J C, Kahn, A

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Characterization and metabolic regulation of a liver-specific 5.4-kilobase mRNA whose synthesis is transcriptionally induced by carbohydrates and repressed by glucagon and cyclic A... von Pichard, A L, Munnich, A, Meienhofer, M C, Vaulont, S, Simon, M P, Marie, J, Dreyfus, J C, Kahn, A

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Phosphofructokinase in Human Blood Cells von Meienhofer, Marie-Claire, Lagrange, Jean-Leon, Cottreau, Dominique, Lenoir, Gilbert, Dreyfus, Jean-Claude, Kahn, Axel

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Enquêter en terrain sensible. Risques et défis méthodologiques dans les études internationales

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Advances in hereditary red cell enzyme anomalies von Kahn, A, Kaplan, J C, Dreyfus, J C

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