Sı́lvia Martras

Retinoids, ω‐hydroxyfatty acids and cytotoxic aldehydes as physiological substrates, and H2‐receptor antagonists as pharmacological inhibitors, of human class IV alcohol dehydrogenase

J. Farrés, X. Parés, A. Allali-Hassani, 1998, FEBS letters.

Alcohol dehydrogenase 2 is a major hepatic enzyme for human retinol metabolism

B. Persson, J. Farrés, O. Gallego, 2007, Cellular and Molecular Life Sciences.

Molecular Basis for Differential Substrate Specificity in Class IV Alcohol Dehydrogenases

B. Persson, H. Jörnvall, J. Farrés, 2000, The Journal of Biological Chemistry.

Human aldose reductase and human small intestine aldose reductase are efficient retinal reductases: consequences for retinoid metabolism.

T. Flynn, J. Farrés, O. Gallego, 2003, The Biochemical journal.

Stimulation of retinoic acid production and growth by ubiquitously expressed alcohol dehydrogenase Adh3

G. Duester, J. Farrés, X. Parés, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Kinetics of human alcohol dehydrogenase with ring-oxidized retinoids: effect of Tween 80.

R. Álvarez, A. D. de Lera, J. Farrés, 2004, Archives of biochemistry and biophysics.