L. O'Brien

Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications.

J. Ibdah, M. Bennett, P. Rinaldo, 1999, Seminars in perinatology.

Sequestration of the active site by interdomain shifting. Crystallographic and spectroscopic evidence for distinct conformations of L-3-hydroxyacyl-CoA dehydrogenase.

L. Banaszak, A. Strauss, J. Barycki, 2000, The Journal of biological chemistry.

Pig heart short chain L‐3‐hydroxyacyl‐CoA dehydrogenase revisited: Sequence analysis and crystal structure determination

L. Banaszak, J. Birktoft, A. Strauss, 1999, Protein science : a publication of the Protein Society.

Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family study.

J. Vockley, M. Bennett, R. Boriack, 2000, The Journal of pediatrics.

Biochemical characterization and crystal structure determination of human heart short chain L-3-hydroxyacyl-CoA dehydrogenase provide insights into catalytic mechanism.

L. Banaszak, R. Sanishvili, A. Strauss, 1999, Biochemistry.

Glutamate 170 of Human l-3-Hydroxyacyl-CoA Dehydrogenase Is Required for Proper Orientation of the Catalytic Histidine and Structural Integrity of the Enzyme*

L. Banaszak, A. Strauss, J. Barycki, 2001, The Journal of Biological Chemistry.