F. Dai

Adenosine deaminase prefers a distinct sugar ring conformation for binding and catalysis: kinetic and structural studies.

M. Nicklaus, L. Anderson, V. Marquez, 2000, Biochemistry.

Synthesis of Conformationally Restricted Carbocyclic Nucleosides: The Role of the O(4′)-Atom in the Key Hydration Step of Adenosine Deaminase

C. George, M. Nicklaus, V. Marquez, 1999 .

Conformationally restricted nucleosides. The reaction of adenosine deaminase with substrates built on a bicyclo[3.1.0]hexane template.

C. George, M. Nicklaus, V. Marquez, 1999, Nucleosides & nucleotides.

Synthesis of Conformationally Restricted Carbocyclic Nucleosides: The Role of the O(4′)-Atom in the Key Hydration Step of Adenosine Deaminase.

Victor E. Marquez, Marc C. Nicklaus, Clifford George, 2000 .

Fluorometric determination of 2'-beta-fluoro-2',3'-dideoxyadenosine 5'-triphosphate, the active metabolite of a new anti-human immunodeficiency virus drug, in human lymphocytes.

R. Yarchoan, J. Kelley, L. Welles, 2001, Analytical biochemistry.