John I. Davis

Mutations in MCT1 cDNA in patients with symptomatic deficiency in lactate transport

Natalya Merezhinskaya, William N. Fishbein, John I. Davis et al. · Muscle & Nerve · 2000 · 110 citations · Full text

Levels of adenylate deaminase, adenylate kinase, and creatine kinase in frozen human muscle biopsy specimens relative to type 1/type 2 fiber distribution: Evidence for a carrier state of myoadenylate deaminase deficiency

William N. Fishbein, John I. Davis, Vernon W. Armbrustmacher et al. · Annals of Neurology · 1984 · 24 citations

Mechanobiology, Muscle Physiology, Muscle Function +11

Levels of adenosine deaminase, AMP deaminase, and adenylate kinase in cultured human lymphoblast lines: Exquisite sensitivity of AMP deaminase to adenosine deaminase inhibitors

William N. Fishbein, John I. Davis, John W. Winkert et al. · Biochemical Medicine · 1981 · 17 citations

Signal Transduction, Amp Deaminase, Adenosine Deaminase +6

Immunologic distinction of human muscle adenylate deaminase from the isozyme(s) in human peripheral blood cells: Implications for myoadenylate deaminase deficiency

William N. Fishbein, John I. Davis, K. Nagarajan et al. · Archives of Biochemistry and Biophysics · 1980 · 15 citations

Immunologic Distinction, Muscle Function, Biochemistry +9

Clinical assay of the human erythrocyte lactate transporter

William N. Fishbein, John I. Davis, John W. Foellmer et al. · Biochemical Medicine and Metabolic Biology · 1988 · 12 citations

Medical Diagnostics, Medicine, Physiology +6