Immunochemical Characterization of Variant Medium-Chain Acyl-CoA Dehydrogenase in Fibroblasts from Patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

Ulrich K. Laemmli · Nature · 1970 · 251.6K citations

Life Sciences, Microbiology, Molecular Biology +14

Measurement of protein using bicinchoninic acid

Pam Smith, Randall I. Krohn, Greg T. Hermanson et al. · Analytical Biochemistry · 1985 · 18.4K citations

Life Sciences, Biochemistry, Molecular Biology +10

Purification and characterization of short-chain, medium-chain, and long-chain acyl-CoA dehydrogenases from rat liver mitochondria. Isolation of the holo- and apoenzymes and conversion of the apoenzyme to the holoenzyme.

Yasuyuki Ikeda, Kazuko Okamura‐Ikeda, Kay Tanaka · Journal of Biological Chemistry · 1985 · 220 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +11

In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase

Steen Kølvraa, N. Gregersen, E. Christensen et al. · Clinica Chimica Acta · 1982 · 167 citations

Life Sciences, Biochemistry, Cellular Metabolism +10

Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutation.

Ichiro Yokota, Yasuhiro Indo, Paul M. Coates et al. · Journal of Clinical Investigation · 1990 · 102 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17