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Gerontology|January 1, 1991
Spontaneous degradation and enzymatic repair of aspartyl and asparaginyl residues in aging red cell proteins analyzed by computer simulationJ D Lowenson, S ClarkeThe Journal of Biological Chemistry|January 25, 1983
Membrane protein carboxyl methylation increases with human erythrocyte age. Evidence for an increase in the number of methylatable sitesJ R Barber, S ClarkeProceedings of the National Academy of Sciences of the United States of America|May 1, 1987
Conversion of isoaspartyl peptides to normal peptides: implications for the cellular repair of damaged proteinsP N McFadden, S ClarkeMuscle & Nerve|February 1, 1988
Multifocal acquired demyelinating neuropathy masquerading as motor neuron diseaseG J Parry, S ClarkeThe Journal of Biological Chemistry|March 25, 1992
Recognition of D-aspartyl residues in polypeptides by the erythrocyte L-isoaspartyl/D-aspartyl protein methyltransferase. Implications for the repair hypothesisJ D Lowenson, S ClarkeAnatomy and Embryology|February 1, 1996
Nineteenth century research on naturally occurring cell death and related phenomenaP G Clarke, S ClarkeThe Journal of Biological Chemistry|September 10, 1984
Synthetic peptide substrates for the erythrocyte protein carboxyl methyltransferase. Detection of a new site of methylation at isomerized L-aspartyl residuesE D Murray, S ClarkeBiochemistry|October 19, 1993
Characterization of plant L-isoaspartyl methyltransferases that may be involved in seed survival: purification, cloning, and sequence analysis of the wheat germ enzymeM B Mudgett, S ClarkeJournal of Human Genetics|September 25, 1999
Polymorphic forms of the protein L-isoaspartate (D-aspartate) O-methyltransferase involved in the repair of age-damaged proteinsC G DeVry, S ClarkeThe Biochemical Journal|April 1, 1986
Carboxyl methylation of human erythrocyte band 3 in intact cells. Relation to anion transport activityL L Lou, S ClarkePageof 101