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Journal of Molecular Biology|May 20, 1992
RNase T1 mutant Glu46Gln binds the inhibitors 2'GMP and 2'AMP at the 3' subsiteJ Granzin, R Puras-Lutzke, O Landt, et al.
Protein Engineering|September 1, 1993
Trp59 to Tyr substitution enhances the catalytic activity of RNase T1 and of the Tyr to Trp variants in positions 24, 42 and 45H P Grunert, O Landt, M Zirpel-Giesebrecht, et al.
Neuro-Degenerative Diseases|December 4, 2009
8-OHdG in cerebrospinal fluid as a marker of oxidative stress in various neurodegenerative diseasesK Gmitterová, U Heinemann, J Gawinecka, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2009
The appearance of pyrrolysine in tRNAHis guanylyltransferase by neutral evolutionIlka U Heinemann, Patrick O'Donoghue, Catherine Madinger, et al.
European Journal of Pediatrics|August 1, 1995
Ketamine and strychnine treatment of an infant with nonketotic hyperglycinaemiaH Tegtmeyer-Metzdorf, B Roth, M Günther, et al.
IUBMB Life|October 1, 2024
Characterization of a novel heterozygous variant in the histidyl-tRNA synthetase gene associated with Charcot-Marie-Tooth disease type 2WSarah D P Wilhelm, Angelica A Moresco, Alberto D Rivero, et al.
IUBMB Life|March 29, 2025
Yeast models for Charcot-Marie-Tooth disease-causing aminoacyl-tRNA synthetase alleles reveal the cellular basis of diseaseMaria Mahmood, Emma Little, Nicole Girard, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|January 29, 2000
Sodium bromide: effects on different patterns of epileptiform activity, extracellular pH changes and GABAergic inhibitionH Meierkord, F Grünig, U Gutschmidt, et al.
Neurobiology of Disease|July 12, 2012
Peri-infarct blood-brain barrier dysfunction facilitates induction of spreading depolarization associated with epileptiform dischargesE G Lapilover, K Lippmann, S Salar, et al.
Epilepsia|September 22, 2000
Alterations of glial cell function in temporal lobe epilepsyU Heinemann, S Gabriel, R Jauch, et al.
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