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- Determination of S-methylmethionine in plant products by use of an automatic amino-acid analyser. E. G. Kovatcheva
, Analyst
, 1979
, 104
, 79
- Stable organophosphorus analogues of S-adenosylmethionine and S-methylmethionine. Kirill V. Alferov, Yurii N. Zhukov, Elena N. Khurs, Radii M. Khomutov
, Mendeleev Commun.
, 2003
, 13
, 243
- Comparative metabolite profiling of foxglove aphids (Aulacorthum solani Kaltenbach) on leaves of resistant and susceptible soybean strains. Dan Sato, Masahiro Sugimoto, Hiromichi Akashi, Masaru Tomita, Tomoyoshi Soga
, Mol. BioSyst.
, 2014
, 10
, 909
- A bicyclic S-adenosylmethionine regeneration system applicable with different nucleosides or nucleotides as cofactor building blocks. Désirée Popadić, Dipali Mhaindarkar, Mike H. N. Dang Thai, Helen C. Hailes, Silja Mordhorst, Jennifer N. Andexer
, RSC Chem. Biol.
, 2021
, 2
, 883
- Sources and sinks of chloromethane in a salt marsh ecosystem: constraints from concentration and stable isotope measurements of laboratory incubation experiments. Frank Keppler, Amelie Ninja Röhling, Nicole Jaeger, Moritz Schroll, Simon Christoph Hartmann, Markus Greule
, Environ. Sci.: Processes Impacts
, 2020
, 22
, 627
- One-electron reduction of sulphonium salts in aqueous solution: a pulse radiolysis study. Marija Bonifačić, Elke Anklam
, J. Chem. Soc., Perkin Trans. 2
, 1991
, 243
- The stereochemical course of methyl group transfer catalysed by the S-methylmethionine: homocysteine transferase from jack beans. Gunnar Grue-Sørensen, Ebbe Kelstrup, Anders Kjær, Jørgen Øgaard Madsen
, J. Chem. Soc., Chem. Commun.
, 1980
, 19
- Diastereospecific, enzymically catalysed transmethylation from S-methyl-L-methionine to L-homocysteine, a naturally occurring process. Gunnar Grue-Sørensen, Ebbe Kelstrup, Anders Kjær, Jørgen Øgaard Madsen
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 1091
- The biosynthesis of nitrogen-, sulfur-, and high-carbon chain-containing sugars. Chia-I. Lin, Reid M. McCarty, Hung-wen Liu
, Chem. Soc. Rev.
, 2013
, 42
, 4377
- Isolation, biological activity, biosynthesis and synthetic studies towards the rubromycin family of natural products. Darcy J. Atkinson, Margaret A. Brimble
, Nat. Prod. Rep.
, 2015
, 32
, 811