Liying Jiang
Affiliations: | Analytical Chemistry and Environmental Science | Stockholm University, Stockholm, Stockholms län, Sweden |
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Parents
Sign in to add mentorLeopold Ilag | grad student | 2015 | Stockholm University |
David Anthony Cowan | post-doc | (Chemistry Tree) |
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Publications
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Karlsson O, Jiang L, Ersson L, et al. (2015) Environmental neurotoxin interaction with proteins: Dose-dependent increase of free and protein-associated BMAA (β-N-methylamino-L-alanine) in neonatal rat brain. Scientific Reports. 5: 15570 |
Xie X, Backman D, Lebedev AT, et al. (2015) Primordial soup was edible: abiotically produced Miller-Urey mixture supports bacterial growth. Scientific Reports. 5: 14338 |
Xie X, Backman D, Lebedev AT, et al. (2015) Primordial soup was edible: Abiotically produced Miller-Urey mixture supports bacterial growth Scientific Reports. 5 |
Jiang L, Kiselova N, Rosén J, et al. (2014) Quantification of neurotoxin BMAA (β-N-methylamino-L-alanine) in seafood from Swedish markets. Scientific Reports. 4: 6931 |
Jiang L, Dziedzic P, Spacil Z, et al. (2014) Abiotic synthesis of amino acids and self-crystallization under prebiotic conditions. Scientific Reports. 4: 6769 |
Karlsson O, Jiang L, Andersson M, et al. (2014) Protein association of the neurotoxin and non-protein amino acid BMAA (β-N-methylamino-L-alanine) in the liver and brain following neonatal administration in rats. Toxicology Letters. 226: 1-5 |
Jiang L, Eriksson J, Lage S, et al. (2014) Diatoms: a novel source for the neurotoxin BMAA in aquatic environments. Plos One. 9: e84578 |
Jiang L, Johnston E, Aberg KM, et al. (2013) Strategy for quantifying trace levels of BMAA in cyanobacteria by LC/MS/MS. Analytical and Bioanalytical Chemistry. 405: 1283-92 |
Banack SA, Metcalf JS, Jiang L, et al. (2012) Cyanobacteria produce N-(2-aminoethyl)glycine, a backbone for peptide nucleic acids which may have been the first genetic molecules for life on Earth. Plos One. 7: e49043 |
Jiang L, Aigret B, De Borggraeve WM, et al. (2012) Selective LC-MS/MS method for the identification of BMAA from its isomers in biological samples. Analytical and Bioanalytical Chemistry. 403: 1719-30 |