"Characterization of a full-length cDNA encoding human liver S-adenosylmethionine synthetase: tissue-specific gene expression and mRNA levels in hepatopathies."
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Biochem. J.293:481-486(1993) [PubMed] [Europe PMC] [Abstract]

"Molecular cloning and nucleotide sequence of cDNA encoding the human liver S-adenosylmethionine synthetase."
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"The DNA sequence and comparative analysis of human chromosome 10."
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Nature429:375-381(2004) [PubMed] [Europe PMC] [Abstract]

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"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]

"Initial characterization of the human central proteome."
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"Crystal structure of the human s-adenosylmethionine synthetase 1 in complex with the product."
Structural genomics consortium (SGC)
Submitted (2007-07) to the PDB data bank

"Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency."
Ubagai T. , Lei K.-J. , Huang S. , Mudd S.H. , Levy H.L. , Chou J.Y.
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"Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency."
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"Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene."
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Am. J. Hum. Genet.60:540-546(1997) [PubMed] [Europe PMC] [Abstract]

"Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations."
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Am. J. Hum. Genet.66:347-355(2000) [PubMed] [Europe PMC] [Abstract]