<HashMap><database>MetabolomicsWorkbench</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>http://www.metabolomicsworkbench.org/rest/study/study_id/ST000524/mwtab</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><technology_type>Mass Spectrometry</technology_type><technology_type>ESI</technology_type><disease>Heart Disease</disease><full_dataset_link>http://www.metabolomicsworkbench.org/data/DRCCMetadata.php?Mode=Study&amp;StudyID=ST000524</full_dataset_link><study_factor>group:Old-Placebo | Time point:Post</study_factor><study_factor>group:Old-Curcumin | Time point:Pre</study_factor><study_factor>group:young | Time point:Baseline</study_factor><study_factor>group:Old-Curcumin | Time point:Post</study_factor><study_factor>group:Old-Placebo | Time point:Pre</study_factor><tissue>Blood</tissue><sample_protocol>Reversed phase POSITIVE ION MODE.</sample_protocol><repository>MetabolomicsWorkbench</repository><data_protocol></data_protocol><omics_type>Metabolomics</omics_type><species>Homo Sapiens</species><submitter_affiliation>Mayo Clinic</submitter_affiliation><metabolite_name>Taurine</metabolite_name><metabolite_name>alpha-Amino-N-butyric-acid</metabolite_name><metabolite_name>Hydroxyproline</metabolite_name><metabolite_name>Serine</metabolite_name><metabolite_name>Proline</metabolite_name><metabolite_name>Carnosine</metabolite_name><metabolite_name>Aspartic Acid</metabolite_name><metabolite_name>1-Methylhistidine</metabolite_name><metabolite_name>Leucine</metabolite_name><metabolite_name>Glycine</metabolite_name><metabolite_name>Cystine</metabolite_name><metabolite_name>Cystathionine 1</metabolite_name><metabolite_name>Phosphoethanolamine</metabolite_name><metabolite_name>Histidine</metabolite_name><metabolite_name>allo-Isoleucine</metabolite_name><metabolite_name>Arginine</metabolite_name><metabolite_name>Anserine</metabolite_name><metabolite_name>beta-Alanine</metabolite_name><metabolite_name>3-Methylhistidine</metabolite_name><metabolite_name>Isoleucine</metabolite_name><metabolite_name>Cystathionine 2</metabolite_name><metabolite_name>Tyrosine</metabolite_name><metabolite_name>beta-Aminoisobutyric-acid</metabolite_name><metabolite_name>Ethanolamine</metabolite_name><metabolite_name>Alanine</metabolite_name><metabolite_name>gamma-Amino-N-butyric-acid</metabolite_name><metabolite_name>Phenylalanine</metabolite_name><metabolite_name>Threonine</metabolite_name><metabolite_name>Methionine</metabolite_name><metabolite_name>Tryptophan</metabolite_name><metabolite_name>Citrulline</metabolite_name><metabolite_name>Hydroxylysine 1</metabolite_name><metabolite_name>Glutamic Acid</metabolite_name><metabolite_name>Hydroxylysine 2</metabolite_name><metabolite_name>Lysine</metabolite_name><metabolite_name>Valine</metabolite_name><metabolite_name>Sarcosine</metabolite_name><metabolite_name>alpha-Aminoadipic-acid</metabolite_name><metabolite_name>Asparagine</metabolite_name><metabolite_name>Ornithine</metabolite_name><metabolite_name>Homocystine</metabolite_name><metabolite_name>Glutamine</metabolite_name><name_synonyms>Amino Acid, Acid, Natural yellow 3, amino acids, function., E 100, Aminokarbonsaeure, 5-dione, Aminosaeure, Aminocarbonsaeure, 7-bis(4-hydroxy-3-methoxyphenyl)-, C.I. 75300, C.I. Natural Yellow 3, Amino, Kacha haldi, Curcumin, (E, Turmeric yellow, 6-Heptadiene-3, Phytosome, Turmeric Yellow, Diferuloylmethane, E)-, concentration, Turmeric, 1, Acids, Yellow, Curcumin Phytosome, Adults, adult, Mervia</name_synonyms><sample_synonyms>backward, reversed.</sample_synonyms></additional><is_claimable>false</is_claimable><name>Effects of Curcumin Supplementation on the Amino Acid Concentration of Older Adults: Relation to Vascular Function (part 1)</name><description/><dates><publication></publication></dates><accession>ST000524</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>