{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000218","ANALYSIS_ID":"AN000322","VERSION":"1","CREATED_ON":"2016-09-17"},

"PROJECT":{"PROJECT_TITLE":"Hirschprung Associated Enterocolitis Studies","PROJECT_SUMMARY":"Assess for correlations between SCFA content and history of HAEC","INSTITUTE":"University of Michigan","DEPARTMENT":"Surgery","LABORATORY":"Teitelbaum Lab","LAST_NAME":"Teitelbaum","FIRST_NAME":"Daniel","ADDRESS":"Ann Arbor, MI","EMAIL":"dttbm@umich.edu","PHONE":"734-936-8464"},

"STUDY":{"STUDY_TITLE":"Role of Microbiome in Psoriatic Arthritis (SCFA in PsA)","STUDY_SUMMARY":"To investigate associations of gut and skin microbiota diversity with psoriatic pathogenesis.Characterize the abundance and diversity of gut microbiota in with never-treated, new-onset psoriatic arthritis (PsA). Methods: 16s rRNA pyrosequencing was utilized to compare the community composition of microbiota in PsA patients, psoriasis patients and healthy, matched controls. from patients with PsA, psoriasis of the skin (Ps), new-onset rheumatoid (NORA) and healthy controls were assessed for the presence and levels of fecal immunoglobulin A (sIgA) and various proteins and pro-inflammatory cytokines","INSTITUTE":"University of Michigan","DEPARTMENT":"Biomedical Research Core Facilities","LABORATORY":"Metabolomics core","LAST_NAME":"Kachman","FIRST_NAME":"Maureen","ADDRESS":"6300 Brehm Tower, 1000 Wall Street, Ann Arbor, MI 48105-5714","EMAIL":"mkachman@umich.edu","PHONE":"-","NUM_GROUPS":"4","TOTAL_SUBJECTS":"89"},

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"TREATMENT":{"TREATMENT_SUMMARY":"-"},

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"MS_METABOLITE_DATA":{
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