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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Wruck, W; Kashofer, K; Rehman, S; Daskalaki, A; Berg, D; Gralka, E; Jozefczuk, J; Drews, K; Pandey, V; Regenbrecht, C; Wierling, C; Turano, P; Korf, U; Zatloukal, K; Lehrach, H; Westerhoff, HV; Adjaye, J.
Multi-omic profiles of human non-alcoholic fatty liver disease tissue highlight heterogenic phenotypes.
Sci Data. 2015; 2(S 01):150068-150068 Doi: 10.1038/sdata.2015.68 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Kashofer Karl
Zatloukal Kurt
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Abstract:
Non-alcoholic fatty liver disease (NAFLD) is a consequence of sedentary life style and high fat diets with an estimated prevalence of about 30% in western countries. It is associated with insulin resistance, obesity, glucose intolerance and drug toxicity. Additionally, polymorphisms within, e.g., APOC3, PNPLA3, NCAN, TM6SF2 and PPP1R3B, correlate with NAFLD. Several studies have already investigated later stages of the disease. This study explores the early steatosis stage of NAFLD with the aim of identifying molecular mechanisms underlying the etiology of NAFLD. We analyzed liver biopsies and serum samples from patients with high- and low-grade steatosis (also pre-disease states) employing transcriptomics, ELISA-based serum protein analyses and metabolomics. Here, we provide a detailed description of the various related datasets produced in the course of this study. These datasets may help other researchers find new clues for the etiology of NAFLD and the mechanisms underlying its progression to more severe disease states.
Find related publications in this database (using NLM MeSH Indexing)
Apolipoprotein C-III - genetics
Biopsy -
Chondroitin Sulfate Proteoglycans - genetics
Genetic Association Studies -
Genetic Predisposition to Disease -
Humans -
Lectins, C-Type - genetics
Lipase - genetics
Liver - metabolism
Liver - pathology
Membrane Proteins - genetics
Nerve Tissue Proteins - genetics
Non-alcoholic Fatty Liver Disease - etiology
Non-alcoholic Fatty Liver Disease - genetics
Polymorphism, Single Nucleotide -
Protein Phosphatase 1 - genetics

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