Julian Geiger
Roskilde University
8 Papers
4 Citations
Julian Geiger is an academic researcher from Roskilde University. The author has contributed to research in topics: microRNA & Insulin. The author has an hindex of 4, co-authored 6 publications.
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Papers
MicroRNAs in metabolism
TL;DR: This review emphasizes current ideas and controversies within miRNA research in metabolism, and emphasizes their importance as both endocrine signalling molecules and potentially disease markers.
Interplay of mitochondrial metabolism and microRNAs.
TL;DR: The focus of this review is on miRNAs and mitomiRs with influence on mitochondrial metabolism and their possible pathophysiological impact.
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Hyperandrogenism and Metabolic Syndrome Are Associated With Changes in Serum-Derived microRNAs in Women With Polycystic Ovary Syndrome.
Anja Elaine Sørensen,Anja Elaine Sørensen,Pernille Bækgaard Udesen,Grzegorz J. Maciag,Julian Geiger,Negar Saliani,Andrzej S. Januszewski,Guozhi Jiang,Ronald C.W. Ma,Anandwardhan A. Hardikar,Marie Louise Muff Wissing,Anne Lis Mikkelsen Englund,Louise Torp Dalgaard +12 more
TL;DR: This study is the first to report comprehensive miRNA profiling in different subgroups of PCOS women with respect to MetS and suggests that circulating miRNAs might be useful as diagnostic biomarkers of MetS for a different subset of PCos.
Isolation and Analysis of Mitochondrial Small RNAs from Rat Liver Tissue and HepG2 Cells.
TL;DR: The described procedure depicts a simple way of isolating and quantifying mitomiRs in tissue and cell culture samples and applies the Normfinder algorithm to identify the suitable reference miRNAs to use as normalizers for mitochondrial input and data analysis.
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Physiological phenotyping of mammalian cell lines by enzymatic activity fingerprinting of key carbohydrate metabolic enzymes: a pilot and feasibility study
TL;DR: In this paper, the authors applied semi-high throughput enzyme activity assays that were originally designed for plant samples and tested their feasibility in extracts of six frequently used mammalian cell lines (Caco2, HaCaT, C2C12, HEK293, HepG2 and INS-1E).