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Lea H. Gregersen

Researcher at Francis Crick Institute

Publications -  18
Citations -  7327

Lea H. Gregersen is an academic researcher from Francis Crick Institute. The author has contributed to research in topics: RNA polymerase II & Gene. The author has an hindex of 13, co-authored 16 publications receiving 5641 citations. Previous affiliations of Lea H. Gregersen include Max Planck Society & University of Copenhagen.

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Circular RNAs are a large class of animal RNAs with regulatory potency

TL;DR: It is found that a human circRNA, antisense to the cerebellar degeneration-related protein 1 transcript (CDR1as), is densely bound by microRNA (miRNA) effector complexes and harbours 63 conserved binding sites for the ancient miRNA miR-7.
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Mechanisms and Evolution of Oxidative Sulfur Metabolism in Green Sulfur Bacteria

TL;DR: The last common ancestor of currently known GSB was probably photoautotrophic, hydrogenotrophic and contained SQR but not DSR or SOX, and the predominance of the Chlorobium–Chlorobaculum–Prosthecochloris lineage among cultured GSB could be due to the horizontally acquired DSR and SOX systems.
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MiR-203 controls proliferation, migration and invasive potential of prostate cancer cell lines.

TL;DR: It is shown that miR-203 is downregulated in clinical primary prostatic tumors compared tonormal prostate tissue, and in metastatic prostate cancer cell lines compared to normal epithelial prostatic cells, and could be a potentially new prognostic marker and therapeutic target in metastatics prostate cancer.
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MOV10 Is a 5′ to 3′ RNA Helicase Contributing to UPF1 mRNA Target Degradation by Translocation along 3′ UTRs

TL;DR: It is demonstrated that MOV10 has an ATP-dependent 5' to 3' in vitro RNA unwinding activity and the RNA-binding sites of MOV10 and its helicase mutants are determined using PAR-CLIP, which reveals that MOV 10 and UPF1 bind to RNA in close proximity.
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MicroRNA-145 Targets YES and STAT1 in Colon Cancer Cells

TL;DR: The study identifies and validates new cancer-relevant direct targets of miR-145 in colon cancer cells and adds important mechanistic understanding of the tumor-suppressive functions of mi R-145.