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Molecular Aspects of Medicine|August 2, 2024
Extracellular vesicles transport RNA between cells: Unraveling their dual role in diagnostics and therapeuticsZahra Payandeh, Benyapa Tangruksa, Jane Synnergren, et al.
Chemistry & Biology|December 3, 2014
Effects of pharmacological AMP deaminase inhibition and Ampd1 deletion on nucleotide levels and AMPK activation in contracting skeletal muscleCatheline Plaideau, Yu-Chiang Lai, Samanta Kviklyte, et al.
Frontiers in Pharmacology|May 13, 2022
A Combined Human in Silico and CRISPR/Cas9-Mediated in Vivo Zebrafish Based Approach to Provide Phenotypic Data for Supporting Early Target ValidationMatthew J Winter, Yosuke Ono, Jonathan S Ball, et al.
Biochemical and Biophysical Research Communications|March 15, 2008
The role of mitochondrial glycerol-3-phosphate acyltransferase-1 in regulating lipid and glucose homeostasis in high-fat diet fed miceMisak Yazdi, Andrea Ahnmark, Lena William-Olsson, et al.
American Journal of Physiology. Endocrinology and Metabolism|July 9, 2009
Central NMU signaling in body weight and energy balance regulation: evidence from NMUR2 deletion and chronic central NMU treatment in miceEmil Egecioglu, Karolina Ploj, Xiufeng Xu, et al.
Nature Communications|November 23, 2022
Sphingosine 1-phosphate mediates adiponectin receptor signaling essential for lipid homeostasis and embryogenesisMario Ruiz, Ranjan Devkota, Dimitra Panagaki, et al.
Stem Cells (Dayton, Ohio)|April 2, 2019
CRISPR-Knockout Screen Identifies Dmap1 as a Regulator of Chemically Induced Reprogramming and Differentiation of Cardiac ProgenitorsJason S L Yu, Giorgia Palano, Cindy Lim, et al.
Nature Communications|March 15, 2024
Regulation of meiotic telomere dynamics through membrane fluidity promoted by AdipoR2-ELOVL2Jingjing Zhang, Mario Ruiz, Per-Olof Bergh, et al.
Nucleic Acids Research|July 23, 2018
Decoding non-random mutational signatures at Cas9 targeted sitesAmir Taheri-Ghahfarokhi, Benjamin J M Taylor, Roberto Nitsch, et al.
Ebiomedicine|March 4, 2018
Therapeutic Genome Editing With CRISPR/Cas9 in a Humanized Mouse Model Ameliorates α1-antitrypsin Deficiency PhenotypeMikael Bjursell, Michelle J Porritt, Elke Ericson, et al.
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