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Benjamin L. Parker
Researcher at University of Melbourne
Publications - 101
Citations - 5026
Benjamin L. Parker is an academic researcher from University of Melbourne. The author has contributed to research in topics: Phosphorylation & Skeletal muscle. The author has an hindex of 33, co-authored 92 publications receiving 3582 citations. Previous affiliations of Benjamin L. Parker include Garvan Institute of Medical Research & University of Southern Denmark.
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Journal ArticleDOI
Extracellular Vesicles Provide a Means for Tissue Crosstalk during Exercise
Martin Whitham,Martin Whitham,Benjamin L. Parker,Martin Friedrichsen,Janne R. Hingst,Marit Hjorth,Marit Hjorth,William E. Hughes,William E. Hughes,Casey L. Egan,Lena Cron,Kevin I. Watt,Rhiannon P. Kuchel,Navind Jayasooriah,Navind Jayasooriah,Emma Estevez,Tim Petzold,Catherine M. Suter,Paul Gregorevic,Bente Kiens,Erik A. Richter,David E. James,Jørgen F. P. Wojtaszewski,Mark A. Febbraio,Mark A. Febbraio +24 more
TL;DR: A new paradigm by which tissue crosstalk during exercise can exert systemic biological effects is identified, identified by employing arteriovenous balance studies across the contracting human limb to identify several novel candidate myokines released into circulation independently of classical secretion.
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Functional screening in human cardiac organoids reveals a metabolic mechanism for cardiomyocyte cell cycle arrest
Richard J. Mills,Drew M. Titmarsh,Xaver Koenig,Xaver Koenig,Benjamin L. Parker,James G. Ryall,Gregory A. Quaife-Ryan,Holly K. Voges,Mark P. Hodson,Charles Ferguson,Lauren Drowley,Alleyn T. Plowright,Elise J. Needham,Qing-Dong Wang,Paul Gregorevic,Mei Xin,Walter G. Thomas,Robert G. Parton,Lars K. Nielsen,Bradley S. Launikonis,David E. James,David A. Elliott,Enzo R. Porrello,James E. Hudson +23 more
TL;DR: It is found that simulating the postnatal switch in metabolic substrates from carbohydrates to fatty acids promoted a switch in metabolism, DNA damage response, and cell cycle arrest in hPSC-CM, and under optimized maturation conditions, functional and molecular characterization revealed that a switch to fatty acid metabolism was a central driver of cardiac maturation.
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Simultaneous Glycan-Peptide Characterization Using Hydrophilic Interaction Chromatography and Parallel Fragmentation by CID, Higher Energy Collisional Dissociation, and Electron Transfer Dissociation MS Applied to the N-Linked Glycoproteome of Campylobacter jejuni
Nichollas E. Scott,Benjamin L. Parker,Angela Connolly,Jana Paulech,Alistair V.G. Edwards,Ben Crossett,Linda Falconer,Daniel Kolarich,Steven P. Djordjevic,Steven P. Djordjevic,Peter Højrup,Nicolle H. Packer,Martin R. Larsen,Stuart J. Cordwell,Stuart J. Cordwell +14 more
TL;DR: The data demonstrate that peptide-centric approaches coupled to novel mass spectrometric fragmentation techniques may be suitable for application to eukaryotic glycoproteins for simultaneous elucidation of glycan structures and peptide sequence.
Journal ArticleDOI
Global Phosphoproteomic Analysis of Human Skeletal Muscle Reveals a Network of Exercise-Regulated Kinases and AMPK Substrates
Nolan J. Hoffman,Benjamin L. Parker,Rima Chaudhuri,Kelsey H. Fisher-Wellman,Maximilian Kleinert,Sean J. Humphrey,Pengyi Yang,Mira Holliday,Sophie Trefely,Daniel J. Fazakerley,Jacqueline Stöckli,James G. Burchfield,Thomas E. Jensen,Raja Jothi,Bente Kiens,Jørgen F. P. Wojtaszewski,Erik A. Richter,David E. James +17 more
TL;DR: A global analysis of protein phosphorylation in human skeletal muscle biopsies from untrained healthy males before and after a single high-intensity exercise bout revealed 1,004 unique exercise-regulated phosphosites on 562 proteins, exposing the unexplored complexity of acute exercise signaling.
Journal ArticleDOI
Selective enrichment of sialic acid-containing glycopeptides using titanium dioxide chromatography with analysis by HILIC and mass spectrometry
Giuseppe Palmisano,Sara Eun Lendal,Kasper Engholm-Keller,Rikke Leth-Larsen,Benjamin L. Parker,Benjamin L. Parker,Martin R. Larsen +6 more
TL;DR: A protocol for the selective enrichment of SA-containing glycopeptides using a combination of titanium dioxide (TiO2) and hydrophilic interaction liquid chromatography (HILIC) and the efficiency of the method is illustrated by the identification of 1,632 unique formerly sialylated glycoproteins.