Author

E. Zanoteli

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Physiology· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Approach:statistical model· 2 Approach:biophysical modeling· 1 Research Focus:cell signaling & trafficking· 1

Frequent Co-Authors

J. Ochala· 3 shared A. D'Amico· 1 shared A. Hau· 1 shared A. Oldfors· 1 shared A. S. Deshmukh· 1 shared A. Van de Loock· 1 shared A. Weyns· 1 shared B. Stocks· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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3 shared papersPhysiology

J. Ochala

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Author profile →

3 papers

Recent·Most cited

Human skeletal muscle fiber heterogeneity beyond myosin heavy chains

R. Moreno-Justicia, T. Van der Stede, B. Stocks, J. Laitila, R. A. Seaborne, A. Van de Loock, E. Lievens, D. Samodova, L. Marin-Arraiza, O. Dmytriyeva, R. Browaeys, K. Van Vossel, L. Moesgaard, N. Yigit, J. Anckaert, , A. S. Deshmukh

This study identifies sources of skeletal muscle fiber heterogeneity beyond myosin heavy chains using transcriptomic and proteomic data from human muscle fibers.

bioRxiv · Sep 7, 2023Physiology

Human light meromyosin mutations linked to skeletal myopathies disrupt the coiled coil structure and myosin head sequestration

G. Carrington, A. Hau, S. Kosta, H. Dugdale, F. Muntoni, A. D'Amico, P. Van den Bergh, N. Romero, E. Malfatti, J. J. Vilchez, A. Oldfors, S. Pajusalu, K. Ounap, M. Giralt-Pujol, E. Zanoteli, , J. Ochala

This study investigates how mutations in MYH7 and MYH2 genes affect myosin structure and function, finding that they disrupt coiled-coil structure and increase ATP consumption without affecting contractile function.

bioRxiv · May 15, 2023 · PreprintPhysiology

Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy

J. A. Ross, Y. Levy, M. Ripolone, J. S. Kolb, M. Turmaine, M. Holt, M. Moggio, C. Fiorillo, J. Lindqvist, N. Figeac, P. Zammit, H. Jungbluth, J. Vissing, N. Witting, H. Granzier, , J. Ochala

This study identifies nuclear defects in nemaline myopathy caused by impaired contractility and cytoskeletal organisation in muscle fibres.

bioRxiv · Jan 28, 2019Cell Biology