Author

M. Mol

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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Cell Biology· 2

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:electrophysiology· 1 Assay:proteomics· 1

Frequent Co-Authors

A. Dakwar· 1 shared A. Hoy· 1 shared A. O. Verkerk· 1 shared B. J. van Meer· 1 shared C. Grandela· 1 shared C. L. Mummery· 1 shared D. Bertinetti· 1 shared D. C. Miller· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperCell Biology

A. Dakwar

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2 papers

Recent·Most cited

Allosteric modulation of protein kinase A in individuals affected by NLPD-PKA , a neurodegenerative disease in which the RIβ-L50R variant is expressed

T. Benjamin-Zukerman, V. Pane, R. Safadi-Safa, M. Solomon, V. Lev-Ram, M. Aboraya, A. Dakwar, D. Bertinetti, A. Hoy, M. Mol, J. van Swieten, F. W. Herberg, R. Maillard, R. Ilouz

This study investigates the RIβ-L50R variant in NLPD-PKA, showing it causes misfolding, disrupts PKA holoenzyme assembly, and increases C-subunit nuclear translocation, with a potential therapeutic strategy to reduce dissociation.

bioRxiv · Jun 30, 2024 · PreprintCell Biology

Isogenic sets of hiPSC-CMs harboring KCNH2 mutations capture location-related phenotypic differences

K. O. Brandao, L. van den Brink, D. C. Miller, C. Grandela, B. J. van Meer, M. Mol, L. G. J. Tertoolen, C. L. Mummery, L. Sala, A. O. Verkerk, R. P. Davis

The paper uses hiPSC-CMs with KCNH2 mutations to show phenotypic differences based on mutation location, supporting their use in risk stratification for LQT2.

bioRxiv · Nov 18, 2019Cell Biology