Stefan P. Conijn
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
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Found 16 publications
The titin N2A-MARP signalosome constrains muscle longitudinal hypertrophy in response to stretch.
Journal: eLife
Published: July 30, 2026
Kbtbd13 knockdown restores muscle function in a clinically relevant mouse model of nemaline myopathy type 6.
Journal: Science translational medicine
Published: June 24, 2026
The titin N2A-MARP signalosome constrains muscle longitudinal hypertrophy in response to stretch.
Journal: bioRxiv : the preprint server for biology
Published: July 16, 2025
Super-relaxed myosins contribute to respiratory muscle hibernation in mechanically ventilated patients.
Journal: Science translational medicine
Published: July 31, 2024
Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle disease.
Journal: Science translational medicine
Published: April 03, 2024
KBTBD13 is an actin-binding protein that modulates muscle kinetics.
Journal: The Journal of clinical investigation
Published: February 01, 2024
Cardiac troponin T N-domain variant destabilizes the actin interface resulting in disturbed myofilament function.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: May 30, 2023
Replacement Fibrosis in the Diaphragm of Mechanically Ventilated Critically Ill Patients.
Journal: American journal of respiratory and critical care medicine
Published: September 30, 2022
COVID-19 is associated with distinct myopathic features in the diaphragm of critically ill patients.
COVID-19 is associated with distinct myopathic features in the diaphragm of critically ill patients.
Journal: BMJ open respiratory research
Published: July 14, 2021
Muscle ankyrin repeat protein 1 (MARP1) locks titin to the sarcomeric thin filament and is a passive force regulator.
Journal: The Journal of general physiology
Published: March 23, 2021
Pathogenic variants in TNNC2 cause congenital myopathy due to an impaired force response to calcium.
Pathogenic variants in TNNC2 cause congenital myopathy due to an impaired force response to calcium.
Journal: The Journal of clinical investigation
Published: November 10, 2020
Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy.
Journal: Acta neuropathologica communications
Published: June 22, 2020
Last Updated: 09/26/2026