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Mathias Gautel

King's College London
Randall Division of Cell and Molecular Biophysics
Max Planck Society

211

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20358

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Out-of-Frame Mutations in ACTN2 Last Exon Cause a Dominant Distal Myopathy With Facial Weakness

2021 Neurology Genetics
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Sub-diffraction error mapping for localization microscopy images

2021 bioRxiv
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Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure.

2021 JAMA Cardiology
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The spectrum of neurodevelopmental, neuromuscular and neurodegenerative disorders due to defective autophagy

2021 Autophagy
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When is an obscurin variant pathogenic? The impact of Arg4344Gln and Arg4444Trp variants on protein-protein interactions and protein stability.

2021 Human Molecular Genetics
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Structure of the thin filament in native skeletal muscles reveals its interaction with nebulin and two distinct conformations of myosin

2021 bioRxiv
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The molecular basis for sarcomere organization in vertebrate skeletal muscle

2021 Cell
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Sub-diffraction error mapping for localisation microscopy images.

2021 Nature Communications
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Myopalladin knockout mice develop cardiac dilation and show a maladaptive response to mechanical pressure overload

2021 eLife
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The molecular basis for sarcomere organization in vertebrate skeletal muscle

2021 Microscopy and Microanalysis
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