Katja Gehmlich
0000-0003-4019-1844
Oxford University
5 papers found
Refreshing results…
Familial atrial fibrillation mutation M1875T-SCN5A increases early sodium current and dampens the effect of flecainide
Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant
HspB1 phosphorylation regulates its intramolecular dynamics and mechanosensitive molecular chaperone interaction with filamin C
Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion
Phosphorylation of HspB1 regulates its mechanosensitive molecular chaperone interaction with native filamin C
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