Stephanie Tennstedt
Luebeck, SH 23562, Germany
Last Updated: 09/26/2026
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Found 11 publications
Nexilin in cardiomyopathy: unveiling its diverse roles with special focus on endocardial fibroelastosis.
Journal: Heart failure reviews
Published: July 01, 2024
Identification of a functional missense variant in the matrix metallopeptidase 10 (MMP10) gene in two families with premature myocardial infarction.
Journal: Scientific reports
Published: December 03, 2023
H-ABC- and dystonia-causing TUBB4A mutations show distinct pathogenic effects.
Journal: Science advances
Published: March 11, 2022
Identification of a Functional PDE5A Variant at the Chromosome 4q27 Coronary Artery Disease Locus in an Extended Myocardial Infarction Family.
Journal: Circulation
Published: August 23, 2021
A novel, in-frame KMT2B deletion in a patient with apparently isolated, generalized dystonia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: June 14, 2017
Stimulators of the soluble guanylyl cyclase: promising functional insights from rare coding atherosclerosis-related GUCY1A3 variants.
Journal: Basic research in cardiology
Published: April 20, 2016
Classification of ADAMTS binding sites: The first step toward selective ADAMTS7 inhibitors.
Journal: Biochemical and biophysical research communications
Published: February 03, 2016
A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.
Journal: European journal of medical genetics
Published: September 09, 2013
Dysfunctional nitric oxide signalling increases risk of myocardial infarction.
Journal: Nature
Published: March 22, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026