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Katja Gehmlich

Showing results (51-60 of 65) with videos related to

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Journal of Molecular and Cellular Cardiology|July 27, 2018
Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletionMehroz Ehsan, Matthew Kelly, Charlotte Hooper, et al.
Circulation|March 19, 2003
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathyChristian Geier, Andreas Perrot, Cemil Ozcelik, et al.
Science Advances|September 5, 2025
Mechanosensitive biochemical imprinting of the talin interaction with DLC1 regulates RhoA activity and cardiomyocyte remodelingEmilie Marhuenda, Ioannis Xanthis, Poppy O Smith, et al.
Cells|March 11, 2023
Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in <i>ACTN2</i>Sophie Broadway-Stringer, He Jiang, Kirsty Wadmore, et al.
Basic Research in Cardiology|February 27, 2021
Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variantHe Jiang, Charlotte Hooper, Matthew Kelly, et al.
Science Advances|May 28, 2019
HspB1 phosphorylation regulates its intramolecular dynamics and mechanosensitive molecular chaperone interaction with filamin CMiranda P Collier, T Reid Alderson, Carin P de Villiers, et al.
Human Molecular Genetics|May 29, 2008
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathyChristian Geier, Katja Gehmlich, Elisabeth Ehler, et al.
Cardiovascular Research|May 27, 2026
A titin truncating variant linked to atrial fibrillation increases atrial profibrotic signalling and cholinergic sensitivityMax J Cumberland, Albert Dasí, Naeramit Sontayananon, et al.
Circulation. Cardiovascular Genetics|September 15, 2016
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular NoncompactionRobert Hastings, Carin P de Villiers, Charlotte Hooper, et al.
Scientific Reports|March 25, 2025
An ALPK3 truncation variant causing autosomal dominant hypertrophic cardiomyopathy is partially rescued by mavacamtenLisa Leinhos, Paul Robinson, Giulia Poloni, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Journal of Molecular and Cellular Cardiology|July 27, 2018
Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletionMehroz Ehsan, Matthew Kelly, Charlotte Hooper, et al.
Circulation|March 19, 2003
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathyChristian Geier, Andreas Perrot, Cemil Ozcelik, et al.
Science Advances|September 5, 2025
Mechanosensitive biochemical imprinting of the talin interaction with DLC1 regulates RhoA activity and cardiomyocyte remodelingEmilie Marhuenda, Ioannis Xanthis, Poppy O Smith, et al.
Cells|March 11, 2023
Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in <i>ACTN2</i>Sophie Broadway-Stringer, He Jiang, Kirsty Wadmore, et al.
Basic Research in Cardiology|February 27, 2021
Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variantHe Jiang, Charlotte Hooper, Matthew Kelly, et al.
Science Advances|May 28, 2019
HspB1 phosphorylation regulates its intramolecular dynamics and mechanosensitive molecular chaperone interaction with filamin CMiranda P Collier, T Reid Alderson, Carin P de Villiers, et al.
Human Molecular Genetics|May 29, 2008
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathyChristian Geier, Katja Gehmlich, Elisabeth Ehler, et al.
Cardiovascular Research|May 27, 2026
A titin truncating variant linked to atrial fibrillation increases atrial profibrotic signalling and cholinergic sensitivityMax J Cumberland, Albert Dasí, Naeramit Sontayananon, et al.
Circulation. Cardiovascular Genetics|September 15, 2016
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular NoncompactionRobert Hastings, Carin P de Villiers, Charlotte Hooper, et al.
Scientific Reports|March 25, 2025
An ALPK3 truncation variant causing autosomal dominant hypertrophic cardiomyopathy is partially rescued by mavacamtenLisa Leinhos, Paul Robinson, Giulia Poloni, et al.
Pageof 7