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Sandra D Laufer

Showing results (11-20 of 21) with videos related to

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Cold Spring Harbor Molecular Case Studies|July 15, 2022
A biallelic loss-of-function variant in MYZAP is associated with a recessive form of severe dilated cardiomyopathyAles Maver, Tamara Zigman, Ashraf Yusuf Rangrez, et al.
Stem Cell Research|August 10, 2021
Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathyNele Warnecke, Bärbel M Ulmer, Sandra D Laufer, et al.
Circulation|September 5, 2020
An Important Role for DNMT3A-Mediated DNA Methylation in Cardiomyocyte Metabolism and ContractilityAlexandra Madsen, Grit Höppner, Julia Krause, et al.
JCI Insight|March 9, 2026
Lysine-specific histone demethylase 1a regulates nephron development and long-term transcriptional programmingNicola Wanner, Julia Keller, Nastassia Liaukouskaya, et al.
Current Protocols in Stem Cell Biology|September 21, 2020
Cell Banking of hiPSCs: A Practical Guide to Cryopreservation and Quality Control in Basic ResearchAya Shibamiya, Elisabeth Schulze, Dana Krauß, et al.
EMBO Molecular Medicine|August 8, 2022
Disease modeling of a mutation in α-actinin 2 guides clinical therapy in hypertrophic cardiomyopathyMaksymilian Prondzynski, Marc D Lemoine, Antonia Tl Zech, et al.
EMBO Molecular Medicine|November 5, 2019
Disease modeling of a mutation in α-actinin 2 guides clinical therapy in hypertrophic cardiomyopathyMaksymilian Prondzynski, Marc D Lemoine, Antonia Tl Zech, et al.
Redox Biology|September 28, 2024
Physioxia rewires mitochondrial complex composition to protect stem cell viabilityJanice Raabe, Ilka Wittig, Patrick Laurette, et al.
The Journal of Clinical Investigation|April 4, 2023
Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathyFabian Braun, Ahmed Abed, Dominik Sellung, et al.
The EMBO Journal|October 28, 2025
Proteolytic profiling of human plasma reveals an immunoactive complement C3 fragmentFatih Demir, Elina Kovalenko, Moritz Lassé, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Cold Spring Harbor Molecular Case Studies|July 15, 2022
A biallelic loss-of-function variant in MYZAP is associated with a recessive form of severe dilated cardiomyopathyAles Maver, Tamara Zigman, Ashraf Yusuf Rangrez, et al.
Stem Cell Research|August 10, 2021
Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathyNele Warnecke, Bärbel M Ulmer, Sandra D Laufer, et al.
Circulation|September 5, 2020
An Important Role for DNMT3A-Mediated DNA Methylation in Cardiomyocyte Metabolism and ContractilityAlexandra Madsen, Grit Höppner, Julia Krause, et al.
JCI Insight|March 9, 2026
Lysine-specific histone demethylase 1a regulates nephron development and long-term transcriptional programmingNicola Wanner, Julia Keller, Nastassia Liaukouskaya, et al.
Current Protocols in Stem Cell Biology|September 21, 2020
Cell Banking of hiPSCs: A Practical Guide to Cryopreservation and Quality Control in Basic ResearchAya Shibamiya, Elisabeth Schulze, Dana Krauß, et al.
EMBO Molecular Medicine|August 8, 2022
Disease modeling of a mutation in α-actinin 2 guides clinical therapy in hypertrophic cardiomyopathyMaksymilian Prondzynski, Marc D Lemoine, Antonia Tl Zech, et al.
EMBO Molecular Medicine|November 5, 2019
Disease modeling of a mutation in α-actinin 2 guides clinical therapy in hypertrophic cardiomyopathyMaksymilian Prondzynski, Marc D Lemoine, Antonia Tl Zech, et al.
Redox Biology|September 28, 2024
Physioxia rewires mitochondrial complex composition to protect stem cell viabilityJanice Raabe, Ilka Wittig, Patrick Laurette, et al.
The Journal of Clinical Investigation|April 4, 2023
Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathyFabian Braun, Ahmed Abed, Dominik Sellung, et al.
The EMBO Journal|October 28, 2025
Proteolytic profiling of human plasma reveals an immunoactive complement C3 fragmentFatih Demir, Elina Kovalenko, Moritz Lassé, et al.
Pageof 3