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Thomas Meitinger

Showing results (231-240 of 508) with videos related to

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Nature Genetics|January 15, 2013
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial diseaseCornelia Kornblum, Thomas J Nicholls, Tobias B Haack, et al.
Plos One|May 31, 2014
Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndromeEva C Schulte, Katharina Schramm, Claudia Schurmann, et al.
Nature Genetics|July 20, 2007
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regionsJuliane Winkelmann, Barbara Schormair, Peter Lichtner, et al.
Journal of Lipid Research|May 18, 2017
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoformsSalome Mack, Stefan Coassin, Rico Rueedi, et al.
Frontiers in Genetics|April 29, 2015
Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiencyUwe Ahting, Johannes A Mayr, Arnaud V Vanlander, et al.
The EMBO Journal|May 17, 2018
Interplay of cell-cell contacts and RhoA/MRTF-A signaling regulates cardiomyocyte identityTatjana Dorn, Jessica Kornherr, Elvira I Parrotta, et al.
Nature Communications|January 11, 2022
Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosisMarkus Scholz, Katrin Horn, Janne Pott, et al.
American Journal of Human Genetics|July 21, 2015
TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain DeficienciesChristopher A Powell, Robert Kopajtich, Aaron R D'Souza, et al.
Nature Genetics|May 2, 2006
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarizationDan E Arking, Arne Pfeufer, Wendy Post, et al.
Circulation|February 8, 2013
Calmodulin mutations associated with recurrent cardiac arrest in infantsLia Crotti, Christopher N Johnson, Elisabeth Graf, et al.
Pageof 51

Showing results (231-240 of 508) with videos related to

Sort By:
Pageof 51
Nature Genetics|January 15, 2013
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial diseaseCornelia Kornblum, Thomas J Nicholls, Tobias B Haack, et al.
Plos One|May 31, 2014
Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndromeEva C Schulte, Katharina Schramm, Claudia Schurmann, et al.
Nature Genetics|July 20, 2007
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regionsJuliane Winkelmann, Barbara Schormair, Peter Lichtner, et al.
Journal of Lipid Research|May 18, 2017
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoformsSalome Mack, Stefan Coassin, Rico Rueedi, et al.
Frontiers in Genetics|April 29, 2015
Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiencyUwe Ahting, Johannes A Mayr, Arnaud V Vanlander, et al.
The EMBO Journal|May 17, 2018
Interplay of cell-cell contacts and RhoA/MRTF-A signaling regulates cardiomyocyte identityTatjana Dorn, Jessica Kornherr, Elvira I Parrotta, et al.
Nature Communications|January 11, 2022
Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosisMarkus Scholz, Katrin Horn, Janne Pott, et al.
American Journal of Human Genetics|July 21, 2015
TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain DeficienciesChristopher A Powell, Robert Kopajtich, Aaron R D'Souza, et al.
Nature Genetics|May 2, 2006
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarizationDan E Arking, Arne Pfeufer, Wendy Post, et al.
Circulation|February 8, 2013
Calmodulin mutations associated with recurrent cardiac arrest in infantsLia Crotti, Christopher N Johnson, Elisabeth Graf, et al.
Pageof 51