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Thomas Meitinger

Showing results (161-170 of 508) with videos related to

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European Journal of Human Genetics : EJHG|April 27, 2022
Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genesKatinka Breuer, Korbinian M Riedhammer, Nicole Müller, et al.
Anesthesiology|March 28, 2009
Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass graftingAmanda A Fox, Charles D Collard, Stanton K Shernan, et al.
Molecular Vision|August 2, 2017
Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous familiesAsmat Ullah, Muhammad Umair, Maryam Yousaf, et al.
Brain : a Journal of Neurology|December 3, 2015
Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegenerationEliska Holzerova, Katharina Danhauser, Tobias B Haack, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2015
Frequency and clinical correlates of somatic Ying Yang 1 mutations in sporadic insulinomasUrs D Lichtenauer, Guido Di Dalmazi, Emily P Slater, et al.
Nature Genetics|November 9, 2010
Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiencyTobias B Haack, Katharina Danhauser, Birgit Haberberger, et al.
Neurogenetics|September 5, 2009
Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's diseaseAnne S Soehn, Thomas Franck, Saskia Biskup, et al.
European Heart Journal|June 16, 2026
Genetic screening of children for familial hypercholesterolaemia: the VRONI studyRaphael S Schmieder, Lea D Schlieben, Artem Amosov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 7, 2007
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndromeJuliane Winkelmann, Peter Lichtner, Barbara Schormair, et al.
American Journal of Human Genetics|January 8, 2005
Linkage disequilibrium patterns and tagSNP transferability among European populationsJakob C Mueller, Elin Lõhmussaar, Reedik Mägi, et al.
Pageof 51

Showing results (161-170 of 508) with videos related to

Sort By:
Pageof 51
European Journal of Human Genetics : EJHG|April 27, 2022
Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genesKatinka Breuer, Korbinian M Riedhammer, Nicole Müller, et al.
Anesthesiology|March 28, 2009
Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass graftingAmanda A Fox, Charles D Collard, Stanton K Shernan, et al.
Molecular Vision|August 2, 2017
Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous familiesAsmat Ullah, Muhammad Umair, Maryam Yousaf, et al.
Brain : a Journal of Neurology|December 3, 2015
Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegenerationEliska Holzerova, Katharina Danhauser, Tobias B Haack, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2015
Frequency and clinical correlates of somatic Ying Yang 1 mutations in sporadic insulinomasUrs D Lichtenauer, Guido Di Dalmazi, Emily P Slater, et al.
Nature Genetics|November 9, 2010
Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiencyTobias B Haack, Katharina Danhauser, Birgit Haberberger, et al.
Neurogenetics|September 5, 2009
Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's diseaseAnne S Soehn, Thomas Franck, Saskia Biskup, et al.
European Heart Journal|June 16, 2026
Genetic screening of children for familial hypercholesterolaemia: the VRONI studyRaphael S Schmieder, Lea D Schlieben, Artem Amosov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 7, 2007
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndromeJuliane Winkelmann, Peter Lichtner, Barbara Schormair, et al.
American Journal of Human Genetics|January 8, 2005
Linkage disequilibrium patterns and tagSNP transferability among European populationsJakob C Mueller, Elin Lõhmussaar, Reedik Mägi, et al.
Pageof 51