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Thomas Meitinger

Showing results (251-260 of 508) with videos related to

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Circulation. Cardiovascular Genetics|March 5, 2015
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2Iris C R M Kolder, Michael W T Tanck, Pieter G Postema, et al.
Journal of Medical Genetics|April 14, 2012
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencingTobias B Haack, Birgit Haberberger, Eva-Maria Frisch, et al.
Plos One|April 18, 2014
Mapping the genetic architecture of gene regulation in whole bloodKatharina Schramm, Carola Marzi, Claudia Schurmann, et al.
Neuromolecular Medicine|February 15, 2015
A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD)Felix Grassmann, Ulrike Friedrich, Sascha Fauser, et al.
Cardiovascular Diabetology|June 12, 2024
Bidirectional modulation of TCA cycle metabolites and anaplerosis by metformin and its combination with SGLT2iMakoto Harada, Jonathan Adam, Marcela Covic, et al.
The Journal of Clinical Investigation|August 18, 2015
RAP1-mediated MEK/ERK pathway defects in Kabuki syndromeNina Bögershausen, I-Chun Tsai, Esther Pohl, et al.
Plos Computational Biology|February 4, 2020
DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learningJanine Arloth, Gökcen Eraslan, Till F M Andlauer, et al.
Plos One|December 16, 2014
MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathyLore Becker, Eva Kling, Evelyn Schiller, et al.
American Journal of Human Genetics|July 19, 2016
Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile HepatopathyRobert Kopajtich, Kei Murayama, Andreas R Janecke, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 27, 2021
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouseCaroline A Biagosch, Silvia Vidali, Michael Faerberboeck, et al.
Pageof 51

Showing results (251-260 of 508) with videos related to

Sort By:
Pageof 51
Circulation. Cardiovascular Genetics|March 5, 2015
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2Iris C R M Kolder, Michael W T Tanck, Pieter G Postema, et al.
Journal of Medical Genetics|April 14, 2012
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencingTobias B Haack, Birgit Haberberger, Eva-Maria Frisch, et al.
Plos One|April 18, 2014
Mapping the genetic architecture of gene regulation in whole bloodKatharina Schramm, Carola Marzi, Claudia Schurmann, et al.
Neuromolecular Medicine|February 15, 2015
A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD)Felix Grassmann, Ulrike Friedrich, Sascha Fauser, et al.
Cardiovascular Diabetology|June 12, 2024
Bidirectional modulation of TCA cycle metabolites and anaplerosis by metformin and its combination with SGLT2iMakoto Harada, Jonathan Adam, Marcela Covic, et al.
The Journal of Clinical Investigation|August 18, 2015
RAP1-mediated MEK/ERK pathway defects in Kabuki syndromeNina Bögershausen, I-Chun Tsai, Esther Pohl, et al.
Plos Computational Biology|February 4, 2020
DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learningJanine Arloth, Gökcen Eraslan, Till F M Andlauer, et al.
Plos One|December 16, 2014
MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathyLore Becker, Eva Kling, Evelyn Schiller, et al.
American Journal of Human Genetics|July 19, 2016
Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile HepatopathyRobert Kopajtich, Kei Murayama, Andreas R Janecke, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 27, 2021
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouseCaroline A Biagosch, Silvia Vidali, Michael Faerberboeck, et al.
Pageof 51