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Human Molecular Genetics
|
September 25, 2020
Coenzyme Q10 modulates sulfide metabolism and links the mitochondrial respiratory chain to pathways associated to one carbon metabolism
Pilar González-García, Agustín Hidalgo-Gutiérrez, Cristina Mascaraque, et al.
Plos One
|
March 29, 2016
Association between DNA Methylation in Whole Blood and Measures of Glucose Metabolism: KORA F4 Study
Jennifer Kriebel, Christian Herder, Wolfgang Rathmann, et al.
Mitochondrion
|
March 31, 2025
An inherited mtDNA rearrangement, mimicking a single large-scale deletion, associated with MIDD and a primary cardiological phenotype
Piervito Lopriore, Andrea Legati, Christiane Michaela Neuhofer, et al.
European Journal of Human Genetics : EJHG
|
October 9, 2014
A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency
Monika Oláhová, Tobias B Haack, Charlotte L Alston, et al.
European Journal of Medical Genetics
|
August 29, 2020
Paroxysmal and non-paroxysmal dystonia in 3 patients with biallelic ECHS1 variants: Expanding the neurological spectrum and therapeutic approaches
Sabine Illsinger, G Christoph Korenke, Sylvia Boesch, et al.
Cells
|
December 24, 2021
Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA
Jana Key, Sylvia Torres-Odio, Nina C Bach, et al.
Journal of Medical Genetics
|
April 3, 2021
Whole genome and exome sequencing identify <i>NDUFV2</i> mutations as a new cause of progressive cavitating leukoencephalopathy
Zhimei Liu, Li Zhang, Changhong Ren, et al.
Genetic Epidemiology
|
June 3, 2021
Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study
Alina Bauer, Astrid Zierer, Christian Gieger, et al.
The Journal of Investigative Dermatology
|
April 18, 2014
An integrated epigenetic and transcriptomic analysis reveals distinct tissue-specific patterns of DNA methylation associated with atopic dermatitis
Elke Rodríguez, Hansjörg Baurecht, Anna Franziska Wahn, et al.
American Journal of Human Genetics
|
November 13, 2012
DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduria
Katharina Danhauser, Sven W Sauer, Tobias B Haack, et al.
Page
of 40
Search research articles
Search
Showing results (151-160 of 395) with videos related to
Sort By:
Page
of 40
Human Molecular Genetics
|
September 25, 2020
Coenzyme Q10 modulates sulfide metabolism and links the mitochondrial respiratory chain to pathways associated to one carbon metabolism
Pilar González-García, Agustín Hidalgo-Gutiérrez, Cristina Mascaraque, et al.
Plos One
|
March 29, 2016
Association between DNA Methylation in Whole Blood and Measures of Glucose Metabolism: KORA F4 Study
Jennifer Kriebel, Christian Herder, Wolfgang Rathmann, et al.
Mitochondrion
|
March 31, 2025
An inherited mtDNA rearrangement, mimicking a single large-scale deletion, associated with MIDD and a primary cardiological phenotype
Piervito Lopriore, Andrea Legati, Christiane Michaela Neuhofer, et al.
European Journal of Human Genetics : EJHG
|
October 9, 2014
A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency
Monika Oláhová, Tobias B Haack, Charlotte L Alston, et al.
European Journal of Medical Genetics
|
August 29, 2020
Paroxysmal and non-paroxysmal dystonia in 3 patients with biallelic ECHS1 variants: Expanding the neurological spectrum and therapeutic approaches
Sabine Illsinger, G Christoph Korenke, Sylvia Boesch, et al.
Cells
|
December 24, 2021
Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA
Jana Key, Sylvia Torres-Odio, Nina C Bach, et al.
Journal of Medical Genetics
|
April 3, 2021
Whole genome and exome sequencing identify <i>NDUFV2</i> mutations as a new cause of progressive cavitating leukoencephalopathy
Zhimei Liu, Li Zhang, Changhong Ren, et al.
Genetic Epidemiology
|
June 3, 2021
Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study
Alina Bauer, Astrid Zierer, Christian Gieger, et al.
The Journal of Investigative Dermatology
|
April 18, 2014
An integrated epigenetic and transcriptomic analysis reveals distinct tissue-specific patterns of DNA methylation associated with atopic dermatitis
Elke Rodríguez, Hansjörg Baurecht, Anna Franziska Wahn, et al.
American Journal of Human Genetics
|
November 13, 2012
DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduria
Katharina Danhauser, Sven W Sauer, Tobias B Haack, et al.
Page
of 40