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Diabetes
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June 11, 2016
Bezafibrate Improves Insulin Sensitivity and Metabolic Flexibility in STZ-Induced Diabetic Mice
Andras Franko, Peter Huypens, Susanne Neschen, et al.
Plos Genetics
|
October 11, 2008
Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus
Stephan Weidinger, Christian Gieger, Elke Rodriguez, et al.
American Journal of Human Genetics
|
February 7, 2015
COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency
Gloria Brea-Calvo, Tobias B Haack, Daniela Karall, et al.
JAMA
|
May 9, 2013
Identification of genetic loci associated with Helicobacter pylori serologic status
Julia Mayerle, Caroline M den Hoed, Claudia Schurmann, et al.
Brain : a Journal of Neurology
|
April 30, 2025
Pleiotropic effects of MORC2 derive from its epigenetic signature
Fatemeh Peymani, Tomohiro Ebihara, Dmitrii Smirnov, et al.
Brain : a Journal of Neurology
|
October 30, 2015
LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population
Monika Oláhová, Steven A Hardy, Julie Hall, et al.
American Journal of Human Genetics
|
September 2, 2014
Mutations in APOPT1, encoding a mitochondrial protein, cause cavitating leukoencephalopathy with cytochrome c oxidase deficiency
Laura Melchionda, Tobias B Haack, Steven Hardy, et al.
Journal of Inherited Metabolic Disease
|
May 4, 2022
How to proceed after "negative" exome: A review on genetic diagnostics, limitations, challenges, and emerging new multiomics techniques
Saskia B Wortmann, Machteld M Oud, Mariëlle Alders, et al.
Nature Communications
|
June 13, 2017
Genetic diagnosis of Mendelian disorders via RNA sequencing
Laura S Kremer, Daniel M Bader, Christian Mertes, et al.
Neurology
|
May 9, 2014
Novel (ovario) leukodystrophy related to AARS2 mutations
Cristina Dallabona, Daria Diodato, Sietske H Kevelam, et al.
Page
of 40
Search research articles
Search
Showing results (281-290 of 396) with videos related to
Sort By:
Page
of 40
Diabetes
|
June 11, 2016
Bezafibrate Improves Insulin Sensitivity and Metabolic Flexibility in STZ-Induced Diabetic Mice
Andras Franko, Peter Huypens, Susanne Neschen, et al.
Plos Genetics
|
October 11, 2008
Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus
Stephan Weidinger, Christian Gieger, Elke Rodriguez, et al.
American Journal of Human Genetics
|
February 7, 2015
COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency
Gloria Brea-Calvo, Tobias B Haack, Daniela Karall, et al.
JAMA
|
May 9, 2013
Identification of genetic loci associated with Helicobacter pylori serologic status
Julia Mayerle, Caroline M den Hoed, Claudia Schurmann, et al.
Brain : a Journal of Neurology
|
April 30, 2025
Pleiotropic effects of MORC2 derive from its epigenetic signature
Fatemeh Peymani, Tomohiro Ebihara, Dmitrii Smirnov, et al.
Brain : a Journal of Neurology
|
October 30, 2015
LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population
Monika Oláhová, Steven A Hardy, Julie Hall, et al.
American Journal of Human Genetics
|
September 2, 2014
Mutations in APOPT1, encoding a mitochondrial protein, cause cavitating leukoencephalopathy with cytochrome c oxidase deficiency
Laura Melchionda, Tobias B Haack, Steven Hardy, et al.
Journal of Inherited Metabolic Disease
|
May 4, 2022
How to proceed after "negative" exome: A review on genetic diagnostics, limitations, challenges, and emerging new multiomics techniques
Saskia B Wortmann, Machteld M Oud, Mariëlle Alders, et al.
Nature Communications
|
June 13, 2017
Genetic diagnosis of Mendelian disorders via RNA sequencing
Laura S Kremer, Daniel M Bader, Christian Mertes, et al.
Neurology
|
May 9, 2014
Novel (ovario) leukodystrophy related to AARS2 mutations
Cristina Dallabona, Daria Diodato, Sietske H Kevelam, et al.
Page
of 40