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Thomas Meitinger

Showing results (111-120 of 508) with videos related to

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American Journal of Human Genetics|May 22, 2012
Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosisDaniele Ghezzi, Enrico Baruffini, Tobias B Haack, et al.
Plos Genetics|December 2, 2008
Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serumChristian Gieger, Ludwig Geistlinger, Elisabeth Altmaier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 22, 2014
DYT16 revisited: exome sequencing identifies PRKRA mutations in a European dystonia familyMichael Zech, Florian Castrop, Barbara Schormair, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
Spectrum of combined respiratory chain defectsJohannes A Mayr, Tobias B Haack, Peter Freisinger, et al.
Neurobiology of Aging|December 21, 2019
SQSTM1/p62 variants in 486 patients with familial ALS from Germany and SwedenRüstem Yilmaz, Kathrin Müller, David Brenner, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humansAnne-Kathrin Wermter, André Scherag, David Meyre, et al.
International Journal of Molecular Medicine|February 3, 2007
The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomaliesEmanuele Panza, Giorgio Gimelli, Mario Passalacqua, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 15, 2007
Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populationsKamil Sedlacek, Katharina Neureuther, Jakob C Mueller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 11, 2006
Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolateFlorian D Vogl, Irene Pichler, Susanna Adel, et al.
Child and Adolescent Psychiatry and Mental Health|November 19, 2008
Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosaTimo Dirk Müller, Kathrin Reichwald, Günter Brönner, et al.
Pageof 51

Showing results (111-120 of 508) with videos related to

Sort By:
Pageof 51
American Journal of Human Genetics|May 22, 2012
Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosisDaniele Ghezzi, Enrico Baruffini, Tobias B Haack, et al.
Plos Genetics|December 2, 2008
Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serumChristian Gieger, Ludwig Geistlinger, Elisabeth Altmaier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 22, 2014
DYT16 revisited: exome sequencing identifies PRKRA mutations in a European dystonia familyMichael Zech, Florian Castrop, Barbara Schormair, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
Spectrum of combined respiratory chain defectsJohannes A Mayr, Tobias B Haack, Peter Freisinger, et al.
Neurobiology of Aging|December 21, 2019
SQSTM1/p62 variants in 486 patients with familial ALS from Germany and SwedenRüstem Yilmaz, Kathrin Müller, David Brenner, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humansAnne-Kathrin Wermter, André Scherag, David Meyre, et al.
International Journal of Molecular Medicine|February 3, 2007
The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomaliesEmanuele Panza, Giorgio Gimelli, Mario Passalacqua, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 15, 2007
Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populationsKamil Sedlacek, Katharina Neureuther, Jakob C Mueller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 11, 2006
Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolateFlorian D Vogl, Irene Pichler, Susanna Adel, et al.
Child and Adolescent Psychiatry and Mental Health|November 19, 2008
Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosaTimo Dirk Müller, Kathrin Reichwald, Günter Brönner, et al.
Pageof 51