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Thomas Meitinger

Showing results (1-10 of 536) with videos related to

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Genetic Epidemiology|February 18, 2011
Sampling GWAS subjects from risk populationsKonrad Oexle, Thomas Meitinger
Human Molecular Genetics|January 30, 2003
An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondriaKonstanze Hörtnagel, Holger Prokisch, Thomas Meitinger
European Journal of Human Genetics : EJHG|October 9, 2008
STAT3 single-nucleotide polymorphisms and STAT3 mutations associated with hyper-IgE syndrome are not responsible for increased serum IgE serum levels in asthma familiesMatthias Wjst, Peter Lichtner, Thomas Meitinger, et al.
International Review of Neurobiology|November 12, 2013
Mitochondrial membrane protein-associated neurodegeneration (MPAN)Monika Hartig, Holger Prokisch, Thomas Meitinger, et al.
Current Drug Targets|April 21, 2012
Pantothenate kinase-associated neurodegenerationMonika B Hartig, Holger Prokisch, Thomas Meitinger, et al.
Mitochondrion|August 27, 2005
Mechanisms for multiple intracellular localization of human mitochondrial proteinsJakob Christian Mueller, Christophe Andreoli, Holger Prokisch, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
A population-based epidemiological and genetic study of X-linked retinitis pigmentosaHolger Prokisch, Monika Hartig, Rosa Hellinger, et al.
Frontiers in Genetics|April 11, 2018
<i>MAP2</i> - A Candidate Gene for Epilepsy, Developmental Delay and Behavioral Abnormalities in a Patient With Microdeletion 2q34Dominik S Westphal, Stephanie Andres, Christine Makowski, et al.
International Journal of Molecular Epidemiology and Genetics|June 21, 2011
Effect of genome-wide simultaneous hypotheses tests on the discovery rateSusana Eyheramendy, Christian Gieger, Maris Laan, et al.
Cardiovascular Research|January 20, 2011
Genome-wide association studies of atrial fibrillation: past, present, and futureMoritz F Sinner, Patrick T Ellinor, Thomas Meitinger, et al.
Pageof 54

Showing results (1-10 of 536) with videos related to

Sort By:
Pageof 54
Genetic Epidemiology|February 18, 2011
Sampling GWAS subjects from risk populationsKonrad Oexle, Thomas Meitinger
Human Molecular Genetics|January 30, 2003
An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondriaKonstanze Hörtnagel, Holger Prokisch, Thomas Meitinger
European Journal of Human Genetics : EJHG|October 9, 2008
STAT3 single-nucleotide polymorphisms and STAT3 mutations associated with hyper-IgE syndrome are not responsible for increased serum IgE serum levels in asthma familiesMatthias Wjst, Peter Lichtner, Thomas Meitinger, et al.
International Review of Neurobiology|November 12, 2013
Mitochondrial membrane protein-associated neurodegeneration (MPAN)Monika Hartig, Holger Prokisch, Thomas Meitinger, et al.
Current Drug Targets|April 21, 2012
Pantothenate kinase-associated neurodegenerationMonika B Hartig, Holger Prokisch, Thomas Meitinger, et al.
Mitochondrion|August 27, 2005
Mechanisms for multiple intracellular localization of human mitochondrial proteinsJakob Christian Mueller, Christophe Andreoli, Holger Prokisch, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
A population-based epidemiological and genetic study of X-linked retinitis pigmentosaHolger Prokisch, Monika Hartig, Rosa Hellinger, et al.
Frontiers in Genetics|April 11, 2018
<i>MAP2</i> - A Candidate Gene for Epilepsy, Developmental Delay and Behavioral Abnormalities in a Patient With Microdeletion 2q34Dominik S Westphal, Stephanie Andres, Christine Makowski, et al.
International Journal of Molecular Epidemiology and Genetics|June 21, 2011
Effect of genome-wide simultaneous hypotheses tests on the discovery rateSusana Eyheramendy, Christian Gieger, Maris Laan, et al.
Cardiovascular Research|January 20, 2011
Genome-wide association studies of atrial fibrillation: past, present, and futureMoritz F Sinner, Patrick T Ellinor, Thomas Meitinger, et al.
Pageof 54