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Thomas Meitinger

Showing results (371-380 of 508) with videos related to

Pageof 51
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Cell|January 16, 2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.
Kidney International|December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Nature Genetics|December 21, 2010
Common variants in P2RY11 are associated with narcolepsyBirgitte R Kornum, Minae Kawashima, Juliette Faraco, et al.
Plos One|September 19, 2014
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 lociClaire L Simpson, Robert Wojciechowski, Konrad Oexle, et al.
Circulation. Cardiovascular Genetics|August 11, 2017
Fifteen Genetic Loci Associated With the Electrocardiographic P WaveIngrid E Christophersen, Jared W Magnani, Xiaoyan Yin, et al.
Nature Genetics|February 10, 2009
New susceptibility locus for coronary artery disease on chromosome 3q22.3Jeanette Erdmann, Anika Grosshennig, Peter S Braund, et al.
Plos Genetics|October 15, 2011
Genetic determinants of serum testosterone concentrations in menClaes Ohlsson, Henri Wallaschofski, Kathryn L Lunetta, et al.
Nature Genetics|September 10, 2013
Systematic identification of trans eQTLs as putative drivers of known disease associationsHarm-Jan Westra, Marjolein J Peters, Tõnu Esko, et al.
Nature Genetics|July 15, 2009
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestryEmelia J Benjamin, Kenneth M Rice, Dan E Arking, et al.
Nature Genetics|December 9, 2008
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohortsYurii S Aulchenko, Samuli Ripatti, Ida Lindqvist, et al.
Pageof 51

Showing results (371-380 of 508) with videos related to

Sort By:
Pageof 51
Cell|January 16, 2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.
Kidney International|December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Nature Genetics|December 21, 2010
Common variants in P2RY11 are associated with narcolepsyBirgitte R Kornum, Minae Kawashima, Juliette Faraco, et al.
Plos One|September 19, 2014
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 lociClaire L Simpson, Robert Wojciechowski, Konrad Oexle, et al.
Circulation. Cardiovascular Genetics|August 11, 2017
Fifteen Genetic Loci Associated With the Electrocardiographic P WaveIngrid E Christophersen, Jared W Magnani, Xiaoyan Yin, et al.
Nature Genetics|February 10, 2009
New susceptibility locus for coronary artery disease on chromosome 3q22.3Jeanette Erdmann, Anika Grosshennig, Peter S Braund, et al.
Plos Genetics|October 15, 2011
Genetic determinants of serum testosterone concentrations in menClaes Ohlsson, Henri Wallaschofski, Kathryn L Lunetta, et al.
Nature Genetics|September 10, 2013
Systematic identification of trans eQTLs as putative drivers of known disease associationsHarm-Jan Westra, Marjolein J Peters, Tõnu Esko, et al.
Nature Genetics|July 15, 2009
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestryEmelia J Benjamin, Kenneth M Rice, Dan E Arking, et al.
Nature Genetics|December 9, 2008
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohortsYurii S Aulchenko, Samuli Ripatti, Ida Lindqvist, et al.
Pageof 51