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Peter Nürnberg

Showing results (61-70 of 517) with videos related to

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Pharmacogenomics|May 1, 2007
Sex-dependent genetic markers of CYP3A4 expression and activity in human liver microsomesMarkus Schirmer, Albert Rosenberger, Kathrin Klein, et al.
Plos One|July 9, 2016
Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and LimitationsAmit Tiwari, Johannes Lemke, Janine Altmueller, et al.
Nucleic Acids Research|August 30, 2007
Efficacy assessment of SNP sets for genome-wide disease association studiesAndreas Wollstein, Alexander Herrmann, Michael Wittig, et al.
Human Genetics|January 20, 2009
New genetic evidence for involvement of the dopamine system in migraine with auraUnda Todt, Christian Netzer, Mohammad Toliat, et al.
Molecular Medicine (Cambridge, Mass.)|December 13, 2002
A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10Markus Pfister, Tímea Tóth, Holger Thiele, et al.
American Journal of Primatology|April 27, 2002
Multiple sirehood in free-ranging twin rhesus macaques (Macaca mulatta)Fred B Bercovitch, Anja Widdig, John D Berard, et al.
International Journal of Cancer|June 10, 2003
Distinct methylation profiles of glioma subtypesKaren Uhlmann, Klaus Rohde, Constanze Zeller, et al.
American Journal of Medical Genetics. Part A|December 8, 2015
A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutationGökhan Yigit, Dagmar Wieczorek, Nina Bögershausen, et al.
Epilepsy Research|October 26, 2002
Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsyThomas Sander, Mohammad Reza Toliat, Armin Heils, et al.
European Journal of Human Genetics : EJHG|March 1, 2007
Identification of a candidate genetic variant for the high prevalence of type II diabetes in PolynesiansSean Myles, Eva Hradetzky, Johannes Engelken, et al.
Pageof 52

Showing results (61-70 of 517) with videos related to

Sort By:
Pageof 52
Pharmacogenomics|May 1, 2007
Sex-dependent genetic markers of CYP3A4 expression and activity in human liver microsomesMarkus Schirmer, Albert Rosenberger, Kathrin Klein, et al.
Plos One|July 9, 2016
Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and LimitationsAmit Tiwari, Johannes Lemke, Janine Altmueller, et al.
Nucleic Acids Research|August 30, 2007
Efficacy assessment of SNP sets for genome-wide disease association studiesAndreas Wollstein, Alexander Herrmann, Michael Wittig, et al.
Human Genetics|January 20, 2009
New genetic evidence for involvement of the dopamine system in migraine with auraUnda Todt, Christian Netzer, Mohammad Toliat, et al.
Molecular Medicine (Cambridge, Mass.)|December 13, 2002
A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10Markus Pfister, Tímea Tóth, Holger Thiele, et al.
American Journal of Primatology|April 27, 2002
Multiple sirehood in free-ranging twin rhesus macaques (Macaca mulatta)Fred B Bercovitch, Anja Widdig, John D Berard, et al.
International Journal of Cancer|June 10, 2003
Distinct methylation profiles of glioma subtypesKaren Uhlmann, Klaus Rohde, Constanze Zeller, et al.
American Journal of Medical Genetics. Part A|December 8, 2015
A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutationGökhan Yigit, Dagmar Wieczorek, Nina Bögershausen, et al.
Epilepsy Research|October 26, 2002
Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsyThomas Sander, Mohammad Reza Toliat, Armin Heils, et al.
European Journal of Human Genetics : EJHG|March 1, 2007
Identification of a candidate genetic variant for the high prevalence of type II diabetes in PolynesiansSean Myles, Eva Hradetzky, Johannes Engelken, et al.
Pageof 52