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David B Goldstein

Showing results (131-140 of 338) with videos related to

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American Journal of Human Genetics|April 5, 2011
A genome-wide comparison of the functional properties of rare and common genetic variants in humansQianqian Zhu, Dongliang Ge, Jessica M Maia, et al.
Genomics|August 2, 2011
A whole-genome analysis of premature termination codonsElizabeth T Cirulli, Erin L Heinzen, Fred S Dietrich, et al.
Journal of Virology|May 14, 2010
Counteraction of HLA-C-mediated immune control of HIV-1 by NefAnke Specht, Amalio Telenti, Raquel Martinez, et al.
The Lancet. Neurology|November 15, 2016
MicroRNAs in epilepsy: pathophysiology and clinical utilityDavid C Henshall, Hajo M Hamer, R Jeroen Pasterkamp, et al.
Ebiomedicine|February 9, 2017
Whole Exome Sequencing Reveals Severe Thrombophilia in Acute Unprovoked Idiopathic Fatal Pulmonary EmbolismMatt Halvorsen, Ying Lin, Barbara A Sampson, et al.
The Journal of Infectious Diseases|August 8, 2008
The HCP5 single-nucleotide polymorphism: a simple screening tool for prediction of hypersensitivity reaction to abacavirSara Colombo, Andri Rauch, Margalida Rotger, et al.
Pharmacogenetics and Genomics|September 27, 2006
A common polymorphism in the SCN1A gene associates with phenytoin serum levels at maintenance doseSarah K Tate, Rinki Singh, Chin-Chuan Hung, et al.
Gastroenterology|January 5, 2011
Inosine triphosphate protects against ribavirin-induced adenosine triphosphate loss by adenylosuccinate synthase functionYuki Hitomi, Elizabeth T Cirulli, Jacques Fellay, et al.
Genome Biology|July 6, 2010
Screening the human exome: a comparison of whole genome and whole transcriptome sequencingElizabeth T Cirulli, Abanish Singh, Kevin V Shianna, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2020
Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnosesKelly Schoch, Queenie K-G Tan, Nicholas Stong, et al.
Pageof 34

Showing results (131-140 of 338) with videos related to

Sort By:
Pageof 34
American Journal of Human Genetics|April 5, 2011
A genome-wide comparison of the functional properties of rare and common genetic variants in humansQianqian Zhu, Dongliang Ge, Jessica M Maia, et al.
Genomics|August 2, 2011
A whole-genome analysis of premature termination codonsElizabeth T Cirulli, Erin L Heinzen, Fred S Dietrich, et al.
Journal of Virology|May 14, 2010
Counteraction of HLA-C-mediated immune control of HIV-1 by NefAnke Specht, Amalio Telenti, Raquel Martinez, et al.
The Lancet. Neurology|November 15, 2016
MicroRNAs in epilepsy: pathophysiology and clinical utilityDavid C Henshall, Hajo M Hamer, R Jeroen Pasterkamp, et al.
Ebiomedicine|February 9, 2017
Whole Exome Sequencing Reveals Severe Thrombophilia in Acute Unprovoked Idiopathic Fatal Pulmonary EmbolismMatt Halvorsen, Ying Lin, Barbara A Sampson, et al.
The Journal of Infectious Diseases|August 8, 2008
The HCP5 single-nucleotide polymorphism: a simple screening tool for prediction of hypersensitivity reaction to abacavirSara Colombo, Andri Rauch, Margalida Rotger, et al.
Pharmacogenetics and Genomics|September 27, 2006
A common polymorphism in the SCN1A gene associates with phenytoin serum levels at maintenance doseSarah K Tate, Rinki Singh, Chin-Chuan Hung, et al.
Gastroenterology|January 5, 2011
Inosine triphosphate protects against ribavirin-induced adenosine triphosphate loss by adenylosuccinate synthase functionYuki Hitomi, Elizabeth T Cirulli, Jacques Fellay, et al.
Genome Biology|July 6, 2010
Screening the human exome: a comparison of whole genome and whole transcriptome sequencingElizabeth T Cirulli, Abanish Singh, Kevin V Shianna, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2020
Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnosesKelly Schoch, Queenie K-G Tan, Nicholas Stong, et al.
Pageof 34