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David B Goldstein

Showing results (191-200 of 338) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 20, 2007
Review of evidence for genetic testing for CYP450 polymorphisms in management of patients with nonpsychotic depression with selective serotonin reuptake inhibitorsMugdha Thakur, Iris Grossman, Douglas C McCrory, et al.
Hepatology (Baltimore, Md.)|October 9, 2010
IL28B genotype is associated with differential expression of intrahepatic interferon-stimulated genes in patients with chronic hepatitis CThomas J Urban, Alexander J Thompson, Shelton S Bradrick, et al.
Gastroenterology|July 13, 2010
An IL28B polymorphism determines treatment response of hepatitis C virus genotype 2 or 3 patients who do not achieve a rapid virologic responseAlessandra Mangia, Alexander J Thompson, Rosanna Santoro, et al.
American Journal of Human Genetics|May 7, 2002
Founding mothers of Jewish communities: geographically separated Jewish groups were independently founded by very few female ancestorsMark G Thomas, Michael E Weale, Abigail L Jones, et al.
Epilepsia|June 4, 2011
Genomic microdeletions associated with epilepsy: not a contraindication to resective surgeryClaudia B Catarino, Dalia Kasperavičiūtė, Maria Thom, et al.
Frontiers in Physiology|October 5, 2020
A Novel Kv7.3 Variant in the Voltage-Sensing S<sub>4</sub> Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and <i>in vitro</i> Rescue by β-HydroxybutyrateFrancesco Miceli, Lidia Carotenuto, Vincenzo Barrese, et al.
Journal of Clinical Immunology|April 15, 2016
Dominant Splice Site Mutations in PIK3R1 Cause Hyper IgM Syndrome, Lymphadenopathy and Short StatureSlavé Petrovski, Roberta E Parrott, Joseph L Roberts, et al.
Gastroenterology|June 16, 2010
Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reductionAlexander J Thompson, Jacques Fellay, Keyur Patel, et al.
Nature|August 18, 2009
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearanceDongliang Ge, Jacques Fellay, Alexander J Thompson, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca<sup>2+</sup> regulationMatthew Halvorsen, Laura Gould, Xiaohan Wang, et al.
Pageof 34

Showing results (191-200 of 338) with videos related to

Sort By:
Pageof 34
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 20, 2007
Review of evidence for genetic testing for CYP450 polymorphisms in management of patients with nonpsychotic depression with selective serotonin reuptake inhibitorsMugdha Thakur, Iris Grossman, Douglas C McCrory, et al.
Hepatology (Baltimore, Md.)|October 9, 2010
IL28B genotype is associated with differential expression of intrahepatic interferon-stimulated genes in patients with chronic hepatitis CThomas J Urban, Alexander J Thompson, Shelton S Bradrick, et al.
Gastroenterology|July 13, 2010
An IL28B polymorphism determines treatment response of hepatitis C virus genotype 2 or 3 patients who do not achieve a rapid virologic responseAlessandra Mangia, Alexander J Thompson, Rosanna Santoro, et al.
American Journal of Human Genetics|May 7, 2002
Founding mothers of Jewish communities: geographically separated Jewish groups were independently founded by very few female ancestorsMark G Thomas, Michael E Weale, Abigail L Jones, et al.
Epilepsia|June 4, 2011
Genomic microdeletions associated with epilepsy: not a contraindication to resective surgeryClaudia B Catarino, Dalia Kasperavičiūtė, Maria Thom, et al.
Frontiers in Physiology|October 5, 2020
A Novel Kv7.3 Variant in the Voltage-Sensing S<sub>4</sub> Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and <i>in vitro</i> Rescue by β-HydroxybutyrateFrancesco Miceli, Lidia Carotenuto, Vincenzo Barrese, et al.
Journal of Clinical Immunology|April 15, 2016
Dominant Splice Site Mutations in PIK3R1 Cause Hyper IgM Syndrome, Lymphadenopathy and Short StatureSlavé Petrovski, Roberta E Parrott, Joseph L Roberts, et al.
Gastroenterology|June 16, 2010
Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reductionAlexander J Thompson, Jacques Fellay, Keyur Patel, et al.
Nature|August 18, 2009
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearanceDongliang Ge, Jacques Fellay, Alexander J Thompson, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca<sup>2+</sup> regulationMatthew Halvorsen, Laura Gould, Xiaohan Wang, et al.
Pageof 34