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David B Goldstein

Showing results (241-250 of 338) with videos related to

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Annals of Neurology|February 2, 2006
UCHL-1 is not a Parkinson's disease susceptibility geneDaniel G Healy, Patrick M Abou-Sleiman, Juan P Casas, et al.
Brain Communications|August 16, 2021
Alternating hemiplegia of childhood: evolution over time and mouse model corroborationJulie Uchitel, Keri Wallace, Linh Tran, et al.
Nature Metabolism|March 24, 2021
Serine biosynthesis defect due to haploinsufficiency of PHGDH causes retinal diseaseKevin Eade, Marin L Gantner, Joseph A Hostyk, et al.
Nature Neuroscience|June 29, 2021
Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variantsMathew Halvorsen, Jack Samuels, Ying Wang, et al.
Annals of Neurology|December 19, 2022
Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe EpilepsyPiero Perucca, Kate Stanley, Natasha Harris, et al.
Gastroenterology|July 20, 2010
A polymorphism near IL28B is associated with spontaneous clearance of acute hepatitis C virus and jaundiceHans L Tillmann, Alex J Thompson, Keyur Patel, et al.
Journal of the American Society of Nephrology : JASN|May 16, 2019
Exome-Based Rare-Variant Analyses in CKDSophia Cameron-Christie, Charles J Wolock, Emily Groopman, et al.
Epilepsia|April 18, 2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyGianpiero L Cavalleri, Nicole M Walley, Nicole Soranzo, et al.
American Journal of Respiratory and Critical Care Medicine|January 19, 2017
An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary FibrosisSlavé Petrovski, Jamie L Todd, Michael T Durheim, et al.
Genome Research|April 4, 2019
A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALSSahar Gelfman, Sarah Dugger, Cristiane de Araujo Martins Moreno, et al.
Pageof 34

Showing results (241-250 of 338) with videos related to

Sort By:
Pageof 34
Annals of Neurology|February 2, 2006
UCHL-1 is not a Parkinson's disease susceptibility geneDaniel G Healy, Patrick M Abou-Sleiman, Juan P Casas, et al.
Brain Communications|August 16, 2021
Alternating hemiplegia of childhood: evolution over time and mouse model corroborationJulie Uchitel, Keri Wallace, Linh Tran, et al.
Nature Metabolism|March 24, 2021
Serine biosynthesis defect due to haploinsufficiency of PHGDH causes retinal diseaseKevin Eade, Marin L Gantner, Joseph A Hostyk, et al.
Nature Neuroscience|June 29, 2021
Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variantsMathew Halvorsen, Jack Samuels, Ying Wang, et al.
Annals of Neurology|December 19, 2022
Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe EpilepsyPiero Perucca, Kate Stanley, Natasha Harris, et al.
Gastroenterology|July 20, 2010
A polymorphism near IL28B is associated with spontaneous clearance of acute hepatitis C virus and jaundiceHans L Tillmann, Alex J Thompson, Keyur Patel, et al.
Journal of the American Society of Nephrology : JASN|May 16, 2019
Exome-Based Rare-Variant Analyses in CKDSophia Cameron-Christie, Charles J Wolock, Emily Groopman, et al.
Epilepsia|April 18, 2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyGianpiero L Cavalleri, Nicole M Walley, Nicole Soranzo, et al.
American Journal of Respiratory and Critical Care Medicine|January 19, 2017
An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary FibrosisSlavé Petrovski, Jamie L Todd, Michael T Durheim, et al.
Genome Research|April 4, 2019
A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALSSahar Gelfman, Sarah Dugger, Cristiane de Araujo Martins Moreno, et al.
Pageof 34