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B Goldstein

Showing results (1241-1250 of 1,434) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 19, 2021
Amyloidogenic Processing of Amyloid Precursor Protein Drives Stretch-Induced Disruption of Axonal Transport in hiPSC-Derived NeuronsRodrigo S Chaves, My Tran, Andrew R Holder, et al.
Cancer Prevention Research (Philadelphia, Pa.)|October 3, 2018
High Prevalence of Hereditary Cancer Syndromes and Outcomes in Adults with Early-Onset Pancreatic CancerSarah A Bannon, Maria F Montiel, Jennifer B Goldstein, et al.
Neurology|November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosisPaloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.
Annals of Internal Medicine|November 27, 2018
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome SequencingHila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, et al.
The Journal of Infectious Diseases|October 5, 2010
Determinants of protection among HIV‐exposed seronegative persons: an overviewMichael M Lederman, Galit Alter, Demetre C Daskalakis, et al.
Science (New York, N.Y.)|October 4, 2003
Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS miceA M Clement, M D Nguyen, E A Roberts, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 27, 2009
CYP2C9*1B promoter polymorphisms, in linkage with CYP2C19*2, affect phenytoin autoinduction of clearance and maintenance doseAmarjit S Chaudhry, Thomas J Urban, Jatinder K Lamba, et al.
Nature Genetics|December 21, 2004
A single-nucleotide polymorphism tagging set for human drug metabolism and transportKourosh R Ahmadi, Mike E Weale, Zhengyu Y Xue, et al.
Plos Genetics|November 30, 2017
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutationsXiaolin Zhu, Raghavendra Padmanabhan, Brett Copeland, et al.
Nephrology (Carlton, Vic.)|May 23, 2018
Left ventricular strain analysis using cardiac magnetic resonance imaging in patients undergoing in-centre nocturnal haemodialysisJann P Ong, Ron Wald, Marc B Goldstein, et al.
Pageof 144

Showing results (1241-1250 of 1,434) with videos related to

Sort By:
Pageof 144
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 19, 2021
Amyloidogenic Processing of Amyloid Precursor Protein Drives Stretch-Induced Disruption of Axonal Transport in hiPSC-Derived NeuronsRodrigo S Chaves, My Tran, Andrew R Holder, et al.
Cancer Prevention Research (Philadelphia, Pa.)|October 3, 2018
High Prevalence of Hereditary Cancer Syndromes and Outcomes in Adults with Early-Onset Pancreatic CancerSarah A Bannon, Maria F Montiel, Jennifer B Goldstein, et al.
Neurology|November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosisPaloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.
Annals of Internal Medicine|November 27, 2018
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome SequencingHila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, et al.
The Journal of Infectious Diseases|October 5, 2010
Determinants of protection among HIV‐exposed seronegative persons: an overviewMichael M Lederman, Galit Alter, Demetre C Daskalakis, et al.
Science (New York, N.Y.)|October 4, 2003
Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS miceA M Clement, M D Nguyen, E A Roberts, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 27, 2009
CYP2C9*1B promoter polymorphisms, in linkage with CYP2C19*2, affect phenytoin autoinduction of clearance and maintenance doseAmarjit S Chaudhry, Thomas J Urban, Jatinder K Lamba, et al.
Nature Genetics|December 21, 2004
A single-nucleotide polymorphism tagging set for human drug metabolism and transportKourosh R Ahmadi, Mike E Weale, Zhengyu Y Xue, et al.
Plos Genetics|November 30, 2017
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutationsXiaolin Zhu, Raghavendra Padmanabhan, Brett Copeland, et al.
Nephrology (Carlton, Vic.)|May 23, 2018
Left ventricular strain analysis using cardiac magnetic resonance imaging in patients undergoing in-centre nocturnal haemodialysisJann P Ong, Ron Wald, Marc B Goldstein, et al.
Pageof 144