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Showing results (471-480 of 495) with videos related to

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Plos One|March 26, 2013
Glycoform-selective prion formation in sporadic and familial forms of prion diseaseXiangzhu Xiao, Jue Yuan, Stéphane Haïk, et al.
Diagnostics (Basel, Switzerland)|October 23, 2021
The ERG1A K<sup>+</sup> Channel Is More Abundant in <i>Rectus abdominis</i> Muscle from Cancer Patients Than that from Healthy HumansSandra Zampieri, Marco Sandri, Joseph L Cheatwood, et al.
Parkinsonism & Related Disorders|February 25, 2012
PARK2 variability in Polish Parkinson's disease patients--interaction with mitochondrial haplogroupsKatarzyna Gaweda-Walerych, Krzysztof Safranow, Barbara Jasinska-Myga, et al.
Molecular Cell|August 5, 2022
S-nitrosylation is required for β<sub>2</sub>AR desensitization and experimental asthmaFabio V Fonseca, Thomas M Raffay, Kunhong Xiao, et al.
Parkinsonism & Related Disorders|September 2, 2009
LINGO1 rs9652490 is associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Owen A Ross, Christian Wider, et al.
European Journal of Neurology|December 17, 2010
SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction studyC Wider, C Vilariño-Güell, M G Heckman, et al.
Parkinsonism & Related Disorders|July 28, 2009
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunctionAndreas Puschmann, Owen A Ross, Carles Vilariño-Güell, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 25, 2018
Antiretroviral Drug Metabolism in Humanized PXR-CAR-CYP3A-NOG MiceJoEllyn M McMillan, Denise A Cobb, Zhiyi Lin, et al.
Neurology|September 7, 2007
Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5C Wider, S Melquist, M Hauf, et al.
Molecular Cell|December 5, 2020
A Role for the Mre11-Rad50-Xrs2 Complex in Gene Expression and Chromosome OrganizationRomain Forey, Antoine Barthe, Mireille Tittel-Elmer, et al.
Pageof 50

Showing results (471-480 of 495) with videos related to

Sort By:
Pageof 50
Plos One|March 26, 2013
Glycoform-selective prion formation in sporadic and familial forms of prion diseaseXiangzhu Xiao, Jue Yuan, Stéphane Haïk, et al.
Diagnostics (Basel, Switzerland)|October 23, 2021
The ERG1A K<sup>+</sup> Channel Is More Abundant in <i>Rectus abdominis</i> Muscle from Cancer Patients Than that from Healthy HumansSandra Zampieri, Marco Sandri, Joseph L Cheatwood, et al.
Parkinsonism & Related Disorders|February 25, 2012
PARK2 variability in Polish Parkinson's disease patients--interaction with mitochondrial haplogroupsKatarzyna Gaweda-Walerych, Krzysztof Safranow, Barbara Jasinska-Myga, et al.
Molecular Cell|August 5, 2022
S-nitrosylation is required for β<sub>2</sub>AR desensitization and experimental asthmaFabio V Fonseca, Thomas M Raffay, Kunhong Xiao, et al.
Parkinsonism & Related Disorders|September 2, 2009
LINGO1 rs9652490 is associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Owen A Ross, Christian Wider, et al.
European Journal of Neurology|December 17, 2010
SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction studyC Wider, C Vilariño-Güell, M G Heckman, et al.
Parkinsonism & Related Disorders|July 28, 2009
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunctionAndreas Puschmann, Owen A Ross, Carles Vilariño-Güell, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 25, 2018
Antiretroviral Drug Metabolism in Humanized PXR-CAR-CYP3A-NOG MiceJoEllyn M McMillan, Denise A Cobb, Zhiyi Lin, et al.
Neurology|September 7, 2007
Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5C Wider, S Melquist, M Hauf, et al.
Molecular Cell|December 5, 2020
A Role for the Mre11-Rad50-Xrs2 Complex in Gene Expression and Chromosome OrganizationRomain Forey, Antoine Barthe, Mireille Tittel-Elmer, et al.
Pageof 50