Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Lea

Showing results (401-410 of 439) with videos related to

Pageof 44
Sort By:
Plos Genetics|January 23, 2008
The genetic structure of Pacific IslandersJonathan S Friedlaender, Françoise R Friedlaender, Floyd A Reed, et al.
Biochemistry|August 10, 2016
Chaperonin-Based Biolayer Interferometry To Assess the Kinetic Stability of Metastable, Aggregation-Prone ProteinsWendy A Lea, Pierce T O'Neil, Alexandra J Machen, et al.
Epilepsy Research|March 15, 2021
The MinION as a cost-effective technology for diagnostic screening of the SCN1A gene in epilepsy patientsThi Tuyet Dieu Ngo, Rodney A Lea, Neven Maksemous, et al.
Scientific Reports|October 1, 2021
Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney diseaseNgan K Tran, Rodney A Lea, Samuel Holland, et al.
Neurogenetics|April 15, 2005
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraineR A Lea, D R Nyholt, R P Curtain, et al.
The Journal of Biological Chemistry|March 27, 2014
Biochemical, cellular, and biophysical characterization of a potent inhibitor of mutant isocitrate dehydrogenase IDH1Mindy I Davis, Stefan Gross, Min Shen, et al.
Human Genetics|November 17, 2009
Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aboriginesHung-Pin Tu, Albert Min-Shan Ko, Shu-Jung Wang, et al.
Human Molecular Genetics|May 21, 2013
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 geneTeresa Esposito, Rod A Lea, Bridget H Maher, et al.
Frontiers in Molecular Neuroscience|August 5, 2022
Investigation of <i>CACNA1I</i> Cav3.3 Dysfunction in Hemiplegic MigraineNeven Maksemous, Claire D Blayney, Heidi G Sutherland, et al.
Plos Genetics|October 17, 2015
A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder MarkersMiles C Benton, Rodney A Lea, Donia Macartney-Coxson, et al.
Pageof 44

Showing results (401-410 of 439) with videos related to

Sort By:
Pageof 44
Plos Genetics|January 23, 2008
The genetic structure of Pacific IslandersJonathan S Friedlaender, Françoise R Friedlaender, Floyd A Reed, et al.
Biochemistry|August 10, 2016
Chaperonin-Based Biolayer Interferometry To Assess the Kinetic Stability of Metastable, Aggregation-Prone ProteinsWendy A Lea, Pierce T O'Neil, Alexandra J Machen, et al.
Epilepsy Research|March 15, 2021
The MinION as a cost-effective technology for diagnostic screening of the SCN1A gene in epilepsy patientsThi Tuyet Dieu Ngo, Rodney A Lea, Neven Maksemous, et al.
Scientific Reports|October 1, 2021
Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney diseaseNgan K Tran, Rodney A Lea, Samuel Holland, et al.
Neurogenetics|April 15, 2005
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraineR A Lea, D R Nyholt, R P Curtain, et al.
The Journal of Biological Chemistry|March 27, 2014
Biochemical, cellular, and biophysical characterization of a potent inhibitor of mutant isocitrate dehydrogenase IDH1Mindy I Davis, Stefan Gross, Min Shen, et al.
Human Genetics|November 17, 2009
Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aboriginesHung-Pin Tu, Albert Min-Shan Ko, Shu-Jung Wang, et al.
Human Molecular Genetics|May 21, 2013
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 geneTeresa Esposito, Rod A Lea, Bridget H Maher, et al.
Frontiers in Molecular Neuroscience|August 5, 2022
Investigation of <i>CACNA1I</i> Cav3.3 Dysfunction in Hemiplegic MigraineNeven Maksemous, Claire D Blayney, Heidi G Sutherland, et al.
Plos Genetics|October 17, 2015
A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder MarkersMiles C Benton, Rodney A Lea, Donia Macartney-Coxson, et al.
Pageof 44