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

Nathan Pankratz

Showing results (41-50 of 173) with videos related to

Pageof 18
Sort By:
The Journal of Molecular Diagnostics : JMD|June 11, 2021
Prediction of False-Positive Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Molecular Results in a High-Throughput Open-Platform SystemRyan J Martinez, Nathan Pankratz, Matthew Schomaker, et al.
BMC Medical Genetics|April 2, 2010
Maternal inheritance and mitochondrial DNA variants in familial Parkinson's diseaseDavid K Simon, Nathan Pankratz, Diane K Kissell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2022
Genetic drivers of Cushing's disease: Frequency and associated phenotypesLaura C Hernández-Ramírez, Nathan Pankratz, John Lane, et al.
Thrombosis Research|June 15, 2018
Pleiotropic effects of n-6 and n-3 fatty acid-related genetic variants on circulating hemostatic variablesLu-Chen Weng, Weihua Guan, Lyn M Steffen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 16, 2004
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's diseaseWilliam C Nichols, Sean K Uniacke, Nathan Pankratz, et al.
Journal of Nutrigenetics and Nutrigenomics|January 31, 2015
The associations between 6-n-propylthiouracil (PROP) intensity and taste intensities differ by TAS2R38 haplotypeMary E Fischer, Karen J Cruickshanks, James S Pankow, et al.
Human Molecular Genetics|August 2, 2023
Predicted leukocyte telomere length and risk of myeloid neoplasmsShannon M Sullivan, Ben Cole, John Lane, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2009
Alpha-synuclein and familial Parkinson's diseaseNathan Pankratz, William C Nichols, Veronika E Elsaesser, et al.
Neuroscience Letters|September 26, 2006
Mutations in DJ-1 are rare in familial Parkinson diseaseNathan Pankratz, Michael W Pauciulo, Veronika E Elsaesser, et al.
Plos One|April 13, 2018
Evaluation of the relationship between plasma lipids and abdominal aortic aneurysm: A Mendelian randomization studyLu-Chen Weng, Nicholas S Roetker, Pamela L Lutsey, et al.
Pageof 18

Showing results (41-50 of 173) with videos related to

Sort By:
Pageof 18
The Journal of Molecular Diagnostics : JMD|June 11, 2021
Prediction of False-Positive Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Molecular Results in a High-Throughput Open-Platform SystemRyan J Martinez, Nathan Pankratz, Matthew Schomaker, et al.
BMC Medical Genetics|April 2, 2010
Maternal inheritance and mitochondrial DNA variants in familial Parkinson's diseaseDavid K Simon, Nathan Pankratz, Diane K Kissell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2022
Genetic drivers of Cushing's disease: Frequency and associated phenotypesLaura C Hernández-Ramírez, Nathan Pankratz, John Lane, et al.
Thrombosis Research|June 15, 2018
Pleiotropic effects of n-6 and n-3 fatty acid-related genetic variants on circulating hemostatic variablesLu-Chen Weng, Weihua Guan, Lyn M Steffen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 16, 2004
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's diseaseWilliam C Nichols, Sean K Uniacke, Nathan Pankratz, et al.
Journal of Nutrigenetics and Nutrigenomics|January 31, 2015
The associations between 6-n-propylthiouracil (PROP) intensity and taste intensities differ by TAS2R38 haplotypeMary E Fischer, Karen J Cruickshanks, James S Pankow, et al.
Human Molecular Genetics|August 2, 2023
Predicted leukocyte telomere length and risk of myeloid neoplasmsShannon M Sullivan, Ben Cole, John Lane, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2009
Alpha-synuclein and familial Parkinson's diseaseNathan Pankratz, William C Nichols, Veronika E Elsaesser, et al.
Neuroscience Letters|September 26, 2006
Mutations in DJ-1 are rare in familial Parkinson diseaseNathan Pankratz, Michael W Pauciulo, Veronika E Elsaesser, et al.
Plos One|April 13, 2018
Evaluation of the relationship between plasma lipids and abdominal aortic aneurysm: A Mendelian randomization studyLu-Chen Weng, Nicholas S Roetker, Pamela L Lutsey, et al.
Pageof 18