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Nathan Pankratz

Showing results (51-60 of 173) with videos related to

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Plos Genetics|July 5, 2012
Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulationAlexandra Dumitriu, Jeanne C Latourelle, Tiffany C Hadzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2011
Genomewide linkage study of modifiers of LRRK2-related Parkinson's diseaseJeanne C Latourelle, Audrey E Hendricks, Nathan Pankratz, et al.
Journal of the American Society of Nephrology : JASN|January 23, 2016
Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities StudyAdrienne Tin, Morgan E Grams, Foram N Ashar, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2019
Large Genomic Aberrations in Corticotropinomas Are Associated With Greater AggressivenessChristina Tatsi, Nathan Pankratz, John Lane, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|November 5, 2019
Replication of Newly Identified Genetic Associations Between Abdominal Aortic Aneurysm and SMYD2, LINC00540, PCIF1/MMP9/ZNF335, and ERGWeihong Tang, Athanasios Saratzis, Jack Pattee, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 29, 2022
Proteomics Analysis of Genetic Liability of Abdominal Aortic Aneurysm Identifies Plasma Neogenin and Kit Ligand: The ARIC StudyBrian T Steffen, James S Pankow, Faye L Norby, et al.
Lancet (London, England)|February 1, 2005
Genetic screening for a single common LRRK2 mutation in familial Parkinson's diseaseWilliam C Nichols, Nathan Pankratz, Dena Hernandez, et al.
Journal of the Endocrine Society|August 31, 2022
Whole Exome Sequencing in Patients With Ectopic Posterior PituitaryTatiane S Silva, Fabio R Faucz, Laura C Hernández-Ramírez, et al.
The Journal of Clinical Endocrinology and Metabolism|April 2, 2020
Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing's Disease With or Without an MEN4 PhenotypeFanny Chasseloup, Nathan Pankratz, John Lane, et al.
Human Genetics|November 6, 2008
Genomewide association study for susceptibility genes contributing to familial Parkinson diseaseNathan Pankratz, Jemma B Wilk, Jeanne C Latourelle, et al.
Pageof 18

Showing results (51-60 of 173) with videos related to

Sort By:
Pageof 18
Plos Genetics|July 5, 2012
Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulationAlexandra Dumitriu, Jeanne C Latourelle, Tiffany C Hadzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2011
Genomewide linkage study of modifiers of LRRK2-related Parkinson's diseaseJeanne C Latourelle, Audrey E Hendricks, Nathan Pankratz, et al.
Journal of the American Society of Nephrology : JASN|January 23, 2016
Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities StudyAdrienne Tin, Morgan E Grams, Foram N Ashar, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2019
Large Genomic Aberrations in Corticotropinomas Are Associated With Greater AggressivenessChristina Tatsi, Nathan Pankratz, John Lane, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|November 5, 2019
Replication of Newly Identified Genetic Associations Between Abdominal Aortic Aneurysm and SMYD2, LINC00540, PCIF1/MMP9/ZNF335, and ERGWeihong Tang, Athanasios Saratzis, Jack Pattee, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 29, 2022
Proteomics Analysis of Genetic Liability of Abdominal Aortic Aneurysm Identifies Plasma Neogenin and Kit Ligand: The ARIC StudyBrian T Steffen, James S Pankow, Faye L Norby, et al.
Lancet (London, England)|February 1, 2005
Genetic screening for a single common LRRK2 mutation in familial Parkinson's diseaseWilliam C Nichols, Nathan Pankratz, Dena Hernandez, et al.
Journal of the Endocrine Society|August 31, 2022
Whole Exome Sequencing in Patients With Ectopic Posterior PituitaryTatiane S Silva, Fabio R Faucz, Laura C Hernández-Ramírez, et al.
The Journal of Clinical Endocrinology and Metabolism|April 2, 2020
Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing's Disease With or Without an MEN4 PhenotypeFanny Chasseloup, Nathan Pankratz, John Lane, et al.
Human Genetics|November 6, 2008
Genomewide association study for susceptibility genes contributing to familial Parkinson diseaseNathan Pankratz, Jemma B Wilk, Jeanne C Latourelle, et al.
Pageof 18