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Tracy Campbell

Showing results (21-30 of 47) with videos related to

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European Journal of Human Genetics : EJHG|April 10, 2014
Predictive testing for inherited prion disease: report of 22 years experienceJane Owen, Jon Beck, Tracy Campbell, et al.
Lancet (London, England)|February 8, 2011
Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assayJulie Ann Edgeworth, Michael Farmer, Anita Sicilia, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Genetic susceptibility, evolution and the kuru epidemicSimon Mead, Jerome Whitfield, Mark Poulter, et al.
American Journal of Human Genetics|March 20, 2024
Population structure and migration in the Eastern Highlands of Papua New Guinea, a region impacted by the kuru epidemicLiam Quinn, Jerome Whitfield, Michael P Alpers, et al.
Science (New York, N.Y.)|April 12, 2003
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemicsSimon Mead, Michael P H Stumpf, Jerome Whitfield, et al.
The New England Journal of Medicine|January 19, 2017
Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129Tzehow Mok, Zane Jaunmuktane, Susan Joiner, et al.
Neurobiology of Aging|March 2, 2015
Rare structural genetic variation in human prion diseasesAna Lukic, James Uphill, Craig A Brown, et al.
Acta Neuropathologica|September 12, 2020
Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt-Jakob diseaseLuke C Dabin, Fernando Guntoro, Tracy Campbell, et al.
The New England Journal of Medicine|November 20, 2009
A novel protective prion protein variant that colocalizes with kuru exposureSimon Mead, Jerome Whitfield, Mark Poulter, et al.
Journal of Alzheimer'S Disease : JAD|July 4, 2025
Inherited prion disease caused by a novel frameshift mutation of <i>PRNP</i> resulting in protein truncation at codon 157Leah Holm-Mercer, Tze How Mok, Danielle Sequeira, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|April 10, 2014
Predictive testing for inherited prion disease: report of 22 years experienceJane Owen, Jon Beck, Tracy Campbell, et al.
Lancet (London, England)|February 8, 2011
Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assayJulie Ann Edgeworth, Michael Farmer, Anita Sicilia, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Genetic susceptibility, evolution and the kuru epidemicSimon Mead, Jerome Whitfield, Mark Poulter, et al.
American Journal of Human Genetics|March 20, 2024
Population structure and migration in the Eastern Highlands of Papua New Guinea, a region impacted by the kuru epidemicLiam Quinn, Jerome Whitfield, Michael P Alpers, et al.
Science (New York, N.Y.)|April 12, 2003
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemicsSimon Mead, Michael P H Stumpf, Jerome Whitfield, et al.
The New England Journal of Medicine|January 19, 2017
Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129Tzehow Mok, Zane Jaunmuktane, Susan Joiner, et al.
Neurobiology of Aging|March 2, 2015
Rare structural genetic variation in human prion diseasesAna Lukic, James Uphill, Craig A Brown, et al.
Acta Neuropathologica|September 12, 2020
Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt-Jakob diseaseLuke C Dabin, Fernando Guntoro, Tracy Campbell, et al.
The New England Journal of Medicine|November 20, 2009
A novel protective prion protein variant that colocalizes with kuru exposureSimon Mead, Jerome Whitfield, Mark Poulter, et al.
Journal of Alzheimer'S Disease : JAD|July 4, 2025
Inherited prion disease caused by a novel frameshift mutation of <i>PRNP</i> resulting in protein truncation at codon 157Leah Holm-Mercer, Tze How Mok, Danielle Sequeira, et al.
Pageof 5