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F Wadsworth

Showing results (121-130 of 137) with videos related to

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Journal of Neuropathology and Experimental Neurology|August 22, 2008
First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutationThomas E F Webb, Suvankar Pal, Durrenajaf Siddique, et al.
Nature Communications|July 10, 2014
Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peakedMalin K Sandberg, Huda Al-Doujaily, Bernadette Sharps, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 9, 2020
Highly infectious prions are not directly neurotoxicIryna Benilova, Madeleine Reilly, Cassandra Terry, et al.
Nature Communications|September 12, 2013
Amyloid-β nanotubes are associated with prion protein-dependent synaptotoxicityAndrew J Nicoll, Silvia Panico, Darragh B Freir, et al.
Plos Pathogens|February 20, 2025
Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patientFuquan Zhang, Susan Joiner, Jacqueline M Linehan, et al.
Neurobiology of Aging|June 5, 2018
Evaluating the causality of novel sequence variants in the prion protein gene by exampleTze How Mok, Carolin Koriath, Zane Jaunmuktane, et al.
Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.
Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.
Molecular Psychiatry|March 6, 2021
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.
Journal of Neurogenetics|January 10, 2025
The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's diseaseLeah Holm-Mercer, Thomas Coysh, Tze How Mok, et al.
Pageof 14

Showing results (121-130 of 137) with videos related to

Sort By:
Pageof 14
Journal of Neuropathology and Experimental Neurology|August 22, 2008
First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutationThomas E F Webb, Suvankar Pal, Durrenajaf Siddique, et al.
Nature Communications|July 10, 2014
Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peakedMalin K Sandberg, Huda Al-Doujaily, Bernadette Sharps, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 9, 2020
Highly infectious prions are not directly neurotoxicIryna Benilova, Madeleine Reilly, Cassandra Terry, et al.
Nature Communications|September 12, 2013
Amyloid-β nanotubes are associated with prion protein-dependent synaptotoxicityAndrew J Nicoll, Silvia Panico, Darragh B Freir, et al.
Plos Pathogens|February 20, 2025
Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patientFuquan Zhang, Susan Joiner, Jacqueline M Linehan, et al.
Neurobiology of Aging|June 5, 2018
Evaluating the causality of novel sequence variants in the prion protein gene by exampleTze How Mok, Carolin Koriath, Zane Jaunmuktane, et al.
Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.
Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.
Molecular Psychiatry|March 6, 2021
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.
Journal of Neurogenetics|January 10, 2025
The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's diseaseLeah Holm-Mercer, Thomas Coysh, Tze How Mok, et al.
Pageof 14