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F Hill

Showing results (671-680 of 780) with videos related to

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Protein Expression and Purification|July 5, 2001
Expression of the amino-terminal domain of platelet glycoprotein Ib alpha: exploitation of a calmodulin tag for determination of its functional activityC Q Li, P Ye, Cao Zf, et al.
Plos One|September 3, 2010
Glycosaminoglycan sulphation affects the seeded misfolding of a mutant prion proteinVictoria A Lawson, Brooke Lumicisi, Jeremy Welton, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2008
Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type miceJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
The EMBO Journal|November 29, 2002
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion proteinEmmanuel A Asante, Jacqueline M Linehan, Melanie Desbruslais, et al.
The Journal of Bone and Joint Surgery. American Volume|April 9, 2025
Open Reduction of Hip Dislocation Is Associated with Higher Rates of Proximal Femoral Growth Disturbance in Patients with Arthrogryposis Multiplex Congenita Than Idiopathic DDH: A Dual-Center Retrospective Cohort StudyTristen N Taylor, Rishi Sinha, Nihar N Pathare, et al.
Free Radical Biology & Medicine|March 3, 2009
Formation of dopamine-mediated alpha-synuclein-soluble oligomers requires methionine oxidationSu Ling Leong, Chi L L Pham, Denise Galatis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 18, 2014
Cognitive impairment in rapid-onset dystonia-parkinsonismJared F Cook, Deborah F Hill, Beverly M Snively, et al.
The American Journal of Pathology|June 17, 1998
An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathyP Piccardo, J P Langeveld, A F Hill, et al.
Science (New York, N.Y.)|November 13, 2004
Human prion protein with valine 129 prevents expression of variant CJD phenotypeJonathan D F Wadsworth, Emmanuel A Asante, Melanie Desbruslais, et al.
Neurology|August 31, 2012
Psychiatric disorders in rapid-onset dystonia-parkinsonismAllison Brashear, Jared F Cook, Deborah F Hill, et al.
Pageof 78

Showing results (671-680 of 780) with videos related to

Sort By:
Pageof 78
Protein Expression and Purification|July 5, 2001
Expression of the amino-terminal domain of platelet glycoprotein Ib alpha: exploitation of a calmodulin tag for determination of its functional activityC Q Li, P Ye, Cao Zf, et al.
Plos One|September 3, 2010
Glycosaminoglycan sulphation affects the seeded misfolding of a mutant prion proteinVictoria A Lawson, Brooke Lumicisi, Jeremy Welton, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2008
Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type miceJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
The EMBO Journal|November 29, 2002
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion proteinEmmanuel A Asante, Jacqueline M Linehan, Melanie Desbruslais, et al.
The Journal of Bone and Joint Surgery. American Volume|April 9, 2025
Open Reduction of Hip Dislocation Is Associated with Higher Rates of Proximal Femoral Growth Disturbance in Patients with Arthrogryposis Multiplex Congenita Than Idiopathic DDH: A Dual-Center Retrospective Cohort StudyTristen N Taylor, Rishi Sinha, Nihar N Pathare, et al.
Free Radical Biology & Medicine|March 3, 2009
Formation of dopamine-mediated alpha-synuclein-soluble oligomers requires methionine oxidationSu Ling Leong, Chi L L Pham, Denise Galatis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 18, 2014
Cognitive impairment in rapid-onset dystonia-parkinsonismJared F Cook, Deborah F Hill, Beverly M Snively, et al.
The American Journal of Pathology|June 17, 1998
An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathyP Piccardo, J P Langeveld, A F Hill, et al.
Science (New York, N.Y.)|November 13, 2004
Human prion protein with valine 129 prevents expression of variant CJD phenotypeJonathan D F Wadsworth, Emmanuel A Asante, Melanie Desbruslais, et al.
Neurology|August 31, 2012
Psychiatric disorders in rapid-onset dystonia-parkinsonismAllison Brashear, Jared F Cook, Deborah F Hill, et al.
Pageof 78