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

Fiona J Sorrell

Showing results (1-10 of 18) with videos related to

Pageof 2
Sort By:
Free Radical Biology & Medicine|June 10, 2015
Structural basis of Keap1 interactions with Nrf2Peter Canning, Fiona J Sorrell, Alex N Bullock
The Biochemical Journal|March 13, 2019
Solution structures and biophysical analysis of full-length group A PAKs reveal they are monomeric and auto-inhibited in <i>cis</i>Fiona J Sorrell, Lena Marie Kilian, Jonathan M Elkins
Journal of Pharmaceutical and Biomedical Analysis|April 9, 2010
Development of a differential scanning fluorimetry based high throughput screening assay for the discovery of affinity binders against an anthrax proteinFiona J Sorrell, Gemma K Greenwood, Kristian Birchall, et al.
Structure (London, England : 1993)|February 9, 2016
Family-wide Structural Analysis of Human Numb-Associated Protein KinasesFiona J Sorrell, Marta Szklarz, Kamal R Abdul Azeez, et al.
The Biochemical Journal|March 20, 2014
Structural and biochemical characterization of the KLHL3-WNK kinase interaction important in blood pressure regulationFrances-Rose Schumacher, Fiona J Sorrell, Dario R Alessi, et al.
The Biochemical Journal|October 1, 2017
Structural complexity in the KCTD family of Cullin3-dependent E3 ubiquitin ligasesDaniel M Pinkas, Caroline E Sanvitale, Joshua C Bufton, et al.
Chemmedchem|July 17, 2010
Improved 2,4-diarylthiazole-based antiprion agents: switching the sense of the amide group at C5 leads to an increase in potencyMark J Thompson, Jennifer C Louth, Gemma K Greenwood, et al.
Chemmedchem|December 15, 2010
Structure-activity relationship refinement and further assessment of indole-3-glyoxylamides as a lead series against prion diseaseMark J Thompson, Jennifer C Louth, Steven Ferrara, et al.
Chemmedchem|February 7, 2023
Systematic Potency and Property Assessment of VHL Ligands and Implications on PROTAC DesignJohannes Krieger, Fiona J Sorrell, Ansgar A Wegener, et al.
European Journal of Medicinal Chemistry|July 6, 2011
Discovery of 6-substituted indole-3-glyoxylamides as lead antiprion agents with enhanced cell line activity, improved microsomal stability and low toxicityMark J Thompson, Jennifer C Louth, Steven Ferrara, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Free Radical Biology & Medicine|June 10, 2015
Structural basis of Keap1 interactions with Nrf2Peter Canning, Fiona J Sorrell, Alex N Bullock
The Biochemical Journal|March 13, 2019
Solution structures and biophysical analysis of full-length group A PAKs reveal they are monomeric and auto-inhibited in <i>cis</i>Fiona J Sorrell, Lena Marie Kilian, Jonathan M Elkins
Journal of Pharmaceutical and Biomedical Analysis|April 9, 2010
Development of a differential scanning fluorimetry based high throughput screening assay for the discovery of affinity binders against an anthrax proteinFiona J Sorrell, Gemma K Greenwood, Kristian Birchall, et al.
Structure (London, England : 1993)|February 9, 2016
Family-wide Structural Analysis of Human Numb-Associated Protein KinasesFiona J Sorrell, Marta Szklarz, Kamal R Abdul Azeez, et al.
The Biochemical Journal|March 20, 2014
Structural and biochemical characterization of the KLHL3-WNK kinase interaction important in blood pressure regulationFrances-Rose Schumacher, Fiona J Sorrell, Dario R Alessi, et al.
The Biochemical Journal|October 1, 2017
Structural complexity in the KCTD family of Cullin3-dependent E3 ubiquitin ligasesDaniel M Pinkas, Caroline E Sanvitale, Joshua C Bufton, et al.
Chemmedchem|July 17, 2010
Improved 2,4-diarylthiazole-based antiprion agents: switching the sense of the amide group at C5 leads to an increase in potencyMark J Thompson, Jennifer C Louth, Gemma K Greenwood, et al.
Chemmedchem|December 15, 2010
Structure-activity relationship refinement and further assessment of indole-3-glyoxylamides as a lead series against prion diseaseMark J Thompson, Jennifer C Louth, Steven Ferrara, et al.
Chemmedchem|February 7, 2023
Systematic Potency and Property Assessment of VHL Ligands and Implications on PROTAC DesignJohannes Krieger, Fiona J Sorrell, Ansgar A Wegener, et al.
European Journal of Medicinal Chemistry|July 6, 2011
Discovery of 6-substituted indole-3-glyoxylamides as lead antiprion agents with enhanced cell line activity, improved microsomal stability and low toxicityMark J Thompson, Jennifer C Louth, Steven Ferrara, et al.
Pageof 2