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Showing results (151-160 of 158) with videos related to

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Elife|June 3, 2015
An internal thioester in a pathogen surface protein mediates covalent host bindingMiriam Walden, John M Edwards, Aleksandra M Dziewulska, et al.
Nature Communications|February 2, 2023
Tautomerism unveils a self-inhibition mechanism of crystallizationWeiwei Tang, Taimin Yang, Cristian A Morales-Rivera, et al.
Molecular Genetics and Metabolism|December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementiaM J Kovach, B Waggoner, S M Leal, et al.
Neurology|July 15, 2011
Randomized, blinded trial of weekend vs daily prednisone in Duchenne muscular dystrophyD M Escolar, L P Hache, P R Clemens, et al.
Neurology|March 10, 2012
Pentoxifylline as a rescue treatment for DMD: a randomized double-blind clinical trialD M Escolar, A Zimmerman, T Bertorini, et al.
Neurology|December 14, 2005
Tolerance of high-dose (3,000 mg/day) coenzyme Q10 in ALSK L Ferrante, J Shefner, H Zhang, et al.
International Journal of Pharmaceutics|November 3, 2025
Quality by digital design in action: a workflow for crystallisation and isolationIan Houson, Humera Siddique, Magdalene W S Chong, et al.
International Journal of Pharmaceutics|April 26, 2025
Quality by digital design to accelerate sustainable medicines developmentChantal L Mustoe, Alice J Turner, Stephanie J Urwin, et al.
Pageof 16

Showing results (151-160 of 158) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 158 results.
Elife|June 3, 2015
An internal thioester in a pathogen surface protein mediates covalent host bindingMiriam Walden, John M Edwards, Aleksandra M Dziewulska, et al.
Nature Communications|February 2, 2023
Tautomerism unveils a self-inhibition mechanism of crystallizationWeiwei Tang, Taimin Yang, Cristian A Morales-Rivera, et al.
Molecular Genetics and Metabolism|December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementiaM J Kovach, B Waggoner, S M Leal, et al.
Neurology|July 15, 2011
Randomized, blinded trial of weekend vs daily prednisone in Duchenne muscular dystrophyD M Escolar, L P Hache, P R Clemens, et al.
Neurology|March 10, 2012
Pentoxifylline as a rescue treatment for DMD: a randomized double-blind clinical trialD M Escolar, A Zimmerman, T Bertorini, et al.
Neurology|December 14, 2005
Tolerance of high-dose (3,000 mg/day) coenzyme Q10 in ALSK L Ferrante, J Shefner, H Zhang, et al.
International Journal of Pharmaceutics|November 3, 2025
Quality by digital design in action: a workflow for crystallisation and isolationIan Houson, Humera Siddique, Magdalene W S Chong, et al.
International Journal of Pharmaceutics|April 26, 2025
Quality by digital design to accelerate sustainable medicines developmentChantal L Mustoe, Alice J Turner, Stephanie J Urwin, et al.
Pageof 16