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A Quinlan

Showing results (161-170 of 268) with videos related to

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Molecular Biology of the Cell|August 8, 2008
Glial fibrillary acidic protein filaments can tolerate the incorporation of assembly-compromised GFAP-delta, but with consequences for filament organization and alphaB-crystallin associationMing-Der Perng, Shu-Fang Wen, Terry Gibbon, et al.
Investigative Ophthalmology & Visual Science|September 1, 1996
Expression of Crystallins, Pax6, Filensin, CP49, MIP, and MP20 in lens-derived cell linesE Krausz, R C Augusteyn, R A Quinlan, et al.
Journal of Cell Science|April 1, 1995
Vimentin and CP49/filensin form distinct networks in the lens which are independently modulated during lens fibre cell differentiationA Sandilands, A R Prescott, J M Carter, et al.
Molecular Biology of the Cell|August 19, 2007
FGF-2 release from the lens capsule by MMP-2 maintains lens epithelial cell viabilityFrederique M D Tholozan, Christopher Gribbon, Zheng Li, et al.
Inorganic Chemistry|April 26, 2005
Characterization of the low-energy electronic excited states of benzoyl-substituted ruthenocenesCynthia T Sanderson, Jessica A Quinlan, Richard C Conover, et al.
Investigative Ophthalmology & Visual Science|March 28, 2006
The C terminus of lens aquaporin 0 interacts with the cytoskeletal proteins filensin and CP49Kristie M Lindsey Rose, Robert G Gourdie, Alan R Prescott, et al.
Advanced Nanobiomed Research|January 19, 2026
Self-Assembled Verteporfin Nanoparticles for Photodynamic and Light-Independent Therapy in GlioblastomaJohn A Quinlan, Kaylin Baumiller, Anandita Gaur, et al.
Clinical and Experimental Immunology|August 20, 2010
Use of bioluminescence imaging to track neutrophil migration and its inhibition in experimental colitisC T Murphy, G Moloney, L J Hall, et al.
American Journal of Human Genetics|July 11, 2006
The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27Ming Der Perng, Mu Su, Shu Fang Wen, et al.
Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology|February 2, 2013
Design and evaluation of a chronic EMG multichannel detection system for long-term recordings of hindlimb muscles in behaving miceVicki M Tysseling, Lindsay Janes, Rebecca Imhoff, et al.
Pageof 27

Showing results (161-170 of 268) with videos related to

Sort By:
Pageof 27
Molecular Biology of the Cell|August 8, 2008
Glial fibrillary acidic protein filaments can tolerate the incorporation of assembly-compromised GFAP-delta, but with consequences for filament organization and alphaB-crystallin associationMing-Der Perng, Shu-Fang Wen, Terry Gibbon, et al.
Investigative Ophthalmology & Visual Science|September 1, 1996
Expression of Crystallins, Pax6, Filensin, CP49, MIP, and MP20 in lens-derived cell linesE Krausz, R C Augusteyn, R A Quinlan, et al.
Journal of Cell Science|April 1, 1995
Vimentin and CP49/filensin form distinct networks in the lens which are independently modulated during lens fibre cell differentiationA Sandilands, A R Prescott, J M Carter, et al.
Molecular Biology of the Cell|August 19, 2007
FGF-2 release from the lens capsule by MMP-2 maintains lens epithelial cell viabilityFrederique M D Tholozan, Christopher Gribbon, Zheng Li, et al.
Inorganic Chemistry|April 26, 2005
Characterization of the low-energy electronic excited states of benzoyl-substituted ruthenocenesCynthia T Sanderson, Jessica A Quinlan, Richard C Conover, et al.
Investigative Ophthalmology & Visual Science|March 28, 2006
The C terminus of lens aquaporin 0 interacts with the cytoskeletal proteins filensin and CP49Kristie M Lindsey Rose, Robert G Gourdie, Alan R Prescott, et al.
Advanced Nanobiomed Research|January 19, 2026
Self-Assembled Verteporfin Nanoparticles for Photodynamic and Light-Independent Therapy in GlioblastomaJohn A Quinlan, Kaylin Baumiller, Anandita Gaur, et al.
Clinical and Experimental Immunology|August 20, 2010
Use of bioluminescence imaging to track neutrophil migration and its inhibition in experimental colitisC T Murphy, G Moloney, L J Hall, et al.
American Journal of Human Genetics|July 11, 2006
The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27Ming Der Perng, Mu Su, Shu Fang Wen, et al.
Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology|February 2, 2013
Design and evaluation of a chronic EMG multichannel detection system for long-term recordings of hindlimb muscles in behaving miceVicki M Tysseling, Lindsay Janes, Rebecca Imhoff, et al.
Pageof 27