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A Quinlan

Showing results (81-90 of 268) with videos related to

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Gene|July 4, 1998
Identification and functional analysis of the mouse lens filensin gene promoterS Masaki, Y Kamachi, R A Quinlan, et al.
European Journal of Cell Biology|July 1, 1983
Identification and characterization of axopodial tubulins from Echinosphaerium nucleofilumM Little, R A Quinlan, E J Hoffman, et al.
Experimental Cell Research|September 1, 1993
Network incorporation of intermediate filament molecules differs between preexisting and newly assembling filamentsX Lu, R A Quinlan, J B Steel, et al.
Cell Stress & Chaperones|April 10, 2017
The functional roles of the unstructured N- and C-terminal regions in αB-crystallin and other mammalian small heat-shock proteinsJohn A Carver, Aidan B Grosas, Heath Ecroyd, et al.
Journal of Cell Science|July 1, 1994
Identification of two N-terminal non-alpha-helical domain motifs important in the assembly of glial fibrillary acidic proteinJ E Ralton, X Lu, A M Hutcheson, et al.
Plos One|November 19, 2011
Multiple sites in αB-crystallin modulate its interactions with desmin filaments assembled in vitroScott A Houck, Andrew Landsbury, John I Clark, et al.
Journal of Experimental Psychology. General|October 20, 2022
Does a brief exposure to literary fiction improve social ability? Assessing the evidential value of published studies with a p-curveJoshua A Quinlan, Jessica K Padgett, Amin Khajehnassiri, et al.
Seminars in Cardiothoracic and Vascular Anesthesia|August 12, 2021
Perioperative and Anesthetic Considerations in Tetralogy of Fallot With Pulmonary AtresiaCasey A Quinlan, Gregory J Latham, Denise Joffe, et al.
BMJ Open Ophthalmology|July 26, 2023
Multimorbidity due to novel pathogenic variants in the <i>WFS1/RP1/NOD2</i> genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British familyVanita Berry, Alexander Ionides, Michalis Georgiou, et al.
Biochemical and Biophysical Research Communications|February 7, 2001
Mapping of the human CP49 gene and identification of an intragenic polymorphic marker to allow genetic linkage analysis in autosomal dominant congenital cataractJ M Carter, W H McLean, S West, et al.
Pageof 27

Showing results (81-90 of 268) with videos related to

Sort By:
Pageof 27
Gene|July 4, 1998
Identification and functional analysis of the mouse lens filensin gene promoterS Masaki, Y Kamachi, R A Quinlan, et al.
European Journal of Cell Biology|July 1, 1983
Identification and characterization of axopodial tubulins from Echinosphaerium nucleofilumM Little, R A Quinlan, E J Hoffman, et al.
Experimental Cell Research|September 1, 1993
Network incorporation of intermediate filament molecules differs between preexisting and newly assembling filamentsX Lu, R A Quinlan, J B Steel, et al.
Cell Stress & Chaperones|April 10, 2017
The functional roles of the unstructured N- and C-terminal regions in αB-crystallin and other mammalian small heat-shock proteinsJohn A Carver, Aidan B Grosas, Heath Ecroyd, et al.
Journal of Cell Science|July 1, 1994
Identification of two N-terminal non-alpha-helical domain motifs important in the assembly of glial fibrillary acidic proteinJ E Ralton, X Lu, A M Hutcheson, et al.
Plos One|November 19, 2011
Multiple sites in αB-crystallin modulate its interactions with desmin filaments assembled in vitroScott A Houck, Andrew Landsbury, John I Clark, et al.
Journal of Experimental Psychology. General|October 20, 2022
Does a brief exposure to literary fiction improve social ability? Assessing the evidential value of published studies with a p-curveJoshua A Quinlan, Jessica K Padgett, Amin Khajehnassiri, et al.
Seminars in Cardiothoracic and Vascular Anesthesia|August 12, 2021
Perioperative and Anesthetic Considerations in Tetralogy of Fallot With Pulmonary AtresiaCasey A Quinlan, Gregory J Latham, Denise Joffe, et al.
BMJ Open Ophthalmology|July 26, 2023
Multimorbidity due to novel pathogenic variants in the <i>WFS1/RP1/NOD2</i> genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British familyVanita Berry, Alexander Ionides, Michalis Georgiou, et al.
Biochemical and Biophysical Research Communications|February 7, 2001
Mapping of the human CP49 gene and identification of an intragenic polymorphic marker to allow genetic linkage analysis in autosomal dominant congenital cataractJ M Carter, W H McLean, S West, et al.
Pageof 27