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M Jablonski

Showing results (81-90 of 186) with videos related to

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AAPS Pharmscitech|March 10, 2018
P-glycoprotein Restricts Ocular Penetration of Loperamide across the Blood-Ocular Barriers: a Comparative Study in Mdr1a Knock-out and Wild Type Sprague Dawley RatsAkshaya Tatke, Karthik Yadav Janga, Bharathi Avula, et al.
Pharmaceutics|July 30, 2020
Enhanced Corneal Penetration of a Poorly Permeable Drug Using Bioadhesive Multiple Microemulsion TechnologyMohamed Moustafa Ibrahim, Doaa Nabih Maria, XiangDi Wang, et al.
Molecular Vision|November 25, 2016
Genetic and immunohistochemical analysis of HSPA5 in mouse and human retinasSumana R Chintalapudi, XiaoFei Wang, Huiling Li, et al.
Anesthesia and Analgesia|June 8, 2018
Decision Support Tool Improves Real and Perceived Anesthesiology Resident Relief EquityMonica Bhutiani, Patrick M Jablonski, Jesse M Ehrenfeld, et al.
Nanomaterials (Basel, Switzerland)|December 29, 2018
In Situ Gel of Triamcinolone Acetonide-Loaded Solid Lipid Nanoparticles for Improved Topical Ocular Delivery: Tear Kinetics and Ocular Disposition StudiesAkshaya Tatke, Narendar Dudhipala, Karthik Yadav Janga, et al.
Molecular Vision|March 28, 2015
Presence of rd8 mutation does not alter the ocular phenotype of late-onset retinal degeneration mouse modelBhubanananda Sahu, Venkata R M Chavali, Akhila Alapati, et al.
Molecular Vision|October 7, 2011
Complex interactions of Tyrp1 in the eyeHong Lu, Liyuan Li, Edmond R Watson, et al.
Frontiers in Aging Neuroscience|June 1, 2016
Isolation and Molecular Profiling of Primary Mouse Retinal Ganglion Cells: Comparison of Phenotypes from Healthy and Glaucomatous RetinasSumana R Chintalapudi, Levon Djenderedjian, Andrew B Stiemke, et al.
Human Molecular Genetics|February 26, 2011
A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degenerationVenkata R M Chavali, Naheed W Khan, Catherine A Cukras, et al.
American Journal of Medical Genetics. Part A|January 18, 2005
Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in the BBS4 geneAlessandro Iannaccone, Kirk Mykytyn, Antonio M Persico, et al.
Pageof 19

Showing results (81-90 of 186) with videos related to

Sort By:
Pageof 19
AAPS Pharmscitech|March 10, 2018
P-glycoprotein Restricts Ocular Penetration of Loperamide across the Blood-Ocular Barriers: a Comparative Study in Mdr1a Knock-out and Wild Type Sprague Dawley RatsAkshaya Tatke, Karthik Yadav Janga, Bharathi Avula, et al.
Pharmaceutics|July 30, 2020
Enhanced Corneal Penetration of a Poorly Permeable Drug Using Bioadhesive Multiple Microemulsion TechnologyMohamed Moustafa Ibrahim, Doaa Nabih Maria, XiangDi Wang, et al.
Molecular Vision|November 25, 2016
Genetic and immunohistochemical analysis of HSPA5 in mouse and human retinasSumana R Chintalapudi, XiaoFei Wang, Huiling Li, et al.
Anesthesia and Analgesia|June 8, 2018
Decision Support Tool Improves Real and Perceived Anesthesiology Resident Relief EquityMonica Bhutiani, Patrick M Jablonski, Jesse M Ehrenfeld, et al.
Nanomaterials (Basel, Switzerland)|December 29, 2018
In Situ Gel of Triamcinolone Acetonide-Loaded Solid Lipid Nanoparticles for Improved Topical Ocular Delivery: Tear Kinetics and Ocular Disposition StudiesAkshaya Tatke, Narendar Dudhipala, Karthik Yadav Janga, et al.
Molecular Vision|March 28, 2015
Presence of rd8 mutation does not alter the ocular phenotype of late-onset retinal degeneration mouse modelBhubanananda Sahu, Venkata R M Chavali, Akhila Alapati, et al.
Molecular Vision|October 7, 2011
Complex interactions of Tyrp1 in the eyeHong Lu, Liyuan Li, Edmond R Watson, et al.
Frontiers in Aging Neuroscience|June 1, 2016
Isolation and Molecular Profiling of Primary Mouse Retinal Ganglion Cells: Comparison of Phenotypes from Healthy and Glaucomatous RetinasSumana R Chintalapudi, Levon Djenderedjian, Andrew B Stiemke, et al.
Human Molecular Genetics|February 26, 2011
A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degenerationVenkata R M Chavali, Naheed W Khan, Catherine A Cukras, et al.
American Journal of Medical Genetics. Part A|January 18, 2005
Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in the BBS4 geneAlessandro Iannaccone, Kirk Mykytyn, Antonio M Persico, et al.
Pageof 19