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AAPS Pharmscitech
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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 Rats
Akshaya Tatke, Karthik Yadav Janga, Bharathi Avula, et al.
Pharmaceutics
|
July 30, 2020
Enhanced Corneal Penetration of a Poorly Permeable Drug Using Bioadhesive Multiple Microemulsion Technology
Mohamed Moustafa Ibrahim, Doaa Nabih Maria, XiangDi Wang, et al.
Molecular Vision
|
November 25, 2016
Genetic and immunohistochemical analysis of HSPA5 in mouse and human retinas
Sumana R Chintalapudi, XiaoFei Wang, Huiling Li, et al.
Anesthesia and Analgesia
|
June 8, 2018
Decision Support Tool Improves Real and Perceived Anesthesiology Resident Relief Equity
Monica 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 Studies
Akshaya 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 model
Bhubanananda Sahu, Venkata R M Chavali, Akhila Alapati, et al.
Molecular Vision
|
October 7, 2011
Complex interactions of Tyrp1 in the eye
Hong 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 Retinas
Sumana 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 degeneration
Venkata 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 gene
Alessandro Iannaccone, Kirk Mykytyn, Antonio M Persico, et al.
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of 19
Search research articles
Search
Showing results (81-90 of 186) with videos related to
Sort By:
Page
of 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 Rats
Akshaya Tatke, Karthik Yadav Janga, Bharathi Avula, et al.
Pharmaceutics
|
July 30, 2020
Enhanced Corneal Penetration of a Poorly Permeable Drug Using Bioadhesive Multiple Microemulsion Technology
Mohamed Moustafa Ibrahim, Doaa Nabih Maria, XiangDi Wang, et al.
Molecular Vision
|
November 25, 2016
Genetic and immunohistochemical analysis of HSPA5 in mouse and human retinas
Sumana R Chintalapudi, XiaoFei Wang, Huiling Li, et al.
Anesthesia and Analgesia
|
June 8, 2018
Decision Support Tool Improves Real and Perceived Anesthesiology Resident Relief Equity
Monica 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 Studies
Akshaya 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 model
Bhubanananda Sahu, Venkata R M Chavali, Akhila Alapati, et al.
Molecular Vision
|
October 7, 2011
Complex interactions of Tyrp1 in the eye
Hong 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 Retinas
Sumana 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 degeneration
Venkata 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 gene
Alessandro Iannaccone, Kirk Mykytyn, Antonio M Persico, et al.
Page
of 19