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Ricardo F Frausto

Showing results (1-10 of 37) with videos related to

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Investigative Ophthalmology & Visual Science|November 8, 2014
Transcriptome analysis of the human corneal endotheliumRicardo F Frausto, Cynthia Wang, Anthony J Aldave
Cureus|August 25, 2023
Nanocrystalline Silver Layer of Knitted Polyester Outperforms Other Silver-Containing Wound Dressings in an In Vitro Wound ModelJonathan Hus, Ricardo F Frausto, Joel Grunhut, et al.
Cell Transplantation|September 5, 2015
Transcriptomic Analysis of Cultured Corneal Endothelial Cells as a Validation for Their Use in Cell Replacement TherapyRicardo F Frausto, Derek J Le, Anthony J Aldave
Glia|May 2, 2008
A novel method to establish microglia-free astrocyte cultures: comparison of matrix metalloproteinase expression profiles in pure cultures of astrocytes and microgliaStephen J Crocker, Ricardo F Frausto, J Lindsay Whitton, et al.
Vision Research|May 1, 2014
Posterior polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosumMichelle S Jang, Ashley N Roldan, Ricardo F Frausto, et al.
Cornea|June 29, 2013
Pre-Descemet corneal dystrophy and X-linked ichthyosis associated with deletion of Xp22.31 containing the STS geneCrystal Hung, Reed I Ayabe, Cynthia Wang, et al.
Journal of Neuroimmunology|October 30, 2007
Myelin oligodendrocyte glycoprotein peptide-induced experimental allergic encephalomyelitis and T cell responses are unaffected by immunoproteasome deficiencyRicardo F Frausto, Stephen J Crocker, Boreth Eam, et al.
Ophthalmic Genetics|October 1, 2013
X-linked Megalocornea Associated with the Novel CHRDL1 Gene Mutation p.(Pro56Leu*8)Jonathan Han, Jonathan W Young, Ricardo F Frausto, et al.
Molecular Vision|April 6, 2013
Exclusion of pathogenic promoter region variants and identification of novel nonsense mutations in the zinc finger E-box binding homeobox 1 gene in posterior polymorphous corneal dystrophyPejman Bakhtiari, Ricardo F Frausto, Ashley N Roldan, et al.
Ophthalmic Genetics|April 20, 2018
Confirmation and refinement of the heterozygous deletion of the small leucine-rich proteoglycans associated with posterior amorphous corneal dystrophyAleck E Cervantes, Katherine M Gee, Martha F Whiting, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Investigative Ophthalmology & Visual Science|November 8, 2014
Transcriptome analysis of the human corneal endotheliumRicardo F Frausto, Cynthia Wang, Anthony J Aldave
Cureus|August 25, 2023
Nanocrystalline Silver Layer of Knitted Polyester Outperforms Other Silver-Containing Wound Dressings in an In Vitro Wound ModelJonathan Hus, Ricardo F Frausto, Joel Grunhut, et al.
Cell Transplantation|September 5, 2015
Transcriptomic Analysis of Cultured Corneal Endothelial Cells as a Validation for Their Use in Cell Replacement TherapyRicardo F Frausto, Derek J Le, Anthony J Aldave
Glia|May 2, 2008
A novel method to establish microglia-free astrocyte cultures: comparison of matrix metalloproteinase expression profiles in pure cultures of astrocytes and microgliaStephen J Crocker, Ricardo F Frausto, J Lindsay Whitton, et al.
Vision Research|May 1, 2014
Posterior polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosumMichelle S Jang, Ashley N Roldan, Ricardo F Frausto, et al.
Cornea|June 29, 2013
Pre-Descemet corneal dystrophy and X-linked ichthyosis associated with deletion of Xp22.31 containing the STS geneCrystal Hung, Reed I Ayabe, Cynthia Wang, et al.
Journal of Neuroimmunology|October 30, 2007
Myelin oligodendrocyte glycoprotein peptide-induced experimental allergic encephalomyelitis and T cell responses are unaffected by immunoproteasome deficiencyRicardo F Frausto, Stephen J Crocker, Boreth Eam, et al.
Ophthalmic Genetics|October 1, 2013
X-linked Megalocornea Associated with the Novel CHRDL1 Gene Mutation p.(Pro56Leu*8)Jonathan Han, Jonathan W Young, Ricardo F Frausto, et al.
Molecular Vision|April 6, 2013
Exclusion of pathogenic promoter region variants and identification of novel nonsense mutations in the zinc finger E-box binding homeobox 1 gene in posterior polymorphous corneal dystrophyPejman Bakhtiari, Ricardo F Frausto, Ashley N Roldan, et al.
Ophthalmic Genetics|April 20, 2018
Confirmation and refinement of the heterozygous deletion of the small leucine-rich proteoglycans associated with posterior amorphous corneal dystrophyAleck E Cervantes, Katherine M Gee, Martha F Whiting, et al.
Pageof 4