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Benjamin R Lin

Showing results (21-30 of 27) with videos related to

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Molecular Vision|October 20, 2017
Elucidating the molecular basis of PPCD: Effects of decreased ZEB1 expression on corneal endothelial cell functionMarina Zakharevich, Jaffer M Kattan, Judy L Chen, et al.
Molecular Vision|January 21, 2016
Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophyJudy L Chen, Benjamin R Lin, Katherine M Gee, et al.
Plos One|June 17, 2016
Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24Benjamin R Lin, Derek J Le, Yabin Chen, et al.
Stem Cells Translational Medicine|April 25, 2014
Crosstalk between adrenergic and toll-like receptors in human mesenchymal stem cells and keratinocytes: a recipe for impaired wound healingMohan R Dasu, Sandra R Ramirez, Thi Dinh La, et al.
Ophthalmology|January 30, 2023
Clinical Outcomes after Ocular Trauma with Orbeez Gel Pellet ProjectilesBenjamin R Lin, Hasenin Al-Khersan, Tyler Rowsey, et al.
Ophthalmology|July 12, 2023
ReplyBenjamin R Lin, Hasenin Al-Khersan, Tyler Rowsey, et al.
Clinical Ophthalmology (Auckland, N.Z.)|December 22, 2022
Outcomes in Patients with Suprachoroidal Hemorrhage After Anterior Segment SurgeryJason Fan, Julia L Hudson, Parastou Pakravan, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Molecular Vision|October 20, 2017
Elucidating the molecular basis of PPCD: Effects of decreased ZEB1 expression on corneal endothelial cell functionMarina Zakharevich, Jaffer M Kattan, Judy L Chen, et al.
Molecular Vision|January 21, 2016
Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophyJudy L Chen, Benjamin R Lin, Katherine M Gee, et al.
Plos One|June 17, 2016
Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24Benjamin R Lin, Derek J Le, Yabin Chen, et al.
Stem Cells Translational Medicine|April 25, 2014
Crosstalk between adrenergic and toll-like receptors in human mesenchymal stem cells and keratinocytes: a recipe for impaired wound healingMohan R Dasu, Sandra R Ramirez, Thi Dinh La, et al.
Ophthalmology|January 30, 2023
Clinical Outcomes after Ocular Trauma with Orbeez Gel Pellet ProjectilesBenjamin R Lin, Hasenin Al-Khersan, Tyler Rowsey, et al.
Ophthalmology|July 12, 2023
ReplyBenjamin R Lin, Hasenin Al-Khersan, Tyler Rowsey, et al.
Clinical Ophthalmology (Auckland, N.Z.)|December 22, 2022
Outcomes in Patients with Suprachoroidal Hemorrhage After Anterior Segment SurgeryJason Fan, Julia L Hudson, Parastou Pakravan, et al.
Pageof 3