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H A Allen

Showing results (41-50 of 46) with videos related to

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Internal Medicine Journal|September 18, 2014
High proportion of rare and compound epidermal growth factor receptor mutations in an Australian population of non-squamous non-small-cell lung cancerE Stone, H A Allen, T Saghaie, et al.
Investigative Ophthalmology & Visual Science|December 13, 2012
Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophyEdwin H A Allen, Sarah D Atkinson, Haihui Liao, et al.
Gene Therapy|August 21, 2015
CRISPR/Cas9 DNA cleavage at SNP-derived PAM enables both in vitro and in vivo KRT12 mutation-specific targetingD G Courtney, J E Moore, S D Atkinson, et al.
Investigative Ophthalmology & Visual Science|January 16, 2014
Development of allele-specific gene-silencing siRNAs for TGFBI Arg124Cys in lattice corneal dystrophy type IDavid G Courtney, Sarah D Atkinson, Johnny E Moore, et al.
Investigative Ophthalmology & Visual Science|May 8, 2014
siRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophyDavid G Courtney, Sarah D Atkinson, Edwin H A Allen, et al.
Human Molecular Genetics|January 14, 2016
Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophyEdwin H A Allen, David G Courtney, Sarah D Atkinson, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Internal Medicine Journal|September 18, 2014
High proportion of rare and compound epidermal growth factor receptor mutations in an Australian population of non-squamous non-small-cell lung cancerE Stone, H A Allen, T Saghaie, et al.
Investigative Ophthalmology & Visual Science|December 13, 2012
Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophyEdwin H A Allen, Sarah D Atkinson, Haihui Liao, et al.
Gene Therapy|August 21, 2015
CRISPR/Cas9 DNA cleavage at SNP-derived PAM enables both in vitro and in vivo KRT12 mutation-specific targetingD G Courtney, J E Moore, S D Atkinson, et al.
Investigative Ophthalmology & Visual Science|January 16, 2014
Development of allele-specific gene-silencing siRNAs for TGFBI Arg124Cys in lattice corneal dystrophy type IDavid G Courtney, Sarah D Atkinson, Johnny E Moore, et al.
Investigative Ophthalmology & Visual Science|May 8, 2014
siRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophyDavid G Courtney, Sarah D Atkinson, Edwin H A Allen, et al.
Human Molecular Genetics|January 14, 2016
Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophyEdwin H A Allen, David G Courtney, Sarah D Atkinson, et al.
Pageof 5