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Stephen J Tuft

Showing results (61-70 of 96) with videos related to

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Ophthalmic Research|February 9, 2008
Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech familiesPetra Liskova, Gordon K Klintworth, Brandy L Bowling, et al.
Annals of Human Genetics|December 3, 2014
Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3Cerys J Evans, Petra Liskova, Lubica Dudakova, et al.
Progress in Retinal and Eye Research|August 1, 2020
TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated diseaseMichael P Fautsch, Eric D Wieben, Keith H Baratz, et al.
Stem Cells Translational Medicine|January 21, 2014
Three-year outcomes of cultured limbal epithelial allografts in aniridia and Stevens-Johnson syndrome evaluated using the Clinical Outcome Assessment in Surgical Trials assessment toolAlex J Shortt, Catey Bunce, Hannah J Levis, et al.
Eye (London, England)|February 26, 2024
A comparison of keratoconus progression following collagen cross-linkage using standard or personalised keratometry thresholdsJi-Peng Olivia Li, Howard P Maile, Catey Bunce, et al.
Eye (London, England)|February 19, 2026
Influence of inflammatory and metabolic factors on keratoconus risk: a causal inference analysisPirro G Hysi, Alison J Hardcastle, Alice E Davidson, et al.
Investigative Ophthalmology & Visual Science|January 8, 2015
Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconusAlice E Davidson, Edmondo Borasio, Petra Liskova, et al.
Molecular Vision|October 26, 2007
Molecular analysis of the VSX1 gene in familial keratoconusPetra Liskova, Neil D Ebenezer, Pirro G Hysi, et al.
American Journal of Ophthalmology|January 18, 2005
Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophyMohamed F El-Ashry, Mai M Abd El-Aziz, Osama Shalaby, et al.
Human Mutation|February 14, 2015
Mutations in collagen, type XVII, alpha 1 (COL17A1) cause epithelial recurrent erosion dystrophy (ERED)Frida Jonsson, Berit Byström, Alice E Davidson, et al.
Pageof 10

Showing results (61-70 of 96) with videos related to

Sort By:
Pageof 10
Ophthalmic Research|February 9, 2008
Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech familiesPetra Liskova, Gordon K Klintworth, Brandy L Bowling, et al.
Annals of Human Genetics|December 3, 2014
Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3Cerys J Evans, Petra Liskova, Lubica Dudakova, et al.
Progress in Retinal and Eye Research|August 1, 2020
TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated diseaseMichael P Fautsch, Eric D Wieben, Keith H Baratz, et al.
Stem Cells Translational Medicine|January 21, 2014
Three-year outcomes of cultured limbal epithelial allografts in aniridia and Stevens-Johnson syndrome evaluated using the Clinical Outcome Assessment in Surgical Trials assessment toolAlex J Shortt, Catey Bunce, Hannah J Levis, et al.
Eye (London, England)|February 26, 2024
A comparison of keratoconus progression following collagen cross-linkage using standard or personalised keratometry thresholdsJi-Peng Olivia Li, Howard P Maile, Catey Bunce, et al.
Eye (London, England)|February 19, 2026
Influence of inflammatory and metabolic factors on keratoconus risk: a causal inference analysisPirro G Hysi, Alison J Hardcastle, Alice E Davidson, et al.
Investigative Ophthalmology & Visual Science|January 8, 2015
Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconusAlice E Davidson, Edmondo Borasio, Petra Liskova, et al.
Molecular Vision|October 26, 2007
Molecular analysis of the VSX1 gene in familial keratoconusPetra Liskova, Neil D Ebenezer, Pirro G Hysi, et al.
American Journal of Ophthalmology|January 18, 2005
Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophyMohamed F El-Ashry, Mai M Abd El-Aziz, Osama Shalaby, et al.
Human Mutation|February 14, 2015
Mutations in collagen, type XVII, alpha 1 (COL17A1) cause epithelial recurrent erosion dystrophy (ERED)Frida Jonsson, Berit Byström, Alice E Davidson, et al.
Pageof 10