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Cerys J Evans

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

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Cornea|January 28, 2017
Copper in Keratoconic CorneasLubica Dudakova, Cerys J Evans, Petra Liskova
BMC Ophthalmology|September 19, 2018
Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 geneCerys J Evans, Lubica Dudakova, Pavlina Skalicka, et al.
Acta Ophthalmologica|May 3, 2019
Paraproteinemic keratopathy associated with monoclonal gammopathy of undetermined significance (MGUS): clinical findings in twelve patients including recurrence after keratoplastyPavlina Skalicka, Lubica Dudakova, Michalis Palos, et al.
Cornea|May 27, 2016
Spectrum of Clinical Signs and Genetic Characterization of Gelatinous Drop-Like Corneal Dystrophy in a Colombian FamilySara Morantes, Cerys J Evans, Ana V Valencia, et al.
Investigative Ophthalmology & Visual Science|October 14, 2016
Genotype-Phenotype Correlation for TGFBI Corneal Dystrophies Identifies p.(G623D) as a Novel Cause of Epithelial Basement Membrane DystrophyCerys J Evans, Alice E Davidson, Nicole Carnt, 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.
European Journal of Human Genetics : EJHG|October 29, 2015
Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3Petra Liskova, Cerys J Evans, Alice E Davidson, et al.
American Journal of Human Genetics|March 3, 2018
Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4Petra Liskova, Lubica Dudakova, Cerys J Evans, et al.
Experimental Eye Research|March 10, 2019
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosisLubica Dudakova, Cerys J Evans, Nikolas Pontikos, et al.
American Journal of Human Genetics|January 11, 2016
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2Alice E Davidson, Petra Liskova, Cerys J Evans, et al.
Pageof 1

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

Sort By:
Pageof 1
Cornea|January 28, 2017
Copper in Keratoconic CorneasLubica Dudakova, Cerys J Evans, Petra Liskova
BMC Ophthalmology|September 19, 2018
Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 geneCerys J Evans, Lubica Dudakova, Pavlina Skalicka, et al.
Acta Ophthalmologica|May 3, 2019
Paraproteinemic keratopathy associated with monoclonal gammopathy of undetermined significance (MGUS): clinical findings in twelve patients including recurrence after keratoplastyPavlina Skalicka, Lubica Dudakova, Michalis Palos, et al.
Cornea|May 27, 2016
Spectrum of Clinical Signs and Genetic Characterization of Gelatinous Drop-Like Corneal Dystrophy in a Colombian FamilySara Morantes, Cerys J Evans, Ana V Valencia, et al.
Investigative Ophthalmology & Visual Science|October 14, 2016
Genotype-Phenotype Correlation for TGFBI Corneal Dystrophies Identifies p.(G623D) as a Novel Cause of Epithelial Basement Membrane DystrophyCerys J Evans, Alice E Davidson, Nicole Carnt, 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.
European Journal of Human Genetics : EJHG|October 29, 2015
Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3Petra Liskova, Cerys J Evans, Alice E Davidson, et al.
American Journal of Human Genetics|March 3, 2018
Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4Petra Liskova, Lubica Dudakova, Cerys J Evans, et al.
Experimental Eye Research|March 10, 2019
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosisLubica Dudakova, Cerys J Evans, Nikolas Pontikos, et al.
American Journal of Human Genetics|January 11, 2016
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2Alice E Davidson, Petra Liskova, Cerys J Evans, et al.
Pageof 1