Related Experiment Video

Updated: May 9, 2026

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia
06:15

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia

Published on: August 9, 2024

Corneal endothelial findings in a Czech patient with compound heterozygous mutations in KERA

Lubica Dudakova1, Michalis Palos, Alison J Hardcastle

  • 1Laboratory of the Biology and Pathology of the Eye, Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague .

Ophthalmic Genetics
|July 10, 2013
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Establishing a Severe Corneal Inflammation Model in Rats Based on Corneal Epithelium Curettage Combined with Corneal Sutures
04:48

Establishing a Severe Corneal Inflammation Model in Rats Based on Corneal Epithelium Curettage Combined with Corneal Sutures

Published on: November 22, 2024

Related Experiment Videos

Last Updated: May 9, 2026

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia
06:15

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia

Published on: August 9, 2024

Establishing a Severe Corneal Inflammation Model in Rats Based on Corneal Epithelium Curettage Combined with Corneal Sutures
04:48

Establishing a Severe Corneal Inflammation Model in Rats Based on Corneal Epithelium Curettage Combined with Corneal Sutures

Published on: November 22, 2024

Related Concept Videos

The Retinoblastoma Gene01:20

The Retinoblastoma Gene

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The Retinoblastoma Gene01:20

The Retinoblastoma Gene

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...

Articles linked to this work by shared authors, journal, and citation graph.

Widening the Spectrum of Disease Expression due to Heterozygous Variants in EFEMP1.

JAMA ophthalmology·2026

Clinical and molecular features of PRCD-associated retinopathy.

Acta ophthalmologica·2026

The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

HGG advances·2026

Identification of a Duplication in the RP17 Locus in an Individual With Pathogenic CEP290 Variants: Implications for RP17 Variant Classification.

Investigative ophthalmology & visual science·2026

Paediatric Keratoconus: An ERN-EYE Clinical Consensus Statement on Diagnosis, Treatment and Follow-Up Care.

Ophthalmology and therapy·2026

Radial outer retina reflectivity (RORR) sign in LAMP2-associated retinopathy.

Acta ophthalmologica·2026

Could thiamine supplementation delay the progression of retinal dystrophy in Rogers syndrome?

Ophthalmic genetics·2026

A novel PRPF31 variant associated with autosomal dominant retinitis pigmentosa in Japanese families.

Ophthalmic genetics·2026

Crystalline maculopathy as a clue to a neurocutaneous syndrome.

Ophthalmic genetics·2026

Genetic findings and clinical features of extreme refractive errors in Thai children using whole genome sequencing.

Ophthalmic genetics·2026

Beyond corneal structure in Noonan syndrome: topographic, tomographic, and optical findings.

Ophthalmic genetics·2026

Isolated rod-cone dystrophy in homozygous IFT140 missense allele p.Tyr923Asp.

Ophthalmic genetics·2026

Plasmonic Foam-Enabled Dual-Modal Biohybrid Chemical Sensor.

Advanced materials (Deerfield Beach, Fla.)·2026

Plasmon-enhanced molecularly imprinted photoelectrochemical sensor for non-invasive lactate monitoring in sweat.

Chemical communications (Cambridge, England)·2026

Structural insights into target detection by the Serratia type III CRISPR complex and its deployment in SNP identification.

The Journal of biological chemistry·2026

Cefalexin fingerprinting in water using graphene oxide/gold nanoparticle-modified silica photonic microsphere SERS substrates.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy·2026

Portable cyanide monitoring using a benzothiazolium-based ratiometric fluorescent probe coupled with smartphone imaging, test strips, and living cell imaging.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy·2026

Mass Spectral Investigation of Carbamates Using EI and CI Techniques.

Journal of mass spectrometry : JMS·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies
Jove
Visualize
Contact Us