Corneal nerves in health and disease

MA Al-Aqaba, VK Dhillon, I Mohammed… - Progress in retinal and …, 2019 - Elsevier
The cornea is the most sensitive structure in the human body. Corneal nerves adapt to
maintain transparency and contribute to corneal health by mediating tear secretion and …

[HTML][HTML] Congenital aniridia beyond black eyes: from phenotype and novel genetic mechanisms to innovative therapeutic approaches

A Daruich, M Duncan, MP Robert, N Lagali… - Progress in retinal and …, 2023 - Elsevier
Congenital PAX6-aniridia, initially characterized by the absence of the iris, has progressively
been shown to be associated with other developmental ocular abnormalities and systemic …

Cultivated autologous limbal epithelial cell (CALEC) transplantation: Development of manufacturing process and clinical evaluation of feasibility and safety

UV Jurkunas, J Yin, LK Johns, S Li, H Negre… - Science …, 2023 - science.org
To treat unilateral limbal stem cell (LSC) deficiency, we developed cultivated autologous
limbal epithelial cells (CALEC) using an innovative xenobiotic-free, serum-free, antibiotic …

BCLA CLEAR-Contact lens complications

F Stapleton, M Bakkar, N Carnt, R Chalmers… - Contact Lens and …, 2021 - Elsevier
Contact lens-related complications are common, affecting around one third of wearers,
although most are mild and easily managed. Contact lenses have well-defined anatomical …

Global consensus on the management of limbal stem cell deficiency

SX Deng, F Kruse, JAP Gomes, CC Chan, S Daya… - Cornea, 2020 - journals.lww.com
Purpose: In recent decades, the medical and surgical treatment of limbal stem cell deficiency
(LSCD) has evolved significantly through the incorporation of innovative pharmacological …

[HTML][HTML] Congenital aniridia–A comprehensive review of clinical features and therapeutic approaches

ECS Landsend, N Lagali, TP Utheim - Survey of ophthalmology, 2021 - Elsevier
Congenital aniridia is a rare genetic eye disorder with total or partial absence of the iris from
birth. In most cases the genetic origin of aniridia is a mutation in the PAX6 gene, leading to …

Human limbal epithelial stem cell regulation, bioengineering and function

C Bonnet, S González, JAS Roberts… - Progress in retinal and …, 2021 - Elsevier
The corneal epithelium is continuously renewed by limbal stem/progenitor cells (LSCs), a
cell population harbored in a highly regulated niche located at the limbus. Dysfunction …

BCLA CLEAR–Medical use of contact lenses

DS Jacobs, KG Carrasquillo, PD Cottrell… - Contact Lens and …, 2021 - Elsevier
The medical use of contact lenses is a solution for many complex ocular conditions,
including high refractive error, irregular astigmatism, primary and secondary corneal ectasia …

Molecular characteristics and spatial distribution of adult human corneal cell subtypes

AJ Ligocki, W Fury, C Gutierrez, C Adler, T Yang… - Scientific reports, 2021 - nature.com
Bulk RNA sequencing of a tissue captures the gene expression profile from all cell types
combined. Single-cell RNA sequencing identifies discrete cell-signatures based on …

Induced pluripotent stem-cell-derived corneal epithelium for transplant surgery: a single-arm, open-label, first-in-human interventional study in Japan

T Soma, Y Oie, H Takayanagi, S Matsubara, T Yamada… - The Lancet, 2024 - thelancet.com
Background The loss of corneal epithelial stem cells from the limbus at the edge of the
cornea has severe consequences for vision, with the pathological manifestations of a limbal …