[HTML][HTML] 10q26–The enigma in age-related macular degeneration
DA Merle, M Sen, A Armento, CM Stanton… - Progress in Retinal and …, 2023 - Elsevier
Despite comprehensive research efforts over the last decades, the pathomechanisms of age-
related macular degeneration (AMD) remain far from being understood. Large-scale …
related macular degeneration (AMD) remain far from being understood. Large-scale …
Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes
A Villaplana-Velasco, M Pigeyre, J Engelmann… - Communications …, 2023 - nature.com
There is increasing evidence that the complexity of the retinal vasculature measured as
fractal dimension, Df, might offer earlier insights into the progression of coronary artery …
fractal dimension, Df, might offer earlier insights into the progression of coronary artery …
Ocular and neural genes jointly regulate the visuospatial working memory in ADHD children
Y Zhao, Y Zhong, W Chen, S Chang, Q Cao… - Behavioral and Brain …, 2023 - Springer
Objective Working memory (WM) deficits have frequently been linked to attention deficit
hyperactivity disorder (ADHD). Despite previous studies suggested its high heritability, its …
hyperactivity disorder (ADHD). Despite previous studies suggested its high heritability, its …
A mouse model of brittle cornea syndrome caused by mutation in Zfp469
CM Stanton, AS Findlay, C Drake… - Disease Models & …, 2021 - journals.biologists.com
Brittle cornea syndrome (BCS) is a rare recessive condition characterised by extreme
thinning of the cornea and sclera. BCS results from loss-of-function mutations in the poorly …
thinning of the cornea and sclera. BCS results from loss-of-function mutations in the poorly …
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation
Fuchs endothelial corneal dystrophy (FECD) is a leading indication for corneal
transplantation, but its molecular etiology remains poorly understood. We performed …
transplantation, but its molecular etiology remains poorly understood. We performed …
Colocalization of corneal resistance factor GWAS loci with GTEx e/sQTLs highlights plausible candidate causal genes for keratoconus postnatal corneal stroma …
X Jiang, T Boutin, V Vitart - Frontiers in genetics, 2023 - frontiersin.org
Background: Genome-wide association studies (GWAS) for corneal resistance factor (CRF)
have identified 100s of loci and proved useful to uncover genetic determinants for …
have identified 100s of loci and proved useful to uncover genetic determinants for …
[HTML][HTML] Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulation
Fuchs endothelial corneal dystrophy (FECD) is a leading indication for corneal
transplantation, but its molecular pathophysiology remains poorly understood. We …
transplantation, but its molecular pathophysiology remains poorly understood. We …
[PDF][PDF] Revisión Bibliográfica: Determinar los factores biomecánicos de la córnea relacionados con la aparición del Queratocono
JF JIMENEZ RAMIREZ - 2022 - repositorio.uan.edu.co
Revisión Bibliografica: determinar los factores de la biomecánica de la córnea relacionados
con la aparición de queratocono Page 1 1 Revisión Bibliográfica: Determinar los factores …
con la aparición de queratocono Page 1 1 Revisión Bibliográfica: Determinar los factores …
[PDF][PDF] SUNNY CHOUDHARY
CS KUMAR - 2021 - krishikosh.egranth.ac.in
Macrotyloma is a genus of 32 wild species belonging to the Fabaceae family, with
chromosome numbers of 20, 22, and 24.(Allen and Allen 1981). Macrotyloma uniflorum is …
chromosome numbers of 20, 22, and 24.(Allen and Allen 1981). Macrotyloma uniflorum is …