[HTML][HTML] The role of Müller cells in diabetic macular edema

D Lai, Y Wu, C Shao, Q Qiu - Investigative Ophthalmology & …, 2023 - tvst.arvojournals.org
Diabetic macular edema (DME) is a common complication of diabetic retinopathy and is the
leading cause of vision loss in diabetic patients. Various factors, such as metabolic disorders …

Nonmechanical roles of dystrophin and associated proteins in exercise, neuromuscular junctions, and brains

B Nichols, S Takeda, T Yokota - Brain sciences, 2015 - mdpi.com
Dystrophin-glycoprotein complex (DGC) is an important structural unit in skeletal muscle that
connects the cytoskeleton (f-actin) of a muscle fiber to the extracellular matrix (ECM) …

Astrogliosis and impaired aquaporin‐4 and dystrophin systems in idiopathic normal pressure hydrocephalus

PK Eide, HA Hansson - Neuropathology and Applied …, 2018 - Wiley Online Library
Aims Idiopathic normal pressure hydrocephalus (iNPH) is one subtype of dementia that may
improve following drainage of cerebrospinal fluid (CSF). This prospective observational …

Dp71 contribution to the molecular scaffold anchoring aquaporine‐4 channels in brain macroglial cells

M Belmaati Cherkaoui, O Vacca, C Izabelle, A Boulay… - Glia, 2021 - Wiley Online Library
Intellectual disability in Duchenne muscular dystrophy has been associated with the loss of
dystrophin‐protein 71, Dp71, the main dystrophin‐gene product in the adult brain. Dp71 …

Non-invasive evaluation of retinal vascular alterations in a mouse model of optic neuritis using laser speckle flowgraphy and optical coherence tomography …

SE Buscho, F Xia, S Shi, JL Lin, B Szczesny, W Zhang… - Cells, 2023 - mdpi.com
Optic neuritis, a characteristic feature of multiple sclerosis (MS), involves the inflammation of
the optic nerve and the degeneration of retinal ganglion cells (RGCs). Although previous …

Dystrophin Dp71 isoforms are differentially expressed in the mouse brain and retina: report of new alternative splicing and a novel nomenclature for Dp71 isoforms

J Aragón, M González-Reyes, J Romo-Yáñez… - Molecular …, 2018 - Springer
Multiple dystrophin Dp71 isoforms have been identified in rats, mice, and humans and in
several cell line models. These Dp71 isoforms are produced by the alternative splicing of …

Animal models for researching approaches to therapy of Duchenne muscular dystrophy

MI Zaynitdinova, AV Lavrov, SA Smirnikhina - Transgenic Research, 2021 - Springer
Duchenne muscular dystrophy (DMD) is a relatively widespread genetic disease which
develops as a result of a mutation in the gene DMD encoding dystrophin. In this review …

Potential role of the methylation of VEGF gene promoter in response to hypoxia in oxygen‐induced retinopathy: beneficial effect of the absence of AQP4

F Pisani, M Cammalleri, M Dal Monte… - Journal of Cellular …, 2018 - Wiley Online Library
Hypoxia‐dependent accumulation of vascular endothelial growth factor (VEGF) plays a
major role in retinal diseases characterized by neovessel formation. In this study, we …

[HTML][HTML] Retinal dystrophins and the retinopathy of Duchenne muscular dystrophy

MTS Barboni, A Joachimsthaler, MJ Roux… - Progress in Retinal and …, 2023 - Elsevier
Duchenne muscular dystrophy (DMD) is caused by X-linked inherited or de novo DMD gene
mutations predominantly affecting males who develop early-onset muscle degeneration …

Dysfunction of 67-kDa laminin receptor disrupts BBB integrity via impaired dystrophin/AQP4 complex and p38 MAPK/VEGF activation following status epilepticus

H Park, SH Choi, MJ Kong, TC Kang - Frontiers in Cellular …, 2019 - frontiersin.org
Status epilepticus (SE, a prolonged seizure activity) impairs brain-blood barrier (BBB)
integrity, which results in secondary complications following SE. The non-integrin 67-kDa …