Results 201 to 210 of about 72,734 (313)

Discharge patterns of retinal ganglion cells in rodent models of degenerative retinal diseases [PDF]

, 2012
Menzler, Jacob
core  

Disrupted energy metabolism is associated with retinal ganglion cell degeneration in autosomal dominant optic atrophy. [PDF]

Sci Adv
Kang EY, Tseng YJ, Peng WH, Hung HC, Lin PH, Montales KP, Sherman E, Peregrin J, Wang EH, Kang C, Teng YC, Huang CY, Tsai CL, Chang IY, Chen J, Tezel G, He Y, Li TD, Stiles L, Shirihai O, Tsang SH, Lai CC, Tsai CN, Lin CS, Wang NK.   +24 more
europepmc   +1 more source

The influence of TLR4 signaling on retinal ganglion cell survival and angiogenic response in a mouse model of oxygen-induced retinopathy. [PDF]

Biochem Biophys Rep
Munemasa Y.
europepmc   +1 more source

Moutan Cortex Extract Mediates Diabetic Retinopathy by Blocking the ROS‑Triggered HIF‐1α/VEGF Axis in Retinal Pigment Epithelial Cells

eFood, Volume 7, Issue 4, August 2026.
Schematic diagram of the mechanism by which Moutan Cortex extract (MCE) ameliorates DR. MCE alleviates retinal structural damage and reduces neovascular lesions by downregulating the ROS/HIF‐1α/VEGF signaling axis. ABSTRACT Moutan Cortex is a functional food ingredient with multiple health benefits, but its effects on diabetic retinopathy (DR) remain ...
Mei‐rong Li, Xian‐yi Zhang, Wan‐ying Zhang, Nan Chen, Wei‐wei Lv, Tian‐yu Liu, Xu Guo, Ying‐ying Chen, Meng‐qi Zhang, Shu‐tao Sun, Mu‐xuan Wang, Qi‐dong Ren, Chao Liu, Jin‐yue Sun   +13 more
wiley   +1 more source

Enzymatic Disruption of the Internal Limiting Membrane Enhances Transplanted Retinal Ganglion Cell Survival. [PDF]

Invest Ophthalmol Vis Sci
Stavropoulos D, Liu CC, Chen CY, Mirzaliyeva L, Rao M, Wang S, Zhao C, Lin YL, Talebian N, Rosin B, Lo J, Pi S, Johnson TV, Sahel JA, Chang KC.   +14 more
europepmc   +1 more source

Prognostic Factors for Postoperative Complications. An Aggregate Protocol for 10 Observational Studies From the Danish TRIPLE‐A Cohort of 1.2 Million Surgeries

Acta Anaesthesiologica Scandinavica, Volume 70, Issue 7, August 2026.
ABSTRACT Background Postoperative complications substantially increase morbidity, mortality and healthcare costs. Understanding prognostic factors is essential for risk stratification, targeted prevention strategies, and development of prediction models.
Anders Peder Højer Karlsen, Asta Prescott, Caroline Folkersen, Jens Laigaard, Atena Saito, Caroline Lando Klammer, Mik Wetterslev, Emil Ipsen Ørskov, Mathilde Fahrendorff, Rebecca Kiær, Helene Holm Laigaard, Nichlas Hovmand, Lars Hyldborg Lundstrøm, Sebastian Buhl Rasmussen, Anders Kehlet Nørskov, Markus Harboe Olsen   +15 more
wiley   +1 more source

An image-computable spatio-chromatic receptive field model of the midget retinal ganglion cell mosaic across the retina. [PDF]

J Comput Neurosci
Cottaris NP, Wandell BA, Brainard DH.
europepmc   +1 more source

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1465-1478, July 2026.
ABSTRACT Cockayne syndrome (CS) is an ultrarare genetic disorder associated with genes encoding proteins involved in DNA repair. The clinical course of CS involves neurodevelopmental and neurodegenerative features, including swallowing and communication impairments.
Abigail M. Spoden, Katlyn E. McGrattan, Peter B. Kang   +2 more
wiley   +1 more source

Systemic Inflammation Aggravates Retinal Ganglion Cell Vulnerability to Optic Nerve Trauma in Adult Rats. [PDF]

Int J Mol Sci
Rovere G, Caja-Matas Y, Vidal-Villegas B, Bernal-Garro JM, Sobrado-Calvo P, Salinas-Navarro M, Nucci C, Villegas-Pérez MP, Vidal-Sanz M, Agudo-Barriuso M, Nadal-Nicolás FM.   +10 more
europepmc   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source