Deep learning-enabled filter-free fluorescence microscope. [PDF]
Dai B +12 more
europepmc +1 more source
Super-resolution fluorescence microscope
Ko Sugawara +2 more
openaire +2 more sources
Development and design of a spatially and temporally resolved fluorescence fluctuation microscope for the analysis of molecular mobilities and interactions [PDF]
Gerrit L. Heuvelman
openalex +1 more source
NR4A1 Exerts Pro‐Tumor Role in Glioblastoma via Inducing xCT/GPX4‐Regulated Ferroptosis
ABSTRACT Purpose This study investigates NR4A1's paradoxical roles in glioblastoma (GBM) progression, focusing on its mechanistic link to ferroptosis regulation. We aimed to resolve conflicting reports of NR4A1 as both an oncogene and a tumor suppressor by defining its transcriptional control over xCT/GPX4‐mediated iron homeostasis and its clinical ...
Peng Tao +10 more
wiley +1 more source
Knowledge-enhanced protein subcellular localization prediction from 3D fluorescence microscope images. [PDF]
Zeng GH +5 more
europepmc +1 more source
Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome
ABSTRACT Objective Rett syndrome (RTT) is a devastating neurodevelopmental disorder with developmental regression affecting motor, sensory, and cognitive functions. Sensory disruptions contribute to the complex behavioral and cognitive difficulties and represent an important target for therapeutic interventions.
Alex Joseph Simon +12 more
wiley +1 more source
3D-printed fiber-bundle fluorescence microscope for quantifying single-cell responses to high-power radiofrequency sources. [PDF]
O'Connor SP +9 more
europepmc +1 more source
SURG-24. Intraoperative Assessment of Glioma Using Miniaturized Epi-fluorescence Widefield Microscope: A Prospective Comparative Study of Ex-vivo and In-vivo Applications [PDF]
Xiefeng Wang +11 more
openalex +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source
Intramolecular Fluorescence Correlation Spectroscopy in a Feedback Tracking Microscope [PDF]
Kevin McHale, Hideo Mabuchi
openalex +1 more source

