Results 191 to 200 of about 1,071,713 (341)

Deep learning-enabled filter-free fluorescence microscope. [PDF]

open access: yesSci Adv
Dai B   +12 more
europepmc   +1 more source

Super-resolution fluorescence microscope

open access: yesDrug Delivery System, 2014
Ko Sugawara   +2 more
openaire   +2 more sources

NR4A1 Exerts Pro‐Tumor Role in Glioblastoma via Inducing xCT/GPX4‐Regulated Ferroptosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
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

Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
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]

open access: yesBiomed Opt Express
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]

open access: bronze
Xiefeng Wang   +11 more
openalex   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
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

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