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
Longitudinal changes in salivary biomarkers in Parkinson’s disease (PD) from early (T0) to 4‐year follow‐up (T1), quantified by ELISA: oligomeric and total α‐synuclein, total and phosphorylated tau, MAP1LC3B (autophagy), and TNFa (inflammation). Blue arrows indicate direction of change at T1 vs T0 (up = increase; down = decrease).
Maria Ilenia De Bartolo +13 more
wiley +1 more source
Evaluation of Human Hair Absorption and Retention. [PDF]
Yun J, Kim SH, Yoo H, Park KH.
europepmc +1 more source
LIGHT-MASS ABSORPTION DURING PHOTOSYNTHESIS [PDF]
Earle Augustus Spessard
openalex +1 more source
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann +6 more
wiley +1 more source
Inverse design of periodic cavities in anechoic coatings with gradient changes of radii and distances via a conditional generative adversarial network. [PDF]
Sun Y, Fu J, Wu Y, Chen J, Tao M.
europepmc +1 more source
Remarks on the uses of the globules in relation to absorption, secretion, and morbid deposition; but here especially for the diagnosis of tubercle of the lungs or elsewhere [PDF]
Thomas Hodgson Watts
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
Ultraviolet A absorption coefficients of contact lenses for use in contact lens assisted corneal crosslinking for thin Corneas. [PDF]
Ogbuehi KC +3 more
europepmc +1 more source

