NR4A1 Exerts Pro‐Tumor Role in Glioblastoma via Inducing xCT/GPX4‐Regulated Ferroptosis
Annals 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
A THEORY FOR CLOSE-IN FALLOUT FROM LAND-SURFACE NUCLEAR BURSTS [PDF]
, 1961 Albert D. Anderson
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Assessing a Mitochondrial Disease Treatment via a Novel Statistical Technique for Accelerometer Data
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Therapeutic development for mitochondrial diseases, rare genetic disorders with pathogenic defects of oxidative phosphorylation, is hindered by unsatisfactory outcome measures. To address this problem, we provide the first clinical application of a novel, bias‐adjusted outcome measure of acceleration across a range of subjects ...
Ian W. McKeague +8 more
wiley +1 more source
Theory of Neutron Chain Reactions Volume II, Part I: Homogeneous Nuclear Chain Reactions
, 1951 Alvin M. Weinberg, L.C. Noderer
openalex +2 more sources
Perturbation Theory Applied to the Nuclear Many-Body Problem [PDF]
, 1961 J. S. Levinger +3 more
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CSF Mitochondrial DNA: Biomarker of Body Composition and Energy Metabolism in Parkinson's Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Cerebrospinal fluid (CSF) cell‐free mitochondrial DNA (cf‐mtDNA) is a potential biomarker for Parkinson's disease (PD), but its clinical relevance remains unclear. We investigated associations between CSF cf‐mtDNA levels, body composition, nutritional status, and metabolic biomarkers in PD. Methods CSF cf‐mtDNA levels, defined as the
Yasuaki Mizutani +11 more
wiley +1 more source
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco +18 more
wiley +1 more source
Bohr: Physique atomique et connaissance humaine/Becker: Theorie der Elektrizität Bd. I/Schaefer und Päsler: Einführung in die Theoret. Physik Bd. I/MacDonald: Thermoelectricity: An Introduction to the Principles/Brillouin: Science and Information Theory/Bradley: Shock Waves in Chemistry and Physics/Pirani und Yarwood: Principles of Vacuum Engineering/Chase: Nuclear Pulse Spectrometry [PDF]
, 1962 Klaus Pöschl +7 more
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Comments on Fermi's Statistical Theory of High Energy Nuclear Events [PDF]
, 1961 K. B. Fenton
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