Results 181 to 190 of about 6,153,427 (293)
Regulatory mechanism of heme-regulated inhibitor through autophosphorylation-driven activation and heme-induced deactivation. [PDF]
Oka T +5 more
europepmc +1 more source
Chronobiology of Cancer: How Aging Fuels Oncogenesis at the Molecular Level
This graphical abstract illustrates the key biological pathways linking aging with cancer development and progression. In the upper left, cumulative exposure to ultraviolet radiation, toxins, and reactive oxygen species (ROS) causes DNA damage and genomic instability, whereas age‐related decline in repair mechanisms, such as ATM/ATR, BER, and NER ...
Anu Singh, Aroonima Misra, Sufian Zaheer
wiley +1 more source
Function within disorder: Small heat shock proteins use different functional regions to chaperone tau aggregation. [PDF]
Cervantes M +5 more
europepmc +1 more source
SPG4 and Dementia: Expanding the Clinical Spectrum
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
Bicyclo[1.1.1]pentane as a Phenyl Isosteric Replacement. [PDF]
Saar A +9 more
europepmc +1 more source
Some remarks on a terminal value problem
Some theorems concerning the existence and uniqueness of solutions of the differential equations with deviating arguments \(x'(t)=f(t,x[\sigma_ 1(t)],...,x[\sigma_ k(t)]),\) which satisfy the ''terminal'' condition \(\lim_{t\to \infty}x(t)=\xi\) where \(\xi \in R^ n\) or \({\mathbb{C}}^ n\) are obtained.
openaire +2 more sources
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
The Cox-Aalen Rate Model for Recurrent Events With an Informative Terminal Event. [PDF]
Yue M, Chen X, Chen J, Sun L.
europepmc +1 more source
ABSTRACT Objective High‐resolution MRI enables detailed assessment of intracranial vessel wall pathology in moyamoya vasculopathy. We aimed to classify adult moyamoya vasculopathy etiologies using high‐resolution MRI and to examine subtype‐specific associations between high‐resolution MRI features and ischemic infarction.
Guangsong Han +8 more
wiley +1 more source
Genetic variants of Ehrlichia canis detected in two dogs in Japan. [PDF]
Taira M +6 more
europepmc +1 more source

