N6-methyladenosine RNA modification regulates microglial phagocytosis in the APP/PS1 mouse model of Alzheimer's disease. [PDF]
Qu X, Lin L, Li Y, Chen Y, Chen Y.
europepmc +1 more source
Long‐Term Follow‐Up of Chemotherapy‐Associated Biological Aging in Women With Early Breast Cancer
Women threated with adjuvant chemotherapy for early breast cancer have sustained long‐term increase in p16INK4a,, a robust marker of cell senescence, suggesting a chemotherapy‐associated age acceleration. p16INK4a as well as other biomarkers may identify patients at greatest risk for senescence‐related diseases of aging.
Hyman B. Muss +12 more
wiley +1 more source
Regulation of Skeletogenic Pathways by m6A RNA Modification: A Comprehensive Review. [PDF]
Ahi EP.
europepmc +1 more source
Exploratory Analysis of ELP1 Expression in Whole Blood From Patients With Familial Dysautonomia
ABSTRACT Background Familial dysautonomia (FD) is a hereditary neurodevelopmental disorder caused by aberrant splicing of the ELP1 gene, leading to a tissue‐specific reduction in ELP1 protein expression. Preclinical models indicate that increasing ELP1 levels can mitigate disease manifestations.
Alejandra González‐Duarte +13 more
wiley +1 more source
RNA Modification and Digestive Tract Tumors: A Review. [PDF]
Liu Y, Zhang S, Liu K, Gu X, Hu X.
europepmc +1 more source
Bacteriophage T4-included anticodon-loop nuclease detected in a host strain restrictive to RNA ligase mutants [PDF]
Borasio, Gian Domenico +2 more
core
Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron +5 more
wiley +1 more source
Targeting m<sup>6</sup>A RNA Modification in Tumor Therapeutics. [PDF]
Mao Z, Li M, Wang S.
europepmc +1 more source
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi +2 more
wiley +1 more source
Aberrant NSUN1 activity connects m<sup>5</sup>C-RNA modification to TDP-43 neurotoxicity in ALS/FTD. [PDF]
Parra-Torres M +8 more
europepmc +1 more source

