Age mosaic of gut epithelial cells prevents aging. [PDF]
Qin P, Wang Q, Wu Y, You Q, Li M, Guo Z.
europepmc +1 more source
Extracellular Matrix Signaling Cues: Biological Functions, Diseases, and Therapeutic Targets
Targeting ECM dysregulation: therapeutic strategies for disease intervention. Dysregulated ECM composition and biomechanics contribute to disease pathogenesis in cancer and fibrotic disorders. Physical modulation: Nanomedicine‐based strategies tune ECM physical properties (e.g., density, stiffness) to enhance drug penetration and therapeutic efficacy ...
Tian Zhao+11 more
wiley +1 more source
Lamin variants cause cardiac arrhythmogenicity in Drosophila.
van Wijk SW+7 more
europepmc +1 more source
Optimizing Proximity Proteomics on the EvoSep‐timsTOF LC–MS System
ABSTRACT Proximity‐dependent biotinylation (BioID) is a powerful means of exploring the cellular environments in which proteins reside. Expressing a protein of interest (bait) fused to a biotin ligase and adding biotin induces the covalent biotinylation of proximal partners (preys), which are recovered on streptavidin beads and identified by MS ...
Julia Kitaygorodsky+8 more
wiley +1 more source
Phosphatidylcholine suppresses inflammatory responses in LPS-stimulated MG6 microglial cells by inhibiting NF-κB/JNK/p38 MAPK signaling. [PDF]
Mizuno S+7 more
europepmc +1 more source
ZNF224 enhances the oncogenic function of p21 via p53 and AKT pathways in melanoma
KRAB zinc finger protein ZNF224 acts as an oncogenic factor in melanoma cells, enhancing p21 cytosolic retention and impairing nuclear p21 cytostatic activity through stimulation of the AKT pathway. Furthermore, ZNF224 regulates transcriptional expression levels of p21 via p53.
Leandra Sepe+12 more
wiley +1 more source
Lamin A/C regulates cerebellar granule cell maturation. [PDF]
Vilardo L+15 more
europepmc +1 more source
SFPQ subcellular mislocalisation entails altered cancer cell function
Clinical and Translational Medicine, Volume 15, Issue 8, August 2025.
Libang Yang+8 more
wiley +1 more source
A Novel LAMA2 Mutation (c.7412G>A) Was Found in a Chinese Patient With Congenital Muscular Dystrophy
ABSTRACT Congenital muscular dystrophy (CMD) is a genetic muscle disorder characterised by muscle weakness and degeneration, either present at birth or emerging in middle age, often leading to progressive disability. MDC1A is a subtype of CMD caused by mutations in the LAMA2 gene.
Meifang Zhao+5 more
wiley +1 more source
Downregulation of Nesprin1 by Runx2 deficiency is critical for the development of skeletal laminopathy-like pathology. [PDF]
Saito A+9 more
europepmc +1 more source