Mark Screen

Altered Ribostasis: RNA-Protein Granules in Degenerative Disorders

The role of liquid–liquid phase separation in aggregation of the TDP-43 low-complexity domain

Biomolecular condensates: organizers of cellular biochemistry

Oxidative stress, aging, and diseases

Atomic structures of TDP-43 LCD segments and insights into reversible or pathogenic aggregation

C9orf72 Dipeptide Repeats Impair the Assembly, Dynamics, and Function of Membrane-Less Organelles

Macrolides sensitize EGFR-TKI-induced non-apoptotic cell death via blocking autophagy flux in pancreatic cancer cell lines

The VCP/p97 system at a glance: connecting cellular function to disease pathogenesis

Quality Control of Membraneless Organelles

Decoding ALS: from genes to mechanism

Considerations and Challenges in Studying Liquid-Liquid Phase Separation and Biomolecular Condensates

Altered gene expression and spongiotrophoblast differentiation in placenta from a mouse model of diabetes in pregnancy

Formation and Maturation of Phase-Separated Liquid Droplets by RNA-Binding Proteins

A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation

Increased susceptibility of HIF-1α heterozygous-null mice to cardiovascular malformations associated with maternal diabetes

Phase Separation by Low Complexity Domains Promotes Stress Granule Assembly and Drives Pathological Fibrillization

Liquid phase condensation in cell physiology and disease

Welander distal myopathy is caused by a mutation in the RNA‐binding protein TIA1

Cathepsin proteases have distinct roles in trophoblast function and vascular remodelling