Exploring the role of lamin in normal aging
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria - ScienceDirect
Cells | Free Full-Text | Progerin, an Aberrant Spliced Form of Lamin A, Is a Potential Therapeutic Target for HGPS
CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy
Progeria (Hutchinson-Gilford Progeria Syndrome — HGPS): Symptoms & Causes
Prelamin A causes progeria through cell-extrinsic mechanisms and prevents cancer invasion | Nature Communications
Permanent farnesylation of lamin A mutants linked to progeria impairs its phosphorylation at serine 22 during interphase | Aging
Progerin - Wikipedia
Prelamin A and progerin differ in their processing. A simplified model... | Download Scientific Diagram
Progeria - Wikipedia
JCI - Interruption of progerin–lamin A/C binding ameliorates Hutchinson-Gilford progeria syndrome phenotype
Cos'è la progeria - A.I.Pro.Sa.B.
Cardiovascular Progerin Suppression and Lamin A Restoration Rescue Hutchinson-Gilford Progeria Syndrome | Circulation
Progeria Gene Implicated in Normal Aging | National Institutes of Health (NIH)
Biogenesis of lamin A and progerin in the cell. The left picture... | Download Scientific Diagram
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome | Nature
IJMS | Free Full-Text | Small-Molecule Therapeutic Perspectives for the Treatment of Progeria
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson–Gilford progeria syndrome | PNAS
Progeria
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson–Gilford progeria syndrome | PNAS
Studying the Molecular Mechanism of Post-Translational Modification of Lamin A in Hutchinson-Gilford Progeria Syndrome
Cos'è la progeria - A.I.Pro.Sa.B.
Lamin A Truncation in Hutchinson-Gilford Progeria | Science
Fatti rapidi | La Progeria Research Foundation
