A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
LMNA mutations in progeria patients. The diagram shows the structure of... | Download Scientific Diagram
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics
Gene Positioning
Children living with progeria - MedCrave online
David R. Liu on Twitter: "The mutation (discovered by @NIHDirector's lab in 2003) results in progerin, a toxic protein that damages nuclei. So providing more healthy LMNA is not a solution, and
Progeria
Genes | Free Full-Text | Splicing Variants, Protein-Protein Interactions, and Drug Targeting in Hutchinson-Gilford Progeria Syndrome and Small Cell Lung Cancer
Gene Editing Reverses Premature Aging – Developmental Biology Research Highlights, University of Otago, New Zealand
Progeria | Definition, Types, Symptoms, Syndrome, & Facts | Britannica
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria - ScienceDirect
Hutchinson–Gilford Progeria Syndrome (HGPS)
About Progeria
The Disorder That Makes One Age 7 Times Faster | Hutchinson-Gilford Progeria Syndrome and its Recent Advances | Science Repository | Open Access Journals
The Curious Case of Ageing
Progeria Syndrome
Hutchinson-Gilford Progeria Syndrome | IntechOpen
Lamin A Truncation in Hutchinson-Gilford Progeria | Science
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
Pharmacotherapy to gene editing: potential therapeutic approaches for Hutchinson–Gilford progeria syndrome | SpringerLink
Progeria: old before their time - ScienceDirect
Progerin - Wikipedia
Interview: CRISPR Base Editors Offer First One-Time Treatment for the Lethal Premature-ageing Disease Progeria - CRISPR Medicine
Development of a new drug for progeria syndrome; Past, Present and Future
LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome | Journal of Medical Genetics
