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Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newborn | European Journal of Human Genetics
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Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson–Gilford progeria syndrome | PNAS
Permanent farnesylation of lamin A mutants linked to progeria impairs its phosphorylation at serine 22 during interphase | Aging
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JCI Insight - Nuclear membrane ruptures underlie the vascular pathology in a mouse model of Hutchinson-Gilford progeria syndrome
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LMNA mutations in progeria patients. The diagram shows the structure of... | Download Scientific Diagram
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A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
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A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
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Genes | Free Full-Text | Splicing Variants, Protein-Protein Interactions, and Drug Targeting in Hutchinson-Gilford Progeria Syndrome and Small Cell Lung Cancer
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The flavonoid morin alleviates nuclear deformation in aged cells by disrupting progerin-lamin A/C binding - ScienceDirect
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Mislocalization of centromeres in atypical-progeria-patient fibroblasts... | Download Scientific Diagram
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Prelamin A and progerin differ in their processing. A simplified model... | Download Scientific Diagram
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Speeding up the clock: The past, present and future of progeria - Swahari - 2016 - Development, Growth & Differentiation - Wiley Online Library
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Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics
![Francis Villatoro on X: "#Nature In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice (by David R. Liu et al.) https://t.co/YvqGq0aSGg Progeria is typically caused by a dominant-negative C•G-to-T•A mutation (c.1824 Francis Villatoro on X: "#Nature In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice (by David R. Liu et al.) https://t.co/YvqGq0aSGg Progeria is typically caused by a dominant-negative C•G-to-T•A mutation (c.1824](https://pbs.twimg.com/media/ErH8k88XUAAIsxU.png)
Francis Villatoro on X: "#Nature In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice (by David R. Liu et al.) https://t.co/YvqGq0aSGg Progeria is typically caused by a dominant-negative C•G-to-T•A mutation (c.1824
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A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
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