Detection of nuclear STING in cultured human cells and in the normal and cancer tissues. [PDF]
iScienceVo N, Chen E, Sidorova JM.
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Computational Predictions and In Silico Structural Characterization of Putative Progerin-Interacting Peptides [PDF]
openProgeria is one of the rarest diseases in the world, affecting about one in every 20 million people. Progeria is caused by a single mutation in the LMNA gene, which creates an abnormal splicing site that leads to the removal of 50 amino acids from ...
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Antagonistic contributions of A-type and B-type lamins to LBR localization and dynamics. [PDF]
NucleusOdell J +3 more
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Why and How Are Infants with Hutchinson-Gilford Progeria Syndrome Born Without Severe Manifestations? [PDF]
Med Sci (Basel)Erokhina MA +3 more
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The impact of alterations in lamin A on genome integrity. [PDF]
Mutat Res Rev Mutat ResDiCintio AJ, Waldman AS.
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Epidural hematoma in a pediatric patient with Hutchinson-Gilford progeria syndrome: management considerations: a case report. [PDF]
Chin Neurosurg JOzmarasali AI, Sivas ZZ, Uguz I, Oto A.
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Hutchinson-Gilford progeria syndrome alters the endothelial genetic response to laminar shear stress. [PDF]
Front PhysiolKennedy CC, Carter JL, Truskey GA.
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Lonafarnib clinical trials demonstrate uncoupling of the muscle-bone unit in Hutchinson-Gilford Progeria Syndrome. [PDF]
J Bone Miner ResKreienkamp RJ +8 more
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Progerin regulates actin cytoskeletal remodeling and inhibits EMT and metastasis in triple‑negative breast cancer cells. [PDF]
Int J OncolHuang X, Luo W, Liu W, Liu X, Chen W.
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Elevated SUN1 promotes migratory cell polarity defects through mechanically coupling microtubules to the nuclear lamina. [PDF]
Commun BiolLi Y +7 more
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