Lysophosphatidic acid receptor LPA 3 prevents oxidative stress and cellular senescence in Hutchinson...
Lysophosphatidic acid receptor LPA 3 prevents oxidative stress and cellular senescence in Hutchinson-Gilford progeria syndrome
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England
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Language
English
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England
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Hutchinson-Gilford progeria syndrome (HGPS) is a rare laminopathy that produces a mutant form of prelamin A, known as Progerin, resulting in premature aging. HGPS cells show morphological abnormalities of the nuclear membrane, reduced cell proliferation rates, accumulation of reactive oxygen species (ROS), and expression of senescence markers. Lyso...
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Lysophosphatidic acid receptor LPA 3 prevents oxidative stress and cellular senescence in Hutchinson-Gilford progeria syndrome
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TN_cdi_crossref_primary_10_1111_acel_13064
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1111_acel_13064
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ISSN
1474-9718
E-ISSN
1474-9726
DOI
10.1111/acel.13064