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Paper Details

Bone dysplasia in Hutchinson-Gilford progeria syndrome is associated with dysregulated differentiation and function of bone cell populations.
Aging Cell
3
2023
Bone dysplasia, Cultured, G608G, HGPS, Hutchinson-Gilford progeria syndrome, KI, KI osteoblasts, KI osteoclasts, KI transcripts, LMNA, Lmna, adipogenic genes, bone, bone cell populations, bone deterioration, bone dysplasia, c.1824C, cardiovascular defects, cryptic splice donor site, growth deficiency, lamin A, lipodystrophy, marrow-derived precursors, mice, mouse, osteoblast, osteoclasts, patients, premature aging disorder, premature aging disorders, progerin protein, sclerotic dermis, wild-type
Author NameAffiliation
Narisu NarisuCenter for Precision Health Research, National Human Genome Research Institute
Tingfen YanCenter for Precision Health Research, National Human Genome Research Institute
Michael R ErdosCenter for Precision Health Research, National Human Genome Research Institute
Michael R ErdosCenter for Precision Health Research, National Human Genome Research Institute
Francis S CollinsCenter for Precision Health Research, National Human Genome Research Institute
Francis S CollinsCenter for Precision Health Research, National Human Genome Research Institute
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Release 1.2