about
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndromeGenome-scale expression profiling of Hutchinson-Gilford progeria syndrome reveals widespread transcriptional misregulation leading to mesodermal/mesenchymal defects and accelerated atherosclerosis.Nucleolar expansion and elevated protein translation in premature aging.
P4510
description
Zelllinie
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ceall-líne
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cell line
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cellijn van een Homo sapiens
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lignée cellulaire
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name
AG11513
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AG11513
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AG11513
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AG11513
@ga
AG11513
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এজি১১৫১৩
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type
label
AG11513
@de
AG11513
@en
AG11513
@fr
AG11513
@ga
AG11513
@nl
এজি১১৫১৩
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prefLabel
AG11513
@de
AG11513
@en
AG11513
@fr
AG11513
@ga
AG11513
@nl
এজি১১৫১৩
@bn