(Q54743960)

English

AG11498

cell line

In more languages

Statements

1 reference

Cellosaurus release 47

13 October 2023

finite cell line

1 reference

Cellosaurus release 47

13 October 2023

described by source

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

1 reference

Cellosaurus release 47

13 October 2023

Genome-scale expression profiling of Hutchinson-Gilford progeria syndrome reveals widespread transcriptional misregulation leading to mesodermal/mesenchymal defects and accelerated atherosclerosis

1 reference

Cellosaurus release 47

13 October 2023

Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition

1 reference

Cellosaurus release 47

13 October 2023

Nucleolar expansion and elevated protein translation in premature aging

1 reference

Cellosaurus release 47

13 October 2023

established from medical condition

1 reference

Cellosaurus release 47

13 October 2023

derived from organism type

1 reference

Cellosaurus release 47

13 October 2023

http://purl.obolibrary.org/obo/CLO_0021565

1 reference

Cellosaurus release 47

13 October 2023

Identifiers

Cell Line Ontology ID

1 reference

Cellosaurus release 47

13 October 2023

1 reference

Cellosaurus release 47

13 October 2023

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