AG06297 (Q54740296)

From Wikidata

Jump to navigation Jump to search

cell line

AG06297A
AG06297B
AG06297C

Language	Label	Description	Also known as
English	AG06297	cell line	AG06297A AG06297B AG06297C

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

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

Mitotic misregulation and human aging

1 reference

Cellosaurus release 47

13 October 2023

Aging of Hutchinson-Gilford progeria syndrome fibroblasts is characterised by hyperproliferation and increased apoptosis

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_0035510

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

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q54740296&oldid=1990990507"