IBS Publications Repository: Base Editing in Progeria

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IBS Publications RepositoryCenter for Genome Engineering(유전체 교정 연구단)1. Journal Papers (저널논문)

Base Editing in Progeria

DC Field	Value	Language
dc.contributor.author	Jin‑Soo Kim	-
dc.contributor.author	Eriksson, Maria	-
dc.date.accessioned	2021-07-05T02:30:15Z	-
dc.date.accessioned	2021-07-05T02:30:15Z	-
dc.date.available	2021-07-05T02:30:15Z	-
dc.date.available	2021-07-05T02:30:15Z	-
dc.date.created	2021-04-21	-
dc.date.issued	2021-04-08	-
dc.identifier.issn	0028-4793	-
dc.identifier.uri	https://pr.ibs.re.kr/handle/8788114/9839	-
dc.description.abstract	The Hutchinson?Gilford progeria syndrome is an autosomal dominant disease caused by a single point mutation in LMNA, which encodes the lamin A and C proteins. Recent experiments have shown that life span in a mouse model of the disease was extended through DNA base editing.	-
dc.language	영어	-
dc.publisher	MASSACHUSETTS MEDICAL SOC	-
dc.title	Base Editing in Progeria	-
dc.type	Article	-
dc.type.rims	ART	-
dc.identifier.wosid	000637799800016	-
dc.identifier.scopusid	2-s2.0-85103876458	-
dc.identifier.rimsid	75407	-
dc.contributor.affiliatedAuthor	Jin‑Soo Kim	-
dc.identifier.doi	10.1056/NEJMcibr2100661	-
dc.identifier.bibliographicCitation	NEW ENGLAND JOURNAL OF MEDICINE, v.384, no.14, pp.1364 - 1366	-
dc.relation.isPartOf	NEW ENGLAND JOURNAL OF MEDICINE	-
dc.citation.title	NEW ENGLAND JOURNAL OF MEDICINE	-
dc.citation.volume	384	-
dc.citation.number	14	-
dc.citation.startPage	1364	-
dc.citation.endPage	1366	-
dc.type.docType	Editorial Material	-
dc.description.journalClass	1	-
dc.description.journalClass	1	-
dc.description.isOpenAccess	N	-
dc.description.journalRegisteredClass	scie	-
dc.description.journalRegisteredClass	scopus	-
dc.relation.journalResearchArea	General & Internal Medicine	-
dc.relation.journalWebOfScienceCategory	Medicine, General & Internal	-