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Map2k6 is a potent genetic modifier of arterial rupture in vascular Ehlers-Danlos syndrome mice.

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Bibliographic Details
Title:	Map2k6 is a potent genetic modifier of arterial rupture in vascular Ehlers-Danlos syndrome mice.
Authors:	Bowen CJ; Department of Genetic Medicine and., Sorber R; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Calderón Giadrosic JF; Department of Genetic Medicine and., Doyle JJ; Department of Genetic Medicine and.; Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, USA., Rykiel G; Department of Genetic Medicine and., Burger Z; Department of Genetic Medicine and., Zhang X; Department of Genetic Medicine and., Espinoza Camejo WA; Department of Genetic Medicine and., Anderson N; Department of Genetic Medicine and., Sabnis S; Department of Bioengineering, Northeastern University, Boston, Massachusetts, USA., Bellini C; Department of Bioengineering, Northeastern University, Boston, Massachusetts, USA., MacFarlane EG; Department of Genetic Medicine and.; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Dietz HC; Department of Genetic Medicine and.; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Howard Hughes Medical Institute, Chevy Chase, Maryland, USA.
Source:	JCI insight [JCI Insight] 2025 Jan 21; Vol. 10 (5). Date of Electronic Publication: 2025 Jan 21.
Publication Type:	Journal Article; Research Support, N.I.H., Extramural
Journal Info:	Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 101676073 Publication Model: Electronic Cited Medium: Internet ISSN: 2379-3708 (Electronic) Linking ISSN: 23793708 NLM ISO Abbreviation: JCI Insight Subsets: MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	2379-3708
DOI:	10.1172/jci.insight.187315