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

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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
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DbLabel: MEDLINE Ultimate
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PubType: Academic Journal
PubTypeId: academicJournal
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  Data: Map2k6 is a potent genetic modifier of arterial rupture in vascular Ehlers-Danlos syndrome mice.
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  Data: <searchLink fieldCode="AU" term="%22Bowen+CJ%22">Bowen CJ</searchLink>; Department of Genetic Medicine and.<br /><searchLink fieldCode="AU" term="%22Sorber+R%22">Sorber R</searchLink>; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Calderón+Giadrosic+JF%22">Calderón Giadrosic JF</searchLink>; Department of Genetic Medicine and.<br /><searchLink fieldCode="AU" term="%22Doyle+JJ%22">Doyle JJ</searchLink>; Department of Genetic Medicine and.; Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Rykiel+G%22">Rykiel G</searchLink>; Department of Genetic Medicine and.<br /><searchLink fieldCode="AU" term="%22Burger+Z%22">Burger Z</searchLink>; Department of Genetic Medicine and.<br /><searchLink fieldCode="AU" term="%22Zhang+X%22">Zhang X</searchLink>; Department of Genetic Medicine and.<br /><searchLink fieldCode="AU" term="%22Espinoza+Camejo+WA%22">Espinoza Camejo WA</searchLink>; Department of Genetic Medicine and.<br /><searchLink fieldCode="AU" term="%22Anderson+N%22">Anderson N</searchLink>; Department of Genetic Medicine and.<br /><searchLink fieldCode="AU" term="%22Sabnis+S%22">Sabnis S</searchLink>; Department of Bioengineering, Northeastern University, Boston, Massachusetts, USA.<br /><searchLink fieldCode="AU" term="%22Bellini+C%22">Bellini C</searchLink>; Department of Bioengineering, Northeastern University, Boston, Massachusetts, USA.<br /><searchLink fieldCode="AU" term="%22MacFarlane+EG%22">MacFarlane EG</searchLink>; Department of Genetic Medicine and.; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Dietz+HC%22">Dietz HC</searchLink>; 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.
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  Data: <searchLink fieldCode="JN" term="%22101676073%22">JCI insight</searchLink> [JCI Insight] 2025 Jan 21; Vol. 10 (5). <i>Date of Electronic Publication: </i>2025 Jan 21.
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  Data: Journal Article; Research Support, N.I.H., Extramural
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22American+Society+for+Clinical+Investigation%22">American Society for Clinical Investigation </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101676073 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2379-3708 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2223793708%22">23793708 </searchLink><i>NLM ISO Abbreviation: </i>JCI Insight <i>Subsets: </i>MEDLINE
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        Value: 10.1172/jci.insight.187315
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        Text: English
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      – TitleFull: Map2k6 is a potent genetic modifier of arterial rupture in vascular Ehlers-Danlos syndrome mice.
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              Text: 2025 Jan 21
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