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A mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition.

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Title: A mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition.
Authors: Gao CW; Department of Genetic Medicine.; Department of Molecular Biology and Genetics, and., Lin W; Department of Genetic Medicine., Riddle RC; Department of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Department of Orthopaedics, University of Maryland School of Medicine, Baltimore, Maryland, USA.; Research and Development Service, Baltimore Veterans Administration Medical Center, Baltimore, Maryland, USA., Kushwaha P; Department of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Boukas L; Department of Genetic Medicine.; Department of Biostatistics, Johns Hopkins University School of Public Health, Baltimore, Maryland, USA., Björnsson HT; Department of Genetic Medicine.; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Faculty of Medicine, University of Iceland, Reykjavík, Iceland.; Landspítali University Hospital, Reykjavík, Iceland., Hansen KD; Department of Genetic Medicine.; Department of Biostatistics, Johns Hopkins University School of Public Health, Baltimore, Maryland, USA.; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Fahrner JA; Department of Genetic Medicine.; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Source: JCI insight [JCI Insight] 2024 Jan 09; Vol. 9 (1). Date of Electronic Publication: 2024 Jan 09.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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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PubType: Academic Journal
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  Data: A mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition.
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  Data: <searchLink fieldCode="AU" term="%22Gao+CW%22">Gao CW</searchLink>; Department of Genetic Medicine.; Department of Molecular Biology and Genetics, and.<br /><searchLink fieldCode="AU" term="%22Lin+W%22">Lin W</searchLink>; Department of Genetic Medicine.<br /><searchLink fieldCode="AU" term="%22Riddle+RC%22">Riddle RC</searchLink>; Department of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Department of Orthopaedics, University of Maryland School of Medicine, Baltimore, Maryland, USA.; Research and Development Service, Baltimore Veterans Administration Medical Center, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Kushwaha+P%22">Kushwaha P</searchLink>; Department of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Boukas+L%22">Boukas L</searchLink>; Department of Genetic Medicine.; Department of Biostatistics, Johns Hopkins University School of Public Health, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Björnsson+HT%22">Björnsson HT</searchLink>; Department of Genetic Medicine.; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Faculty of Medicine, University of Iceland, Reykjavík, Iceland.; Landspítali University Hospital, Reykjavík, Iceland.<br /><searchLink fieldCode="AU" term="%22Hansen+KD%22">Hansen KD</searchLink>; Department of Genetic Medicine.; Department of Biostatistics, Johns Hopkins University School of Public Health, Baltimore, Maryland, USA.; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Fahrner+JA%22">Fahrner JA</searchLink>; Department of Genetic Medicine.; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
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  Data: <searchLink fieldCode="JN" term="%22101676073%22">JCI insight</searchLink> [JCI Insight] 2024 Jan 09; Vol. 9 (1). <i>Date of Electronic Publication: </i>2024 Jan 09.
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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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      – Type: doi
        Value: 10.1172/jci.insight.173392
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      – Code: eng
        Text: English
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      – TitleFull: A mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition.
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            NameFull: Gao CW
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            NameFull: Lin W
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            – D: 09
              M: 01
              Text: 2024 Jan 09
              Type: published
              Y: 2024
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