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Loss of tissue-type plasminogen activator causes multiple developmental anomalies.

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Title: Loss of tissue-type plasminogen activator causes multiple developmental anomalies.
Authors: Uguen K; CHU Sainte-Justine Azrieli Research Centre, Montreal H3T 1C5, Canada.; Department of Medical Genetics, CHRU Brest, Brest F 29200, France.; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest F-29200, France., Frey T; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich 8952, Switzerland., Muthaffar O; Department of Pediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia., Décarie JC; Department of Medical Imaging, CHU Sainte-Justine, Montreal, Quebec H3T 1C5, Canada.; Department of Radiology, Radio-Oncology and Nuclear Medicine, Université de Montréal, Montreal, Quebec H3C 3J7, Canada., Ameziane N; Arcensus GmbH, Rostock 18119, Germany., Boissel S; CHU Sainte-Justine Azrieli Research Centre, Montreal H3T 1C5, Canada., Baradaran-Heravi Y; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich 8952, Switzerland., Rauch A; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich 8952, Switzerland.; University Children's Hospital Zurich, Zurich 8032, Switzerland.; University of Zurich Research Priority Program ITINERARE: Innovative Therapies in Rare Diseases, Zurich 8952, Switzerland.; University of Zurich Research Priority Program AdaBD: Adaptive Brain Circuits in Development and Learning, Zurich 8952, Switzerland., Oprea G; Arcensus GmbH, Rostock 18119, Germany., Rad A; Arcensus GmbH, Rostock 18119, Germany., Steindl K; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich 8952, Switzerland., Michaud JL; CHU Sainte-Justine Azrieli Research Centre, Montreal H3T 1C5, Canada.; Department of Pediatrics, Université de Montréal, Montreal H3C 3J7, Canada.; Department of Neurosciences, Université de Montréal, Montreal H3C 3J7, Canada.
Source: Brain communications [Brain Commun] 2024 Nov 16; Vol. 6 (6), pp. fcae408. Date of Electronic Publication: 2024 Nov 16 (Print Publication: 2024).
Publication Type: Journal Article
Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 101755125 Publication Model: eCollection Cited Medium: Internet ISSN: 2632-1297 (Electronic) Linking ISSN: 26321297 NLM ISO Abbreviation: Brain Commun Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Loss of tissue-type plasminogen activator causes multiple developmental anomalies.
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  Data: <searchLink fieldCode="AU" term="%22Uguen+K%22">Uguen K</searchLink>; CHU Sainte-Justine Azrieli Research Centre, Montreal H3T 1C5, Canada.; Department of Medical Genetics, CHRU Brest, Brest F 29200, France.; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest F-29200, France.<br /><searchLink fieldCode="AU" term="%22Frey+T%22">Frey T</searchLink>; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich 8952, Switzerland.<br /><searchLink fieldCode="AU" term="%22Muthaffar+O%22">Muthaffar O</searchLink>; Department of Pediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Décarie+JC%22">Décarie JC</searchLink>; Department of Medical Imaging, CHU Sainte-Justine, Montreal, Quebec H3T 1C5, Canada.; Department of Radiology, Radio-Oncology and Nuclear Medicine, Université de Montréal, Montreal, Quebec H3C 3J7, Canada.<br /><searchLink fieldCode="AU" term="%22Ameziane+N%22">Ameziane N</searchLink>; Arcensus GmbH, Rostock 18119, Germany.<br /><searchLink fieldCode="AU" term="%22Boissel+S%22">Boissel S</searchLink>; CHU Sainte-Justine Azrieli Research Centre, Montreal H3T 1C5, Canada.<br /><searchLink fieldCode="AU" term="%22Baradaran-Heravi+Y%22">Baradaran-Heravi Y</searchLink>; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich 8952, Switzerland.<br /><searchLink fieldCode="AU" term="%22Rauch+A%22">Rauch A</searchLink>; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich 8952, Switzerland.; University Children's Hospital Zurich, Zurich 8032, Switzerland.; University of Zurich Research Priority Program ITINERARE: Innovative Therapies in Rare Diseases, Zurich 8952, Switzerland.; University of Zurich Research Priority Program AdaBD: Adaptive Brain Circuits in Development and Learning, Zurich 8952, Switzerland.<br /><searchLink fieldCode="AU" term="%22Oprea+G%22">Oprea G</searchLink>; Arcensus GmbH, Rostock 18119, Germany.<br /><searchLink fieldCode="AU" term="%22Rad+A%22">Rad A</searchLink>; Arcensus GmbH, Rostock 18119, Germany.<br /><searchLink fieldCode="AU" term="%22Steindl+K%22">Steindl K</searchLink>; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich 8952, Switzerland.<br /><searchLink fieldCode="AU" term="%22Michaud+JL%22">Michaud JL</searchLink>; CHU Sainte-Justine Azrieli Research Centre, Montreal H3T 1C5, Canada.; Department of Pediatrics, Université de Montréal, Montreal H3C 3J7, Canada.; Department of Neurosciences, Université de Montréal, Montreal H3C 3J7, Canada.
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  Data: <searchLink fieldCode="JN" term="%22101755125%22">Brain communications</searchLink> [Brain Commun] 2024 Nov 16; Vol. 6 (6), pp. fcae408. <i>Date of Electronic Publication: </i>2024 Nov 16 (<i>Print Publication: </i>2024).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Oxford+University+Press%22">Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101755125 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>2632-1297 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2226321297%22">26321297 </searchLink><i>NLM ISO Abbreviation: </i>Brain Commun <i>Subsets: </i>PubMed not MEDLINE
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