Pex1 loss-of-function in zebrafish is viable and recapitulates hallmarks of Zellweger spectrum disorders.

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Title: Pex1 loss-of-function in zebrafish is viable and recapitulates hallmarks of Zellweger spectrum disorders.
Authors: Heins-Marroquin U; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., Hodzic Z; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., da Silva BSC; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., Hendriks A; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., Gavotto F; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., Warmoes MO; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., Schlicker L; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., Omri S; Child Health and Human Development Axis, Research Institute of the McGill University Health Centre, Montréal, QC, Canada., Jäger C; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., Glaab E; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., Braverman NE; Child Health and Human Development Axis, Research Institute of the McGill University Health Centre, Montréal, QC, Canada.; Division of Medical Genetics, Department of Pediatrics and Human Genetics, McGill University, Montreal, QC, Canada., Cordero-Maldonado ML; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg., Linster CL; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Source: Frontiers in molecular neuroscience [Front Mol Neurosci] 2025 Nov 05; Vol. 18, pp. 1634536. Date of Electronic Publication: 2025 Nov 05 (Print Publication: 2025).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101477914 Publication Model: eCollection Cited Medium: Print ISSN: 1662-5099 (Print) Linking ISSN: 16625099 NLM ISO Abbreviation: Front Mol Neurosci Subsets: PubMed not MEDLINE
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  Data: Pex1 loss-of-function in zebrafish is viable and recapitulates hallmarks of Zellweger spectrum disorders.
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  Data: <searchLink fieldCode="AU" term="%22Heins-Marroquin+U%22">Heins-Marroquin U</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Hodzic+Z%22">Hodzic Z</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22da+Silva+BSC%22">da Silva BSC</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Hendriks+A%22">Hendriks A</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Gavotto+F%22">Gavotto F</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Warmoes+MO%22">Warmoes MO</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Schlicker+L%22">Schlicker L</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Omri+S%22">Omri S</searchLink>; Child Health and Human Development Axis, Research Institute of the McGill University Health Centre, Montréal, QC, Canada.<br /><searchLink fieldCode="AU" term="%22Jäger+C%22">Jäger C</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Glaab+E%22">Glaab E</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Braverman+NE%22">Braverman NE</searchLink>; Child Health and Human Development Axis, Research Institute of the McGill University Health Centre, Montréal, QC, Canada.; Division of Medical Genetics, Department of Pediatrics and Human Genetics, McGill University, Montreal, QC, Canada.<br /><searchLink fieldCode="AU" term="%22Cordero-Maldonado+ML%22">Cordero-Maldonado ML</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.<br /><searchLink fieldCode="AU" term="%22Linster+CL%22">Linster CL</searchLink>; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
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  Data: <searchLink fieldCode="JN" term="%22101477914%22">Frontiers in molecular neuroscience</searchLink> [Front Mol Neurosci] 2025 Nov 05; Vol. 18, pp. 1634536. <i>Date of Electronic Publication: </i>2025 Nov 05 (<i>Print Publication: </i>2025).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101477914 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1662-5099 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216625099%22">16625099 </searchLink><i>NLM ISO Abbreviation: </i>Front Mol Neurosci <i>Subsets: </i>PubMed not MEDLINE
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