Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis.

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Title: Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis.
Authors: Burkhalter MD; Department of Experimental and Clinical Pharmacology and Pharmacogenomics, University of Tübingen, Tübingen, Germany.; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany., Sridhar A; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA., Sampaio P; CEDOC Chronic Diseases Research Center, NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisboa, Portugal., Jacinto R; CEDOC Chronic Diseases Research Center, NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisboa, Portugal., Burczyk MS; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany., Donow C; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany., Angenendt M; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany., Hempel M; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Walther P; Central Facility for Electron Microscopy, Ulm University, Ulm, Germany., Pennekamp P; Department of General Pediatrics, University Hospital Muenster, Muenster, Germany., Omran H; Department of General Pediatrics, University Hospital Muenster, Muenster, Germany., Lopes SS; CEDOC Chronic Diseases Research Center, NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisboa, Portugal., Ware SM; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA., Philipp M; Department of Experimental and Clinical Pharmacology and Pharmacogenomics, University of Tübingen, Tübingen, Germany.; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany.
Corporate Authors: Competence Network for Congenital Heart Defects Investigators
Source: The Journal of clinical investigation [J Clin Invest] 2019 May 16; Vol. 129 (7), pp. 2841-2855. Date of Electronic Publication: 2019 May 16.
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: 7802877 Publication Model: Electronic Cited Medium: Internet ISSN: 1558-8238 (Electronic) Linking ISSN: 00219738 NLM ISO Abbreviation: J Clin Invest Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis.
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  Data: <searchLink fieldCode="AU" term="%22Burkhalter+MD%22">Burkhalter MD</searchLink>; Department of Experimental and Clinical Pharmacology and Pharmacogenomics, University of Tübingen, Tübingen, Germany.; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Sridhar+A%22">Sridhar A</searchLink>; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.<br /><searchLink fieldCode="AU" term="%22Sampaio+P%22">Sampaio P</searchLink>; CEDOC Chronic Diseases Research Center, NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisboa, Portugal.<br /><searchLink fieldCode="AU" term="%22Jacinto+R%22">Jacinto R</searchLink>; CEDOC Chronic Diseases Research Center, NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisboa, Portugal.<br /><searchLink fieldCode="AU" term="%22Burczyk+MS%22">Burczyk MS</searchLink>; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Donow+C%22">Donow C</searchLink>; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Angenendt+M%22">Angenendt M</searchLink>; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Hempel+M%22">Hempel M</searchLink>; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.<br /><searchLink fieldCode="AU" term="%22Walther+P%22">Walther P</searchLink>; Central Facility for Electron Microscopy, Ulm University, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Pennekamp+P%22">Pennekamp P</searchLink>; Department of General Pediatrics, University Hospital Muenster, Muenster, Germany.<br /><searchLink fieldCode="AU" term="%22Omran+H%22">Omran H</searchLink>; Department of General Pediatrics, University Hospital Muenster, Muenster, Germany.<br /><searchLink fieldCode="AU" term="%22Lopes+SS%22">Lopes SS</searchLink>; CEDOC Chronic Diseases Research Center, NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisboa, Portugal.<br /><searchLink fieldCode="AU" term="%22Ware+SM%22">Ware SM</searchLink>; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.<br /><searchLink fieldCode="AU" term="%22Philipp+M%22">Philipp M</searchLink>; Department of Experimental and Clinical Pharmacology and Pharmacogenomics, University of Tübingen, Tübingen, Germany.; Institute of Biochemistry and Molecular Biology, Ulm University, Ulm, Germany.
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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>7802877 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1558-8238 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200219738%22">00219738 </searchLink><i>NLM ISO Abbreviation: </i>J Clin Invest <i>Subsets: </i>MEDLINE
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