Publications by authors named "Aleksandar Rakovic"

39Publications

Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?

Parkinsonism Relat Disord 2020 02 30;71:44-45. Epub 2020 Jan 30.

Edmond J. Safra Program in Parkinson's Disease and Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, Toronto, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2020.01.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109519PMC
February 2020

iPS models of Parkin and PINK1.

Biochem Soc Trans 2015 Apr;43(2):302-7

*Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.

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http://dx.doi.org/10.1042/BST20150010DOI Listing
April 2015

THAP1, the gene mutated in DYT6 dystonia, autoregulates its own expression.

Biochim Biophys Acta 2014 Nov 1;1839(11):1196-204. Epub 2014 Aug 1.

Sektion für Funktionelle Genetik am Institut für Humangenetik, University of Luebeck, Luebeck 23538, Germany.

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http://dx.doi.org/10.1016/j.bbagrm.2014.07.019DOI Listing
November 2014

Dichloroacetate prevents restenosis in preclinical animal models of vessel injury.

Nature 2014 May 20;509(7502):641-4. Epub 2014 Apr 20.

1] TSI-laboratory, University Heart Center Hamburg, Martinistraße 52, 20246 Hamburg, Germany [2] Cardiovascular Research Center Hamburg (CVRC) and DZHK (German Center for Cardiovascular Research), partner site Hamburg/Kiel/Luebeck, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany [3] Cardiovascular Surgery, University Heart Center Hamburg, Martinistraße 52, 20246 Hamburg, Germany [4] Department of Cardiothoracic Surgery and Stanford Cardiovascular Institute, Stanford University, 300 Pasteur Drive, Stanford, California 94305, USA.

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http://www.uniklinika.de/media/file/5423.FolienSchrepfer.pdf
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http://www.nature.com/doifinder/10.1038/nature13232
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http://dx.doi.org/10.1038/nature13232DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323184PMC
May 2014

ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome.

Neurobiol Aging 2012 Aug 31;33(8):1843.e1-7. Epub 2012 Jan 31.

Section of Clinical and Molecular Neurogenetics, Department of Neurology, University of Lübeck, Lübeck, Germany.

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http://linkinghub.elsevier.com/retrieve/pii/S019745801100580
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http://dx.doi.org/10.1016/j.neurobiolaging.2011.12.035DOI Listing
August 2012

PINK1-Interacting Proteins: Proteomic Analysis of Overexpressed PINK1.

Parkinsons Dis 2011 Mar 16;2011:153979. Epub 2011 Mar 16.

Section of Clinical and Molecular Neurogenetics, Department of Neurology, University of Lübeck, Maria-Goeppert-Straße 1, 23562 Lübeck, Germany.

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http://dx.doi.org/10.4061/2011/153979DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062077PMC
March 2011

Mutations in PINK1 and Parkin impair ubiquitination of Mitofusins in human fibroblasts.

PLoS One 2011 Mar 8;6(3):e16746. Epub 2011 Mar 8.

Section of Clinical and Molecular Neurogenetics, Department of Neurology, University of Lübeck, Lübeck, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0016746PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050809PMC
March 2011

Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.

Mov Disord 2010 Aug;25(11):1577-82

Section of Clinical and Molecular Neurogenetics, Department of Neurology, University of Luübeck, Luübeck, Germany.

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http://dx.doi.org/10.1002/mds.22857DOI Listing
August 2010

Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients.

Hum Mol Genet 2010 Aug 27;19(16):3124-37. Epub 2010 May 27.

Section of Clinical and Molecular Neurogenetics, Department of Neurology, University of Lübeck, 23562 Lübeck, Germany.

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http://hmg.oxfordjournals.org/content/19/16/3124.full.pdf
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http://www.hmg.oxfordjournals.org/cgi/doi/10.1093/hmg/ddq215
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http://dx.doi.org/10.1093/hmg/ddq215DOI Listing
August 2010

Allele-specific detection of C-1562T polymorphism in the matrix metalloproteinase-9 gene: genotyping by MADGE.

Clin Biochem 2006 Jun 3;39(6):630-2. Epub 2006 Feb 3.

Vinca Institute of Nuclear Sciences, Laboratory for Radiobiology and Molecular Genetics, PO Box 522, 11001 Belgrade, Serbia and Montenegro, UK.

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http://dx.doi.org/10.1016/j.clinbiochem.2006.01.005DOI Listing
June 2006