Oliver Brandau

Oliver Brandau

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Oliver Brandau

Oliver Brandau

Publications by authors named "Oliver Brandau"

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30Publications

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De novo mutation of emopamil binding protein () gene in a girl with Conradi-Hünermann-Happle syndrome.

Clin Case Rep 2019 Aug 28;7(8):1522-1525. Epub 2019 Jun 28.

Department of Dermatology Medical University of Vienna Vienna Austria.

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http://dx.doi.org/10.1002/ccr3.2213DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692985PMC
August 2019

A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature.

J Appl Genet 2019 May 1;60(2):151-162. Epub 2019 Feb 1.

Department of Pediatrics, University of Szeged, Temesvári krt. 35-37, Szeged, 6726, Hungary.

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http://dx.doi.org/10.1007/s13353-019-00486-yDOI Listing
May 2019

Novel causative variants in patients with achromatopsia.

Ophthalmic Genet 2018 12 5;39(6):678-683. Epub 2018 Oct 5.

e King Khaled Eye Specialist Hospital , Vitreoretinal Division , Riyadh , Saudi Arabia.

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https://www.tandfonline.com/doi/full/10.1080/13816810.2018.1
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http://dx.doi.org/10.1080/13816810.2018.1522653DOI Listing
December 2018

Schmerzhafte Knoten.

J Dtsch Dermatol Ges 2016 Jun;14(6):627-629

Abteilung für Allgemeine Dermatologie und Dermato-Onkologie, Universitätsklinik für Dermatologie, Medizinische Universität Wien.

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http://dx.doi.org/10.1111/ddg.12923_gDOI Listing
June 2016

Painful nodules.

J Dtsch Dermatol Ges 2016 Jun;14(6):627-629

Division of General Dermatology and Dermatooncology, Department of Dermatology, Medical University Vienna, Vienna, Austria.

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http://dx.doi.org/10.1111/ddg.12923DOI Listing
June 2016

A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis-lymphedema-telangiectasia syndrome by Whole Exome Sequencing.

Mol Cell Probes 2016 Feb 26;30(1):18-21. Epub 2015 Nov 26.

Centre for Arab Genomic Studies, Dubai, United Arab Emirates. Electronic address:

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http://dx.doi.org/10.1016/j.mcp.2015.11.005DOI Listing
February 2016

Distal myosin heavy chain-7 myopathy due to the novel transition c.5566G>A (p.E1856K) with high interfamilial cardiac variability and putative anticipation.

Neuromuscul Disord 2014 Aug 4;24(8):721-5. Epub 2014 Jun 4.

Institute of Medical Genetics, Medical University of Vienna, Währinger Strasse 10, 1090 Vienna, Austria.

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http://dx.doi.org/10.1016/j.nmd.2014.05.010DOI Listing
August 2014

Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompaction.

Int J Cardiol 2014 May 15;173(3):532-5. Epub 2014 Mar 15.

Centre for Medical Research, University of Western Australia and Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands, Western Australia 6009, Australia.

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http://dx.doi.org/10.1016/j.ijcard.2014.03.025DOI Listing
May 2014

Amniotic fluid stem cells to study mTOR signaling in differentiation.

Organogenesis 2012 Jul-Sep;8(3):96-100. Epub 2012 Jul 1.

Medical Genetics, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.4161/org.22038DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527322PMC
July 2013

Complete loss of murine Xin results in a mild cardiac phenotype with altered distribution of intercalated discs.

Cardiovasc Res 2010 Mar 19;85(4):739-50. Epub 2009 Oct 19.

Department of Molecular Cell Biology, Institute for Cell Biology, University of Bonn, Ulrich-Haberland-Str. 61a, Bonn D-53121, Germany.

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https://academic.oup.com/cardiovascres/article-lookup/doi/10
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http://dx.doi.org/10.1093/cvr/cvp345DOI Listing
March 2010

Murine CXCL14 is dispensable for dendritic cell function and localization within peripheral tissues.

Mol Cell Biol 2007 Feb 27;27(3):983-92. Epub 2006 Nov 27.

Department of Medical Biochemistry and Immunology, Henry Wellcome Building, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, United Kingdom.

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http://dx.doi.org/10.1128/MCB.01648-06DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1800689PMC
February 2007

ESAM supports neutrophil extravasation, activation of Rho, and VEGF-induced vascular permeability.

J Exp Med 2006 Jul 3;203(7):1671-7. Epub 2006 Jul 3.

Max-Planck-Institute for Molecular Biomedicine and Institute of Cell Biology, University of Münster, D-48149 Münster, Germany.

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http://dx.doi.org/10.1084/jem.20060565DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118342PMC
July 2006

Tenomodulin is necessary for tenocyte proliferation and tendon maturation.

Mol Cell Biol 2005 Jan;25(2):699-705

Max Planck Institute for Biochemistry, Department of Molecular Medicine, Am Klopferspitz 18, 82152 Martinsried, Germany.

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http://dx.doi.org/10.1128/MCB.25.2.699-705.2005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC543433PMC
January 2005

The murine Ten-m/Odz genes show distinct but overlapping expression patterns during development and in adult brain.

Gene Expr Patterns 2003 Aug;3(4):397-405

Department of Experimental Pathology, Lund University, 22185 Lund, Sweden.

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http://dx.doi.org/10.1016/s1567-133x(03)00087-5DOI Listing
August 2003

PINCH2 is a new five LIM domain protein, homologous to PINCHand localized to focal adhesions.

Exp Cell Res 2003 Apr;284(2):239-50

Max Planck Institute for Biochemistry, Department of Molecular Medicine, Martinsried, Germany.

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http://dx.doi.org/10.1016/s0014-4827(02)00039-3DOI Listing
April 2003

Genomic organization of profilin-III and evidence for a transcript expressed exclusively in testis.

Gene 2002 Jan;283(1-2):219-25

Department of Experimental Pathology, Lund University, S-22185, Lund, Sweden.

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http://dx.doi.org/10.1016/s0378-1119(01)00855-1DOI Listing
January 2002