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Experimental Neurology|May 31, 2008
Parkinson patient fibroblasts show increased alpha-synuclein expressionHans-Hermann Hoepken, Suzana Gispert, Mekhman Azizov, et al.
European Journal of Human Genetics : EJHG|May 8, 2014
Genome-wide UPD screening in patients with intellectual disabilityChristopher Schroeder, Arif Bülent Ekici, Ute Moog, et al.
International Journal of Medical Microbiology : IJMM|December 15, 2016
Influence of Platelet-rich Plasma on the immune response of human monocyte-derived dendritic cells and macrophages stimulated with Aspergillus fumigatusKristin Czakai, Marcus Dittrich, Martin Kaltdorf, et al.
American Journal of Medical Genetics. Part A|January 19, 2010
Four unrelated patients with Lubs X-linked mental retardation syndrome and different Xq28 duplicationsOliver Bartsch, Konstanze Gebauer, Stanislav Lechno, et al.
Investigative Ophthalmology & Visual Science|August 30, 2011
Gene expression profiling of the retina after transcorneal electrical stimulation in wild-type Brown Norway ratsGabriel Willmann, Karin Schäferhoff, Manuel D Fischer, et al.
Molecular and Cellular Probes|November 13, 2012
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissectionsUshanthine Kathiravel, Britta Keyser, Sabine Hoffjan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 13, 2007
Nuclear localization of ataxin-3 is required for the manifestation of symptoms in SCA3: in vivo evidenceUlrike Bichelmeier, Thorsten Schmidt, Jeannette Hübener, et al.
Human Molecular Genetics|May 27, 2008
Sex differences in a transgenic rat model of Huntington's disease: decreased 17beta-estradiol levels correlate with reduced numbers of DARPP32+ neurons in malesFelix J Bode, Michael Stephan, Hendrik Suhling, et al.
International Journal of Cancer|March 26, 2013
Engraftment of low numbers of pediatric acute lymphoid and myeloid leukemias into NOD/SCID/IL2Rcγnull mice reflects individual leukemogenecity and highly correlates with clinical outcomeJeanette Woiterski, Martin Ebinger, Kai E Witte, et al.
European Journal of Human Genetics : EJHG|February 18, 2011
De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardationUte Grasshoff, Michael Bonin, Ina Goehring, et al.
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