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Plos One|March 4, 2014
Impairment of Drosophila orthologs of the human orphan protein C19orf12 induces bang sensitivity and neurodegenerationArcangela Iuso, Ody C M Sibon, Matteo Gorza, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|May 4, 2010
Clinical implementation of volumetric intensity-modulated arc therapy (VMAT) with ERGO++Dirk Wolff, Florian Stieler, Brigitte Hermann, et al.
Clinical & Translational Immunology|January 17, 2017
High thioredoxin-1 levels in rheumatoid arthritis patients diminish binding and signalling of the monoclonal antibody TregalizumabKatharina Heim, Benjamin Dälken, Stefanie Faust, et al.
Acta Neuropathologica|May 5, 2011
Expression analysis of dopaminergic neurons in Parkinson's disease and aging links transcriptional dysregulation of energy metabolism to cell deathMatthias Elstner, Christopher M Morris, Katharina Heim, et al.
European Journal of Human Genetics : EJHG|June 14, 2012
Impact of common regulatory single-nucleotide variants on gene expression profiles in whole bloodDivya Mehta, Katharina Heim, Christian Herder, et al.
Immunology and Cell Biology|December 17, 2014
A specific CD4 epitope bound by tregalizumab mediates activation of regulatory T cells by a unique signaling pathwayBianca Helling, Martin König, Benjamin Dälken, et al.
European Journal of Human Genetics : EJHG|August 30, 2012
Dilution of candidates: the case of iron-related genes in restless legs syndromeKonrad Oexle, Barbara Schormair, Janina S Ried, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 2, 2010
Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performanceGeorg Winterer, Kirstin Mittelstrass, Ina Giegling, et al.
American Journal of Human Genetics|October 11, 2011
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulationMonika B Hartig, Arcangela Iuso, Tobias Haack, et al.
Atherosclerosis|August 8, 2009
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery diseasePatrick Linsel-Nitschke, Jörg Heeren, Zouhair Aherrahrou, et al.
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