Georg Auburger

Klinik für Neurologie Goethe-Universität Frankfurt am Main, Germany 
"Georg Auburger"
Mean distance: 15.82 (cluster 11)
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Maletzko A, Key J, Wittig I, et al. (2021) Increased presence of nuclear DNAJA3 and upregulation of cytosolic STAT1 and of nucleic acid sensors trigger innate immunity in the ClpP-null mouse. Neurogenetics
Valek L, Tran B, Wilken-Schmitz A, et al. (2021) Prodromal sensory neuropathy in Pink1 SNCA double mutant Parkinson mice. Neuropathology and Applied Neurobiology
Auburger G, Graeber MB, Ptáček LJ. (2021) Welcoming articles on genotype-dependent clinical features and diagnostics. Neurogenetics
Torres-Odio S, Lei Y, Gispert S, et al. (2021) Loss of Mitochondrial Protease CLPP Activates Type I IFN Responses through the Mitochondrial DNA-cGAS-STING Signaling Axis. Journal of Immunology (Baltimore, Md. : 1950)
Rodriguez-Graña T, Rodríguez-Labrada R, Santana-Porbén S, et al. (2021) Weight loss is correlated with disease severity in Spinocerebellar ataxia type 2: a cross-sectional cohort study. Nutritional Neuroscience. 1-9
Canet-Pons J, Sen NE, Arsovic A, et al. (2021) Atxn2-CAG100-KnockIn mouse spinal cord shows progressive TDP43 pathology associated with cholesterol biosynthesis suppression. Neurobiology of Disease. 105289
Almaguer-Mederos LE, Pérez-Ávila I, Aguilera-Rodríguez R, et al. (2021) Body Mass Index Is Significantly Associated With Disease Severity in Spinocerebellar Ataxia Type 2 Patients. Movement Disorders : Official Journal of the Movement Disorder Society
Guzman-Parra J, Streit F, Forstner AJ, et al. (2021) Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families. Translational Psychiatry. 11: 31
Velázquez-Pérez L, Rodriguez-Labrada R, González-Garcés Y, et al. (2020) Prodromal Spinocerebellar Ataxia Type 2 Subjects Have Quantifiable Gait and Postural Sway Deficits. Movement Disorders : Official Journal of the Movement Disorder Society
Key J, Sen NE, Arsović A, et al. (2020) Systematic Surveys of Iron Homeostasis Mechanisms Reveal Ferritin Superfamily and Nucleotide Surveillance Regulation to be Modified by PINK1 Absence. Cells. 9
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