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Lehrstuhl für Humangenetik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Institute of Human Genetics
Overview
Publications
(514)
Research Grants
(37)
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Journal article
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Mutations in IL36RN in patients with generalized pustular psoriasis (2013)
Koerber A, Moessner R, Renner R, Sticht H, Wilsmann-Theis D, Schulz P, Sticherling M, et al.
Journal article
Biallelic SEMA3A defects cause a novel type of syndromic short stature (2013)
Hofmann K, Zweier M, Sticht H, Zweier C, Wittmann W, Hoyer J, Uebe S, et al.
Journal article
Role of α-synuclein in adult neurogenesis and neuronal maturation in the dentate gyrus. (2012)
Winner B, Regensburger M, Prots I, Winkler J
Journal article
α-Synuclein induces alterations in adult neurogenesis in Parkinson disease models via p53-mediated repression of Notch1. (2012)
Desplats P, Spencer B, Crews L, Pathel P, Morvinski-Friedmann D, Kosberg K, Roberts S, et al.
Journal article
LRRK2 knockout mice have an intact dopaminergic system but display alterations in exploratory and motor co-ordination behaviors. (2012)
Winner B, Prots I, Hinkle KM, Yue M, Bahareh B, Dächsel JC, Lincoln SJ, et al.
Journal article, Review article
Patients with unstable angina pectoris show an increased frequency of the Fc gamma RIIa R131 allele (2012)
Raaz-Schrauder D, Ekici AB, Munoz LE, Klinghammer L, Voll RE, Leusen JH, Van De Winkel JG, et al.
Journal article
Fluoxetine rescues impaired hippocampal neurogenesis in a transgenic A53T synuclein mouse model. (2012)
Kohl Z, Winner B, Ubhi K, Rockenstein E, Mante M, Muench M, Barlow C, et al.
Journal article
Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein (2012)
May VEL, Nuber S, Marxreiter F, Riess O, Winner B, Winkler J
Journal article
Variants in ASB10 are associated with open-angle glaucoma (2012)
Pasutto F, Keller KE, Weisschuh N, Sticht H, Samples JR, Yang YF, Zenkel M, et al.
Journal article
Functional null mutations in the gonosomal homologue gene TBL1Y are associated with non-syndromic coarctation of the aorta (2012)
Tagariello A, Breuer C, Birkner Y, Schmidt S, Koch AM, Cesnjevar R, Rueffer A, et al.
Journal article
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