Rheinische Friedrich-Wilhelms-Universität Bonn

University / College


Location: Bonn, Germany (DE) DE

ISNI: 0000000122403300

ROR: https://ror.org/041nas322

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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Abstract

Journal

In vivo characterization of human myofibrillar myopathy genes in zebrafish (2015) Buehrdel JB, Hirth S, Kessler M, Westphal S, Forster M, Manta L, Wiche G, et al. Journal article Sequence-specific activation of the DNA sensor cGAS by Y-form DNA structures as found in primary HIV-1 cDNA (2015) Herzner AM, Hagmann CA, Goldeck M, Wolter S, Kuebler K, Wittmann S, Gramberg T, et al. Journal article Cranial and cerebral signs in the diagnosis of spina bifida between 18 and 22 weeks of gestation: a German multicentre study (2015) Bahlmann F, Reinhard I, Schramm T, Geipel A, Gembruch U, Von Kaisenberg CS, Schmitz R, et al. Journal article Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8 (2015) Boycott KM, Beaulieu CL, Kernohan KD, Gebril OH, Mhanni A, Chudley AE, Redl D, et al. Journal article Evidence-based health services research--a short review and implications (2015) Grässel E, Donath C, Hollederer A, Drexler H, Kornhuber J, Zobel A, Kolominsky-Rabas P Journal article Myofibrillar instability exacerbated by acute exercise in filaminopathy (2015) Chevessier F, Schuld J, Orfanos Z, Plank AC, Wolf L, Maerkens A, Unger A, et al. Journal article Subjective cognitive decline is related to CSF biomarkers of AD in patients with MCI (2015) Wolfsgruber S, Jessen F, Koppara A, Kleineidam L, Schmidtke K, Froelich L, Kurz A, et al. Journal article Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome (2015) Kuechler A, Zink AM, Wieland T, Luedecke HJ, Cremer K, Salviati L, Magini P, et al. Journal article Gaps Between Aims and Achievements in Therapeutic Modification of Neuronal Damage ("Neuroprotection") (2015) Wiendl H, Elger C, Foerstl H, Hartung HP, Oertel W, Reichmann H, Schwab S Journal article A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis (2015) Buch S, Stickel F, Trepo E, Way M, Herrmann A, Nischalke HD, Brosch M, et al. Journal article