Prof. Dr. Heinrich Sticht



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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Unpublished / Preprint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

From
To

Abstract

Journal

Confirmation of mutations inPROSCas a novel cause of vitamin B 6 -dependent epilepsy (2017) Plecko B, Zweier M, Begemann A, Mathis D, Schmitt B, Striano P, Baethmann M, et al. Journal article Role of the N-terminus for the stability of an amyloid-β fibril with three-fold symmetry (2017) Söldner C, Sticht H, Horn A Journal article Protective capacity of neutralizing and non-neutralizing antibodies against glycoprotein B of cytomegalovirus (2017) Bootz A, Karbach A, Spindler J, Kropff B, Reuter N, Sticht H, Winkler T, et al. Journal article Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation (2017) Asadollahi R, Zweier M, Gogoll L, Schiffmann R, Sticht H, Steindl K, Rauch A Journal article Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID (2017) Redler S, Strom TM, Wieland T, Cremer K, Engels H, Distelmaier F, Schaper J, et al. Journal article AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability (2017) Brechet A, Buchert R, Schwenk J, Boudkkazi S, Zolles G, Siquier-Pernet K, Schaber I, et al. Journal article Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and Microcephaly (2017) Tawamie H, Martianov I, Wohlfahrt N, Buchert R, Mengus G, Uebe S, Janiri L, et al. Journal article Crystal Structure of the Extracellular Domain of the Human Dendritic Cell Surface Marker CD83 (2017) Heilingloh C, Klingl S, Egerer-Sieber C, Schmid B, Weiler S, Mühl-Zürbes P, Hofmann J, et al. Journal article, Original article Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders (2017) Reuter M, Tawamie H, Buchert R, Gebril OH, Froukh T, Thiel C, Uebe S, et al. Journal article Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes (2017) Sighart R, Rech J, Hueber A, Blank N, Löhr S, Reis A, Sticht H, Hüffmeier U Journal article