Institut für Biochemie


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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Unpublished / Preprint

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Abstract

Journal

Cardiac outflow tract development relies on the complex function of Sox4 and Sox11 in multiple cell types (2014) Paul M, Harvey RP, Wegner M, Sock E Journal article The influence of pre-analytical conditions on platelet-derived microparticles (2014) Eckstein F, Xiang W, Weiss DR, Zimmermann R, Strasser EF Journal article Autophagy modulates SNCA/?-synuclein release, thereby generating a hostile microenvironment (2014) Pöhler AM, Xiang W, Spitzer P, May VEL, Meixner H, Rockenstein E, Chutna O, et al. Journal article The conformational stability of nonfibrillar amyloid-β peptide oligomers critically depends on the C-terminal peptide length (2014) Socher E, Sticht H, Horn A Journal article, Original article In vivo targeting of adult neural stem cells in the dentate gyrus by a split-cre approach (2014) Beckervordersandforth R, Deshpande A, Schäffner I, Huttner H, Lepier A, Lie DC, Goetz M Journal article The Ca2+ sensor protein swiprosin-1/EFhd2 is present in neurites and involved in kinesin-mediated transport in neurons (2014) Purohit P, Perez-Branguli F, Prots I, Borger E, Gunn-Moore F, Welzel O, Loy K, et al. Journal article ?-Synuclein impairs oligodendrocyte progenitor maturation in multiple system atrophy (2014) May VEL, Ettle B, Pöhler AM, Nuber S, Ubhi K, Rockenstein E, Winner B, et al. Journal article MRTF-A controls vessel growth and maturation by increasing the expression of CCN1 and CCN2 (2014) Hinkel R, Trenkwalder T, Petersen B, Husada W, Gesenhues F, Lee S, Hannappel E, et al. Journal article Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia (2014) Perez-Branguli F, Mishra HK, Prots I, Havlicek S, Kohl Z, Saul D, Rummel C, et al. Journal article Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations (2014) Basel-Vanagaite L, Yilmaz R, Tang S, Reuter M, Rahner N, Grange DK, Mortenson M, et al. Journal article