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Unpublished / Preprint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

Nociception in the Glycine Receptor Deficient Mutant Mouse Spastic (2022) Grömer TW, Triller A, Zeilhofer HU, Becker K, Eulenburg V, Becker CM Journal article Astrogenesis in the murine dentate gyrus is a life-long and dynamic process (2022) Schneider J, Weigel J, Wittmann MT, Svehla P, Ehrt S, Zheng F, Elmzzahi T, et al. Journal article The Putative Bromodomain Protein PfBDP7 of the Human Malaria Parasite Plasmodium Falciparum Cooperates With PfBDP1 in the Silencing of Variant Surface Antigen Expression (2022) Quinn J, Jeninga M, Limm K, Pareek K, Meißgeier T, Bachmann A, Duffy MF, Petter M Journal article Common RUNX3 missense variant contributes to psoriatic arthritis by modifying differentiation of CD8(+) T-cells (2022) Kerker I, Löhr S, Uebe S, Popp B, Vasileiou G, Bowes J, Kirchner P, et al. Conference contribution Metabotropic Glutamate Receptors at Ribbon Synapses in the Retina and Cochlea (2022) Klotz-Weigand LJ, Enz R Journal article, Review article Viroporins: Structure, function, and their role in the life cycle of SARS-CoV-2 (2022) Breitinger U, Farag NS, Sticht H, Breitinger HG Journal article, Review article Differential vulnerability of adult neurogenic niches to dosage of the neurodevelopmental-disorder linked gene Foxg1 (2022) Schäffner I, Wittmann MT, Vogel T, Lie DC Journal article The crystal structure of the varicella-zoster Orf24-Orf27 nuclear egress complex spotlights multiple determinants of herpesvirus subfamily specificity (2022) Schweininger J, Kriegel M, Häge S, Conrad M, Alkhashrom S, Lösing J, Weiler S, et al. Journal article Transcription factor Zfp276 drives oligodendroglial differentiation and myelination by switching off the progenitor cell program (2022) Aberle T, Piefke S, Hillgärtner S, Tamm ER, Wegner M, Küspert M Journal article Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly (2022) Kloeckner C, Murray JPF, Tavasoli M, Sticht H, Stoltenburg-Didinger G, Scholle LM, Bakhtiari S, et al. Journal article