Sabine Maria Hölter

25PUBLICATIONS
179CO-AUTHORS
Neurology and neuromuscular diseasesBiomolecular modelling and designEpigenetics (incl. genome methylation and epigenomics)Molecular targetsCellular nervous system
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Publications (25)

|Nov 01, 2025
Neuropathy-associated Tecpr2 mutation knock-in mice reveal endolysosomal loss of function phenotypes in neurons and microglia.

Debjani Bhattacharya, Patricia da Silva-Buttkus, Karsten Nalbach

|Jan 23, 2025
Muscarinic receptor agonists and positive allosteric modulators in animal models of psychosis: protocol for a systematic review and meta-analysis.

Spyridon Siafis, Nobuyuki Nomura, Johannes Schneider-Thoma

|Dec 05, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes.

Tim P Hasenbein, Sarah Hoelzl, Zachary D Smith

|Jun 18, 2024
Comparative Phenotyping of Mice Reveals Canonical and Noncanonical Physiological Functions of TRα and TRβ.

Georg Sebastian Hönes, Daniela Geist, Christina Wenzek

|May 24, 2024
A brain-enriched circular RNA controls excitatory neurotransmission and restricts sensitivity to aversive stimuli.

Sebastian A Giusti, Natalia S Pino, Camila Pannunzio

|Feb 05, 2024
A patient-enriched MEIS1 coding variant causes a restless legs syndrome-like phenotype in mice.

Chia-Luen Leu, Daniel D Lam, Aaro V Salminen

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Frequent Collaborators

13 joint publications

Martin Hrabé de Angelis

9 joint publications

Valerie Gailus-Durner

9 joint publications

Lore Becker

8 joint publications

Helmut Fuchs