Sabine M. Hölter
Helmholtz Zentrum München Institut für Entwicklungsgenetik
79 papers found
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AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease
UploadKnockout mouse models as a resource for the study of rare diseases
UploadParkinson's disease motor symptoms rescue by CRISPRa‐reprogramming astrocytes into GABAergic neurons
Download from doi.orgPost-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk
Download from doi.orgCharacterising a homozygous two‐exon deletion in UQCRH : comparing human and mouse phenotypes
Download from doi.orgDose-dependent long-term effects of a single radiation event on behaviour and glial cells
UploadDusp8 affects hippocampal size and behavior in mice and humans
Download from www.nature.comGeneration and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant Mice
Download from doi.orgSLIRP Regulates the Rate of Mitochondrial Protein Synthesis and Protects LRPPRC from Degradation
Download from doi.orgMIM-Induced Membrane Bending Promotes Dendritic Spine Initiation
UploadMTO1-Deficient Mouse Model Mirrors the Human Phenotype Showing Complex I Defect and Cardiomyopathy
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