Kristin Moreth
Neuherberg, BY 85764, Germany
Last Updated: 09/26/2026
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Found 25 publications
Creld1 regulates myocardial development and function.
Journal: Journal of molecular and cellular cardiology
Published: December 05, 2020
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes.
Journal: Mammalian genome : official journal of the International Mammalian Genome Society
Published: October 23, 2019
The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice?
Journal: Biochemical and biophysical research communications
Published: July 30, 2018
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 gene.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: July 06, 2018
Biglycan is a new high-affinity ligand for CD14 in macrophages.
Journal: Matrix biology : journal of the International Society for Matrix Biology
Published: April 30, 2018
Mesenchymal TNFR2 promotes the development of polyarthritis and comorbid heart valve stenosis.
Journal: JCI insight
Published: November 27, 2017
Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse Clinic.
Journal: Behavioural brain research
Published: June 01, 2017
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant mice.
Journal: Journal of biomedical science
Published: March 03, 2017
The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.
Journal: G3 (Bethesda, Md.)
Published: November 06, 2016
Every-other-day feeding extends lifespan but fails to delay many symptoms of aging in mice.
Journal: Nature communications
Published: November 01, 2016
Serum Response Factor (SRF) Ablation Interferes with Acute Stress-Associated Immediate and Long-Term Coping Mechanisms.
Journal: Molecular neurobiology
Published: September 09, 2016
Last Updated: 09/26/2026