Wolfgang Hans

Neuherberg, BY 85764, Germany

Last Updated: 09/26/2026

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Found 33 publications

A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes.

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?

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.

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

Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data.

Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data.

Journal: PLoS biology

Published: December 04, 2017

Genetic and Molecular Insights Into Genotype-Phenotype Relationships in Osteopathia Striata With Cranial Sclerosis (OSCS) Through the Analysis of Novel Mouse Wtx Mutant Alleles.

Genetic and Molecular Insights Into Genotype-Phenotype Relationships in Osteopathia Striata With Cranial Sclerosis (OSCS) Through the Analysis of Novel Mouse Wtx Mutant Alleles.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Published: June 30, 2017

Fgf9 Y162C Mutation Alters Information Processing and Social Memory in Mice.

Fgf9 Y162C Mutation Alters Information Processing and Social Memory in Mice.

Journal: Molecular neurobiology

Published: January 16, 2017

The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.

The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.

Journal: G3 (Bethesda, Md.)

Published: November 06, 2016

Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation.

Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation.

Journal: Mammalian genome : official journal of the International Mammalian Genome Society

Published: June 27, 2016

Hyperoxaluria Requires TNF Receptors to Initiate Crystal Adhesion and Kidney Stone Disease.

Hyperoxaluria Requires TNF Receptors to Initiate Crystal Adhesion and Kidney Stone Disease.

Journal: Journal of the American Society of Nephrology : JASN

Published: April 27, 2016

Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant Mice.

Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant Mice.

Journal: PloS one

Published: November 20, 2015

Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.

Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.

Journal: Mammalian genome : official journal of the International Mammalian Genome Society

Published: October 01, 2015

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.

Journal: Nature genetics

Published: February 02, 2015

Showing 1-12 of 33

Last Updated: 09/26/2026