Genome-wide expression profiling analysis of a Hmgn2 and Hmgn1/2 double knock out mutant mouse model

A recessive point mutation is responsible for pleiotropic effects in a scube3 mutant mouse

Transcriptome analysis of Cox4-2 knockout mice after OVA challenge

Transcriptome analysis of Prdm11 knockout mice after OVA challenge

Cancerous inhibitor of Protein Phosphatase 2A is a novel cell-autonomous regulator governing both T-and B-cell activation in vivo

Mildly compromised tetrahydrobiopterin biosynthesis mouse mutants exhibit abnormal body fat distribution and abdominal obesity

Genome-wide expression profiling analysis of a time course of differentiating adipocytes

Uncoupling Malt1 threshold function from paracaspase activity results in destructive autoimmune inflammation

Jag1K295*/+ as a mouse model for Alagille syndrome

Uromodulin-retention in thick ascending limb affects SCD1 in neighboring S3 proximal tubule in males: transcriptome studies in mouse models of Uromodulin-associated kidney disease

MiR-34a is dispensable for normal development but its loss accelerates medulloblastoma formation

Mice lacking DUF1220 protein domains are hyperactive  and show reduced fecundity

Genome-wide expression profiling analysis of the Ali35 mutant mouseline carrying a mutation in the Shc2 gene

ENU derived mouse line AEA001: A model for osteoporosis carrying a mutation in Ednra

Decrease of Parkin and CD36 expression and body weight correlate with an increase of non-esterified fatty acids in a mouse model for TDP-43 pathology

IFIT2 mediates IFN signaling

Generation and standardized, systemic phenotypic analysis of Kctd1 mutant mice

ENU mutagenesis derived Ednray129F-/- mice as a new model for human velocardiofacial syndrome/DiGeorg syndrome (VCFS/DGS)

Peroxidasin is essential for eye development

Differential Kinetics of Antigen Dependency of CD4+ and CD8+ T Cells