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PRECISION PATHOBIOLOGY FOR DISEASE MODELS (PATHBIO)
MODEL MATCHMAKING VIA THE RARE DISEASES MODELS & MECHANISMS NETWORK (RDMM-EUROPE)
FROM MOUSE TO HUMAN: DECIPHERING NEURODEVELOPMENTAL ANOMALIES
MOLECULAR AND BEHAVIORAL CHARACTERIZATION OF A NOVEL MOUSE MODEL OF SNYDER-ROBINSON SYNDROME: A PATH TOWARDS THERAPEUTIC DEVELOPMENT
DdCBE Mediates Efficient and Inheritable Modifications in Mouse Mitochondrial Genome
CULLIN4 REGULATES COLORECTAL CANCER EXPANSION THROUGH THE MODULATION OF INTRACELLULAR SMAD3 TRAFFICKING
TAFAZZIN DEFICIENCY IMPAIRS MITOCHONDRIAL METABOLISM AND FUNCTION OF LIPOPOLYSACCHARIDE ACTIVATED B LYMPHOCYTES IN MICE
Ensuring global access to IMPC-generated mouse resources distributed by US public repositories
Revealing Candidate Inherited Retinal Disorder Genes through Genome-wide Screening of Knockout Mice
IDENTIFICATION OF SUBTLE PHENO-DEVIANTS SUGGESTS Zic2-ASSOCIATED HPE-PHENOTYPES ARE SEMI-DOMINANT AND INFLUENCED BY GENETIC MODIFIERS
NORMAL VS. ABNORMAL: LOOKING FOR BORDER VALUE IN CT SCANS OF MOUSE SKULLS
NEUROBIOLOGY & BEHAVIOUR UNIT SERVICE AT CZECH CENTRE FOR PHENOGENOMICS
Potential new therapies targeting NSCLC heterogeneity
STANDARDIZED BEHAVIORAL CHARACTERIZATION OF MOUSE MODELS OF GENETIC DISEASES WITH INTELLECTUAL DISABILITIES
CHARACTERIZATION OF THE ROLE OF NON-CANONICAL POLY A POLYMERASE TENT5A IN MINERALIZE TISSUES.
PRECISE LOW INVASIVE ORTHOTOPIC PLACEMENT OF CARCINOMA CELLS INTO THE MOUSE MAMMARY FAT PAD USING TRANSILLUMINATION
LACE1 DEFICIENCY ACCERLERATES BROWNING OF INGUINAL WHITE ADIPOSE TISSUE IN MICE
FUNCTIONAL CHARACTERIZATION OF NONCODING CIRCULAR RNAS IN MOUSE GENOME
BIOIMAGING & EMBRYOLOGY UNIT OF CZECH CENTRE FOR PHENOGENOMICS
Long-term effects of low-dose radiation on behavior and hippocampal microglial morphotypes in mice
LIVE MOUSE TRACKER: A TOOL TO PROFILE SOCIAL BEHAVIORS AT THE INDIVIDUAL LEVEL IN MICE LIVING IN A GROUP
PHENOTYPING AND PRECLINICAL STUDIES IN THE MOUSE MODEL AT PHENOMIN-ICS
ASCC2 AS A NOVEL REGULATOR OF CARDIAC DEVELOPMENT
TWENTY-ONE-COLOR FULL SPECTRUM FLOW CYTOMETRY PANEL FOR IMPC IMMUNOPHENOTYPING OF MAJOR CELL SUBSETS IN MOUSE SPLEEN
UTILIZATION OF CLINICAL CHEMISTRY ASSAY PANELS FOR PHENOTYPING MOUSE MODELS AT THE CCP
Uncovering the dosage-dependent roles of Arid1a in gastric tumorigenesis for combinatorial drug therapy
GENERATION OF ANIMAL MODELS (MOUSE OR RAT) OF RARE DISEASES AT PHENOMIN-ICS
CELPHEDIA, the French national reference infrastructure for animal research on rare diseases.
TOUCH SCREEN POTENTIALS FOR EVALUATION OF COGNITIVE ABILITIES
CCP VALIDATION OF BODY COMPOSITION MODEL FOR ADULT MOUSE FOR IMPC
PATERNAL MITOCHONDRIA ARE IMPORTANT FOR OFFSPRING METABOLIC HEALTH
DISRUPTION OF PATERNAL CIRCADIAN RHYTHM AFFECTS METABOLIC HEALTH IN MALE OFFSPRING VIA NONGERM CELL FACTORS
New “Histo3D” HREM-based imaging system for Qualitative and Quantitative Data in phenotyping Altered Embryos and Adult Mice
SECOND LINE PHENOTYPING TO CHARACTERIZE A SPONTANEOUS DEGENERATIVE MITRAL VALVE DISEASE IN FVB MICE
Biochemical, histological and behavioral characterization of a new mouse model of Niemann-Pick C2 disease
Predicting early lethal genes in the mouse
LIPIDOMIC AND METABOLOMIC ANALYSIS OF HYPERBILIRUBINEMIC PLASMA
INVESTIGATING REPLICATION REPAIR DEFICIENT TUMOURS USING GENETIC DRIVERS IN MOUSE MODELS
Myelin regulatory factor is required for mouse embryonic development
A PILOT HAPLO-ESSENTIAL PHENOTYPING PIPELINE
SEMA4D DEFICIENCY IMPROVED METABOLIC PHENOTYPE THROUGH IMMATURE B CELL DEVELOPMENT IN DIET-INDUCD OBESITY
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