about
CIN85 regulates dopamine receptor endocytosis and governs behaviour in miceCardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms.Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics ProjectINFRAFRONTIER: a European resource for studying the functional basis of human diseasePrinciples and application of LIMS in mouse clinicsCIP2A Promotes T-Cell Activation and Immune Response to Listeria monocytogenes InfectionIn vivo functional requirement of the mouse Ifitm1 gene for germ cell development, interferon mediated immune response and somitogenesisMTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathy.Post-stroke inhibition of induced NADPH oxidase type 4 prevents oxidative stress and neurodegenerationUromodulin retention in thick ascending limb of Henle's loop affects SCD1 in neighboring proximal tubule: renal transcriptome studies in mouse models of uromodulin-associated kidney diseaseAbnormal brain iron metabolism in Irp2 deficient mice is associated with mild neurological and behavioral impairmentsPrdm5 regulates collagen gene transcription by association with RNA polymerase II in developing boneNeurobeachin, a regulator of synaptic protein targeting, is associated with body fat mass and feeding behavior in mice and body-mass index in humansA broad phenotypic screen identifies novel phenotypes driven by a single mutant allele in Huntington's disease CAG knock-in mice.Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processesThe mouse Trm1-like gene is expressed in neural tissues and plays a role in motor coordination and exploratory behavioureIF6 coordinates insulin sensitivity and lipid metabolism by coupling translation to transcriptionMissing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epitheliaRestless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalonDoes enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse linesMouse Phenotype Database Integration Consortium: integration [corrected] of mouse phenome data resourcesLarge-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous systemLoss of the actin remodeler Eps8 causes intestinal defects and improved metabolic status in miceInterplay between H1 and HMGN epigenetically regulates OLIG1&2 expression and oligodendrocyte differentiation.Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutationGeneration and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant MiceOverexpression of the mitochondrial methyltransferase TFB1M in the mouse does not impact mitoribosomal methylation status or hearing.Pleiotropic functions for transcription factor zscan10.A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.High mobility group N proteins modulate the fidelity of the cellular transcriptional profile in a tissue- and variant-specific manner.Requirement of the RNA-editing enzyme ADAR2 for normal physiology in miceMouse phenotyping.Innovations in phenotyping of mouse models in the German Mouse Clinic.Rapamycin extends murine lifespan but has limited effects on aging.A robust and reliable non-invasive test for stress responsivity in mice.Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.MausDB: an open source application for phenotype data and mouse colony management in large-scale mouse phenotyping projects.Pleiotropic effects in Eya3 knockout mice.An ENU mutagenesis-derived mouse model with a dominant Jak1 mutation resembling phenotypes of systemic autoimmune disease.Mechanisms controlling anaemia in Trypanosoma congolense infected mice.
P50
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P50
description
hulumtuese
@sq
onderzoeker
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researcher
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հետազոտող
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name
Valérie Gailus-Durner
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Valérie Gailus-Durner
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Valérie Gailus-Durner
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Valérie Gailus-Durner
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Valérie Gailus-Durner
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type
label
Valérie Gailus-Durner
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Valérie Gailus-Durner
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Valérie Gailus-Durner
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Valérie Gailus-Durner
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Valérie Gailus-Durner
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altLabel
Valerie Gailus-Durner
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Valérie Gailus-Durner
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Valérie Gailus-Durner
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Valérie Gailus-Durner
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Valérie Gailus-Durner
@nl
Valérie Gailus-Durner
@sl