about
MTO1-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 neurodegenerationAbnormal brain iron metabolism in Irp2 deficient mice is associated with mild neurological and behavioral impairmentsNeurobeachin, a regulator of synaptic protein targeting, is associated with body fat mass and feeding behavior in mice and body-mass index in humansCreatine improves health and survival of miceA broad phenotypic screen identifies novel phenotypes driven by a single mutant allele in Huntington's disease CAG knock-in mice.Genetic evidence for the adhesion protein IgSF9/Dasm1 to regulate inhibitory synapse development independent of its intracellular domainDll1 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 behaviourTransient neuromotor phenotype in transgenic spastic mice expressing low levels of glycine receptor beta-subunit: an animal model of startle disease.Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse linesLarge-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous systemA humanized version of Foxp2 affects cortico-basal ganglia circuits in miceGeneration 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 miceThe German Mouse Clinic: a platform for systemic phenotype analysis of mouse models.Mouse phenotyping.Innovations in phenotyping of mouse models in the German Mouse Clinic.Rapamycin extends murine lifespan but has limited effects on aging.Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice.Pleiotropic effects in Eya3 knockout mice.Mitochondrial dysfunction and decrease in body weight of a transgenic knock-in mouse model for TDP-43.Aberrant methylation of tRNAs links cellular stress to neuro-developmental disorders.Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant mice.MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention.Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathologyLife span extension by targeting a link between metabolism and histone acetylation in Drosophila.The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.Neuron-glia communication via EphA4/ephrin-A3 modulates LTP through glial glutamate transport.Systemic first-line phenotyping.Every-other-day feeding extends lifespan but fails to delay many symptoms of aging in mice.MiR-34a deficiency accelerates medulloblastoma formation in vivo.MIM-Induced Membrane Bending Promotes Dendritic Spine Initiation.The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing.Meis1: effects on motor phenotypes and the sensorimotor system in miceDJ-1-deficient mice show less TH-positive neurons in the ventral tegmental area and exhibit non-motoric behavioural impairments.
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Lore Becker
@ast
Lore Becker
@en
Lore Becker
@es
Lore Becker
@nl
Lore Becker
@sl
type
label
Lore Becker
@ast
Lore Becker
@en
Lore Becker
@es
Lore Becker
@nl
Lore Becker
@sl
prefLabel
Lore Becker
@ast
Lore Becker
@en
Lore Becker
@es
Lore Becker
@nl
Lore Becker
@sl
P106
P21
P31
P496
0000-0002-6890-4984
P569
2000-01-01T00:00:00Z