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The mammalian gene function resource: the International Knockout Mouse ConsortiumMouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics ProjectReciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication SyndromesRepression of osteoblast maturation by ERRα accounts for bone loss induced by estrogen deficiencyThe cell proliferation antigen Ki-67 organises heterochromatinAnalysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinicsConditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegenerationHyperactivation of Alk induces neonatal lethality in knock-in AlkF1178L miceA mu-delta opioid receptor brain atlas reveals neuronal co-occurrence in subcortical networks.Rfx6 maintains the functional identity of adult pancreatic β cells.Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction.Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss.Site-specific recombinases for manipulation of the mouse genome.Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.Efficient and rapid generation of large genomic variants in rats and mice using CRISMEREDeciphering the Role of Oncogenic MITFE318K in Senescence Delay and Melanoma Progression.Modeling human disease in rodents by CRISPR/Cas9 genome editing.GDNF acts through PEA3 to regulate cell body positioning and muscle innervation of specific motor neuron pools.Influence of growth factors on neuronal differentiation.Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.Myeloproliferative neoplasm induced by constitutive expression of JAK2V617F in knock-in mice.Nox4 genetic inhibition in experimental hypertension and metabolic syndrome.Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse.Biochemical and immunohistochemical studies with specific polyclonal antibodies directed against bovine myelin/oligodendrocyte glycoprotein.A study of the potential of the embryonic rat telencephalon to generate oligodendrocytes.Absence of TI-VAMP/Vamp7 leads to increased anxiety in mice.Etr-r3/mNapor, encoding an ELAV-type RNA binding protein, is expressed in differentiating cells in the developing rodent forebrain.Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy.Highly-efficient, fluorescent, locus directed cre and FlpO deleter mice on a pure C57BL/6N genetic background.Developmental expression of the C1G5F2 antigen in cultured rat oligodendroglial cells.A new mouse model of ARX dup24 recapitulates the patients' behavioural and fine motor alterations.Counterregulation between thymic stromal lymphopoietin– and IL-23–driven immune axes shapes skin inflammation in mice with epidermal barrier defectsCharacterization and Validation of Cre-Driver Mouse LinesReg-2 is a motoneuron neurotrophic factor and a signalling intermediate in the CNTF survival pathwayThe Regulation of the Expression, Phosphorylation, and Protein Associations of pp125FAKduring Rat Brain DevelopmentA new oligodendrocyte specific plasma membrane surface protein identified by a monoclonal antibody produced in vitroCbs overdosage is necessary and sufficient to induce cognitive phenotypes in mouse models of Down syndrome and interacts genetically with Dyrk1aTUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesisSevere head dysgenesis resulting from imbalance between anterior and posterior ontogenetic programsTransgenic mouse models expressing human and macaque prion protein exhibit similar prion susceptibility on a strain-dependent manner
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description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Marie-Christine Birling
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Marie-Christine Birling
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Marie-Christine Birling
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Marie-Christine Birling
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Marie-Christine Birling
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type
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Marie-Christine Birling
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Marie-Christine Birling
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Marie-Christine Birling
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Marie-Christine Birling
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Marie-Christine Birling
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prefLabel
Marie-Christine Birling
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Marie-Christine Birling
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Marie-Christine Birling
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Marie-Christine Birling
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Marie-Christine Birling
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P106
P21
P31
P496
0000-0002-3372-8108