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Skin progenitor cells contribute to bleomycin-induced skin fibrosis
Characterization of PTZ-induced seizure susceptibility in a down syndrome mouse model that overexpresses CSTB
Prmt2 regulates the lipopolysaccharide-induced responses in lungs and macrophages
Surveying the Down syndrome mouse model resource identifies critical regions responsible for chronic otitis media
Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndrome
Highly-efficient, fluorescent, locus directed cre and FlpO deleter mice on a pure C57BL/6N genetic background
Dyrk1A induces pancreatic beta cell mass expansion and improves glucose tolerance
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome
The in vivo Down syndrome genomic library in mouse
Standardized Post-Mortem Examination and Fixation Procedures for Mutant and Treated Mice
Cognition and hippocampal plasticity in the mouse is altered by monosomy of a genomic region implicated in Down syndrome
Pharmacological correction of excitation/inhibition imbalance in Down syndrome mouse models
Distinct fibroblast lineages determine dermal architecture in skin development and repair
Missense mutation in the second RNA binding domain reveals a role for Prkra (PACT/RAX) during skull development
The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model
Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy
LXR-Mediated ABCA1 Expression and Function Are Modulated by High Glucose and PRMT2

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