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Skin progenitor cells contribute to bleomycin-induced skin fibrosis
Surveying the Down syndrome mouse model resource identifies critical regions responsible for chronic otitis media
Prmt2 regulates the lipopolysaccharide-induced responses in lungs and macrophages
Characterization of PTZ-induced seizure susceptibility in a down syndrome mouse model that overexpresses CSTB
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling 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
The in vivo Down syndrome genomic library in mouse
Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndrome
Standardized Post-Mortem Examination and Fixation Procedures for Mutant and Treated Mice
The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model
DYRK1A overexpression decreases plasma lecithin:cholesterol acyltransferase activity and apolipoprotein A-I levels
DYRK1A: a master regulatory protein controlling brain growth
LXR-Mediated ABCA1 Expression and Function Are Modulated by High Glucose and PRMT2
La révolution de la génomique fonctionnelle
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

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