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Olson-Lorin

Skeletal stem cell fate defects caused by Pdgfrb activating mutation.

Sweet Dre-ams about intersectional genetics.

Mosaic Mutant Analysis Identifies PDGFRα/PDGFRβ as Negative Regulators of Adipogenesis.

Fibroblast-specific Stat1 deletion enhances the myofibroblast phenotype during tissue repair.

Dysregulated mesenchymal PDGFR-β drives kidney fibrosis.

Complementary Wnt Sources Regulate Lymphatic Vascular Development via PROX1-Dependent Wnt/β-Catenin Signaling.