Integrin-alpha9 is required for fibronectin matrix assembly during lymphatic valve morphogenesis. Read more about Integrin-alpha9 is required for fibronectin matrix assembly during lymphatic valve morphogenesis.
Essential role of TGF-beta signaling in glucose-induced cell hypertrophy. Read more about Essential role of TGF-beta signaling in glucose-induced cell hypertrophy.
A cilium is not a cilium is not a cilium: signaling contributes to ciliary morphological diversity. Read more about A cilium is not a cilium is not a cilium: signaling contributes to ciliary morphological diversity.
Cofilin activity downstream of Pak1 regulates cell protrusion efficiency by organizing lamellipodium and lamella actin networks. Read more about Cofilin activity downstream of Pak1 regulates cell protrusion efficiency by organizing lamellipodium and lamella actin networks.
G'rab'bing the microenvironment for invasion. Read more about G'rab'bing the microenvironment for invasion.
Catch the KIF5B train to the apical surface. Read more about Catch the KIF5B train to the apical surface.
An essential role for 14-3-3 proteins in brassinosteroid signal transduction in Arabidopsis. Read more about An essential role for 14-3-3 proteins in brassinosteroid signal transduction in Arabidopsis.
Quantitative modeling in cell biology: what is it good for? Read more about Quantitative modeling in cell biology: what is it good for?
Sprouty genes control diastema tooth development via bidirectional antagonism of epithelial-mesenchymal FGF signaling. Read more about Sprouty genes control diastema tooth development via bidirectional antagonism of epithelial-mesenchymal FGF signaling.
ERK and MMPs sequentially regulate distinct stages of epithelial tubule development. Read more about ERK and MMPs sequentially regulate distinct stages of epithelial tubule development.
