Receptor tyrosine kinases of the Ryk and Ror families were initially classified as orphan receptors because their ligands were unknown. They are now known to contain functional extracellular Wnt-binding domains and are implicated in Wnt-signal transduction in multiple species. Although their signaling mechanisms still remain to be resolved in detail, both Ryk and Ror control important developmental processes in different tissues. However, whereas many other Wnt-signaling responses affect cell proliferation and differentiation, Ryk and Ror are mostly associated with controlling processes that rely on the polarized migration of cells. Here we discuss what is currently known about the involvement of this exciting class of receptors in developm...
BackgroundThe noncanonical Wnt receptor and tyrosine kinase Ror2 has been associated with recessive ...
Mutations in the receptor tyrosine kinase Ror2 account for Brachydactyly type B and Robinow Syndrome...
Mutations in the receptor tyrosine kinase Ror2 account for Brachydactyly type B and Robinow Syndrome...
The receptor tyrosine kinase-like orphan receptor (Ror) proteins are conserved tyrosine kinase recep...
Receptor tyrosine kinase-like orphan receptor (Ror) proteins are a conserved family of tyrosine kina...
AbstractThe Ryk receptor belongs to the atypical receptor tyrosine kinase family. It is a new member...
Background: Ror2 is an orphan receptor, belonging to the Ror family of receptor tyrosine kinases. Al...
Background and aims: Wnt signaling has central role during embryonic development and adult tissue ho...
AbstractThe Ryk receptor belongs to the atypical receptor tyrosine kinase family. It is a new member...
Members of the Wnt family and their receptors, the Frizzleds, are key regulators of pivotal developm...
Summary: WNTs play key roles in development and disease, signaling through Frizzled (FZD) seven-pass...
Background: Ror2 is an orphan receptor, belonging to the Ror family of receptor tyrosine kinases. Al...
BackgroundThe noncanonical Wnt receptor and tyrosine kinase Ror2 has been associated with recessive ...
BackgroundThe noncanonical Wnt receptor and tyrosine kinase Ror2 has been associated with recessive ...
Background: Ror2 is an orphan receptor, belonging to the Ror family of receptor tyrosine kinases. Al...
BackgroundThe noncanonical Wnt receptor and tyrosine kinase Ror2 has been associated with recessive ...
Mutations in the receptor tyrosine kinase Ror2 account for Brachydactyly type B and Robinow Syndrome...
Mutations in the receptor tyrosine kinase Ror2 account for Brachydactyly type B and Robinow Syndrome...
The receptor tyrosine kinase-like orphan receptor (Ror) proteins are conserved tyrosine kinase recep...
Receptor tyrosine kinase-like orphan receptor (Ror) proteins are a conserved family of tyrosine kina...
AbstractThe Ryk receptor belongs to the atypical receptor tyrosine kinase family. It is a new member...
Background: Ror2 is an orphan receptor, belonging to the Ror family of receptor tyrosine kinases. Al...
Background and aims: Wnt signaling has central role during embryonic development and adult tissue ho...
AbstractThe Ryk receptor belongs to the atypical receptor tyrosine kinase family. It is a new member...
Members of the Wnt family and their receptors, the Frizzleds, are key regulators of pivotal developm...
Summary: WNTs play key roles in development and disease, signaling through Frizzled (FZD) seven-pass...
Background: Ror2 is an orphan receptor, belonging to the Ror family of receptor tyrosine kinases. Al...
BackgroundThe noncanonical Wnt receptor and tyrosine kinase Ror2 has been associated with recessive ...
BackgroundThe noncanonical Wnt receptor and tyrosine kinase Ror2 has been associated with recessive ...
Background: Ror2 is an orphan receptor, belonging to the Ror family of receptor tyrosine kinases. Al...
BackgroundThe noncanonical Wnt receptor and tyrosine kinase Ror2 has been associated with recessive ...
Mutations in the receptor tyrosine kinase Ror2 account for Brachydactyly type B and Robinow Syndrome...
Mutations in the receptor tyrosine kinase Ror2 account for Brachydactyly type B and Robinow Syndrome...