AbstractLeft–right asymmetry is initiated during chick embryogenesis in small domains near Hensen's node. Subsequently, broad asymmetric gene expression domains are established in the lateral plate mesoderm, ultimately determining the directionality of morphogenetic events. The transfer of asymmetric information from the node to the lateral plate is mediated by Caronte (Car), a novel member of the Cerberus/Dan gene family, which induces targets by antagonizing symmetrically expressed BMP signals. In addition, BMP antagonism by Car induces asymmetric expression of Lefty in the midline, preventing spread of left-sided signals to the contralateral side
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Although recently our understanding of how the LR asymmetry is generated in vertebrate embryos has s...
AbstractThe earliest known left-right asymmetric genes are expressed at Hensen's node during chick g...
AbstractLeft–right asymmetry is initiated during chick embryogenesis in small domains near Hensen's ...
AbstractBackground: Most of the molecules known to regulate left–right asymmetry in vertebrate embry...
The TGF-beta-related molecule Nodal plays an essential and conserved role in left-right patterning o...
AbstractWhile significant progress has been made in understanding the molecular events underlying th...
AbstractLeft–right asymmetry in vertebrate embryos is first recognisable using molecular markers tha...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Many bilaterally symmetrical animals develop genetically-programmed left-right asymmetries. In verte...
The formation of the asymmetric left-right (LR) body axis is one of the fundamental aspects of verte...
AbstractDuring left–right (L–R) axis formation, Nodal is expressed in the node and has a central rol...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Although recently our understanding of how the LR asymmetry is generated in vertebrate embryos has s...
AbstractThe earliest known left-right asymmetric genes are expressed at Hensen's node during chick g...
AbstractLeft–right asymmetry is initiated during chick embryogenesis in small domains near Hensen's ...
AbstractBackground: Most of the molecules known to regulate left–right asymmetry in vertebrate embry...
The TGF-beta-related molecule Nodal plays an essential and conserved role in left-right patterning o...
AbstractWhile significant progress has been made in understanding the molecular events underlying th...
AbstractLeft–right asymmetry in vertebrate embryos is first recognisable using molecular markers tha...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Many bilaterally symmetrical animals develop genetically-programmed left-right asymmetries. In verte...
The formation of the asymmetric left-right (LR) body axis is one of the fundamental aspects of verte...
AbstractDuring left–right (L–R) axis formation, Nodal is expressed in the node and has a central rol...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Development of visceral left–right asymmetry in bilateria is based on initial symmetry breaking foll...
Although recently our understanding of how the LR asymmetry is generated in vertebrate embryos has s...
AbstractThe earliest known left-right asymmetric genes are expressed at Hensen's node during chick g...