AbstractGpr161 (also known as RE2) is an orphan G protein-coupled receptor (GPCR) that is expressed during embryonic development in zebrafish. Determining its biological function has proven difficult due to lack of knowledge regarding its natural or synthetic ligands. Here, we show that targeted knockdown of gpr161 disrupts asymmetric gene expression in the lateral plate mesoderm, resulting in aberrant looping of the heart tube. This is associated with elevated Ca2+ levels in cells lining the Kupffer's vesicle and normalization of Ca2+ levels, by over-expression of ncx1 or pmca-RNA, is able to partially rescue the cardiac looping defect in gpr161 knockdown embryos. Taken together, these data support a model in which gpr161 plays an essentia...
The Adhesion family of G protein-coupled receptors (AdGCPRs) is a unique set of cell-surface recepto...
Mutations in the G protein–coupled receptor GPR126/ADGRG6 cause human diseases, including defective ...
Congenital heart diseases (CHDs) are the most common type of human birth defect and often feature st...
AbstractGpr161 (also known as RE2) is an orphan G protein-coupled receptor (GPCR) that is expressed ...
SummaryIn vertebrates, the morphogenetic assembly of the primitive heart tube requires the medial mi...
GPR22 is an orphan G protein-coupled receptor (GPCR). Since the ligand of the receptor is currently ...
GPR22 is an orphan G protein-coupled receptor (GPCR). Since the ligand of the receptor is currently ...
SummaryWhile many factors that modulate the morphogenesis and patterning of the embryonic heart have...
<div><p>GPR22 is an orphan G protein-coupled receptor (GPCR). Since the ligand of the receptor is cu...
In vertebrates, the morphogenetic assembly of the primitive heart tube requires the medial migration...
Gpr126 is an adhesion G protein-coupled receptor (GPCR) that is required for peripheral nervous sys...
SummaryIn vertebrates, the morphogenetic assembly of the primitive heart tube requires the medial mi...
In vertebrates, the morphogenetic assembly of the primitive heart tube requires the medial migration...
Adhesion-GPCRs provide essential cell-cell and cell-matrix interactions in development, and have bee...
Glucocorticoids (GCs) play important roles in developmental and physiological processes through the ...
The Adhesion family of G protein-coupled receptors (AdGCPRs) is a unique set of cell-surface recepto...
Mutations in the G protein–coupled receptor GPR126/ADGRG6 cause human diseases, including defective ...
Congenital heart diseases (CHDs) are the most common type of human birth defect and often feature st...
AbstractGpr161 (also known as RE2) is an orphan G protein-coupled receptor (GPCR) that is expressed ...
SummaryIn vertebrates, the morphogenetic assembly of the primitive heart tube requires the medial mi...
GPR22 is an orphan G protein-coupled receptor (GPCR). Since the ligand of the receptor is currently ...
GPR22 is an orphan G protein-coupled receptor (GPCR). Since the ligand of the receptor is currently ...
SummaryWhile many factors that modulate the morphogenesis and patterning of the embryonic heart have...
<div><p>GPR22 is an orphan G protein-coupled receptor (GPCR). Since the ligand of the receptor is cu...
In vertebrates, the morphogenetic assembly of the primitive heart tube requires the medial migration...
Gpr126 is an adhesion G protein-coupled receptor (GPCR) that is required for peripheral nervous sys...
SummaryIn vertebrates, the morphogenetic assembly of the primitive heart tube requires the medial mi...
In vertebrates, the morphogenetic assembly of the primitive heart tube requires the medial migration...
Adhesion-GPCRs provide essential cell-cell and cell-matrix interactions in development, and have bee...
Glucocorticoids (GCs) play important roles in developmental and physiological processes through the ...
The Adhesion family of G protein-coupled receptors (AdGCPRs) is a unique set of cell-surface recepto...
Mutations in the G protein–coupled receptor GPR126/ADGRG6 cause human diseases, including defective ...
Congenital heart diseases (CHDs) are the most common type of human birth defect and often feature st...