Guo, Chaoshe

A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis. [electronic resource] - The Journal of clinical investigation Apr 2011 - 1585-95 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

1558-8238

10.1172/JCI44630 doi


Animals
Base Sequence
Cardiovascular Abnormalities--genetics
Cardiovascular System--embryology
Cell Proliferation
Cell Survival--genetics
Chromosomes, Human, Pair 22--genetics
Craniofacial Abnormalities--genetics
DNA Primers--genetics
DiGeorge Syndrome--genetics
Disease Models, Animal
Facial Bones--embryology
Fibroblast Growth Factor 8--deficiency
Homeodomain Proteins--genetics
Humans
Intracellular Signaling Peptides and Proteins--deficiency
Mice
Mice, 129 Strain
Mice, Inbred C57BL
Mice, Knockout
Mice, Transgenic
Morphogenesis--genetics
Mutation
Nuclear Proteins--deficiency
Protein Tyrosine Phosphatases--deficiency
Skull--embryology
T-Box Domain Proteins--deficiency