Publication | Open Access
Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly
174
Citations
21
References
2008
Year
Transcriptional RegulationDevelopmental BiologyNodal Signaling StrengthSignaling PathwayGenetic DisorderCell SignalingGeneticsAutophagyHuman Heart DefectsGenomic MechanismGene ExpressionMedicineEpigenetics
| Year | Citations | |
|---|---|---|
Page 1
Page 1