Pages that link to "Q36743869"
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The following pages link to Wnt/β-catenin signaling enables developmental transitions during valvulogenesis (Q36743869):
Displaying 15 items.
- Embryonic Ethanol Exposure Dysregulates BMP and Notch Signaling, Leading to Persistent Atrio-Ventricular Valve Defects in Zebrafish (Q27328758) (← links)
- Calcium sensing receptor protects high glucose-induced energy metabolism disorder via blocking gp78-ubiquitin proteasome pathway (Q32872021) (← links)
- Loss of Axin2 results in impaired heart valve maturation and subsequent myxomatous valve disease. (Q39030652) (← links)
- Tissue specific requirements for WNT11 in developing outflow tract and dorsal mesenchymal protrusion (Q41588615) (← links)
- Hemodynamic Forces Sculpt Developing Heart Valves through a KLF2-WNT9B Paracrine Signaling Axis. (Q47619529) (← links)
- Increased canonical WNT/β-catenin signalling and myxomatous valve disease (Q50325560) (← links)
- Hippo Signaling Plays an Essential Role in Cell State Transitions during Cardiac Fibroblast Development. (Q54114587) (← links)
- The Role of Hedgehog Signalling in the Formation of the Ventricular Septum. (Q55363953) (← links)
- Mutations in and genes cause congenital heart defects by tissue-specific perturbation of Wnt/β-catenin signaling (Q58114035) (← links)
- The proximal segment of the embryonic outflow (conus) does not participate in aortic vestibule development (Q60924957) (← links)
- A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A (Q63976740) (← links)
- Myocardial β-Catenin-BMP2 signaling promotes mesenchymal cell proliferation during endocardial cushion formation (Q91367103) (← links)
- Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort (Q91559690) (← links)
- New imaging techniques project the cellular and molecular alterations underlying bicuspid aortic valve development (Q92073745) (← links)
- Developmental origins for semilunar valve stenosis identified in mice harboring congenital heart disease-associated GATA4 mutation (Q92354322) (← links)