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Modulation of noncanonical TGF-β signaling prevents cleft palate in Tgfbr2 mutant mice

Patients with mutations in either TGF-β receptor type I (TGFBR1) or TGF-β receptor type II (TGFBR2), such as those with Loeys-Dietz syndrome, have craniofacial defects and signs of elevated TGF-β signaling. Similarly, mutations in TGF-β receptor gene family members cause craniofacial deformities, su...

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Hlavní autoři: Iwata, Jun-ichi, Hacia, Joseph G., Suzuki, Akiko, Sanchez-Lara, Pedro A., Urata, Mark, Chai, Yang
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Clinical Investigation 2012
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3287237/
https://ncbi.nlm.nih.gov/pubmed/22326956
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI61498
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