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Summary Anatomy Item Literature (209) Expression Attributions Wiki
XB-ANAT-1512

Papers associated with endochondral bone (and snai2)

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Inhibition of the serine protease HtrA1 by SerpinE2 suggests an extracellular proteolytic pathway in the control of neural crest migration., Pera EM., Elife. April 18, 2024; 12                                               


Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease., Getwan M., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):                                                   


Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.                              


The extreme anterior domain is an essential craniofacial organizer acting through Kinin-Kallikrein signaling., Jacox L., Cell Rep. July 24, 2014; 8 (2): 596-609.                            


Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis., Tazumi S., Dev Biol. October 15, 2010; 346 (2): 170-80.                                


Ectopic Hoxa2 induction after neural crest migration results in homeosis of jaw elements in Xenopus., Pasqualetti M., Development. December 1, 2000; 127 (24): 5367-78.          

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