Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Anatomy Item Literature (2231) Expression Attributions Wiki
XB-ANAT-3282

Papers associated with posterior hypothalamus (and bmp7.1)

Limit to papers also referencing gene:
Show all posterior hypothalamus papers
???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

BMP signalling controls the construction of vertebrate mucociliary epithelia., Cibois M., Development. July 1, 2015; 142 (13): 2352-63.                        


Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints., Genikhovich G., Cell Rep. March 17, 2015; 10 (10): 1646-1654.            


Transient expression of Ngn3 in Xenopus endoderm promotes early and ectopic development of pancreatic beta and delta cells., Oropeza D., Genesis. March 1, 2012; 50 (3): 271-85.                        


Regulation of chemotropic guidance of nerve growth cones by microRNA., Han L., Mol Brain. November 3, 2011; 4 40.              


Gsx transcription factors repress Iroquois gene expression., Winterbottom EF., Dev Dyn. June 1, 2011; 240 (6): 1422-9.        


SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.                              


Expression cloning of Xenopus zygote arrest 2 (Xzar2) as a novel epidermalization-promoting factor in early embryos of Xenopus laevis., Nakajima Y., Genes Cells. May 1, 2009; 14 (5): 583-95.                    


Robust stability of the embryonic axial pattern requires a secreted scaffold for chordin degradation., Inomata H., Cell. September 5, 2008; 134 (5): 854-65.                  


Integrating patterning signals: Wnt/GSK3 regulates the duration of the BMP/Smad1 signal., Fuentealba LC., Cell. November 30, 2007; 131 (5): 980-93.      


CDMP1/GDF5 has specific processing requirements that restrict its action to joint surfaces., Thomas JT., J Biol Chem. September 8, 2006; 281 (36): 26725-33.              


Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.            


Tsukushi functions as an organizer inducer by inhibition of BMP activity in cooperation with chordin., Ohta K., Dev Cell. September 1, 2004; 7 (3): 347-358.        


The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.                  


In Xenopus embryos, BMP heterodimers are not required for mesoderm induction, but BMP activity is necessary for dorsal/ventral patterning., Eimon PM., Dev Biol. December 1, 1999; 216 (1): 29-40.          


Xenopus GDF6, a new antagonist of noggin and a partner of BMPs., Chang C., Development. August 1, 1999; 126 (15): 3347-57.              


Direct binding of follistatin to a complex of bone-morphogenetic protein and its receptor inhibits ventral and epidermal cell fates in early Xenopus embryo., Iemura S., Proc Natl Acad Sci U S A. August 4, 1998; 95 (16): 9337-42.            


Cloning and expression of three members of the zebrafish Bmp family: Bmp2a, Bmp2b and Bmp4., Martínez-Barberá JP., Gene. October 1, 1997; 198 (1-2): 53-9.


Differential expression of Xenopus BMPs in early embryos and tissues., Suzuki A., Zoolog Sci. February 1, 1993; 10 (1): 175-8.

???pagination.result.page??? 1