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Summary Expression Phenotypes Gene Literature (30) GO Terms (4) Nucleotides (73) Proteins (40) Interactants (244) Wiki
XB-GENEPAGE-5959292

Papers associated with hoxb7



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Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS, Collodel MG, Lopez IA, Roa C, Hochbaum D, Hukriede NA, Cirio MC., Sci Rep. October 4, 2023; 13 (1): 16671.                                          

Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration., Patel JH, Schattinger PA, Takayoshi EE, Wills AE., Dev Biol. March 1, 2022; 483 157-168.                  

Cellular response to spinal cord injury in regenerative and non-regenerative stages in Xenopus laevis., Edwards-Faret G, González-Pinto K, Cebrián-Silla A, Peñailillo J, García-Verdugo JM, Larraín J., Neural Dev. February 2, 2021; 16 (1): 2.                              

Therapeutic Rationale to Target Highly Expressed Aurora kinase A Conferring Poor Prognosis in Cholangiocarcinoma., Ding X, Huang T, Peng C, Ahn KS, Andersen JB, Lewinska M, Cao Y, Xu G, Chen G, Kong B, Friess H, Shen S, Roberts LR, Wang L, Zou X., J Cancer. February 3, 2020; 11 (8): 2241-2251.              

What are the roles of retinoids, other morphogens, and Hox genes in setting up the vertebrate body axis?, Durston AJ., Genesis. July 1, 2019; 57 (7-8): e23296.            

Two Tier Hox Collinearity Mediates Vertebrate Axial Patterning., Durston AJ., Front Cell Dev Biol. January 1, 2018; 6 102.        

Role of remodeling and spacing factor 1 in histone H2A ubiquitination-mediated gene silencing., Zhang Z, Zhang Z, Jones AE, Wu W, Kim J, Kang Y, Bi X, Gu Y, Popov IK, Renfrow MB, Vassylyeva MN, Vassylyev DG, Giles KE, Chen D, Kumar A, Fan Y, Tong Y, Liu CF, An W, Chang C, Luo J, Chow LT, Wang H., Proc Natl Acad Sci U S A. September 19, 2017; 114 (38): E7949-E7958.                          

Comprehensive analyses of hox gene expression in Xenopus laevis embryos and adult tissues., Kondo M, Yamamoto T, Takahashi S, Taira M., Dev Growth Differ. August 1, 2017; 59 (6): 526-539.                                

Molecular insights into the origin of the Hox-TALE patterning system., Hudry B, Thomas-Chollier M, Volovik Y, Duffraisse M, Dard A, Frank D, Technau U, Merabet S., Elife. March 18, 2014; 3 e01939.                                    

FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos., Murgan S, Castro Colabianchi AM, Monti RJ, Boyadjián López LE, Aguirre CE, Stivala EG, Carrasco AE, López SL., PLoS One. January 1, 2014; 9 (10): e110559.                              

Notch destabilises maternal beta-catenin and restricts dorsal-anterior development in Xenopus., Acosta H, López SL, Revinski DR, Carrasco AE., Development. June 1, 2011; 138 (12): 2567-79.                          

Lhx1 is required for specification of the renal progenitor cell field., Cirio MC, Hui Z, Haldin CE, Cosentino CC, Stuckenholz C, Chen X, Hong SK, Dawid IB, Hukriede NA., PLoS One. April 15, 2011; 6 (4): e18858.                          

TMEPAI, a transmembrane TGF-beta-inducible protein, sequesters Smad proteins from active participation in TGF-beta signaling., Watanabe Y, Itoh S, Goto T, Ohnishi E, Inamitsu M, Itoh F, Satoh K, Wiercinska E, Yang W, Shi L, Tanaka A, Nakano N, Mommaas AM, Shibuya H, Ten Dijke P, Kato M., Mol Cell. January 15, 2010; 37 (1): 123-34.                                      

Beta-catenin is necessary to keep cells of ureteric bud/Wolffian duct epithelium in a precursor state., Marose TD, Merkel CE, McMahon AP, Carroll TJ., Dev Biol. February 1, 2008; 314 (1): 112-26.    

Smads oppose Hox transcriptional activities., Li X, Nie S, Chang C, Qiu T, Cao X., Exp Cell Res. April 1, 2006; 312 (6): 854-64.

The doublesex-related gene, XDmrt4, is required for neurogenesis in the olfactory system., Huang X, Hong CS, O'Donnell M, Saint-Jeannet JP., Proc Natl Acad Sci U S A. August 9, 2005; 102 (32): 11349-54.                        

Morphometry and estimated bulk oxygen diffusion in larvae of Xenopus laevis under chronic carbon monoxide exposure., Territo PR, Altimiras J., J Comp Physiol B. March 1, 2001; 171 (2): 145-53.

Xenopus embryonic E2F is required for the formation of ventral and posterior cell fates during early embryogenesis., Suzuki A, Hemmati-Brivanlou A., Mol Cell. February 1, 2000; 5 (2): 217-29.                      

Graded retinoid responses in the developing hindbrain., Godsave SF, Koster CH, Getahun A, Mathu M, Hooiveld M, van der Wees J, Hendriks J, Durston AJ., Dev Dyn. September 1, 1998; 213 (1): 39-49.

Differential effects of retinoic acid and a retinoid antagonist on the spatial distribution of the homeoprotein Hoxb-7 in vertebrate embryos., López SL, Dono R, Zeller R, Carrasco AE., Dev Dyn. December 1, 1995; 204 (4): 457-71.      

Nucleolar localisation of three Hox homeoproteins., Corsetti MT, Levi G, Lancia F, Sanseverino L, Ferrini S, Boncinelli E, Corte G., J Cell Sci. January 1, 1995; 108 ( Pt 1) 187-93.          

Expression patterns of Hoxb genes in the Xenopus embryo suggest roles in anteroposterior specification of the hindbrain and in dorsoventral patterning of the mesoderm., Godsave S, Dekker EJ, Holling T, Pannese M, Boncinelli E, Durston A., Dev Biol. December 1, 1994; 166 (2): 465-76.              

Characterization of the Xenopus Hox 2.4 gene and identification of control elements in its intron., Bittner D, De Robertis EM, Cho KW., Dev Dyn. January 1, 1993; 196 (1): 11-24.            

Retinoic acid induces changes in the localization of homeobox proteins in the antero-posterior axis of Xenopus laevis embryos., López SL, Carrasco AE., Mech Dev. February 1, 1992; 36 (3): 153-64.          

The Xenopus laevis Hox 2.1 homeodomain protein is expressed in a narrow band of the hindbrain., Jegalian BG, De Robertis EM., Int J Dev Biol. December 1, 1990; 34 (4): 453-6.    

Endonucleolytic cleavage of a maternal homeo box mRNA in Xenopus oocytes., Brown BD, Harland RM., Genes Dev. November 1, 1990; 4 (11): 1925-35.

Duplicated homeobox genes in Xenopus., Fritz AF, Cho KW, Wright CV, Jegalian BG, De Robertis EM., Dev Biol. February 1, 1989; 131 (2): 584-8.

Xenopus homeobox-containing cDNAs expressed in early development., Fritz A, De Robertis EM., Nucleic Acids Res. February 25, 1988; 16 (4): 1453-69.    

A homeo-box-containing gene expressed during oogenesis in Xenopus., Müller MM, Carrasco AE, DeRobertis EM., Cell. November 1, 1984; 39 (1): 157-62.

Long-term growth and differentiation of Xenopus oocytes in a defined medium., Wallace RA, Misulovin Z., Proc Natl Acad Sci U S A. November 1, 1978; 75 (11): 5534-8.

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