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Summary Anatomy Item Literature (2048) Expression Attributions Wiki
XB-ANAT-131

Papers associated with liver (and myh6)

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Liver Specification in the Absence of Cardiac Differentiation Revealed by Differential Sensitivity to Wnt/β Catenin Pathway Activation., Haworth K., Front Physiol. January 1, 2019; 10 155.              


Distinct MHC class I-like interacting invariant T cell lineage at the forefront of mycobacterial immunity uncovered in Xenopus., Edholm ES., Proc Natl Acad Sci U S A. April 24, 2018; 115 (17): E4023-E4031.          


Carboxy terminus of GATA4 transcription factor is required for its cardiogenic activity and interaction with CDK4., Gallagher JM., Mech Dev. November 1, 2014; 134 31-41.            


Cyclin D2 is a GATA4 cofactor in cardiogenesis., Yamak A., Proc Natl Acad Sci U S A. January 28, 2014; 111 (4): 1415-20.          


The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            


Cloning and expression analysis of interferon-γ-inducible-lysosomal thiol reductase gene in South African clawed frog (Xenopus laevis)., Cui XW., Int Immunopharmacol. December 1, 2011; 11 (12): 2091-7.  


Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus., Smith SJ., Mech Dev. January 1, 2011; 128 (5-6): 303-15.                            


IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis., Zhu W., Nature. July 17, 2008; 454 (7202): 345-9.                        


The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis., Huot ME., Mol Biol Cell. September 1, 2005; 16 (9): 4350-61.                  


The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart., Smith SJ., Dev Dyn. April 1, 2005; 232 (4): 1003-12.            


Two myogenin-related genes are differentially expressed in Xenopus laevis myogenesis and differ in their ability to transactivate muscle structural genes., Charbonnier F., J Biol Chem. January 11, 2002; 277 (2): 1139-47.              


The small muscle-specific protein Csl modifies cell shape and promotes myocyte fusion in an insulin-like growth factor 1-dependent manner., Palmer S., J Cell Biol. May 28, 2001; 153 (5): 985-98.                    


Xenopus NK cells identified by novel monoclonal antibodies., Horton TL., Eur J Immunol. February 1, 2000; 30 (2): 604-13.


T-cell and natural killer cell development in thymectomized Xenopus., Horton JD., Immunol Rev. December 1, 1998; 166 245-58.


The Xenopus GATA-4/5/6 genes are associated with cardiac specification and can regulate cardiac-specific transcription during embryogenesis., Jiang Y., Dev Biol. March 15, 1996; 174 (2): 258-70.          


Molecular cloning and linkage analysis of the Japanese medaka fish complement Bf/C2 gene., Kuroda N., Immunogenetics. January 1, 1996; 44 (6): 459-67.


Fourth component of Xenopus laevis complement: cDNA cloning and linkage analysis of the frog MHC., Mo R., Immunogenetics. January 1, 1996; 43 (6): 360-9.


Isolation of Xenopus LMP-7 homologues. Striking allelic diversity and linkage to MHC., Namikawa C., J Immunol. August 15, 1995; 155 (4): 1964-71.


Isolation of the Xenopus complement factor B complementary DNA and linkage of the gene to the frog MHC., Kato Y., J Immunol. November 15, 1994; 153 (10): 4546-54.


Induction of cardiac muscle differentiation in isolated animal pole explants of Xenopus laevis embryos., Logan M., Development. July 1, 1993; 118 (3): 865-75.              


Cloning of the cDNA encoding a myosin heavy chain B isoform of Xenopus nonmuscle myosin with an insert in the head region., Bhatia-Dey N., Proc Natl Acad Sci U S A. April 1, 1993; 90 (7): 2856-9.


Lethal graft-versus-host reaction induced by parental cells in the clawed frog, Xenopus laevis., Nakamura T., Transplantation. October 1, 1985; 40 (4): 393-7.

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