Papers associated with anterior (and myh6)

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	Characterization of convergent thickening, a major convergence force producing morphogenic movement in amphibians., Shook DR., Elife. April 11, 2022; 11
	A systemic cell cycle block impacts stage-specific histone modification profiles during Xenopus embryogenesis., Pokrovsky D., PLoS Biol. September 1, 2021; 19 (9): e3001377.
	Generation of anisotropic strain dysregulates wild-type cell division at the interface between host and oncogenic tissue., Moruzzi M., Curr Biol. August 9, 2021; 31 (15): 3409-3418.e6.
	Disabled-2: a positive regulator of the early differentiation of myoblasts., Shang N., Cell Tissue Res. September 1, 2020; 381 (3): 493-508.
	Vangl2 coordinates cell rearrangements during gut elongation., Dush MK., Dev Dyn. July 1, 2019; 248 (7): 569-582.
	Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis., Schwenty-Lara J., Dev Dyn. June 1, 2019; 248 (6): 465-476.
	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.
	Id genes are essential for early heart formation., Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.
	The CapZ interacting protein Rcsd1 is required for cardiogenesis downstream of Wnt11a in Xenopus laevis., Hempel A., Dev Biol. April 1, 2017; 424 (1): 28-39.
	Analysis of Craniocardiac Malformations in Xenopus using Optical Coherence Tomography., Deniz E., Sci Rep. February 14, 2017; 7 42506.
	A thioredoxin fold protein Sh3bgr regulates Enah and is necessary for proper sarcomere formation., Jang DG., Dev Biol. September 1, 2015; 405 (1): 1-9.
	Contractile activity is required for Z-disc sarcomere maturation in vivo., Geach TJ., Genesis. May 1, 2015; 53 (5): 299-307.
	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.
	Nkx2.5 is involved in myeloid cell differentiation at anterior ventral blood islands in the Xenopus embryo., Sakata H., Dev Growth Differ. October 1, 2014; 56 (8): 544-54.
	Comparative analysis reveals distinct and overlapping functions of Mef2c and Mef2d during cardiogenesis in Xenopus laevis., Guo Y., PLoS One. January 17, 2014; 9 (1): e87294.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Early development of the thymus in Xenopus laevis., Lee YH, Lee YH., Dev Dyn. February 1, 2013; 242 (2): 164-78.
	SHP-2 acts via ROCK to regulate the cardiac actin cytoskeleton., Langdon Y., Development. March 1, 2012; 139 (5): 948-57.
	Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning., Fakhro KA., Proc Natl Acad Sci U S A. February 15, 2011; 108 (7): 2915-20.
	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.
	Focal adhesion kinase is essential for cardiac looping and multichamber heart formation., Doherty JT., Genesis. August 1, 2010; 48 (8): 492-504.
	The BMP pathway acts to directly regulate Tbx20 in the developing heart., Mandel EM., Development. June 1, 2010; 137 (11): 1919-29.
	Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.
	Paralysis and delayed Z-disc formation in the Xenopus tropicalis unc45b mutant dicky ticker., Geach TJ., BMC Dev Biol. January 22, 2010; 10 75.
	FoxO genes are dispensable during gastrulation but required for late embryogenesis in Xenopus laevis., Schuff M., Dev Biol. January 15, 2010; 337 (2): 259-73.
	Morphogenesis of the primitive gut tube is generated by Rho/ROCK/myosin II-mediated endoderm rearrangements., Reed RA., Dev Dyn. December 1, 2009; 238 (12): 3111-25.
	Neural ectoderm-secreted FGF initiates the expression of Nkx2.5 in cardiac progenitors via a p38 MAPK/CREB pathway., Keren-Politansky A., Dev Biol. November 15, 2009; 335 (2): 374-84.
	Notch activates Wnt-4 signalling to control medio-lateral patterning of the pronephros., Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.
	Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis., Gessert S., Dev Biol. October 15, 2009; 334 (2): 395-408.
	Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Morphogenetic movements driving neural tube closure in Xenopus require myosin IIB., Rolo A., Dev Biol. March 15, 2009; 327 (2): 327-38.
	DM-GRASP/ALCAM/CD166 is required for cardiac morphogenesis and maintenance of cardiac identity in first heart field derived cells., Gessert S., Dev Biol. September 1, 2008; 321 (1): 150-61.
	IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis., Zhu W., Nature. July 17, 2008; 454 (7202): 345-9.
	Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline., Christine KS., Dev Cell. April 1, 2008; 14 (4): 616-23.
	A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis., Shibata T., Mech Dev. January 1, 2008; 125 (3-4): 284-98.
	The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros., Wingert RA., PLoS Genet. October 1, 2007; 3 (10): 1922-38.
	Myoskeletin, a factor related to Myocardin, is expressed in somites and required for hypaxial muscle formation in Xenopus., Zhao H., Int J Dev Biol. January 1, 2007; 51 (4): 315-20.
	Xtn3 is a developmentally expressed cardiac and skeletal muscle-specific novex-3 titin isoform., Brown DD., Gene Expr Patterns. October 1, 2006; 6 (8): 913-8.
	TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
	Genetic screens for mutations affecting development of Xenopus tropicalis., Goda T., PLoS Genet. June 1, 2006; 2 (6): e91.
	Retinoic acid signaling is essential for formation of the heart tube in Xenopus., Collop AH., Dev Biol. March 1, 2006; 291 (1): 96-109.
	Spatio-temporal expression of MRF4 transcripts and protein during Xenopus laevis embryogenesis., Della Gaspera B., Dev Dyn. February 1, 2006; 235 (2): 524-9.
	p38 MAP kinase regulates the expression of XMyf5 and affects distinct myogenic programs during Xenopus development., Keren A., Dev Biol. December 1, 2005; 288 (1): 73-86.
	SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C., Dev Dyn. December 1, 2005; 234 (4): 878-91.
	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.
	Developmental expression and comparative genomic analysis of Xenopus cardiac myosin heavy chain genes., Garriock RJ., Dev Dyn. August 1, 2005; 233 (4): 1287-93.
	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.
	Wnt11-R, a protein closely related to mammalian Wnt11, is required for heart morphogenesis in Xenopus., Garriock RJ., Dev Biol. March 1, 2005; 279 (1): 179-92.
	Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.

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