Papers associated with left (and dlx5)

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	The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains., Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
	Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates., Baxi AB., iScience. September 15, 2023; 26 (9): 107665.
	Ash2l, an obligatory component of H3K4 methylation complexes, regulates neural crest development., Mohammadparast S., Dev Biol. December 1, 2022; 492 14-24.
	Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease., Coppenrath K., Genesis. December 1, 2021; 59 (12): e23453.
	Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development., Tavares ALP., Development. September 1, 2021; 148 (17):
	Fibroblast dedifferentiation as a determinant of successful regeneration., Lin TY., Dev Cell. May 17, 2021; 56 (10): 1541-1551.e6.
	Xenopus leads the way: Frogs as a pioneering model to understand the human brain., Exner CRT., Genesis. February 1, 2021; 59 (1-2): e23405.
	Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM., Dis Model Mech. March 3, 2020; 13 (3):
	A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation., Hou K., Cells. May 15, 2019; 8 (5):
	Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.
	Bone regeneration after traumatic skull injury in Xenopus tropicalis., Muñoz D., Mech Dev. December 1, 2018; 154 153-161.
	Ketamine Modulates Zic5 Expression via the Notch Signaling Pathway in Neural Crest Induction., Shi Y, Shi Y., Front Mol Neurosci. February 7, 2018; 11 9.
	Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development., Neilson KM., Dev Biol. January 15, 2017; 421 (2): 171-182.
	Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.
	The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus., Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.
	A gene expression map of the larval Xenopus laevis head reveals developmental changes underlying the evolution of new skeletal elements., Square T., Dev Biol. January 15, 2015; 397 (2): 293-304.
	Development of the vertebrate tailbud., Beck CW., Wiley Interdiscip Rev Dev Biol. January 1, 2015; 4 (1): 33-44.
	Xenopus Nkx6.3 is a neural plate border specifier required for neural crest development., Zhang Z., PLoS One. December 15, 2014; 9 (12): e115165.
	Early neural crest induction requires an initial inhibition of Wnt signals., Steventon B., Dev Biol. May 1, 2012; 365 (1): 196-207.
	Analyzing the function of a hox gene: an evolutionary approach., Michaut L., Dev Growth Differ. December 1, 2011; 53 (9): 982-93.
	Conserved expression of mouse Six1 in the pre-placodal region (PPR) and identification of an enhancer for the rostral PPR., Sato S., Dev Biol. August 1, 2010; 344 (1): 158-71.
	Xhairy2 functions in Xenopus lens development by regulating p27(xic1) expression., Murato Y., Dev Dyn. September 1, 2009; 238 (9): 2179-92.
	Cloning and expression analysis of the anterior parahox genes, Gsh1 and Gsh2 from Xenopus tropicalis., Illes JC., Dev Dyn. January 1, 2009; 238 (1): 194-203.
	Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
	GABAergic specification in the basal forebrain is controlled by the LIM-hd factor Lhx7., Bachy I., Dev Biol. March 15, 2006; 291 (2): 218-26.
	The divergent DSL ligand Dll3 does not activate Notch signaling but cell autonomously attenuates signaling induced by other DSL ligands., Ladi E., J Cell Biol. September 12, 2005; 170 (6): 983-92.
	An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation., Matsuo-Takasaki M., Development. September 1, 2005; 132 (17): 3885-94.
	The doublesex-related gene, XDmrt4, is required for neurogenesis in the olfactory system., Huang X., Proc Natl Acad Sci U S A. August 9, 2005; 102 (32): 11349-54.
	Phylogenetic footprinting and genome scanning identify vertebrate BMP response elements and new target genes., von Bubnoff A., Dev Biol. May 15, 2005; 281 (2): 210-26.
	Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus., Chen JA., Mech Dev. March 1, 2005; 122 (3): 307-31.
	Expression cloning screening of a unique and full-length set of cDNA clones is an efficient method for identifying genes involved in Xenopus neurogenesis., Voigt J., Mech Dev. March 1, 2005; 122 (3): 289-306.
	Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.
	Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor., Brugmann SA., Development. December 1, 2004; 131 (23): 5871-81.
	A restrictive role for Hedgehog signalling during otic specification in Xenopus., Koebernick K., Dev Biol. August 15, 2003; 260 (2): 325-38.
	Dlx proteins position the neural plate border and determine adjacent cell fates., Woda JM., Development. January 1, 2003; 130 (2): 331-42.
	Defining pallial and subpallial divisions in the developing Xenopus forebrain., Bachy I., Mech Dev. September 1, 2002; 117 (1-2): 163-72.
	Conserved and divergent patterns of Reelin expression in the zebrafish central nervous system., Costagli A., J Comp Neurol. August 12, 2002; 450 (1): 73-93.
	Transgenic Xenopus embryos reveal that anterior neural development requires continued suppression of BMP signaling after gastrulation., Hartley KO., Dev Biol. October 1, 2001; 238 (1): 168-84.
	Misexpression of Polycomb-group proteins in Xenopus alters anterior neural development and represses neural target genes., Yoshitake Y., Dev Biol. November 15, 1999; 215 (2): 375-87.
	The Xenopus Emx genes identify presumptive dorsal telencephalon and are induced by head organizer signals., Pannese M., Mech Dev. April 1, 1998; 73 (1): 73-83.
	Xwnt-8 and lithium can act upon either dorsal mesodermal or neurectodermal cells to cause a loss of forebrain in Xenopus embryos., Fredieu JR., Dev Biol. June 1, 1997; 186 (1): 100-14.
	Cellular and molecular interactions in the development of the Xenopus olfactory system., Reiss JO., Semin Cell Dev Biol. April 1, 1997; 8 (2): 171-9.
	Patterns of distal-less gene expression and inductive interactions in the head of the direct developing frog Eleutherodactylus coqui., Fang H., Dev Biol. October 10, 1996; 179 (1): 160-72.
	Xenopus Distal-less related homeobox genes are expressed in the developing forebrain and are induced by planar signals., Papalopulu N., Development. March 1, 1993; 117 (3): 961-75.

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