Papers associated with primordium (and lhx1)

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	Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.
	Adrenergic receptor signaling induced by Klf15, a regulator of regeneration enhancer, promotes kidney reconstruction., Suzuki N., Proc Natl Acad Sci U S A. August 16, 2022; 119 (33): e2204338119.
	The Wnt/PCP formin Daam1 drives cell-cell adhesion during nephron development., Krneta-Stankic V., Cell Rep. July 6, 2021; 36 (1): 109340.
	Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals in Xenopus laevis., Ding Y., Proc Natl Acad Sci U S A. April 11, 2017; 114 (15): E3081-E3090.
	Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
	Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
	E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE., Dev Cell. February 9, 2015; 32 (3): 345-57.
	Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.
	Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification., Yasuoka Y., Nat Commun. July 9, 2014; 5 4322.
	Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis., Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.
	ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3., Hoff S., Nat Genet. August 1, 2013; 45 (8): 951-6.
	Regulation of primitive hematopoiesis by class I histone deacetylases., Shah RR., Dev Dyn. February 1, 2013; 242 (2): 108-21.
	Microarray-based identification of Pitx3 targets during Xenopus embryogenesis., Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.
	Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus., Rankin SA, Rankin SA., Development. August 1, 2012; 139 (16): 3010-20.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
	Dynamic in vivo binding of transcription factors to cis-regulatory modules of cer and gsc in the stepwise formation of the Spemann-Mangold organizer., Sudou N., Development. May 1, 2012; 139 (9): 1651-61.
	Involvement of the eukaryotic initiation factor 6 and kermit2/gipc2 in Xenopus laevis pronephros formation., Tussellino M., Int J Dev Biol. January 1, 2012; 56 (5): 357-62.
	Xenopus as a model system for the study of GOLPH2/GP73 function: Xenopus GOLPH2 is required for pronephros development., Li L., PLoS One. January 1, 2012; 7 (6): e38939.
	Non-canonical wnt signals antagonize and canonical wnt signals promote cell proliferation in early kidney development., McCoy KE., Dev Dyn. June 1, 2011; 240 (6): 1558-66.
	A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer., Rankin SA, Rankin SA., Dev Biol. March 15, 2011; 351 (2): 297-310.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	The RNA-binding protein bicaudal C regulates polycystin 2 in the kidney by antagonizing miR-17 activity., Tran U., Development. April 1, 2010; 137 (7): 1107-16.
	XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis., Lee SJ., Mech Dev. January 1, 2010; 127 (1-2): 49-61.
	Embryogenesis and laboratory maintenance of the foam-nesting túngara frogs, genus Engystomops (= Physalaemus)., Romero-Carvajal A., Dev Dyn. June 1, 2009; 238 (6): 1444-54.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.
	Requirement of Wnt/beta-catenin signaling in pronephric kidney development., Lyons JP., Mech Dev. January 1, 2009; 126 (3-4): 142-59.
	Expression cloning in Xenopus identifies RNA-binding proteins as regulators of embryogenesis and Rbmx as necessary for neural and muscle development., Dichmann DS., Dev Dyn. July 1, 2008; 237 (7): 1755-66.
	Upstream stimulatory factors, USF1 and USF2 are differentially expressed during Xenopus embryonic development., Fujimi TJ., Gene Expr Patterns. July 1, 2008; 8 (6): 376-381.
	Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan., Coolen M., PLoS One. April 18, 2007; 2 (4): e374.
	ADMP2 is essential for primitive blood and heart development in Xenopus., Kumano G., Dev Biol. November 15, 2006; 299 (2): 411-23.
	FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.
	An amphioxus LIM-homeobox gene, AmphiLim1/5, expressed early in the invaginating organizer region and later in differentiating cells of the kidney and central nervous system., Langeland JA., Int J Biol Sci. January 1, 2006; 2 (3): 110-6.
	The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos., Callery EM., Dev Biol. February 15, 2005; 278 (2): 542-59.
	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.
	Adult and embryonic blood and endothelium derive from distinct precursor populations which are differentially programmed by BMP in Xenopus., Walmsley M., Development. December 1, 2002; 129 (24): 5683-95.
	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.
	Identification of NKL, a novel Gli-Kruppel zinc-finger protein that promotes neuronal differentiation., Lamar E., Development. April 1, 2001; 128 (8): 1335-46.
	A study of Xlim1 function in the Spemann-Mangold organizer., Kodjabachian L., Int J Dev Biol. January 1, 2001; 45 (1): 209-18.
	A role for Xlim-1 in pronephros development in Xenopus laevis., Chan TC., Dev Biol. December 15, 2000; 228 (2): 256-69.
	Synergism between Pax-8 and lim-1 in embryonic kidney development., Carroll TJ., Dev Biol. October 1, 1999; 214 (1): 46-59.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	Xenopus brain factor-2 controls mesoderm, forebrain and neural crest development., Gómez-Skarmeta JL., Mech Dev. January 1, 1999; 80 (1): 15-27.
	XIPOU 2 is a potential regulator of Spemann's Organizer., Witta SE., Development. March 1, 1997; 124 (6): 1179-89.
	Expression of murine Lhx5 suggests a role in specifying the forebrain., Sheng HZ., Dev Dyn. February 1, 1997; 208 (2): 266-77.
	Analysis of Dishevelled signalling pathways during Xenopus development., Sokol SY., Curr Biol. November 1, 1996; 6 (11): 1456-67.
	v-erbA and citral reduce the teratogenic effects of all-trans retinoic acid and retinol, respectively, in Xenopus embryogenesis., Schuh TJ., Development. November 1, 1993; 119 (3): 785-98.
	Expression of LIM class homeobox gene Xlim-3 in Xenopus development is limited to neural and neuroendocrine tissues., Taira M., Dev Biol. September 1, 1993; 159 (1): 245-56.

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