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Summary Anatomy Item Literature (3426) Expression Attributions Wiki
XB-ANAT-726

Papers associated with sensory system (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.                                          

Evo-Devo of Urbilateria and its larval forms., De Robertis EM., Dev Biol. July 1, 2022; 487 10-20.        

Xenopus leads the way: Frogs as a pioneering model to understand the human brain., Exner CRT., Genesis. February 1, 2021; 59 (1-2): e23405.          

Tissue-Specific Gene Inactivation in Xenopus laevis: Knockout of lhx1 in the Kidney with CRISPR/Cas9., DeLay BD., Genetics. February 1, 2018; 208 (2): 673-686.                        

Peroxiredoxin1, a novel regulator of pronephros development, influences retinoic acid and Wnt signaling by controlling ROS levels., Chae S., Sci Rep. August 21, 2017; 7 (1): 8874.                    

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.                                    

TRPP2-dependent Ca2+ signaling in dorso-lateral mesoderm is required for kidney field establishment in Xenopus., Futel M., J Cell Sci. March 1, 2015; 128 (5): 888-99.                      

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.                                              

Characterization of the hypothalamus of Xenopus laevis during development. I. The alar regions., Domínguez L., J Comp Neurol. March 1, 2013; 521 (4): 725-59.                                                  

Variation in the schedules of somite and neural development in frogs., Sáenz-Ponce N., Proc Natl Acad Sci U S A. December 11, 2012; 109 (50): 20503-7.    

Microarray-based identification of Pitx3 targets during Xenopus embryogenesis., Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.                          

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.                                              

Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.                              

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.      

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.                

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.                          

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.                    

LIM-homeodomain genes as territory markers in the brainstem of adult and developing Xenopus laevis., Moreno N., J Comp Neurol. May 9, 2005; 485 (3): 240-54.

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.                  

LIM-homeodomain genes as developmental and adult genetic markers of Xenopus forebrain functional subdivisions., Moreno N., J Comp Neurol. April 19, 2004; 472 (1): 52-72.                    

Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.                    

Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.                    

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.            

RNA interference for the organizer-specific gene Xlim-1 in Xenopus embryos., Nakano H., Biochem Biophys Res Commun. August 2, 2000; 274 (2): 434-9.      

The mutated human gene encoding hepatocyte nuclear factor 1beta inhibits kidney formation in developing Xenopus embryos., Wild W., Proc Natl Acad Sci U S A. April 25, 2000; 97 (9): 4695-700.            

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.              

Differential expression of non-muscle myosin heavy chain genes during Xenopus embryogenesis., Bhatia-Dey N., Mech Dev. November 1, 1998; 78 (1-2): 33-6.

Frzb-1 is a secreted antagonist of Wnt signaling expressed in the Spemann organizer., Leyns L., Cell. March 21, 1997; 88 (6): 747-56.              

XIPOU 2 is a potential regulator of Spemann's Organizer., Witta SE., Development. March 1, 1997; 124 (6): 1179-89.                

The LIM homeodomain protein Lim-1 is widely expressed in neural, neural crest and mesoderm derivatives in vertebrate development., Karavanov AA., Int J Dev Biol. April 1, 1996; 40 (2): 453-61.          

The LIM class homeobox gene lim5: implied role in CNS patterning in Xenopus and zebrafish., Toyama R., Dev Biol. August 1, 1995; 170 (2): 583-93.            

Expression of the LIM class homeobox gene Xlim-1 in pronephros and CNS cell lineages of Xenopus embryos is affected by retinoic acid and exogastrulation., Taira M., Development. June 1, 1994; 120 (6): 1525-36.        

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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