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Summary Expression Phenotypes Gene Literature (74) GO Terms (4) Nucleotides (150) Proteins (35) Interactants (505) Wiki
XB-GENEPAGE-490553

Papers associated with rab40b



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A retinoic acid receptor expressed in the early development of Xenopus laevis., Ellinger-Ziegelbauer H, Dreyer C., Genes Dev. January 1, 1991; 5 (1): 94-104.              

Structure, localization and transcriptional properties of two classes of retinoic acid receptor alpha fusion proteins in acute promyelocytic leukemia (APL): structural similarities with a new family of oncoproteins., Kastner P, Perez A, Lutz Y, Rochette-Egly C, Gaub MP, Durand B, Lanotte M, Berger R, Chambon P., EMBO J. February 1, 1992; 11 (2): 629-42.

All-trans and 9-cis retinoic acid induction of CRABPII transcription is mediated by RAR-RXR heterodimers bound to DR1 and DR2 repeated motifs., Durand B, Saunders M, Leroy P, Leid M, Chambon P., Cell. October 2, 1992; 71 (1): 73-85.

Two isoforms of retinoic acid receptor alpha expressed during Xenopus development respond to retinoic acid., Sharpe CR., Mech Dev. November 1, 1992; 39 (1-2): 81-93.

Multiple parameters control the selectivity of nuclear receptors for their response elements. Selectivity and promiscuity in response element recognition by retinoic acid receptors and retinoid X receptors., Mader S, Leroy P, Chen JY, Chambon P., J Biol Chem. January 5, 1993; 268 (1): 591-600.

The pattern of retinoic acid receptor gamma (RAR gamma) expression in normal development of Xenopus laevis and after manipulation of the main body axis., Ellinger-Ziegelbauer H, Dreyer C., Mech Dev. April 1, 1993; 41 (1): 33-46.

Chimeric retinoic acid/thyroid hormone receptors implicate RAR-alpha 1 as mediating growth inhibition by retinoic acid., Schilthuis JG, Gann AA, Brockes JP., EMBO J. September 1, 1993; 12 (9): 3459-66.

The retinoid ligand 4-oxo-retinoic acid is a highly active modulator of positional specification., Pijnappel WW, Hendriks HF, Folkers GE, van den Brink CE, Dekker EJ, Edelenbosch C, van der Saag PT, Durston AJ., Nature. November 25, 1993; 366 (6453): 340-4.

Regional specificity of RAR gamma isoforms in Xenopus development., Pfeffer PL, De Robertis EM., Mech Dev. February 1, 1994; 45 (2): 147-53.          

Activation function 2 (AF-2) of retinoic acid receptor and 9-cis retinoic acid receptor: presence of a conserved autonomous constitutive activating domain and influence of the nature of the response element on AF-2 activity., Durand B, Saunders M, Gaudon C, Roy B, Losson R, Chambon P., EMBO J. November 15, 1994; 13 (22): 5370-82.

Characterization of cDNAs encoding the chick retinoic acid receptor gamma 2 and preferential distribution of retinoic acid receptor gamma transcripts during chick skin development., Michaille JJ, Blanchet S, Kanzler B, Garnier JM, Dhouailly D., Dev Dyn. December 1, 1994; 201 (4): 334-43.

The androgen receptor mRNA is up-regulated by testosterone in both the Harderian gland and thumb pad of the frog, Rana esculenta., Varriale B, Serino I., J Steroid Biochem Mol Biol. December 1, 1994; 51 (5-6): 259-65.

Two isoforms of Xenopus retinoic acid receptor gamma 2 (B) exhibit differential expression and sensitivity to retinoic acid during embryogenesis., Crawford MJ, Liversage RA, Varmuza SL., Dev Genet. January 1, 1995; 17 (4): 291-302.

Endogenous retinoic acid receptor (RAR)-retinoid X receptor (RXR) heterodimers are the major functional forms regulating retinoid-responsive elements in adult human keratinocytes. Binding of ligands to RAR only is sufficient for RAR-RXR heterodimers to confer ligand-dependent activation of hRAR beta 2/RARE (DR5)., Xiao JH, Durand B, Chambon P, Voorhees JJ., J Biol Chem. February 17, 1995; 270 (7): 3001-11.

Effects of retinoic acid on Xenopus embryos., Old RW, Smith DP, Mason CS, Marklew S, Jones EA., Biochem Soc Symp. January 1, 1996; 62 157-74.

Retinoic acid receptors and nuclear orphan receptors in the development of Xenopus laevis., Dreyer C, Ellinger-Ziegelbauer H., Int J Dev Biol. February 1, 1996; 40 (1): 255-62.        

Retinoid X receptor-selective ligands produce malformations in Xenopus embryos., Minucci S, Saint-Jeannet JP, Toyama R, Scita G, DeLuca LM, Tiara M, Levin AA, Ozato K, Dawid IB., Proc Natl Acad Sci U S A. March 5, 1996; 93 (5): 1803-7.

Novel retinoic acid receptor ligands in Xenopus embryos., Blumberg B, Bolado J, Derguini F, Craig AG, Moreno TA, Chakravarti D, Heyman RA, Buck J, Evans RM., Proc Natl Acad Sci U S A. May 14, 1996; 93 (10): 4873-8.

Retinoid X receptor (RXR) within the RXR-retinoic acid receptor heterodimer binds its ligand and enhances retinoid-dependent gene expression., Minucci S, Leid M, Toyama R, Saint-Jeannet JP, Peterson VJ, Horn V, Ishmael JE, Bhattacharyya N, Dey A, Dawid IB, Ozato K., Mol Cell Biol. February 1, 1997; 17 (2): 644-55.

Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ, Apekin V, Sive H., Dev Biol. December 1, 1997; 192 (1): 1-16.              

Inhibition of retinoic acid receptor-mediated signalling alters positional identity in the developing hindbrain., van der Wees J, Schilthuis JG, Koster CH, Diesveld-Schipper H, Folkers GE, van der Saag PT, Dawson MI, Shudo K, van der Burg B, Durston AJ., Development. February 1, 1998; 125 (3): 545-56.              

Retinoid receptor-induced alteration of the chromatin assembled on a ligand-responsive promoter in Xenopus oocytes., Minucci S, Wong J, Blanco JC, Shi YB, Shi YB, Wolffe AP, Ozato K., Mol Endocrinol. March 1, 1998; 12 (3): 315-24.

Molecular cloning of xSRC-3, a novel transcription coactivator from Xenopus, that is related to AIB1, p/CIP, and TIF2., Kim HJ, Lee SK, Na SY, Choi HS, Lee JW, Lee JW., Mol Endocrinol. July 1, 1998; 12 (7): 1038-47.

Metabolism to a response pathway selective retinoid ligand during axial pattern formation., Pijnappel WW, Folkers GE, de Jonge WJ, Verdegem PJ, de Laat SW, Lugtenburg J, Hendriks HF, van der Saag PT, Durston AJ., Proc Natl Acad Sci U S A. December 22, 1998; 95 (26): 15424-9.

The role of the 5' untranslated region of an mRNA in translation regulation during development., van der Velden AW, Thomas AA., Int J Biochem Cell Biol. January 1, 1999; 31 (1): 87-106.

The putative nuclear receptor mediator TIF1alpha is tightly associated with euchromatin., Remboutsika E, Lutz Y, Gansmuller A, Vonesch JL, Losson R, Chambon P., J Cell Sci. June 1, 1999; 112 ( Pt 11) 1671-83.

Active repression of RAR signaling is required for head formation., Koide T, Downes M, Chandraratna RA, Blumberg B, Umesono K., Genes Dev. August 15, 2001; 15 (16): 2111-21.            

The germ cell nuclear factor is required for retinoic acid signaling during Xenopus development., Barreto G, Borgmeyer U, Dreyer C., Mech Dev. April 1, 2003; 120 (4): 415-28.            

Active repression by unliganded retinoid receptors in development: less is sometimes more., Weston AD, Blumberg B, Underhill TM., J Cell Biol. April 28, 2003; 161 (2): 223-8.

Retinoic acid receptor alpha fusion to PML affects its transcriptional and chromatin-remodeling properties., Segalla S, Rinaldi L, Kilstrup-Nielsen C, Badaracco G, Minucci S, Pelicci PG, Landsberger N., Mol Cell Biol. December 1, 2003; 23 (23): 8795-808.

Multiple points of interaction between retinoic acid and FGF signaling during embryonic axis formation., Shiotsugu J, Katsuyama Y, Arima K, Baxter A, Koide T, Song J, Chandraratna RA, Blumberg B., Development. June 1, 2004; 131 (11): 2653-67.              

Spatiotemporal retinoid-X receptor activation detected in live vertebrate embryos., Luria A, Furlow JD., Proc Natl Acad Sci U S A. June 15, 2004; 101 (24): 8987-92.          

Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K, Shiotsugu J, Niu R, Khandpur R, Martinez M, Shin Y, Koide T, Cho KW, Kitayama A, Ueno N, Chandraratna RA, Blumberg B., Dev Dyn. February 1, 2005; 232 (2): 414-31.                          

Neofunctionalization in vertebrates: the example of retinoic acid receptors., Escriva H, Bertrand S, Germain P, Robinson-Rechavi M, Umbhauer M, Cartry J, Duffraisse M, Holland L, Gronemeyer H, Laudet V., PLoS Genet. July 1, 2006; 2 (7): e102.                  

Retinoic acid signalling is required for specification of pronephric cell fate., Cartry J, Nichane M, Ribes V, Colas A, Riou JF, Pieler T, Dollé P, Bellefroid EJ, Umbhauer M., Dev Biol. November 1, 2006; 299 (1): 35-51.                  

Inhibition of histone deacetylase as a new mechanism of teratogenesis., Menegola E, Di Renzo F, Broccia ML, Giavini E., Birth Defects Res C Embryo Today. December 1, 2006; 78 (4): 345-53.

Tpt1 activates transcription of oct4 and nanog in transplanted somatic nuclei., Koziol MJ, Garrett N, Gurdon JB., Curr Biol. May 1, 2007; 17 (9): 801-7.        

Exploring nervous system transcriptomes during embryogenesis and metamorphosis in Xenopus tropicalis using EST analysis., Fierro AC, Thuret R, Coen L, Perron M, Demeneix BA, Wegnez M, Gyapay G, Weissenbach J, Wincker P, Mazabraud A, Pollet N., BMC Genomics. May 16, 2007; 8 118.        

XRab40 and XCullin5 form a ubiquitin ligase complex essential for the noncanonical Wnt pathway., Lee RH, Iioka H, Ohashi M, Iemura S, Natsume T, Kinoshita N., EMBO J. August 8, 2007; 26 (15): 3592-606.

Arsenic as an endocrine disruptor: arsenic disrupts retinoic acid receptor-and thyroid hormone receptor-mediated gene regulation and thyroid hormone-mediated amphibian tail metamorphosis., Davey JC, Nomikos AP, Wungjiranirun M, Sherman JR, Ingram L, Batki C, Lariviere JP, Hamilton JW., Environ Health Perspect. February 1, 2008; 116 (2): 165-72.                

Retinoid signaling can repress blastula Wnt signaling and impair dorsal development in Xenopus embryo., Li S, Lou X, Wang J, Liu B, Ma L, Su Z, Ding X., Differentiation. October 1, 2008; 76 (8): 897-907.            

A microarray screen for direct targets of Zic1 identifies an aquaporin gene, aqp-3b, expressed in the neural folds., Cornish EJ, Hassan SM, Martin JD, Li S, Merzdorf CS., Dev Dyn. May 1, 2009; 238 (5): 1179-94.                

Developmental expression of retinoic acid receptors (RARs)., Dollé P., Nucl Recept Signal. May 12, 2009; 7 e006.            

The target of the NSD family of histone lysine methyltransferases depends on the nature of the substrate., Li Y, Trojer P, Xu CF, Cheung P, Kuo A, Drury WJ, Qiao Q, Neubert TA, Xu RM, Gozani O, Reinberg D., J Biol Chem. December 4, 2009; 284 (49): 34283-95.              

XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis., Lee SJ, Kim S, Choi SC, Han JK., Mech Dev. January 1, 2010; 127 (1-2): 49-61.                  

Retinoid signalling is required for information transfer from mesoderm to neuroectoderm during gastrulation., Lloret-Vilaspasa F, Jansen HJ, de Roos K, Chandraratna RA, Zile MH, Stern CD, Durston AJ., Int J Dev Biol. January 1, 2010; 54 (4): 599-608.                

A role for all-trans-retinoic acid in the early steps of lymphatic vasculature development., Marino D, Dabouras V, Brändli AW, Detmar M., J Vasc Res. January 1, 2011; 48 (3): 236-51.

Teratogenic effects of triphenyltin on embryos of amphibian (Xenopus tropicalis): a phenotypic comparison with the retinoid X and retinoic acid receptor ligands., Yu L, Zhang X, Yuan J, Cao Q, Liu J, Zhu P, Shi H., J Hazard Mater. September 15, 2011; 192 (3): 1860-8.

Analyzing the function of a hox gene: an evolutionary approach., Michaut L, Jansen HJ, Bardine N, Durston AJ, Gehring WJ., Dev Growth Differ. December 1, 2011; 53 (9): 982-93.                  

RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm., Janesick A, Shiotsugu J, Taketani M, Blumberg B., Development. March 1, 2012; 139 (6): 1213-24.                        

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