Papers associated with mst1

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	Variation in the DNA methylation pattern of expressed and nonexpressed genes in chicken., Cooper DN, Errington LH, Clayton RM., DNA. January 1, 1983; 2 (2): 131-40.
	Analysis of expression of adenovirus DNA (fragments) by microinjection in Xenopus oocytes. Independent synthesis of minor early region 2 proteins., Asselbergs FA, Smart JE, Mathews MB., J Mol Biol. January 15, 1983; 163 (2): 209-38.
	Regulation of adenovirus transcription by an E1a gene in microinjected Xenopus laevis oocytes., Jones NC, Richter JD, Weeks DL, Smith LD., Mol Cell Biol. December 1, 1983; 3 (12): 2131-42.
	Adenovirus E1a gene product expressed at high levels in Escherichia coli is functional., Ferguson B, Jones N, Richter J, Rosenberg M., Science. June 22, 1984; 224 (4655): 1343-6.
	Transformed Xenopus embryos as a transient expression system to analyze gene expression at the midblastula transition., Etkin LD, Balcells S., Dev Biol. March 1, 1985; 108 (1): 173-8.
	A first exon-encoded domain of E1A sufficient for posttranslational modification, nuclear-localization, and induction of adenovirus E3 promoter expression in Xenopus oocytes., Richter JD, Young P, Jones NC, Krippl B, Rosenberg M, Ferguson B., Proc Natl Acad Sci U S A. December 1, 1985; 82 (24): 8434-8.
	Trans effect of the E1 region of adenoviruses on the expression of a prokaryotic gene in mammalian cells: resistance to 5' -CCGG- 3' methylation., Langner KD, Weyer U, Doerfler W., Proc Natl Acad Sci U S A. March 1, 1986; 83 (6): 1598-1602.
	Adenovirus E1A requires synthesis of a cellular protein to establish a stable transcription complex in injected Xenopus laevis oocytes., Richter JD, Hurst HC, Jones NC., Mol Cell Biol. September 1, 1987; 7 (9): 3049-56.
	Reactivation of the methylation-inactivated late E2A promoter of adenovirus type 2 by E1A (13 S) functions., Weisshaar B, Langner KD, Jüttermann R, Müller U, Zock C, Klimkait T, Doerfler W., J Mol Biol. July 20, 1988; 202 (2): 255-70.
	Rapid turnover of adenovirus E1A is determined through a co-translational mechanism that requires an aminoterminal domain., Slavicek JM, Jones NC, Richter JD., EMBO J. October 1, 1988; 7 (10): 3171-80.
	Phosphorylation of serine residue 89 of human adenovirus E1A proteins is responsible for their characteristic electrophoretic mobility shifts, and its mutation affects biological function., Smith CL, Debouck C, Rosenberg M, Culp JS., J Virol. April 1, 1989; 63 (4): 1569-77.
	In vivo photocrosslinking reveals that transcription factor binding to the mammalian ATF recognition sequence is required for E1A-induced transactivation in injected Xenopus laevis oocytes., Richter JD., Nucleic Acids Res. June 26, 1989; 17 (12): 4503-16.
	Identification of four nuclear transport signal-binding proteins that interact with diverse transport signals., Yamasaki L, Kanda P, Lanford RE., Mol Cell Biol. July 1, 1989; 9 (7): 3028-36.
	A karyophilic signal sequence in adenovirus type 5 E1A is functional in Xenopus oocytes but not in somatic cells., Slavicek JM, Jones NC, Richter JD., J Virol. September 1, 1989; 63 (9): 4047-50.
	Comparison of diverse transport signals in synthetic peptide-induced nuclear transport., Lanford RE, Feldherr CM, White RG, Dunham RG, Kanda P., Exp Cell Res. January 1, 1990; 186 (1): 32-8.
	Activation in vitro of RNA polymerase II and III directed transcription by baculovirus produced E1A protein., Patel G, Jones NC., Nucleic Acids Res. May 25, 1990; 18 (10): 2909-15.
	The degradation sequence of adenovirus E1A consists of the amino-terminal tetrapeptide Met-Arg-His-Ile., Simon R, Richter JD., Mol Cell Biol. November 1, 1990; 10 (11): 5609-15.
	Isolation of the human cdk2 gene that encodes the cyclin A- and adenovirus E1A-associated p33 kinase., Tsai LH, Harlow E, Meyerson M., Nature. September 12, 1991; 353 (6340): 174-7.
	Antibodies specific for the human retinoblastoma protein identify a family of related polypeptides., Hu QJ, Bautista C, Edwards GM, Defeo-Jones D, Jones RE, Harlow E., Mol Cell Biol. November 1, 1991; 11 (11): 5792-9.
	xP2, a new member of the P-domain peptide family of potential growth factors, is synthesized in Xenopus laevis skin., Hauser F, Roeben C, Hoffmann W., J Biol Chem. July 15, 1992; 267 (20): 14451-5.
	Structure and expression of the Xenopus retinoblastoma gene., Destrée OH, Lam KT, Peterson-Maduro LJ, Eizema K, Diller L, Gryka MA, Frebourg T, Shibuya E, Friend SH., Dev Biol. September 1, 1992; 153 (1): 141-9.
	Analysis of a developmentally regulated nuclear localization signal in Xenopus., Standiford DM, Richter JD., J Cell Biol. September 1, 1992; 118 (5): 991-1002.
	The mouse one P-domain (pS2) and two P-domain (mSP) genes exhibit distinct patterns of expression., Lefebvre O, Wolf C, Kédinger M, Chenard MP, Tomasetto C, Chambon P, Rio MC., J Cell Biol. July 1, 1993; 122 (1): 191-8.
	Transcriptional elongation by RNA polymerase II is stimulated by transactivators., Yankulov K, Blau J, Purton T, Roberts S, Bentley DL., Cell. June 3, 1994; 77 (5): 749-59.
	Analysis of ATF2 gene expression during early Xenopus laevis development., Villarreal XC, Richter JD., Gene. February 14, 1995; 153 (2): 225-9.
	The Xenopus homologue of hepatocyte growth factor-like protein is specifically expressed in the presumptive neural plate during gastrulation., Aberger F, Schmidt G, Richter K., Mech Dev. January 1, 1996; 54 (1): 23-37.
	Cloning and expression of Xenopus HGF-like protein (HLP) and Ron/HLP receptor implicate their involvement in early neural development., Nakamura T, Aoki S, Takahashi T, Matsumoto K, Kiyohara T, Nakamura T., Biochem Biophys Res Commun. July 16, 1996; 224 (2): 564-73.
	Involvement of Livertine, a hepatocyte growth factor family member, in neural morphogenesis., Ruiz i Altaba A, Théry C., Mech Dev. December 1, 1996; 60 (2): 207-20.
	A member of the Met/HGF-receptor family is expressed in a BMP-4-like pattern in the ectoderm of Xenopus gastrulae., Aberger F, Weidinger G, Richter K., Biochem Biophys Res Commun. February 3, 1997; 231 (1): 191-5.
	A role for Xenopus Gli-type zinc finger proteins in the early embryonic patterning of mesoderm and neuroectoderm., Marine JC, Bellefroid EJ, Pendeville H, Martial JA, Pieler T., Mech Dev. May 1, 1997; 63 (2): 211-25.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V, Pollet N, Delius H, Vingron M, Pfister R, Nitsch R, Blumenstock C, Niehrs C., Mech Dev. October 1, 1998; 77 (2): 95-141.
	Xenopus NF-Y pre-sets chromatin to potentiate p300 and acetylation-responsive transcription from the Xenopus hsp70 promoter in vivo., Li Q, Herrler M, Landsberger N, Kaludov N, Ogryzko VV, Nakatani Y, Wolffe AP., EMBO J. November 2, 1998; 17 (21): 6300-15.
	XBF-1, a winged helix transcription factor with dual activity, has a role in positioning neurogenesis in Xenopus competent ectoderm., Bourguignon C, Li J, Papalopulu N., Development. December 1, 1998; 125 (24): 4889-900.
	C-Terminal binding protein is a transcriptional repressor that interacts with a specific class of vertebrate Polycomb proteins., Sewalt RG, Gunster MJ, van der Vlag J, Satijn DP, Otte AP., Mol Cell Biol. January 1, 1999; 19 (1): 777-87.
	p300 stimulates transcription instigated by ligand-bound thyroid hormone receptor at a step subsequent to chromatin disruption., Li Q, Imhof A, Collingwood TN, Urnov FD, Wolffe AP., EMBO J. October 15, 1999; 18 (20): 5634-52.
	Neuralization of the Xenopus embryo by inhibition of p300/ CREB-binding protein function., Kato Y, Shi Y, Shi Y, He X., J Neurosci. November 1, 1999; 19 (21): 9364-73.
	The p300/CBP acetyltransferases function as transcriptional coactivators of beta-catenin in vertebrates., Hecht A, Vleminckx K, Vleminckx K, Stemmler MP, van Roy F, Kemler R., EMBO J. April 17, 2000; 19 (8): 1839-50.
	The transcriptional coactivator CBP interacts with beta-catenin to activate gene expression., Takemaru KI, Moon RT., J Cell Biol. April 17, 2000; 149 (2): 249-54.
	Dome formation and tubule morphogenesis by Xenopus kidney A6 cell cultures exposed to microgravity simulated with a 3D-clinostat and to hypergravity., Ichigi J, Asashima M., In Vitro Cell Dev Biol Anim. January 1, 2001; 37 (1): 31-44.
	Xiro-1 controls mesoderm patterning by repressing bmp-4 expression in the Spemann organizer., Glavic A, Gómez-Skarmeta JL, Mayor R., Dev Dyn. November 1, 2001; 222 (3): 368-76.
	The homeoprotein Xiro1 is required for midbrain-hindbrain boundary formation., Glavic A, Gómez-Skarmeta JL, Mayor R., Development. April 1, 2002; 129 (7): 1609-21.
	Regulation of GRIP1 and CBP Coactivator activity by Rho GDI modulates estrogen receptor transcriptional enhancement., Su LF, Wang Z, Garabedian MJ., J Biol Chem. October 4, 2002; 277 (40): 37037-44.
	Xiro homeoproteins coordinate cell cycle exit and primary neuron formation by upregulating neuronal-fate repressors and downregulating the cell-cycle inhibitor XGadd45-gamma., de la Calle-Mustienes E, Glavic A, Modolell J, Gómez-Skarmeta JL., Mech Dev. November 1, 2002; 119 (1): 69-80.
	Dual effect of lysine-rich polypeptides on the activity of protein kinase CK2., Romero-Oliva F, Jacob G, Allende JE., J Cell Biochem. May 15, 2003; 89 (2): 348-55.
	Adenovirus protein VII condenses DNA, represses transcription, and associates with transcriptional activator E1A., Johnson JS, Osheim YN, Xue Y, Emanuel MR, Lewis PW, Bankovich A, Beyer AL, Engel DA., J Virol. June 1, 2004; 78 (12): 6459-68.
	PR72, a novel regulator of Wnt signaling required for Naked cuticle function., Creyghton MP, Roël G, Eichhorn PJ, Hijmans EM, Maurer I, Destrée O, Bernards R., Genes Dev. February 1, 2005; 19 (3): 376-86.
	A dual requirement for Iroquois genes during Xenopus kidney development., Alarcón P, Rodríguez-Seguel E, Fernández-González A, Rubio R, Gómez-Skarmeta JL., Development. October 1, 2008; 135 (19): 3197-207.
	Integration of telencephalic Wnt and hedgehog signaling center activities by Foxg1., Danesin C, Peres JN, Johansson M, Snowden V, Cording A, Papalopulu N, Houart C., Dev Cell. April 1, 2009; 16 (4): 576-87.
	The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx., Rodríguez-Seguel E, Alarcón P, Gómez-Skarmeta JL., Dev Biol. May 15, 2009; 329 (2): 258-68.
	The adenoviral E1A protein displaces corepressors and relieves gene repression by unliganded thyroid hormone receptors in vivo., Sato Y, Ding A, Heimeier RA, Yousef AF, Mymryk JS, Walfish PG, Shi YB., Cell Res. June 1, 2009; 19 (6): 783-92.

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