Papers associated with h4c4

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	Histone gene number in relation to C-value in amphibians., Hilder VA, Livesey RN, Turner PC, Vlad MT., Nucleic Acids Res. November 11, 1981; 9 (21): 5737-46.
	The genes coding for histone H3 and H4 in Neurospora crassa are unique and contain intervening sequences., Woudt LP, Pastink A, Kempers-Veenstra AE, Jansen AE, Mager WH, Planta RJ., Nucleic Acids Res. August 25, 1983; 11 (16): 5347-60.
	Transcription of a cloned Xenopus laevis H4 histone gene in the homologous frog oocyte system depends on an evolutionary conserved sequence motif in the -50 region., Clerc RG, Bucher P, Strub K, Birnstiel ML., Nucleic Acids Res. December 20, 1983; 11 (24): 8641-57.
	Assembly of transcriptionally active chromatin in Xenopus oocytes requires specific DNA binding factors., Gargiulo G, Razvi F, Worcel A., Cell. September 1, 1984; 38 (2): 511-21.
	A protein kinase from Xenopus eggs specific for ribosomal protein S6., Erikson E, Maller JL., Proc Natl Acad Sci U S A. February 1, 1985; 82 (3): 742-6.
	Level of histone H4 mRNA in Xenopus laevis embryonic cells cultured in the absence of cell adhesion., Atsuchi Y, Tashiro K, Yamana K, Shiokawa K., J Embryol Exp Morphol. November 1, 1986; 98 175-85.
	Antisense oligodeoxyribonucleotide-directed cleavage of maternal mRNA in Xenopus oocytes and embryos., Shuttleworth J, Matthews G, Dale L, Baker C, Colman A., Gene. December 10, 1988; 72 (1-2): 267-75.
	The assembly of regularly spaced nucleosomes in the Xenopus oocyte S-150 extract is accompanied by deacetylation of histone H4., Shimamura A, Worcel A., J Biol Chem. August 25, 1989; 264 (24): 14524-30.
	The maternal store of the xlgv7 mRNA in full-grown oocytes is not required for normal development in Xenopus., Kloc M, Miller M, Carrasco AE, Eastman E, Etkin L., Development. December 1, 1989; 107 (4): 899-907.
	Effects of oligo sequence and chemistry on the efficiency of oligodeoxyribonucleotide-mediated mRNA cleavage., Baker C, Holland D, Edge M, Colman A., Nucleic Acids Res. June 25, 1990; 18 (12): 3537-43.
	Xenopus laevis sperm proteins, previously identified as surface proteins with egg coat binding capability, are indeed histone H4, histone H3, and sperm specific protein SP2., Bernardini G, Donne ID, Norreri S, Negri A, Milzani A., J Exp Zool. August 15, 1992; 263 (2): 210-4.
	Histone H4 acetylation and transcription in amphibian chromatin., Sommerville J, Baird J, Turner BM., J Cell Biol. January 1, 1993; 120 (2): 277-90.
	A more efficient and specific strategy in the ablation of mRNA in Xenopus laevis using mixtures of antisense oligos., Morgan R, Edge M, Colman A., Nucleic Acids Res. September 25, 1993; 21 (19): 4615-20.
	Chromatin transitions during early Xenopus embryogenesis: changes in histone H4 acetylation and in linker histone type., Dimitrov S, Almouzni G, Dasso M, Wolffe AP., Dev Biol. November 1, 1993; 160 (1): 214-27.
	Anterior neurectoderm is progressively induced during gastrulation: the role of the Xenopus homeobox gene orthodenticle., Blitz IL, Cho KW., Development. April 1, 1995; 121 (4): 993-1004.
	Xwnt-8b: a maternally expressed Xenopus Wnt gene with a potential role in establishing the dorsoventral axis., Cui Y, Brown JD, Moon RT, Christian JL., Development. July 1, 1995; 121 (7): 2177-86.
	Developmentally regulated chromatin acetylation and histone H1(0) accumulation., Seigneurin D, Grunwald D, Lawrence JJ, Khochbin S., Int J Dev Biol. August 1, 1995; 39 (4): 597-603.
	Progressive maturation of chromatin structure regulates HSP70.1 gene expression in the preimplantation mouse embryo., Thompson EM, Legouy E, Christians E, Renard JP., Development. October 1, 1995; 121 (10): 3425-37.
	The Xvent-2 homeobox gene is part of the BMP-4 signalling pathway controlling [correction of controling] dorsoventral patterning of Xenopus mesoderm., Onichtchouk D, Gawantka V, Dosch R, Delius H, Hirschfeld K, Blumenstock C, Niehrs C., Development. October 1, 1996; 122 (10): 3045-53.
	Expression of a dominant-negative Wnt blocks induction of MyoD in Xenopus embryos., Hoppler S, Brown JD, Moon RT., Genes Dev. November 1, 1996; 10 (21): 2805-17.
	Combinatorial signalling by Xwnt-11 and Xnr3 in the organizer epithelium., Glinka A, Delius H, Blumenstock C, Niehrs C., Mech Dev. December 1, 1996; 60 (2): 221-31.
	Smad5 induces ventral fates in Xenopus embryo., Suzuki A, Chang C, Yingling JM, Wang XF, Hemmati-Brivanlou A., Dev Biol. April 15, 1997; 184 (2): 402-5.
	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.
	Regulated unmasking of in vivo synthesized maternal mRNA at oocyte maturation. A role for the chaperone nucleoplasmin., Meric F, Matsumoto K, Wolffe AP., J Biol Chem. May 9, 1997; 272 (19): 12840-6.
	Early expression of a novel nucleotide receptor in the neural plate of Xenopus embryos., Bogdanov YD, Dale L, King BF, Whittock N, Burnstock G., J Biol Chem. May 9, 1997; 272 (19): 12583-90.
	Xenopus LIM motif-containing protein kinase, Xlimk1, is expressed in the developing head structure of the embryo., Takahashi T, Aoki S, Koshimizu U, Matsumoto K, Nakamura T., Dev Dyn. June 1, 1997; 209 (2): 196-205.
	Xenopus Pax-2 displays multiple splice forms during embryogenesis and pronephric kidney development., Heller N, Brändli AW., Mech Dev. December 1, 1997; 69 (1-2): 83-104.
	The homeobox gene PV.1 mediates specification of the prospective neural ectoderm in Xenopus embryos., Ault KT, Xu RH, Kung HF, Jamrich M., Dev Biol. December 1, 1997; 192 (1): 162-71.
	Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K, Kishi M, Matsui M, Nakanishi S, Sasai Y., Development. February 1, 1998; 125 (4): 579-87.
	A Xenopus homologue of aml-1 reveals unexpected patterning mechanisms leading to the formation of embryonic blood., Tracey WD, Pepling ME, Horb ME, Thomsen GH, Gergen JP., Development. April 1, 1998; 125 (8): 1371-80.
	Requirement for Xvent-1 and Xvent-2 gene function in dorsoventral patterning of Xenopus mesoderm., Onichtchouk D, Glinka A, Niehrs C., Development. April 1, 1998; 125 (8): 1447-56.
	The Xcad-2 gene can provide a ventral signal independent of BMP-4., Pillemer G, Yelin R, Epstein M, Gont L, Frumkin Y, Yisraeli JK, Steinbeisser H, Fainsod A., Mech Dev. June 1, 1998; 74 (1-2): 133-43.
	Xenopus Zic family and its role in neural and neural crest development., Nakata K, Nagai T, Aruga J, Mikoshiba K., Mech Dev. July 1, 1998; 75 (1-2): 43-51.
	Transcriptionally active Xenopus laevis somatic 5 S ribosomal RNA genes are packaged with hyperacetylated histone H4, whereas transcriptionally silent oocyte genes are not., Howe L, Ranalli TA, Allis CD, Ausió J., J Biol Chem. August 14, 1998; 273 (33): 20693-6.
	Misexpression of the catenin p120(ctn)1A perturbs Xenopus gastrulation but does not elicit Wnt-directed axis specification., Paulson AF, Fang X, Ji H, Reynolds AB, McCrea PD., Dev Biol. March 15, 1999; 207 (2): 350-63.
	XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M, Brown JD, Bates R, Kimelman D, Moon RT., Development. June 1, 1999; 126 (14): 3159-70.
	Patterning of the mesoderm involves several threshold responses to BMP-4 and Xwnt-8., Marom K, Fainsod A, Steinbeisser H., Mech Dev. September 1, 1999; 87 (1-2): 33-44.
	Functional analysis of the SIN3-histone deacetylase RPD3-RbAp48-histone H4 connection in the Xenopus oocyte., Vermaak D, Wade PA, Jones PL, Shi YB, Wolffe AP., Mol Cell Biol. September 1, 1999; 19 (9): 5847-60.
	Purification and properties of the Xenopus Hat1 acetyltransferase: association with the 14-3-3 proteins in the oocyte nucleus., Imhof A, Wolffe AP., Biochemistry. October 5, 1999; 38 (40): 13085-93.
	Inhibition of transcription of class II, but not class III and I, genes in Xenopus postblastular embryos overexpressed with the TBP-binding protein, Dr1 (NC2beta)., Nagano M, Shiokawa K., Biochem Biophys Res Commun. November 30, 1999; 265 (3): 644-51.
	Is chordin a long-range- or short-range-acting factor? Roles for BMP1-related metalloproteases in chordin and BMP4 autofeedback loop regulation., Blitz IL, Shimmi O, Wünnenberg-Stapleton K, O'Connor MB, Cho KW., Dev Biol. July 1, 2000; 223 (1): 120-38.
	The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD, Hallagan SE, McGrew LL, Miller JR, Moon RT., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.
	Xoom is required for epibolic movement of animal ectodermal cells in Xenopus laevis gastrulation., Hasegawa K, Kinoshita T., Dev Growth Differ. August 1, 2000; 42 (4): 337-46.
	The homeodomain transcription factor Xvent-2 mediates autocatalytic regulation of BMP-4 expression in Xenopus embryos., Schuler-Metz A, Knöchel S, Kaufmann E, Knöchel W., J Biol Chem. November 3, 2000; 275 (44): 34365-74.
	The pitx2 homeobox protein is required early for endoderm formation and nodal signaling. ., Faucourt M, Houliston E, Besnardeau L, Kimelman D, Lepage T., Dev Biol. January 15, 2001; 229 (2): 287-306.
	The histone H4 acetyltransferase MOF uses a C2HC zinc finger for substrate recognition., Akhtar A, Becker PB., EMBO Rep. February 1, 2001; 2 (2): 113-8.
	Critical role for the histone H4 N terminus in nucleosome remodeling by ISWI., Clapier CR, Längst G, Corona DF, Becker PB, Nightingale KP., Mol Cell Biol. February 1, 2001; 21 (3): 875-83.
	foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA, Akers L, Moody SA., Dev Biol. April 15, 2001; 232 (2): 439-57.
	Methylation of histone H4 at arginine 3 facilitating transcriptional activation by nuclear hormone receptor., Wang H, Huang ZQ, Xia L, Feng Q, Erdjument-Bromage H, Strahl BD, Briggs SD, Allis CD, Wong J, Tempst P, Zhang Y., Science. August 3, 2001; 293 (5531): 853-7.
	The APC regulator CDH1 is essential for the progression of embryonic cell cycles in Xenopus., Zhou Y, Ching YP, Ng RW, Jin DY., Biochem Biophys Res Commun. May 31, 2002; 294 (1): 120-6.

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