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Summary Expression Phenotypes Gene Literature (204) GO Terms (11) Nucleotides (2488) Proteins (54) Interactants (1082) Wiki
XB--480346

Papers associated with actc1



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The Xenopus GATA-4/5/6 genes are associated with cardiac specification and can regulate cardiac-specific transcription during embryogenesis., Jiang Y, Evans T., Dev Biol. March 15, 1996; 174 (2): 258-70.          


Activation of the cardiac alpha-actin promoter depends upon serum response factor, Tinman homologue, Nkx-2.5, and intact serum response elements., Chen CY, Croissant J, Majesky M, Topouzis S, McQuinn T, Frankovsky MJ, Schwartz RJ., Dev Genet. January 1, 1996; 19 (2): 119-30.


Caudalization of neural fate by tissue recombination and bFGF., Cox WG, Hemmati-Brivanlou A., Development. December 1, 1995; 121 (12): 4349-58.                


Anti-dorsalizing morphogenetic protein is a novel TGF-beta homolog expressed in the Spemann organizer., Moos M, Wang S, Krinks M., Development. December 1, 1995; 121 (12): 4293-301.                  


Disruption of BMP signals in embryonic Xenopus ectoderm leads to direct neural induction., Hawley SH, Wünnenberg-Stapleton K, Hashimoto C, Laurent MN, Watabe T, Blumberg BW, Cho KW., Genes Dev. December 1, 1995; 9 (23): 2923-35.                


Nodal-related signals induce axial mesoderm and dorsalize mesoderm during gastrulation., Jones CM, Kuehn MR, Hogan BL, Smith JC, Wright CV., Development. November 1, 1995; 121 (11): 3651-62.                


Androgen regulation of a laryngeal-specific myosin heavy chain mRNA isoform whose expression is sexually differentiated., Catz DS, Fischer LM, Kelley DB., Dev Biol. October 1, 1995; 171 (2): 448-57.              


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.        


Bone morphogenetic protein 2 in the early development of Xenopus laevis., Clement JH, Fettes P, Knöchel S, Lef J, Knöchel W., Mech Dev. August 1, 1995; 52 (2-3): 357-70.            


FGF is a prospective competence factor for early activin-type signals in Xenopus mesoderm induction., Cornell RA, Musci TJ, Kimelman D., Development. August 1, 1995; 121 (8): 2429-37.


Functional conservation of the Wnt signaling pathway revealed by ectopic expression of Drosophila dishevelled in Xenopus., Rothbächer U, Laurent MN, Blitz IL, Watabe T, Marsh JL, Cho KW., Dev Biol. August 1, 1995; 170 (2): 717-21.    


Induction of dorsal mesoderm by soluble, mature Vg1 protein., Kessler DS, Melton DA., Development. July 1, 1995; 121 (7): 2155-64.            


Androgen-directed development of the Xenopus laevis larynx: control of androgen receptor expression and tissue differentiation., Fischer LM, Catz D, Kelley DB., Dev Biol. July 1, 1995; 170 (1): 115-26.            


Role of MAP kinase in mesoderm induction and axial patterning during Xenopus development., LaBonne C, Burke B, Whitman M., Development. May 1, 1995; 121 (5): 1475-86.


Patterning of the mesoderm in Xenopus: dose-dependent and synergistic effects of Brachyury and Pintallavis., O'Reilly MA, Smith JC, Cunliffe V., Development. May 1, 1995; 121 (5): 1351-9.                  


Localized BMP-4 mediates dorsal/ventral patterning in the early Xenopus embryo., Schmidt JE, Suzuki A, Ueno N, Kimelman D., Dev Biol. May 1, 1995; 169 (1): 37-50.              


Cardiac myosin heavy chain expression during heart development in Xenopus laevis., Cox WG, Neff AW., Differentiation. April 1, 1995; 58 (4): 269-80.                


The Xenopus homologue of Otx2 is a maternal homeobox gene that demarcates and specifies anterior body regions., Pannese M, Polo C, Andreazzoli M, Vignali R, Kablar B, Barsacchi G, Boncinelli E., Development. March 1, 1995; 121 (3): 707-20.                      


The SH2-containing protein-tyrosine phosphatase SH-PTP2 is required upstream of MAP kinase for early Xenopus development., Tang TL, Freeman RM, O'Reilly AM, Neel BG, Sokol SY., Cell. February 10, 1995; 80 (3): 473-83.              


XIdx, a dominant negative regulator of bHLH function in early Xenopus embryos., Wilson R, Mohun T., Mech Dev. February 1, 1995; 49 (3): 211-22.          


Ventral expression of GATA-1 and GATA-2 in the Xenopus embryo defines induction of hematopoietic mesoderm., Kelley C, Yee K, Harland R, Zon LI., Dev Biol. September 1, 1994; 165 (1): 193-205.            


The location of the third cleavage plane of Xenopus embryos partitions morphogenetic information in animal quartets., Chung HM, Yokota H, Dent A, Malacinski GM, Neff AW., Int J Dev Biol. September 1, 1994; 38 (3): 421-8.


Effect of an inhibitory mutant of the FGF receptor on mesoderm-derived alpha-smooth muscle actin-expressing cells in Xenopus embryo., Saint-Jeannet JP, Thiery JP, Koteliansky VE., Dev Biol. August 1, 1994; 164 (2): 374-82.          


Mesodermal patterning by a gradient of the vertebrate homeobox gene goosecoid., Niehrs C, Steinbeisser H, De Robertis EM., Science. February 11, 1994; 263 (5148): 817-20.


Activin-mediated mesoderm induction requires FGF., Cornell RA, Kimelman D., Development. February 1, 1994; 120 (2): 453-62.


Suramin and heparin: aspecific inhibitors of mesoderm induction in the Xenopus laevis embryo., Cardellini P, Polo C, Coral S., Mech Dev. January 1, 1994; 45 (1): 73-87.


XFKH2, a Xenopus HNF-3 alpha homologue, exhibits both activin-inducible and autonomous phases of expression in early embryos., Bolce ME, Hemmati-Brivanlou A, Harland RM., Dev Biol. December 1, 1993; 160 (2): 413-23.              


The MyoD binding site is dispensable for cardiac actin gene expression in the somites of later stage Xenopus embryos., Su XL, Woodland HR., FEBS Lett. November 29, 1993; 335 (1): 41-6.


Competence prepattern in the animal hemisphere of the 8-cell-stage Xenopus embryo., Kinoshita K, Bessho T, Asashima M., Dev Biol. November 1, 1993; 160 (1): 276-84.        


Expression of tenascin mRNA in mesoderm during Xenopus laevis embryogenesis: the potential role of mesoderm patterning in tenascin regionalization., Umbhauer M, Riou JF, Spring J, Smith JC, Boucaut JC., Development. September 1, 1992; 116 (1): 147-57.            


Ventrolateral regionalization of Xenopus laevis mesoderm is characterized by the expression of alpha-smooth muscle actin., Saint-Jeannet JP, Levi G, Girault JM, Koteliansky V, Thiery JP., Development. August 1, 1992; 115 (4): 1165-73.          


DVR-4 (bone morphogenetic protein-4) as a posterior-ventralizing factor in Xenopus mesoderm induction., Jones CM, Lyons KM, Lapan PM, Wright CV, Hogan BL., Development. June 1, 1992; 115 (2): 639-47.


Localized expression of a Xenopus POU gene depends on cell-autonomous transcriptional activation and induction-dependent inactivation., Frank D, Harland RM., Development. June 1, 1992; 115 (2): 439-48.            


Analysis of mRNAs under translational control during Xenopus embryogenesis: isolation of new ribosomal protein clones., Loreni F, Francesconi A, Jappelli R, Amaldi F., Nucleic Acids Res. April 25, 1992; 20 (8): 1859-63.


Cloning of a second type of activin receptor and functional characterization in Xenopus embryos., Mathews LS, Vale WW, Kintner CR., Science. March 27, 1992; 255 (5052): 1702-5.


Protein kinase C isozymes have distinct roles in neural induction and competence in Xenopus., Otte AP, Moon RT., Cell. March 20, 1992; 68 (6): 1021-9.


Transient expression of XMyoD in non-somitic mesoderm of Xenopus gastrulae., Frank D, Harland RM., Development. December 1, 1991; 113 (4): 1387-93.        


Developmental and regional expression of thyroid hormone receptor genes during Xenopus metamorphosis., Kawahara A, Baker BS, Tata JR., Development. August 1, 1991; 112 (4): 933-43.            


Localized and inducible expression of Xenopus-posterior (Xpo), a novel gene active in early frog embryos, encoding a protein with a 'CCHC' finger domain., Sato SM, Sargent TD., Development. July 1, 1991; 112 (3): 747-53.            


Xenopus embryos contain a somite-specific, MyoD-like protein that binds to a promoter site required for muscle actin expression., Taylor MV, Gurdon JB, Hopwood ND, Towers N, Mohun TJ., Genes Dev. July 1, 1991; 5 (7): 1149-60.


A family of muscle gene promoter element (CArG) binding activities in Xenopus embryos: CArG/SRE discrimination and distribution during myogenesis., Taylor MV., Nucleic Acids Res. May 25, 1991; 19 (10): 2669-75.


Xenopus Myf-5 marks early muscle cells and can activate muscle genes ectopically in early embryos., Hopwood ND, Pluck A, Gurdon JB., Development. February 1, 1991; 111 (2): 551-60.                


Gene activation in the amphibian mesoderm., Hopwood ND, Gurdon JB., Dev Suppl. January 1, 1991; 1 95-104.


Localization of specific mRNAs in Xenopus embryos by whole-mount in situ hybridization., Hemmati-Brivanlou A, Frank D, Bolce ME, Brown BD, Sive HL, Harland RM., Development. October 1, 1990; 110 (2): 325-30.  


Muscle-specific (CArG) and serum-responsive (SRE) promoter elements are functionally interchangeable in Xenopus embryos and mouse fibroblasts., Taylor M, Treisman R, Garrett N, Mohun T., Development. May 1, 1989; 106 (1): 67-78.


Mesoderm-inducing properties of INT-2 and kFGF: two oncogene-encoded growth factors related to FGF., Paterno GD, Gillespie LL, Dixon MS, Slack JM, Heath JK., Development. May 1, 1989; 106 (1): 79-83.


The CArG promoter sequence is necessary for muscle-specific transcription of the cardiac actin gene in Xenopus embryos., Mohun TJ, Taylor MV, Garrett N, Gurdon JB., EMBO J. April 1, 1989; 8 (4): 1153-61.


The presence of fibroblast growth factor in the frog egg: its role as a natural mesoderm inducer., Kimelman D, Abraham JA, Haaparanta T, Palisi TM, Kirschner MW., Science. November 18, 1988; 242 (4881): 1053-6.


Proteins regulating actin assembly in oogenesis and early embryogenesis of Xenopus laevis: gelsolin is the major cytoplasmic actin-binding protein., Ankenbauer T, Kleinschmidt JA, Vandekerckhove J, Franke WW., J Cell Biol. October 1, 1988; 107 (4): 1489-98.                  


A third striated muscle actin gene is expressed during early development in the amphibian Xenopus laevis., Mohun T, Garrett N, Stutz F, Sophr G., J Mol Biol. July 5, 1988; 202 (1): 67-76.

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