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Summary Expression Phenotypes Gene Literature (192) GO Terms (4) Nucleotides (1093) Proteins (40) Interactants (779) Wiki
XB--6469704

Papers associated with acta4



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Actin in Xenopus oocytes., Clark TG, Merriam RW., J Cell Biol. May 1, 1978; 77 (2): 427-38.

Diversity of expression of non-muscle actin in amphibia., Vandekerckhove J, Franke WW, Weber K., J Mol Biol. October 25, 1981; 152 (2): 413-26.

Ultrastructural studies on the replication of herpes simplex virus in PK and XTC-2 cells., Ciampor F, Szántó J., Acta Virol. January 1, 1982; 26 (1-2): 67-72.

The 5S ribosomal RNA gene clusters in Tetrahymena thermophila: strain differences, chromosomal localization, and loss during micronuclear ageing., Allen SL, Ervin PR, McLaren NC, Brand RE., Mol Gen Genet. January 1, 1984; 197 (2): 244-53.

Cell type-specific activation of actin genes in the early amphibian embryo., Mohun TJ, Brennan S, Dathan N, Fairman S, Gurdon JB., Nature. October 25, 1984; 311 (5988): 716-21.

Activation of muscle-specific actin genes in Xenopus development by an induction between animal and vegetal cells of a blastula., Gurdon JB, Fairman S, Mohun TJ, Brennan S., Cell. July 1, 1985; 41 (3): 913-22.                      

Actin genes in Xenopus and their developmental control., Gurdon JB, Mohun TJ, Brennan S, Cascio S., J Embryol Exp Morphol. November 1, 1985; 89 Suppl 125-36.    

[Movements of cellular material of the dorsal wall in clawed-toad embryos during gastrulation and neurulation]., Petrov KV, Belousov LV., Ontogenez. January 1, 1986; 17 (1): 78-83.

A monoclonal antibody against alpha-smooth muscle actin: a new probe for smooth muscle differentiation., Skalli O, Ropraz P, Trzeciak A, Benzonana G, Gillessen D, Gabbiani G., J Cell Biol. December 1, 1986; 103 (6 Pt 2): 2787-96.

Expression of Xenopus N-CAM RNA in ectoderm is an early response to neural induction., Kintner CR, Melton DA., Development. March 1, 1987; 99 (3): 311-25.                  

Effects of substitution of putative transmembrane segments on nicotinic acetylcholine receptor function., Tobimatsu T, Fujita Y, Fukuda K, Tanaka K, Mori Y, Konno T, Mishina M, Numa S., FEBS Lett. September 28, 1987; 222 (1): 56-62.

Synergistic induction of mesoderm by FGF and TGF-beta and the identification of an mRNA coding for FGF in the early Xenopus embryo., Kimelman D, Kirschner M., Cell. December 4, 1987; 51 (5): 869-77.

Different regulatory elements are required for cell-type and stage specific expression of the Xenopus laevis skeletal muscle actin gene upon injection in X.laevis oocytes and embryos., Steinbeisser H, Hofmann A, Stutz F, Trendelenburg MF., Nucleic Acids Res. April 25, 1988; 16 (8): 3223-38.

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.

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.                  

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.

Amphibian (urodele) myotomes display transitory anterior/posterior and medial/lateral differentiation patterns., Neff AW, Malacinski GM, Chung HM., Dev Biol. April 1, 1989; 132 (2): 529-43.  

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.

The appearance of acetylated alpha-tubulin during early development and cellular differentiation in Xenopus., Chu DT, Klymkowsky MW., Dev Biol. November 1, 1989; 136 (1): 104-17.                  

Cleavage plane determination in amphibian eggs., Sawai T, Yomota A., Ann N Y Acad Sci. January 1, 1990; 582 40-9.

The Xenopus MyoD gene: an unlocalised maternal mRNA predates lineage-restricted expression in the early embryo., Harvey RP., Development. April 1, 1990; 108 (4): 669-80.

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.  

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.

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.

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.

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.          

A Xenopus homebox gene defines dorsal-ventral domains in the developing brain., Saha MS, Michel RB, Gulding KM, Grainger RM., Development. May 1, 1993; 118 (1): 193-202.              

Determination of the sequence requirements for the expression of a Xenopus borealis embryonic/larval skeletal actin gene., Lakin ND, Boardman M, Woodland HR., Eur J Biochem. June 1, 1993; 214 (2): 425-35.

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.        

Diluted and undiluted Mercox severely destroy unfixed endothelial cells. A light and electron microscopic study using cultured endothelial cells and tadpole tail fin vessels., Gassner J, Lametschwandtner A, Weiger T, Bauer HC., Scanning Microsc. January 1, 1994; 8 (3): 721-32; discussion 732-4.

Differential expression of a Distal-less homeobox gene Xdll-2 in ectodermal cell lineages., Dirksen ML, Morasso MI, Sargent TD, Jamrich M., Mech Dev. April 1, 1994; 46 (1): 63-70.          

Functional independence of monomeric CHIP28 water channels revealed by expression of wild-type mutant heterodimers., Shi LB, Skach WR, Verkman AS., J Biol Chem. April 8, 1994; 269 (14): 10417-22.

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.          

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.              

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.                      

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.              

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.

Patterning of the neural ectoderm of Xenopus laevis by the amino-terminal product of hedgehog autoproteolytic cleavage., Lai CJ, Ekker SC, Beachy PA, Moon RT., Development. August 1, 1995; 121 (8): 2349-60.            

Efficient hormone-inducible protein function in Xenopus laevis., Kolm PJ, Sive HL., Dev Biol. September 1, 1995; 171 (1): 267-72.  

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.                

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.                

A truncated FGF receptor blocks neural induction by endogenous Xenopus inducers., Launay C, Fromentoux V, Shi DL, Boucaut JC., Development. March 1, 1996; 122 (3): 869-80.                

Analysis of MyoD, myogenin, and muscle-specific gene mRNAs in regenerating Xenopus skeletal muscle., Nicolas N, Gallien CL, Chanoine C., Dev Dyn. September 1, 1996; 207 (1): 60-8.

A Xenopus nodal-related gene that acts in synergy with noggin to induce complete secondary axis and notochord formation., Lustig KD, Kroll K, Sun E, Ramos R, Elmendorf H, Kirschner MW., Development. October 1, 1996; 122 (10): 3275-82.                

Cytoplasmic polyadenylation of activin receptor mRNA and the control of pattern formation in Xenopus development., Simon R, Wu L, Richter JD., Dev Biol. October 10, 1996; 179 (1): 239-50.              

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