The Xenopus IP3 receptor: Structure, function, and localization in oocytes and eggs
暂无分享,去创建一个
K. Mikoshiba | H. Okano | T. Michikawa | T. Nakagawa | J. Aruga | T. Furuichi | S. Kume | S. Nakade | A. Muto
[1] C. Larabell,et al. Inositol lipid hydrolysis contributes to the Ca2+ wave in the activating egg of Xenopus laevis. , 1992, Developmental biology.
[2] S. W. Sernett,et al. Isolation, characterization, and localization of the inositol 1,4,5-trisphosphate receptor protein in Xenopus laevis oocytes. , 1992, The Journal of biological chemistry.
[3] W. R. Buck,et al. Synergistic release of calcium in sea urchin eggs by caffeine and ryanodine. , 1992, Experimental cell research.
[4] K. Mikoshiba,et al. Molecular cloning and characterization of the inositol 1,4,5-trisphosphate receptor in Drosophila melanogaster. , 1992, The Journal of biological chemistry.
[5] A. Martelli,et al. Nuclear localization and signalling activity of phosphoinositidase Cβ in Swiss 3T3 cells , 1992, Nature.
[6] K. Mikoshiba,et al. Block of Ca2+ wave and Ca2+ oscillation by antibody to the inositol 1,4,5-trisphosphate receptor in fertilized hamster eggs. , 1992, Science.
[7] M. Welsh,et al. Inositol trisphosphate is required for the propagation of calcium waves in Xenopus oocytes. , 1992, The Journal of biological chemistry.
[8] David E. Clapham,et al. Molecular mechanisms of intracellular calcium excitability in X. laevis oocytes , 1992, Cell.
[9] W. Busa,et al. Lithium-sensitive production of inositol phosphates during amphibian embryonic mesoderm induction. , 1992, Science.
[10] K. Campbell,et al. Cortical localization of a calcium release channel in sea urchin eggs , 1992, The Journal of cell biology.
[11] V. Centonze,et al. Confocal microscopy of fertilization-induced calcium dynamics in sea urchin eggs. , 1992, Developmental biology.
[12] C. Sardet,et al. Ryanodine Activates Sea Urchin Eggs , 1992, Development, growth & differentiation.
[13] K. Mikoshiba,et al. Differential Localization of Alternative Spliced Transcripts Encoding Inositol 1,4,5‐Trisphosphate Receptors in Mouse Cerebellum and Hippocampus: In Situ Hybridization Study , 1991, Journal of neurochemistry.
[14] M. Terasaki,et al. Organization of the sea urchin egg endoplasmic reticulum and its reorganization at fertilization , 1991, The Journal of cell biology.
[15] E. Sigel,et al. The polarized distribution of poly(A+)-mRNA-induced functional ion channels in the Xenopus oocyte plasma membrane is prevented by anticytoskeletal drugs , 1991, The Journal of cell biology.
[16] Y. Ikawa,et al. Independent inactivation of MPF and cytostatic factor (Mos) upon fertilization of Xenopus eggs , 1991, Nature.
[17] K. Mikoshiba,et al. The subtypes of the mouse inositol 1,4,5-trisphosphate receptor are expressed in a tissue-specific and developmentally specific manner. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[18] K. Mikoshiba,et al. Involvement of the C-terminus of the inositol 1,4,5-trisphosphate receptor in Ca2+ release analysed using region-specific monoclonal antibodies. , 1991, The Biochemical journal.
[19] K. Mikoshiba,et al. Structure-function relationships of the mouse inositol 1,4,5-trisphosphate receptor. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[20] J. Lechleiter,et al. Subcellular patterns of calcium release determined by G protein-specific residues of muscarinic receptors , 1991, Nature.
[21] D. Clapham,et al. Spiral calcium wave propagation and annihilation in Xenopus laevis oocytes. , 1991, Science.
[22] R. Huganir,et al. Inositol 1,4,5-trisphosphate receptor is phosphorylated by cyclic AMP-dependent protein kinase at serines 1755 and 1589. , 1991, Biochemical and biophysical research communications.
[23] D. Fesquet,et al. An okadaic acid-sensitive phosphatase negatively controls the cyclin degradation pathway in amphibian eggs , 1991, Molecular and cellular biology.
[24] L. Jaffe,et al. Evidence for the involvement of a pertussis toxin-insensitive G-protein in egg activation of the frog, Xenopus laevis. , 1991, Developmental biology.
[25] K. Mikoshiba,et al. Structural and functional characterization of inositol 1,4,5-trisphosphate receptor channel from mouse cerebellum. , 1991, The Journal of biological chemistry.
[26] A. Murray,et al. Cyclin is degraded by the ubiquitin pathway , 1991, Nature.
[27] T. Rakow,et al. Multiple stores of calcium are released in the sea urchin egg during fertilization. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[28] T. Südhof,et al. The ligand binding site and transduction mechanism in the inositol‐1,4,5‐triphosphate receptor. , 1990, The EMBO journal.
[29] D. Capco,et al. Nonspecific effects of oligodeoxynucleotide injection in Xenopus oocytes: a reevaluation of previous D7 mRNA ablation experiments. , 1990, Development.
[30] S. Orrenius,et al. An inositol 1,4,5-trisphosphate-sensitive Ca2+ pool in liver nuclei. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[31] S. Snyder,et al. The inositol 1,4,5,-trisphosphate receptor in cerebellar Purkinje cells: quantitative immunogold labeling reveals concentration in an ER subcompartment , 1990, The Journal of cell biology.
[32] T. Südhof,et al. Structure and expression of the rat inositol 1,4,5-trisphosphate receptor. , 1990, The Journal of biological chemistry.
[33] A. Markwick,et al. Angiotensin II-induced calcium mobilization in oocytes by signal transfer through gap junctions. , 1990, Science.
[34] K. Mikoshiba,et al. Expressed cerebellar-type inositol 1,4,5-trisphosphate receptor, P400, has calcium release activity in a fibroblast L cell line , 1990, Neuron.
[35] A. Colman,et al. Effects of oligo sequence and chemistry on the efficiency of oligodeoxyribonucleotide-mediated mRNA cleavage. , 1990, Nucleic acids research.
[36] A. Fujiwara,et al. Fertilization Membrane Formation in Sea Urchin Eggs Induced by Drugs Known to Cause Ca2+Release from Isolated Sarcoplasmic Reticulum , 1990, Development, growth & differentiation.
[37] K. Mikoshiba,et al. Immunogold localization of inositol 1, 4, 5-trisphosphate (InsP3) receptor in mouse cerebellar Purkinje cells using three monoclonal antibodies. , 1990, Cell structure and function.
[38] D. Melton,et al. The stability, toxicity and effectiveness of unmodified and phosphorothioate antisense oligodeoxynucleotides in Xenopus oocytes and embryos. , 1990, Nucleic acids research.
[39] R. Nuccitelli,et al. Inositol 1,4,5-trisphosphate-induced calcium release in the organelle layers of the stratified, intact egg of Xenopus laevis , 1990, The Journal of cell biology.
[40] R. Huganir,et al. Calcium flux mediated by purified inositol 1,4,5-trisphosphate receptor in reconstituted lipid vesicles is allosterically regulated by adenine nucleotides. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[41] K. Mikoshiba,et al. A cerebellar Purkinje cell marker P400 protein is an inositol 1,4,5‐trisphosphate (InsP3) receptor protein. Purification and characterization of InsP3 receptor complex. , 1990, The EMBO journal.
[42] G. Woude,et al. Specific proteolysis of the c-mos proto-oncogene product by calpain on fertilization of Xenopus eggs , 1989, Nature.
[43] G. Woude,et al. The c-mos proto-oncogene product is a cytostatic factor responsible for meiotic arrest in vertebrate eggs , 1989, Nature.
[44] R. Huganir,et al. Purified inositol 1,4,5-trisphosphate receptor mediates calcium flux in reconstituted lipid vesicles , 1989, Nature.
[45] Teiichi Furuichi,et al. Primary structure and functional expression of the inositol 1,4,5-trisphosphate-binding protein P400 , 1989, Nature.
[46] K. Kao,et al. The Location of Dorsal Information in Frog Early Development , 1989, Development, growth & differentiation.
[47] Michael J. Berridge,et al. Inositol phosphates and cell signalling , 1989, Nature.
[48] K. Mikoshiba,et al. Nucleotide sequence of cDNA encoding P400 protein in the mouse cerebellum. , 1989, Nucleic acids research.
[49] H. Takeshima,et al. Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor , 1989, Nature.
[50] K. Mikoshiba,et al. Developmental expression and intracellular location of P400 protein characteristic of Purkinje cells in the mouse cerebellum. , 1989, Developmental biology.
[51] W. Busa,et al. Lithium-induced teratogenesis in frog embryos prevented by a polyphosphoinositide cycle intermediate or a diacylglycerol analog. , 1989, Developmental biology.
[52] D. Capco,et al. Activators of protein kinase C trigger cortical granule exocytosis, cortical contraction, and cleavage furrow formation in Xenopus laevis oocytes and eggs , 1989, The Journal of cell biology.
[53] T. Iwamatsu. Exocytosis of Cortical Alveoli and Its Initiation Time in Medaka Eggs Induced by Microinjection of Various Agents , 1989, Development, growth & differentiation.
[54] K. Mikoshiba,et al. Purification and Characterization of P400 Protein, a Glycoprotein Characteristic of Purkinje Cell, from Mouse Cerebellum , 1988, Journal of neurochemistry.
[55] R. Kado,et al. G-proteins and egg activation. , 1988, Cell differentiation and development : the official journal of the International Society of Developmental Biologists.
[56] S. Supattapone,et al. Cyclic AMP-dependent phosphorylation of a brain inositol trisphosphate receptor decreases its release of calcium. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[57] Busa Wb. Roles for the Phosphatidylinositol Cycle in Early Development , 1988 .
[58] R. Kado,et al. Fertilization events induced by neurotransmitters after injection of mRNA in Xenopus eggs. , 1988, Science.
[59] D. Smith,et al. Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase. , 1988, Gene.
[60] Y. Oron,et al. Differences in receptor-evoked membrane electrical responses in native and mRNA-injected Xenopus oocytes. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[61] D. Kline,et al. Calcium-dependent events at fertilization of the frog egg: injection of a calcium buffer blocks ion channel opening, exocytosis, and formation of pronuclei. , 1988, Developmental biology.
[62] S. Miyazaki. Inositol 1,4,5-trisphosphate-induced calcium release and guanine nucleotide-binding protein-mediated periodic calcium rises in golden hamster eggs , 1988, The Journal of cell biology.
[63] K. Mullis,et al. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. , 1988, Science.
[64] S H Snyder,et al. Solubilization, purification, and characterization of an inositol trisphosphate receptor. , 1988, The Journal of biological chemistry.
[65] J. Gerhart,et al. Subcortical rotation in Xenopus eggs: an early step in embryonic axis specification. , 1987, Developmental biology.
[66] H. Okayama,et al. High-efficiency transformation of mammalian cells by plasmid DNA. , 1987, Molecular and cellular biology.
[67] D. Melton. Translocation of a localized maternal mRNA to the vegetal pole of Xenopus oocytes , 1987, Nature.
[68] L. Jaffe,et al. A cholera toxin-sensitive G-protein stimulates exocytosis in sea urchin eggs. , 1987, Developmental biology.
[69] Y. Hiramoto,et al. The Wave Pattern of Free Calcium Release Upon Fertilization in Medaka and Sand Dollar Eggs , 1986, Development, growth & differentiation.
[70] Y. Igusa,et al. Temporal and spatial dynamics of the periodic increase in intracellular free calcium at fertilization of golden hamster eggs. , 1986, Developmental biology.
[71] L. Jaffe,et al. Regulation of cortical vesicle exocytosis in sea urchin eggs by inositol 1,4,5-trisphosphate and GTP-binding protein , 1986, The Journal of cell biology.
[72] D. L. Weeks,et al. Identification and cloning of localized maternal RNAs from xenopus eggs , 1985, Cell.
[73] J. Williamson,et al. Activation of frog (Xenopus laevis) eggs by inositol trisphosphate. I. Characterization of Ca2+ release from intracellular stores , 1985, The Journal of cell biology.
[74] R. Nuccitelli,et al. An elevated free cytosolic Ca2+ wave follows fertilization in eggs of the frog, Xenopus laevis , 1985, The Journal of cell biology.
[75] A. Picard,et al. Inositol 1,4,5‐triphosphate microinjection triggers activation, but not meiotic maturation in amphibian and starfish oocytes , 1985, FEBS letters.
[76] M. Whitaker,et al. Inositol 1,4,5-trisphosphate microinjection activates sea urchin eggs , 1984, Nature.
[77] P. Greengard,et al. Phosphorylation of the nicotinic acetylcholine receptor by an endogenous tyrosine-specific protein kinase. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[78] G. Reynolds,et al. Calcium transients during early development in single starfish (Asterias forbesi) oocytes , 1984, The Journal of cell biology.
[79] M. Charbonneau,et al. The onset of activation responsiveness during maturation coincides with the formation of the cortical endoplasmic reticulum in oocytes of Xenopus laevis. , 1984, Developmental biology.
[80] P. Andreuccetti,et al. The modifications of cortical endoplasmic reticulum during in vitro maturation of Xenopus laevis oocytes and its involvement in cortical granule exocytosis. , 1984, The Journal of experimental zoology.
[81] M. Kozak. Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs. , 1984, Nucleic acids research.
[82] L. Jaffe. Sources of calcium in egg activation: a review and hypothesis. , 1983, Developmental biology.
[83] Wim G. J. Hol,et al. Predicted nucleotide-binding properties of p21 protein and its cancer-associated variant , 1983, Nature.
[84] D. Gardiner,et al. Membrane junctions in xenopus eggs: their distribution suggests a role in calcium regulation , 1983, The Journal of cell biology.
[85] M. Kirschner,et al. A major developmental transition in early xenopus embryos: I. characterization and timing of cellular changes at the midblastula stage , 1982, Cell.
[86] R. Doolittle,et al. A simple method for displaying the hydropathic character of a protein. , 1982, Journal of molecular biology.
[87] P. Cobbold,et al. Free Ca2+ increases in exponential phases during mouse oocyte activation , 1981, Nature.
[88] R. Steinhardt,et al. Dual ionic controls for the activation of protein synthesis at fertilization , 1980, Nature.
[89] F. Sanger,et al. DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[90] R. Zucker,et al. Intracellular calcium release at fertilization in the sea urchin egg. , 1977, Developmental biology.
[91] R. Elinson. Site of sperm entry and a cortical contraction associated with egg activation in the frog Rana pipiens. , 1975, Developmental biology.
[92] J. Dumont. Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals , 1972, Journal of morphology.
[93] U. K. Laemmli,et al. Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.
[94] L. Sternberger,et al. THE UNLABELED ANTIBODY ENZYME METHOD OF IMMUNOHISTOCHEMISTRY PREPARATION AND PROPERTIES OF SOLUBLE ANTIGEN-ANTIBODY COMPLEX (HORSERADISH PEROXIDASE-ANTIHORSERADISH PEROXIDASE) AND ITS USE IN IDENTIFICATION OF SPIROCHETES , 1970, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[95] K. Mikoshiba,et al. Distribution of inositol 1,4,5‐trisphosphate receptor mRNA in mouse tissues , 1990, FEBS letters.
[96] Y. Hiramoto,et al. Free calcium wave upon activation in Xenopus eggs. , 1987, Developmental biology.
[97] R. Elinson,et al. ANIMAL/VEGETAL DIFFERENCES IN CORTICAL GRANULE EXOCYTOSIS DURING ACTIVATION OF THE FROG EGG * , 1980, Development, growth & differentiation.
[98] T. G. Hollinger,et al. Artificial fertilization of gametes from the South African clawed frog, Xenopus laevis , 1980 .