The DOI matches its Crossref record; 399 of the 399 references it cites were found in a registry or an index.
Calcium at Fertilization and in Early Development
Open accessAbstract
Fertilization calcium waves are introduced, and the evidence from which we can infer general mechanisms of these waves is presented. The two main classes of hypotheses put forward to explain the generation of the fertilization calcium wave are set out, and it is concluded that initiation of the fertilization calcium wave can be most generally explained in invertebrates by a mechanism in which an activating substance enters the egg from the sperm on sperm-egg fusion, activating the egg by stimulating phospholipase C activation through a src family kinase pathway and in mammals by the diffusion of a sperm-specific phospholipase C from sperm to egg on sperm-egg fusion. The fertilization calcium wave is then set into the context of cell cycle control, and the mechanism of repetitive calcium spiking in mammalian eggs is investigated. Evidence that calcium signals control cell division in early embryos is reviewed, and it is concluded that calcium signals are essential at all three stages of cell division in early embryos. Evidence that phosphoinositide signaling pathways control the resumption of meiosis during oocyte maturation is considered. It is concluded on balance that the evidence points to a need for phosphoinositide/calcium signaling during resumption of meiosis. Changes to the calcium signaling machinery occur during meiosis to enable the production of a calcium wave in the mature oocyte when it is fertilized; evidence that the shape and structure of the endoplasmic reticulum alters dynamically during maturation and after fertilization is reviewed, and the link between ER dynamics and the cytoskeleton is discussed. There is evidence that calcium signaling plays a key part in the development of patterning in early embryos. Morphogenesis in ascidian, frog, and zebrafish embryos is briefly described to provide the developmental context in which calcium signals act. Intracellular calcium waves that may play a role in axis formation in ascidian are discussed. Evidence that the Wingless/calcium signaling pathway is a strong ventralizing signal in Xenopus, mediated by phosphoinositide signaling, is adumbrated. The central role that calcium channels play in morphogenetic movements during gastrulation and in ectodermal and mesodermal gene expression during late gastrulation is demonstrated. Experiments in zebrafish provide a strong indication that calcium signals are essential for pattern formation and organogenesis.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Calcium's Role in Mechanotransduction during Muscle Development
Benavides Damm, T., & Egli, M. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000356667 · Cited by 14,502
Stages of embryonic development of the zebrafish
Kimmel, C. B., Ballard, W. W., Kimmel, S. R., Ullmann, B., & Schilling, T. F. (1995) · Developmental Dynamics · doi:10.1002/aja.1002030302 · Cited by 12,037
Down-Regulation of Na+/K+ATPase Activity by Human Parvovirus B19 Capsid Protein VP1
Almilaji, A., Szteyn, K., Fein, E., Pakladok, T., Munoz, C., Elvira, B., Towhid, S. T., Alesutan, I., Shumilina, E., Bock, C.-T., et al. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350083 · Cited by 8,675
Inositol trisphosphate and calcium signalling
Berridge, M. J. (1993) · Nature · doi:10.1038/361315a0 · Cited by 6,545
The versatility and universality of calcium signalling
Berridge, M. J., Lipp, P., & Bootman, M. D. (2000) · Nature Reviews Molecular Cell Biology · doi:10.1038/35036035 · Cited by 5,701
Streb, H., Irvine, R. F., Berridge, M. J., & Schulz, I. (1983) · Nature · doi:10.1038/306067a0 · Cited by 2,593
A molecular mechanism for the effect of lithium on development.
Klein, P. S., & Melton, D. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8455 · Cited by 2,301
Lithium amplifies agonist-dependent phosphatidylinositol responses in brain and salivary glands
Berridge, M. J., Downes, C. P., & Hanley, M. R. (1982) · Biochemical Journal · doi:10.1042/bj2060587 · Cited by 2,136
Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells
Nauli, S. M., Alenghat, F. J., Luo, Y., Williams, E., Vassilev, P., Li, X., Elia, A. E. H., Lu, W., Brown, E. M., Quinn, S. J., et al. (2003) · Nature Genetics · doi:10.1038/ng1076 · Cited by 2,057
Clapham, D. E. (1995) · Cell · doi:10.1016/0092-8674(95)90408-5 · Cited by 1,959
Calcium Sparks: Elementary Events Underlying Excitation-Contraction Coupling in Heart Muscle
Cheng, H., Lederer, W. J., & Cannell, M. B. (1993) · Science · doi:10.1126/science.8235594 · Cited by 1,935
Nonaka, S., Tanaka, Y., Okada, Y., Takeda, S., Harada, A., Kanai, Y., Kido, M., & Hirokawa, N. (1998) · Cell · doi:10.1016/s0092-8674(00)81705-5 · Cited by 1,617
A genomic regulatory network for development
Davidson, E. H., Rast, J. P., Oliveri, P., Ransick, A., Calestani, C., Yuh, C.-H., Minokawa, T., Amore, G., Hinman, V., Arenas-Mena, C., et al. (2002) · Science · doi:10.1126/science.1069883 · Cited by 1,567
Evans, T., Rosenthal, E. T., Youngblom, J., Distel, D., & Hunt, T. (1983) · Cell · doi:10.1016/0092-8674(83)90420-8 · Cited by 1,516
A Human Syndrome Caused by Immotile Cilia
Afzelius, B. A. (1976) · Science · doi:10.1126/science.1084576 · Cited by 1,257
Inositol Trisphosphate and Calcium Signaling
BERRIDGE, M. J. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb26646.x · Cited by 1,031
Neural and developmental actions of lithium: A unifying hypothesis
Berridge, M. J., Downes, C. P., & Hanley, M. R. (1989) · Cell · doi:10.1016/0092-8674(89)90026-3 · Cited by 1,014
Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation
Heisenberg, C.-P., Tada, M., Rauch, G.-J., Saúde, L., Concha, M. L., Geisler, R., Stemple, D. L., Smith, J. C., & Wilson, S. W. (2000) · Nature · doi:10.1038/35011068 · Cited by 1,013
PLCζ: a sperm-specific trigger of Ca2+ oscillations in eggs and embryo development
Saunders, C. M., Larman, M. G., Parrington, J., Cox, L. J., Royse, J., Blayney, L. M., Swann, K., & Lai, F. A. (2002) · Development · doi:10.1242/dev.129.15.3533 · Cited by 1,010
Zebrafish Prickle, a Modulator of Noncanonical Wnt/Fz Signaling, Regulates Gastrulation Movements
Veeman, M. T., Slusarski, D. C., Kaykas, A., Louie, S. H., & Moon, R. T. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00240-9 · Cited by 945
Cell-permeant caged InsP3 ester shows that Ca2+ spike frequency can optimize gene expression
Li, W.-H., Llopis, J., Whitney, M., Zlokarnik, G., & Tsien, R. Y. (1998) · Nature · doi:10.1038/31965 · Cited by 844
FORMATION AND FUNCTION OF SPEMANN'S ORGANIZER
Harland, R., & Gerhart, J. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.611 · Cited by 839
Bending the MDCK Cell Primary Cilium Increases Intracellular Calcium
Praetorius, H. A., & Spring, K. R. (2001) · Journal of Membrane Biology · doi:10.1007/s00232-001-0075-4 · Cited by 828
Calcium Induced Release of Calcium from the Sarcoplasmic Reticulum of Skinned Skeletal Muscle Fibres
ENDO, M., TANAKA, M., & OGAWA, Y. (1970) · Nature · doi:10.1038/228034a0 · Cited by 814
Two Populations of Node Monocilia Initiate Left-Right Asymmetry in the Mouse
McGrath, J., Somlo, S., Makova, S., Tian, X., & Brueckner, M. (2003) · Cell · doi:10.1016/s0092-8674(03)00511-7 · Cited by 797
Dishevelled controls cell polarity during Xenopus gastrulation
Wallingford, J. B., Rowning, B. A., Vogeli, K. M., Rothbächer, U., Fraser, S. E., & Harland, R. M. (2000) · Nature · doi:10.1038/35011077 · Cited by 751
Comparative Biology of Calcium Signaling during Fertilization and Egg Activation in Animals
Stricker, S. A. (1999) · Developmental Biology · doi:10.1006/dbio.1999.9340 · Cited by 712
Kline, D., & Kline, J. T. (1992) · Developmental Biology · doi:10.1016/0012-1606(92)90265-i · Cited by 693
Mechanism and function of signal transduction by the Wnt/β-catenin and Wnt/Ca2+ pathways
Miller, J. R., Hocking, A. M., Brown, J. D., & Moon, R. T. (1999) · Oncogene · doi:10.1038/sj.onc.1203245 · Cited by 691
Berridge, M. J., & Galione, A. (1988) · The FASEB Journal · doi:10.1096/fasebj.2.15.2847949 · Cited by 685
Determination of left–right patterning of the mouse embryo by artificial nodal flow
Nonaka, S., Shiratori, H., Saijoh, Y., & Hamada, H. (2002) · Nature · doi:10.1038/nature00849 · Cited by 682
Slusarski, D. C., Corces, V. G., & Moon, R. T. (1997) · Nature · doi:10.1038/37138 · Cited by 680 · cited 6×
“Expressing a rat Frizzled-2 receptor in zebrafish embryos also enhances the endogenous transients (495).”
BackgroundInfluentialTada, M., & Smith, J. C. (2000) · Development · doi:10.1242/dev.127.10.2227 · Cited by 675
Smith, W. C., & Harland, R. M. (1991) · Cell · doi:10.1016/0092-8674(91)90070-f · Cited by 647
Schatten, G. (1994) · Developmental Biology · doi:10.1006/dbio.1994.1256 · Cited by 636
Activation of the Wnt Signaling Pathway: A Molecular Mechanism for Lithium Action
Hedgepeth, C. M., Conrad, L. J., Zhang, J., Huang, H.-C., Lee, V. M. Y., & Klein, P. S. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8552 · Cited by 636
Ca 2+ -Induced Ca 2+ Release in Sea Urchin Egg Homogenates: Modulation by Cyclic ADP-Ribose
Galione, A., Lee, H. C., & Busa, W. B. (1991) · Science · doi:10.1126/science.1909457 · Cited by 618
WNTs modulate cell fate and behavior during vertebrate development
Moon, R. (1997) · Trends in Genetics · doi:10.1016/s0168-9525(97)01093-7 · Cited by 600
Clapper, D. L., Walseth, T. F., Dargie, P. J., & Lee, H. C. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47970-7 · Cited by 569
Specific and high-affinity binding of inositol phosphates to an isolated pleckstrin homology domain
Lemmon, M. A., Ferguson, K. M., O'Brien, R., Sigler, P. B., & Schlessinger, J. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.23.10472 · Cited by 566
Intracellular pH and Activation of Sea Urchin Eggs after Fertilisation
Johnson, J. D., Epel, D., & Paul, M. (1976) · Nature · doi:10.1038/262661a0 · Cited by 556
Mutation of an axonemal dynein affects left–right asymmetry in inversus viscerum mice
Supp, D. M., Witte, D. P., Potter, S. S., & Brueckner, M. (1997) · Nature · doi:10.1038/40140 · Cited by 554
A free calcium wave traverses the activating egg of the medaka, Oryzias latipes.
Gilkey, J. C., Jaffe, L. F., Ridgway, E. B., & Reynolds, G. T. (1978) · The Journal of cell biology · doi:10.1083/jcb.76.2.448 · Cited by 546
Calcium Rises Abruptly and Briefly Throughout the Cell at the Onset of Anaphase
Poenie, M., Alderton, J., Steinhardt, R., & Tsien, R. (1986) · Science · doi:10.1126/science.3755550 · Cited by 539
Tanaka, Y., Okada, Y., & Hirokawa, N. (2005) · Nature · doi:10.1038/nature03494 · Cited by 535
Cell Membrane Resealing by a Vesicular Mechanism Similar to Neurotransmitter Release
Steinhardt, R. A., Bi, G., & Alderton, J. M. (1994) · Science · doi:10.1126/science.7904084 · Cited by 528
Intracellular calcium release at fertilization in the sea urchin egg
Steinhardt, R., Zucker, R., & Schatten, G. (1977) · Developmental Biology · doi:10.1016/0012-1606(77)90084-7 · Cited by 523
Miyazaki, S., Shirakawa, H., Nakada, K., & Honda, Y. (1993) · Developmental Biology · doi:10.1006/dbio.1993.1168 · Cited by 522
Mechanisms of convergence and extension by cell intercalation
Keller, R., Davidson, L., Edlund, A., Elul, T., Ezin, M., Shook, D., & Skoglund, P. (2000) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2000.0626 · Cited by 519
Kühl, M., Sheldahl, L. C., Malbon, C. C., & Moon, R. T. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.17.12701 · Cited by 517
Hirose, K., Kadowaki, S., Tanabe, M., Takeshima, H., & Iino, M. (1999) · Science · doi:10.1126/science.284.5419.1527 · Cited by 513
Extracellular matrix remodelling and cellular differentiation
Streuli, C. (1999) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(99)00026-5 · Cited by 512
Injected Wnt RNA induces a complete body axis in Xenopus embryos
Sokol, S., Christian, J. L., Moon, R. T., & Melton, D. A. (1991) · Cell · doi:10.1016/0092-8674(91)90069-b · Cited by 506
Miyazaki, S.-I., Yuzaki, M., Nakada, K., Shirakawa, H., Nakanishi, S., Nakade, S., & Mikoshiba, K. (1992) · Science · doi:10.1126/science.1321497 · Cited by 500
Fertilization Defects in Sperm from Mice Lacking Fertilin β
Cho, C., O'Dell Bunch, D., Faure, J.-E., Goulding, E. H., Eddy, E. M., Primakoff, P., & Myles, D. G. (1998) · Science · doi:10.1126/science.281.5384.1857 · Cited by 499
The gamete fusion process is defective in eggs of Cd9-deficient mice
Kaji, K., Oda, S., Shikano, T., Ohnuki, T., Uematsu, Y., Sakagami, J., Tada, N., Miyazaki, S., & Kudo, A. (2000) · Nature Genetics · doi:10.1038/73502 · Cited by 491
Lee, H. C., & Aarhus, R. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.5.2152 · Cited by 475
Sheldahl, L. C., Park, M., Malbon, C. C., & Moon, R. T. (1999) · Current Biology · doi:10.1016/s0960-9822(99)80310-8 · Cited by 475
A frizzled homolog functions in a vertebrate Wnt signaling pathway
Yang-Snyder, J., Miller, J. R., Brown, J. D., Lai, C.-J., & Moon, R. T. (1996) · Current Biology · doi:10.1016/s0960-9822(02)70716-1 · Cited by 469
Ectodermal Patterning in Vertebrate Embryos
Sasai, Y., & De Robertis, E. M. (1997) · Developmental Biology · doi:10.1006/dbio.1996.8445 · Cited by 463
Activation of Sea-Urchin Eggs by a Calcium Ionophore
Steinhardt, R. A., & Epel, D. D. (1974) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.71.5.1915 · Cited by 461
NAADP Mobilizes Ca2+ from Reserve Granules, Lysosome-Related Organelles, in Sea Urchin Eggs
Churchill, G. C., Okada, Y., Thomas, J. M., Genazzani, A. A., Patel, S., & Galione, A. (2002) · Cell · doi:10.1016/s0092-8674(02)01082-6 · Cited by 457
Fast block to polyspermy in sea urchin eggs is electrically mediated
JAFFE, L. A. (1976) · Nature · doi:10.1038/261068a0 · Cited by 455
A common sequence of calcium and pH signals in the mitogenic stimulation of eukaryotic cells
Hesketh, T. R., Moore, J. P., Morris, J. D. H., Taylor, M. V., Rogers, J., Smith, G. A., & Metcalfe, J. C. (1985) · Nature · doi:10.1038/313481a0 · Cited by 449
Swann, K. (1990) · Development · doi:10.1242/dev.110.4.1295 · Cited by 447
Lorca, T., Cruzalegui, F. H., Fesquet, D., Cavadore, J.-C., Méry, J., Means, A., & Dorée, M. (1993) · Nature · doi:10.1038/366270a0 · Cited by 446
Physiological functions of cyclic ADP-ribose and NAADP as calcium messengers
Lee, H. C. (2001) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.41.1.317 · Cited by 433
The Ion Channel Polycystin-2 Is Required for Left-Right Axis Determination in Mice
Pennekamp, P., Karcher, C., Fischer, A., Schweickert, A., Skryabin, B., Horst, J., Blum, M., & Dworniczak, B. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00869-2 · Cited by 425
Egg-to-Embryo Transition Is Driven by Differential Responses to Ca2+ Oscillation Number
Ducibella, T., Huneau, D., Angelichio, E., Xu, Z., Schultz, R. M., Kopf, G. S., Fissore, R., Madoux, S., & Ozil, J.-P. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0788 · Cited by 417
ADP-ribosyl Cyclase and CD38 Catalyze the Synthesis of a Calcium-mobilizing Metabolite from NADP+
Aarhus, R., Graeff, R. M., Dickey, D. M., Walseth, T. F., & Hon, C. L. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.51.30327 · Cited by 416
Verlhac, M.-H., Kubiak, J. Z., Clarke, H. J., & Maro, B. (1994) · Development · doi:10.1242/dev.120.4.1017 · Cited by 408
Torres, M. A., Yang-Snyder, J. A., Purcell, S. M., DeMarais, A. A., McGrew, L. L., & Moon, R. T. (1996) · The Journal of cell biology · doi:10.1083/jcb.133.5.1123 · Cited by 405
Modulation of Embryonic Intracellular Ca2+Signaling byWnt-5A
Slusarski, D. C., Yang-Snyder, J., Busa, W. B., & Moon, R. T. (1997) · Developmental Biology · doi:10.1006/dbio.1996.8463 · Cited by 404
Levin, M., Thorlin, T., Robinson, K. R., Nogi, T., & Mercola, M. (2002) · Cell · doi:10.1016/s0092-8674(02)00939-x · Cited by 403
Activity-dependent homeostatic specification of transmitter expression in embryonic neurons
Borodinsky, L. N., Root, C. M., Cronin, J. A., Sann, S. B., Gu, X., & Spitzer, N. C. (2004) · Nature · doi:10.1038/nature02518 · Cited by 401
The Immunophilin FKBP12 Functions as a Common Inhibitor of the TGFβ Family Type I Receptors
Wang, T., Li, B.-Y., Danielson, P. D., Shah, P. C., Rockwell, S., Lechleider, R. J., Martin, J., Manganaro, T., & Donahoe, P. K. (1996) · Cell · doi:10.1016/s0092-8674(00)80116-6 · Cited by 388
Is calcium ionophore a universal activator for unfertilised eggs?
Steinhardt, R. A., Epel, D. D., Carroll, E. J., & Yanagimachi, R. (1974) · Nature · doi:10.1038/252041a0 · Cited by 386
Localization of endoplasmic reticulum in living and glutaraldehyde-fixed cells with fluorescent dyes
Terasaki, M., Song, J., Wong, J. R., Weiss, M. J., & Chen, L. B. (1984) · Cell · doi:10.1016/0092-8674(84)90530-0 · Cited by 385
Conserved function for embryonic nodal cilia
Essner, J. J., Vogan, K. J., Wagner, M. K., Tabin, C. J., Yost, H. J., & Brueckner, M. (2002) · Nature · doi:10.1038/418037a · Cited by 375
Calcium oscillations in mammalian eggs triggered by a soluble sperm protein
Parrington, J., Swann, K., Shevchenko, V. I., Sesay, A. K., & Lai, F. A. (1996) · Nature · doi:10.1038/379364a0 · Cited by 373
Multiphoton microscopy in biological research
Williams, R. M., Zipfel, W. R., & Webb, W. W. (2001) · Current Opinion in Chemical Biology · doi:10.1016/s1367-5931(00)00241-6 · Cited by 370
Mechanisms of calcium signaling by cyclic ADP-ribose and NAADP
Lee, H. C. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.4.1133 · Cited by 367
Egg Activation at Fertilization: Where It All Begins
Runft, L. L., Jaffe, L. A., & Mehlmann, L. M. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0600 · Cited by 364
Gerasimenko, O. V., Gerasimenko, J. V., Tepikin, A. V., & Petersen, O. H. (1995) · Cell · doi:10.1016/0092-8674(95)90494-8 · Cited by 364
A study of the mechanics of gastrulation
Holtfreter, J. (1944) · Journal of Experimental Zoology · doi:10.1002/jez.1400950203 · Cited by 352
Dishevelled activates Ca2+ flux, PKC, and CamKII in vertebrate embryos
Sheldahl, L. C., Slusarski, D. C., Pandur, P., Miller, J. R., Kühl, M., & Moon, R. T. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211094 · Cited by 350
Evolution of Gamete Recognition Proteins
Vacquier, V. D. (1998) · Science · doi:10.1126/science.281.5385.1995 · Cited by 350
Mlodzik, M. (2002) · Trends in Genetics · doi:10.1016/s0168-9525(02)02770-1 · Cited by 341
The G s -Linked Receptor GPR3 Maintains Meiotic Arrest in Mammalian Oocytes
Mehlmann, L. M., Saeki, Y., Tanaka, S., Brennan, T. J., Evsikov, A. V., Pendola, F. L., Knowles, B. B., Eppig, J. J., & Jaffe, L. A. (2004) · Science · doi:10.1126/science.1103974 · Cited by 337
An elevated free cytosolic Ca2+ wave follows fertilization in eggs of the frog, Xenopus laevis.
Busa, W. B., & Nuccitelli, R. (1985) · The Journal of cell biology · doi:10.1083/jcb.100.4.1325 · Cited by 335
A nodal-related gene defines a physical and functional domain within the Spemann organizer
Smith, W. C., McKendry, R., Ribisi, S., & Harland, R. M. (1995) · Cell · doi:10.1016/0092-8674(95)90050-0 · Cited by 329
Moon, R. T., Campbell, R. M., Christian, J. L., McGrew, L. L., Shih, J., & Fraser, S. (1993) · Development · doi:10.1242/dev.119.1.97 · Cited by 329
The role of Ppt/Wnt5 in regulating cell shape and movement during zebrafish gastrulation
Kilian, B., Mansukoski, H., Barbosa, F. C., Ulrich, F., Tada, M., & Heisenberg, C.-P. (2003) · Mechanisms of Development · doi:10.1016/s0925-4773(03)00004-2 · Cited by 326
Lighting the fuse at fertilization
Whitaker, M., & Swann, K. (1993) · Development · doi:10.1242/dev.117.1.1 · Cited by 323
Self-citationThe Wnt/calcium pathway activates NF-AT and promotes ventral cell fate in Xenopus embryos
Saneyoshi, T., Kume, S., Amasaki, Y., & Mikoshiba, K. (2002) · Nature · doi:10.1038/417295a · Cited by 322 · cited 13×
“A constitutively active, calcineurin-independent NF-AT ventralizes embryos (457), inhibiting activin-induced morphogenesis in an echo of the consequences of Wnt-5A overexpression (387).”
BackgroundResultInfluentialIon Channels in Sperm Physiology
Darszon, A., Labarca, P., Nishigaki, T., & Espinosa, F. (1999) · Physiological Reviews · doi:10.1152/physrev.1999.79.2.481 · Cited by 321
Verlhac, M.-H., Kubiak, J. Z., Weber, M., Géraud, G., Colledge, W. H., Evans, M. J., & Maro, B. (1996) · Development · doi:10.1242/dev.122.3.815 · Cited by 320
Flirting in Little Space: The ER/Mitochondria Ca 2+ Liaison
Rizzuto, R., Duchen, M. R., & Pozzan, T. (2004) · Science's STKE · doi:10.1126/stke.2152004re1 · Cited by 319
Environmental-Dependent Acceleration of a Developmental Switch: The Floral Transition
Simpson, G. G., & Dean, C. (2000) · Science's STKE · doi:10.1126/stke.2000.18.pe1 · Cited by 318
Du, S. J., Purcell, S. M., Christian, J. L., McGrew, L. L., & Moon, R. T. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.5.2625 · Cited by 314
Galione, A., McDougall, A., Busa, W. B., Willmott, N., Gillot, I., & Whitaker, M. (1993) · Science · doi:10.1126/science.8392748 · Cited by 310
Self-citationCalcium Mobilization by Dual Receptors During Fertilization of Sea Urchin Eggs
Lee, H. C., Aarhus, R., & Walseth, T. F. (1993) · Science · doi:10.1126/science.8392749 · Cited by 293
Cox, L. J., Larman, M. G., Saunders, C. M., Hashimoto, K., Swann, K., & Lai, F. A. (2002) · Reproduction · doi:10.1530/rep.0.1240611 · Cited by 286
Calcium-regulated exocytosis is required for cell membrane resealing.
Bi, G. Q., Alderton, J. M., & Steinhardt, R. A. (1995) · The Journal of cell biology · doi:10.1083/jcb.131.6.1747 · Cited by 285
The generation of diversity and pattern in animal development
Gurdon, J. B. (1992) · Cell · doi:10.1016/0092-8674(92)90465-o · Cited by 280
Kawakami, Y., Raya, Á., Raya, R. M., Rodríguez-Esteban, C., & Belmonte, J. C. I. (2005) · Nature · doi:10.1038/nature03512 · Cited by 271
Westfall, T. A., Brimeyer, R., Twedt, J., Gladon, J., Olberding, A., Furutani-Seiki, M., & Slusarski, D. C. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200303107 · Cited by 270
Dorsalization and neural induction: properties of the organizer in Xenopus laevis
Smith, J. C., & Slack, J. M. W. (1983) · Development · doi:10.1242/dev.78.1.299 · Cited by 270
Role for sperm in spatial patterning of the early mouse embryo
Piotrowska, K., & Zernicka-Goetz, M. (2001) · Nature · doi:10.1038/35054069 · Cited by 264
Frizzled-7 signalling controls tissue separation during Xenopus gastrulation
Winklbauer, R., Medina, A., Swain, R. K., & Steinbeisser, H. (2001) · Nature · doi:10.1038/35101621 · Cited by 263 · cited 1×
“This appears to involve the regulation of cell-cell adhesion by the Wnt/Ca pathway (618).”
BackgroundMammalian Sperm Acrosome: Formation, Contents, and Function
Abou-Haila, A., & Tulsiani, D. R. P. (2000) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2000.1880 · Cited by 259
A two-cilia model for vertebrate left-right axis specification: Figure 1.
Tabin, C. J., & Vogan, K. J. (2003) · Genes & Development · doi:10.1101/gad.1053803 · Cited by 258
Miller, J. R., Rowning, B. A., Larabell, C. A., Yang-Snyder, J. A., Bates, R. L., & Moon, R. T. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.146.2.427 · Cited by 254
Spontaneous neuronal calcium spikes and waves during early differentiation
Gu, X., Olson, E., & Spitzer, N. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-11-06325.1994 · Cited by 253
Miyazaki, S. (1988) · The Journal of cell biology · doi:10.1083/jcb.106.2.345 · Cited by 253
The path of calcium in cytosolic calcium oscillations: a unifying hypothesis.
Jaffe, L. F. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.21.9883 · Cited by 247
Intracellular free calcium rise triggers nuclear envelope breakdown in the sea urchin embryo
Steinhardt, R. A., & Alderton, J. (1988) · Nature · doi:10.1038/332364a0 · Cited by 242
van der Wal, J., Habets, R., Várnai, P., Balla, T., & Jalink, K. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m007194200 · Cited by 241
Recombinant Phospholipase Cζ Has High Ca2+ Sensitivity and Induces Ca2+ Oscillations in Mouse Eggs
Kouchi, Z., Fukami, K., Shikano, T., Oda, S., Nakamura, Y., Takenawa, T., & Miyazaki, S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313801200 · Cited by 241
Roderick, H. L., Lechleiter, J. D., & Camacho, P. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.149.6.1235 · Cited by 239
The mechanism of facilitated cell membrane resealing
Togo, T., Alderton, J. M., Bi, G.-Q., & Steinhardt, R. A. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.5.719 · Cited by 238
Meiotic Arrest in the Mouse Follicle Maintained by a G s Protein in the Oocyte
Mehlmann, L. M., Jones, T. L. Z., & Jaffe, L. A. (2002) · Science · doi:10.1126/science.1073978 · Cited by 237
Notch activity acts as a sensor for extracellular calcium during vertebrate left–right determination
Raya, Á., Kawakami, Y., Rodríguez-Esteban, C., Ibañes, M., Rasskin-Gutman, D., Rodríguez-León, J., Büscher, D., Feijó, J. A., & Izpisúa Belmonte, J. C. (2004) · Nature · doi:10.1038/nature02190 · Cited by 236
Notch signaling regulates left–right asymmetry determination by inducing Nodal expression
Krebs, L. T., Iwai, N., Nonaka, S., Welsh, I. C., Lan, Y., Jiang, R., Saijoh, Y., O'Brien, T. P., Hamada, H., & Gridley, T. (2003) · Genes & Development · doi:10.1101/gad.1084703 · Cited by 235
Activation of rabbit oocytes: the impact of the Ca2+ signal regime on development
Ozil, J.-P., & Huneau, D. (2001) · Development · doi:10.1242/dev.128.6.917 · Cited by 234
Dumollard, R., Marangos, P., Fitzharris, G., Swann, K., Duchen, M., & Carroll, J. (2004) · Development · doi:10.1242/dev.01181 · Cited by 233
Willmott, N., Sethi, J. K., Walseth, T. F., Lee, H. C., White, A. M., & Galione, A. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.7.3699 · Cited by 232
Cyclic ADP ribose activation of the ryanodine receptor is mediated by calmodulin
Lee, H. C., Aarhus, R., Graeff, R., Gurnack, M. E., & Walseth, T. F. (1994) · Nature · doi:10.1038/370307a0 · Cited by 227
Integrins in cell adhesion and signaling.
Akiyama, S. K. (1996) · PubMed · Cited by 226
Gerasimenko, J. V., Maruyama, Y., Yano, K., Dolman, N. J., Tepikin, A. V., Petersen, O. H., & Gerasimenko, O. V. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200306134 · Cited by 222
Calcium signalling during embryonic development
Webb, S. E., & Miller, A. L. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1149 · Cited by 221
Kühl, M., Geis, K., Sheldahl, L. C., Pukrop, T., Moon, R. T., & Wedlich, D. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00416-6 · Cited by 220
Wallingford, J. B., & Harland, R. M. (2001) · Development · doi:10.1242/dev.128.13.2581 · Cited by 217
Eto, K., Puzon-McLaughlin, W., Sheppard, D., Sehara-Fujisawa, A., Zhang, X.-P., & Takada, Y. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m001953200 · Cited by 214
PIP3, PIP2, and Cell Movement—Similar Messages, Different Meanings?
Insall, R. H., & Weiner, O. D. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00086-7 · Cited by 213
Akt inhibits Myt1 in the signalling pathway that leads to meiotic G2/M-phase transition
Okumura, E., Fukuhara, T., Yoshida, H., Hanada, S.-I., Kozutsumi, R., Mori, M., Tachibana, K., & Kishimoto, T. (2002) · Nature Cell Biology · doi:10.1038/ncb741 · Cited by 213
Concerted Evolution in an Egg Receptor for a Rapidly Evolving Abalone Sperm Protein
Swanson, W. J., & Vacquier, V. D. (1998) · Science · doi:10.1126/science.281.5377.710 · Cited by 210
Kinesin- and Myosin-driven Steps of Vesicle Recruitment for Ca2+-regulated Exocytosis
Bi, G.-Q., Morris, R. L., Liao, G., Alderton, J. M., Scholey, J. M., & Steinhardt, R. A. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.138.5.999 · Cited by 208
Fertilization increases the polyphosphoinositide content of sea urchin eggs
Turner, P. R., Sheetz, M. P., & Jaffe, L. A. (1984) · Nature · doi:10.1038/310414a0 · Cited by 207
Clandinin, T. R., DeModena, J. A., & Sternberg, P. W. (1998) · Cell · doi:10.1016/s0092-8674(00)80945-9 · Cited by 205
Gap Junctions Are Involved in the Early Generation of Left–Right Asymmetry
Levin, M., & Mercola, M. (1998) · Developmental Biology · doi:10.1006/dbio.1998.9024 · Cited by 204
Thorn, P., Gerasimenko, O., & Petersen, O. H. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06478.x · Cited by 201
Bioelectric Responses of the Echinoderm Egg to Fertilization
Steinhardt, R. A., Lundin, L., & Mazia, D. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.10.2426 · Cited by 201
pH regulates the polymerization of actin in the sea urchin egg cortex.
Begg, D. A., & Rebhun, L. I. (1979) · The Journal of cell biology · doi:10.1083/jcb.83.1.241 · Cited by 201
Identification and localization of polycystin, the PKD1 gene product.
Geng, L., Segal, Y., Peissel, B., Deng, N., Pei, Y., Carone, F., Rennke, H. G., Glücksmann-Kuis, A. M., Schneider, M. C., Ericsson, M., et al. (1996) · Journal of Clinical Investigation · doi:10.1172/jci119090 · Cited by 200
Damsky, C., Sutherland, A., & Fisher, S. (1993) · The FASEB Journal · doi:10.1096/fasebj.7.14.8224605 · Cited by 194
Solovyova, N. (2002) · The EMBO Journal · doi:10.1093/emboj/21.4.622 · Cited by 191
PtdIns(4,5)P2 Functions at the Cleavage Furrow during Cytokinesis
Field, S. J., Madson, N., Kerr, M. L., Galbraith, K. A. A., Kennedy, C. E., Tahiliani, M., Wilkins, A., & Cantley, L. C. (2005) · Current Biology · doi:10.1016/j.cub.2005.06.059 · Cited by 187
Jones, K. T., Carroll, J., & Whittingham, D. G. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.12.6671 · Cited by 184
Busa, W. B., & Gimlich, R. L. (1989) · Developmental Biology · doi:10.1016/0012-1606(89)90228-5 · Cited by 182
Native Polycystin 2 Functions as a Plasma Membrane Ca2+-Permeable Cation Channel in Renal Epithelia
Luo, Y., Vassilev, P. M., Li, X., Kawanabe, Y., & Zhou, J. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.7.2600-2607.2003 · Cited by 182
Raya, Á., Kawakami, Y., Rodrı́guez-Esteban, C., Büscher, D., Koth, C. M., Itoh, T., Morita, M., Raya, R. M., Dubova, I., Bessa, J. G., et al. (2003) · Genes & Development · doi:10.1101/gad.1084403 · Cited by 182
Arendt, D., & Nübler-Jung, K. (1997) · Mechanisms of Development · doi:10.1016/s0925-4773(96)00620-x · Cited by 181
Nuclear calcium signalling by individual cytoplasmic calcium puffs
Lipp, P. (1997) · The EMBO Journal · doi:10.1093/emboj/16.23.7166 · Cited by 181
Nuccitelli, R., Yim, D. L., & Smart, T. (1993) · Developmental Biology · doi:10.1006/dbio.1993.1179 · Cited by 181
Activation and Inactivation of Ca Release by NAADP
Aarhus, R., Dickey, D. M., Graeff, R. M., Gee, K. R., Walseth, T. F., & Lee, H. C. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.15.8513 · Cited by 180
Cell-cycle calcium transients driven by cyclic changes in inositol trisphosphate levels
Ciapa, B., Pesando, D., Wilding, M., & Whitaker, M. (1994) · Nature · doi:10.1038/368875a0 · Cited by 179
Self-citationEpel, D., Steinhardt, R., Humphreys, T., & Mazia, D. (1974) · Developmental Biology · doi:10.1016/0012-1606(74)90127-4 · Cited by 179
Levin, M., & Mercola, M. (1999) · Development · doi:10.1242/dev.126.21.4703 · Cited by 179
PIP2 Hydrolysis and Calcium Release Are Required for Cytokinesis in Drosophila Spermatocytes
Wong, R., Hadjiyanni, I., Wei, H.-C., Polevoy, G., McBride, R., Sem, K.-P., & Brill, J. A. (2005) · Current Biology · doi:10.1016/j.cub.2005.06.060 · Cited by 177
Normal Fertilization Occurs with Eggs Lacking the Integrin α6β1 and Is Cd9-Dependent
Miller, B. J., Georges-Labouesse, E., Primakoff, P., & Myles, D. G. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.149.6.1289 · Cited by 177
Jellerette, T., He, C. L., Wu, H., Parys, J. B., & Fissore, R. A. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9675 · Cited by 176
Lorca, T., Galas, S., Fesquet, D., Devault, A., Cavadore, J. C., & Dorée, M. (1991) · The EMBO Journal · doi:10.1002/j.1460-2075.1991.tb07741.x · Cited by 175
Eisen, A., Kiehart, D. P., Wieland, S. J., & Reynolds, G. T. (1984) · The Journal of cell biology · doi:10.1083/jcb.99.5.1647 · Cited by 175
Mehlmann, L. M., Mikoshiba, K., & Kline, D. (1996) · Developmental Biology · doi:10.1006/dbio.1996.0322 · Cited by 174
Deguchi, R., Shirakawa, H., Oda, S., Mohri, T., & Miyazaki, S. (2000) · Developmental Biology · doi:10.1006/dbio.1999.9573 · Cited by 172
Left-Right Asymmetry Determination in Vertebrates
Mercola, M., & Levin, M. (2001) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.17.1.779 · Cited by 171
NO is necessary and sufficient for egg activation at fertilization
Kuo, R. C., Baxter, G. T., Thompson, S. H., Stricker, S. A., Patton, C., Bonaventura, J., & Epel, D. (2000) · Nature · doi:10.1038/35020577 · Cited by 170
Baitinger, C., Alderton, J., Poenie, M., Schulman, H., & Steinhardt, R. A. (1990) · The Journal of cell biology · doi:10.1083/jcb.111.5.1763 · Cited by 169
Carroll, J., & Swann, K. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)49895-5 · Cited by 166
Choi, S.-C., & Han, J.-K. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0602 · Cited by 165
Wang, S., Luo, Y., Wilson, P. D., Witman, G. B., & Zhou, J. (2004) · Journal of the American Society of Nephrology · doi:10.1097/01.asn.0000113793.12558.1d · Cited by 165
Gordo, A. C., Rodrigues, P., Kurokawa, M., Jellerette, T., Exley, G. E., Warner, C., & Fissore, R. (2002) · Biology of Reproduction · doi:10.1095/biolreprod66.6.1828 · Cited by 165
Swann, K. (1992) · Biochemical Journal · doi:10.1042/bj2870079 · Cited by 165
Antero-posterior tissue polarity links mesoderm convergent extension to axial patterning
Ninomiya, H., Elinson, R. P., & Winklbauer, R. (2004) · Nature · doi:10.1038/nature02620 · Cited by 163
Chambers, E. L., & de Armendi, J. (1979) · Experimental Cell Research · doi:10.1016/0014-4827(79)90575-5 · Cited by 163
Axis determination by inhibition of Wnt signaling in Xenopus
Itoh, K., & Sokol, S. Y. (1999) · Genes & Development · doi:10.1101/gad.13.17.2328 · Cited by 163
The activation of sea urchin eggs by the divalent ionophores A23187 and X-537A
Chambers, E. L., Pressman, B. C., & Rose, B. (1974) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(74)90181-8 · Cited by 162
Late onset of renal and hepatic cysts in Pkd1-targeted heterozygotes
Lu, W., Fan, X., Basora, N., Babakhanlou, H., Law, T., Rifai, N., Harris, P. C., Perez-Atayde, A. R., Rennke, H. G., & Zhou, J. (1999) · Nature Genetics · doi:10.1038/5944 · Cited by 160
Stimulation of the Na/H exchanger of sea urchin eggs by phorbol ester
Swann, K., & Whitaker, M. (1985) · Nature · doi:10.1038/314274a0 · Cited by 160
Self-citationCalcium signaling during convergent extension in Xenopus
Wallingford, J. B., Ewald, A. J., Harland, R. M., & Fraser, S. E. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00201-9 · Cited by 158
Cyclins and their partners: from a simple idea to complicated reality.
Hunt, T. (1991) · PubMed · Cited by 156
Patterns of free calcium in zebrafish embryos
Créton, R., Speksnijder, J. E., & Jaffe, L. F. (1998) · Journal of Cell Science · doi:10.1242/jcs.111.12.1613 · Cited by 155
Sperm Deliver a New Second Messenger
Churchill, G. C., O'Neill, J. S., Masgrau, R., Patel, S., Thomas, J. M., Genazzani, A. A., & Galione, A. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00002-2 · Cited by 153
Carroll, J., Swann, K., Whittingham, D. G., & Whitaker, M. (1994) · Development · doi:10.1242/dev.120.12.3507 · Cited by 153
Self-citationTwigg, J., Patel, R., & Whitaker, M. (1988) · Nature · doi:10.1038/332366a0 · Cited by 150
Self-citationEvans, J. P., Kopf, G. S., & Schultz, R. M. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8611 · Cited by 149
Chini, E. N., Beers, K. W., & Dousa, T. P. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.7.3216 · Cited by 147
Hiiragi, T., & Solter, D. (2004) · Nature · doi:10.1038/nature02595 · Cited by 145
Nixon, V. L., Levasseur, M., McDougall, A., & Jones, K. T. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00811-4 · Cited by 143
Imaging of multicellular large-scale rhythmic calcium waves during zebrafish gastrulation
Gilland, E., Miller, A. L., Karplus, E., Baker, R., & Webb, S. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.1.157 · Cited by 143
The first cleavage of the mouse zygote predicts the blastocyst axis
Płusa, B., Hadjantonakis, A., Gray, D., Piotrowska-Nitsche, K., Jędrusik, A., Papaioannou, V. E., Glover, D. M., & Zernicka‐Goetz, M. (2005) · Nature · doi:10.1038/nature03388 · Cited by 142
Patterning of the embryo: the first spatial decisions in the life of a mouse
Zernicka‐Goetz, M. (2002) · Development · doi:10.1242/dev.129.4.815 · Cited by 142
Kline, D., & Kline, J. T. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)37088-7 · Cited by 141
Wyrick, R. E., Nishihara, T., & Hedrick, J. L. (1974) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.71.5.2067 · Cited by 141
Homa, S. T., Carroll, J., & Swann, K. (1993) · Human Reproduction · doi:10.1093/oxfordjournals.humrep.a138240 · Cited by 140
Patel, R., Holt, M., Philipova, R., Moss, S. J., Schulman, H., Hidaka, H., & Whitaker, M. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.12.7958 · Cited by 139
Self-citationMehlmann, L. M., Carpenter, G. F., Rhee, S. G., & Jaffe, L. A. (1998) · Developmental Biology · doi:10.1006/dbio.1998.9051 · Cited by 138
Lillie, F. R. (1919) · Transactions of the American Microscopical Society · doi:10.2307/3221556 · Cited by 138
依田, 綾., Oda, S., Shikano, T., Kouchi, Z., Awaji, T., Shirakawa, H., Kinoshita, K., & Miyazaki, S. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2003.12.028 · Cited by 137
Cited by
The endoplasmic reticulum: structure, function and response to cellular signaling
Schwarz, D. S., & Blower, M. D. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2052-6 · Cited by 1,613
Metadata
- Authors
- Whitaker, M.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2006-01
- Volume
- 86
- Issue
- 1
- Pages
- 25-88
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2132204920
- Cited by
- 512
- References
- 399
- FWCI
- 5.00
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.