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• W2009088673 abstract "Next article No AccessEarly History and Mechanics of the Chick Blastoderm: A ReviewDorothea RudnickDorothea Rudnick Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The Quarterly Review of Biology Volume 19, Number 3Sep., 1944 Published in association with Stony Brook University Article DOIhttps://doi.org/10.1086/394693 Views: 3Total views on this site Citations: 65Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Brian K. Hall Germ layers, the neural crest and emergent organization in development and evolution, genesis 139 (Apr 2018): e23103.https://doi.org/10.1002/dvg.23103Sabine Brauckmann Axes, planes and tubes, or the geometry of embryogenesis, Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 42, no.44 (Dec 2011): 381–390.https://doi.org/10.1016/j.shpsc.2011.07.009Mareike Pieper, Gerald W. Eagleson, Werner Wosniok, Gerhard Schlosser Origin and segregation of cranial placodes in Xenopus laevis, Developmental Biology 360, no.22 (Dec 2011): 257–275.https://doi.org/10.1016/j.ydbio.2011.09.024J.H. Yuan, J.S. Gao, Z.F. Zhan, H.W. Liu, W.J. Jin, Z.D. Li Development-promoting effect of chicken embryo membrane on chicken ovarian cortical pieces of different age, Poultry Science 88, no.1111 (Nov 2009): 2415–2421.https://doi.org/10.3382/ps.2008-00555Ann Foley Cardiac lineage selection: integrating biological complexity into computational models, WIREs Systems Biology and Medicine 1, no.33 (Nov 2009): 334–347.https://doi.org/10.1002/wsbm.43My Sjödal, Thomas Edlund, Lena Gunhaga Time of Exposure to BMP Signals Plays a Key Role in the Specification of the Olfactory and Lens Placodes Ex Vivo, Developmental Cell 13, no.11 (Jul 2007): 141–149.https://doi.org/10.1016/j.devcel.2007.04.020Rosa M. Guzzo, Ann C. Foley, Yessenia M. Ibarra, Mark Mercola Signaling Pathways in Embryonic Heart Induction, (Jan 2007): 117–151.https://doi.org/10.1016/S1574-3349(07)18005-4Lucía Rodríguez-Gallardo, Luisa Sánchez-Arrones, Pedro Fernández-Garre, Luis Puelles Agreement and disagreement among fate maps of the chick neural plate, Brain Research Reviews 49, no.22 (Sep 2005): 191–201.https://doi.org/10.1016/j.brainresrev.2004.12.032Sujata Bhattacharyya, Andrew P. Bailey, Marianne Bronner-Fraser, Andrea Streit Segregation of lens and olfactory precursors from a common territory: cell sorting and reciprocity of Dlx5 and Pax6 expression, Developmental Biology 271, no.22 (Jul 2004): 403–414.https://doi.org/10.1016/j.ydbio.2004.04.010J. W. Witkin, D. Dao, I. Livne, I. C. Dunn, X. L. Zhou, K. Pula, A. J. Silverman Early Expression of Chicken Gonadotropin-Releasing Hormone-1 in the Developing Chick, Journal of Neuroendocrinology 15, no.99 (Aug 2003): 865–870.https://doi.org/10.1046/j.1365-2826.2003.01073.xAndrea Streit Extensive Cell Movements Accompany Formation of the Otic Placode, Developmental Biology 249, no.22 (Sep 2002): 237–254.https://doi.org/10.1006/dbio.2002.0739Charles P. Ordahl Fate Map, (Jan 2002).https://doi.org/10.1002/047120918X.emb0523J. E. Fortune Activation of Primordial Follicles, (Jan 2002): 11–21.https://doi.org/10.1007/978-3-662-04960-0_2Clare V.H. Baker, Marianne Bronner-Fraser Vertebrate Cranial Placodes I. Embryonic Induction, Developmental Biology 232, no.11 (Apr 2001): 1–61.https://doi.org/10.1006/dbio.2001.0156Curtis R. Altmann, Ali H. Brivanlou Neural patterning in the vertebrate embryo, (Jan 2001): 447–482.https://doi.org/10.1016/S0074-7696(01)03013-3K.E. Whitlock, M. Westerfield The olfactory placodes of the zebrafish form by convergence of cellular fields at the edge of the neural plate, Development 127, no.1717 (Sep 2000): 3645–3653.https://doi.org/10.1242/dev.127.17.3645Vidya Patwardhan, Sonalis Fernandez, Michael Montgomery, Judith Litvin The rostro-caudal position of cardiac myocytes affect their fate, Developmental Dynamics 218, no.11 (May 2000): 123–135.https://doi.org/10.1002/(SICI)1097-0177(200005)218:1<123::AID-DVDY11>3.0.CO;2-6J.E Fortune, R.A Cushman, C.M Wahl, S Kito The primordial to primary follicle transition, Molecular and Cellular Endocrinology 163, no.1-21-2 (May 2000): 53–60.https://doi.org/10.1016/S0303-7207(99)00240-3Jodi L. Smith, Gary C. Schoenwolf 3 Getting Organized: New Insights into the Organizer of Higher Vertebrates, (Jan 1998): 79–110.https://doi.org/10.1016/S0070-2153(08)60365-8Martin Catala, Marie-Aimée Teillet, Nicole M. Le Douarin Organization and development of the tail bud analyzed with the quail-chick chimaera system, Mechanisms of Development 51, no.11 (May 1995): 51–65.https://doi.org/10.1016/0925-4773(95)00350-AJodi L. Smith, Katherine M. Gesteland, Gary C. Schoenwolf Prospective fate map of the mouse primitive streak at 7.5 days of gestation, Developmental Dynamics 201, no.33 (Feb 2005): 279–289.https://doi.org/10.1002/aja.1002010310Virginio Garcia-Martinez, Ignacio S. Alvarez, Gary C. Schoenwolf Locations of the ectodermal and nonectodermal subdivisions of the epiblast at stages 3 and 4 of avian gastrulation and neurulation, Journal of Experimental Zoology 267, no.44 (Nov 1993): 431–446.https://doi.org/10.1002/jez.1402670409Paolo Di Nardo, Marilena Minieri, Arnaldo Carbone, Nicola Maggiano, Rosella Micheletti, Giuseppe Peruzzi, Giuseppe Tallarida Myocardial expression of atrial natriuretic factor gene in early stages of hamster cardiomyopathy, Molecular and Cellular Biochemistry 125, no.22 (Aug 1993): 179–192.https://doi.org/10.1007/BF00936447Gary C. Schoenwolf, Virginio Garcia-Martinez, Mark S. Dias Mesoderm movement and fate during avian gastrulation and neurulation, Developmental Dynamics 193, no.33 (Feb 2005): 235–248.https://doi.org/10.1002/aja.1001930304Hilde Bortier, Lucien C. A. Vakaet Mesoblast Anlage Fields in the Upper Layer of the Chicken Blastoderm at Stage 5V, (Jan 1992): 1–7.https://doi.org/10.1007/978-1-4615-3458-7_1Gary C. Schoenwolf, Philip Sheard Fate mapping the avian epiblast with focal injections of a fluorescent-histochemical marker: Ectodermal derivatives, Journal of Experimental Zoology 255, no.33 (Sep 1990): 323–339.https://doi.org/10.1002/jez.1402550309Gary C. Schoenwolf, Hilde Bortier, Lucien Vakaet Fate mapping the avian neural plate with quail/chick chimeras: Origin of prospective median wedge cells, Journal of Experimental Zoology 249, no.33 (Mar 1989): 271–278.https://doi.org/10.1002/jez.1402490305Jean-Paul Thiery, Jean-Loup Duband, Sylvie Dufour, Pierre Savagner, Beat A. Imhof Roles of Fibronectins in Embryogenesis, (Jan 1989): 181–212.https://doi.org/10.1016/B978-0-12-508470-3.50012-2J. M. Doménech-Mateu, X. Gonzalez-Compta Horseshoe kidney: A new theory on lts embrogenesis based on the study of a 16-mm human embryo, The Anatomical Record 222, no.44 (Jan 2005): 408–417.https://doi.org/10.1002/ar.1092220413S L Warren, W J Nelson Nonmitogenic morphoregulatory action of pp60v-src on multicellular epithelial structures, Molecular and Cellular Biology 7, no.44 (Apr 1987): 1326–1337.https://doi.org/10.1128/mcb.7.4.1326-1337.1987Pio Fioroni Weiterführende Literatur, (Jan 1987): 402–415.https://doi.org/10.1007/978-3-642-96983-6_16Esmond J. Sanders Mesoderm Migration in the Early Chick Embryo, (Jan 1986): 449–480.https://doi.org/10.1007/978-1-4613-2141-5_12M. K. KHARE, S. CHOUDHURY Establishment of the Neural Differentiation Pattern in the Prospective Prosencephalic Ectoderm of the Chick Embryo (Gallus domesticus). (neural induction/neural differentiation/prosencephalic differentiation/eye potency field), Development, Growth and Differentiation 27, no.11 (Feb 1985): 83–93.https://doi.org/10.1111/j.1440-169X.1985.00083.xANN ANDREW DEVELOPMENTAL RELATIONSHIPS OF NEUROENDOCRINE CELLS , Biomedical Research 6, no.44 (Jan 1985): 191–196.https://doi.org/10.2220/biomedres.6.191Robert W. Keane, Leah A. Lipsich, Joan S. Brugge Differentiation and transformation of neural plate cells, Developmental Biology 103, no.11 (May 1984): 38–52.https://doi.org/10.1016/0012-1606(84)90005-8Glenn C. Rosenquist Epiblast origin and early migration of neural crest cells in the chick embryo, Developmental Biology 87, no.22 (Oct 1981): 201–211.https://doi.org/10.1016/0012-1606(81)90143-3A. Leikola Hensen's node — The ’Organizer’ of the amniote embryo, Experientia 32, no.33 (Mar 1976): 269–277.https://doi.org/10.1007/BF01940787 The erythroid cells and haemoglobins of the chick embryo, Philosophical Transactions of the Royal Society of London. B, Biological Sciences 266, no.877877 (Jan 1997): 225–305.https://doi.org/10.1098/rstb.1973.0050Alan M. Cohen Factors directing the expression of sympathetic nerve traits in cells of neural crest origin, Journal of Experimental Zoology 179, no.22 (Feb 1972): 167–182.https://doi.org/10.1002/jez.1401790204Gerard Nicolet Avian Gastrulation, (Jan 1971): 231–262.https://doi.org/10.1016/B978-0-12-028609-6.50010-8Hefzibah Eyal-Giladi, Moshe Wolk The inducing capacities of the primary hypoblast as revealed by transfilter induction studies, Wilhelm Roux' Archiv f�r Entwicklungsmechanik der Organismen 165, no.33 (Sep 1970): 226–241.https://doi.org/10.1007/BF01380786Nelson T. Spratt, Hermann Haas Germ layer formation and the role of the primitive streak in the chick. I. Basic architecture and morphogenetic tissue movements, Journal of Experimental Zoology 158, no.11 (Feb 1965): 9–38.https://doi.org/10.1002/jez.1401580103Nelson T. Spratt, Hermann Haas Integrative mechanisms in development of the early chick blastoderm. I. Regulative potentiality of separated parts, Journal of Experimental Zoology 145, no.22 (Nov 1960): 97–137.https://doi.org/10.1002/jez.1401450202Nelson T. Spratt, Hermann Haas Importance of morphogenetic movements in the lower surface of the young chick blastoderm, Journal of Experimental Zoology 144, no.33 (Aug 1960): 257–275.https://doi.org/10.1002/jez.1401440305Nelson T. Spratt, Hermann Haas Morphogenetic movements in the lower surface of the unincubated and early chick blastoderm, Journal of Experimental Zoology 144, no.22 (Jul 1960): 139–157.https://doi.org/10.1002/jez.1401440204Shakuntala Chaube On axiation and symmetry in transplanted wing of the chick, Journal of Experimental Zoology 140, no.11 (Feb 1959): 29–77.https://doi.org/10.1002/jez.1401400104G. E. H. Foxon SOME POSSIBLE CAUSES OF CONGENITAL HEART MALFORMATION, Heart 21, no.11 (Jan 1959): 51–64.https://doi.org/10.1136/hrt.21.1.51YOSHITO OGAWA, TAKATADA KAWAHARA, JIROO MIURA Serological Determination of Developing Muscle Protein in Chick Embryo, Nature 181, no.46094609 (Mar 1958): 621–622.https://doi.org/10.1038/181621a0Casimer T. Grabowski The induction of secondary embryos in the early chick blastoderm by grafts of Hensen's node, American Journal of Anatomy 101, no.11 (Jul 1957): 101–133.https://doi.org/10.1002/aja.1001010106Nelson T. Spratt Analysis of the organizer center in the early chick embryo. III. Regulative properties of the chorda and somite centers, Journal of Experimental Zoology 135, no.22 (Jul 1957): 319–353.https://doi.org/10.1002/jez.1401350207Nelson T. Spratt Analysis of the organizer center in the early chick embryo. II. Studies of the mechanics of notochord elongation and somite formation, Journal of Experimental Zoology 134, no.33 (Apr 1957): 577–612.https://doi.org/10.1002/jez.1401340309I.L. Kosin, Emile St. Pierre Studies on Pre-Incubation Warming of Chicken and Turkey Eggs ,, Poultry Science 35, no.66 (Nov 1956): 1384–1392.https://doi.org/10.3382/ps.0351384James D. Ebert, R. A. Tolman, A. M. Mun, J. F. Albright THE MOLECULAR BASIS OF THE FIRST HEART BEATS, Annals of the New York Academy of Sciences 60, no.77 (Jun 1955): 968–985.https://doi.org/10.1111/j.1749-6632.1955.tb40083.xNelson T. Spratt Analysis of the organizer center in the early chick embryo. I. Localization of prospective notochord and somite cells, Journal of Experimental Zoology 128, no.11 (Feb 1955): 121–163.https://doi.org/10.1002/jez.1401280106Ronald C. Fraser Studies on the hypoblast of the young chick embryo., Journal of Experimental Zoology 126, no.33 (Aug 1954): 349–399.https://doi.org/10.1002/jez.1401260302Sumner I. Zacks Esterases in the early chick embryo, The Anatomical Record 118, no.33 (Mar 1954): 509–537.https://doi.org/10.1002/ar.1091180304Gert Andres Experiments on the fate of dissociated embryonic cells (chick) disseminated by the vascular route. Part II. Teratomas, Journal of Experimental Zoology 122, no.33 (Apr 1953): 507–539.https://doi.org/10.1002/jez.1401220309Clifford Grobstein, Edgar Zwilling Modification of growth and differentiation of chorio-allantoic grafts of chick blastoderm pieces after cultivation at a glassclot interface, Journal of Experimental Zoology 122, no.22 (Mar 1953): 259–284.https://doi.org/10.1002/jez.1401220204Mary E. Rawles TRANSPLANTATION OF NORMAL EMBRYONIC TISSUES, Annals of the New York Academy of Sciences 55, no.22 (Aug 1952): 302–312.https://doi.org/10.1111/j.1749-6632.1952.tb26546.xNelson T. Spratt Localization of the prospective neural plate in the early chick blastoderm, Journal of Experimental Zoology 120, no.11 (Jun 1952): 109–130.https://doi.org/10.1002/jez.1401200105Byron S. Wenger Determination of structural patterns in the spinal cord of the chick embryo studied by transplantations between brachial and adjacent levels, Journal of Experimental Zoology 116, no.11 (Feb 1951): 123–163.https://doi.org/10.1002/jez.1401160106 The effects of antero-posterior reversal of lengths of the primitive streak in the chick, Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 234, no.613613 (Jun 1950): 317–338.https://doi.org/10.1098/rstb.1950.0004DONALD PAUL COSTELLO Growth and Development, (Jan 1949): 115–153.https://doi.org/10.1016/B978-1-4832-0000-2.50008-1Nelson T. Spratt Regression and shortening of the primitive streak in the explanted chick blastoderm, Journal of Experimental Zoology 104, no.11 (Feb 1947): 69–100.https://doi.org/10.1002/jez.1401040105Nelson T. Spratt Formation of the primitive streak in the explanted chick blastoderm marked with carbon particles, Journal of Experimental Zoology 103, no.22 (Nov 1946): 259–304.https://doi.org/10.1002/jez.1401030204" @default.
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