spacer gif spacer gif spacer gif spacer gif spacer gif
QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Summary Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bauer, D. V.
Right arrow Articles by Moody, S. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bauer, D. V.
Right arrow Articles by Moody, S. A.
Social Bookmarking
Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?
Blumberg, B., Wright, C. V. E., De Robertis, E. M. and Cho, K. W. Y (1991). Organizer-specific homeobox genes in Xenopus laevis embryos. Science 253, 194-196.[Abstract/Free Full Text]

Cho, K. W. Y., Blumberg, B., Steinbesser, H. and De Robertis, E. M (1991). Molecular nature of Spemann's Organizer: the role of the Xenopus homeobox gene goosecoid. Cell 67, 1111-1120.[Medline]

Christian, J. L., Olson, D. J. and Moon, R. T (1992). Xwnt-8 modifies the character of mesoderm induced by bFGF in isolated Xenopus ectoderm. EMBO J 11, 33-41.[Medline]

Dale, L. and Slack, J. M. W (1987). Fate map for the 32 cell stage of Xenopus laevis. Development 99, 197-210.[Abstract]

Dirksen, M. L. and Jamrich, M (1992). A novel, activin-inducible, blastopore lip-specific gene of Xenopus laevis contains a fork head DNA-binding domain. Genes Dev 6, 599-608.[Abstract/Free Full Text]

Elinson, R. P. and Kao, K. R (1989). The location of dorsal information in frog early development. Dev. Growth Differ 31, 357-369.

Gallagher, B. C., Hainski, A. M. and Moody, S. A (1991). Autonomous differentiation of dorsal axial structures from an animal cap cleavage stage blastomere in Xenopus. Development 112, 1103-1114.[Abstract]

Gimlich, R. L (1986). Acquisition of developmental autonomy in the equatorial region of the Xenopus embryo. Dev. Biol 115, 340-352.[Medline]

Hainski, A. M. and Moody, S. A (1992). Xenopus maternal RNAs from a dorsal animal blastomere induce a secondary axis in host embryos. Development 116, 347-355.[Medline]

Hirose, G. and Jacobson, M (1979). Clonal organization of the central nervous system of the frog. I. Clones stemming from individual blastomeres of the 16-cell and earlier stages. Dev. Biol 71, 191-202.[Medline]

Huang, S. and Moody, S. A (1992). Does lineage determine the dopamine phenotypein the tadpole hypothalamus?: A quantitative analysis. J. Neurosci 12, 1351-1362.[Abstract]

Huang, S. and Moody, S. A (1993). The retinal fate of Xenopus cleavage stage progenitors is dependent upon blastomere position and competence: Studies of normal and regulated clones. J. Neurosci 13, 3193-3210.[Abstract]

Jacobson, M (1983). Clonal organization of the central nervous system of the frog. III.Clones stemming from the individual blastomeres of the 128-, 256-, and 512-cell stages. J. Neurosci 2, 1019-1038.

Jacobson, M. and Hirose, G (1978). Origin of the retina from both sides of the embryonic brain: a contribution to the problem of crossing at the optic chiasma. Science 202, 637-639.[Abstract/Free Full Text]

Jacobson, M. and Hirose, G (1981). Clonal organization of the central nervous system of the frog. II. Clones stemming from individual blastomeres of the 32-and 64-cell stages. J Neurosci 1, 271-284.[Abstract]

Jones, E. A. and Woodland, H. R (1987). The development of animal cap cells in Xenopus : a measure of the start of animal cap competence to form mesoderm. Development 101, 557-563.[Abstract]

Kageura, H (1990). Spatial distribution of the capacity to initiate a secondary embryo in the 32-cell embryo of Xenopus laevis. Dev. Biol 142, 432-438.[Medline]

Keller, R. E (1975). Vital dye mapping of the gastrula and neurula of Xenopus laevis . I. Prospective areas and morphogenetic movements of the superficial layer. Dev.Biol 42, 222-241.[Medline]

Keller, R. E (1976). Vital dye mapping of the gastrula and neurula of Xenopus laevis . II. Prospective areas and morphogenetic movements of the deep layer. Dev. Biol 51, 118-137.[Medline]

Keller, R. E (1978). Time-lapse cinemicrographic analysis of superficial cell behaviorduring and prior to gastrulation in Xenopus laevis. J. Morph 157, 223-248.

Keller, R. E (1980). The cellular basis of epiboly: An SEM study of deep-cell rearrangement during gastrulation in Xenopus laevis. J. Embryol. Exp. Morph 60, 201-234.[Medline]

Kimelman, D. and Kirschner, M (1987). Synergistic induction of mesoderm by FGF and TGF-and the identification of an mRNA coding for FGF in the early Xenopus embryo. Cell 51, 869-877.[Medline]

Kimmel, C. B. and Law, R. D (1985). Cell lineage of zebrafish blastomeres. III. Clonal analyses of the blastula and gastrula stages. Dev. Biol 108, 94-101.[Medline]

Masho, R (1988). Fates of animal-dorsal blastomeres of eight-cell stage Xenopus embryos vary according to the specific pattern of the third cleavage plane. Dev. Growth Differ 30, 347-359.[Medline]

Moody, S. A (1987). Fates of the blastomeres of the 16-cell stage Xenopus embryo. Dev. Biol 119, 560-578.[Medline]

Moody, S. A (1987). Fates of the blastomeres of the 32-cell stage Xenopus embryo. Dev. Biol 122, 300-319.[Medline]

Moody, S. A. and Kline, M. J (1990). Segregation of fate during cleavage of frog ( Xenopus laevis ) blastomeres. Anat. Embryol 182, 347-362.[Medline]

Nakamura, O. and Kishiyama, K (1971). Prospective fates of blastomeres at the 32-cell stage of Xenopus laevis embryos. Proc. Japan Acad 47, 407-412.

Newport, J. and Kirschner, M (1982). A major developmental transition in early Xenopus embryos: I. Characterization and timing of cellular changes at the midblastula stage. Cell 30, 675-686.[Medline]

Rosa, F., Roberts, A. B., Danielpour, D., Dart, L.L., Sporn, M. B., and Dawid, I. B (1988). Mesoderm induction in amphibians: The role of TGF-2-like factors. Science 239, 783-785.[Abstract/Free Full Text]

Shih, J. and Keller, R (1992). The epithelium of the dorsal marginal zone of Xenopus has organizer properties. Development 116, 887-899.[Abstract]

Shih, J. and Keller, R (1992). Cell motility driving mediolateral intercalation in explants of Xenopus laevis. Development 116, 901-914.[Abstract]

Slack, J. M. W., Darlington, B. G., Heath, J. K., and Godsave, S. F (1987). Mesoderm induction in early Xenopus embryos by heparin-binding growth factor. Nature 326, 197-200.[Medline]

Smith, J. C (1987). A mesoderm-inducing factor is produced by a Xenopus cell line. Development 99, 3-14.[Abstract/Free Full Text]

Smith, W. C. and Harland, R. M (1991). Injected Xwnt-8 RNA induces a complete body axis in Xenopus embryos. Cell 67, 753-765.[Medline]

Smith, W. C. and Harland, R. M (1992). Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos. Cell 70, 829-840.[Medline]

Sokol, S. Y (1993). Mesoderm formation in Xenopus ectodermal explants overexpressing Xwnt-8: evidence for a cooperating signal reaching the animal pole by gastrulation. Development 118, 1335-1342.[Abstract]

Sokol, S. Y. and Melton, D. A (1991). Preexistent pattern in Xenopus animal pole cells revealed by induction with activin. Nature 351, 409-411.[Medline]

Sokol, S. Y. and Melton, D. A (1992). Interaction of Wnt and activin in dorsal mesoderm induction in Xenopus. Dev. Biol 154, 348-355.[Medline]

Steinbesser, H., De Robertis, E. M., Ku, M., Kessler, D. S. and Melton, D. A (1993). Xenopus axis formation: induction of goosecoid by injected Xwnt-8 and activin mRNAs. Development 118, 499-507.[Abstract]

Taira, M., Jamrich, M., Good, P. J. and Dawid, I. B (1992). The LIM domain-containing homeobox gene Xlim-1 is expressed specifically in the organizer region of Xenopus gastrula. Genes Dev 6, 356-66.[Abstract/Free Full Text]

Takasaki, H (1987). Fates and roles of the presumptive organizer region in the 32-cell embryo in normal development of Xenopus laevis. Dev.Growth Differ 29, 141-152.[Medline]

Warga, R. M. and Kimmel, C. B (1990). Cell movements during epiboly and gastrulation in zebrafish. Development 108, 569-580.[Abstract/Free Full Text]

Wetts, R. and Fraser, S. E (1989). Slow intermixing of cells during Xenopus embryogenesis contributes to the consistency of the blastomere fate map. Development 105, 9-15.[Abstract]

Wilson, P. and Keller, R (1991). Cell rearrangement during gastrulation of Xenopus : direct observation of cultured explants. Development 112, 289-300.[Abstract]
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
 DevelopmentHome page
N. Martynova, F. Eroshkin, G. Ermakova, A. Bayramov, J. Gray, R. Grainger, and A. Zaraisky
Patterning the forebrain: FoxA4a/Pintallavis and Xvent2 determine the posterior limit of Xanf1 expression in the neural plate
Development, May 15, 2004; 131(10): 2329 - 2338.
[Abstract] [Full Text] [PDF]

Home page
 DevelopmentHome page
M. S. Murakami, S. A. Moody, I. O. Daar, and D. K. Morrison
Morphogenesis during Xenopus gastrulation requires Wee1-mediated inhibition of cell proliferation
Development, February 1, 2004; 131(3): 571 - 580.
[Abstract] [Full Text] [PDF]

Home page
 DevelopmentHome page
A. C. Silva, M. Filipe, K.-M. Kuerner, H. Steinbeisser, and J. A. Belo
Endogenous Cerberus activity is required for anterior head specification in Xenopus
Development, October 15, 2003; 130(20): 4943 - 4953.
[Abstract] [Full Text] [PDF]

Home page
 DevelopmentHome page
M. Walmsley, A. Ciau-Uitz, and R. Patient
Adult and embryonic blood and endothelium derive from distinct precursor populations which are differentially programmed by BMP in Xenopus
Development, March 14, 2003; 129(24): 5683 - 5695.
[Abstract] [Full Text] [PDF]

Home page
 Genes Dev.Home page
Y. Yamanaka, T. Mizuno, Y. Sasai, M. Kishi, H. Takeda, C.-H. Kim, M. Hibi, and T. Hirano
A novel homeobox gene, dharma, can induce the organizer in a non-cell-autonomous manner
Genes & Dev., August 1, 1998; 12(15): 2345 - 2353.
[Abstract] [Full Text]

Home page
 ScienceHome page
G. L. Henry and D. A. Melton
Mixer, a Homeobox Gene Required for Endoderm Development
Science, July 3, 1998; 281(5373): 91 - 96.
[Abstract] [Full Text]

Home page
 DevelopmentHome page
M. Deardorff, C Tan, L. Conrad, and P. Klein
Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis
Development, January 7, 1998; 125(14): 2687 - 2700.
[Abstract] [PDF]

Home page
 Genes Dev.Home page
M. Brannon, M. Gomperts, L. Sumoy, R. T. Moon, and D. Kimelman
A beta -catenin/XTcf-3 complex binds to the siamois promoter to regulate dorsal axis specification in Xenopus
Genes & Dev., September 15, 1997; 11(18): 2359 - 2370.
[Abstract] [Full Text] [PDF]

Home page
 DevelopmentHome page
M. Laurent, I. Blitz, C Hashimoto, U Rothbacher, and K. Cho
The Xenopus homeobox gene twin mediates Wnt induction of goosecoid in establishment of Spemann's organizer
Development, January 12, 1997; 124(23): 4905 - 4916.
[Abstract] [PDF]

Home page
 DevelopmentHome page
S Darras, Y Marikawa, R. Elinson, and P Lemaire
Animal and vegetal pole cells of early Xenopus embryos respond differently to maternal dorsal determinants: implications for the patterning of the organiser
Development, January 11, 1997; 124(21): 4275 - 4286.
[Abstract] [PDF]

Home page
 DevelopmentHome page
S. Witta and S. Sato
XIPOU 2 is a potential regulator of Spemann's Organizer
Development, January 3, 1997; 124(6): 1179 - 1189.
[Abstract] [PDF]

Home page
 DevelopmentHome page
M. Vodicka and J. Gerhart
Blastomere derivation and domains of gene expression in the Spemann Organizer of Xenopus laevis
Development, January 11, 1995; 121(11): 3505 - 3518.
[Abstract] [PDF]

Home page
 DevelopmentHome page
C Domingo and R Keller
Induction of notochord cell intercalation behavior and differentiation by progressive signals in the gastrula of Xenopus laevis
Development, January 10, 1995; 121(10): 3311 - 3321.
[Abstract] [PDF]

This Article
Right arrow Summary Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bauer, D. V.
Right arrow Articles by Moody, S. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bauer, D. V.
Right arrow Articles by Moody, S. A.
Social Bookmarking
Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?