Cited by 443

The DOI matches its Crossref record; 99 of the 99 references it cites were found in a registry or an index.

Structure and function of the notochord: an essential organ for chordate development

Stemple, Derek L.·2005·Development

Open this paper in CoChat — free account

Abstract

The notochord is the defining structure of the chordates, and has essential roles in vertebrate development. It serves as a source of midline signals that pattern surrounding tissues and as a major skeletal element of the developing embryo. Genetic and embryological studies over the past decade have informed us about the development and function of the notochord. In this review, I discuss the embryonic origin, signalling roles and ultimate fate of the notochord, with an emphasis on structural aspects of notochord biology.

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

Crossref · 10.1242/dev.01812

Cites

99 of 99 references verified0 citation errors · 0 not checkable

Statistics

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.

The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio
Haffter, P., Granato, M., Brand, M., Mullins, M. C., Hammerschmidt, M., Kane, D. A., Odenthal, J., J. M. van Eeden, F., Jiang, Y.-J., Heisenberg, C.-P., et al. (1996) · Development · doi:10.1242/dev.123.1.1 · Cited by 1,662
MATRIX PROTEOGLYCANS: From Molecular Design to Cellular Function
Iozzo, R. V. (1998) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.67.1.609 · Cited by 1,637
A genetic screen for mutations affecting embryogenesis in zebrafish
Driever, W., Solnica-Krezel, L., Schier, A. F., Neuhauss, S. C. F., Malicki, J., Stemple, D. L., Stainier, D. Y. R., Zwartkruis, F., Abdelilah, S., Rangini, Z., et al. (1996) · Development · doi:10.1242/dev.123.1.37 · Cited by 1,337
Self-citation
Form and function: The laminin family of heterotrimers
Colognato, H., & Yurchenco, P. D. (2000) · Developmental Dynamics · doi:10.1002/(sici)1097-0177(200006)218:2<213::aid-dvdy1>3.0.co;2-r · Cited by 1,244
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
Self-citation
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
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
über Induktion von Embryonalanlagen durch Implantation artfremder Organisatoren
Spemann, H., & Mangold, H. (1924) · Archiv für Mikroskopische Anatomie und Entwicklungsmechanik · doi:10.1007/bf02108176 · Cited by 828
sonic hedgehog and vascular endothelial growth factor Act Upstream of the Notch Pathway during Arterial Endothelial Differentiation
Lawson, N. D., Vogel, A. M., & Weinstein, B. M. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00198-3 · Cited by 813
The EGF-CFC Protein One-Eyed Pinhead Is Essential for Nodal Signaling
Gritsman, K., Zhang, J., Cheng, S., Heckscher, E., Talbot, W. S., & Schier, A. F. (1999) · Cell · doi:10.1016/s0092-8674(00)80720-5 · Cited by 713
Control of cell pattern in the developing nervous system: Polarizing activity of the floor plate and notochord
Yamada, T., Placzek, M., Tanaka, H., Dodd, J., & Jessell, T. M. (1991) · Cell · doi:10.1016/0092-8674(91)90247-v · Cited by 707
Supramolecular assembly of basement membranes
Timpl, R., & Brown, J. C. (1996) · BioEssays · doi:10.1002/bies.950180208 · Cited by 699
DORSAL-VENTRAL PATTERNING AND NEURAL INDUCTION IN XENOPUS EMBRYOS
De Robertis, E. M., & Kuroda, H. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.011403.154124 · Cited by 671
SOX9 Binds DNA, Activates Transcription, and Coexpresses with Type II Collagen during Chondrogenesis in the Mouse
Ng, L.-J., Wheatley, S., Muscat, G. E. O., Conway-Campbell, J., Bowles, J., Wright, E., Bell, D. M., Tam, P. P. L., Cheah, K. S. E., & Koopman, P. (1997) · Developmental Biology · doi:10.1006/dbio.1996.8487 · Cited by 666
Identification of separate slow and fast muscle precursor cells in vivo, prior to somite formation
Devoto, S. H., Melançon, E., Eisen, J. S., & Westerfield, M. (1996) · Development · doi:10.1242/dev.122.11.3371 · Cited by 666
Zebrafish organizer development and germ-layer formation require nodal-related signals
Feldman, B., Gates, M. A., Egan, E. S., Dougan, S. T., Rennebeck, G., Sirotkin, H. I., Schier, A. F., & Talbot, W. S. (1998) · Nature · doi:10.1038/26013 · Cited by 663
Identification of a potent Xenopus mesoderm-inducing factor as a homologue of activin A
Smith, J. C., Price, B. M. J., Nimmen, K. V., & Huylebroeck, D. (1990) · Nature · doi:10.1038/345729a0 · Cited by 657
The protein product of the zebrafish homologue of the mouse T gene is expressed in nuclei of the germ ring and the notochord of the early embryo
Schulte-Merker, S., Ho, R. K., Herrmann, B. G., & NÜsslein-Volhard, C. (1992) · Development · doi:10.1242/dev.116.4.1021 · Cited by 644
no tail (ntl) is the zebrafish homologue of the mouse T (Brachyury) gene
Schulte-Merker, S., Eeden, F. J. M. V., Halpern, M. E., Kimmel, C. B., & Nüsslein-Volhard, C. (1994) · Development · doi:10.1242/dev.120.4.1009 · Cited by 623
Cartilage proteoglycans
Knudson, C. B., & Knudson, W. (2001) · Seminars in Cell & Developmental Biology · doi:10.1006/scdb.2000.0243 · Cited by 600
Anteroposterior patterning in hemichordates and the origins of the chordate nervous system
Lowe, C. J., Wu, M., Salic, A., Evans, L., Lander, E., Stange-Thomann, N., Gruber, C. E., Gerhart, J., & Kirschner, M. (2003) · Cell · doi:10.1016/s0092-8674(03)00469-0 · Cited by 531
Angiogenic network formation in the developing vertebrate trunk
Isogai, S., Lawson, N. D., Torrealday, S., Horiguchi, M., & Weinstein, B. M. (2003) · Development · doi:10.1242/dev.00733 · Cited by 519
Nodal signalling in vertebrate development
Schier, A. F., & Shen, M. M. (2000) · Nature · doi:10.1038/35000126 · Cited by 515
Parallel expression ofSox9 andCol2a1 in cells undergoing chondrogenesis
Zhao, Q., Eberspaecher, H., Lefebvre, V., & de Crombrugghe, B. (1997) · Developmental Dynamics · doi:10.1002/(sici)1097-0177(199708)209:4<377::aid-aja5>3.0.co;2-f · Cited by 508
Zebrafish trilobite identifies new roles for Strabismus in gastrulation and neuronal movements
Jessen, J. R., Topczewski, J., Bingham, S., Sepich, D. S., Marlow, F., Chandrasekhar, A., & Solnica-Krezel, L. (2002) · Nature Cell Biology · doi:10.1038/ncb828 · Cited by 504
Graded changes in dose of a Xenopus activin A homologue elicit stepwise transitions in embryonic cell fate
Green, J. B. A., & Smith, J. C. (1990) · Nature · doi:10.1038/347391a0 · Cited by 504
Responses of embryonic xenopus cells to activin and FGF are separated by multiple dose thresholds and correspond to distinct axes of the mesoderm
Green, J. B. A., New, H. V., & Smith, J. C. (1992) · Cell · doi:10.1016/0092-8674(92)90550-v · Cited by 480
A homeobox gene essential for zebrafish notochord development
Talbot, W. S., Trevarrow, B., Halpern, M. E., Melby, A. E., Farr, G., Postlethwait, J. H., Jowett, T., Kimmel, C. B., & Kimelman, D. (1995) · Nature · doi:10.1038/378150a0 · Cited by 465 · cited 4×
“Genetic screens in zebrafish have identified two loci, floating head (flh) and bozozok (dharma – Zebrafish Information Network), as being essential for this transition to occur (Amacher and Kimmel, 1998; Fekany et al., 1999; Solnica-Krezel et al., 1996; Talbot et al., 1995).”
BackgroundInfluential
Control of cell pattern in the neural tube: Motor neuron induction by diffusible factors from notochord and floor plate
Yamada, T., Pfaff, S. L., Edlund, T., & Jessell, T. M. (1993) · Cell · doi:10.1016/0092-8674(93)90248-o · Cited by 465
Positional Cloning Identifies Zebrafish one-eyed pinhead as a Permissive EGF-Related Ligand Required during Gastrulation
Zhang, J., Talbot, W. S., & Schier, A. F. (1998) · Cell · doi:10.1016/s0092-8674(00)80918-6 · Cited by 459
The Zebrafish Glypican Knypek Controls Cell Polarity during Gastrulation Movements of Convergent Extension
Topczewski, J., Sepich, D. S., Myers, D. C., Walker, C., Amores, A., Lele, Z., Hammerschmidt, M., Postlethwait, J., & Solnica-Krezel, L. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00005-3 · Cited by 455
Induction of a second neural axis by the mouse node
Beddington, R. S. P. (1994) · Development · doi:10.1242/dev.120.3.613 · Cited by 436
The cyclops mutation blocks specification of the floor plate of the zebrafish central nervous system
Hatta, K., Kimmel, C. B., Ho, R. K., & Walker, C. (1991) · Nature · doi:10.1038/350339a0 · Cited by 426
Notochord to endoderm signaling is required for pancreas development
Kim, S. K., Hebrok, M., & Melton, D. A. (1997) · Development · doi:10.1242/dev.124.21.4243 · Cited by 405
The one-eyed pinhead gene functions in mesoderm and endoderm formation in zebrafish and interacts with no tail
Schier, A. F., Neuhauss, S. C. F., Helde, K. A., Talbot, W. S., & Driever, W. (1997) · Development · doi:10.1242/dev.124.2.327 · Cited by 359
Mutations affecting cell fates and cellular rearrangements during gastrulation in zebrafish
Solnica-Krezel, L., Stemple, D. L., Mountcastle-Shah, E., Rangini, Z., Neuhauss, S. C. F., Malicki, J., Schier, A. F., Stainier, D. Y. R., Zwartkruis, F., Abdelilah, S., et al. (1996) · Development · doi:10.1242/dev.123.1.67 · Cited by 320
Self-citation
Induction of a specific muscle cell type by a hedgehog-like protein in zebrafish
Currie, P. D., & Ingham, P. W. (1996) · Nature · doi:10.1038/382452a0 · Cited by 320
Basal lamina assembly
Yurchenco, P. D., & O'Rear, J. J. (1994) · Current Opinion in Cell Biology · doi:10.1016/0955-0674(94)90093-0 · Cited by 317
Control of dorsoventral patterning of somitic derivatives by notochord and floor plate.
Pourquié, O., Coltey, M., Teillet, M. A., Ordahl, C., & Le Douarin, N. M. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.11.5242 · Cited by 310
The zebrafish slow-muscle-omitted gene product is required for Hedgehog signal transduction and the development of slow muscle identity
Barresi, M. J. F., Stickney, H. L., & Devoto, S. H. (2000) · Development · doi:10.1242/dev.127.10.2189 · Cited by 303
Vessel Patterning in the Embryo of the Zebrafish: Guidance by Notochord
Fouquet, B., Weinstein, B. M., Serluca, F. C., & Fishman, M. C. (1997) · Developmental Biology · doi:10.1006/dbio.1996.8495 · Cited by 300
Mutations affecting morphogenesis during gastrulation and tail formation in the zebrafish, Danio rerio
Hammerschmidt, M., Pelegri, F., Mullins, M. C., Kane, D. A., Brand, M., Eeden, F. J. M. V., Furutani-Seiki, M., Granato, M., Haffter, P., Heisenberg, C.-P., et al. (1996) · Development · doi:10.1242/dev.123.1.143 · Cited by 286
The mechanics of notochord elongation, straightening and stiffening in the embryo of Xenopus laevis
Adams, D. S., Keller, R., & Koehl, M. A. R. (1990) · Development · doi:10.1242/dev.110.1.115 · Cited by 274
Induction of floor plate differentiation by contact-dependent, homeogenetic signals
Placzek, M., Jessell, T. M., & Dodd, J. (1993) · Development · doi:10.1242/dev.117.1.205 · Cited by 273
Defective Glomerulogenesis in the Absence of Laminin α5 Demonstrates a Developmental Role for the Kidney Glomerular Basement Membrane
Miner, J. H., & Li, C. (2000) · Developmental Biology · doi:10.1006/dbio.1999.9546 · Cited by 270
Prickle 1 regulates cell movements during gastrulation and neuronal migration in zebrafish
Carreira-Barbosa, F., Concha, M. L., Takeuchi, M., Ueno, N., Wilson, S. W., & Tada, M. (2003) · Development · doi:10.1242/dev.00567 · Cited by 269
Nodal signaling patterns the organizer
Gritsman, K., Talbot, W. S., & Schier, A. F. (2000) · Development · doi:10.1242/dev.127.5.921 · Cited by 265
Heparan sulfate proteoglycans in invasion and metastasis
Sanderson, R. D. (2001) · Seminars in Cell & Developmental Biology · doi:10.1006/scdb.2000.0241 · Cited by 262
The formation of the mesoderm in urodelean amphibians: V. Its regional induction by the endoderm
Boterenbrood, E. C., & Nieuwkoop, P. D. (1973) · Wilhelm Roux' Archiv f�r Entwicklungsmechanik der Organismen · doi:10.1007/bf00575837 · Cited by 247
Zebrafish mutants identify an essential role for laminins in notochord formation
Parsons, M. J., Pollard, S. M., Saúde, L., Feldman, B., Coutinho, P., Hirst, E. M. A., & Stemple, D. L. (2002) · Development · doi:10.1242/dev.129.13.3137 · Cited by 243
Self-citation
Collagen II Is Essential for the Removal of the Notochord and the Formation of Intervertebral Discs
Aszódi, A., Chan, D., Hunziker, E., Bateman, J. F., & Fässler, R. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.5.1399 · Cited by 241
The ascidian tadpole larva: comparative molecular development and genomics
Satoh, N. (2003) · Nature Reviews Genetics · doi:10.1038/nrg1042 · Cited by 239
Mutations affecting the formation of the notochord in the zebrafish, Danio rerio
Odenthal, J., Haffter, P., Vogelsang, E., Brand, M., Eeden, F. J. M. V., Furutani-Seiki, M., Granato, M., Hammerschmidt, M., Heisenberg, C.-P., Jiang, Y.-J., et al. (1996) · Development · doi:10.1242/dev.123.1.103 · Cited by 238
Characterizing the zebrafish organizer: microsurgical analysis at the early-shield stage
Shih, J., & Fraser, S. E. (1996) · Development · doi:10.1242/dev.122.4.1313 · Cited by 231
Expression of a type II collagen gene in the zebrafish embryonic axis
Yan, Y., Hatta, K., Riggleman, B., & Postlethwait, J. H. (1995) · Developmental Dynamics · doi:10.1002/aja.1002030308 · Cited by 229
Maternally controlled β-catenin-mediated signaling is required for organizer formation in the zebrafish
Kelly, C., Chin, A. J., Leatherman, and, D. J. K., & Weinberg, E. S. (2000) · Development · doi:10.1242/dev.127.18.3899 · Cited by 215
Formation and differentiation of the avian sclerotome
Christ, B., Huang, R., & Scaal, M. (2004) · Anatomy and Embryology · doi:10.1007/s00429-004-0408-z · Cited by 201
Mutations affecting development of the notochord in zebrafish
Stemple, D. L., Solnica-Krezel, L., Zwartkruis, F., Neuhauss, S. C. F., Schier, A. F., Malicki, J., Stainier, D. Y. R., Abdelilah, S., Rangini, Z., Mountcastle-Shah, E., et al. (1996) · Development · doi:10.1242/dev.123.1.117 · Cited by 198
Self-citation
The zebrafish bozozok locus encodes Dharma, a homeodomain protein essential for induction of gastrula organizer and dorsoanterior embryonic structures
Fekany, K., Yamanaka, Y., Leung, T., Sirotkin, H. I., Topczewski, J., Gates, M. A., Hibi, M., Renucci, A., Stemple, D., Radbill, A., et al. (1999) · Development · doi:10.1242/dev.126.7.1427 · Cited by 198
Self-citation
The prickle-Related Gene in Vertebrates Is Essential for Gastrulation Cell Movements
Takeuchi, M., Nakabayashi, J., Sakaguchi, T., Yamamoto, T. S., Takahashi, H., Takeda, H., & Ueno, N. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00245-8 · Cited by 194
Combinatorial signals from the neural tube, floor plate and notochord induce myogenic bHLH gene expression in the somite
Münsterberg, A. E., & Lassar, A. B. (1995) · Development · doi:10.1242/dev.121.3.651 · Cited by 192
Sox5 and Sox6 are required for notochord extracellular matrix sheath formation, notochord cell survival and development of the nucleus pulposus of intervertebral discs
Smits, P., & Lefebvre, V. (2003) · Development · doi:10.1242/dev.00331 · Cited by 187
Control of dorsoventral pattern in vertebrate neural development: induction and polarizing properties of the floor plate
Placzek, M., Yamada, T., Tessier-Lavigne, M., Jessell, T., & Dodd, J. (1991) · Development · doi:10.1242/dev.113.supplement_2.105 · Cited by 176
Role of the floor plate in axonal patterning in the zebrafish CNS
Hatta, K. (1992) · Neuron · doi:10.1016/0896-6273(92)90027-b · Cited by 167
Left-right asymmetry of a nodal-related gene is regulated by dorsoanterior midline structures during Xenopus development
Lohr, J. L., Danos, M. C., & Yost, H. J. (1997) · Development · doi:10.1242/dev.124.8.1465 · Cited by 162
Vertebrate mesendoderm induction and patterning
Kimelman, D., & Griffin, K. J. (2000) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(00)00095-2 · Cited by 158
Ascidian prickle Regulates Both Mediolateral and Anterior-Posterior Cell Polarity of Notochord Cells
Jiang, D., Munro, E., & Smith, W. C. (2005) · Current Biology · doi:10.1016/j.cub.2004.12.041 · Cited by 155
Wnt signaling and dorso-ventral axis specification in vertebrates
Sokol, S. Y. (1999) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(99)80061-6 · Cited by 151
The chordate amphioxus: an emerging model organism for developmental biology
Holland, L. Z., Laudet, V., & Schubert, M. (2004) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-004-4075-2 · Cited by 148
Getting into the Golgi
Bannykh, S. I., Nishimura, N., & Balch, W. E. (1998) · Trends in Cell Biology · doi:10.1016/s0962-8924(97)01184-7 · Cited by 144
Coatomer (COPI)-coated vesicles: role in intracellular transport and protein sorting
Cosson, P., & Letourneur, F. (1997) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(97)80023-3 · Cited by 142
Linkage of cardiac left-right asymmetry and dorsal-anterior development in Xenopus
Danos, M. C., & Yost, H. J. (1995) · Development · doi:10.1242/dev.121.5.1467 · Cited by 139
A comparative molecular approach to mesodermal patterning in basal deuterostomes: the expression pattern of Brachyury in the enteropneust hemichordate Ptychodera flava
Peterson, K. J., Cameron, R. A., Tagawa, K., Satoh, N., & Davidson, E. H. (1999) · Development · doi:10.1242/dev.126.1.85 · Cited by 138
Axis-inducing activities and cell fates of the zebrafish organizer
Saúde, L., Woolley, K., Martin, P. B., Driever, W., & Stemple, D. L. (2000) · Development · doi:10.1242/dev.127.16.3407 · Cited by 118
Self-citation
Notochord Patterning of the Endoderm
Cleaver, O., & Krieg, P. A. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0214 · Cited by 114
Nodal-related signals establish mesendodermal fate and trunk neural identity in zebrafish
Feldman, B., Dougan, S. T., Schier, A. F., & Talbot, W. S. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00469-3 · Cited by 112
Transplantation experiments on developing teleosts (Fundulus and Perca)
OPPENHEIMER, J. M. (1936) · Journal of Experimental Zoology · doi:10.1002/jez.1400720304 · Cited by 110
Requirement of the Manx Gene for Expression of Chordate Features in a Tailless Ascidian Larva
Swalla, B. J., & Jeffery, W. R. (1996) · Science · doi:10.1126/science.274.5290.1205 · Cited by 107
Regulation of membrane traffic in animal cells by COPI
Lowe, M., & Kreis, T. E. (1998) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/s0167-4889(98)00046-9 · Cited by 102
Effect of the notochord on proliferation and differentiation in the neural tube of the chick embryo
van Straaten, H. W. M., Hekking, J. W. M., Beursgens, J. P. W. M., Terwindt‐Rouwenhorst, E., & Drukker, J. (1989) · Development · doi:10.1242/dev.107.4.793 · Cited by 102
Mechanical Design of Fiber-Wound Hydraulic Skeletons: The Stiffening and Straightening of Embryonic Notochords
Koehl, M. A. R., Quillin, K. J., & Pell, C. A. (2000) · American Zoologist · doi:10.1668/0003-1569(2000)040[0028:mdofwh]2.0.co;2 · Cited by 93
The Biochemically and Immunologically Distinct CSPG of Notochord Is a Product of the Aggrecan Gene
Domowicz, M. S., Li, H., Hennig, A., Henry, J. G., Vertel, B. M., & Schwartz, N. B. (1995) · Developmental Biology · doi:10.1006/dbio.1995.1312 · Cited by 78
Differential Requirements for COPI Transport during Vertebrate Early Development
Coutinho, P., Parsons, M. J., Thomas, K. A., Hirst, E. M. A., Saúde, L., Campos, I., Williams, P., & Stemple, D. L. (2004) · Developmental Cell · doi:10.1016/j.devcel.2004.07.020 · Cited by 77
Self-citation
Promoting notochord fate and repressing muscle development in zebrafish axial mesoderm
Amacher, S. L., & Kimmel, C. B. (1998) · Development · doi:10.1242/dev.125.8.1397 · Cited by 77
The When and Where of Floor Plate Induction
Dodd, J., Jessell, T. M., & Placzek, M. (1998) · Science · doi:10.1126/science.282.5394.1654 · Cited by 66
Genetic approaches to inflorescence and leaf development in maize
Veit, B. E., Greene, B. A., Lowe, B., Mathern, J., Sinha, N. R., Vollbrecht, E., Walko, R. M., & Hake, S. (1991) · Development · doi:10.1242/dev.113.supplement_1.105 · Cited by 65
Mutations affecting tail and notochord development in the ascidian Ciona savignyi
Nakatani, Y., Moody, R. G., & Smith, W. C. (1999) · Development · doi:10.1242/dev.126.15.3293 · Cited by 65
Notochord Regulates Cardiac Lineage in Zebrafish Embryos
Goldstein, A. M., & Fishman, M. C. (1998) · Developmental Biology · doi:10.1006/dbio.1998.8976 · Cited by 63
A Three-Dimensional Model of the Mouse at Embryonic Day 9
Brune, R., Bard, J., Dubreuil, C., Guest, E., Hill, W., Kaufman, M. H., Stark, M. H., Davidson, D. R., & Baldock, R. (1999) · Developmental Biology · doi:10.1006/dbio.1999.9500 · Cited by 59
Endoderm patterning by the notochord: development of the hypochord in Xenopus
Cleaver, O. B., Seufert, D. W., & Krieg, P. A. (2000) · Development · doi:10.1242/dev.127.4.869 · Cited by 58
Blood Vessel Patterning at the Embryonic Midline
Hogan, K. A., & Bautch, V. L. (2004) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(04)62003-5 · Cited by 56
Isolation of developmental mutants of the ascidian Ciona savignyi
Moody, R., Davis, S. W., Cubas, F., & Smith, W. C. (1999) · Molecular and General Genetics MGG · doi:10.1007/s004380051075 · Cited by 53
Analyzing gene regulation in ascidian embryos: new tools for new perspectives
Gregorio, A. D., & Levine, M. (2002) · Differentiation · doi:10.1046/j.1432-0436.2002.700402.x · Cited by 48
Two Types of Bilateral Symmetry in the Metazoa: Chordate and Bilaterian
Jefferies, R. P. S. (2007) · Novartis Foundation symposium · doi:10.1002/9780470514160.ch7 · Cited by 44
Sequence analysis of zebrafish chondromodulin-1 and expression profile in the notochord and chondrogenic regions during cartilage morphogenesis
Sachdev, S. W., Dietz, U. H., Oshima, Y., et al. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00417-8 · Cited by 39
Biosynthetic protein transport through the early secretory pathway
Nickel, W., & Wieland, F. (1998) · Histochemistry and Cell Biology · doi:10.1007/s004180050249 · Cited by 35
Pieter Nieuwkoop's contributions to the understanding of meso-endoderm induction and neural induction in chordate development
Gerhart, J. C. (1999) · The International Journal of Developmental Biology · doi:10.1387/ijdb.10668970 · Cited by 15
Effects of an additional notochord on the proliferation and differentiation of the neural tube in the chick embryo
van Straaten, H. W. M., & Drukker, J. (1989) · Cell Differentiation and Development · doi:10.1016/0922-3371(89)90614-x · Cited by 8
Ascidian gene-expression profiles
Jeffery, W. R. (2002) · Genome biology · doi:10.1186/gb-2002-3-10-reviews1030 · Cited by 5

Development of the annelid axochord: Insights into notochord evolution
Lauri, A., Brunet, T., Handberg-Thorsager, M., Fischer, A. H. L., Simakov, O., Steinmetz, P. R. H., Tomer, R., Keller, P. J., & Arendt, D. (2014) · Science · doi:10.1126/science.1253396 · Cited by 104
The words of the regulatory code are arranged in a variable manner in highly conserved enhancers
Rastegar, S., Hess, I., Dickmeis, T., Nicod, J. C., Ertzer, R., Hadzhiev, Y., Thies, W.-G., Scherer, G., & Strähle, U. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.03.034 · Cited by 56
FoxA transcription factors are essential for the development of dorsal axial structures
Dal-Pra, S., Thisse, C., & Thisse, B. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2010.12.018 · Cited by 35

See all 443

Authors: Stemple, D. L.
Venue: Development
Publisher: The Company of Biologists
Published: 2005-06-01
Volume: 132
Issue: 11
Pages: 2503-2512
ISSN: 0950-1991 (ISSN-L)
1477-9129
DOI: 10.1242/dev.01812
OpenAlex: W1989388378
Cited by: 443
References: 99
FWCI: 5.53
Type: journal article
Language: en
Open access: closed

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.

Structure and function of the notochord: an essential organ for chordate development

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Metadata

Record

About these checks

Data sources