The DOI matches its Crossref record; 94 of the 94 references it cites were found in a registry or an index.
Endogenous patterns of TGFβ superfamily signaling during early Xenopus development
Abstract
Transforming growth factor β (TGFβ) superfamily signaling has been implicated in patterning of the early Xenopus embryo. Upon ligand stimulation, TGFβ receptors phosphorylate Smad proteins at carboxy-terminal SS(V/M)S consensus motifs. Smads 1/5/8, activated by bone morphogenetic protein (BMP) signaling, induce ventral mesoderm whereas Smad2, activated by activin-like ligands, induces dorsal mesoderm. Although ectopic expression studies are consistent with roles for TGFβ signals in early Xenopus embryogenesis, when and where BMP and activin-like signaling pathways are active endogenously has not been directly examined. In this study, we investigate the temporal and spatial activation of TGFβ superfamily signaling in early Xenopus development by using antibodies specific for the type I receptor-phosphorylated forms of Smad1/5/8 and Smad2. We find that Smad1/5/8 and two distinct isoforms of Smad2, full-length Smad2 and Smad2Δexon3, are phosphorylated in early embryos. Both Smad1/5/8 and Smad2/Smad2Δexon3 are activated after, but not before, the mid-blastula transition (MBT). Endogenous activation of Smad2/Smad2Δexon3 requires zygotic transcription, while Smad1/5/8 activation at MBT appears to involve transcription-independent regulation. We also find that the competence of embryonic cells to respond to TGFβ superfamily ligands is temporally regulated and may be a determinant of early patterning. Levels of phospho-Smad1/5/8 and of phospho- Smad2/Smad2Δexon3 are asymmetrically distributed across both the animal-vegetal and dorsoventral axes. The timing of the development of these asymmetries differs for phospho- Smad1/5/8 and for phospho-Smad2/Smad2Δexon3, and the spatial distribution of phosphorylation of each Smad changes dramatically as gastrulation begins. We discuss the implications of our results for endogenous functions of BMP and activin-like signals as candidate morphogens regulating primary germ layer formation and dorsoventral patterning of the early Xenopus embryo.
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
Antibodies, a laboratory manual
(1989) · Biomedicine & Pharmacotherapy · doi:10.1016/0753-3322(89)90130-3 · Cited by 12,366
Massagué, J. (1998) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.67.1.753 · Cited by 7,556
Dennler, S. (1998) · The EMBO Journal · doi:10.1093/emboj/17.11.3091 · Cited by 1,793
Newport, J., & Kirschner, M. (1982) · Cell · doi:10.1016/0092-8674(82)90272-0 · Cited by 1,628
Normal Table of Xenopus Laevis.
Johnson, K. E. (1968) · PubMed Central · Cited by 1,220
Smith, W. C., & Harland, R. M. (1992) · Cell · doi:10.1016/0092-8674(92)90316-5 · Cited by 1,178
Xenopus chordin: A novel dorsalizing factor activated by organizer-specific homeobox genes
SASAI, Y. (1994) · Cell · doi:10.1016/0092-8674(94)90068-x · Cited by 1,118
Smith, J. C., Price, B. M. J., Green, J. B. A., Weigel, D., & Herrmann, B. G. (1991) · Cell · doi:10.1016/0092-8674(91)90573-h · Cited by 971
SARA, a FYVE Domain Protein that Recruits Smad2 to the TGFβ Receptor
Tsukazaki, T., Chiang, T. A., Davison, A. F., Attisano, L., & Wrana, J. L. (1998) · Cell · doi:10.1016/s0092-8674(00)81701-8 · Cited by 968
Mesoderm induction in early Xenopus embryos by heparin-binding growth factors
Slack, J. M. W., Darlington, B. G., Heath, J. K., & Godsave, S. F. (1987) · Nature · doi:10.1038/326197a0 · Cited by 933
Kimelman, D., & Kirschner, M. (1987) · Cell · doi:10.1016/0092-8674(87)90110-3 · Cited by 874
A SMAD ubiquitin ligase targets the BMP pathway and affects embryonic pattern formation
Zhu, H., Kavsak, P., Abdollah, S., Wrana, J. L., & Thomsen, G. H. (1999) · Nature · doi:10.1038/23293 · Cited by 845
Eppert, K., Scherer, S. W., Ozcelik, H., Pirone, R., Hoodless, P., Kim, H., Tsui, L.-C., Bapat, B., Gallinger, S., Andrulis, I. L., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)80128-2 · Cited by 845
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
Induction of epidermis and inhibition of neural fate by Bmp-4
Wilson, P. A., & Hemmati-Brivanlou, A. (1995) · Nature · doi:10.1038/376331a0 · Cited by 787
Kroll, K. L., & Amaya, E. (1996) · Development · doi:10.1242/dev.122.10.3173 · Cited by 778
Hemmati-Brivanlou, A., Kelly, O. G., & Melton, D. A. (1994) · Cell · doi:10.1016/0092-8674(94)90320-4 · Cited by 757
Weeks, D. L., & Melton, D. A. (1987) · Cell · doi:10.1016/0092-8674(87)90109-7 · Cited by 743
Macías-Silva, M., Abdollah, S., Hoodless, P. A., Pirone, R., Attisano, L., & Wrana, J. L. (1996) · Cell · doi:10.1016/s0092-8674(00)81817-6 · Cited by 735
Regulation of neural induction by the Chd and Bmp-4 antagonistic patterning signals in Xenopus
Sasai, Y., Lu, B., Steinbeisser, H., & De Robertis, E. M. (1995) · Nature · doi:10.1038/376333a0 · Cited by 716
MADR1, a MAD-Related Protein That Functions in BMP2 Signaling Pathways
Hoodless, P. A., Haerry, T., Abdollah, S., Stapleton, M., O'Connor, M. B., Attisano, L., & Wrana, J. L. (1996) · Cell · doi:10.1016/s0092-8674(00)81250-7 · Cited by 696
A transcriptional partner for MAD proteins in TGF-β signalling
Chen, X., Rubock, M. J., & Whitman, M. (1996) · Nature · doi:10.1038/383691a0 · Cited by 684
Self-citationThomsen, G., Woolf, T., Whitman, M., Sokol, S., Vaughan, J., Vale, W., & Melton, D. A. (1990) · Cell · doi:10.1016/0092-8674(90)90445-k · Cited by 592
Self-citationKretzschmar, M., Liu, F., Hata, A., Doody, J., & Massagué, J. (1997) · Genes & Development · doi:10.1101/gad.11.8.984 · Cited by 574
Bone morphogenetic protein 4: a ventralizing factor in early Xenopus development
Dale, L., Howes, G., Price, B. M. J., & Smith, J. C. (1992) · Development · doi:10.1242/dev.115.2.573 · Cited by 571
Smad4 and FAST-1 in the assembly of activin-responsive factor
Chen, X., Weisberg, E., Fridmacher, V., Watanabe, M., Naco, G., & Whitman, M. (1997) · Nature · doi:10.1038/38008 · Cited by 565
Self-citationHemmati-Brivanlou, A., & Melton, D. A. (1992) · Nature · doi:10.1038/359609a0 · Cited by 534
Labbé, E., Silvestri, C., Hoodless, P. A., Wrana, J. L., & Attisano, L. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80119-7 · Cited by 517
Inhibition of activin receptor signaling promotes neuralization in Xenopus
Hemmati-Brivanlou, A., & Melton, D. A. (1994) · Cell · doi:10.1016/0092-8674(94)90319-0 · Cited by 485
Abdollah, S., Macı́as-Silva, M., Tsukazaki, T., Hayashi, H., Attisano, L., & Wrana, J. L. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.44.27678 · Cited by 481
Green, J. B. A., New, H. V., & Smith, J. C. (1992) · Cell · doi:10.1016/0092-8674(92)90550-v · Cited by 480
Smads and early developmental signaling by the TGFβ superfamily
Whitman, M. (1998) · Genes & Development · doi:10.1101/gad.12.16.2445 · Cited by 478
Self-citationJones, C. M., Lyons, K. M., An, P. M. L., Wright, C. V. E., & Hogan, B. L. M. (1992) · Development · doi:10.1242/dev.115.2.639 · Cited by 477
Specific Activation of Smad1 Signaling Pathways by the BMP7 Type I Receptor, ALK2
Macı́as-Silva, M., Hoodless, P. A., Tang, S. J., Buchwald, M., & Wrana, J. L. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.40.25628 · Cited by 476
The Role of Maternal VegT in Establishing the Primary Germ Layers in Xenopus Embryos
Zhang, J., Houston, D. W., King, M. L., Payne, C., Wylie, C., & Heasman, J. (1998) · Cell · doi:10.1016/s0092-8674(00)81592-5 · Cited by 470
Graff, J. M., Thies, R. S., Song, J. J., Celeste, A. J., & Melton, D. A. (1994) · Cell · doi:10.1016/0092-8674(94)90409-x · Cited by 451
Suzuki, A., Thies, R. S., Yamaji, N., Song, J. J., Wozney, J. M., Murakami, K., & Ueno, N. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.22.10255 · Cited by 447
Xenopus Mad Proteins Transduce Distinct Subsets of Signals for the TGFβ Superfamily
Graff, J. M., Bansal, A., & Melton, D. A. (1996) · Cell · doi:10.1016/s0092-8674(00)81249-0 · Cited by 424
Nodal-related signals induce axial mesoderm and dorsalize mesoderm during gastrulation
Jones, C. M., Kuehn, M. R., Hogan, B. L. M., Smith, J. C., & Wright, C. V. E. (1995) · Development · doi:10.1242/dev.121.11.3651 · Cited by 421
Processed Vg1 protein is an axial mesoderm inducer in xenopus
Thomsen, G. H., & Melton, D. A. (1993) · Cell · doi:10.1016/0092-8674(93)80045-g · Cited by 413
Persson, U., Izumi, H., Souchelnytskyi, S., Itoh, S., Grimsby, S., Engström, U., Heldin, C.-H., Funa, K., & ten Dijke, P. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00954-5 · Cited by 398
Souchelnytskyi, S., Tamaki, K., Engström, U., Wernstedt, C., ten Dijke, P., & Heldin, C.-H. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.44.28107 · Cited by 382
Disruption of BMP signals in embryonic Xenopus ectoderm leads to direct neural induction.
Hawley, S. H., Wünnenberg-Stapleton, K., Hashimoto, C., Laurent, M. N., Watabe, T., Blumberg, B. W., & Cho, K. W. (1995) · Genes & Development · doi:10.1101/gad.9.23.2923 · Cited by 368
Liu, X., Sun, Y., Constantinescu, S. N., Karam, E., Weinberg, R. A., & Lodish, H. F. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.20.10669 · Cited by 357
Xsox17α and -β Mediate Endoderm Formation in Xenopus
Hudson, C., Clements, D., Friday, R. V., Stott, D., & Woodland, H. R. (1997) · Cell · doi:10.1016/s0092-8674(00)80423-7 · Cited by 346
Ubiquitin-dependent degradation of TGF-β-activated Smad2
Lo, R. S., & Massagué, J. (1999) · Nature Cell Biology · doi:10.1038/70258 · Cited by 344
A novel mesoderm inducer, Madr2, functions in the activin signal transduction pathway.
Baker, J. C., & Harland, R. M. (1996) · Genes & Development · doi:10.1101/gad.10.15.1880 · Cited by 340
Activin signalling and response to a morphogen gradient
Gurdon, J. B., Harger, P., Mitchell, A., & Lemaire, P. (1994) · Nature · doi:10.1038/371487a0 · Cited by 327
Nishimura, R., Kato, Y., Chen, D., Harris, S. E., Mundy, G. R., & Yoneda, T. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.4.1872 · Cited by 318
Zhang, J., & King, M. L. (1996) · Development · doi:10.1242/dev.122.12.4119 · Cited by 308
Mesoderm induction in Xenopus is a zygotic event regulated by maternal VegT via TGFβ growth factors
Kofron, M., Demel, T., Xanthos, J., Lohr, J., Sun, B., Sive, H., Osada, S.-I., Wright, C., Wylie, C., & Heasman, J. (1999) · Development · doi:10.1242/dev.126.24.5759 · Cited by 264
Alternatively Spliced Variant of Smad2 Lacking Exon 3
Yagi, K., Goto, D., Hamamoto, T., Takenoshita, S., Kato, M., & Miyazono, K. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.2.703 · Cited by 234
Patterning the Xenopus blastula
Heasman, J. (1997) · Development · doi:10.1242/dev.124.21.4179 · Cited by 232
Mesoderm induction by activin requires FGF-mediated intracellular signals
LaBonne, C., & Whitman, M. (1994) · Development · doi:10.1242/dev.120.2.463 · Cited by 228
Self-citationLocalized BMP-4 Mediates Dorsal/Ventral Patterning in the Early Xenopus Embryo
Schmidt, J. E., Suzuki, A., Ueno, N., & Kimelman, D. (1995) · Developmental Biology · doi:10.1006/dbio.1995.1124 · Cited by 226
Watabe, T., Kim, S., Candia, A., Rothbächer, U., Hashimoto, C., Inoue, K., & Cho, K. W. (1995) · Genes & Development · doi:10.1101/gad.9.24.3038 · Cited by 224
Yamamoto, N., Akiyama, S., Katagiri, T., Namiki, M., Kurokawa, T., & Suda, T. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.7325 · Cited by 219
Activin-mediated mesoderm induction requires FGF
Cornell, R. A., & Kimelman, D. (1994) · Development · doi:10.1242/dev.120.2.453 · Cited by 209
Lustig, K. D., Kroll, K. L., Sun, E. E., & Kirschner, M. W. (1996) · Development · doi:10.1242/dev.122.12.4001 · Cited by 203
Stennard, F., Carnac, G., & Gurdon, J. B. (1996) · Development · doi:10.1242/dev.122.12.4179 · Cited by 199
Maternal β-catenin establishes a ‘dorsal signal’ in early Xenopus embryos
Wylie, C., Kofron, M., Payne, C., Anderson, R., Hosobuchi, M., Joseph, E., & Heasman, J. (1996) · Development · doi:10.1242/dev.122.10.2987 · Cited by 195
TGF-β signals and a prepattern in Xenopus laevis endodermal development
Henry, G. L., Brivanlou, I. H., Kessler, D. S., Hemmati-Brivanlou, A., & Melton, D. A. (1996) · Development · doi:10.1242/dev.122.3.1007 · Cited by 193
Horb, M. E., & Thomsen, G. H. (1997) · Development · doi:10.1242/dev.124.9.1689 · Cited by 193
Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis
Osada, S.-I., & Wright, C. V. E. (1999) · Development · doi:10.1242/dev.126.14.3229 · Cited by 186
Jones, E. A., & Woodland, H. R. (1987) · Development · doi:10.1242/dev.101.3.557 · Cited by 185
Mode of action of VegT in mesoderm and endoderm formation
Clements, D., Friday, R. V., & Woodland, H. R. (1999) · Development · doi:10.1242/dev.126.21.4903 · Cited by 183
derrière: a TGF-β family member required for posterior development in Xenopus
Sun, B. I., Bush, S. M., Collins-Racie, L. A., LaVallie, E. R., DiBlasio-Smith, E. A., Wolfman, N. M., McCoy, J. M., & Sive, H. L. (1999) · Development · doi:10.1242/dev.126.7.1467 · Cited by 179
Thomsen, G. H. (1996) · Development · doi:10.1242/dev.122.8.2359 · Cited by 171
Anterior Endomesoderm Specification inXenopusby Wnt/β-catenin and TGF-β Signalling Pathways
Zorn, A. M., Butler, K., & Gurdon, J. B. (1999) · Developmental Biology · doi:10.1006/dbio.1999.9257 · Cited by 170
Secretion and mesoderm‐inducing activity of the TGF‐beta‐related domain of Xenopus Vg1.
Dale, L., Matthews, G. M., & Colman, A. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb06136.x · Cited by 170
Spatial response to fibroblast growth factor signalling in Xenopus embryos
Christen, B., & Slack, J. M. W. (1999) · Development · doi:10.1242/dev.126.1.119 · Cited by 167
Xnr4:AXenopusNodal-Related Gene Expressed in the Spemann Organizer
Joseph, E. M., & Melton, D. A. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8510 · Cited by 163
Smad5 Induces Ventral Fates inXenopusEmbryo
Suzuki, A., Chang, C., Yingling, J. M., Wang, X.-F., & Hemmati‐Brivanlou, A. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8548 · Cited by 153
Smad8 mediates the signaling of the receptor serine kinase
Chen, Y., Bhushan, A., & Vale, W. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.24.12938 · Cited by 152
Induction of dorsal mesoderm by soluble, mature Vg1 protein
Kessler, D. S., & Melton, D. A. (1995) · Development · doi:10.1242/dev.121.7.2155 · Cited by 151
Schulte-Merker, S., Smith, J. C., & Dale, L. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06660.x · Cited by 146
Jones, C. M., Dale, L., Hogan, B. L. M., Wright, C. V. E., & Smith, J. C. (1996) · Development · doi:10.1242/dev.122.5.1545 · Cited by 145
Oda, S., Nishimatsu, S., Murakami, K., & Ueno, N. (1995) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1995.1699 · Cited by 143
Genes for bone morphogenetic proteins are differentially transcribed in early amphibian embryos
Nishimatsu, S., Suzuki, A., Shoda, A., Murakami, K., & Ueno, N. (1992) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(05)81574-8 · Cited by 130
A two-step model for the fate determination of presumptive endodermal blastomeres in Xenopus embryos
Yasuo, H., & Lemaire, P. (1999) · Current Biology · doi:10.1016/s0960-9822(99)80391-1 · Cited by 126
Localized synthesis of the Vg1 protein during early Xenopus development
Tannahill, D., & Melton, D. A. (1989) · Development · doi:10.1242/dev.106.4.775 · Cited by 125
Stack, J. H., & Newport, J. W. (1997) · Development · doi:10.1242/dev.124.16.3185 · Cited by 116
FAST-1 is a key maternal effector of mesoderm inducers in the early Xenopus embryo
Watanabe, M., & Whitman, M. (1999) · Development · doi:10.1242/dev.126.24.5621 · Cited by 115
Self-citationYeo, C., Chen, X., & Whitman, M. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.37.26584 · Cited by 112
Self-citationBone morphogenetic protein 2 in the early development of Xenopus laevis
Clement, J. H., Fettes, P., Knöchel, S., Lef, J., & Knöchel, W. (1995) · Mechanisms of Development · doi:10.1016/0925-4773(95)00413-u · Cited by 102
Zygotic Transcription Is Required to Block a Maternal Program of Apoptosis inXenopusEmbryos
Sible, J. C., Anderson, J. A., Lewellyn, A. L., & Maller, J. L. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8683 · Cited by 102
Cooperation between the activin and Wnt pathways in the spatial control of organizer gene expression
Crease, D. J., Dyson, S., & Gurdon, J. B. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.8.4398 · Cited by 101
LaBonne, C., & Whitman, M. (1997) · Developmental Biology · doi:10.1006/dbio.1996.8497 · Cited by 97
Self-citationPeng, H. B. (1991) · Cited by 89
Armes, N., & Smith, J. C. (1997) · Development · doi:10.1242/dev.124.19.3797 · Cited by 82
Activin signalling has a necessary function in Xenopus early development
Dyson, S., & Gurdon, J. B. (1997) · Current Biology · doi:10.1016/s0960-9822(06)00030-3 · Cited by 77
Dominant-Negative Smad2 Mutants Inhibit Activin/Vg1 Signaling and Disrupt Axis Formation in Xenopus
Hoodless, P. A., Tsukazaki, T., Nishimatsu, S., Attisano, L., Wrana, J. L., & Thomsen, G. H. (1999) · Developmental Biology · doi:10.1006/dbio.1998.9168 · Cited by 76
XBMPRII, a novel Xenopus type II receptor mediating BMP signaling in embryonic tissues
Frisch, A., & Wright, C. V. E. (1998) · Development · doi:10.1242/dev.125.3.431 · Cited by 60
Takenoshita, S., Mogi, A., Nagashima, M., Ke, Y., Yagi, K., Hanyu, A., Nagamachi, Y., Miyazono, K., & Hagiwara, K. (1998) · Genomics · doi:10.1006/geno.1997.5149 · Cited by 54
Cited by
Inman, G. J., Nicolás, F. J., Callahan, J. F., Harling, J. D., Gaster, L. M., Reith, A. D., Laping, N. J., & Hill, C. S. (2002) · Molecular Pharmacology · doi:10.1124/mol.62.1.65 · Cited by 1,634
Small non-coding RNAs in animal development
Stefani, G., & Slack, F. J. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2347 · Cited by 1,368
TGF-beta receptor-activated p38 MAP kinase mediates Smad-independent TGF-beta responses
Yu, L. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf366 · Cited by 721
The establishment of spemann's organizer and patterning of the vertebrate embryo
De Robertis, E. M., Larraín, J., Oelgeschläger, M., & Wessely, O. (2000) · Nature Reviews Genetics · doi:10.1038/35042039 · Cited by 429
Nodal Signals to Smads through Cripto-Dependent and Cripto-Independent Mechanisms
Yeo, C.-Y., & Whitman, M. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00249-0 · Cited by 377
Self-citation
Metadata
- Authors
- Faure, S., Lee, M. A., Keller, T., Dijke, P. T., & Whitman, M.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2000-07-01
- Volume
- 127
- Issue
- 13
- Pages
- 2917-2931
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2165857084
- Cited by
- 257
- References
- 94
- FWCI
- 7.77
- 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.