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Cited by 1,029

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Maize yellow stripe1 encodes a membrane protein directly involved in Fe(III) uptake

Curie, Catherine, Panaviene, Zivile, Loulergue, Clarisse, Dellaporta, Stephen L., Briat, Jean-Francois, Walker, Elsbeth L.·2001·Nature
DOI 10.1038/35053080
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Crossref · 10.1038/35053080

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Research works printed but not linked: 21

  1. Briat, J. -F. & Lobreaux, S. Iron transport and storage in plants. Trends Plant Sci. 2, 187– 193 (1997). · DOI · Paper page
  2. Mori, S. Iron acquisition by plants. Curr. Opin. Plant Biol. 2, 250–253 (1999). · DOI · Paper page
  3. Eide, D., Broderius, M., Fett, J. & Guerinot, M. L. A novel iron-regulated metal transporter from plants identified by functional expression in yeast. Proc. Natl Acad. Sci. USA 93, 5624– 5628 (1996). · DOI · Paper page
  4. Yi, Y. & Guerinot, M. L. Genetic evidence that induction of root Fe[iii] chelate reductase activity is necessary for iron uptake under iron deficiency. Plant J. 10, 835–844 (1996). · DOI · Paper page
  5. Robinson, N. J., Procter, C. M., Connolly, E. L. & Guerinot, M. L. A ferric-chelate reductase for iron uptake from soils. Nature 397, 694–697 (1999). · DOI · Paper page
  6. Tagaki, S., Nomoto, K. & Takemoto, T. Physiological aspect of mugineic acid, a possible phytosiderophore of graminaceous plants. J. Plant Nutr. 7, 469–477 (1984). · DOI · Paper page
  7. von Wiren, N., Mori, S., Marschner, H. & Romheld, V. Iron inefficiency in maize mutant ys1 (Zea mays L. cv Yellow-Stripe) is caused by a defect in uptake of iron phytosiderophores. Plant Physiol. 106, 71–77 ( 1994). · DOI · Paper page
  8. von Wiren, N., Marchner, H. & Romheld, V. Uptake kinetics of iron-phytosiderophores in two maize genotypes differing in iron efficiency. Physiol. Plant. 93, 611–616 (1995). · DOI
  9. Hopkins, B. G., Jolley, V. D. & Brown, J. C. Plant utilization of iron solubilized by oat phytosiderophore. J. Plant Nutr. 15, 1599– 1612 (1992). · DOI
  10. Jolley, V. D. & Brown, J. C. Differential response of Fe-efficient corn and Fe-inefficient corn and oat to phytosiderophore released by Fe-efficient Coker 227 oat. J. Plant Nutr. 14, 45– 58 (1991). · doi:10.1080/01904169109364182
  11. Dellaporta, S. L. & Moreno, M. in The Maize Handbook (eds Freeling, M. & Walbot, V.) 219–233 (Springer, New York, 1993).
  12. Loulergue, C., Lebrun, M. & Briat, J. F. Expression cloning in Fe2+ transport defective yeast of a novel maize MYC transcription factor. Gene 225, 47–57 ( 1998). · doi:10.1016/s0378-1119(98)00531-9
  13. Mori, S. et al. Why are young rice plants highly susceptible to iron deficiency? Plant Soil 130, 143–156 (1991). · doi:10.1007/bf00011869
  14. von Wiren, N. et al. Nicotianamine chelates both Fe[iii] and Fe[ii ]. Implications for metal transport in plants. Plant Physiol. 119, 1107–1114 ( 1999). · DOI · Paper page
  15. Stephan, U. W., Schmidke, I. & Pich, A. Phloem translocation of Fe, Cu, Mn, and Zn in Ricinus seedlings in relation to the concentrations of nicotianamine, an endogenous chelator of divalent metal-ions, in different seedling parts. Plant Soil 165, 181–188 (1994). · DOI
  16. Stephan, U. W., Schmidke, I., Stephan, V. W. & Scholz, G. The nicotianamine molecule is made-to-measure for complexation of metal micronutrients in plants. Biometals 9, 84– 90 (1996). · DOI
  17. Minet, M., Dufour, M. E. & Lacroute, F. Complementation of Saccharomyces cerevisiae auxotrophic mutants by Arabidopsis thaliana cDNAs. Plant J. 2, 417–422 (1992). · DOI · Paper page
  18. von Wiren, N., Gibrat, R. & Briat, J.-F. In vitro characterization of iron-phytosiderophore interaction with maize root plasma membranes: evidences for slow association kinetics. Biochem. Biophys. Acta 1371, 143– 155 (1998). · DOI
  19. Thoiron, S., Pascal, N. & Briat, J.-F. Impact of iron deficiency and iron re-supply during the early stages of vegetative development in maize (Zea mays L.). Plant Cell Env. 20, 1051–1060 (1997). · doi:10.1111/j.1365-3040.1997.tb00681.x
  20. Hirokawa, T., Boon-Chieng, S. & Mitaku, S. SOSUI: Classification and secondary structure prediction system for membrane proteins. Bioinformatics 14, 378–379 (1998). · DOI · Paper page
  21. Bagnaresi, P. et al. Cloning and characterization of a maize cytochrome-b 5 reductase with Fe3+-chelate reduction capability. Biochem. J. 338, 499–505 (1999). · doi:10.1042/bj3380499

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Metadata

Authors
Curie, C., Panaviene, Z., Loulergue, C., Dellaporta, S. L., Briat, J.-F., & Walker, E. L.
Venue
Nature
Publisher
Springer Science and Business Media LLC
Published
2001-01
Volume
409
Issue
6818
Pages
346-349
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
DOI
10.1038/35053080
OpenAlex
W1588913699
Cited by
1,029
References
2
FWCI
37.53
Type
journal article
Language
en
Open access
closed
Licence
www.springer.com/tdm (tdm)

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CoChat. (2026). Citation check: Maize yellow stripe1 encodes a membrane protein directly involved in Fe(III) uptake. https://app.cochat.ai/papers/10.1038/35053080
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Curie, C., Panaviene, Z., Loulergue, C., Dellaporta, S. L., Briat, J.-F., & Walker, E. L. (2001). Maize yellow stripe1 encodes a membrane protein directly involved in Fe(III) uptake. Nature. https://doi.org/10.1038/35053080

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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.