The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Cystinosin, the protein defective in cystinosis, is a H+-driven lysosomal cystine transporter
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Cites
Sato, H., Tamba, M., Ishii, T., & Bannai, S. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.17.11455 · Cited by 1,109
Molecular Biology of Mammalian Plasma Membrane Amino Acid Transporters
PALACÍN, M., ESTÉVEZ, R., BERTRAN, J., & ZORZANO, A. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.4.969 · Cited by 823
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis
Town, M., Jean, G., Cherqui, S., Attard, M., Forestier, L., Whitmore, S. A., Callen, D. F., Gribouval, O., Broyer, M., Bates, G. P., et al. (1998) · Nature Genetics · doi:10.1038/ng0498-319 · Cited by 639
Vacuolar and Plasma Membrane Proton-Adenosinetriphosphatases
Nelson, N., & Harvey, W. R. (1999) · Physiological Reviews · doi:10.1152/physrev.1999.79.2.361 · Cited by 421
Cystine Transport Is Defective in Isolated Leukocyte Lysosomes from Patients with Cystinosis
Gahl, W. A., Bashan, N., Tietze, F., Bernardini, I., & Schulman, J. D. (1982) · Science · doi:10.1126/science.7112129 · Cited by 360
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT
Feliubadaló, L., Font, M., Purroy, J., Rousaud, F., Estivill, X., Nunes, V., Golomb, E., Centola, M., Aksentijevich, I., Kreiss, Y., et al. (1999) · Nature Genetics · doi:10.1038/12652 · Cited by 337
Rapid separation of particulate components and soluble cytoplasm of isolated rat-liver cells
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A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases
Verheijen, F. W., Verbeek, E., Aula, N., Beerens, C. E. M. T., Havelaar, A. C., Joosse, M., Peltonen, L., Aula, P., Galjaard, H., van der Spek, P. J., et al. (1999) · Nature Genetics · doi:10.1038/70585 · Cited by 293
Sorting of soluble ER proteins in yeast.
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The cytoskeleton of digitonin-treated rat hepatocytes.
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Cited by
Lipid peroxidation and ferroptosis: The role of GSH and GPx4
Ursini, F., & Maiorino, M. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.02.027 · Cited by 1,954
Amino acid transporters revisited: New views in health and disease
Kandasamy, P., Gyimesi, G., Kanai, Y., & Hediger, M. A. (2018) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2018.05.003 · Cited by 484
Parkinson’s disease-risk protein TMEM175 is a proton-activated proton channel in lysosomes
Hu, M., Li, P., Wang, C., Feng, X., Geng, Q., Chen, W., Marthi, M., Zhang, W., Gao, C., Reid, W., et al. (2022) · Cell · doi:10.1016/j.cell.2022.05.021 · Cited by 254
Schröder, B. A., Wrocklage, C., Hasilik, A., & Saftig, P. (2010) · PROTEOMICS · doi:10.1002/pmic.201000196 · Cited by 226
SLC7A11 is an unconventional H+ transporter in lysosomes
Zhou, N., Chen, J., Hu, M., Wen, N., Cai, W., Li, P., Zhao, L., Meng, Y., Zhao, D., Yang, X., et al. (2025) · Cell · doi:10.1016/j.cell.2025.04.004 · Cited by 105
Metadata
- Authors
- Kalatzis, V.
- Venue
- The EMBO Journal
- Published
- 2001-11-01
- Volume
- 20
- Issue
- 21
- Pages
- 5940-5949
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- OpenAlex
- W2166434963
- Cited by
- 331
- References
- 35
- FWCI
- 5.40
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: Cystinosin, the protein defective in cystinosis, is a H+-driven lysosomal cystine transporter. https://app.cochat.ai/papers/10.1093/emboj/20.21.5940
- The paper
- Kalatzis, V. (2001). Cystinosin, the protein defective in cystinosis, is a H+-driven lysosomal cystine transporter. The EMBO Journal. https://doi.org/10.1093/emboj/20.21.5940
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.
