The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
The cell biology of lysosomal storage disorders
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Citations
Cites
Orchestrating the unfolded protein response in health and disease
Kaufman, R. J. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0216886 · Cited by 1,015
Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease.
Hollak, C. E., van Weely, S., van Oers, M. H., & Aerts, J. M. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117084 · Cited by 896 · cited 1×
“For example, changes in the levels of serum chitotriosidase 67 or chemokine CCL18 (REF.68) are characteristic of Gaucher disease,but the relationship between glucosylceramide accumulation and the secretion of these compounds is unknown.”
Cholesterol homeostasis and function in neurons of the central nervous system
Pfrieger, F. W. (2003) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-003-3018-7 · Cited by 453
Zhou, X. Y., Morreau, H., Rottier, R., Davis, D., Bonten, E., Gillemans, N., Wenger, D., Grosveld, F. G., Doherty, P., & Suzuki, K. (1995) · Genes & Development · doi:10.1101/gad.9.21.2623 · Cited by 131
Leimig, T., Mann, L., Martin, M. D. P., Bonten, E., Persons, D., Knowles, J., Allay, J. A., Cunningham, J., Nienhuis, A. W., Smeyne, R., et al. (2002) · Blood · doi:10.1182/blood.v99.9.3169 · Cited by 75
Cited by
von Moos, N., Burkhardt-Holm, P., & Köhler, A. (2012) · Environmental Science & Technology · doi:10.1021/es302332w · Cited by 1,697
Inclusion formation and neuronal cell death through neuron-to-neuron transmission of α-synuclein
Desplats, P., Lee, H.-J., Bae, E.-J., Patrick, C., Rockenstein, E., Crews, L., Spencer, B., Masliah, E., & Lee, S.-J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903691106 · Cited by 1,485
Pharmacological modulation of autophagy: therapeutic potential and persisting obstacles
Galluzzi, L., Bravo-San Pedro, J. M., Levine, B., Green, D. R., & Kroemer, G. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.22 · Cited by 842
Autophagy and lysosomal dysfunction as emerging mechanisms of nanomaterial toxicity
Stern, S. T., Adiseshaiah, P. P., & Crist, R. M. (2012) · Particle and Fibre Toxicology · doi:10.1186/1743-8977-9-20 · Cited by 836
Lysosomal storage disorders: The cellular impact of lysosomal dysfunction
Platt, F. M., Boland, B., & van der Spoel, A. C. (2012) · Journal of Cell Biology · doi:10.1083/jcb.201208152 · Cited by 689
Metadata
- Authors
- Futerman, A. H., & van Meer, G.
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2004-07
- Volume
- 5
- Issue
- 7
- Pages
- 554-565
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- OpenAlex
- W2076107153
- Cited by
- 796
- References
- 5
- FWCI
- 2.87
- Type
- journal article
- Language
- en
- Open access
- green
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- Futerman, A. H., & van Meer, G. (2004). The cell biology of lysosomal storage disorders. Nature Reviews Molecular Cell Biology. https://doi.org/10.1038/nrm1423
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.