The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
CXCL10 Is Critical for the Progression and Maintenance of Depigmentation in a Mouse Model of Vitiligo
Open accessAbstract
Neutralizing CXCL10 reverses established vitiligo.
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Citations
Cites
Gene Expression Omnibus: NCBI gene expression and hybridization array data repository
Edgar, R. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.1.207 · Cited by 13,288
Cited by
Bergqvist, C., & Ezzedine, K. (2020) · Dermatology · doi:10.1159/000506103 · Cited by 799
Chow, M. T., Ozga, A. J., Servis, R. L., Frederick, D. T., Lo, J. A., Fisher, D. E., Freeman, G. J., Boland, G. M., & Luster, A. D. (2019) · Immunity · doi:10.1016/j.immuni.2019.04.010 · Cited by 716
“The CXCR3 chemokine system also plays important roles in the positioning of T cells within secondary lymphoid organs and peripheral tissue, facilitating the interactions of T cells with antigen-loaded activated dendritic cells (DCs), promoting T cell activation and differentiation, as well as assisting the process of…”
Self-citationCD49a Expression Defines Tissue-Resident CD8 + T Cells Poised for Cytotoxic Function in Human Skin
Cheuk, S., Schlums, H., Gallais Sérézal, I., Martini, E., Chiang, S. C., Marquardt, N., Gibbs, A., Detlofsson, E., Introini, A., Forkel, M., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.01.009 · Cited by 678
“, 2008), whereas vitiligo presents with persistent depigmentations attributed to local interferon-g (IFN-g) production and T cell-mediated killing of melanocytes (Harris et al., 2012; Rashighi et al., 2014; van den Boorn et al., 2009).”
Metzemaekers, M., Vanheule, V., Janssens, R., Struyf, S., & Proost, P. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01970 · Cited by 328
Emerging Topical and Systemic JAK Inhibitors in Dermatology
Solimani, F., Meier, K., & Ghoreschi, K. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02847 · Cited by 308
Metadata
- Authors
- Rashighi, M., Agarwal, P., Richmond, J. M., Harris, T. H., Dresser, K., Su, M.-W., Zhou, Y., Deng, A., Hunter, C. A., Luster, A. D., & Harris, J. E.
- Venue
- Science Translational Medicine
- Published
- 2014-02-12
- Volume
- 6
- Issue
- 223
- Pages
- 223ra23-223ra23
- ISSN
- 1946-6234 (ISSN-L)
- 1946-6242
- OpenAlex
- W2060069128
- Cited by
- 518
- References
- 1
- FWCI
- 13.78
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: CXCL10 Is Critical for the Progression and Maintenance of Depigmentation in a Mouse Model of Vitiligo. https://app.cochat.ai/papers/10.1126/scitranslmed.3007811
- The paper
- Rashighi, M., Agarwal, P., Richmond, J. M., Harris, T. H., Dresser, K., Su, M.-W., Zhou, Y., Deng, A., Hunter, C. A., Luster, A. D., & Harris, J. E. (2014). CXCL10 Is Critical for the Progression and Maintenance of Depigmentation in a Mouse Model of Vitiligo. Science Translational Medicine. https://doi.org/10.1126/scitranslmed.3007811
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.
