The DOI matches its Crossref record; 158 of the 158 references it cites were found in a registry or an index.
Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease
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Cites
Naldini, L., Blömer, U., Gage, F. H., Trono, D., & Verma, I. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11382 · Cited by 1,499
PDZ Domains and the Organization of Supramolecular Complexes
Sheng, M., & Sala, C. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1 · Cited by 1,200
Defective myosin VIIA gene responsible for Usher syndrome type IB
Well, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M. D., et al. (1995) · Nature · doi:10.1038/374060a0 · Cited by 1,068
Myosins: a diverse superfamily
Sellers, J. R. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/s0167-4889(00)00005-7 · Cited by 848
Nagase, T. (1998) · DNA Research · doi:10.1093/dnares/5.1.31 · Cited by 842
Mechanism and role of PDZ domains in signaling complex assembly
Harris, B. Z., & Lim, W. A. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.18.3219 · Cited by 830
The ankyrin repeat: a diversity of interactions on a common structural framework
Sedgwick, S. G., & Smerdon, S. J. (1999) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(99)01426-7 · Cited by 820
Lewis, P. F., & Emerman, M. (1994) · Journal of Virology · doi:10.1128/jvi.68.1.510-516.1994 · Cited by 797
Will Retinal Implants Restore Vision?
Zrenner, E. (2002) · Science · doi:10.1126/science.1067996 · Cited by 724
Molecular basis of mechanosensory transduction
Gillespie, P. G., & Walker, R. G. (2001) · Nature · doi:10.1038/35093011 · Cited by 706
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When cilia go bad: cilia defects and ciliopathies
Fliegauf, M., Benzing, T., & Omran, H. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2278 · Cited by 1,257
The Evolution of Extracellular Matrix
Özbek, S., Balasubramanian, P. G., Chiquet-Ehrismann, R., Tucker, R. P., & Adams, J. C. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-03-0251 · Cited by 347
A comprehensive review of retinal gene therapy
Boye, S. E., Boye, S. L., Lewin, A. S., & Hauswirth, W. W. (2013) · Molecular Therapy · doi:10.1038/mt.2012.280 · Cited by 262
Maerker, T., van Wijk, E., Overlack, N., Kersten, F. F. J., McGee, J., Goldmann, T., Sehn, E., Roepman, R., Walsh, E. J., Kremer, H., et al. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddm285 · Cited by 259
Usher syndrome: Animal models, retinal function of Usher proteins, and prospects for gene therapy
Williams, D. S. (2008) · Vision Research · doi:10.1016/j.visres.2007.08.015 · Cited by 188
Metadata
- Authors
- Reiners, J., Nagel-Wolfrum, K., Jürgens, K., Märker, T., & Wolfrum, U.
- Venue
- Experimental Eye Research
- Publisher
- Elsevier BV
- Published
- 2006-07
- Volume
- 83
- Issue
- 1
- Pages
- 97-119
- ISSN
- 0014-4835 (ISSN-L)
- OpenAlex
- W2076400021
- Cited by
- 305
- References
- 158
- FWCI
- 7.49
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease. https://app.cochat.ai/papers/10.1016/j.exer.2005.11.010
- The paper
- Reiners, J., Nagel-Wolfrum, K., Jürgens, K., Märker, T., & Wolfrum, U. (2006). Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease. Experimental Eye Research. https://doi.org/10.1016/j.exer.2005.11.010
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.