The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
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Citations
Cites
Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites
Nielsen, H., Engelbrecht, J., Brunak, S., & von Heijne, G. (1997) · Protein Engineering Design and Selection · doi:10.1093/protein/10.1.1 · Cited by 5,356
Cell Adhesion: The Molecular Basis of Tissue Architecture and Morphogenesis
Gumbiner, B. M. (1996) · Cell · doi:10.1016/s0092-8674(00)81279-9 · Cited by 3,471
Morphogenetic roles of classic cadherins
Takeichi, M. (1995) · Current Opinion in Cell Biology · doi:10.1016/0955-0674(95)80102-2 · Cited by 1,450
SMART: a web-based tool for the study of genetically mobile domains
Schultz, J. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.231 · Cited by 1,378
[31] PHD: Predicting one-dimensional protein structure by profile-based neural networks
Rost, B. (1996) · Methods in Enzymology · doi:10.1016/s0076-6879(96)66033-9 · Cited by 1,274
MOLECULAR AND FUNCTIONAL ANALYSIS OF CADHERIN-BASED ADHERENS JUNCTIONS
Yap, A. S., Brieher, W. M., & Gumbiner, B. M. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.119 · Cited by 805
Nollet, F., Kools, P., & van Roy, F. (2000) · Journal of Molecular Biology · doi:10.1006/jmbi.2000.3777 · Cited by 698
Cadherin superfamily genes: functions, genomic organization, and neurologic diversity
Yagi, T., & Takeichi, M. (2000) · Genes & Development · doi:10.1101/gad.14.10.1169 · Cited by 637
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
Bolz, H., von Brederlow, B., Ramírez, A., Bryda, E. C., Kutsche, K., Nothwang, H. G., Seeliger, M., Cabrera, M. D. C.-S., Vila, M. C., Molina, O. P., et al. (2001) · Nature Genetics · doi:10.1038/83667 · Cited by 497
Self-citationNotch signalling pathway mediates hair cell development in mammalian cochlea
Lanford, P. J., Lan, Y., Jiang, R., Lindsell, C., Weinmaster, G., Gridley, T., & Kelley, M. W. (1999) · Nature Genetics · doi:10.1038/6804 · Cited by 485
Cited by
Curtin, J. A., Quint, E., Tsipouri, V., Arkell, R. M., Cattanach, B., Copp, A. J., Henderson, D. J., Spurr, N., Stanier, P., Fisher, E. M., et al. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00374-9 · Cited by 631
Self-citationBoeda, B. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf689 · Cited by 447
Mlodzik, M. (2002) · Trends in Genetics · doi:10.1016/s0168-9525(02)02770-1 · Cited by 341
Reiners, J., Nagel-Wolfrum, K., Jürgens, K., Märker, T., & Wolfrum, U. (2006) · Experimental Eye Research · doi:10.1016/j.exer.2005.11.010 · Cited by 305
Weil, D. (2003) · Human Molecular Genetics · doi:10.1093/hmg/12.5.463 · Cited by 294
Metadata
- Authors
- Palma, F. D., Holme, R. H., Bryda, E. C., Belyantseva, I. A., Pellegrino, R., Kachar, B., Steel, K. P., & Noben-Trauth, K.
- Venue
- Nature Genetics
- Published
- 2001-01
- Volume
- 27
- Issue
- 1
- Pages
- 103-107
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1514414732
- Cited by
- 431
- References
- 22
- FWCI
- 17.16
- Type
- journal article
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
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Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. https://app.cochat.ai/papers/10.1038/83660
- The paper
- Palma, F. D., Holme, R. H., Bryda, E. C., Belyantseva, I. A., Pellegrino, R., Kachar, B., Steel, K. P., & Noben-Trauth, K. (2001). Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. Nature Genetics. https://doi.org/10.1038/83660
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.
