The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity
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Citations
Cites
Novel myosin heavy chain encoded by murine dilute coat colour locus
Mercer, J. A., Seperack, P. K., Strobel, M. C., Copeland, N. G., & Jenkins, N. A. (1991) · Nature · doi:10.1038/349709a0 · Cited by 535
Huber, L. A., Pimplikar, S., Parton, R. G., Virta, H., Zerial, M., & Simons, K. (1993) · The Journal of cell biology · doi:10.1083/jcb.123.1.35 · Cited by 465
Self-citationThe Rab8 GTPase regulates apical protein localization in intestinal cells
Sato, T., Mushiake, S., Kato, Y., Sato, K., Sato, M., Takeda, N., Ozono, K., Miki, K., Kubo, Y., Tsuji, A., et al. (2007) · Nature · doi:10.1038/nature05929 · Cited by 344
Ménasché, G., Ho, C. H., Sanal, O., Feldmann, J., Tezcan, I., Ersoy, F., Houdusse, A., Fischer, A., & Basile, G. D. S. (2003) · Journal of Clinical Investigation · doi:10.1172/jci18264 · Cited by 291
Ménasché, G., Ho, C. H., Sanal, O., Feldmann, J., Tezcan, I., Ersoy, F., Houdusse, A., Fischer, A., & Basile, G. D. S. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200318264 · Cited by 289
Human myosin-Vc is a novel class V myosin expressed in epithelial cells
Rodriguez, O. C., & Cheney, R. E. (2002) · Journal of Cell Science · doi:10.1242/jcs.115.5.991 · Cited by 180
Myosin Vb Interacts with Rab8a on a Tubular Network Containing EHD1 and EHD3
Roland, J. T., Kenworthy, A. K., Peranen, J., Caplan, S., & Goldenring, J. R. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-02-0169 · Cited by 169
Rab11a and myosin Vb are required for bile canalicular formation in WIF-B9 cells
Wakabayashi, Y., Dutt, P., Lippincott-Schwartz, J., & Arias, I. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503702102 · Cited by 159
Tako, E., Glahn, R. P., Welch, R. M., Lei, X. G., Yasuda, K., & Miller, D. D. (2007) · British Journal Of Nutrition · doi:10.1017/s0007114507825128 · Cited by 158
Microvillous inclusion disease (microvillous atrophy)
Ruemmele, F. M., Schmitz, J., & Goulet, O. (2006) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-1-22 · Cited by 149
Self-citation
Cited by
The myosin superfamily at a glance
Hartman, M. A., & Spudich, J. A. (2012) · Journal of Cell Science · doi:10.1242/jcs.094300 · Cited by 337
Promises and challenges of organoid-guided precision medicine
Bose, S., Clevers, H., & Shen, X. (2021) · Med · doi:10.1016/j.medj.2021.08.005 · Cited by 213
Myosin motors at neuronal synapses: drivers of membrane transport and actin dynamics
Kneussel, M., & Wagner, W. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3445 · Cited by 191
Tzaban, S., Massol, R. H., Yen, E., Hamman, W., Frank, S. R., Lapierre, L. A., Hansen, S. H., Goldenring, J. R., Blumberg, R. S., & Lencer, W. I. (2009) · Journal of Cell Biology · doi:10.1083/jcb.200809122 · Cited by 169
Polarized Protein Transport and Lumen Formation During Epithelial Tissue Morphogenesis
Blasky, A. J., Mangan, A., & Prekeris, R. (2015) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100814-125323 · Cited by 78
Metadata
- Authors
- Müller, T., Hess, M. W., Schiefermeier, N., Pfaller, K., Ebner, H. L., Heinz-Erian, P., Ponstingl, H., Partsch, J., Röllinghoff, B., Köhler, H., Berger, T., Lenhartz, H., Schlenck, B., Houwen, R. J., Taylor, C. J., Zoller, H., Lechner, S., Goulet, O., Utermann, G., Ruemmele, F. M., Huber, L. A., & Janecke, A. R.
- Venue
- Nature Genetics
- Published
- 2008-08-24
- Volume
- 40
- Issue
- 10
- Pages
- 1163-1165
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2037437691
- Cited by
- 381
- References
- 14
- FWCI
- 7.75
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. https://app.cochat.ai/papers/10.1038/ng.225
- The paper
- Müller, T., Hess, M. W., Schiefermeier, N., Pfaller, K., Ebner, H. L., Heinz-Erian, P., Ponstingl, H., Partsch, J., Röllinghoff, B., Köhler, H., Berger, T., Lenhartz, H., Schlenck, B., Houwen, R. J., Taylor, C. J., Zoller, H., Lechner, S., Goulet, O., Utermann, G., . . . Janecke, A. R. (2008). MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. Nature Genetics. https://doi.org/10.1038/ng.225
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.