The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
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Citations
Cites
A protein related to extracellular matrix proteins deleted in the mouse mutant reeler
D'Arcangelo, G., G. Miao, G., Chen, S.-C., Scares, H. D., Morgan, J. I., & Curran, T. (1995) · Nature · doi:10.1038/374719a0 · Cited by 1,748
Messenger RNA degradation in eukaryotes
Sachs, A. B. (1993) · Cell · doi:10.1016/0092-8674(93)80043-e · Cited by 846
Scrambler and yotari disrupt the disabled gene and produce a reeler -like phenotype in mice
Sheldon, M., Rice, D. S., D'Arcangelo, G., Yoneshima, H., Nakajima, K., Mikoshiba, K., Howell, B. W., Cooper, J. A., Goldowitz, D., & Curran, T. (1997) · Nature · doi:10.1038/39601 · Cited by 638
Research works printed but not linked: 19
- Fukuyama, Y., Osawa, M. & Suzuki, H. Congenital muscular dystrophy of the Fukuyama type—clinical, genetic and pathological considerations. Brain Dev. 3, 1–30 (1981). · DOI · Paper page
- Toda, T. et al. Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33. Nature Genet. 5, 283–286 (1993). · DOI
- Toda, T. et al. Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium. Am. J. Hum. Genet. 55, 946–950 (1994).
- Toda, T. et al. Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb. Am. J. Hum. Genet. 59, 1313–1320 (1996).
- Kobayashi, K. et al. Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD). Hum. Genet. (in the press). · doi:10.1007/s004390050824
- Miyake, M. et al. YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31. Genomics 40, 284–293 (1997). · DOI
- Nakai, K. & Kanehisa, M. Aknowledge base for predicting protein localization sites in eukaryotic cells. Genomics 14, 897–911 (1992). · DOI · Paper page
- Hofmann, K. & Stoffel, W. TMbase—A database of membrane spanning protein segments. Biol. Chem. Hoppe Seyler 374, 166 (1993).
- Ervasti, J. M. & Campbell, K. P. Membrane organization of the dystrophin–glycoprotein complex. Cell 66, 1121–1131 (1991). · DOI · Paper page
- Campbell, K. P. Three muscular dystrophies: loss of cytoskeleton–extracellular matrix linkage. Cell 80, 675–679 (1995). · DOI · Paper page
- Worton, R. Muscular dystrophies: disease of the dystrophin–glycoprotein complex. Science 270, 755–756 (1995). · DOI · Paper page
- Matsumura, K., Nonaka, I. & Campbell, K. P. Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy. Lancet 341, 521–522 (1993). · doi:10.1016/0140-6736(93)90279-p
- Hayashi, K. Y. et al. Abnormal localization of laminin subunits in muscular dystrophies. J. Neurol. Sci. 119, 53–64 (1993). · DOI
- Nakano, I., Funahashi, M., Takada, K. & Toda, T. Are beaches in the glia limitans the primary cause of the micropolygria in Fukuyama-type congenital muscular dystrophy (FCMD)?—Pathological study of the cerebral cortex of an FCMD fetus. Acta Neuropathol. 91, 313–321 (1996). · DOI
- Ishii, H., Hayashi, Y. K., Nonaka, I. & Arahata, K. Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy. Neuromuscul. Disord. 7, 191–197 (1997). · doi:10.1016/s0960-8966(97)00462-8
- Reiner, O. et al. Isolation of a Miller-Dieker lissencephaly gene containing G-protein β-subunit-like repeats. Nature 364, 717–721 (1993). · DOI · Paper page
- des Portes, V. et al. Anovel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lisencephaly syndrome. Cell 92, 51–61 (1998). · DOI · Paper page
- 1. Gleeson, J. G. et al. doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 92, 63–72 (1998). · DOI · Paper page
- Bannai, M. et al. Discrimination of human HLA-DRB1 alleles by PCR-SSCP (single-strand conformation polymorphism) method. Eur. J. Immunogenet. 21, 1–9 (1994). · DOI
Cited by
The sequence of the human genome
Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., et al. (2001) · Science · doi:10.1126/science.1058040 · Cited by 13,909
Emery, A. E. (2002) · The Lancet · doi:10.1016/s0140-6736(02)07815-7 · Cited by 1,667
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
Rust, S., Rosier, M., Funke, H., Real, J., Amoura, Z., Piette, J.-C., Deleuze, J.-F., Brewer, H. B., Duverger, N., Denèfle, P., et al. (1999) · Nature Genetics · doi:10.1038/11921 · Cited by 1,433
Interspersed repeats and other mementos of transposable elements in mammalian genomes
Smit, A. F. (1999) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(99)00031-3 · Cited by 949
DNA hypomethylation and human diseases
Wilson, A. S., Power, B. E., & Molloy, P. L. (2007) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2006.08.007 · Cited by 804
Metadata
- Authors
- Kobayashi, K., Nakahori, Y., Miyake, M., Matsumura, K., Kondo-Iida, E., Nomura, Y., Segawa, M., Yoshioka, M., Saito, K., Osawa, M., Hamano, K., Sakakihara, Y., Nonaka, I., Nakagome, Y., Kanazawa, I., Nakamura, Y., Tokunaga, K., & Toda, T.
- Venue
- Nature
- Published
- 1998-07
- Volume
- 394
- Issue
- 6691
- Pages
- 388-392
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1528429662
- Cited by
- 802
- References
- 3
- FWCI
- 12.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
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- CoChat. (2026). Citation check: An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. https://app.cochat.ai/papers/10.1038/28653
- The paper
- Kobayashi, K., Nakahori, Y., Miyake, M., Matsumura, K., Kondo-Iida, E., Nomura, Y., Segawa, M., Yoshioka, M., Saito, K., Osawa, M., Hamano, K., Sakakihara, Y., Nonaka, I., Nakagome, Y., Kanazawa, I., Nakamura, Y., Tokunaga, K., & Toda, T. (1998). An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature. https://doi.org/10.1038/28653
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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.