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Cited by 802

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

Kobayashi, Kazuhiro, Nakahori, Yutaka, Miyake, Masashi, Matsumura, Kiichiro, Kondo-Iida, Eri, Nomura, Yoshiko, Segawa, Masaya, Yoshioka, Mieko, Saito, Kayoko, Osawa, Makiko, Hamano, Kenzo, Sakakihara, Youichi, Nonaka, Ikuya, Nakagome, Yasuo, Kanazawa, Ichiro, Nakamura, Yusuke, Tokunaga, Katsushi, Toda, Tatsushi·1998·Nature

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Citations

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Show all 3 references

Research works printed but not linked: 19

  1. 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
  2. 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
  3. 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).
  4. 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).
  5. Kobayashi, K. et al. Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD). Hum. Genet. (in the press). · doi:10.1007/s004390050824
  6. 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
  7. Nakai, K. & Kanehisa, M. Aknowledge base for predicting protein localization sites in eukaryotic cells. Genomics 14, 897–911 (1992). · DOI · Paper page
  8. Hofmann, K. & Stoffel, W. TMbase—A database of membrane spanning protein segments. Biol. Chem. Hoppe Seyler 374, 166 (1993).
  9. Ervasti, J. M. & Campbell, K. P. Membrane organization of the dystrophin–glycoprotein complex. Cell 66, 1121–1131 (1991). · DOI · Paper page
  10. Campbell, K. P. Three muscular dystrophies: loss of cytoskeleton–extracellular matrix linkage. Cell 80, 675–679 (1995). · DOI · Paper page
  11. Worton, R. Muscular dystrophies: disease of the dystrophin–glycoprotein complex. Science 270, 755–756 (1995). · DOI · Paper page
  12. 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
  13. Hayashi, K. Y. et al. Abnormal localization of laminin subunits in muscular dystrophies. J. Neurol. Sci. 119, 53–64 (1993). · DOI
  14. 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
  15. 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
  16. 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
  17. 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
  18. 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
  19. 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

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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).

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