The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Mutations in the integrin α7 gene cause congenital myopathy
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Citations
Cites
Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy
Helbling-Leclerc, A., Zhang, X., Topaloglu, H., Cruaud, C., Tesson, F., Weissenbach, J., Tomé, F. M. S., Schwartz, K., Fardeau, M., Tryggvason, K., et al. (1995) · Nature Genetics · doi:10.1038/ng1095-216 · Cited by 632
Absence of integrin α6 leads to epidermolysis bullosa and neonatal death in mice
Georges-Labouesse, E., Messaddeq, N., Yehia, G., Cadalbert, L., Dierich, A., & Le Meur, M. (1996) · Nature Genetics · doi:10.1038/ng0796-370 · Cited by 548
Congenital muscular dystrophy with merosin deficiency.
Tomé, F. M. S., Evangelista, T., Helbling-Leclerc, A., Sunada, Y., Manole, E., Estournet, B., Barois, A., Campbell, K. P., & Fardeau, M. (1994) · PubMed · Cited by 452
Absence of integrin α7 causes a novel form of muscular dystrophy
Mayer, U., Saher, G., Fässler, R., Bornemann, A., Echtermeyer, F., Mark, H. V. D., Miosge, N., Pösch, E., & Mark, K. V. D. (1997) · Nature Genetics · doi:10.1038/ng1197-318 · Cited by 451
Emerin deficiency at the nuclear membrane in patients with Emery-Dreif uss muscular dystrophy
Nagano, A., Koga, R., Ogawa, M., Kurano, Y., Kawada, J., Okada, R., Hayashi, Y. K., Tsukahara, T., & Arahata, K. (1996) · Nature Genetics · doi:10.1038/ng0396-254 · Cited by 341
Self-citationSong, W. K. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.117.3.643 · Cited by 238
Altered expression of the α7β1 integrin in human and murine muscular dystrophies
Hodges, B. L., Hayashi, Y. K., Nonaka, I., Wang, W., Arahata, K., & Kaufman, S. J. (1997) · Journal of Cell Science · doi:10.1242/jcs.110.22.2873 · Cited by 211
Self-citationVachon, P. H., Xu, H., Liu, L., Loechel, F., Hayashi, Y., Arahata, K., Reed, J. C., Wewer, U. M., & Engvall, E. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119716 · Cited by 185
Self-citationRuzzi, L., Gagnoux-Palacios, L., Pinola, M., Belli, S., Meneguzzi, G., D'Alessio, M., & Zambruno, G. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119474 · Cited by 185
Philpot, J., Sewry, C., Pennock, J., & Dubowitz, V. (1995) · Neuromuscular Disorders · doi:10.1016/0960-8966(94)00069-l · Cited by 182
Cited by
Emery, A. E. (2002) · The Lancet · doi:10.1016/s0140-6736(02)07815-7 · Cited by 1,667
Targeting integrin pathways: mechanisms and advances in therapy
Pang, X., He, X., Qiu, Z., Zhang, H., Xie, R., Liu, Z., Gu, Y., Zhao, N., Xiang, Q., & Cui, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01259-6 · Cited by 1,275
Function and Genetics of Dystrophin and Dystrophin-Related Proteins in Muscle
Blake, D. J., Weir, A., Newey, S. E., & Davies, K. E. (2002) · Physiological Reviews · doi:10.1152/physrev.00028.2001 · Cited by 1,242
Striated Muscle Cytoarchitecture: An Intricate Web of Form and Function
Clark, K. A., McElhinny, A. S., Beckerle, M. C., & Gregorio, C. C. (2002) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.18.012502.105840 · Cited by 674
The integrin adhesome: from genes and proteins to human disease
Winograd-Katz, S. E., Fässler, R., Geiger, B., & Legate, K. R. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3769 · Cited by 623
Metadata
- Authors
- Hayashi, Y. K., Chou, F.-L., Engvall, E., Ogawa, M., Matsuda, C., Hirabayashi, S., Yokochi, K., Ziober, B. L., Kramer, R. H., Kaufman, S. J., Ozawa, E., Goto, Y.-I., Nonaka, I., Tsukahara, T., Wang, J.-Z., Hoffman, E. P., & Arahata, K.
- Venue
- Nature Genetics
- Published
- 1998-05
- Volume
- 19
- Issue
- 1
- Pages
- 94-97
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2042799534
- Cited by
- 366
- References
- 24
- FWCI
- 6.75
- 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.
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Mutations in the integrin α7 gene cause congenital myopathy. https://app.cochat.ai/papers/10.1038/ng0598-94
- The paper
- Hayashi, Y. K., Chou, F.-L., Engvall, E., Ogawa, M., Matsuda, C., Hirabayashi, S., Yokochi, K., Ziober, B. L., Kramer, R. H., Kaufman, S. J., Ozawa, E., Goto, Y.-I., Nonaka, I., Tsukahara, T., Wang, J.-Z., Hoffman, E. P., & Arahata, K. (1998). Mutations in the integrin α7 gene cause congenital myopathy. Nature Genetics. https://doi.org/10.1038/ng0598-94
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.
