The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.
A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein
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Citations
Cites
Saiki, R. K., Scharf, S., Faloona, F., Mullis, K. B., Horn, G. T., Erlich, H. A., & Arnheim, N. (1985) · Science · doi:10.1126/science.2999980 · Cited by 8,956
Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
Riordan, J. R., Rommens, J. M., Kerem, B.-S., Alon, N., Rozmahel, R., Grzelczak, Z., Zielenski, J., Lok, S., Plavsic, N., Chou, J.-L., et al. (1989) · Science · doi:10.1126/science.2475911 · Cited by 7,418
Self-citationIdentification of the Cystic Fibrosis Gene: Genetic Analysis
Kerem, B.-S., Rommens, J. M., Buchanan, J. A., Markiewicz, D., Cox, T. K., Chakravarti, A., Buchwald, M., & Tsui, L.-C. (1989) · Science · doi:10.1126/science.2570460 · Cited by 4,142
Self-citationIdentification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
Rommens, J. M., Iannuzzi, M. C., Kerem, B.-S., Drumm, M. L., Melmer, G., Dean, M., Rozmahel, R., Cole, J. L., Kennedy, D., Hidaka, N., et al. (1989) · Science · doi:10.1126/science.2772657 · Cited by 3,253
Self-citationOrkin, S. H., Kazazian, H. H., Antonarakis, S. E., Goff, S. C., Boehm, C. D., Sexton, J. P., Waber, P. G., & Giardina, P. J. V. (1982) · Nature · doi:10.1038/296627a0 · Cited by 926
Self-citationHiguchi, R., von Beroldingen, C. H., Sensabaugh, G. F., & Erlich, H. A. (1988) · Nature · doi:10.1038/332543a0 · Cited by 782
Soria, L. F., Ludwig, E. H., Clarke, H. R., Vega, G. L., Grundy, S. M., & McCarthy, B. J. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.2.587 · Cited by 633
Wong, C., Dowling, C. E., Saiki, R. K., Higuchi, R. G., Erlich, H. A., & Kazazian, H. H. (1987) · Nature · doi:10.1038/330384a0 · Cited by 497
Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots
Youssoufian, H., Kazazian, H. H., Phillips, D. G., Aronis, S., Tsiftis, G., Brown, V. A., & Antonarakis, S. E. (1986) · Nature · doi:10.1038/324380a0 · Cited by 262
Self-citationTight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria
DiLella, A. G., Marvit, J., Lidsky, A. S., Güttler, F., & Woo, S. L. C. (1986) · Nature · doi:10.1038/322799a0 · Cited by 247
Cited by
ABC Transporters: From Microorganisms to Man
Higgins, C. F. (1992) · Annual Review of Cell Biology · doi:10.1146/annurev.cb.08.110192.000435 · Cited by 3,985
Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
Welsh, M. J., & Smith, A. E. (1993) · Cell · doi:10.1016/0092-8674(93)90353-r · Cited by 1,485
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
Mosser, J., Douar, A.-M., Sarde, C.-O., Kioschis, P., Feil, R., Moser, H., Poustka, A.-M., Mandel, J.-L., & Aubourg, P. (1993) · Nature · doi:10.1038/361726a0 · Cited by 1,202
Fawaz, R., Baumann, U., Ekong, U., Fischler, B., Hadzic, N., Mack, C. L., McLin, V. A., Molleston, J. P., Neimark, E., Ng, V. L., et al. (2017) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000001334 · Cited by 555
Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
Zielenski, J., Rozmahel, R., Bozon, D., Kerem, B.-S., Grzelczak, Z., Riordan, J. R., Rommens, J., & Tsui, L.-C. (1991) · Genomics · doi:10.1016/0888-7543(91)90503-7 · Cited by 549
Self-citation
Metadata
- Authors
- Cutting, G. R., Kasch, L. M., Rosenstein, B. J., Zielenski, J., Tsui, L.-C., Antonarakis, S. E., & Kazazian Jr, H. H.
- Venue
- Nature
- Published
- 1990-07
- Volume
- 346
- Issue
- 6282
- Pages
- 366-369
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1986682462
- Cited by
- 398
- References
- 15
- FWCI
- 94.06
- 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: A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein. https://app.cochat.ai/papers/10.1038/346366a0
- The paper
- Cutting, G. R., Kasch, L. M., Rosenstein, B. J., Zielenski, J., Tsui, L.-C., Antonarakis, S. E., & Kazazian Jr, H. H. (1990). A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein. Nature. https://doi.org/10.1038/346366a0
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.
