The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Aberrant CFTR-dependent HCO-3 transport in mutations associated with cystic fibrosis
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Citations
Cites
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
Cited by
Physiology of sweat gland function: The roles of sweating and sweat composition in human health
Baker, L. B. (2019) · Temperature · doi:10.1080/23328940.2019.1632145 · Cited by 732
Electrolyte transport in the mammalian colon: mechanisms and implications for disease
Kunzelmann, K., & Mall, M. (2002) · Physiological Reviews · doi:10.1152/physrev.00026.2001 · Cited by 655
CFTR Function and Prospects for Therapy
Riordan, J. R. (2008) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.75.103004.142532 · Cited by 610
Role of CFTR in epithelial physiology
Saint-Criq, V., & Gray, M. A. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2391-y · Cited by 433
Recent advances in the transmembrane transport of anions
Davis, J. T., Okunola, O., & Quesada, R. (2010) · Chemical Society Reviews · doi:10.1039/b926164h · Cited by 372
Metadata
- Authors
- Choi, J. Y., Muallem, D., Kiselyov, K., Lee, M. G., Thomas, P. J., & Muallem, S.
- Venue
- Nature
- Published
- 2001-03
- Volume
- 410
- Issue
- 6824
- Pages
- 94-97
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1536163743
- Cited by
- 412
- References
- 1
- FWCI
- 27.57
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: Aberrant CFTR-dependent HCO-3 transport in mutations associated with cystic fibrosis. https://app.cochat.ai/papers/10.1038/35065099
- The paper
- Choi, J. Y., Muallem, D., Kiselyov, K., Lee, M. G., Thomas, P. J., & Muallem, S. (2001). Aberrant CFTR-dependent HCO-3 transport in mutations associated with cystic fibrosis. Nature. https://doi.org/10.1038/35065099
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.
