The DOI matches its Crossref record; 16 of the 16 references it cites were found in a registry or an index.
Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis
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Citations
Cites
Airway Surface Dehydration in Cystic Fibrosis: Pathogenesis and Therapy
Boucher, R. C. (2007) · Annual Review of Medicine · doi:10.1146/annurev.med.58.071905.105316 · Cited by 512
Pathology of cystic fibrosis review of the literature and comparison with 146 autopsied cases.
Eh, O., & Esterly, J. R. (1975) · PubMed · Cited by 321
The MUC2 gene product: a human intestinal mucin
Allen, A., Hutton, D. A., & Pearson, J. P. (1998) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(98)00028-4 · Cited by 205
Regulation of Mucin Genes in Chronic Inflammatory Airway Diseases
Voynow, J. A., Gendler, S. J., & Rose, M. C. (2006) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2006-0035sf · Cited by 194
Role of Ca2+/K+ ion exchange in intracellular storage and release of Ca2+
Nguyen, T., Chin, W.-C., & Verdugo, P. (1998) · Nature · doi:10.1038/27686 · Cited by 184
A morphometric study of mucins and small airway plugging in cystic fibrosis
Burgel, P., Montani, D., Danel, C. J., Dusser, D. J., & Nadel, J. A. (2006) · Thorax · doi:10.1136/thx.2006.062190 · Cited by 149
Molecular Mechanism of Mucin Secretion: I. The Role of Intragranular Charge Shielding
Verdugo, P., Deyrup‐Olsen, I., Aitken, M. L., Villalón, M., & Johnson, D. E. (1987) · Journal of Dental Research · doi:10.1177/00220345870660022001 · Cited by 134
Quinton, P. (2001) · Nature Medicine · doi:10.1038/85429 · Cited by 128
Self-citationMucins of the human endocervix
Ilene, K. G. (2001) · Frontiers in bioscience · doi:10.2741/gipson · Cited by 117
Hyposecretion, Not Hyperabsorption, Is the Basic Defect of Cystic Fibrosis Airway Glands
Joo, N. S., Irokawa, T., Robbins, R. C., & Wine, J. J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512766200 · Cited by 97
Cited by
Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele
Middleton, P. G., Mall, M. A., Dřevínek, P., Lands, L. C., McKone, E. F., Polineni, D., Ramsey, B. W., Taylor-Cousar, J. L., Tullis, E., Vermeulen, F., et al. (2019) · New England Journal of Medicine · doi:10.1056/nejmoa1908639 · Cited by 2,198
Elborn, J. S. (2016) · The Lancet · doi:10.1016/s0140-6736(16)00576-6 · Cited by 1,805
O'Sullivan, B. P., & Freedman, S. D. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60327-5 · Cited by 1,320
Progress in therapies for cystic fibrosis
De Boeck, K., & Amaral, M. D. (2016) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(16)00023-0 · Cited by 451
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
Metadata
- Authors
- Quinton, P. M.
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 2008-08
- Volume
- 372
- Issue
- 9636
- Pages
- 415-417
- ISSN
- 0099-5355 (ISSN-L)
- 0140-6736
- OpenAlex
- W1997835226
- Cited by
- 381
- References
- 16
- FWCI
- 15.30
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis. https://app.cochat.ai/papers/10.1016/s0140-6736(08)61162-9
- The paper
- Quinton, P. M. (2008). Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis. The Lancet. https://doi.org/10.1016/s0140-6736(08)61162-9
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.
