The DOI matches its Crossref record; 104 of the 104 references it cites were found in a registry or an index.
SLC9/NHE gene family, a plasma membrane and organellar family of Na+/H+ exchangers
Open accessAbstract
This brief review of the human Na/H exchanger gene family introduces a new classification with three subgroups to the SLC9 gene family. Progress in the structure and function of this gene family is reviewed with structure based on homology to the bacterial Na/H exchanger NhaA. Human diseases which result from genetic abnormalities of the SLC9 family are discussed although the exact role of these transporters in causing any disease is not established, other than poorly functioning NHE3 in congenital Na diarrhea
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Cites
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Renal and intestinal absorptive defects in mice lacking the NHE3 Na+/H+ exchanger
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Identifying autism loci and genes by tracing recent shared ancestry
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Diversity of the mammalian sodium/proton exchanger SLC9 gene family
Orlowski, J., & Grinstein, S. (2004) · Pfl�gers Archiv European Journal of Physiology · doi:10.1007/s00424-003-1110-3 · Cited by 657
Structure of a Na+/H+ antiporter and insights into mechanism of action and regulation by pH
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Evolutionary origins of eukaryotic sodium/proton exchangers
Brett, C. L., Donowitz, M., & Rao, R. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00360.2004 · Cited by 557
Self-citationGrowth Factors Induce Phosphorylation of the Na + /H + Antiporter, a Glycoprotein of 110 kD
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Cited by
Traditional and emerging roles for the SLC9 na+/H+ exchangers
Fuster, D. G., & Alexander, R. T. (2014) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-013-1408-8 · Cited by 159
Self-citationIntestinal brush-border Na+/H+exchanger-3 drives H+-coupled iron absorption in the mouse
Shawki, A., Engevik, M. A., Kim, R. S., Knight, P. B., Baik, R. A., Anthony, S. R., Worrell, R. T., Shull, G. E., & Mackenzie, B. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00167.2016 · Cited by 39
Nikolovska, K., Seidler, U. E., & Stock, C. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.899286 · Cited by 32
Schaschl, H., & Wallner, B. (2020) · BMC Evolutionary Biology · doi:10.1186/s12862-019-1575-0 · Cited by 24
Mouse Slc9a8 Mutants Exhibit Retinal Defects Due to Retinal Pigmented Epithelium Dysfunction
Jadeja, S., Barnard, A. R., McKie, L., Cross, S. H., White, J. K., Robertson, M., Budd, P. S., MacLaren, R. E., & Jackson, I. J. (2015) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.14-15735 · Cited by 13
Metadata
- Authors
- Donowitz, M., Ming Tse, C., & Fuster, D.
- Venue
- Molecular Aspects of Medicine
- Publisher
- Elsevier BV
- Published
- 2013-04
- Volume
- 34
- Issue
- 2-3
- Pages
- 236-251
- ISSN
- 0098-2997 (ISSN-L)
- OpenAlex
- W2034224320
- Cited by
- 275
- References
- 104
- FWCI
- 10.09
- Type
- journal article
- Language
- en
- Open access
- green
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- Donowitz, M., Ming Tse, C., & Fuster, D. (2013). SLC9/NHE gene family, a plasma membrane and organellar family of Na+/H+ exchangers. Molecular Aspects of Medicine. https://doi.org/10.1016/j.mam.2012.05.001
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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.
