PubMed for id: 6508

Year	Number of Results
1989	1
1993	1
1994	2
1998	1
1999	1
2001	6
2002	4
2009	2
2010	1
2011	1
2012	1
2014	1
2016	1
2017	2
2018	1
2019	2
2020	2
2022	1
2023	1
2024	0

1

Investigation of SLA4A3 as a candidate gene for human retinal disease.

Downs LM, Webster AR, Moore AT, Michaelides M, Ali RR, Hardcastle AJ, Mellersh CS. Downs LM, et al. J Negat Results Biomed. 2016 May 23;15:11. doi: 10.1186/s12952-016-0054-z. J Negat Results Biomed. 2016. PMID: 27211793 Free PMC article.

2

Boric acid increases the expression levels of human anion exchanger genes SLC4A2 and SLC4A3.

Akbas F, Aydin Z. Akbas F, et al. Genet Mol Res. 2012 Apr 3;11(2):847-54. doi: 10.4238/2012.April.3.6. Genet Mol Res. 2012. PMID: 22576912 Free article.

3

The AE gene family of Cl/HCO3- exchangers.

Alper SL, Darman RB, Chernova MN, Dahl NK. Alper SL, et al. J Nephrol. 2002 Mar-Apr;15 Suppl 5:S41-53. J Nephrol. 2002. PMID: 12027221 Review.

4

Detection of Cl--HCO3- and Na+-H+ exchangers in human airways epithelium.

Al-Bazzaz FJ, Hafez N, Tyagi S, Gailey CA, Toofanfard M, Alrefai WA, Nazir TM, Ramaswamy K, Dudeja PK. Al-Bazzaz FJ, et al. JOP. 2001 Jul;2(4 Suppl):285-90. JOP. 2001. PMID: 11875273

5

Regulation of Na+-independent Cl-/HCO3- exchangers by pH.

Alper SL, Chernova MN, Stewart AK. Alper SL, et al. JOP. 2001 Jul;2(4 Suppl):171-5. JOP. 2001. PMID: 11875255 Review.

6

Genomic structure of human anion exchanger 3 and its potential role in hereditary neurological disease.

Einum DD, Zhang J, Arneson PJ, Menon AG, Ptacek LJ. Einum DD, et al. Neurogenetics. 1998 Aug;1(4):289-92. doi: 10.1007/s100480050043. Neurogenetics. 1998. PMID: 10732805

7

Expression of the Na+/H+ and Cl-/HCO-3 exchanger isoforms in proximal and distal human airways.

Dudeja PK, Hafez N, Tyagi S, Gailey CA, Toofanfard M, Alrefai WA, Nazir TM, Ramaswamy K, Al-Bazzaz FJ. Dudeja PK, et al. Am J Physiol. 1999 Jun;276(6):L971-8. doi: 10.1152/ajplung.1999.276.6.L971. Am J Physiol. 1999. PMID: 10362722

8

Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36.

Su YR, Klanke CA, Houseal TW, Linn SC, Burk SE, Varvil TS, Otterud BE, Shull GE, Leppert MF, Menon AG. Su YR, et al. Genomics. 1994 Aug;22(3):605-9. doi: 10.1006/geno.1994.1433. Genomics. 1994. PMID: 8001971

9

Molecular cloning, expression, and chromosomal localization of two isoforms of the AE3 anion exchanger from human heart.

Yannoukakos D, Stuart-Tilley A, Fernandez HA, Fey P, Duyk G, Alper SL. Yannoukakos D, et al. Circ Res. 1994 Oct;75(4):603-14. doi: 10.1161/01.res.75.4.603. Circ Res. 1994. PMID: 7923606

10

Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome.

Christiansen MK, Kjær-Sørensen K, Clavsen NC, Dittmann S, Jensen MF, Guldbrandsen HØ, Pedersen LN, Sørensen RH, Lildballe DL, Müller K, Müller P, Vogel K, Rudic B, Borggrefe M, Oxvig C, Aalkjær C, Schulze-Bahr E, Matchkov V, Bundgaard H, Jensen HK. Christiansen MK, et al. Heart Rhythm. 2023 Aug;20(8):1136-1143. doi: 10.1016/j.hrthm.2023.02.010. Epub 2023 Feb 15. Heart Rhythm. 2023. PMID: 36806574 Free article.

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