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Altered gene expression in slc4a11<sup>−/−</sup> mouse cornea highlights SLC4A11 roles.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98921-w
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- Article
Structure and Function of the Band 3 Cl<sup>-</sup>/HCO<sup>-</sup><sup>3</sup> Transporter<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 574, n. 1, p. 75, doi. 10.1111/j.1749-6632.1989.tb25137.x
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- Article
Carbonic anhydrase inhibition prevents and reverts cardiomyocyte hypertrophy.
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- Journal of Physiology, 2007, v. 579, n. 1, p. 127, doi. 10.1113/jphysiol.2006.123638
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- Article
Slc26a6: a cardiac chloride–hydroxyl exchanger and predominant chloride–bicarbonate exchanger of the mouse heart.
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- Journal of Physiology, 2004, v. 561, n. 3, p. 721, doi. 10.1113/jphysiol.2004.077339
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- Article
Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of C0L8A2 mutations in Fuchs endothelial corneal dystrophy.
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- Journal of Human Genetics, 2014, v. 59, n. 8, p. 444, doi. 10.1038/jhg.2014.55
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- Article
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).
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- Nature Genetics, 2006, v. 38, n. 7, p. 755, doi. 10.1038/ng1824
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- Article
Sensors and regulators of intracellular pH.
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- Nature Reviews Molecular Cell Biology, 2010, v. 11, n. 1, p. 50, doi. 10.1038/nrm2820
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- Article
Resistance to cardiomyocyte hypertrophy in ae3<sup>−/−</sup> mice, deficient in the AE3 Cl−/HCO<sub>3</sub><sup>−</sup> exchanger.
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- BMC Cardiovascular Disorders, 2014, v. 14, n. 1, p. 89, doi. 10.1186/1471-2261-14-89
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- Article
Resistance to cardiomyocyte hypertrophy in ae3-/- mice, deficient in the AE3 Cl-/HCO3- exchanger.
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- 2014
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- journal article
Quantification of carbonic anhydrase gene expression in ventricle of hypertrophic and failing human heart.
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- BMC Cardiovascular Disorders, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2261-13-2
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- Article
Quantification of carbonic anhydrase gene expression in ventricle of hypertrophic and failing human heart.
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- 2013
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- journal article
Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-46094-y
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- Article
Defective cell adhesion function of solute transporter, SLC4A11, in endothelial corneal dystrophies.
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- Human Molecular Genetics, 2020, v. 29, n. 1, p. 97, doi. 10.1093/hmg/ddz259
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- Article
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases.
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- Human Molecular Genetics, 2013, v. 22, n. 22, p. 4579, doi. 10.1093/hmg/ddt307
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- Article
Cytosolic H.
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- Journal of Physiology, 2011, v. 589, n. 7, p. 1551, doi. 10.1113/jphysiol.2010.201483
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- Article
Bicarbonate transporters in corals point towards a key step in the evolution of cnidarian calcification.
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- Scientific Reports, 2015, p. 9983, doi. 10.1038/srep09983
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- Article
Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools.
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- 2011
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- journal article
Cover Image, Volume 39, Issue 5.
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- Human Mutation, 2018, v. 39, n. 5, p. i, doi. 10.1002/humu.23432
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- Article
Molecular phenotype of SLC4A11 missense mutants: Setting the stage for personalized medicine in corneal dystrophies.
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- Human Mutation, 2018, v. 39, n. 5, p. 676, doi. 10.1002/humu.23401
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- Article
SLC4A11 Three-Dimensional Homology Model Rationalizes Corneal Dystrophy-Causing Mutations.
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- Human Mutation, 2017, v. 38, n. 3, p. 279, doi. 10.1002/humu.23152
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- Article
Corneal Dystrophy-Causing SLC4 A11 Mutants: Suitability for Folding-Correction Therapy.
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- Human Mutation, 2014, v. 35, n. 9, p. 1082, doi. 10.1002/humu.22601
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- Article
SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
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- Human Molecular Genetics, 2008, v. 17, n. 5, p. 656, doi. 10.1093/hmg/ddm337
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- Article
Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration.
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- Human Molecular Genetics, 2005, v. 14, n. 2, p. 255, doi. 10.1093/hmg/ddi023
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- Article
Molecular mechanism for the red blood cell senescence clock.
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- IUBMB Life, 2018, v. 70, n. 1, p. 32, doi. 10.1002/iub.1703
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- Article
Bicarbonate transport in health and disease.
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- IUBMB Life, 2014, v. 66, n. 9, p. 596, doi. 10.1002/iub.1315
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- Article
Role of N-glycosylation in the expression of human SLC26A2 and A3 anion transport membrane glycoproteins1.
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- Biochemistry & Cell Biology, 2019, v. 97, n. 3, p. 290, doi. 10.1139/bcb-2018-0139
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- Article
Meeting report: The 57th Annual Meeting of the CSMB, Membrane Proteins in Health and Disease<sup>1</sup>.
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- Biochemistry & Cell Biology, 2014, v. 92, n. 6, p. 425, doi. 10.1139/bcb-2014-0131
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- Article
Report on the Bicarbonate Transport Satellite Meeting at the 53rd Annual Meeting of the Canadian Society of Biochemistry, Molecular and Cellular Biology.
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- Biochemistry & Cell Biology, 2011, v. 89, n. 2, p. 83, doi. 10.1139/O10-158
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- Article
Report on the 53rd Annual Meeting of the Canadian Society of Biochemistry, Molecular and Cellular Biology: 'Membrane Proteins in Health and Disease'.
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- Biochemistry & Cell Biology, 2011, v. 89, n. 2, p. 79, doi. 10.1139/O10-157
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- Article
Why bicarbonate?
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- Biochemistry & Cell Biology, 2006, v. 84, n. 6, p. 930, doi. 10.1139/O06-184
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- Article
Bicarbonate transport proteins.
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- Biochemistry & Cell Biology, 2002, v. 80, n. 5, p. 483, doi. 10.1139/o02-152
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- Article
Meeting report: membrane proteins in health and disease.
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- Biochemistry & Cell Biology, 2002, v. 80, n. 5, p. v, doi. 10.1139/o02-162
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- Article