These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 25394471)

  • 1. Human SLC4A11-C functions as a DIDS-stimulatable H⁺(OH⁻) permeation pathway: partial correction of R109H mutant transport.
    Kao L; Azimov R; Abuladze N; Newman D; Kurtz I
    Am J Physiol Cell Physiol; 2015 Jan; 308(2):C176-88. PubMed ID: 25394471
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations.
    Vilas GL; Loganathan SK; Quon A; Sundaresan P; Vithana EN; Casey J
    Hum Mutat; 2012 Feb; 33(2):419-28. PubMed ID: 22072594
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants.
    Kao L; Azimov R; Shao XM; Frausto RF; Abuladze N; Newman D; Aldave AJ; Kurtz I
    Am J Physiol Cell Physiol; 2016 Nov; 311(5):C820-C830. PubMed ID: 27581649
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A biochemical framework for SLC4A11, the plasma membrane protein defective in corneal dystrophies.
    Vilas GL; Morgan PE; Loganathan SK; Quon A; Casey JR
    Biochemistry; 2011 Mar; 50(12):2157-69. PubMed ID: 21288032
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies.
    Loganathan SK; Schneider HP; Morgan PE; Deitmer JW; Casey JR
    Am J Physiol Cell Physiol; 2016 Nov; 311(5):C735-C748. PubMed ID: 27558157
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Corneal dystrophy mutations R125H and R804H disable SLC4A11 by altering the extracellular pH dependence of the intracellular pK that governs H
    Quade BN; Marshall A; Parker MD
    Am J Physiol Cell Physiol; 2022 Oct; 323(4):C990-C1002. PubMed ID: 35993514
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Corneal dystrophy-causing SLC4A11 mutants: suitability for folding-correction therapy.
    Loganathan SK; Casey JR
    Hum Mutat; 2014 Sep; 35(9):1082-91. PubMed ID: 24916015
    [TBL] [Abstract][Full Text] [Related]  

  • 8. SLC4A11 depletion impairs NRF2 mediated antioxidant signaling and increases reactive oxygen species in human corneal endothelial cells during oxidative stress.
    Guha S; Chaurasia S; Ramachandran C; Roy S
    Sci Rep; 2017 Jun; 7(1):4074. PubMed ID: 28642546
    [TBL] [Abstract][Full Text] [Related]  

  • 9. R125H, W240S, C386R, and V507I SLC4A11 mutations associated with corneal endothelial dystrophy affect the transporter function but not trafficking in PS120 cells.
    Li S; Hundal KS; Chen X; Choi M; Ogando DG; Obukhov AG; Bonanno JA
    Exp Eye Res; 2019 Mar; 180():86-91. PubMed ID: 30557570
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fuchs Endothelial Corneal Dystrophy in a Heterozygous Carrier of Congenital Hereditary Endothelial Dystrophy Type 2 with a Novel Mutation in SLC4A11.
    Kim JH; Ko JM; Tchah H
    Ophthalmic Genet; 2015; 36(3):284-6. PubMed ID: 24502824
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular phenotype of SLC4A11 missense mutants: Setting the stage for personalized medicine in corneal dystrophies.
    Alka K; Casey JR
    Hum Mutat; 2018 May; 39(5):676-690. PubMed ID: 29327391
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Defective cell adhesion function of solute transporter, SLC4A11, in endothelial corneal dystrophies.
    Malhotra D; Jung M; Fecher-Trost C; Lovatt M; Peh GSL; Noskov S; Mehta JS; Zimmermann R; Casey JR
    Hum Mol Genet; 2020 Jan; 29(1):97-116. PubMed ID: 31691803
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy.
    Soumittra N; Loganathan SK; Madhavan D; Ramprasad VL; Arokiasamy T; Sumathi S; Karthiyayini T; Rachapalli SR; Kumaramanickavel G; Casey JR; Rajagopal R
    J Hum Genet; 2014 Aug; 59(8):444-53. PubMed ID: 25007886
    [TBL] [Abstract][Full Text] [Related]  

  • 14. SLC4A11 Three-Dimensional Homology Model Rationalizes Corneal Dystrophy-Causing Mutations.
    Badior KE; Alka K; Casey JR
    Hum Mutat; 2017 Mar; 38(3):279-288. PubMed ID: 27925686
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ophthalmic Nonsteroidal Anti-Inflammatory Drugs as a Therapy for Corneal Dystrophies Caused by SLC4A11 Mutation.
    Alka K; Casey JR
    Invest Ophthalmol Vis Sci; 2018 Aug; 59(10):4258-4267. PubMed ID: 30140924
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy.
    Patel SP; Parker MD
    Biomed Res Int; 2015; 2015():475392. PubMed ID: 26451371
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4A11.
    Chiu AM; Mandziuk JJ; Loganathan SK; Alka K; Casey JR
    Invest Ophthalmol Vis Sci; 2015 Dec; 56(13):7739-53. PubMed ID: 26641551
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inhibitory action of DIDS on chloride transport across the amphibian cornea.
    Bentley PJ; McGahan MC
    J Physiol; 1980 Jul; 304():519-27. PubMed ID: 6777484
    [TBL] [Abstract][Full Text] [Related]  

  • 19. AE anion exchangers in atrial tumor cells.
    Papageorgiou P; Shmukler BE; Stuart-Tilley AK; Jiang L; Alper SL
    Am J Physiol Heart Circ Physiol; 2001 Mar; 280(3):H937-45. PubMed ID: 11179033
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected Families.
    Chaurasia S; Ramappa M; Annapurna M; Kannabiran C
    Cornea; 2020 Mar; 39(3):354-357. PubMed ID: 31714402
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.