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 *

177 related articles for article (PubMed ID: 32520610)

  • 21. 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]  

  • 22. IPSC-Derived Corneal Endothelial-like Cells Act as an Appropriate Model System to Assess the Impact of SLC4A11 Variants on Pre-mRNA Splicing.
    Brejchova K; Dudakova L; Skalicka P; Dobrovolny R; Masek P; Putzova M; Moosajee M; Tuft SJ; Davidson AE; Liskova P
    Invest Ophthalmol Vis Sci; 2019 Jul; 60(8):3084-3090. PubMed ID: 31323090
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy.
    Hemadevi B; Veitia RA; Srinivasan M; Arunkumar J; Prajna NV; Lesaffre C; Sundaresan P
    Arch Ophthalmol; 2008 May; 126(5):700-8. PubMed ID: 18474783
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. SLC4A11 function: evidence for H
    Kao L; Azimov R; Shao XM; Abuladze N; Newman D; Zhekova H; Noskov S; Pushkin A; Kurtz I
    Am J Physiol Cell Physiol; 2020 Feb; 318(2):C392-C405. PubMed ID: 31774702
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome.
    Siddiqui S; Zenteno JC; Rice A; Chacón-Camacho O; Naylor SG; Rivera-de la Parra D; Spokes DM; James N; Toomes C; Inglehearn CF; Ali M
    Cornea; 2014 Mar; 33(3):247-51. PubMed ID: 24351571
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia.
    Aldahmesh MA; Khan AO; Meyer BF; Alkuraya FS
    Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4142-5. PubMed ID: 19369245
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel human pathological mutations. Gene symbol: SLC4A11. Disease: Corneal endothelial dystrophy 2.
    Chai SM; Vithana EN; Venkataraman D; Saleh H; Chekkalichintavida NP; al-Sayyed F; Aung T
    Hum Genet; 2010 Jan; 127(1):110. PubMed ID: 20108384
    [No Abstract]   [Full Text] [Related]  

  • 31. Mutations in the Corneal Endothelial Dystrophy-Associated Gene SLC4A11 Render the Cells More Vulnerable to Oxidative Insults.
    Roy S; Praneetha DC; Vendra VP
    Cornea; 2015 Jun; 34(6):668-74. PubMed ID: 25811729
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).
    Vithana EN; Morgan P; Sundaresan P; Ebenezer ND; Tan DT; Mohamed MD; Anand S; Khine KO; Venkataraman D; Yong VH; Salto-Tellez M; Venkatraman A; Guo K; Hemadevi B; Srinivasan M; Prajna V; Khine M; Casey JR; Inglehearn CF; Aung T
    Nat Genet; 2006 Jul; 38(7):755-7. PubMed ID: 16767101
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Observation of nine previously reported and 10 non-reported
    Moazzeni H; Javadi MA; Asgari D; Khani M; Emami M; Moghadam A; Panahi-Bazaz MR; Hosseini Tehrani M; Karimian F; Hosseini B; Nekuie Moghadam T; Hassanpour H; Akbari MT; Elahi E
    Br J Ophthalmol; 2020 Nov; 104(11):1621-1628. PubMed ID: 31420327
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Glutaminolysis is Essential for Energy Production and Ion Transport in Human Corneal Endothelium.
    Zhang W; Li H; Ogando DG; Li S; Feng M; Price FW; Tennessen JM; Bonanno JA
    EBioMedicine; 2017 Feb; 16():292-301. PubMed ID: 28117276
    [TBL] [Abstract][Full Text] [Related]  

  • 36. NH
    Pasternack RA; Quade BN; Marshall A; Parker MD
    Front Physiol; 2024; 15():1440720. PubMed ID: 39206384
    [TBL] [Abstract][Full Text] [Related]  

  • 37. RNA sequencing uncovers alterations in corneal endothelial metabolism, pump and barrier functions of Slc4a11 KO mice.
    Ogando DG; Bonanno JA
    Exp Eye Res; 2022 Jan; 214():108884. PubMed ID: 34871568
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.
    Lopez IA; Rosenblatt MI; Kim C; Galbraith GC; Jones SM; Kao L; Newman D; Liu W; Yeh S; Pushkin A; Abuladze N; Kurtz I
    J Biol Chem; 2009 Sep; 284(39):26882-96. PubMed ID: 19586905
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutational spectrum of the SLC4A11 gene in autosomal recessive congenital hereditary endothelial dystrophy.
    Sultana A; Garg P; Ramamurthy B; Vemuganti GK; Kannabiran C
    Mol Vis; 2007 Jul; 13():1327-32. PubMed ID: 17679935
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.