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 *

165 related articles for article (PubMed ID: 37787991)

  • 61. Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 gene.
    Mehta JS; Hemadevi B; Vithana EN; Arunkumar J; Srinivasan M; Prajna V; Tan DT; Aung T; Sundaresan P
    Cornea; 2010 Mar; 29(3):302-6. PubMed ID: 20118786
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Rescue of the Congenital Hereditary Endothelial Dystrophy Mouse Model by Adeno-Associated Viruse-Mediated
    Shyam R; Ogando DG; Kim ET; Murugan S; Choi M; Bonanno JA
    Ophthalmol Sci; 2022 Mar; 2(1):. PubMed ID: 36051248
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing corneal dystrophy and perceptive deafness in three South American families.
    Romero PT; Donoso R; López P; Miranda A; Rodríguez L; Chrzanowsky D; Asenjo MS; Burgos G; Villegas P; Desir J; Moya G; Herrera LM
    Ophthalmic Genet; 2019 Apr; 40(2):91-98. PubMed ID: 30856043
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Update on the genetics of corneal endothelial dystrophies.
    Kannabiran C; Chaurasia S; Ramappa M; Mootha VV
    Indian J Ophthalmol; 2022 Jul; 70(7):2239-2248. PubMed ID: 35791103
    [TBL] [Abstract][Full Text] [Related]  

  • 65. 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]  

  • 66. pH dependence of the Slc4a11-mediated H
    Quade BN; Marshall A; Parker MD
    Am J Physiol Cell Physiol; 2020 Aug; 319(2):C359-C370. PubMed ID: 32520610
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the Literature.
    Zhu D; Wang J; Wang Y; Jiang Y; Li S; Xiao X; Wang P; Zhang Q
    Int J Mol Sci; 2023 Mar; 24(5):. PubMed ID: 36902444
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Homeostasis of SLC4A11 protein is mediated by endoplasmic reticulum-associated degradation.
    Hara S; Tsujikawa M; Kawasaki S; Nishida K
    Exp Eye Res; 2019 Nov; 188():107782. PubMed ID: 31491427
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Mitochondrial ROS in
    Shyam R; Ogando DG; Bonanno JA
    Front Cell Dev Biol; 2022; 10():878395. PubMed ID: 35557943
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India.
    Hemadevi B; Srinivasan M; Arunkumar J; Prajna NV; Sundaresan P
    BMC Ophthalmol; 2010 Feb; 10():3. PubMed ID: 20144242
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases.
    Vilas GL; Loganathan SK; Liu J; Riau AK; Young JD; Mehta JS; Vithana EN; Casey JR
    Hum Mol Genet; 2013 Nov; 22(22):4579-90. PubMed ID: 23813972
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Structural insights into the conformational changes of BTR1/SLC4A11 in complex with PIP
    Lu Y; Zuo P; Chen H; Shan H; Wang W; Dai Z; Xu H; Chen Y; Liang L; Ding D; Jin Y; Yin Y
    Nat Commun; 2023 Oct; 14(1):6157. PubMed ID: 37788993
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy.
    Tang H; Zhang W; Yan XM; Wang LP; Dong H; Shou T; Lei H; Guo Q
    Int J Mol Med; 2016 Jun; 37(6):1487-500. PubMed ID: 27121161
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Ammonia sensitive SLC4A11 mitochondrial uncoupling reduces glutamine induced oxidative stress.
    Ogando DG; Choi M; Shyam R; Li S; Bonanno JA
    Redox Biol; 2019 Sep; 26():101260. PubMed ID: 31254733
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Enhanced expression of SLC4A11 by tert-Butylhydroquinone is mediated by direct binding of Nrf2 to the promoter of SLC4A11.
    Guha S; Roy S
    Free Radic Biol Med; 2021 May; 167():299-306. PubMed ID: 33744340
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Mouse Slc4a11 expressed in Xenopus oocytes is an ideally selective H+/OH- conductance pathway that is stimulated by rises in intracellular and extracellular pH.
    Myers EJ; Marshall A; Jennings ML; Parker MD
    Am J Physiol Cell Physiol; 2016 Dec; 311(6):C945-C959. PubMed ID: 27681179
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.
    Minear MA; Li YJ; Rimmler J; Balajonda E; Watson S; Allingham RR; Hauser MA; Klintworth GK; Afshari NA; Gregory SG
    Mol Vis; 2013; 19():2508-16. PubMed ID: 24348007
    [TBL] [Abstract][Full Text] [Related]  

  • 78. 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]  

  • 79. A novel nonsense mutation of the SLC4A11 gene in a Korean patient with autosomal recessive congenital hereditary endothelial dystrophy.
    Park SH; Jeong HJ; Kim M; Kim MS
    Cornea; 2013 Jul; 32(7):e181-2. PubMed ID: 23615275
    [No Abstract]   [Full Text] [Related]  

  • 80. Depletion of SLC4A11 causes cell death by apoptosis in an immortalized human corneal endothelial cell line.
    Liu J; Seet LF; Koh LW; Venkatraman A; Venkataraman D; Mohan RR; Praetorius J; Bonanno JA; Aung T; Vithana EN
    Invest Ophthalmol Vis Sci; 2012 Jun; 53(7):3270-9. PubMed ID: 22447871
    [TBL] [Abstract][Full Text] [Related]  

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