Compounds > glutamine

glutamine and Corneal Dystrophies

glutamine has been researched along with Corneal Dystrophies in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bonanno, JA; Choi, MJ; Kim, ET; Li, H; Ogando, DG; Tenessen, JM; Zhang, W1
Bonanno, JA; Feng, M; Li, H; Li, S; Ogando, DG; Price, FW; Tennessen, JM; Zhang, W1
Hou, YC; Hsiao, CH; Hu, FR; Kuo, KT; Wang, IJ1
Chau, HM; Cung, le X; Fujiki, K; Ha, NT; Hasegawa, N; Hiratsuka, Y; Kanai, A; Murakami, A; Thanh, TK1
Affeldt, JA; Aldave, AJ; Gutmark, JG; Klintworth, GK; Meallet, MA; Rao, NA; Small, KW; Udar, N; Yellore, VS1

Other Studies

5 other study(ies) available for glutamine and Corneal Dystrophies

ArticleYear
Conditionally Immortal Slc4a11-/- Mouse Corneal Endothelial Cell Line Recapitulates Disrupted Glutaminolysis Seen in Slc4a11-/- Mouse Model.
    Investigative ophthalmology & visual science, 2017, 07-01, Volume: 58, Issue:9

    Topics: Animals; Anion Transport Proteins; Antigens, Polyomavirus Transforming; Blotting, Western; Cell Line; Cell Proliferation; Corneal Dystrophies, Hereditary; Disease Models, Animal; Endothelium, Corneal; Female; Gas Chromatography-Mass Spectrometry; Glutamine; Ion Transport; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; Real-Time Polymerase Chain Reaction; Symporters

2017
Glutaminolysis is Essential for Energy Production and Ion Transport in Human Corneal Endothelium.
    EBioMedicine, 2017, Volume: 16

    Topics: Adenosine Triphosphate; Amino Acid Transport System X-AG; Animals; Carrier Proteins; Cell Line; Cells, Cultured; Citric Acid Cycle; Corneal Dystrophies, Hereditary; Endothelium, Corneal; Energy Metabolism; Epithelium, Corneal; Fuchs' Endothelial Dystrophy; Gene Expression; Glutamine; Humans; Ion Transport; Mice, Knockout; Microscopy, Fluorescence; Mutation; Rabbits; Reverse Transcriptase Polymerase Chain Reaction; SLC4A Proteins

2017
TGFBI-linked corneal dystrophies treated using superficial lamellar keratectomy combined with phototherapeutic keratectomy.
    Eye (London, England), 2012, Volume: 26, Issue:1

    Topics: Arginine; Corneal Dystrophies, Hereditary; Female; Genotype; Glutamine; Humans; Male; Molecular Sequence Data; Mutation; Photorefractive Keratectomy; Transforming Growth Factor beta1; Treatment Outcome; Visual Acuity

2012
Identification of novel mutations of the CHST6 gene in Vietnamese families affected with macular corneal dystrophy in two generations.
    Cornea, 2003, Volume: 22, Issue:6

    Topics: Adolescent; Adult; Arginine; Base Sequence; Carbohydrate Sulfotransferases; Case-Control Studies; Codon, Terminator; Corneal Dystrophies, Hereditary; Female; Frameshift Mutation; Glutamine; Heterozygote; Humans; Male; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Sulfotransferases; Vietnam

2003
Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.
    American journal of ophthalmology, 2004, Volume: 138, Issue:5

    Topics: Adult; Alanine; Amyloid; Amyloidosis; Aspartic Acid; Cornea; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Exons; Extracellular Matrix Proteins; Female; Glutamine; Haplotypes; Humans; Mutation, Missense; Pedigree; Proline; Transforming Growth Factor beta

2004