Compounds > histidine
Page last updated: 2024-08-17

histidine and Corneal Dystrophies

histidine has been researched along with Corneal Dystrophies in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, J; Wang, D; Yao, Y; Zhang, M1
Aldave, AJ; Kim, BT; Prechanond, A; Rayner, SA; Yellore, VS1
Bhattacharya, SS; Bowling, BL; Ebenezer, ND; Filipec, M; Hardcastle, AJ; Jirsova, K; Klintworth, GK; Liskova, P; Tuft, SJ1
Kim, HM; Kim, JW; Song, JS1

Other Studies

4 other study(ies) available for histidine and Corneal Dystrophies

ArticleYear
Genetic and phenotypic investigation of a Chinese pedigree with lattice corneal dystrophy IIIB subtype.
    Eye science, 2013, Volume: 28, Issue:3

    Topics: Arginine; Asian People; Base Sequence; Cataract; Cornea; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Exons; Extracellular Matrix Proteins; Histidine; Humans; Lens Implantation, Intraocular; Male; Mutation, Missense; Pedigree; Phacoemulsification; Phenotype; Transforming Growth Factor beta

2013
Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene.
    Molecular vision, 2006, Feb-27, Volume: 12

    Topics: Adult; Corneal Dystrophies, Hereditary; Exons; Extracellular Matrix Proteins; Gene Deletion; Heterozygote; Histidine; Humans; Male; Middle Aged; Transforming Growth Factor beta; Visual Acuity

2006
Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families.
    Ophthalmic research, 2008, Volume: 40, Issue:2

    Topics: Adult; Amyloid; Cataract; Cornea; Corneal Dystrophies, Hereditary; Czech Republic; Extracellular Matrix Proteins; Female; Histidine; Humans; Male; Middle Aged; Mutation; Phenotype; Proline; Transforming Growth Factor beta

2008
Phenotypic non-penetrance in granular corneal dystrophy type II.
    Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2008, Volume: 246, Issue:11

    Topics: Adult; Arginine; Base Sequence; Corneal Dystrophies, Hereditary; Corneal Opacity; Epidermis; Extracellular Matrix Proteins; Heterozygote; Histidine; Humans; Keratinocytes; Male; Middle Aged; Mutation; Mutation, Missense; Penetrance; Phenotype; Transforming Growth Factor beta

2008