Compounds > leucine

leucine and Corneal Dystrophies

leucine has been researched along with Corneal Dystrophies in 8 studies

Research

Studies (8)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (12.50)	18.2507
2000's	6 (75.00)	29.6817
2010's	1 (12.50)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Birk, DE; Chen, S	1
Abbott, RL; Crawford, JB; Margolis, TP; Spencer, WH; Warren, JF; Yoon, MK	1
Funayama, T; Kawashima, M; Mashima, Y; Yamada, M	1
Bowling, BL; Jonasson, F; Klintworth, GK; Liu, NP; Smith, CF	1
Aldave, AJ; Chen, MC; Rayner, SA; Sonmez, B; Thonar, EJ; Yellore, VS	1
Aldave, AJ; Bourla, N; Chen, MC; Gorin, MB; Khan, MA; Momi, RS; Rayner, SA; Sampat, KM; Sonmez, B; Yellore, VS	1
Endo, S; Fujiki, K; Hotta, Y; Ishida, N; Kanai, A; Nakayasu, K; Nguyen, TH; Yamaguchi, T	1
Fujiki, K; Hirano, K; Hotta, Y; Kanai, A; Nakamura, M; Yamamoto, N	1

Reviews

1 review(s) available for leucine and Corneal Dystrophies

Article	Year
The regulatory roles of small leucine-rich proteoglycans in extracellular matrix assembly. The FEBS journal, 2013, Volume: 280, Issue:10 Topics: Animals; Chondroitin Sulfate Proteoglycans; Collagen; Cornea; Corneal Dystrophies, Hereditary; Extracellular Matrix; Humans; Keratan Sulfate; Leucine; Lumican; Protein Binding; Protein Interaction Mapping; Protein Transport; Proteoglycans; Tendons	2013

Other Studies

7 other study(ies) available for leucine and Corneal Dystrophies

Article	Year
A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I. American journal of ophthalmology, 2003, Volume: 136, Issue:5 Topics: Adult; Amino Acid Substitution; Arginine; Child, Preschool; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Exons; Extracellular Matrix Proteins; Female; Humans; Keratoplasty, Penetrating; Leucine; Male; Pedigree; Point Mutation; Polymerase Chain Reaction; Recurrence; Reoperation; Sequence Analysis, DNA; Transforming Growth Factor beta; Visual Acuity	2003
[Six cases of late-onset lattice corneal dystrophy associated with gene mutations induced by the transforming growth factor-beta]. Nippon Ganka Gakkai zasshi, 2005, Volume: 109, Issue:2 Topics: Aged; Aged, 80 and over; Arginine; Cornea; Corneal Dystrophies, Hereditary; Exons; Genes, Dominant; Humans; Leucine; Male; Middle Aged; Transforming Growth Factor beta; Transforming Growth Factor beta1	2005
Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland. Molecular vision, 2006, Oct-02, Volume: 12 Topics: Alanine; Carbohydrate Sulfotransferases; Corneal Dystrophies, Hereditary; DNA Transposable Elements; Female; Frameshift Mutation; Heterozygote; Homozygote; Humans; Iceland; Immunohistochemistry; Immunophenotyping; Leucine; Male; Mutation; Pedigree; Polymerase Chain Reaction; Sulfotransferases; Valine	2006
An unusual presentation of macular corneal dystrophy associated with uniparental isodisomy and a novel Leu173Pro mutation. Ophthalmic genetics, 2007, Volume: 28, Issue:3 Topics: Adult; Amino Acid Sequence; Carbohydrate Sulfotransferases; Conserved Sequence; Cornea; Corneal Dystrophies, Hereditary; Genotype; Homozygote; Humans; Keratan Sulfate; Leucine; Male; Mutation; Mutation, Missense; Pedigree; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Proline; Sulfotransferases; Uniparental Disomy	2007
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy. Molecular vision, 2007, Sep-24, Volume: 13 Topics: Amino Acid Substitution; Asparagine; Corneal Dystrophies, Hereditary; Dimethylallyltranstransferase; Female; Humans; Leucine; Male; Mutation; Mutation, Missense; Polymorphism, Single Nucleotide; Proteins; Serine; Valine	2007
Leu518Pro mutation of the beta ig-h3 gene causes lattice corneal dystrophy type I. American journal of ophthalmology, 1999, Volume: 128, Issue:1 Topics: Adolescent; Adult; Base Sequence; Cornea; Corneal Dystrophies, Hereditary; DNA; Exons; Extracellular Matrix Proteins; Female; Humans; Keratoplasty, Penetrating; Leucine; Male; Middle Aged; Molecular Sequence Data; Neoplasm Proteins; Pedigree; Point Mutation; Proline; Transforming Growth Factor beta	1999
Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene. Cornea, 2001, Volume: 20, Issue:5 Topics: Aged; Aged, 80 and over; Amyloidosis; Arginine; Codon; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Extracellular Matrix Proteins; Humans; Leucine; Male; Neoplasm Proteins; Point Mutation; Polymerase Chain Reaction; Transforming Growth Factor beta	2001