leucine and Disomy, Uniparental

leucine has been researched along with Disomy, Uniparental in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Aguirre-Lamban, J; Ayuso, C; Cantalapiedra, D; Lorda-Sanchez, I; Ramos, C; Riveiro-Alvarez, R; Trujillo-Tiebas, MJ; Vallespin, E; Valverde, D	1
Aldave, AJ; Chen, MC; Rayner, SA; Sonmez, B; Thonar, EJ; Yellore, VS	1

Other Studies

2 other study(ies) available for leucine and Disomy, Uniparental

Article	Year
Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease. Molecular vision, 2007, Jan-26, Volume: 13 Topics: Adult; Alleles; Arginine; ATP-Binding Cassette Transporters; Chromosomes, Human, Pair 1; Cytogenetic Analysis; Fathers; Female; Gene Dosage; Haplotypes; Heterozygote; Humans; Karyotyping; Leucine; Macular Degeneration; Male; Microsatellite Repeats; Mutation; Uniparental Disomy	2007
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

Article

Year

Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease.

Molecular vision, 2007, Jan-26, Volume: 13

Topics: Adult; Alleles; Arginine; ATP-Binding Cassette Transporters; Chromosomes, Human, Pair 1; Cytogenetic Analysis; Fathers; Female; Gene Dosage; Haplotypes; Heterozygote; Humans; Karyotyping; Leucine; Macular Degeneration; Male; Microsatellite Repeats; Mutation; Uniparental Disomy

2007

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