leucine has been researched along with Night Blindness in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Azam, M; Collin, RW; Cremers, FP; den Hollander, AI; Hussain, A; Kersten, FF; Keunen, JE; Khan, MI; Kremer, H; Qamar, R; Shah, ST | 1 |
| Achatz, H; Andreasson, S; Berger, W; Brandau, O; Feil, S; Hardcastle, A; Jacobi, FK; Maurer, J; Meindl, A; Pesch, K; Pinckers, A; Pusch, CM; Scharfe, C; Wissinger, B; Zeitz, C | 1 |
| Bech-Hansen, NT; Bergen, AA; Birch, DG; Drack, AV; Gal, A; Jacobson, SG; Koop, B; Maybaum, TA; Musarella, MA; Naylor, MJ; Polomeno, RC; Prinsen, CF; Sparkes, RL; Weleber, RG; Young, RS | 1 |
| Berson, EL; Dryja, TP; Rosner, B; Sandberg, MA; Weigel-DiFranco, C | 1 |
4 other study(ies) available for leucine and Night Blindness
| Article | Year |
|---|---|
CLRN1 mutations cause nonsyndromic retinitis pigmentosa.
Topics: Adult; Audiometry, Pure-Tone; Consanguinity; DNA; Electroretinography; Fundus Oculi; Genes, Recessive; Genetic Linkage; Humans; Intracellular Space; Leucine; Membrane Proteins; Microarray Analysis; Mutation, Missense; Night Blindness; Polymorphism, Single Nucleotide; Proline; Retinitis Pigmentosa; Tissue Distribution; Tryptophan; Young Adult | 2011 |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
Topics: Amino Acid Motifs; Amino Acid Sequence; Brain; Chromosome Mapping; DNA Mutational Analysis; DNA, Complementary; Electroretinography; Eye Proteins; Female; Gene Expression Profiling; Genes; Genetic Heterogeneity; Genetic Markers; Glycosylphosphatidylinositols; Humans; Kidney; Leucine; Male; Models, Molecular; Molecular Sequence Data; Multigene Family; Muscle Proteins; Muscles; Nerve Tissue Proteins; Night Blindness; Organ Specificity; Pedigree; Protein Conformation; Proteoglycans; Repetitive Sequences, Amino Acid; Retina; Reverse Transcriptase Polymerase Chain Reaction; Sequence Deletion; Sequence Homology, Amino Acid; Testis; X Chromosome | 2000 |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
Topics: Adult; Amino Acid Motifs; Amino Acid Sequence; DNA Mutational Analysis; DNA, Complementary; Expressed Sequence Tags; Eye Proteins; Gene Expression Profiling; Genes; Glycosylphosphatidylinositols; Humans; Interneurons; Kidney; Leucine; Male; Molecular Sequence Data; Night Blindness; Organ Specificity; Pedigree; Proteoglycans; Repetitive Sequences, Amino Acid; Retina; Retinal Ganglion Cells; Sequence Alignment; Sequence Homology, Amino Acid; Synaptic Transmission; Vision, Ocular; X Chromosome | 2000 |
Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine.
Topics: Adolescent; Adult; Amino Acid Sequence; Chromosome Aberrations; Chromosome Disorders; Dark Adaptation; Electroretinography; Female; Fundus Oculi; Humans; Leucine; Male; Middle Aged; Molecular Sequence Data; Mutation; Night Blindness; Pedigree; Proline; Retinitis Pigmentosa; Rhodopsin; Visual Fields | 1991 |