phenylalanine has been researched along with Epiphora in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bönnemann, C; Brockmann, K; Gärtner, J; Huebner, A; Kind, B; Koehler, K; Krumbholz, M | 1 |
| Dingerdissen, H; Karagiannis, K; Mazumder, R; Motwani, M; Simonyan, V | 1 |
2 other study(ies) available for phenylalanine and Epiphora
| Article | Year |
|---|---|
Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.
Topics: Amino Acid Substitution; DNA Mutational Analysis; Female; HeLa Cells; Humans; Lacrimal Apparatus Diseases; Leucine; Muscular Atrophy; Musculoskeletal Abnormalities; Nerve Tissue Proteins; Nuclear Pore Complex Proteins; Peripheral Nervous System Diseases; Phenylalanine; Point Mutation; Syndrome; Transfection | 2008 |
Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.
Topics: Abnormalities, Multiple; Amino Acid Substitution; Arginine; Aspartic Acid; Carbohydrate Metabolism; Catalytic Domain; Cluster Analysis; Enzyme Activation; Genetic Variation; Genome, Human; Glycogen Storage Disease; Hearing Loss; Histidine; Humans; Lacrimal Apparatus Diseases; Metabolomics; Molecular Sequence Annotation; Phenylalanine; Polymorphism, Single Nucleotide; Proteome; Proteomics; Structure-Activity Relationship; Syndactyly; Tooth Abnormalities; Tyrosine | 2013 |