phenylalanine has been researched along with Amyloidosis, Hereditary in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Connors, LH; Costello, CE; Lim, A; McComb, ME; Prokaeva, T; Skinner, M | 1 |
| Farsian, FN; Igarashi, P; Naderi, AS | 1 |
| Bergesio, F; Del Pace, S; Frusconi, S; Miliani, A; Minuti, B; Pelo, E; Perfetto, F; Tarquini, R; Torricelli, F | 1 |
3 other study(ies) available for phenylalanine and Amyloidosis, Hereditary
| Article | Year |
|---|---|
Identification of S-sulfonation and S-thiolation of a novel transthyretin Phe33Cys variant from a patient diagnosed with familial transthyretin amyloidosis.
Topics: Amino Acid Sequence; Amyloidosis, Familial; Cysteine; Female; Humans; Middle Aged; Molecular Sequence Data; Mutation, Missense; Oxidative Stress; Peptide Mapping; Phenylalanine; Prealbumin; Protein Conformation; Sequence Analysis, DNA; Spectrometry, Mass, Electrospray Ionization; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | 2003 |
Gastrointestinal amyloidosis associated with transthyretin Phe64Ser mutation.
Topics: Adult; Amino Acid Substitution; Amyloidosis, Familial; Codon; Cytosine; DNA; Exons; Female; Gastrointestinal Diseases; Humans; Male; Pedigree; Phenylalanine; Polymorphism, Single Nucleotide; Prealbumin; Serine; Thymine | 2007 |
A new ATTR Phe64Ile mutation with late-onset multiorgan involvement.
Topics: Aged; Amyloidosis, Familial; Base Sequence; Cardiomyopathies; Codon; DNA Mutational Analysis; Echocardiography; Exons; Humans; Isoleucine; Male; Molecular Sequence Data; Mutation, Missense; Phenylalanine; Prealbumin | 2007 |