Compounds > phenylalanine

phenylalanine and Amyloidosis

phenylalanine has been researched along with Amyloidosis in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (16.67)	18.7374
1990's	0 (0.00)	18.2507
2000's	3 (50.00)	29.6817
2010's	1 (16.67)	24.3611
2020's	1 (16.67)	2.80

Authors

Authors	Studies
Bharath, SR; Cracco, L; Doud, EH; Fernandez, A; Garringer, HJ; Ghetti, B; Hallinan, GI; Hoq, MR; Jacobsen, M; Jiang, W; Li, D; Mosley, AL; Ozcan, KA; Vago, FS; Vidal, R	1
Gazit, E	1
Kelly, JW; Mohamedmohaideen, NN; Palaninathan, SK; Sacchettini, JC; Snee, WC	1
Benson, MD; Dupond, JL; Gil, H; Kantelip, B; Kluve-Beckerman, B; Liepnieks, JJ; Magy, N	1
Balogh, I; Berta, A; Fazakas, F; Losonczy, G; Matesz, K; Sohajda, Z; Takács, L; Tóth, K; Vereb, G	1
Barth, WF; Decker, JL; Waldmann, TA; Willerson, JT	1

Other Studies

6 other study(ies) available for phenylalanine and Amyloidosis

Article	Year
Cryo-EM structures of prion protein filaments from Gerstmann-Sträussler-Scheinker disease. Acta neuropathologica, 2022, Volume: 144, Issue:3 Topics: Amyloid; Amyloidosis; Brain; Cryoelectron Microscopy; Gerstmann-Straussler-Scheinker Disease; Humans; Phenylalanine; Plaque, Amyloid; Prion Proteins; Prions; Protein Subunits	2022
Metabolite amyloids: a new paradigm for inborn error of metabolism disorders. Journal of inherited metabolic disease, 2016, Volume: 39, Issue:4 Topics: Amyloid; Amyloidosis; Humans; Metabolic Diseases; Metabolism, Inborn Errors; Peptides; Phenylalanine; Proteins	2016
Structural insight into pH-induced conformational changes within the native human transthyretin tetramer. Journal of molecular biology, 2008, Oct-24, Volume: 382, Issue:5 Topics: Amyloidosis; Binding Sites; Crystallography, X-Ray; Humans; Hydrogen-Ion Concentration; Models, Molecular; Mutation; Phenylalanine; Prealbumin; Protein Conformation; Protein Structure, Quaternary; Protein Structure, Secondary; Protein Subunits	2008
A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2003, Volume: 10, Issue:1 Topics: Aged; Amyloidosis; Base Sequence; Carpal Tunnel Syndrome; Humans; Male; Pedigree; Peripheral Nervous System Diseases; Phenylalanine; Point Mutation; Polymorphism, Single-Stranded Conformational; Prealbumin; Skin; Tyrosine	2003
TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis. Molecular vision, 2007, Oct-18, Volume: 13 Topics: Amino Acid Substitution; Amyloidosis; Base Sequence; Cornea; Corneal Dystrophies, Hereditary; Extracellular Matrix Proteins; Heterozygote; Humans; Hungary; Keratoplasty, Penetrating; Middle Aged; Mutation; Phenylalanine; Serine; Transforming Growth Factor beta	2007
Primary amyloidosis. Clinical, immunochemical and immunoglobulin metabolism. Studies in fifteen patients. The American journal of medicine, 1969, Volume: 47, Issue:2 Topics: Adult; Agammaglobulinemia; Amyloidosis; Bence Jones Protein; Bone Marrow; Bone Marrow Cells; Electrophoresis; Hemorrhagic Disorders; Hepatomegaly; Humans; Immunoelectrophoresis; Immunoglobulin G; Immunoglobulin M; Kidney; Male; Middle Aged; Multiple Myeloma; Phenylalanine; Salivary Glands; Serum Globulins; Tongue; Xerophthalmia; Xerostomia	1969