threonine has been researched along with Amyloidosis in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (11.11) | 18.7374 |
| 1990's | 4 (44.44) | 18.2507 |
| 2000's | 2 (22.22) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Maitra, S; Vincent, B | 1 |
| Frosch, MP; Greenberg, SM; Nakagawa, K; Sheikh, SI; Snuderl, M | 1 |
| Hanin, G; Podoly, E; Soreq, H | 1 |
| Iwata, M; Matsumura, M; Shimizu, Y; Takeuchi, M; Tokuda, T | 1 |
| Booth, DR; Frustaci, A; Hawkins, PN; Pepys, MB; Tan, SY | 1 |
| De Grandis, D; Ferlini, A; Jacobson, DR; Patrosso, MC; Salvi, F; Vezzoni, P | 1 |
| Canet, D; Dobson, CM; Last, AM; Miranker, A; Robinson, CV; Spencer, A; Sunde, M | 1 |
| Ackermann, A; Baumal, R; Wilson, B | 1 |
| Altland, K; Benson, MD; Koeppen, AH; Wallace, MR | 1 |
2 review(s) available for threonine and Amyloidosis
| Article | Year |
|---|---|
Cdk5-p25 as a key element linking amyloid and tau pathologies in Alzheimer's disease: Mechanisms and possible therapeutic interventions.
Topics: Alzheimer Disease; Amyloid beta-Protein Precursor; Amyloidosis; Calpain; Cyclin-Dependent Kinase 5; Humans; Phosphorylation; Serine; tau Proteins; Threonine | 2022 |
Alanine-to-threonine substitutions and amyloid diseases: butyrylcholinesterase as a case study.
Topics: Alanine; Amino Acid Substitution; Amyloidosis; Animals; Butyrylcholinesterase; Disease; Humans; Threonine | 2010 |
7 other study(ies) available for threonine and Amyloidosis
| Article | Year |
|---|---|
A new Thr49Pro transthyretin gene mutation associated with leptomeningeal amyloidosis.
Topics: Amyloidosis; DNA Mutational Analysis; Humans; Magnetic Resonance Imaging; Male; Meninges; Middle Aged; Mutation; Prealbumin; Proline; Threonine | 2008 |
A case of biopsy-proven leptomeningeal amyloidosis and intravenous Ig-responsive polyneuropathy associated with the Ala25Thr transthyretin gene mutation.
Topics: Alanine; Amino Acid Substitution; Amyloid Neuropathies; Amyloidosis; Brain; Brain Stem; Cerebellum; Humans; Immunoglobulins, Intravenous; Male; Meninges; Middle Aged; Point Mutation; Prealbumin; Threonine | 2006 |
A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.
Topics: Amyloidosis; Angina Pectoris; Cardiomyopathies; DNA; Exons; Female; Genes, Dominant; Genetic Variation; Humans; Italy; Lysine; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Polymerase Chain Reaction; Prealbumin; Threonine | 1995 |
Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis.
Topics: Aged; Amyloidosis; DNA Mutational Analysis; Female; Humans; Italy; Male; Middle Aged; Pedigree; Point Mutation; Polymerase Chain Reaction; Prealbumin; Threonine | 1998 |
Mechanistic studies of the folding of human lysozyme and the origin of amyloidogenic behavior in its disease-related variants.
Topics: Amyloid; Amyloidosis; Aspartic Acid; Histidine; Humans; Isoleucine; Kinetics; Mass Spectrometry; Models, Molecular; Muramidase; Protein Folding; Protons; Recombinant Proteins; Spectrometry, Fluorescence; Threonine | 1999 |
Immunoglobulin biosynthesis in myeloma-associated and casein- and endotoxin-induced murine amyloidosis.
Topics: Amyloid; Amyloidosis; Animals; Carbon Radioisotopes; Caseins; Endotoxins; Fluorescent Antibody Technique; Immune Sera; Immunoglobulins; Kidney; Leucine; Lipopolysaccharides; Liver; Lung; Lymphocytes; Mice; Mice, Inbred Strains; Multiple Myeloma; Myocardium; Plasma Cells; Salmonella typhi; Spleen; Threonine; Tritium; Valine | 1975 |
Familial amyloid polyneuropathy: alanine-for-threonine substitution in the transthyretin (prealbumin) molecule.
Topics: Adult; Aged; Alanine; Amyloidosis; Blotting, Southern; DNA; Female; Humans; Isoelectric Focusing; Male; Myocardium; Nervous System Diseases; Pedigree; Prealbumin; Retinol-Binding Proteins; Threonine | 1990 |