threonine has been researched along with Nervous System Diseases in 9 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (22.22) | 18.7374 |
1990's | 2 (22.22) | 18.2507 |
2000's | 3 (33.33) | 29.6817 |
2010's | 1 (11.11) | 24.3611 |
2020's | 1 (11.11) | 2.80 |
Authors | Studies |
---|---|
Alosco, ML; Aparicio, HJ; Ashton, NJ; Au, R; Blennow, K; Budson, AE; Frank, B; Goldstein, LE; Jun, GR; Karikari, TK; Killiany, R; Kowall, NW; Martin, B; McKee, AC; Mez, J; Morrison, MS; Palmisano, JN; Qiu, WQ; Stein, TD; Steinberg, EG; Stern, RA; Sugarman, MA; Tripodis, Y; Turk, KW; Zetterberg, H | 1 |
Bianco, AC; Deng, Y; Egri, P; Farkas, E; Fekete, C; Gereben, B; Jo, S; Li, Y; Mash, DC; McAninch, EA; Mohácsik, P; Patti, ME; Peeters, RP; Preite, NZ; Zevenbergen, C | 1 |
Cook, SA; Fletcher, CF; Frankel, WN; Herrup, K; Hosford, DA; Letts, VA; Lutz, CM; Miki, T; Mori, Y; Wakamori, M; Zwingman, TA | 1 |
Drenth, JP; Guillet, G; Jansen, JB; Kirby, RL; Taieb, A; te Morsche, RH | 1 |
Aarnoudse, AL; Dieleman, J; Ligthelm, RJ; Molokhia, M; Overbosch, D; Stricker, BH; van der Heiden, IP; van Riemsdijk, MM; van Schaik, RH | 1 |
Indrieri, RJ; Morris, JG; Rogers, QR; Titchenal, CA | 1 |
Castagne, V; Gyger, M; Maire, JC | 1 |
Montini, M; Ongaro, A; Simonutti, M | 1 |
Altland, K; Benson, MD; Koeppen, AH; Wallace, MR | 1 |
1 review(s) available for threonine and Nervous System Diseases
Article | Year |
---|---|
Neurotoxicology and amino acid intake during development: the case of threonine.
Topics: Amino Acids; Animals; Behavior; Behavior, Animal; Brain; Female; Humans; Nervous System Diseases; Nutritional Requirements; Pregnancy; Prenatal Exposure Delayed Effects; Rats; Teratogens; Threonine | 1996 |
1 trial(s) available for threonine and Nervous System Diseases
Article | Year |
---|---|
[Controlled clinical study and clinico-psychological evaluation of a preparation with neurotrophic effects].
Topics: Aged; Arginine; Clinical Trials as Topic; Drug Combinations; Drug Evaluation; Female; Glutamine; Humans; Male; Mental Disorders; Middle Aged; Nervous System Diseases; Organophosphorus Compounds; Serine; Threonine; Tryptophan; Vitamin B 12 | 1977 |
7 other study(ies) available for threonine and Nervous System Diseases
Article | Year |
---|---|
Ante-mortem plasma phosphorylated tau (181) predicts Alzheimer's disease neuropathology and regional tau at autopsy.
Topics: Alzheimer Disease; Amyloid beta-Peptides; Autopsy; Biomarkers; Humans; Nervous System Diseases; tau Proteins; Threonine | 2022 |
Prevalent polymorphism in thyroid hormone-activating enzyme leaves a genetic fingerprint that underlies associated clinical syndromes.
Topics: Adult; Alanine; Amino Acid Substitution; Case-Control Studies; Cerebral Cortex; Gene Frequency; HEK293 Cells; HeLa Cells; Humans; Iodide Peroxidase; Iodothyronine Deiodinase Type II; Male; Microarray Analysis; Nervous System Diseases; Oxidative Stress; Polymorphism, Single Nucleotide; Syndrome; Threonine; Thyroid Diseases; Transcriptome | 2015 |
Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.
Topics: Alanine; Animals; Animals, Newborn; Calbindins; Calcium Channels, N-Type; Cells, Cultured; Cysteine; Disease Models, Animal; Glycine; Green Fluorescent Proteins; Ion Channel Gating; Membrane Potentials; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Mutant Strains; Models, Molecular; Mutation; Nervous System Diseases; Patch-Clamp Techniques; Purkinje Cells; S100 Calcium Binding Protein G; Silver Staining; Threonine; Tyrosine 3-Monooxygenase | 2008 |
SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels.
Topics: Adult; Alanine; Conserved Sequence; Cysteine; Erythromelalgia; Female; Genes, Dominant; Heterozygote; Humans; Male; Mutation; Mutation, Missense; NAV1.7 Voltage-Gated Sodium Channel; Nervous System Diseases; Pedigree; Polymorphism, Genetic; Sodium Channels; Threonine | 2005 |
MDR1 gene polymorphisms are associated with neuropsychiatric adverse effects of mefloquine.
Topics: Adult; Aged; Antimalarials; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 1; Confidence Intervals; Cysteine; Female; Gene Frequency; Genes, MDR; Glycine; Haplotypes; Humans; Male; Mefloquine; Mental Disorders; Middle Aged; Nervous System Diseases; Odds Ratio; Organic Anion Transporters; Polymorphism, Genetic; Reference Values; Threonine; Travel; White People | 2006 |
Threonine imbalance, deficiency and neurologic dysfunction in the kitten.
Topics: Amino Acids; Animals; Cats; Deficiency Diseases; Forelimb; Lameness, Animal; Movement Disorders; Nervous System Diseases; Nutritional Requirements; Specific Pathogen-Free Organisms; Threonine | 1980 |
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 |