arginine has been researched along with Autistic Disorder in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (66.67) | 29.6817 |
2010's | 2 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Abruzzo, PM; Anwar, A; Bolotta, A; Ghezzo, A; Marini, M; Pasha, S; Posar, A; Rabbani, N; Rajpoot, K; Thornalley, PJ; Visconti, P | 1 |
Comoletti, D; De Jaco, A; King, CC; Taylor, P | 1 |
Bolliger, MF; Boucard, AA; Carter, AS; Ko, J; Maher, TA; Milunsky, JM; Newton, S; Powell, CM; Südhof, TC; Tager-Flusberg, H; Zhang, C; Zhao, G | 1 |
Ben-Omran, T; El-Fishawy, P; Ercan-Sencicek, AG; Gabriel, S; Gleeson, JG; Gupta, AR; Harris, RA; Hashem, HS; Hashish, AF; Kara, M; Kayserili, H; Khalil, RO; Matern, D; Meguid, NA; Novarino, G; Rahimi, Y; Sanders, SJ; Schroth, J; Scott, EM; Silhavy, JL; State, MW; Sweetman, L | 1 |
Afridi, SK; Chih, B; Clark, L; Scheiffele, P | 1 |
Colman, RF; Cowley, D; McGown, I; Patterson, D; Sivendran, S; Spiegel, E | 1 |
6 other study(ies) available for arginine and Autistic Disorder
Article | Year |
---|---|
Advanced glycation endproducts, dityrosine and arginine transporter dysfunction in autism - a source of biomarkers for clinical diagnosis.
Topics: Amino Acid Transport Systems, Basic; Arginine; Autistic Disorder; Biomarkers; Child; Female; Glycation End Products, Advanced; Humans; Lysine; Machine Learning; Male; Oxidative Stress; Sensitivity and Specificity; Tyrosine | 2018 |
Trafficking of cholinesterases and neuroligins mutant proteins. An association with autism.
Topics: Acetylcholinesterase; Arginine; Autistic Disorder; Butyrylcholinesterase; Cell Adhesion Molecules, Neuronal; Cell Line; Cysteine; Humans; Membrane Proteins; Mutation; Nerve Tissue Proteins; Protein Transport | 2008 |
A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; Autistic Disorder; Carrier Proteins; Cell Adhesion Molecules, Neuronal; Cell Line; Child, Preschool; Chlorocebus aethiops; COS Cells; Endoplasmic Reticulum; Female; Humans; Male; Membrane Proteins; Mice; Molecular Sequence Data; Mutation, Missense; Protein Folding; Protein Transport; Tryptophan | 2009 |
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy.
Topics: 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Adolescent; Amino Acids, Branched-Chain; Animals; Arginine; Autistic Disorder; Base Sequence; Brain; Child; Child, Preschool; Diet; Epilepsy; Female; Homozygote; Humans; Intellectual Disability; Male; Mice; Mice, Knockout; Molecular Sequence Data; Mutation; Pedigree; Phosphorylation; Protein Folding; Protein Structure, Tertiary; RNA, Messenger; Young Adult | 2012 |
Disorder-associated mutations lead to functional inactivation of neuroligins.
Topics: Animals; Arginine; Aspartic Acid; Autistic Disorder; Carrier Proteins; Cell Adhesion Molecules, Neuronal; Chlorocebus aethiops; COS Cells; Genetic Predisposition to Disease; Hippocampus; Humans; Intellectual Disability; Membrane Proteins; Mutation, Missense; Nerve Tissue Proteins; Neurons; Point Mutation; Protein Transport | 2004 |
Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the equivalent mutant Bacillus subtilis ASL.
Topics: Adenosine Monophosphate; Adenylosuccinate Lyase; Amino Acid Sequence; Arginine; Aspartic Acid; Autistic Disorder; Bacillus subtilis; Circular Dichroism; DNA; Electrophoresis, Polyacrylamide Gel; Family Health; Female; Glutamic Acid; Heterozygote; Hot Temperature; Humans; Hydrogen-Ion Concentration; Kinetics; Male; Models, Chemical; Models, Molecular; Molecular Sequence Data; Mothers; Mutagenesis, Site-Directed; Mutation; Polymerase Chain Reaction; Protein Binding; Sequence Analysis, DNA; Sequence Homology, Amino Acid; Spectrophotometry; Temperature; Thermotoga maritima; Time Factors; Ultraviolet Rays | 2004 |