cysteine has been researched along with Deficiency, Mental in 24 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 15 (62.50) | 18.7374 |
| 1990's | 3 (12.50) | 18.2507 |
| 2000's | 2 (8.33) | 29.6817 |
| 2010's | 2 (8.33) | 24.3611 |
| 2020's | 2 (8.33) | 2.80 |
| Authors | Studies |
|---|---|
| Ades, L; Aleksic, B; Bertoli-Avella, AM; Briere, LC; Dias, KR; Karageorgou, V; Khan, S; Kushima, I; Mancini, GMS; Ordonez, N; Popescu, CA; Roscioli, T; Schot, R; Sleutels, FJGT; Smits, DJ; Sweetser, DA; van der Kaay, DCM; Van Esch, H; Van Mol, C | 1 |
| Ostojic, SM | 1 |
| Chang, CC; Chang, WN; Chen, C; Chen, CF; Huang, CW; Huang, SH; Lu, CH; Lui, CC; Tu, MC; Wang, JJ | 1 |
| Farooq, A; McDonald, CB; Sudol, M | 1 |
| Capone, A; Dailey, W; Drenser, K; Trese, M; Wu, WC | 1 |
| Aldahmesh, MA; Khan, AO; Meyer, B | 1 |
| Irreverre, F; Laster, L; Mudd, SH | 1 |
| Ancker, U; Hellner, KA; Hübner, C; Lenk, U; Oexle, K; Speer, A; Voit, T | 1 |
| Fowler, B; Law, EA | 1 |
| Achatz, H; Berger, W; Cremers, F; Dörner, C; Gal, A; Haasemann, M; Hellebrand, H; Meindl, A; Meitinger, T; van de Pol, D | 1 |
| Bain, M; Chalmers, R; Hammond, J; Jones, M; Patton, MA; Sharland, M | 1 |
| Donnell, GN; Koch, R; Lieberman, E; Shaw, KN | 1 |
| Crawhall, JC; Purkiss, P; Stanbury, JB | 1 |
| Jenner, FA | 1 |
| Ben-Ami, E; Burstein, I; Cohen, BE; Szeinberg, A | 1 |
| Ampola, MG; Bixby, EM; Efron, ML; Meshorer, E | 1 |
| Bir, K; Crawhall, JC; Purkiss, P; Stanbury, JB | 1 |
| Chiang-Teng, C; Clark, SH; Dassell, SW; Scott, CR; Swedberg, KR | 1 |
| Ampola, MG; Bixby, EM; Crawhall, JC; Efron, ML; Parker, R; Sneddon, W; Young, EP | 1 |
| Komrower, GM; Schwarz, V; Wong, PW | 1 |
| Copeland, W; Kelly, S | 1 |
| Humbel, R; Kutter, D | 1 |
| Crawhall, JC; Parker, R; Sneddon, W; Young, EP | 1 |
| Finkelstein, JD; Irreverre, F; Laster, L; Mudd, SH | 1 |
1 review(s) available for cysteine and Deficiency, Mental
| Article | Year |
|---|---|
Molecular insights into the WW domain of the Golabi-Ito-Hall syndrome protein PQBP1.
Topics: Amino Acid Sequence; Carrier Proteins; Cysteine; Disulfides; DNA-Binding Proteins; Humans; Intellectual Disability; Ligands; Molecular Sequence Data; Mutation; Nuclear Proteins; Oxygen; Protein Binding; Protein Conformation; Protein Structure, Tertiary; RNA, Messenger; Sequence Homology, Amino Acid; Syndrome | 2012 |
23 other study(ies) available for cysteine and Deficiency, Mental
| Article | Year |
|---|---|
De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues.
Topics: Autism Spectrum Disorder; Cell Cycle Proteins; Cysteine; DNA Helicases; Humans; Intellectual Disability; Microcephaly; Minichromosome Maintenance Complex Component 6; Neurodevelopmental Disorders; Phenotype; Zinc | 2023 |
Upregulation of AGAT as a Possible Target in Molecular Nutrition.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Cysteine; Developmental Disabilities; Dietary Supplements; Humans; Intellectual Disability; Nutrition Therapy; Speech Disorders; Up-Regulation | 2020 |
Multi-parametric neuroimaging evaluation of cerebrotendinous xanthomatosis and its correlation with neuropsychological presentations.
Topics: Adult; Brain; Case-Control Studies; Cognition Disorders; Cysteine; Diffusion Tensor Imaging; Female; Follow-Up Studies; Humans; Image Processing, Computer-Assisted; Imaging, Three-Dimensional; Intellectual Disability; Magnetic Resonance Imaging; Male; Middle Aged; Organotechnetium Compounds; Tomography, Emission-Computed, Single-Photon; Xanthomatosis, Cerebrotendinous | 2010 |
Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene.
Topics: Amino Acid Sequence; Blindness; Child, Preschool; Cysteine; Deafness; DNA Mutational Analysis; Eye Diseases, Hereditary; Eye Proteins; Female; Genotype; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Molecular Sequence Data; Mutation; Nerve Tissue Proteins; Phenotype; Polymerase Chain Reaction; Retina; Vitreoretinopathy, Proliferative | 2007 |
Correlation of ophthalmic examination with carrier status in females potentially harboring a severe Norrie disease gene mutation.
Topics: Cysteine; Diagnostic Techniques, Ophthalmological; Eye Proteins; Female; Genes, Recessive; Genetic Diseases, X-Linked; Hearing Loss, Sensorineural; Heterozygote; Humans; Intellectual Disability; Male; Molecular Biology; Mutation; Nerve Tissue Proteins; Pedigree; Phenylalanine; Prospective Studies; Retinal Diseases; Severity of Illness Index; Vitreoretinopathy, Proliferative | 2008 |
Sulfite oxidase deficiency in man: demonstration of the enzymatic defect.
Topics: Brain; Cysteine; Cytochromes; Humans; Hydro-Lyases; In Vitro Techniques; Infant; Intellectual Disability; Kidney; Lens, Crystalline; Liver; Male; Metabolism, Inborn Errors; Nervous System Malformations; Oxidoreductases; Sulfates; Sulfites; Thiosulfates; Transferases | 1967 |
A cysteine 3340 substitution in the dystroglycan-binding domain of dystrophin associated with Duchenne muscular dystrophy, mental retardation and absence of the ERG b-wave.
Topics: Binding Sites; Child; Cysteine; Cytoskeletal Proteins; DNA Mutational Analysis; Dystroglycans; Dystrophin; Electroretinography; Humans; Intellectual Disability; Male; Membrane Glycoproteins; Muscle Fibers, Skeletal; Muscle, Skeletal; Muscular Dystrophies; Point Mutation; Retina; Sarcolemma | 1996 |
Beta-mercaptolactate cysteine disulphiduria in a mentally retarded Scottish male.
Topics: Abnormalities, Multiple; Adult; Amino Acid Metabolism, Inborn Errors; Cataract; Chromatography, Ion Exchange; Chromatography, Paper; Chromatography, Thin Layer; Chromosome Aberrations; Chromosome Disorders; Consanguinity; Cysteine; Disulfides; Genes, Recessive; Humans; Intellectual Disability; Lactates; Male; Scotland; Sulfhydryl Compounds | 1976 |
Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins.
Topics: Adult; Amino Acid Sequence; Base Sequence; Blindness; Child; Child, Preschool; Chromosome Mapping; Cysteine; Deafness; DNA; DNA Mutational Analysis; Exons; Genetic Linkage; Humans; Infant; Intellectual Disability; Introns; Male; Molecular Sequence Data; Mucins; Point Mutation; Sequence Homology, Amino Acid; X Chromosome | 1992 |
Balanced translocation (14;20) in a mentally handicapped child with cystinuria.
Topics: Child, Preschool; Chromosomes, Human, Pair 14; Chromosomes, Human, Pair 20; Cysteine; Cystinuria; Female; Heterozygote; Humans; Intellectual Disability; Translocation, Genetic; White People | 1992 |
Cystathioninuria.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carcinoma, Hepatocellular; Child, Preschool; Cysteine; Diet Therapy; Female; Galactosemias; Glycogen; Humans; Infant; Intellectual Disability; Liver Neoplasms; Male; Maple Syrup Urine Disease; Methionine; Middle Aged; Neuroblastoma; Phenylketonurias; Portal Vein; Pyridoxine; Serine; Sulfisoxazole; Tyrosine | 1967 |
Metabolism of sulfur-containing amino acids in a patient excreting -mercaptolactate-cysteine disulfide.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Autoanalysis; Carbon Isotopes; Cysteine; Cystine; Disulfides; Humans; Intellectual Disability; Lactates; Male; Methionine; Sulfur; Sulfur Isotopes; Taurine; Time Factors | 1973 |
Medical research council unit for metabolic studies in psychiatry, Sheffield.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Bipolar Disorder; Catatonia; Circadian Rhythm; Cysteine; Humans; Intellectual Disability; Lithium; Mass Spectrometry; Mental Disorders; Metabolism, Inborn Errors; Periodicity; Phenylketonurias; Sleep; Vasopressins | 1973 |
Cysteine peptiduria in a mentally retarded patient.
Topics: Adolescent; Amino Acids; Autoanalysis; Chromatography, Ion Exchange; Chromatography, Paper; Cysteine; Electrophoresis, Paper; Follow-Up Studies; Glycine; Humans; Intellectual Disability; Ligands; Male; Peptides | 1973 |
Mental deficiency and a new aminoaciduria.
Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Paper; Cysteine; Electrocardiography; Electroencephalography; Eye Abnormalities; Humans; Infections; Intellectual Disability; Intelligence Tests; Male; Middle Aged; Neurologic Examination; Radiography; Seizures; Sulfhydryl Compounds; Sulfides | 1969 |
Sulfur amino acids as precursors of beta-mercaptolactate-cysteine disulfide in human subjects.
Topics: Adult; Anilides; Cysteine; Diet; Dietary Proteins; Disulfides; Electrophoresis; Female; Humans; Intellectual Disability; Lactates; Male; Metabolism; Methionine; Models, Biological; Neomycin; Phthalic Acids; Pyridoxine; Sulfates; Sulfathiazoles; Sulfur; Taurine; Thiosulfates | 1971 |
Cystathioninemia: a benign genetic condition.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Butyrates; Child; Child, Preschool; Congenital Abnormalities; Cysteine; Female; Homozygote; Humans; Intellectual Disability; Keto Acids; Male; Methionine; Pyridoxine | 1970 |
Beta mercaptolactate-cysteine disulfide: analog of cystine in the urine of a mentally retarded patient.
Topics: Amino Acid Metabolism, Inborn Errors; Chemistry, Clinical; Chromatography, Ion Exchange; Cyanides; Cysteine; Cystine; Electrophoresis; Ferrocyanides; Humans; Indicators and Reagents; Intellectual Disability; Lactates; Middle Aged; Spectrum Analysis; Sulfhydryl Compounds | 1968 |
The biosynthesis of cystathionine in patients with homocystinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Brain; Child; Child, Preschool; Chromatography, Ion Exchange; Cysteine; Diet Therapy; Homocystinuria; Humans; Hydro-Lyases; Intellectual Disability; Liver; Rats; Serine; Sulfur Isotopes | 1968 |
A hypothesis on the homocystinuric's response to pyridoxine.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Chemistry, Clinical; Cysteine; Homocystinuria; Humans; Intellectual Disability; Male; Penicillamine; Pyridoxine | 1968 |
Screening for sulfite oxidase deficiency.
Topics: Amino Acids; Chromatography, Thin Layer; Cysteine; Drug Stability; Humans; Intellectual Disability; Mass Screening; Metabolism, Inborn Errors; Methods; Oxidoreductases; Sulfites; Thiosulfates | 1969 |
Beta-mercaptolactate-cysteine disulfide in the urine of a mentally retarded patient.
Topics: Amino Acid Metabolism, Inborn Errors; Chemical Phenomena; Chemistry; Cysteine; Electrophoresis; Humans; Infrared Rays; Intellectual Disability; Spectrophotometry; Sulfhydryl Compounds; Sulfides | 1969 |
Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine.
Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Ion Exchange; Cysteine; Humans; Hydro-Lyases; Intellectual Disability; Liver; Methionine; Sulfates; Urine | 1965 |