adenosine has been researched along with Intellectual Disability in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (57.14) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Bell, R; Feuk, L; Fu, D; Hagelskamp, F; Halvardson, J; Kellner, SM; Kuchinskaya, E; Phelan, B; Proven, M; Ramos, J; Thuresson, AC | 1 |
| Bahi-Buisson, N; Benoist, JF; Ceballos-Picot, I; Desguerre, I; Gitiaux, C; Marie, S; Rio, M; Valayannopoulos, V; Verrieres, S; Vincent, MF | 1 |
| Arnout, J; Eyssen, M; Freson, K; Hoylaerts, MF; Jaeken, J; Van Geet, C; Vermylen, J | 1 |
| Atkin, J; Rundle, AT; Sudell, B | 1 |
| Bradshaw, C; Francke, U; Kernahan, C | 1 |
| Clothier, B; Rundle, AT; Sudell, B | 1 |
| Nyhan, WL; Sweetman, L | 1 |
7 other study(ies) available for adenosine and Intellectual Disability
| Article | Year |
|---|---|
Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorder.
Topics: Active Transport, Cell Nucleus; Adenosine; Adenosine Deaminase; Adolescent; Binding Sites; Cells, Cultured; Child; Child, Preschool; Codon, Terminator; Exome Sequencing; Female; Genetic Predisposition to Disease; Humans; Inosine; Intellectual Disability; Male; Mutation, Missense; Pedigree; Protein Domains; RNA-Binding Proteins; RNA, Transfer | 2020 |
Misleading behavioural phenotype with adenylosuccinate lyase deficiency.
Topics: Adenosine; Adenylosuccinate Lyase; Aminoimidazole Carboxamide; Angelman Syndrome; Behavior; Child; Chromatography, High Pressure Liquid; Consanguinity; Female; Humans; Intellectual Disability; Mutation, Missense; Pedigree; Phenotype; Purine-Pyrimidine Metabolism, Inborn Errors; Ribonucleotides; Sequence Analysis, DNA; Stereotyped Behavior | 2009 |
Genetic variation of the extra-large stimulatory G protein alpha-subunit leads to Gs hyperfunction in platelets and is a risk factor for bleeding.
Topics: Abnormalities, Multiple; Adenosine; Adenylyl Cyclases; Adolescent; Alprostadil; Alternative Splicing; Amino Acid Sequence; Amino Acid Substitution; Bleeding Time; Blood Platelets; Child; Chromogranins; Cyclic AMP; Female; Fingers; Gene Frequency; Genomic Imprinting; GTP-Binding Protein alpha Subunits, Gs; Hemorrhagic Disorders; Heterotrimeric GTP-Binding Proteins; Humans; Hyperkinesis; Hypoparathyroidism; Iloprost; Intellectual Disability; Male; Molecular Sequence Data; Muscle Hypotonia; Mutagenesis, Insertional; Nerve Tissue Proteins; Phenotype; Platelet Aggregation; Platelet Function Tests; Polymorphism, Genetic; Protein Subunits; Repetitive Sequences, Amino Acid; Risk Factors; Second Messenger Systems; Structure-Activity Relationship; Wounds and Injuries | 2001 |
Serum and tissue proteins in tuberous sclerosis. I. Serum and red-cell polymorphic systems.
Topics: Acid Phosphatase; Adenosine; Adult; Alanine Transaminase; Alkaline Phosphatase; Aminohydrolases; Blood Proteins; Erythrocytes; Female; Gene Frequency; Glycoproteins; Haptoglobins; Humans; Intellectual Disability; Leucyl Aminopeptidase; Male; Phenotype; Phosphoglucomutase; Phosphogluconate Dehydrogenase; Phosphotransferases; Polymorphism, Genetic; Tuberous Sclerosis | 1975 |
Del (10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studies.
Topics: Abnormalities, Multiple; Adenosine; Alanine Transaminase; Aminohydrolases; Blood Group Antigens; Blood Proteins; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, 6-12 and X; Cytogenetics; Dermatoglyphics; Erythrocytes; Esterases; Female; Growth Disorders; Head; Heterozygote; Humans; Intellectual Disability; Karyotyping; Polymorphism, Genetic; Syndrome | 1975 |
Haptoglobin phenotype frequencies in mentally retarded persons.
Topics: Acid Phosphatase; Adenine Nucleotides; Adenosine; Alanine Transaminase; Aminohydrolases; Blood Protein Electrophoresis; Blood Proteins; Electrophoresis, Starch Gel; Female; Haptoglobins; Humans; Immunodiffusion; Intellectual Disability; Isoenzymes; L-Lactate Dehydrogenase; Liver Function Tests; Male; Phenotype; Phenytoin; Phosphoglucomutase; Phosphogluconate Dehydrogenase; Phosphotransferases; Primidone | 1972 |
Detailed comparison of the urinary excretion of purines in a patient with the Lesch-Nyhan syndrome and a control subject.
Topics: Adenine; Adenosine; Athetosis; Child; Chromatography, Gel; Chromatography, Ion Exchange; Formamides; Formates; Humans; Hypoxanthines; Imidazoles; Intellectual Disability; Lesch-Nyhan Syndrome; Male; Methods; Purine-Pyrimidine Metabolism, Inborn Errors; Purines; Ribonucleosides; Self Mutilation; Spectrophotometry; Ultraviolet Rays; Xanthines | 1970 |