uric acid has been researched along with Abnormalities, Autosome in 28 studies
Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The frequency of cells with chromosomal aberrations, excluding gaps, per 100 cells, increased significantly from 1." | 1.31 | Cytogenetic alterations and oxidative stress in thyroid cancer patients after iodine-131 therapy. ( Ferreira, TC; Gerber, G; Laires, A; Léonard, A; Limbert, E; Monteiro Gil, O; Oliveira, NG; Rodrigues, AS; Rueff, J, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 22 (78.57) | 18.7374 |
| 1990's | 3 (10.71) | 18.2507 |
| 2000's | 2 (7.14) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (3.57) | 2.80 |
| Authors | Studies |
|---|---|
| Bang, HI | 1 |
| Choi, IH | 1 |
| Park, R | 1 |
| Kobrinsky, NL | 1 |
| Robison, LL | 1 |
| Nesbit, ME | 1 |
| King, CM | 1 |
| Barnett, YA | 1 |
| Mayaudon, H | 1 |
| Burnat, P | 1 |
| Eulry, F | 1 |
| Payen, C | 1 |
| Dupuy, O | 1 |
| Ducorps, M | 1 |
| Bauduceau, B | 1 |
| Monteiro Gil, O | 1 |
| Oliveira, NG | 1 |
| Rodrigues, AS | 1 |
| Laires, A | 1 |
| Ferreira, TC | 1 |
| Limbert, E | 1 |
| Léonard, A | 1 |
| Gerber, G | 1 |
| Rueff, J | 1 |
| Baguette, C | 1 |
| Vermylen, C | 1 |
| Brichard, B | 1 |
| Louis, J | 1 |
| Dahan, K | 1 |
| Vincent, MF | 1 |
| Cornu, G | 1 |
| Persaud, TV | 1 |
| Kihlman, BA | 3 |
| de Vries, A | 1 |
| Sperling, O | 2 |
| Benjamin, D | 1 |
| Weinberg, A | 1 |
| Pinkhas, J | 1 |
| Sturelid, S | 1 |
| Akaoka, I | 1 |
| Nishizawa, T | 1 |
| Yano, E | 1 |
| Takeuchi, A | 1 |
| Nishida, Y | 1 |
| Andersson, HC | 1 |
| Harding, BN | 1 |
| Dunger, DB | 1 |
| Grant, DB | 1 |
| Erdohazi, M | 1 |
| Aukett, A | 1 |
| Bennett, MJ | 1 |
| Hosking, GP | 1 |
| Pant, SS | 1 |
| Moser, HW | 1 |
| Krane, SM | 1 |
| Paulson, GW | 2 |
| Nance, W | 1 |
| Son, C | 1 |
| Son, CD | 1 |
| Nance, WE | 1 |
| Howell, A | 1 |
| Mason, AS | 1 |
| Brown, E | 1 |
| Watts, RW | 1 |
| Chanarin, I | 1 |
| McPherson, K | 1 |
| Ridler, MA | 1 |
| Reed, WB | 1 |
| Nyhan, WL | 1 |
| Fox, IH | 1 |
| Meade, JC | 1 |
| Kelley, WN | 1 |
| Dipalma, JR | 1 |
| Amer, M | 1 |
| el-Shazly, M | 1 |
| Delbarre, F | 1 |
| Auscher, C | 1 |
| Amor, B | 1 |
| de Gery, A | 1 |
| Cartier, P | 1 |
| Hamet, M | 1 |
| Sarto, GE | 1 |
| Van Goor, W | 1 |
| Kooiker, CJ | 1 |
| Mees, EJ | 1 |
| Newcombe, DS | 1 |
| Shapiro, SL | 1 |
| Sheppard, GL | 1 |
| Dreifuss, FE | 1 |
3 reviews available for uric acid and Abnormalities, Autosome
| Article | Year |
|---|---|
Acute nonlymphocytic leukemia.
Topics: Acute Disease; Adolescent; Agranulocytosis; Antineoplastic Agents; Cells, Cultured; Child; Child, Pr | 1980 |
Prenatal diagnosis and its pathologic confirmation.
Topics: alpha-Fetoproteins; Amniocentesis; Amniotic Fluid; Chromosome Aberrations; Chromosome Disorders; Cre | 1976 |
The Lesch-Nyhan syndrome.
Topics: Allopurinol; Animals; Brain; Chromosome Aberrations; Chromosome Disorders; Guanine; Humans; Hypoxant | 1973 |
25 other studies available for uric acid and Abnormalities, Autosome
| Article | Year |
|---|---|
Bone Marrow Gouty Tophi With Plasma Cell Myeloma.
Topics: Aged; Arthritis, Gouty; Bone Marrow; Chromosome Aberrations; Crystallization; Female; Humans; Immuno | 2020 |
Oxidative stress and human ageing.
Topics: Adult; Age Factors; Aged; Aging; Antioxidants; Bilirubin; Cells, Cultured; Chromosome Aberrations; D | 1995 |
[Hereditary xanthinuria, rare cause of hypo-uric acidemia. 2 cases].
Topics: Adult; Aged; Chromosome Aberrations; Chromosome Disorders; Female; Genes, Recessive; Humans; Kidney | 1998 |
Cytogenetic alterations and oxidative stress in thyroid cancer patients after iodine-131 therapy.
Topics: Adult; Aged; Chromosome Aberrations; Female; Humans; Iodine Radioisotopes; Lymphocytes; Male; Micron | 2000 |
Persistent developmental delay despite successful bone marrow transplantation for purine nucleoside phosphorylase deficiency.
Topics: Alternative Splicing; Amino Acid Substitution; Bone Marrow Transplantation; Chromosome Aberrations; | 2002 |
1,3,7,9-tetramethyluric acid--a chromosome-damaging agent occurring as a natural metabolite in certain caffeine-producing plants.
Topics: Adenosine Triphosphate; Animals; Caffeine; Cells, Cultured; Chromatids; Chromosome Aberrations; Chro | 1977 |
Inborn hypouricemia due to isolated renal tubular defect.
Topics: Adult; Calcium; Chromosome Aberrations; Chromosome Disorders; Female; Glomerular Filtration Rate; Hu | 1979 |
Familial hypouricemia due to isolated renal tubular abnormality.
Topics: Chromosome Aberrations; Chromosome Disorders; Genes, Recessive; Humans; Male; Middle Aged; Probeneci | 1978 |
Enhancement by methylated oxypurines of the frequency of induced chromosomal aberrations.
Topics: Animals; Caffeine; Cell Line; Cells, Cultured; Chromosome Aberrations; Chromosomes; Cricetinae; Drug | 1975 |
Familial hypouricaemia due to renal tubular defect of urate transport.
Topics: Adult; Chromosome Aberrations; Chromosome Disorders; Circadian Rhythm; Creatinine; Humans; Male; Ped | 1975 |
Enhancement and reduction by methylated oxypurines of the frequencies of chromatid aberrations induced by camptothecin in root-tip cells of Vicia faba.
Topics: Caffeine; Camptothecin; Chromatids; Chromosome Aberrations; Dose-Response Relationship, Drug; Methyl | 1992 |
Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.
Topics: Brain; Chromosome Aberrations; Chromosome Disorders; Creatinine; Failure to Thrive; Female; Genes, R | 1988 |
Molybdenum co-factor deficiency: an easily missed inborn error of metabolism.
Topics: Aldehyde Oxidase; Aldehyde Oxidoreductases; Chromosome Aberrations; Chromosome Disorders; Coenzymes; | 1988 |
Hyperuricemia in Down's syndrome.
Topics: Adolescent; Adult; Age Factors; Aged; Chemistry, Clinical; Child; Child, Preschool; Chromosome Aberr | 1968 |
Neurologic aspects of typical and atypical Down's syndrome.
Topics: Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Down Syndrome; Electroencepha | 1968 |
Neurologic aspects of typical and atypical Down's syndrome.
Topics: Cataract; Chromosome Aberrations; Down Syndrome; Gait; Humans; Hydroxyindoleacetic Acid; Intelligenc | 1969 |
Red cell size and uric acid in Down's syndrome.
Topics: Bone Marrow Cells; Child; Child, Preschool; Chromosome Aberrations; Cobalt Radioisotopes; Creatinine | 1973 |
[Genetic aspects in dermatology].
Topics: Adult; Alopecia; Amino Acid Metabolism, Inborn Errors; Athetosis; Carotid Body Tumor; Chorea; Chromo | 1970 |
Adenine phosphoribosyltransferase deficiency in man. Report of a second family.
Topics: Adenine; Adenosine Triphosphate; Cells, Cultured; Chromosome Aberrations; Chromosome Disorders; Eryt | 1973 |
Pharmacogenetics.
Topics: Abnormalities, Drug-Induced; Allopurinol; Barbiturates; Chromosome Aberrations; Drug-Related Side Ef | 1974 |
The association of familial hyperbetalipoproteinaemia with Waardenburg's syndrome.
Topics: Abnormalities, Multiple; Adolescent; Adult; Blood Glucose; Child; Cholesterol; Chromosome Aberration | 1974 |
Gout with adenine phosphoribosyl transferase deficiency.
Topics: Adenine; Adolescent; Adult; Aged; Allopurinol; Carbon Radioisotopes; Child; Child, Preschool; Chromo | 1974 |
Prenatal diagnosis of genetic disorders by amniocentesis.
Topics: Adult; Amniotic Fluid; Athetosis; Chorea; Chromosome Aberrations; Chromosome Disorders; Compulsive B | 1970 |
An unusual form of renal disease associated with gout and hypertension.
Topics: Adolescent; Adult; Aged; Biopsy; Cerebrovascular Disorders; Chromosome Aberrations; Chromosome Disor | 1971 |
Treatment of x-linked primary hyperuricemia with allopurinol.
Topics: Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Enzyme Therapy; Hematuria; Humans; M | 1966 |