pteridines has been researched along with Syndrome in 4 studies
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Arachnomelia syndrome is an autosomal recessive inherited disease in cattle." | 5.37 | Arachnomelia syndrome in Simmental cattle is caused by a homozygous 2-bp deletion in the molybdenum cofactor synthesis step 1 gene (MOCS1). ( Buitkamp, J; Götz, KU; Semmer, J, 2011) |
| "Arachnomelia syndrome is an autosomal recessive inherited disease in cattle." | 1.37 | Arachnomelia syndrome in Simmental cattle is caused by a homozygous 2-bp deletion in the molybdenum cofactor synthesis step 1 gene (MOCS1). ( Buitkamp, J; Götz, KU; Semmer, J, 2011) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Buitkamp, J | 1 |
| Semmer, J | 1 |
| Götz, KU | 1 |
| Serrano, M | 1 |
| Lizarraga, I | 1 |
| Reiss, J | 1 |
| Dias, AP | 1 |
| Pérez-Dueñas, B | 1 |
| Vilaseca, MA | 1 |
| Artuch, R | 1 |
| Campistol, J | 1 |
| García-Cazorla, A | 1 |
| Roth, A | 1 |
| Nogues, C | 1 |
| Monnet, JP | 1 |
| Ogier, H | 1 |
| Saudubray, JM | 1 |
| Sahota, A | 1 |
| Leeming, R | 1 |
| Blair, J | 1 |
| Hagberg, B | 1 |
4 other studies available for pteridines and Syndrome
| Article | Year |
|---|---|
Arachnomelia syndrome in Simmental cattle is caused by a homozygous 2-bp deletion in the molybdenum cofactor synthesis step 1 gene (MOCS1).
Topics: Animals; Cattle; Cattle Diseases; Chromosome Mapping; Coenzymes; Gene Deletion; Homozygote; Metallop | 2011 |
Cranial ultrasound and chronological changes in molybdenum cofactor deficiency.
Topics: Atrophy; Brain Diseases; Calcinosis; Coenzymes; Echoencephalography; Humans; Infant, Newborn; Male; | 2007 |
Anatomo-pathological findings in a case of combined deficiency of sulphite oxidase and xanthine oxidase with a defect of molybdenum cofactor.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Brain; Child, Preschool; Coenzymes; Femal | 1985 |
Tetrahydrobiopterin metabolism in the Rett disease.
Topics: Biopterins; Child; Dihydropteridine Reductase; Female; Humans; Intellectual Disability; NADH, NADPH | 1985 |