cytosine has been researched along with Hyperhomocysteinemia in 6 studies
Hyperhomocysteinemia: Condition in which the plasma levels of homocysteine and related metabolites are elevated (
| Excerpt | Relevance | Reference |
|---|---|---|
| "Certain mutations (TT homozygous; CT heterozygous; CC wild-type) of the methylenetetrahydrofolate (MTHFR) gene and long-term levodopa application in patients with Parkinson's disease (PD) support onset of hyperhomocysteinemia." | 7.72 | MTHFR C677T polymorphism, folic acid and hyperhomocysteinemia in levodopa treated patients with Parkinson's disease. ( Kuhn, W; Müller, T; Woitalla, D, 2004) |
| "Certain mutations (TT homozygous; CT heterozygous; CC wild-type) of the methylenetetrahydrofolate (MTHFR) gene and long-term levodopa application in patients with Parkinson's disease (PD) support onset of hyperhomocysteinemia." | 3.72 | MTHFR C677T polymorphism, folic acid and hyperhomocysteinemia in levodopa treated patients with Parkinson's disease. ( Kuhn, W; Müller, T; Woitalla, D, 2004) |
| "The aim of this study was to investigate a possible association among the thermolabile polymorphism, nucleotide 677 cytosine to thymidine point mutation (677 C-->T) of the methylenetetrahydrofolate reductase (MTHFR) gene, hyperhomocysteinemia, serum folate, vitamins B12 and B6, and stroke in children." | 3.70 | Children with stroke: polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin status. ( Artuch, R; Campistol, J; Cardo, E; Colomé, C; Monrós, E; Pineda, M; Vilaseca, MA, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 6 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Woitalla, D | 1 |
| Kuhn, W | 1 |
| Müller, T | 1 |
| Parodi, MB | 1 |
| Di Crecchio, L | 1 |
| Gonzalez-Porras, JR | 1 |
| Martin-Herrero, F | 1 |
| Garcia-Sanz, R | 1 |
| Lopez, ML | 1 |
| Balanzategui, A | 1 |
| Mateos, MV | 1 |
| Pavon, P | 1 |
| Gonzalez, M | 1 |
| Alberca, I | 1 |
| San Miguel, JF | 1 |
| Cardo, E | 1 |
| Monrós, E | 1 |
| Colomé, C | 1 |
| Artuch, R | 1 |
| Campistol, J | 1 |
| Pineda, M | 1 |
| Vilaseca, MA | 1 |
| Couturaud, F | 1 |
| Oger, E | 1 |
| Abalain, JH | 1 |
| Chenu, E | 1 |
| Guias, B | 1 |
| Floch, HH | 1 |
| Mercier, B | 1 |
| Mottier, D | 1 |
| Leroyer, C | 1 |
| Mainou Cid, C | 1 |
| García Giralt, N | 1 |
| Vilaseca Buscà, MA | 1 |
| Ferrer Codina, I | 1 |
| Meco López, JF | 1 |
| Mainou Pintó, A | 1 |
| Pintó Sala, X | 1 |
| Grinberg Vaisman, D | 1 |
| Balcells Comas, S | 1 |
6 other studies available for cytosine and Hyperhomocysteinemia
| Article | Year |
|---|---|
MTHFR C677T polymorphism, folic acid and hyperhomocysteinemia in levodopa treated patients with Parkinson's disease.
Topics: Adult; Aged; Aged, 80 and over; Analysis of Variance; Cytosine; Female; Folic Acid; Humans; Hyperhom | 2004 |
Hyperhomocysteinemia in central retinal vein occlusion in young adults.
Topics: Adult; Case-Control Studies; Cytosine; Female; Genetic Predisposition to Disease; Homozygote; Humans | 2003 |
Hyperhomocysteinemia is a risk factor of recurrent coronary event in young patients irrespective to the MTHFR C677T polymorphism.
Topics: Acute Disease; Adult; Age Factors; Body Mass Index; Cohort Studies; Coronary Disease; Cytosine; Fema | 2007 |
Children with stroke: polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin status.
Topics: Adolescent; Case-Control Studies; Child; Child, Preschool; Cytosine; Female; Folic Acid; Genetic Pre | 2000 |
Methylenetetrahydrofolate reductase C677T genotype and venous thromboembolic disease.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Case-Control Studies; Cytosine; Factor V; Female; France | 2000 |
[Hyperhomocystinemia and 677C T methylenetetrahydrofolate reductase polymorphism as a cardiovascular risk factor in childhood].
Topics: Adolescent; Age Factors; Child; Child, Preschool; Coronary Disease; Cross-Sectional Studies; Cytosin | 2002 |