thymine has been researched along with Cardiomyopathies, Primary in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chalabreysse, L | 1 |
| Senni, F | 1 |
| Bruyère, P | 1 |
| Aime, B | 1 |
| Ollagnier, C | 1 |
| Bozio, A | 1 |
| Bouvagnet, P | 1 |
| Campos, Y | 1 |
| García, A | 1 |
| del Hoyo, P | 1 |
| Jara, P | 1 |
| Martín, MA | 1 |
| Rubio, JC | 1 |
| Berbel, A | 1 |
| Barberá, JR | 1 |
| Ribacoba, R | 1 |
| Astudillo, A | 1 |
| Cabello, A | 1 |
| Ricoy, JR | 1 |
| Arenas, J | 1 |
| Uemichi, T | 1 |
| Gertz, MA | 1 |
| Benson, MD | 1 |
| Hahner, A | 1 |
| Erdmann, J | 1 |
| Kallisch, H | 1 |
| Fleck, E | 1 |
| Regitz-Zagrosek, V | 1 |
4 other studies available for thymine and Cardiomyopathies, Primary
| Article | Year |
|---|---|
A new hypo/oligodontia syndrome: Carvajal/Naxos syndrome secondary to desmoplakin-dominant mutations.
Topics: Adolescent; Amino Acid Sequence; Anodontia; Arrhythmogenic Right Ventricular Dysplasia; Bicuspid; Ca | 2011 |
Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypes.
Topics: Acidosis, Lactic; Adenine; Adult; Biopsy; Cardiomyopathies; Cytosine; DNA, Mitochondrial; Female; Gu | 2003 |
A new transthyretin variant (Ser 24) associated with familial amyloid polyneuropathy.
Topics: Aged; Amyloid Neuropathies; Cardiomyopathies; Codon; Cytosine; DNA; Exons; Family Health; Female; Ge | 1995 |
Identification of genetic variants (g789C>T and G111S) in the human HSPB2 gene.
Topics: Amino Acid Substitution; Cardiomyopathies; Crystallins; Cytosine; Glycine; Heat-Shock Proteins; Huma | 2001 |