thymine has been researched along with Hyperplasia in 1 studies
Hyperplasia: An increase in the number of cells in a tissue or organ without tumor formation. It differs from HYPERTROPHY, which is an increase in bulk without an increase in the number of cells.
Excerpt | Relevance | Reference |
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"To confirm androgen insensitivity syndrome,t he androgen receptor gene should be analyzed for mutations, although the relationship between genotype and phenotype is weak." | 5.31 | [Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome]. ( Argente Oliver, J; González Medeiro, I; Martín Sobrino, MA; Martinez Pérez, J; Muñoz Calvo, MT; Pozo Román, J; Soriano Guillén, L, 2002) |
"To confirm androgen insensitivity syndrome,t he androgen receptor gene should be analyzed for mutations, although the relationship between genotype and phenotype is weak." | 1.31 | [Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome]. ( Argente Oliver, J; González Medeiro, I; Martín Sobrino, MA; Martinez Pérez, J; Muñoz Calvo, MT; Pozo Román, J; Soriano Guillén, L, 2002) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Soriano Guillén, L | 1 |
Muñoz Calvo, MT | 1 |
Martinez Pérez, J | 1 |
Pozo Román, J | 1 |
Martín Sobrino, MA | 1 |
González Medeiro, I | 1 |
Argente Oliver, J | 1 |
1 other study available for thymine and Hyperplasia
Article | Year |
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[Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome].
Topics: Adolescent; Androgen-Insensitivity Syndrome; Exons; Female; Humans; Hyperplasia; Karyotyping; Leydig | 2002 |