cytosine has been researched along with Impaired Glucose Tolerance in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "A cytosine deletion was identified by genomic DNA sequencing of the apo A-I gene of the patient at the third base of codon 184 in the fourth exon, which led to a frame shift mutation and early termination at codon 200." | 1.31 | Apolipoprotein A-I deficiency with accumulated risk for CHD but no symptoms of CHD. ( Hashimoto, Y; Kawamura, M; Kitamura, K; Kotani, K; Mashige, F; Nakahara, K; Okubo, S; Shimada, S; Usuki, Y; Yokota, H; Yumoto, M, 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 |
|---|---|
| Yokota, H | 1 |
| Hashimoto, Y | 1 |
| Okubo, S | 1 |
| Yumoto, M | 1 |
| Mashige, F | 1 |
| Kawamura, M | 1 |
| Kotani, K | 1 |
| Usuki, Y | 1 |
| Shimada, S | 1 |
| Kitamura, K | 1 |
| Nakahara, K | 1 |
1 other study available for cytosine and Impaired Glucose Tolerance
| Article | Year |
|---|---|
Apolipoprotein A-I deficiency with accumulated risk for CHD but no symptoms of CHD.
Topics: Aged; Amino Acid Sequence; Apolipoprotein A-I; Apolipoproteins E; Base Sequence; Cholesterol, HDL; C | 2002 |