cytosine has been researched along with Inborn Errors of Metabolism in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Familial dysalbuminemic hyperthyroxinemia (FDH) is a familial autosomal dominant syndrome caused by abnormal albumin with an increased affinity for thyroxine (T4)." | 7.72 | Artifactually elevated serum-free thyroxine levels measured by equilibrium dialysis in a pregnant woman with familial dysalbuminemic hyperthyroxinemia. ( Hoshikawa, S; Ito, S; Kaise, N; Mori, K; Nakagawa, Y; Yoshida, K, 2004) |
| "Familial dysalbuminemic hyperthyroxinemia (FDH) is a familial autosomal dominant syndrome caused by abnormal albumin with an increased affinity for thyroxine (T4)." | 3.72 | Artifactually elevated serum-free thyroxine levels measured by equilibrium dialysis in a pregnant woman with familial dysalbuminemic hyperthyroxinemia. ( Hoshikawa, S; Ito, S; Kaise, N; Mori, K; Nakagawa, Y; Yoshida, K, 2004) |
| "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 | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hoshikawa, S | 1 |
| Mori, K | 1 |
| Kaise, N | 1 |
| Nakagawa, Y | 1 |
| Ito, S | 1 |
| Yoshida, K | 1 |
| 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 |
2 other studies available for cytosine and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Artifactually elevated serum-free thyroxine levels measured by equilibrium dialysis in a pregnant woman with familial dysalbuminemic hyperthyroxinemia.
Topics: Adult; Amino Acid Substitution; Arginine; Artifacts; Cytosine; Dialysis; Female; Genes, Dominant; Gu | 2004 |
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 |