serine has been researched along with Deficiency, Protein C in 3 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yu, T | 1 |
| Dai, J | 1 |
| Liu, H | 1 |
| Wang, J | 1 |
| Ding, Q | 1 |
| Wang, H | 1 |
| Wang, X | 1 |
| Fu, Q | 1 |
| Gandrille, S | 1 |
| Jude, B | 1 |
| Alhenc-Gelas, M | 1 |
| Emmerich, J | 1 |
| Aiach, M | 1 |
| Wittmann, E | 1 |
| Walter, J | 1 |
| Pabinger-Fasching, I | 1 |
| Watzke, HH | 1 |
3 other studies available for serine and Deficiency, Protein C
| Article | Year |
|---|---|
Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutation.
Topics: Animals; Blood Coagulation; Chlorocebus aethiops; Consanguinity; COS Cells; DNA Mutational Analysis; | 2012 |
First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletion.
Topics: Adult; Alleles; Amino Acid Sequence; Base Sequence; Exons; Female; Gene Deletion; Globins; Humans; I | 1994 |
Symptomatic hereditary type-II protein C deficiency caused by a missense mutation in exon IX of the protein C gene (Gly381 to Ser).
Topics: Adult; Amino Acid Sequence; Base Sequence; Binding Sites; Female; Genotype; Humans; Male; Molecular | 1994 |