alanine has been researched along with Deficiency, Protein C in 2 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Excerpt | Relevance | Reference |
---|---|---|
"The role of two protein C gamma-carboxyglutamic acid domain mutations in familial thrombosis, protein CVermont (Bovill, E." | 3.69 | Molecular mechanism for familial protein C deficiency and thrombosis in protein CVermont (Glu20-->Ala and Val34-->Met). ( Bovill, EG; Long, GL; Lu, D, 1994) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Lu, D | 1 |
Bovill, EG | 1 |
Long, GL | 1 |
Kemahli, S | 1 |
Alhenc-Gelas, M | 1 |
Gandrille, S | 1 |
Aiach, M | 1 |
Akar, N | 1 |
Cin, S | 1 |
2 other studies available for alanine and Deficiency, Protein C
Article | Year |
---|---|
Molecular mechanism for familial protein C deficiency and thrombosis in protein CVermont (Glu20-->Ala and Val34-->Met).
Topics: Alanine; Base Sequence; DNA Primers; Glutamic Acid; Humans; Methionine; Molecular Sequence Data; Mut | 1994 |
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr.
Topics: Alanine; Amino Acid Substitution; Base Sequence; Consanguinity; Genetic Variation; Histidine; Homozy | 1998 |