glycine has been researched along with Factor X Deficiency in 2 studies
Factor X Deficiency: Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Miyata, T | 1 |
| Kojima, T | 1 |
| Suzuki, K | 1 |
| Umeyama, H | 1 |
| Yamazaki, T | 1 |
| Kamiya, T | 1 |
| Toyoda, H | 1 |
| Kato, H | 1 |
| Yin, J | 1 |
| Wang, H | 1 |
| Wang, X | 1 |
2 other studies available for glycine and Factor X Deficiency
| Article | Year |
|---|---|
Factor X Nagoya 1 and Nagoya 2: a CRM- factor X deficiency and a dysfunctional CRM+ factor X deficiency characterized by substitution of Arg306 by Cys and of Gly366 by Ser, respectively.
Topics: Adult; Aged; Alleles; Cysteine; Factor X; Factor X Deficiency; Female; Glycine; Humans; Point Mutati | 1998 |
[Clotting factor X deficiency resulted from an T 58-->G mutation within exon 1 of human factor X gene].
Topics: Base Sequence; Exons; Factor X; Factor X Deficiency; Glycine; Humans; Male; Middle Aged; Mutation, M | 2001 |