glycine has been researched along with Christmas Disease in 6 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "A patient with severe haemophilia B with a glycine-to-valine missense mutation at residue 190 (c25, chymotrypsin numbering) in factor IX (FIX; FIX-G190V or FIX-FuChou) had <1% of normal FIX clotting activity and 36% of normal FIX antigen levels (cross-reacting material- reduced, CRMr)." | 1.37 | Characterisation of factor IX with a glycine-to-valine missense mutation at residue 190 in a patient with severe haemophilia B. ( Hamaguchi, N; Kao, CY; Kao, JT; Lin, CN; Lin, SW; Shen, MC; Yang, SJ; Yang, YL, 2011) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 2 (33.33) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lu, Q | 1 |
| Yang, L | 1 |
| Manithody, C | 1 |
| Wang, X | 1 |
| Rezaie, AR | 1 |
| Kao, CY | 1 |
| Lin, CN | 2 |
| Yang, YL | 1 |
| Hamaguchi, N | 3 |
| Yang, SJ | 1 |
| Shen, MC | 3 |
| Kao, JT | 1 |
| Lin, SW | 3 |
| Smith, KJ | 2 |
| Larson, PJ | 1 |
| Stanfield-Oakley, SA | 1 |
| VanDusen, WJ | 1 |
| Kasper, CK | 1 |
| Monroe, DM | 1 |
| High, KA | 1 |
| Wu, PC | 1 |
| Yu, YS | 1 |
| Breckenridge, RT | 1 |
| Ratnoff, OD | 1 |
1 review available for glycine and Christmas Disease
| Article | Year |
|---|---|
Therapy of hereditary disorders of blood coagulation.
Topics: Abdomen, Acute; Afibrinogenemia; Blood Coagulation Disorders; Blood Transfusion; Cerebral Hemorrhage | 1968 |
5 other studies available for glycine and Christmas Disease
| Article | Year |
|---|---|
Expression and Characterization of Gly-317 Variants of Factor IX Causing Variable Bleeding in Hemophilia B Patients.
Topics: Amino Acid Substitution; Cysteine Endopeptidases; Enzyme Activation; Enzyme Precursors; Factor IX; F | 2015 |
Characterisation of factor IX with a glycine-to-valine missense mutation at residue 190 in a patient with severe haemophilia B.
Topics: Animals; Benzamidines; Factor IX; Gene Transfer Techniques; Glycine; HEK293 Cells; Hemophilia B; Hum | 2011 |
Characterization of a factor IX variant with a glycine207 to glutamic acid mutation.
Topics: Benzamidines; Binding Sites; Calcium; Codon; Computer Simulation; Electrophoresis, Polyacrylamide Ge | 1994 |
Structural integrity of the gamma-carboxyglutamic acid domain of human blood coagulation factor IXa Is required for its binding to cofactor VIIIa.
Topics: Adenine; Amino Acid Sequence; Arginine; Base Sequence; Binding Sites; DNA; DNA Mutational Analysis; | 1996 |
Hemophilia B with mutations at glycine-48 of factor IX exhibited delayed activation by the factor VIIa-tissue factor complex.
Topics: Animals; Blood Coagulation; Cattle; Factor IX; Factor VII; Glycine; Hemophilia B; Humans; Point Muta | 2000 |