serine has been researched along with Factor X Deficiency in 4 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.
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 | 2 (50.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Au, WY | 1 |
| Lam, CC | 1 |
| Cheung, WC | 1 |
| Kwong, YL | 1 |
| Jayandharan, G | 1 |
| Viswabandya, A | 1 |
| Baidya, S | 1 |
| Nair, SC | 1 |
| Shaji, RV | 1 |
| George, B | 1 |
| Chandy, M | 1 |
| Srivastava, A | 1 |
| Bezeaud, A | 1 |
| Miyata, T | 2 |
| Helley, D | 1 |
| Zeng, YZ | 1 |
| Kato, H | 2 |
| Aillaud, MF | 1 |
| Juhan-Vague, I | 1 |
| Guillin, MC | 1 |
| Kojima, T | 1 |
| Suzuki, K | 1 |
| Umeyama, H | 1 |
| Yamazaki, T | 1 |
| Kamiya, T | 1 |
| Toyoda, H | 1 |
4 other studies available for serine and Factor X Deficiency
| Article | Year |
|---|---|
Two novel factor X gene mutations in a Chinese family with factor X deficiency.
Topics: Adult; Amino Acid Substitution; Asian People; Base Sequence; Blood Coagulation Tests; Cytosine; Fact | 2004 |
Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin.
Topics: Arginine; Codon, Nonsense; CpG Islands; DNA Mutational Analysis; DNA Primers; Epitopes; Exons; Facto | 2005 |
Functional consequences of the Ser334-->Pro mutation in a human factor X variant (factor XMarseille).
Topics: Animals; Base Sequence; Calcium; Cattle; DNA; DNA Primers; Factor Va; Factor X; Factor X Deficiency; | 1995 |
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 |