serine has been researched along with Deficiency, Factor 10 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.
| 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 Deficiency, Factor 10
| 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 |