serine has been researched along with Hemochromatosis in 3 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.
Hemochromatosis: A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Hereditary HFE Hemochromatosis is an inherited disorder of iron metabolism that results from mutations in the HFE gene." | 1.37 | Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal). ( Brehm, A; Spínola, C; Spínola, H, 2011) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Oliveira, VC | 1 |
| Caxito, FA | 1 |
| Gomes, KB | 1 |
| Castro, AM | 1 |
| Pardini, VC | 1 |
| Ferreira, AC | 1 |
| Spínola, C | 1 |
| Brehm, A | 1 |
| Spínola, H | 1 |
| Ellory, JC | 1 |
| Hall, AC | 1 |
| Ody, SA | 1 |
| Poli de Figueiredos, CE | 1 |
| Chalder, S | 1 |
| Stuart, J | 1 |
3 other studies available for serine and Hemochromatosis
| Article | Year |
|---|---|
Frequency of the S65C mutation in the hemochromatosis gene in Brazil.
Topics: Adult; Aged; Amino Acid Substitution; Brazil; Cysteine; Female; Gene Frequency; Hemochromatosis; Hem | 2009 |
Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
Topics: Adolescent; Adult; Amino Acid Substitution; Aspartic Acid; Cysteine; Gene Frequency; Genotype; Hemoc | 2011 |
KCl cotransport in HbAA and HbSS red cells: activation by intracellular acidity and disappearance during maturation.
Topics: Anemia, Sickle Cell; Biological Transport; Bumetanide; Carrier Proteins; Choline; Dehydration; Eryth | 1991 |