alanine has been researched along with Erythermalgia in 4 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Excerpt | Relevance | Reference |
---|---|---|
"Primary erythermalgia is a rare disorder characterized by recurrent attacks of red, warm and painful hands, and/or feet." | 1.33 | SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels. ( Drenth, JP; Guillet, G; Jansen, JB; Kirby, RL; Taieb, A; te Morsche, RH, 2005) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Yang, Y | 3 |
Huang, J | 1 |
Mis, MA | 1 |
Estacion, M | 3 |
Macala, L | 1 |
Shah, P | 1 |
Schulman, BR | 1 |
Horton, DB | 1 |
Dib-Hajj, SD | 3 |
Waxman, SG | 3 |
Benke, PJ | 1 |
Te Morsche, RH | 2 |
Eastman, EM | 1 |
Macala, LJ | 1 |
Drenth, JP | 2 |
Tyrrell, L | 1 |
Lin, Z | 1 |
Guillet, G | 1 |
Taieb, A | 1 |
Kirby, RL | 1 |
Jansen, JB | 1 |
4 other studies available for alanine and Erythermalgia
Article | Year |
---|---|
Nav1.7-A1632G Mutation from a Family with Inherited Erythromelalgia: Enhanced Firing of Dorsal Root Ganglia Neurons Evoked by Thermal Stimuli.
Topics: Alanine; Animals; Cells, Cultured; Erythromelalgia; Female; Ganglia, Spinal; Glutamine; HEK293 Cells | 2016 |
NaV1.7 gain-of-function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder mutations and produces symptoms of both disorders.
Topics: Alanine; Animals; Animals, Newborn; Cells, Cultured; Child; Dose-Response Relationship, Radiation; E | 2008 |
A new Nav1.7 mutation in an erythromelalgia patient.
Topics: Alanine; Amino Acid Sequence; Child; Erythromelalgia; Exons; Female; Ganglia, Spinal; HEK293 Cells; | 2013 |
SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels.
Topics: Adult; Alanine; Conserved Sequence; Cysteine; Erythromelalgia; Female; Genes, Dominant; Heterozygote | 2005 |