HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

mevalonate kinase

Mvk Rat RefSeq NM_031063
Also Known As:
ATP-mevalonate 5-phosphotransferase; ERG12 protein, S cerevisiae; LH receptor mRNA-binding protein, human; LHR mRNA binding protein, rat; LRBP protein, human; LRBP protein, rat; MVK protein, human; MvK protein, S cerevisiae; Mvk protein, mouse; Mvk protein, rat; RAR1 protein, S cerevisiae; mevalonate 5-phosphotransferase; mevalonate kinase protein, human; mevalonate kinase protein, mouse; mevalonate kinase protein, rat
Networked: 137 relevant articles (0 outcomes, 3 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Waterham, Hans R: 8 articles (01/2016 - 10/2002)
2. Crovella, Sergio: 7 articles (01/2017 - 07/2010)
3. Waterham, H R: 7 articles (10/2010 - 04/2000)
4. Frenkel, Joost: 6 articles (02/2014 - 07/2002)
5. Frenkel, J: 6 articles (12/2002 - 04/2000)
6. Houten, S M: 6 articles (12/2002 - 04/2000)
7. Houten, Sander M: 5 articles (07/2006 - 10/2002)
8. Wanders, Ronald J A: 5 articles (07/2006 - 10/2002)
9. Wanders, R J: 5 articles (05/2001 - 04/2000)
10. Simon, Anna: 4 articles (01/2019 - 11/2008)

Related Diseases

1. Familial Mediterranean Fever (Periodic Disease)
07/01/2014 - "There was no mutation of the familial Mediterranean fever gene and a diagnosis of partial mevalonate kinase (MVK) deficiency was made. "
07/01/2020 - "In this study, we report homozygote mutations in mevalonate kinase and familial Mediterranean fever genes in a recurrent Kawasaki disease with coronary dilatation."
01/01/2016 - "Mutations in the genes encoding pyrin and mevalonate kinase (MVK) cause distinct interleukin-1β (IL-1β)-mediated autoinflammatory diseases: familial Mediterranean fever (FMF) and hyperimmunoglobulinemia D syndrome (HIDS). "
09/01/2011 - "As autoinflammatory diseases now include TRAPS (TNF receptor-associated periodic syndrome), CAPS (cryopyrin -associated periodic syndromes), FMF(familial Mediterranean fever), MAPS (mevalonate kinase-associated periodic fever syndrome, hyper-IgD syndrome) and many others, and show symptoms and signs of wide variations, we need to make an accurate diagnosis of them to prevent possible complications such as amyloidosis."
08/01/2010 - "These include familial Mediterranean fever due to mutations in the Mediterranean fever (MEFV) gene, hyperimmunoglobulinemia D syndrome due to mutations in the MK gene for mevalonate kinase, cryopyrinopathies such as Muckle-Wells syndrome or neonatal-onset multisystemic inflammatory disease (neonatal-onset multisystemic inflammatory disease or chronic infantile neurological cutaneous and articular (CINCA)) associated with cold-induced autoinflammatory syndrome 1 gene mutations, and tumor necrosis factor receptor-associated periodic syndrome due to mutation of TNF receptor I gene. "
2. Methylmalonic acidemia
3. Ankylosing Spondylitis
4. Mucocutaneous Lymph Node Syndrome (Kawasaki Disease)
5. Coronary Disease (Coronary Heart Disease)

Related Drugs and Biologics

1. Vitamin B 12 (Cyanocobalamin)
2. Lipids
3. Enzymes
4. Terpenes (Terpenoids)
5. Cholesterol
6. Immunoglobulin D (IgD)
7. Mevalonic Acid (Mevalonate)
8. Proteins (Proteins, Gene)
9. isoprene
10. HDL Cholesterol

Related Therapies and Procedures

1. Therapeutics