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MVK gene

Known as: MEVALONATE KINASE, mevalonic aciduria, LH receptor mRNA-binding protein 
National Institutes of Health

Papers overview

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2018
2018
of the 3-hydroxy-3-methylglutaryl coenzyme A (HMGCoA) reductase gene, which had been previeusly isolated by complementation. By… 
2015
2015
Hyperimmunoglobulin D syndrome is a rare autosomal recessive inherited disease characterized by fever attacks, which may be… 
2014
2014
The bilateral primary renal lymphoma (PRL) is a rare disease with a high mortality rate (75% within the first year). We report… 
2013
2013
Abstract: Sweet’s Syndrome, also known as acute febrile neutrophilic dermatosis, is a rare condition with poorly defined… 
2009
2009
Sirs, We observed a 12-year-old boy affected by hyper-IgD syndrome (HIDS) who was successfully treated with etanercept, but… 
2009
2009
Mevalonic aciduria (MVA) is an inborn error of isoprene biosynthesis caused by mevalonate kinase (MVK) gene mutations. Described… 
2009
2009
Structural Studies of Terpenoid Biosynthesis and Bacterial Cell Division. (August 2006) Dong Yang, B.S., Zhe Jiang University… 
2007
2007
Objective To investigate whether the increased interleukin (IL)-1β and IFN-γ secretion in hyperimmunoglobulinemia D and periodic… 
2004