نتایج جستجو برای: MVK mechanism

تعداد نتایج: 565512  

2017
Ekaterina Kazieva Yoko Yamamoto Yoshinori Tajima Keiichi Yokoyama Joanna Katashkina Yousuke Nishio

The inhibition of mevalonate kinase (MVK) by downstream metabolites is an important mechanism in the regulation of isoprenoid production in a broad range of organisms. The first feedback-resistant MVK was previously discovered in the methanogenic archaeon Methanosarcinamazei. Here, we report the cloning, expression, purification, kinetic characterization and inhibition analysis of MVKs from two...

2013
P. Renard

This discussion paper is/has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP if available. Abstract It is now accepted that one of the important pathways of Secondary Organic Aerosol (SOA) formation occurs through aqueous phase chemistry in the atmosphere. However , the liquid phase chemical mechanisms leading to ma...

Journal: :Advanced Materials Interfaces 2023

Abstract First‐principles computations are performed to investigate the catalytic oxidation of CO on a Ti‐decorated Cr 2 TiC O MXene monolayer, through comprehensive analysis charge transfer, electronic density states, and difference interacting systems. By comparing reaction energy barriers, it is found that, rather than traditional Langmuir–Hinshelwood, Eley–Rideal, Mars‐van Krevelen (MvK) me...

2015
B. Ervens P. Renard S. Tlili S. Ravier J.-L. Clément

Laboratory experiments of efficient oligomerization from methyl vinyl ketone (MVK) in the bulk aqueous phase were simulated in a box model. Kinetic data are applied (if known) or fitted to the observed MVK decay and oligomer mass increase. Upon model sensitivity studies, in which unconstrained rate constants were varied over several orders of magnitude, a set of reaction parameters was found th...

Journal: :The FEBS journal 2008
Anil K Nair Matthew A Young K M J Menon

We have shown that hormone-induced downregulation of luteinizing hormone receptor (LHR) in the ovary is post-transcriptionally regulated by an mRNA binding protein. This protein, later identified as mevalonate kinase (MVK), binds to the coding region of LHR mRNA, suppresses its translation, and the resulting ribonucleoprotein complex is targeted for degradation. Mutagenesis and crystallographic...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2017
Paola Maura Tricarico Alessandra Romeo Rossella Gratton Sergio Crovella Fulvio Celsi

BACKGROUND/AIMS Mevalonate Kinase Deficiency (MKD), is a hereditary disease due to mutations in mevalonate kinase gene (MVK). MKD has heterogeneous clinical phenotypes: the correlation between MVK mutations and MKD clinical phenotype is still to be fully elucidated. Deficiency of prenylated proteins has been hypothesized as possible MKD pathogenic mechanism. Based on this hypothesis and conside...

Journal: :Journal of Physical Chemistry C 2021

Introducing a catalyst for dehydrogenation of ethane (EDH) steam cracking represents promising solution with high feasibility to realize efficient ethylene production. We investigated EDH over transition-metal-doped CeO2 catalysts at 873 K in the presence steam. Ce0.8Co0.2O2 exhibited activity and selectivity (ca. 95%). In absence H2O, catalytic dropped rapidly, indicating promotive effect H2O ...

2016
Laurent Messer Ghada Alsaleh Philippe Georgel Raphael Carapito Hans R Waterham Nassim Dali-Youcef Siamak Bahram Jean Sibilia

OBJECTIVE Mevalonate kinase (MVK) deficiency is a rare autosomal recessive auto-inflammatory disorder characterised by recurring episodes of fever associated with multiple non-specific inflammatory symptoms and caused by mutations in the MVK gene. The phenotypic spectrum is wide and depends mostly on the nature of the mutations. Hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS) is a...

2009
M. Harel-Meir Y. Bujanover Y. Anikster

Mevalonic aciduria (MVA) is an inborn error of isoprene biosynthesis caused by mevalonate kinase (MVK) gene mutations. Described below is a case of a Palestinian MVA patient suffering from prolonged fevers as well as from hepatic fibrosis a rare feature of MVA. Also demonstrated is a unique genotype heterozigosity of two novel MVK mutations; V8F (t25a), and F38I (t112a).

2013
Elena Tsitsami Charis Papadopoulou Matthaios Speletas

Hyperimmunoglobulinemia D syndrome is a rare autosomal recessive autoinflammatory disorder caused by mutations in the mevalonate kinase gene (MVK). In a proportion of patients, however, no MVK mutations are detected. Although various standard anti-inflammatory drugs have been tried, until now there is no consensus about how HIDS should be treated. We present a case of HIDS in an 8-year-old girl...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید