نتایج جستجو برای: mtrr

تعداد نتایج: 307  

Journal: :Journal of bacteriology 2009
Jason P Folster Paul J T Johnson Lydgia Jackson Vijaya Dhulipali David W Dyer William M Shafer

The MtrR transcriptional-regulatory protein is known to repress transcription of the mtrCDE operon, which encodes a multidrug efflux pump possessed by Neisseria gonorrhoeae that is important in the ability of gonococci to resist certain hydrophobic antibiotics, detergents, dyes, and host-derived antimicrobials. In order to determine whether MtrR can exert regulatory action on other gonococcal g...

2015
Paul J. T. Johnson William M. Shafer

MtrR is a well-characterized repressor of the Neisseria gonorrhoeae mtrCDE efflux pump operon. However, results from a previous transcriptional profiling study suggested that MtrR also represses or activates expression of at least sixty genes outside of the mtr locus. Evidence that MtrR can directly repress so-called "off target" genes has previously been reported; in particular, MtrR was shown...

Journal: :Cell 2013
Nisha Padmanabhan Dongxin Jia Colleen Geary-Joo Xuchu Wu Anne C. Ferguson-Smith Ernest Fung Mark C. Bieda Floyd F. Snyder Roy A. Gravel James C. Cross Erica D. Watson

The importance of maternal folate consumption for normal development is well established, yet the molecular mechanism linking folate metabolism to development remains poorly understood. The enzyme methionine synthase reductase (Mtrr) is necessary for utilization of methyl groups from the folate cycle. We found that a hypomorphic mutation of the mouse Mtrr gene results in intrauterine growth res...

2014
Boyi Yang Shujun Fan Xueyuan Zhi Da Wang Yongfang Li Yinuo Wang Yanxun Wang Jian Wei Quanmei Zheng Guifan Sun

Prior evidence indicates that homocysteine plays a role in the development of metabolic syndrome (MetS). Methylenetetrahydrofolate reductase (MTHFR) C677T and methionine synthase reductase (MTRR) A66G polymorphisms are common genetic determinants of homocysteine levels. To investigate the associations of the MTHFR C677T and MTRR A66G polymorphisms with MetS, 692 Chinese Han subjects with MetS a...

Journal: :Journal of the neurological sciences 2007
A L Szvetko J Fowdar J Nelson N Colson L Tajouri P A Csurhes M P Pender L R Griffiths

Multiple sclerosis (MS) is a complex neurological disease that affects the central nervous system (CNS) resulting in debilitating neuropathology. Pathogenesis is primarily defined by CNS inflammation and demyelination of nerve axons. Methionine synthase reductase (MTRR) is an enzyme that catalyzes the remethylation of homocysteine (Hcy) to methionine via cobalamin and folate dependant reactions...

2012
Jae-Young Yoo Sook-Young Kim Jung-Ah Hwang Seung-Hyun Hong Aesun Shin Il Ju Choi Yeon-Su Lee

Gastric cancer is ranked as the most common cancer in Koreans. A recent molecular biological study about the folate pathway gene revealed the correlation with a couple of cancer types. In the folate pathway, several genes are involved, including methylenetetrahydrofolate reductase (MTHFR), methyltetrahydrofolate-homocysteine methyltransferase reductase (MTRR), and methyltetrahydrofolate-homocys...

2017
Ping Wang Sanqiang Li Meilin Wang Jing He Shoumin Xi

Methionine synthase reductase (MTRR) is a key regulatory enzyme involved in the folate metabolic pathway. Previous studies investigating the association of MTRR A66G polymorphism with cancer susceptibility reported inconclusive results. We performed the current meta-analysis to obtain a more precise estimation of the possible association. Published literatures were identified from PubMed, Embas...

Journal: :Brazilian dental journal 2015
Márcia Waltrick-Zambuzzi Patricia Nivoloni Tannure Thays Cristine Dos Santos Vieira Leonardo Santos Antunes Fábio Lourenço Romano Willian Fernando Zambuzzi José Mauro Granjeiro Erika Calvano Küchler

The aim of this study was to evaluate the association of the polymorphisms in TCN2 (rs1801198) gene and in MTRR (rs1801394) gene with nonsyndromic cleft lip and/or palate (NSCL/P) in a Brazilian population. Genomic DNA was extracted from buccal cells. The polymorphisms in TCN2 (rs1801198) and MTRR (rs1801394) genes were genotyped by carrying out real-time PCR and Taqman assay. Chi-square test w...

Journal: :Human mutation 2005
Petra Zavadáková Brian Fowler Terttu Suormala Zorka Novotna Peter Mueller Julia B Hennermann Jirí Zeman M Antonia Vilaseca Laura Vilarinho Sven Gutsche Ekkehard Wilichowski Gerd Horneff Viktor Kozich

The cblE type of homocystinuria is a rare autosomal recessive disorder caused by impaired reductive activation of methionine synthase. Although earlier biochemical studies proposed that the methionine synthase enzyme might be activated by two different reducing systems, mutations were reported in only the methionine synthase reductase gene (MTRR) in cblE patients. The pathogenicity of MTRR muta...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007
Fang Fang Zhang Mary Beth Terry Lifang Hou Jinbo Chen Jolanta Lissowska Meredith Yeager Witold Zatonski Stephen Chanock Alfredo Morabia Wong-Ho Chow

Folate deficiency has been implicated in the etiology of stomach cancer through abnormal DNA methylation and disrupted DNA synthesis and repair. Enzyme-coding genes involved in folate metabolism are often polymorphic. In a population-based study of 305 cases and 427 controls in Warsaw, Poland, we evaluated the risk of stomach cancer in relation to polymorphisms in folate-metabolizing genes, inc...

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