Results 111 to 120 of about 4,722 (199)

Impact of mutations in the mtrR, rpdlVD and rrl genes on azithromycin resistance in Neisseria gonorrhoeae

open access: yesPLOS ONE
Introduction Bacterial sexually transmitted infections (STIs) pose a major public health problem. The emergence of antibiotic-resistant strains of Neisseria gonorrhoeae represents a serious threat to successful treatment and epidemiological control. The first extensively drug-resistant (XDR) strains (ceftriaxone-resistant and high-level azithromycin ...
Florian Mauffrey   +5 more
openaire   +6 more sources

Methionine synthase reductase (MTRR) A66G polymorphism is not related to plasma homocysteine concentration and the risk for vascular disease.

open access: yes, 2009
Epidemiological evidence has revealed that hyperhomocysteinemia increases the risk for vascular disease. Methionine Synthase Reductase (MTRR) is one of several key enzymes in the homocysteine metabolic pathway and its mutant forms have been implicated in
Acuto, S   +4 more
core   +1 more source

The MTRR 66A>G polymorphism and maternal risk of birth of a child with Down syndrome in Caucasian women: a case-control study and a meta-analysis.

open access: yes, 2014
We performed a large case-control study and a meta-analysis of the literature to address the role of the methionine synthase reductase (MTRR) c.66A>G polymorphism as a maternal risk factor for the birth of a child with Down Syndrome (DS) among Caucasian ...
Romano, Corrado   +26 more
core   +1 more source

A Neisseria gonorrhoeae strain with a meningococcal mtrR sequence

open access: yesJournal of Medical Microbiology, 2014
Ella, Trembizki   +7 more
openaire   +5 more sources

Association between cobalamin and folate deficiency and the presence of the MTR A2756G and MTRR A66G polymorphisms in pregnant women and their newborns

open access: yes, 2005
A metionina sintase redutase (MTRR) catalisa a redução da cobalamina (Cbl) oxidada a metilcobalamina. Em presença de folato, a metionina sintase (MTR) utiliza a metilcobalamina como cofator na metilação da homocisteína (tHcy) a metionina.
Favaro, Patricia Barbosa
core  

Роль полиморфизма гена MTRR A66G (rs1801394) в развитии хронической фетоплацентарной недостаточности с синдромом задержки развития плода [PDF]

open access: yes, 2012
Изучается роль полиморфизма A66G гена MTRR (methionine synthase reductase) в развитии хронической фетоплацентарной недостаточности (ХФПН) с синдромом задержки развития плода (СЗРП).
Кокорина, О. С.   +1 more
core  

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