نتایج جستجو برای: mtrr

تعداد نتایج: 307  

Journal: :International Journal of Research and Development in Pharmacy & Life Sciences 2018

2012
Bruna Lancia Zampieri Joice Matos Biselli Eny Maria Goloni-Bertollo Hélio Vannucchi Valdemir Melechco Carvalho José Antônio Cordeiro Érika Cristina Pavarino

Studies have shown that the maternal risk for Down syndrome (DS) may be modulated by alterations in folate metabolism. The aim of this study was to evaluate the influence of 12 genetic polymorphisms involved in folate metabolism on maternal risk for DS. In addition, we evaluated the impact of these polymorphisms on serum folate and plasma methylmalonic acid (MMA, an indicator of vitamin B<formu...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
M W Tan L G Rahme J A Sternberg R G Tompkins F M Ausubel

We reported recently that the human opportunistic pathogen Pseudomonas aeruginosa strain PA14 kills Caenorhabditis elegans and that many P. aeruginosa virulence factors (genes) required for maximum virulence in mouse pathogenicity are also required for maximum killing of C. elegans. Here we report that among eight P. aeruginosa PA14 TnphoA mutants isolated that exhibited reduced killing of C. e...

Journal: :Neuroscience & Biobehavioral Reviews 2014
E. Siobhan Mitchell Nelly Conus Jim Kaput

The B vitamins folic acid, vitamin B12 and B6 are essential for neuronal function, and severe deficiencies have been linked to increased risk of neurodevelopmental disorders, psychiatric disease and dementia. Polymorphisms of genes involved in B vitamin absorption, metabolism and function, such as methylene tetrahydrofolate reductase (MTHFR), cystathionine β synthase (CβS), transcobalamin 2 rec...

2018
Zengyu Zhang Lianfang Yu Sufang Li Jun Liu

BACKGROUND Both genetic and environmental factors play a role in the development of autism spectrum disorder (ASD). This case-control study examined the association between childhood ASD and single-nucleotide polymorphisms (SNPs) in genes involved with vitamin B12 and folate metabolism. MATERIAL AND METHODS Genotypes of transcobalamin 2 (TCN2) rs1801198, methionine synthase (MTR) rs1805087, met...

Journal: :Congenital anomalies 2007
Gabriele Tonni Daniela Azzoni Marco Panteghini Alessandro Ventura Pietro Cavalli

Iniencephaly is a rare congenital malformation consisting of a complex alteration of the embryonic development occurring around the third post-fertilization week and characterized by a hyper-retroflexion of the cephalic pole. We report a case of iniencephaly associated with acrania-encephalocele, spina bifida and abnormal ductus venosus in a fetus with trisomy 18 diagnosed at 12 week's gestatio...

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