Folate pathway gene single nucleotide polymorphisms and neural tube defects: a systematic review and meta-analysis

AK Almekkawi, MW AlJardali, HM Daadaa… - Journal of Personalized …, 2022 - mdpi.com
Neural tube defects (NTDs) are congenital abnormalities in the central nervous system. The
exact etiology of NTDs is still not determined, but several genetic and epigenetic factors …

Maternal biomarkers for early prediction of the neural tube defects pregnancies

U Yadav, P Kumar, V Rai - Birth Defects Research, 2021 - Wiley Online Library
Background Neural tube defects (NTD) are one of the most common congenital birth defects.
The reason for the NTD cause is still not completely known, but it is believed that some …

Molecular genetics involved in neural tube defects: recent advances and future prospective for molecular medicine

PR Mishra, M Barik, AK Mahapatra - Neurology India, 2020 - journals.lww.com
Background: Folic acid and multivitamin supplements ((FAMVS) and genetics involvement is
one of the major roles in the development of neural tube defects (NTDs). Objective: Our prior …

[PDF][PDF] Methylene Tetrahydrofolate Reductase (MTHFR) rs868014 Polymorphism Regulated by miR-1203 Associates with Risk and Short Term Outcome of Ischemic …

W He, M Lu, G Li, Z Sun, D Liu, L Gu - Cellular Physiology and …, 2017 - karger.com
Abstract Background/Aims: Genetic polymorphisms of methylene tetrahydrofolate reductase
(MTHFR) were associated with ischemic stroke risk. This study analyzed MTHFR …

Altered methyltetrahydrofolate reductase gene polymorphism in mothers of children with attention deficit and hyperactivity disorder

S Baykal, B Batar, A Nalbantoğlu, Y Albayrak… - Progress in Neuro …, 2019 - Elsevier
Abstract Attention Deficit and Hyperactivity Disorder (ADHD) is one of the most common
psychiatric disorders in childhood and causes significant functional impairments in children …

Hyperhomocysteinemia and pathogenetic mechanisms of ischemic stroke

AM Makhmudovich, RG Sattarovna… - The American Journal …, 2021 - inlibrary.uz
The article is intended to give basic information and the role of homocysteine in the human
body. The amino acid homocysteine is a product of methionine demethylation. When the …

Гипергомоцистеинемия и ишемический инсульт

НВ Пизова, НА Пизов - Медицинский совет, 2017 - cyberleninka.ru
Статья посвящена роли гомоцистеина в организме человека. Аминокислота
гомоцистеин является продуктом деметилирования метионина. При повышении уровня …

[HTML][HTML] Tagging functional polymorphism in 3'untranslated region of methylene tetrahydrofolate reductase and risk of ischemic stroke

J Shi, W He, Y Wang, J Hua - Cellular Physiology and Biochemistry, 2018 - karger.com
Background/Aims: The association between genetic polymorphisms in the exon or
untranslated region of the methylenetetrahydrofolate reductase gene (MTHFR) and the risk …

Association between Fetal MTHFR A1298C (rs1801131) Polymorphism and Neural Tube Defects Risk: A Systematic Review and Meta-Analysis

S Soleimani-Jadidi, B Meibodi, A Javaheri… - Fetal and Pediatric …, 2022 - Taylor & Francis
Background The association of the fetal MTHFR A1298C (rs1801131) polymorphism and
neural tube defects (NTDs) susceptibility has been widely demonstrated, but the results …

Corroborating evidence for the correlation between the MTHFR C677T single nucleotide variant and smoking in Croatian subjects independent of ischemic stroke

AB Martinović, T Križ, I Orešković, AJ van Wijnen… - Gene Reports, 2023 - Elsevier
Hyperhomocysteinaemia is a risk factor for ischemic stroke development. Single nucleotide
variation in the methylenetetrahydrofolate reductase gene (MTHFR, C677T polymorphism, T …