Congenital Heart Disease and Genetic Changes in Folate/Methionine cycles
NK Kuželički, B Doljak - Genes, 2024 - pmc.ncbi.nlm.nih.gov
Congenital heart disease is one of the most common congenital malformations and thus
represents a considerable public health burden. Hence, the identification of individuals and …
represents a considerable public health burden. Hence, the identification of individuals and …
Genetic studies in the Pakistani population reveal novel associations with ventricular septal defects (VSDs)
Background With prevalence up to 4%, Ventricular Septal Defect (VSD) is one of the leading
causes of neonatal deaths. VSD is a common complex genetic disorder that has been …
causes of neonatal deaths. VSD is a common complex genetic disorder that has been …
Association of MTHFR and MS/MTR gene polymorphisms with congenital heart defects in North Indian population (Jammu and Kashmir): a case–control study …
JK Raina, RK Panjaliya, V Dogra, S Sharma, Anupriya… - BMC pediatrics, 2022 - Springer
Abstract Background The risk of Congenital Heart Defects (CHD) is greatly influenced by
variants within the genes involved in folate-homocysteine metabolism. Polymorphism in …
variants within the genes involved in folate-homocysteine metabolism. Polymorphism in …
Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population
Abstract Background Ventricular septal defects (VSDs) are one of the leading causes of
death due to cardiac anomalies during the first months of life. The prevalence of VSD in …
death due to cardiac anomalies during the first months of life. The prevalence of VSD in …
Analysis of genetic polymorphism of methylenetetrahydrofolate reductase in a large ethnic Hakka population in southern China
P Zhao, J Hou, H Wu, M Zhong - Medicine, 2018 - journals.lww.com
Methylenetetrahydrofolate reductase (MTHFR) catalyzes conversion of methylene
tetrahydrofolate to methylte trahydrofolate. MTHFR C677T polymorphism has been regarded …
tetrahydrofolate to methylte trahydrofolate. MTHFR C677T polymorphism has been regarded …
[HTML][HTML] The protective effects of the methylenetetrahydrofolate reductase rs1801131 variant among Saudi smokers
MH Almutairi, NS Al-Numair, NR Parine… - Saudi Journal of …, 2021 - Elsevier
Methylenetetrahydrofolate reductase (MTHFR) polymorphism plays a fundamental role in
susceptibility to various diseases, including cancers and autoimmune diseases. In the …
susceptibility to various diseases, including cancers and autoimmune diseases. In the …
Association between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 …
NN Esmaiel, EA Ashaat, GM Al-Ettribi, A Fayez… - Egyptian Journal of …, 2023 - Springer
Background Stratification analysis studies showed that ethnicity has a significant association
regarding MTHFR C677T variant and congenital heart diseases (CHDs) risk, and many …
regarding MTHFR C677T variant and congenital heart diseases (CHDs) risk, and many …
Design and evaluation of a method for testing polymorphisms of Folate-related genes using the Luminex Liquichip System
X Jiang, T Huang, W Lin, X Li - Genetic Testing and Molecular …, 2020 - liebertpub.com
Purpose: The methylene tetrahydrofolate reductase (MTHFR) C677T, MTHFR A1298C, and
the methionine synthase reductase (MTRR) A66G polymorphisms are the three most …
the methionine synthase reductase (MTRR) A66G polymorphisms are the three most …
The relationship between gene polymorphism of MTRR A66G and lower extremity deep venous thrombosis
J Xu, W Zhou - Hematology, 2018 - Taylor & Francis
Objective: To investigate the relationship between gene polymorphism of MTRR A66G and
lower extremity deep venous thrombosis (DVT). Methods: Two hundred and two patients …
lower extremity deep venous thrombosis (DVT). Methods: Two hundred and two patients …
[PDF][PDF] Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population
SU Shahid, S Hasnain - 2022 - ijponline.biomedcentral.com
Abstract Background: Ventricular septal defects (VSDs) are one of the leading causes of
death due to cardiac anomalies during the first months of life. The prevalence of VSD in …
death due to cardiac anomalies during the first months of life. The prevalence of VSD in …