Co-Occurring Methylenetetrahydrofolate Reductase (MTHFR) rs1801133 and rs1801131 Genotypes as Associative Genetic Modifiers of Clinical Severity in Rett …
J Singh, G Wilkins, E Goodman-Vincent, S Chishti… - Brain Sciences, 2024 - mdpi.com
Aim: Remethylation disorders such as 5, 10-methylenetetrahydrofolate reductase (MTHFR)
deficiency reduce the remethylation of homocysteine to methionine. The resulting …
deficiency reduce the remethylation of homocysteine to methionine. The resulting …
Long daytime napping: A silent danger for hypertensive individuals
J Wu, L Liu, Z Huang, L Wang, F Cai… - European Journal of …, 2024 - Wiley Online Library
Background and purpose Hypertension significantly contributes to stroke. Previous research
has indicated a connection between daytime napping and stroke. Research on the …
has indicated a connection between daytime napping and stroke. Research on the …
Clinical characteristics and thrombophilia associated gene variants in Egyptians with unprovoked venous thromboembolism: three centers experience
Background Thrombophilias are characterized by excessive venous and arterial thrombosis
at regular or unusual sites. It may result from inherited, acquired, or a combination …
at regular or unusual sites. It may result from inherited, acquired, or a combination …
Association of thrombophilic genes (MTHFR, MTR and MTRR) polymorphisms and homocysteine level in relation to the increased risk of thrombosis among COVID-19 …
M El-Ghonaimy, M El-Deeb, S El-Ashwah, M Fouda… - Gene Reports, 2024 - Elsevier
Background Patients with COVID-19 have an increased risk of thrombosis and
coagulopathy. Homocysteine, an amino acid essential to coagulation, is thought to be …
coagulopathy. Homocysteine, an amino acid essential to coagulation, is thought to be …
Methylenetetrahydrofolate reductase gene polymorphisms, lipid profiles, and basic renal functional markers as risk for myocardial infarction: a case-control study and …
S Perović, S Vujović, LK Pojskić, N Garai… - Archives of Biological …, 2024 - serbiosoc.org.rs
Myocardial infarction (MI) is a serious cardiovascular disease and the primary cause of
mortality, with a complex etiopathology. Identifying the genetic basis of myocardial infarction …
mortality, with a complex etiopathology. Identifying the genetic basis of myocardial infarction …
[PDF][PDF] Study of Methylenetetrahydrofolate Reductase C677T gene polymorphism and some biochemical markers for patients with hypertension
NAHM Al-Zubaidi, FA Jabir - Chinese Journal of Laboratory Medicine, 2024 - cjlm.org
The study aims to evaluate the levels of some biochemical in hypertension patients, find out
MTHFRC677T gene polymorphism exist, and whether they are a risk factor for hypertension …
MTHFRC677T gene polymorphism exist, and whether they are a risk factor for hypertension …
A tale of A1298C mutation and recurrent Pulmonary Embolism: a rare association
H Vij, SHM Rizvi - Chest Disease Reports, 2024 - pagepressjournals.org
Abstract Pulmonary Embolism (PE) and Deep Venous Thrombosis (DVT) represent critical
manifestations within the spectrum of Venous Thromboembolic Disease (VTE). The MTHFR …
manifestations within the spectrum of Venous Thromboembolic Disease (VTE). The MTHFR …