Zobrazeno 1 - 10
of 10 109
pro vyhledávání: '"the mthfr"'
Publikováno v:
Reproductive Biology and Endocrinology, Vol 22, Iss 1, Pp 1-17 (2024)
Abstract Background Epidemiological studies have reported that polymorphisms of folate-metabolizing genes have a significant impact on male infertility. However, the results of published studies have come to different conclusions. Objective To determ
Externí odkaz:
https://doaj.org/article/1a85d5747efd4a90b0684878cf18e670
Publikováno v:
International Journal of General Medicine, Vol Volume 17, Pp 6281-6290 (2024)
Zhuoxin Zhang,1 Zuguang Wu,1 Yuwen Zeng,1 Yunlin Li,1 Yingchuan Feng,1 Zhen Gao,1 Yijin Chen2 1Department of Gastrointestinal Surgery, Meizhou People’s Hospital, Meizhou, People’s Republic of China; 2Department of Gastroenterology, Meizhou People
Externí odkaz:
https://doaj.org/article/50c79caefc8b40d5b12e4b98cdb48380
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-5 (2024)
Abstract Mutation of methylenetetrahydrofolate reductase (MTHFR) C677T leads to the decrease of folate utilization and the impairment of spermatogenesis. This study attempts to investigate the association between MTHFR C677T polymorphisms and nonobst
Externí odkaz:
https://doaj.org/article/162e5639f6fc45ea84c56af2b3ede1f2
Publikováno v:
Annals of Human Biology, Vol 51, Iss 1 (2024)
AbstractBackground Chronic hepatitis B virus (HBV) infection is a severe disease affecting the physical and economic well-being of patients. The relationship between polymorphisms in the MTHFR gene and disease progression following HBV infection rema
Externí odkaz:
https://doaj.org/article/14c19d757d2c4362894bde2846f2e7b0
Publikováno v:
Dental Journal, Vol 57, Iss 3, Pp 184-188 (2024)
Background: Cleft lip with or without cleft palate (CL/P) is the most common congenital anomaly found in Indonesia. CL/P is caused by hereditary (genetic) and environmental factors. Environmental factors can result in methylation in the promoter of t
Externí odkaz:
https://doaj.org/article/e54fb6c3235e4de4967df205944e5af3
Publikováno v:
Modern Medicine, Vol 31, Iss 3, Pp 227-236 (2024)
Objectives: Objectives: The current study was designed to evaluate the role of MTHFR gene (rs1801133 and rs1801131) polymorphisms and investigate the serum Homocysteine level in Iraqi patients with CKD. Materials and Methods: Blood samples were coll
Externí odkaz:
https://doaj.org/article/de9dd185dc2444f0803fad457643b071
Autor:
Sura F. Alsaffar, Noor Nihad Baqer
Publikováno v:
Iranian Journal of Medical Sciences, Vol 49, Iss 7, Pp 430-440 (2024)
Background: The methylenetetrahydrofolate reductase (MTHFR) gene is an essential gene in the metabolism of folate-homocysteine. Recently, the level of homocysteine was found to be a significant marker in the follow-up of COVID-19 infection. Thus, thi
Externí odkaz:
https://doaj.org/article/f505f74926414197aadd3639f8d3285c
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background and aims H-type hypertension is essential hypertension combined with high homocysteine, and both synergistically increase the risk of cardiovascular and cerebrovascular events. The aim of this study was to investigate the risk fac
Externí odkaz:
https://doaj.org/article/42882f9da5da49208c68ad304756e8fe
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Analyze the relationship between genetic variations in the MTHFR gene at SNPs (rs1801131 and rs1801133) and the therapy outcomes for Iraqi patients with rheumatoid arthritis (RA). The study was conducted on a cohort of 95 RA Iraqi patients.
Externí odkaz:
https://doaj.org/article/8d17037d576548e5a3e9790c80e43e6d
Publikováno v:
Romanian Journal of Neurology, Vol 23, Iss 2, Pp 166-170 (2024)
Background. Recent data suggests that environmental factors may account for up to 40-50% of the variability in the risk of developing autism spectrum disorder (ASD). Aim. The purpose of this study was to examine the correlation between MTHFR polymorp
Externí odkaz:
https://doaj.org/article/0707f47cd5c441f7ab567c91bd1c5a09