Zobrazeno 1 - 10
of 4 405
pro vyhledávání: '"c677t"'
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:
Crescent Journal of Medical and Biological Sciences, Vol 11, Iss 3, Pp 121-127 (2024)
Objectives: Many single nucleotide polymorphisms affect the incidence of Alzheimer’s disease (AD). This investigation aimed to consider the frequency of the C677T single nucleotide polymorphism of the methylenetetrahydrofolate reductase (MTHFR) gen
Externí odkaz:
https://doaj.org/article/6ef8433e592745fcb4384f24c6da7557
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:
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
Autor:
Fatma Abozeid, Maysaa Zaki, Wafaa Nagah, Amany Ragab, Aya fathy, Dina Elhammady, Hayam Ghazy, Ahmed Yassen, Mohamed Serria, Omar Ammar, Maha Ragab, Manal Nomir
Publikováno v:
Egyptian Liver Journal, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Liver serves as a hub for key metabolic pathways such as folate cycle that provides one-carbon units for a network of metabolic reactions. Methylenetetrahydrofolate reductase (MTHFR) is a rate limiting enzyme in folate metabolism and thus it
Externí odkaz:
https://doaj.org/article/78d1b9f9873f4636bf16992df8cc344a
Autor:
Qiangqiang He, Yaping Wei, Hehao Zhu, Qiongyue Liang, Ping Chen, Shuqun Li, Yun Song, Lishun Liu, Binyan Wang, Xiping Xu, Yuhan Dong
Publikováno v:
Discover Oncology, Vol 15, Iss 1, Pp 1-10 (2024)
Abstract Background and purpose The enzyme methylenetetrahydrofolate reductase (MTHFR) plays a crucial role in directing folate species towards nucleotide synthesis or DNA methylation. The MTHFR polymorphisms C677T and A1298C have been linked to canc
Externí odkaz:
https://doaj.org/article/295a7edcad6f45e49a9303fca24252f1
Publikováno v:
Journal of Pharmacy and Bioallied Sciences, Vol 16, Iss Suppl 3, Pp S2809-S2814 (2024)
This case-control study investigated the correlation between male infertility in India and the methylenetetrahydrofolate reductase (MTHFR) C677T variant. Infertile males were utilized as the case group in the study, whereas fertile individuals served
Externí odkaz:
https://doaj.org/article/811c78e5434a4e6caa3fa0fe95f7b90e
Publikováno v:
International Journal of General Medicine, Vol Volume 17, Pp 1221-1231 (2024)
Qie Guo,1 Jia-Lin Sun,1 Ran Li,2 Xiao Li1 1Department of Clinical Pharmacy, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, People’s Republic of China; 2Department of Infectious Diseases, The Affiliated Hospital of Qingdao Univers
Externí odkaz:
https://doaj.org/article/787ddfe470e24666833032846bd36389
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-9 (2024)
Abstract Background Congenital heart defects (CHDs) are the heart structural malformations present at birth. Septal defects account for 40% of CHD, including atrial, ventricular and atrioventricular septal defects. In Pakistan, the prevalence of CHD
Externí odkaz:
https://doaj.org/article/98a07cd4388b409d9153de0bb08230e0
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Objective To analyse the relationship between the polymorphisms of the H-type hypertensive methylenetetrahydrofolate reductase (MTHFR) C677T gene and neutrophil gelatinase-associated lipocalin (NGAL) in early kidney injury. Method A total of
Externí odkaz:
https://doaj.org/article/736026c76c224a238ea3a9dd6d495d47