Results 101 to 110 of about 5,460 (176)

Relationship between methylenetetrahydrofolate reductase C677T gene polymorphism and neutrophil gelatinase-associated lipocalin in early renal injury in H-type hypertension

open access: yesBMC Cardiovascular Disorders
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.
Chi Zhang   +6 more
doaj   +1 more source

5,10-Methylenetetrahydrofolate reductase C677T gene polymorphism in Behcet's patients with or without ocular involvement

open access: yes, 2005
Background: Increased serum levels of homocysteine (Hcy) have been reported in patients with Behcet's disease ( BD) with an established risk factor for vascular involvement.
Taheri, Serpil   +6 more
core   +1 more source

MOESM1 of Association of parental methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in couples with unexplained recurrent pregnancy loss

open access: yes, 2018
Additional file 1: Table S1.
Nisha Shrestha (4689817)   +9 more
core   +1 more source

Polimorfismo do gene metilenotetra-hidrofolato redutase (MTHFR) e o risco de carcinoma espinocelular de cabeça e pescoço Polymorphism of methylenetetrahydrofolate reductase (MTHFR) gene and risk of head and neck squamous cell carcinoma

open access: yesBrazilian Journal of Otorhinolaryngology, 2010
O polimorfismo C677T do gene metilenotetra-hidrofolato redutase (MTHFR) pode ser um fator de risco para o carcinoma espinocelular de cabeça e pescoço devido a alterações nos níveis de folato que podem induzir alterações na metilação intracelular ...
Juliana Olsen Rodrigues   +6 more
doaj   +1 more source

Pooled analysis for the association between MTHFR C677T genotype frequencies and the risks of NAFLD.

open access: yes, 2016
Pooled analysis for the association between MTHFR C677T genotype frequencies and the risks of NAFLD.
Jing-Na Lin (2634634)   +3 more
core   +1 more source

Evaluating the role of maternal folic acid supplementation in modifying the effects of methylenetetrahydrofolate reductase (C677T and A1298C) gene polymorphisms in oral cleft children

open access: yesJournal of Research in Medical Sciences, 2016
Background: We studied the role of maternal folic acid supplementation in modifying the effects of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) gene polymorphisms in Iranian children with oral clefts.
Asghar Ebadifar   +4 more
doaj   +1 more source

Involvement of the ABCB1 C3435T Variant but Not the MTHFR C677T or MTHFR A1298C Variant in High-Dose Methotrexate-Induced Toxicity in Pediatric Acute Lymphoblastic Leukemia Patients in China [PDF]

open access: yes
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 University ...
Li X, Sun JL, Li R, Guo Q
core  

Einfluss des 5-, 10-Methylentetrahydrofolatreduktase (MTHFR)-Polymorphismus C677T auf den Erfolg einer extrakorporalen Befruchtung

open access: yes, 2011
A retrospective surveillance was performed to ascertain the influence of the 5-,10- Methylenetetrahydrofolate Reductase C677T Mutation on the outcome of IVF and ICSI treatment.
Kresse, Florian
core   +1 more source

MTHFR C677T and A1298C polymorphisms in dementia susceptibility: evidence from a meta-analytic investigation with disease-specific and ethnicity-stratified analyses

open access: yesFrontiers in Aging Neuroscience
BackgroundAlzheimer’s disease (AD) and vascular dementia (VaD) have become significant global health challenges. Recent research evidence indicates a close comorbidity between AD and cerebral small vessel disease.
Yuyao He   +16 more
doaj   +1 more source

Maternal MTHFR C677T genotype and demographic data of the pregnant women and their infants.

open access: yes, 2013
Maternal MTHFR C677T genotype and demographic data of the pregnant women and their infants.
Ursula Brain (362492)   +3 more
core   +1 more source

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