Marrone CD'Amico MVerdone RRizzo ASammarco PFabiano CNiceta MCaltagirone MD'Amico GPagliaro LClinical transplantationPasta L, Marrone C, D'Amico M, et al. MTHFR C677T homo- zygous as risk factor for complications after OLT for cryptogenic cirrhosis. Clin Transplant 2006;20:796-798....
Introduction: Hyperhomocysteinemia is an independent risk factor for cerebrovascular disease and the homozygous C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene can induce hyperhomocysteinemia. However, the association between this 677TT genotype and ischemic stroke still remains contro...
.To the best of our knowledge, this is the first family with multiple AIS patients harboring homozygous MTHFR gene C677T (G80A-RFC1) mutations without associated hyperhomocysteinemia (the latter factor is usually considered as effector of vascular damage in patients with MTHFR C677T mutations)....
These two fruit flies are homozygous for red eye color. 这两种果蝇同型结合形成红眼颜色的品种. 互联网 C 677 T homozygous MTHFR mutation in 4 % , and oral contraceptive use in 22 %. 4%C677T纯合亚甲基四氢叶酸还原酶变异;22%使用口服避孕药. 互联网 The homozygous form is fatal. 纯合子是致...
These two fruit flies arehomozygousfor red eye color. 这两种果蝇同型结合形成红眼颜色的品种. 互联网 C 677 ThomozygousMTHFR mutation in 4 % , and oral contraceptive use in 22 %. 4%C677T纯合亚甲基四氢叶酸还原酶变异;22%使用口服避孕药. ...
protein CThe aim of this study was to evaluate the impact of methylene tetrahydrofolate reductase (MTHFR) rs1801133 (C→T667 transition) on age at first idiopathic portal vein thrombosis (PVT) and to identify clinical and/or laboratory variables influencing age at first PVT, including plasma ...
MTHFR C677T homozygous as risk factor for complications after OLT for cryptogenic cirrhosisdoi:10.1111/j.1399-0012.2006.00564.xLindaInternalPastaInternalCiroInternalMarroneInternalMarioInternalD'AmicoInternalRobertoInternalVerdoneInternalAroldoInternalRizzo...
MTHFR TT, male gender and protein C predicted age at PVT (p?=?0.02, p?=?0.04 and p?=?0.08); MTHFR TT and Child–Pugh score predicted plasma HC (p?=?0.005 and p?=?0.01) as well as low plasma protein C (p?Paul R. J.,Ames...
Background Stroke is a rare disorder in childhood; among its risk factors, C677T mutations in the methylenetetrahydrofolate reductase (MTHFR) gene with secondary hyperhomocysteinemia are considered.关键词: Stroke - Familial - MTHFR gene - C677T mutation - G80A RFC-1 mutation - Homocysteine DOI...
The MTHFR CT polymorphism confers a high risk for stroke in both homozygous and heterozygous T allele carriers with type 2 diabetes. Diabet Med 2006; 23:529-536.Hermans MP, Gala JL, Buysschaert M. The MTHFR CT polymor- phism confers a high risk for stroke in both homozygous and het- ...