PMID: 11865092

Billion S, Tribout B, Cadet E, Queinnec C, Rochette J, Wheatley P, Bataille P
Hyperhomocysteinaemia, folate and vitamin B12 in unsupplemented haemodialysis patients: effect of oral therapy with folic acid and vitamin B12.
Nephrol Dial Transplant. 2002 Mar;17(3):455-61., [PubMed]
Sentences
No. Mutations Sentence Comment
1 ABCC8 p.Cys677Thr
X
ABCC8 p.Cys677Thr 11865092:1:214
status: NEW
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Hyperhomocysteinaemia, a risk factor for atherosclerosis, is common in dialysis patients and particularly in those homozygous for a common polymorphism in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene (C677T transition). Login to comment
4 ABCC8 p.Cys677Thr
X
ABCC8 p.Cys677Thr 11865092:4:36
status: NEW
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The responses were analysed for the C677T genotypes of MTHFR. Login to comment
6 ABCC8 p.Cys677Thr
X
ABCC8 p.Cys677Thr 11865092:6:97
status: NEW
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Plasma tHcy, folate and vitamin B12 were measured in 51 haemodialysis patients genotyped for the C677T MTHFR mutation (homozygotes, TT; heterozygotes, CT; without mutation, CC). Login to comment
19 ABCC8 p.Cys677Thr
X
ABCC8 p.Cys677Thr 11865092:19:116
status: NEW
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(ii) After folate therapy, tHcy levels decreased significantly in all patients and were identical between the three C677T MTHFR genotype subgroups. Login to comment
69 ABCC8 p.Cys677Thr
X
ABCC8 p.Cys677Thr 11865092:69:4
status: NEW
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The C677T polymorphic site was determined by PCR amplification followed by restriction-enzyme digestion of the products and analysed on 2% agarose gels w13x. Login to comment
75 ABCC8 p.Cys677Thr
X
ABCC8 p.Cys677Thr 11865092:75:57
status: NEW
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Results Table 1 shows the genotypic distribution of the (C677T) MTHFR mutation and the main characteristics of patients in the different genotype groups. Login to comment