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Volumn 10, Issue 5, 2001, Pages 433-443

Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); DNA; S ADENOSYLHOMOCYSTEINE; S ADENOSYLMETHIONINE;

EID: 0035282903     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.5.433     Document Type: Article
Times cited : (539)

References (61)
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    • A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells
    • (1998) Proc. Natl Acad. Sci. USA , vol.95 , pp. 13217-13220
    • Bagley, P.J.1    Selhub, J.2
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    • Measurement of plasma and intracellular S-adenosylmethionine and S-adenosylhomocysteine utilizing coulometric electrochemical detection: Alterations with plasma homocysteine and pyridoxal 5′-phosphate concentrations
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.