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5. Metabotype analysis of Mthfd1l-null mouse embryos using desorption electrospray ionization mass spectrometry imaging. Vaughn A; DeHoog RJ; Eberlin LS; Appling DR Anal Bioanal Chem; 2021 May; 413(13):3573-3582. PubMed ID: 33829277 [TBL] [Abstract][Full Text] [Related]
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13. An NTD-associated polymorphism in the 3' UTR of MTHFD1L can affect disease risk by altering miRNA binding. Minguzzi S; Selcuklu SD; Spillane C; Parle-McDermott A Hum Mutat; 2014 Jan; 35(1):96-104. PubMed ID: 24123340 [TBL] [Abstract][Full Text] [Related]
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20. Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects. Hol FA; van der Put NM; Geurds MP; Heil SG; Trijbels FJ; Hamel BC; Mariman EC; Blom HJ Clin Genet; 1998 Feb; 53(2):119-25. PubMed ID: 9611072 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]