Christensen KE - Search Results

1

Magnesium and phosphate ions enable NAD binding to methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase.

Christensen KE, Mirza IA, Berghuis AM, Mackenzie RE. Christensen KE, et al. J Biol Chem. 2005 Oct 7;280(40):34316-23. doi: 10.1074/jbc.M505210200. Epub 2005 Aug 11. J Biol Chem. 2005. PMID: 16100107 Free article.

2

Mammalian mitochondrial methylenetetrahydrofolate dehydrogenase-cyclohydrolase derived from a trifunctional methylenetetrahydrofolate dehydrogenase-cyclohydrolase-synthetase.

Patel H, Christensen KE, Mejia N, MacKenzie RE. Patel H, et al. Among authors: christensen ke. Arch Biochem Biophys. 2002 Jul 1;403(1):145-8. doi: 10.1016/S0003-9861(02)00203-5. Arch Biochem Biophys. 2002. PMID: 12061812

3

The molecular basis of glutamate formiminotransferase deficiency.

Hilton JF, Christensen KE, Watkins D, Raby BA, Renaud Y, de la Luna S, Estivill X, MacKenzie RE, Hudson TJ, Rosenblatt DS. Hilton JF, et al. Among authors: christensen ke. Hum Mutat. 2003 Jul;22(1):67-73. doi: 10.1002/humu.10236. Hum Mutat. 2003. PMID: 12815595

4

Disruption of the mthfd1 gene reveals a monofunctional 10-formyltetrahydrofolate synthetase in mammalian mitochondria.

Christensen KE, Patel H, Kuzmanov U, Mejia NR, MacKenzie RE. Christensen KE, et al. J Biol Chem. 2005 Mar 4;280(9):7597-602. doi: 10.1074/jbc.M409380200. Epub 2004 Dec 16. J Biol Chem. 2005. PMID: 15611115 Free article.

5

Mitochondrial one-carbon metabolism is adapted to the specific needs of yeast, plants and mammals.

Christensen KE, MacKenzie RE. Christensen KE, et al. Bioessays. 2006 Jun;28(6):595-605. doi: 10.1002/bies.20420. Bioessays. 2006. PMID: 16700064 Review.

6

The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects.

Christensen KE, Rohlicek CV, Andelfinger GU, Michaud J, Bigras JL, Richter A, Mackenzie RE, Rozen R. Christensen KE, et al. Hum Mutat. 2009 Feb;30(2):212-20. doi: 10.1002/humu.20830. Hum Mutat. 2009. PMID: 18767138

7

Mitochondrial methylenetetrahydrofolate dehydrogenase, methenyltetrahydrofolate cyclohydrolase, and formyltetrahydrofolate synthetases.

Christensen KE, Mackenzie RE. Christensen KE, et al. Vitam Horm. 2008;79:393-410. doi: 10.1016/S0083-6729(08)00414-7. Vitam Horm. 2008. PMID: 18804703 Review.

8

A novel mouse model for genetic variation in 10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis with impacts on pregnancy and embryonic development.

Christensen KE, Deng L, Leung KY, Arning E, Bottiglieri T, Malysheva OV, Caudill MA, Krupenko NI, Greene ND, Jerome-Majewska L, MacKenzie RE, Rozen R. Christensen KE, et al. Hum Mol Genet. 2013 Sep 15;22(18):3705-19. doi: 10.1093/hmg/ddt223. Epub 2013 May 23. Hum Mol Genet. 2013. PMID: 23704330

9

MTHFD1 formyltetrahydrofolate synthetase deficiency, a model for the MTHFD1 R653Q variant, leads to congenital heart defects in mice.

Christensen KE, Deng L, Bahous RH, Jerome-Majewska LA, Rozen R. Christensen KE, et al. Birth Defects Res A Clin Mol Teratol. 2015 Dec;103(12):1031-8. doi: 10.1002/bdra.23451. Epub 2015 Sep 26. Birth Defects Res A Clin Mol Teratol. 2015. PMID: 26408344

10

Moderate folic acid supplementation and MTHFD1-synthetase deficiency in mice, a model for the R653Q variant, result in embryonic defects and abnormal placental development.

Christensen KE, Hou W, Bahous RH, Deng L, Malysheva OV, Arning E, Bottiglieri T, Caudill MA, Jerome-Majewska LA, Rozen R. Christensen KE, et al. Am J Clin Nutr. 2016 Nov;104(5):1459-1469. doi: 10.3945/ajcn.116.139519. Epub 2016 Oct 5. Am J Clin Nutr. 2016. PMID: 27707701 Free article.

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