| 1 | SHMT1, SHMT2
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| Serine hydroxymethyltransferase 1 and 2: gene sequence variation and functional genomic characterization.
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| Hebbring SJ, Chai Y, Ji Y, Abo RP, Jenkins GD, Fridley B, Zhang J, Eckloff BW, Wieben ED, Weinshilboum RM.
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| J Neurochem 120(6):881-90. doi: 10.1111/j.1471-4159.2012.07646.x. Epub 2012 Feb 6.
2012
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| 2 | SHMT1
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| Polymorphism C1420T of Serine hydroxymethyltransferase gene on maternal risk for Down syndrome.
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| Marucci GH, Zampieri BL, Biselli JM, Valentin S, Bertollo EM, Eberlin MN, Haddad R, Riccio MF, Vannucchi H, Carvalho VM, Pavarino EC.
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| Mol Biol Rep 39(3):2561-6. Epub 2011 Jun 18.
2012
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| 3 | SHMT1
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| Nuclear localization of de novo thymidylate biosynthesis pathway is required to prevent uracil accumulation in DNA.
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| MacFarlane AJ, Anderson DD, Flodby P, Perry CA, Allen RH, Stabler SP, Stover PJ.
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| J Biol Chem 286(51):44015-22. Epub 2011 Nov 4.
2011
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| 4 | SHMT1
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| Shmt1 and de novo thymidylate biosynthesis underlie folate-responsive neural tube defects in mice.
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| Beaudin AE, Abarinov EV, Noden DM, Perry CA, Chu S, Stabler SP, Allen RH, Stover PJ.
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| Am J Clin Nutr 93(4):789-98. Epub 2011 Feb 23.
2011
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| 5 | SHMT1, SHMT2
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| SHMT1 and SHMT2 are functionally redundant in nuclear de novo thymidylate biosynthesis.
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| Anderson DD, Stover PJ.
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| PLoS One 4(6):e5839.
2009
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| 6 | SHMT1
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| Mechanism of the internal ribosome entry site-mediated translation of serine hydroxymethyltransferase 1.
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| Fox JT, Stover PJ.
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| J Biol Chem 284(45):31085-96. Epub 2009 Sep 4.
2009
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| 7 | SHMT1
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| Increased expression of cSHMT, Tbx3 and utrophin in plasma of ovarian and breast cancer patients.
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| Lomnytska M, Dubrovska A, Hellman U, Volodko N, Souchelnytskyi S.
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| Int J Cancer 118(2):412-21.
2006
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| 8 | SHMT1, SHMT2
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| Low serine hydroxymethyltransferase activity in the human placenta has important implications for fetal glycine supply.
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| Lewis RM, Godfrey KM, Jackson AA, Cameron IT, Hanson MA.
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| J Clin Endocrinol Metab 90(3):1594-8. Epub 2004 Dec 14.
2005
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| 9 | SHMT1, SHMT2
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| Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?
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| Heil SG, Van der Put NM, Waas ET, den Heijer M, Trijbels FJ, Blom HJ.
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| Mol Genet Metab 73(2):164-72. 2001
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| 10 | SHMT1
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| Molecular cloning, characterization and alternative splicing of the human cytoplasmic serine hydroxymethyltransferase gene.
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| Girgis S, et al.
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| Gene 210 : 315-324. 1998
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| 11 | SHMT1, SMS
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| Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.
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| Elsea SH, et al.
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| Am J Hum Genet 57 : 1342-1350. 1995
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