Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1996 | 1 |
1997 | 1 |
2002 | 1 |
2004 | 1 |
2005 | 1 |
2007 | 1 |
2023 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
Page 1
Crystal structure and solution characterization of the activation domain of human methionine synthase.
FEBS J. 2007 Feb;274(3):738-50. doi: 10.1111/j.1742-4658.2006.05618.x.
FEBS J. 2007.
PMID: 17288554
Free article.
Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association.
O'Leary VB, Mills JL, Pangilinan F, Kirke PN, Cox C, Conley M, Weiler A, Peng K, Shane B, Scott JM, Parle-McDermott A, Molloy AM, Brody LC; Members of the Birth Defects Research Group.
O'Leary VB, et al.
Mol Genet Metab. 2005 Jul;85(3):220-7. doi: 10.1016/j.ymgme.2005.02.003. Epub 2005 Mar 17.
Mol Genet Metab. 2005.
PMID: 15979034
Item in Clipboard
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Gerhard DS, Wagner L, Feingold EA, Shenmen CM, Grouse LH, Schuler G, Klein SL, Old S, Rasooly R, Good P, Guyer M, Peck AM, Derge JG, Lipman D, Collins FS, Jang W, Sherry S, Feolo M, Misquitta L, Lee E, Rotmistrovsky K, Greenhut SF, Schaefer CF, Buetow K, Bonner TI, Haussler D, Kent J, Kiekhaus M, Furey T, Brent M, Prange C, Schreiber K, Shapiro N, Bhat NK, Hopkins RF, Hsie F, Driscoll T, Soares MB, Casavant TL, Scheetz TE, Brown-stein MJ, Usdin TB, Toshiyuki S, Carninci P, Piao Y, Dudekula DB, Ko MS, Kawakami K, Suzuki Y, Sugano S, Gruber CE, Smith MR, Simmons B, Moore T, Waterman R, Johnson SL, Ruan Y, Wei CL, Mathavan S, Gunaratne PH, Wu J, Garcia AM, Hulyk SW, Fuh E, Yuan Y, Sneed A, Kowis C, Hodgson A, Muzny DM, McPherson J, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madari A, Young AC, Wetherby KD, Granite SJ, Kwong PN, Brinkley CP, Pearson RL, Bouffard GG, Blakesly RW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Griffith M, Griffith OL, Krzywinski MI, Liao N, Morin R, Palmquist D, Petrescu AS, Skalska U, Smailus DE, Stott JM, Schnerch A, Schein JE, Jones SJ, Holt RA, Baross A, Marra MA, Clifto…
See abstract for full author list ➔
Gerhard DS, et al.
Genome Res. 2004 Oct;14(10B):2121-7. doi: 10.1101/gr.2596504.
Genome Res. 2004.
PMID: 15489334
Free PMC article.
Item in Clipboard
Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida.
Doolin MT, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE.
Doolin MT, et al.
Am J Hum Genet. 2002 Nov;71(5):1222-6. doi: 10.1086/344209. Epub 2002 Oct 9.
Am J Hum Genet. 2002.
PMID: 12375236
Free PMC article.
Item in Clipboard
Human methionine synthase. cDNA cloning, gene localization, and expression.
Chen LH, Liu ML, Hwang HY, Chen LS, Korenberg J, Shane B.
Chen LH, et al.
J Biol Chem. 1997 Feb 7;272(6):3628-34.
J Biol Chem. 1997.
PMID: 9013615
Free article.
Item in Clipboard
Defects in human methionine synthase in cblG patients.
Gulati S, Baker P, Li YN, Fowler B, Kruger W, Brody LC, Banerjee R.
Gulati S, et al.
Hum Mol Genet. 1996 Dec;5(12):1859-65. doi: 10.1093/hmg/5.12.1859.
Hum Mol Genet. 1996.
PMID: 8968736
Item in Clipboard
Cite
Cite