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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2007 | 1 |
2009 | 1 |
2012 | 1 |
2020 | 2 |
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2024 | 0 |
PubMed (GeneRIF) for id: 55034
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Impaired expression of the COSMOC/MOCOS gene unit in ASD patient stem cells.
Mol Psychiatry. 2021 May;26(5):1606-1618. doi: 10.1038/s41380-020-0728-2. Epub 2020 Apr 23.
Mol Psychiatry. 2021.
PMID: 32327736
Free PMC article.
The rs594445 in MOCOS gene is associated with risk of autism spectrum disorder.
Taheri M, Noroozi R, Aghaei K, Omrani MD, Ghafouri-Fard S.
Taheri M, et al.
Metab Brain Dis. 2020 Mar;35(3):497-501. doi: 10.1007/s11011-019-00524-y. Epub 2020 Jan 4.
Metab Brain Dis. 2020.
PMID: 31900757
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Polymorphism of genes involved in purine metabolism (XDH, AOX1, MOCOS) in kidney transplant recipients receiving azathioprine.
Kurzawski M, Dziewanowski K, Safranow K, Drozdzik M.
Kurzawski M, et al.
Ther Drug Monit. 2012 Jun;34(3):266-74. doi: 10.1097/FTD.0b013e31824aa681.
Ther Drug Monit. 2012.
PMID: 22495427
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Novel pharmacogenetic markers for treatment outcome in azathioprine-treated inflammatory bowel disease.
Smith MA, Marinaki AM, Arenas M, Shobowale-Bakre M, Lewis CM, Ansari A, Duley J, Sanderson JD.
Smith MA, et al.
Aliment Pharmacol Ther. 2009 Aug 15;30(4):375-84. doi: 10.1111/j.1365-2036.2009.04057.x. Epub 2009 Jun 3.
Aliment Pharmacol Ther. 2009.
PMID: 19500084
Free article.
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Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria.
Peretz H, Naamati MS, Levartovsky D, Lagziel A, Shani E, Horn I, Shalev H, Landau D.
Peretz H, et al.
Mol Genet Metab. 2007 May;91(1):23-9. doi: 10.1016/j.ymgme.2007.02.005. Epub 2007 Mar 23.
Mol Genet Metab. 2007.
PMID: 17368066
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