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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1995 | 1 |
2000 | 1 |
2003 | 1 |
2007 | 1 |
2014 | 1 |
2015 | 1 |
2016 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 221037
6 results
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Page 1
Mutations in JMJD1C are involved in Rett syndrome and intellectual disability.
Genet Med. 2016 Apr;18(4):378-85. doi: 10.1038/gim.2015.100. Epub 2015 Jul 16.
Genet Med. 2016.
PMID: 26181491
Free PMC article.
Novel somatic and germline mutations in intracranial germ cell tumours.
Wang L, Yamaguchi S, Burstein MD, Terashima K, Chang K, Ng HK, Nakamura H, He Z, Doddapaneni H, Lewis L, Wang M, Suzuki T, Nishikawa R, Natsume A, Terasaka S, Dauser R, Whitehead W, Adekunle A, Sun J, Qiao Y, Marth G, Muzny DM, Gibbs RA, Leal SM, Wheeler DA, Lau CC.
Wang L, et al.
Nature. 2014 Jul 10;511(7508):241-5. doi: 10.1038/nature13296. Epub 2014 Jun 4.
Nature. 2014.
PMID: 24896186
Free PMC article.
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A novel variant of the putative demethylase gene, s-JMJD1C, is a coactivator of the AR.
Wolf SS, Patchev VK, Obendorf M.
Wolf SS, et al.
Arch Biochem Biophys. 2007 Apr 1;460(1):56-66. doi: 10.1016/j.abb.2007.01.017. Epub 2007 Feb 5.
Arch Biochem Biophys. 2007.
PMID: 17353003
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Identification and characterization of TRIP8 gene in silico.
Katoh M, Katoh M.
Katoh M, et al.
Int J Mol Med. 2003 Nov;12(5):817-21.
Int J Mol Med. 2003.
PMID: 14533015
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Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro.
Nagase T, Kikuno R, Ishikawa KI, Hirosawa M, Ohara O.
Nagase T, et al.
DNA Res. 2000 Feb 28;7(1):65-73. doi: 10.1093/dnares/7.1.65.
DNA Res. 2000.
PMID: 10718198
Free article.
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Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor.
Lee JW, Choi HS, Gyuris J, Brent R, Moore DD.
Lee JW, et al.
Mol Endocrinol. 1995 Feb;9(2):243-54. doi: 10.1210/mend.9.2.7776974.
Mol Endocrinol. 1995.
PMID: 7776974
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