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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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2004 | 1 |
2014 | 2 |
2016 | 1 |
2017 | 2 |
2024 | 0 |
PubMed (cited) for id: 617492
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Olfactomedin 2 Regulates Smooth Muscle Phenotypic Modulation and Vascular Remodeling Through Mediating Runt-Related Transcription Factor 2 Binding to Serum Response Factor.
Arterioscler Thromb Vasc Biol. 2017 Mar;37(3):446-454. doi: 10.1161/ATVBAHA.116.308606. Epub 2017 Jan 5.
Arterioscler Thromb Vasc Biol. 2017.
PMID: 28062493
Free PMC article.
Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders.
Holt R, Ugur Iseri SA, Wyatt AW, Bax DA, Gold Diaz D, Santos C, Broadgate S, Dunn R, Bruty J, Wallis Y, McMullan D, Ogilvie C, Gerrelli D, Zhang Y, Ragge N.
Holt R, et al.
Hum Genet. 2017 Jan;136(1):119-127. doi: 10.1007/s00439-016-1745-8. Epub 2016 Nov 14.
Hum Genet. 2017.
PMID: 27844144
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Olfactomedin 2, a novel regulator for transforming growth factor-β-induced smooth muscle differentiation of human embryonic stem cell-derived mesenchymal cells.
Shi N, Guo X, Chen SY.
Shi N, et al.
Mol Biol Cell. 2014 Dec 15;25(25):4106-14. doi: 10.1091/mbc.E14-08-1255. Epub 2014 Oct 8.
Mol Biol Cell. 2014.
PMID: 25298399
Free PMC article.
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Deletion of olfactomedin 2 induces changes in the AMPA receptor complex and impairs visual, olfactory, and motor functions in mice.
Sultana A, Nakaya N, Dong L, Abu-Asab M, Qian H, Tomarev SI.
Sultana A, et al.
Exp Neurol. 2014 Nov;261:802-11. doi: 10.1016/j.expneurol.2014.09.002. Epub 2014 Sep 10.
Exp Neurol. 2014.
PMID: 25218043
Free PMC article.
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Bioinformatic approaches for identification and characterization of olfactomedin related genes with a potential role in pathogenesis of ocular disorders.
Mukhopadhyay A, Talukdar S, Bhattacharjee A, Ray K.
Mukhopadhyay A, et al.
Mol Vis. 2004 Apr 20;10:304-14.
Mol Vis. 2004.
PMID: 15123989
Free article.
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