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Results: 13

Cited In for PubMed (Select 11278945)


Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.

Brookes E, Laurent B, Õunap K, Carroll R, Moeschler JB, Field M, Schwartz CE, Gecz J, Shi Y.

Hum Mol Genet. 2015 May 15;24(10):2861-72. doi: 10.1093/hmg/ddv046. Epub 2015 Feb 9.


EMILIN2 regulates platelet activation, thrombus formation, and clot retraction.

Huang M, Sannaningaiah D, Zhao N, Gong Y, Grondolsky J, Hoover-Plow J.

PLoS One. 2015 Feb 6;10(2):e0115284. doi: 10.1371/journal.pone.0115284. eCollection 2015.


Molecular mechanisms of thoracic aortic dissection.

Wu D, Shen YH, Russell L, Coselli JS, LeMaire SA.

J Surg Res. 2013 Oct;184(2):907-24. doi: 10.1016/j.jss.2013.06.007. Epub 2013 Jun 29. Review.


Copy number variation analysis in 98 individuals with PHACE syndrome.

Siegel DH, Shieh JT, Kwon EK, Baselga E, Blei F, Cordisco M, Dobyns WB, Duffy KJ, Garzon MC, Gibbs DL, Grimmer JF, Hayflick SJ, Krol AL, Kwok PY, Lorier R, Matter A, McWeeney S, Metry D, Mitchell S, Pope E, Santoro JL, Stevenson DA, Bayrak-Toydemir P, Wilmot B, Worthey EA, Frieden IJ, Drolet BA, Broeckel U.

J Invest Dermatol. 2013 Mar;133(3):677-84. doi: 10.1038/jid.2012.367. Epub 2012 Oct 25.


The EMILIN/Multimerin family.

Colombatti A, Spessotto P, Doliana R, Mongiat M, Bressan GM, Esposito G.

Front Immunol. 2012 Jan 6;2:93. doi: 10.3389/fimmu.2011.00093. eCollection 2011.


EMILIN-3, peculiar member of elastin microfibril interface-located protein (EMILIN) family, has distinct expression pattern, forms oligomeric assemblies, and serves as transforming growth factor β (TGF-β) antagonist.

Schiavinato A, Becker AK, Zanetti M, Corallo D, Milanetto M, Bizzotto D, Bressan G, Guljelmovic M, Paulsson M, Wagener R, Braghetta P, Bonaldo P.

J Biol Chem. 2012 Mar 30;287(14):11498-515. doi: 10.1074/jbc.M111.303578. Epub 2012 Feb 10.


EMILIN2 (Elastin microfibril interface located protein), potential modifier of thrombosis.

Sa Q, Hoover-Plow JL.

Thromb J. 2011 May 11;9:9. doi: 10.1186/1477-9560-9-9.


Mouse chromosome 17 candidate modifier genes for thrombosis.

Sa Q, Hart E, Nadeau JH, Hoover-Plow JL.

Mamm Genome. 2010 Aug;21(7-8):337-49. doi: 10.1007/s00335-010-9274-6. Epub 2010 Aug 11.


The extracellular matrix glycoprotein elastin microfibril interface located protein 2: a dual role in the tumor microenvironment.

Mongiat M, Marastoni S, Ligresti G, Lorenzon E, Schiappacassi M, Perris R, Frustaci S, Colombatti A.

Neoplasia. 2010 Apr;12(4):294-304.


Regulation of the extrinsic apoptotic pathway by the extracellular matrix glycoprotein EMILIN2.

Mongiat M, Ligresti G, Marastoni S, Lorenzon E, Doliana R, Colombatti A.

Mol Cell Biol. 2007 Oct;27(20):7176-87. Epub 2007 Aug 13.


Structural and functional anatomy of the globular domain of complement protein C1q.

Kishore U, Ghai R, Greenhough TJ, Shrive AK, Bonifati DM, Gadjeva MG, Waters P, Kojouharova MS, Chakraborty T, Agrawal A.

Immunol Lett. 2004 Sep;95(2):113-28. Review. Erratum in: Immunol Lett. 2005 Oct 15;101(1):116.


EMILIN-1 deficiency induces elastogenesis and vascular cell defects.

Zanetti M, Braghetta P, Sabatelli P, Mura I, Doliana R, Colombatti A, Volpin D, Bonaldo P, Bressan GM.

Mol Cell Biol. 2004 Jan;24(2):638-50.

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