van der Lans CA - Search Results

1

The peripheral blood mononuclear cell microRNA signature of coronary artery disease.

Hoekstra M, van der Lans CA, Halvorsen B, Gullestad L, Kuiper J, Aukrust P, van Berkel TJ, Biessen EA. Hoekstra M, et al. Among authors: van der lans ca. Biochem Biophys Res Commun. 2010 Apr 9;394(3):792-7. doi: 10.1016/j.bbrc.2010.03.075. Epub 2010 Mar 15. Biochem Biophys Res Commun. 2010. PMID: 20230787

2

Aorta of ApoE-deficient mice responds to atherogenic stimuli by a prelesional increase and subsequent decrease in the expression of antioxidant enzymes.

't Hoen PA, Van der Lans CA, Van Eck M, Bijsterbosch MK, Van Berkel TJ, Twisk J. 't Hoen PA, et al. Among authors: van der lans ca. Circ Res. 2003 Aug 8;93(3):262-9. doi: 10.1161/01.RES.0000082978.92494.B1. Epub 2003 Jun 26. Circ Res. 2003. PMID: 12829615

3

Differential effects of scavenger receptor BI deficiency on lipid metabolism in cells of the arterial wall and in the liver.

Van Eck M, Twisk J, Hoekstra M, Van Rij BT, Van der Lans CA, Bos IS, Kruijt JK, Kuipers F, Van Berkel TJ. Van Eck M, et al. Among authors: van der lans ca. J Biol Chem. 2003 Jun 27;278(26):23699-705. doi: 10.1074/jbc.M211233200. Epub 2003 Mar 14. J Biol Chem. 2003. PMID: 12639961 Free article.

4

Vascular endothelial growth factor-A induces plaque expansion in ApoE knock-out mice by promoting de novo leukocyte recruitment.

Lucerna M, Zernecke A, de Nooijer R, de Jager SC, Bot I, van der Lans C, Kholova I, Liehn EA, van Berkel TJ, Yla-Herttuala S, Weber C, Biessen EA. Lucerna M, et al. Blood. 2007 Jan 1;109(1):122-9. doi: 10.1182/blood-2006-07-031773. Epub 2006 Sep 21. Blood. 2007. PMID: 16990600 Free article.

5

TREX1 mutations are not associated with sporadic inclusion body myositis.

Cox FM, Boon EM, van der Lans CA, Bakker E, Verschuuren JJ, Badrising UA. Cox FM, et al. Among authors: van der lans ca. Eur J Neurol. 2010 Aug;17(8):1108-9. doi: 10.1111/j.1468-1331.2010.02964.x. Epub 2010 Feb 23. Eur J Neurol. 2010. PMID: 20192983

6

Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein-Taybi and Filippi syndromes.

de Vries TI, Monroe GR, van Belzen MJ, van der Lans CA, Savelberg SM, Newman WG, van Haaften G, Nievelstein RA, van Haelst MM. de Vries TI, et al. Among authors: van der lans ca. Eur J Hum Genet. 2016 Aug;24(9):1363-6. doi: 10.1038/ejhg.2016.14. Epub 2016 Mar 9. Eur J Hum Genet. 2016. PMID: 26956253 Free PMC article.

7

A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening.

Gerkes EH, Fock JM, den Dunnen WF, van Belzen MJ, van der Lans CA, Hoving EW, Fakkert IE, Smith MJ, Evans DG, Olderode-Berends MJ. Gerkes EH, et al. Among authors: van der lans ca. Neurogenetics. 2016 Apr;17(2):83-9. doi: 10.1007/s10048-015-0472-y. Epub 2016 Jan 23. Neurogenetics. 2016. PMID: 26803492 Free PMC article. Review.

8

Erratum.

Wincent J, Luthman A, van Belzen M, van der Lans C, Albert J, Nordgren A, Anderlid BM. Wincent J, et al. Mol Genet Genomic Med. 2016 May 12;4(3):367. doi: 10.1002/mgg3.218. eCollection 2016 May. Mol Genet Genomic Med. 2016. PMID: 27247963 Free PMC article.

9

Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients.

Santen GW, Aten E, Vulto-van Silfhout AT, Pottinger C, van Bon BW, van Minderhout IJ, Snowdowne R, van der Lans CA, Boogaard M, Linssen MM, Vijfhuizen L, van der Wielen MJ, Vollebregt MJ; Coffin-Siris consortium; Breuning MH, Kriek M, van Haeringen A, den Dunnen JT, Hoischen A, Clayton-Smith J, de Vries BB, Hennekam RC, van Belzen MJ. Santen GW, et al. Among authors: van der lans ca. Hum Mutat. 2013 Nov;34(11):1519-28. doi: 10.1002/humu.22394. Epub 2013 Aug 30. Hum Mutat. 2013. PMID: 23929686

10

CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein-Taybi syndrome.

Wincent J, Luthman A, van Belzen M, van der Lans C, Albert J, Nordgren A, Anderlid BM. Wincent J, et al. Mol Genet Genomic Med. 2015 Sep 22;4(1):39-45. doi: 10.1002/mgg3.177. eCollection 2016 Jan. Mol Genet Genomic Med. 2015. PMID: 26788536 Free PMC article.

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

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

10 results

Search Page