Vikkula M - Search Results

1

Ligand oligomerization state controls Tie2 receptor trafficking and angiopoietin-2-specific responses.

Pietilä R, Nätynki M, Tammela T, Kangas J, Pulkki KH, Limaye N, Vikkula M, Koh GY, Saharinen P, Alitalo K, Eklund L. Pietilä R, et al. Among authors: vikkula m. J Cell Sci. 2012 May 1;125(Pt 9):2212-23. doi: 10.1242/jcs.098020. Epub 2012 Feb 22. J Cell Sci. 2012. PMID: 22357955 Free article.

2

Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2.

Vikkula M, Boon LM, Carraway KL 3rd, Calvert JT, Diamonti AJ, Goumnerov B, Pasyk KA, Marchuk DA, Warman ML, Cantley LC, Mulliken JB, Olsen BR. Vikkula M, et al. Cell. 1996 Dec 27;87(7):1181-90. doi: 10.1016/s0092-8674(00)81814-0. Cell. 1996. PMID: 8980225 Free article.

3

Endothelial receptor tyrosine kinases activate the STAT signaling pathway: mutant Tie-2 causing venous malformations signals a distinct STAT activation response.

Korpelainen EI, Kärkkäinen M, Gunji Y, Vikkula M, Alitalo K. Korpelainen EI, et al. Among authors: vikkula m. Oncogene. 1999 Jan 7;18(1):1-8. doi: 10.1038/sj.onc.1202288. Oncogene. 1999. PMID: 9926914

4

Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma.

Jinnin M, Medici D, Park L, Limaye N, Liu Y, Boscolo E, Bischoff J, Vikkula M, Boye E, Olsen BR. Jinnin M, et al. Among authors: vikkula m. Nat Med. 2008 Nov;14(11):1236-46. doi: 10.1038/nm.1877. Epub 2008 Oct 19. Nat Med. 2008. PMID: 18931684 Free PMC article.

5

Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations.

Limaye N, Wouters V, Uebelhoer M, Tuominen M, Wirkkala R, Mulliken JB, Eklund L, Boon LM, Vikkula M. Limaye N, et al. Among authors: vikkula m. Nat Genet. 2009 Jan;41(1):118-24. doi: 10.1038/ng.272. Epub 2008 Dec 14. Nat Genet. 2009. PMID: 19079259 Free PMC article.

6

Recessive primary congenital lymphoedema caused by a VEGFR3 mutation.

Ghalamkarpour A, Holnthoner W, Saharinen P, Boon LM, Mulliken JB, Alitalo K, Vikkula M. Ghalamkarpour A, et al. Among authors: vikkula m. J Med Genet. 2009 Jun;46(6):399-404. doi: 10.1136/jmg.2008.064469. Epub 2009 Mar 15. J Med Genet. 2009. PMID: 19289394

7

From germline towards somatic mutations in the pathophysiology of vascular anomalies.

Limaye N, Boon LM, Vikkula M. Limaye N, et al. Among authors: vikkula m. Hum Mol Genet. 2009 Apr 15;18(R1):R65-74. doi: 10.1093/hmg/ddp002. Hum Mol Genet. 2009. PMID: 19297403 Free PMC article. Review.

8

Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects.

Wouters V, Limaye N, Uebelhoer M, Irrthum A, Boon LM, Mulliken JB, Enjolras O, Baselga E, Berg J, Dompmartin A, Ivarsson SA, Kangesu L, Lacassie Y, Murphy J, Teebi AS, Penington A, Rieu P, Vikkula M. Wouters V, et al. Among authors: vikkula m. Eur J Hum Genet. 2010 Apr;18(4):414-20. doi: 10.1038/ejhg.2009.193. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888299 Free PMC article.

9

Venous malformation-causative TIE2 mutations mediate an AKT-dependent decrease in PDGFB.

Uebelhoer M, Nätynki M, Kangas J, Mendola A, Nguyen HL, Soblet J, Godfraind C, Boon LM, Eklund L, Limaye N, Vikkula M. Uebelhoer M, et al. Among authors: vikkula m. Hum Mol Genet. 2013 Sep 1;22(17):3438-48. doi: 10.1093/hmg/ddt198. Epub 2013 Apr 30. Hum Mol Genet. 2013. PMID: 23633549 Free PMC article.

10

Variable Somatic TIE2 Mutations in Half of Sporadic Venous Malformations.

Soblet J, Limaye N, Uebelhoer M, Boon LM, Vikkula M. Soblet J, et al. Among authors: vikkula m. Mol Syndromol. 2013 Apr;4(4):179-83. doi: 10.1159/000348327. Epub 2013 Mar 26. Mol Syndromol. 2013. PMID: 23801934 Free PMC article.

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