Vikkula M - Search Results

1

Efficient activation of the lymphangiogenic growth factor VEGF-C requires the C-terminal domain of VEGF-C and the N-terminal domain of CCBE1.

Jha SK, Rauniyar K, Karpanen T, Leppänen VM, Brouillard P, Vikkula M, Alitalo K, Jeltsch M. Jha SK, et al. Among authors: vikkula m. Sci Rep. 2017 Jul 7;7(1):4916. doi: 10.1038/s41598-017-04982-1. Sci Rep. 2017. PMID: 28687807 Free PMC article.

2

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

3

A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.

Boon LM, Brouillard P, Irrthum A, Karttunen L, Warman ML, Rudolph R, Mulliken JB, Olsen BR, Vikkula M. Boon LM, et al. Among authors: vikkula m. Am J Hum Genet. 1999 Jul;65(1):125-33. doi: 10.1086/302450. Am J Hum Genet. 1999. PMID: 10364524 Free PMC article.

4

Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.

Irrthum A, Karkkainen MJ, Devriendt K, Alitalo K, Vikkula M. Irrthum A, et al. Among authors: vikkula m. Am J Hum Genet. 2000 Aug;67(2):295-301. doi: 10.1086/303019. Epub 2000 Jun 9. Am J Hum Genet. 2000. PMID: 10856194 Free PMC article.

5

High-resolution physical and transcript map of the locus for venous malformations with glomus cells (VMGLOM) on chromosome 1p21-p22.

Brouillard P, Olsen BR, Vikkula M. Brouillard P, et al. Among authors: vikkula m. Genomics. 2000 Jul 1;67(1):96-101. doi: 10.1006/geno.2000.6232. Genomics. 2000. PMID: 10945476

6

Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YAC.

Irrthum A, Brouillard P, Enjolras O, Gibbs NF, Eichenfield LF, Olsen BR, Mulliken JB, Boon LM, Vikkula M. Irrthum A, et al. Among authors: vikkula m. Eur J Hum Genet. 2001 Jan;9(1):34-8. doi: 10.1038/sj.ejhg.5200576. Eur J Hum Genet. 2001. PMID: 11175297

7

Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas").

Brouillard P, Boon LM, Mulliken JB, Enjolras O, Ghassibé M, Warman ML, Tan OT, Olsen BR, Vikkula M. Brouillard P, et al. Among authors: vikkula m. Am J Hum Genet. 2002 Apr;70(4):866-74. doi: 10.1086/339492. Epub 2002 Feb 13. Am J Hum Genet. 2002. PMID: 11845407 Free PMC article.

8

Vascular malformations: localized defects in vascular morphogenesis.

Brouillard P, Vikkula M. Brouillard P, et al. Among authors: vikkula m. Clin Genet. 2003 May;63(5):340-51. doi: 10.1034/j.1399-0004.2003.00092.x. Clin Genet. 2003. PMID: 12752563 Review.

9

Glomulin is predominantly expressed in vascular smooth muscle cells in the embryonic and adult mouse.

McIntyre BA, Brouillard P, Aerts V, Gutierrez-Roelens I, Vikkula M. McIntyre BA, et al. Among authors: vikkula m. Gene Expr Patterns. 2004 May;4(3):351-8. doi: 10.1016/j.modgep.2003.09.007. Gene Expr Patterns. 2004. PMID: 15053987

10

Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect.

Brouillard P, Ghassibé M, Penington A, Boon LM, Dompmartin A, Temple IK, Cordisco M, Adams D, Piette F, Harper JI, Syed S, Boralevi F, Taïeb A, Danda S, Baselga E, Enjolras O, Mulliken JB, Vikkula M. Brouillard P, et al. Among authors: vikkula m. J Med Genet. 2005 Feb;42(2):e13. doi: 10.1136/jmg.2004.024174. J Med Genet. 2005. PMID: 15689436 Free PMC article.

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