These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
127 related items for PubMed ID: 22621187
1. Cutaneomucosal venous malformations are linked to the TIE2 mutation in a large Chinese family. Shu W, Lin Y, Hua R, Luo Y, He N, Fang L, Tan J, Lu J, Hu Z, Yuan Z. Exp Dermatol; 2012 Jun; 21(6):456-7. PubMed ID: 22621187 [Abstract] [Full Text] [Related]
2. 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. Eur J Hum Genet; 2010 Apr; 18(4):414-20. PubMed ID: 19888299 [Abstract] [Full Text] [Related]
3. Facial cutaneo-mucosal venous malformations can develop independently of mutation of TEK gene but may be associated with excessive expression of Src and p-Src. Brahami N, Subramaniam S, Al-Ddafari MS, Elkaim C, Harmand PO, Sari BE, Lefranc G, Aribi M. J Negat Results Biomed; 2017 Mar 20; 16(1):9. PubMed ID: 28316284 [Abstract] [Full Text] [Related]
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. Nat Genet; 2009 Jan 20; 41(1):118-24. PubMed ID: 19079259 [Abstract] [Full Text] [Related]
6. A Tie2 kinase mutation causing venous malformations increases phosphorylation rates and enhances cooperativity. Kennedy MA, Xu Z, Wu Y, Sohl CD. Biochem Biophys Res Commun; 2019 Feb 19; 509(4):898-902. PubMed ID: 30638931 [Abstract] [Full Text] [Related]
7. Transgenic Expression of A Venous Malformation Related Mutation, TIE2-R849W, Significantly Induces Multiple Malformations of Zebrafish. Du Z, Ma HL, Zhang ZY, Zheng JW, Wang YA. Int J Med Sci; 2018 Feb 19; 15(4):385-394. PubMed ID: 29511374 [Abstract] [Full Text] [Related]
8. STAT1 activation by venous malformations mutant Tie2-R849W antagonizes VEGF-A-mediated angiogenic response partly via reduced bFGF production. Huang YH, Wu MP, Pan SC, Su WC, Chen YW, Wu LW. Angiogenesis; 2013 Jan 19; 16(1):207-22. PubMed ID: 23086340 [Abstract] [Full Text] [Related]
9. Tie2-R849W mutant in venous malformations chronically activates a functional STAT1 to modulate gene expression. Hu HT, Huang YH, Chang YA, Lee CK, Jiang MJ, Wu LW. J Invest Dermatol; 2008 Sep 19; 128(9):2325-33. PubMed ID: 18401423 [Abstract] [Full Text] [Related]
10. Classification and Tie2 mutations in spinal and soft tissue vascular anomalies. Zhou M, Jiang R, Zhao G, Wang L, Wang H, Li W, Li Y, Du X, Bai J. Gene; 2015 Oct 15; 571(1):91-6. PubMed ID: 26115772 [Abstract] [Full Text] [Related]
11. CD10 and CD34 as markers in vascular malformations with PIK3CA and TEK mutations. Moneghini L, Tosi D, Graziani D, Caretti A, Colletti G, Baraldini V, Cattaneo E, Spaccini L, Zocca A, Bulfamante GP. Hum Pathol; 2020 May 15; 99():98-106. PubMed ID: 32272124 [Abstract] [Full Text] [Related]
12. AKT/FOXO1 axis links cross-talking of endothelial cell and pericyte in TIE2-mutated venous malformations. Si Y, Huang J, Li X, Fu Y, Xu R, Du Y, Cheng J, Jiang H. Cell Commun Signal; 2020 Aug 31; 18(1):139. PubMed ID: 32867785 [Abstract] [Full Text] [Related]
14. [Haplotype analysis for mucocutaneous venous malformations in a Chinese Han ethnic family]. Shu W, Lin YK, Hua R, Luo YY, Fang L, Xu SR, He N, Ma J, Hu QP, Li XL, Yuan ZG. Yi Chuan; 2012 Apr 31; 34(4):431-6. PubMed ID: 22522160 [Abstract] [Full Text] [Related]
15. Genetic landscape of common venous malformations in the head and neck. Du Z, Liu JL, You YH, Wang LZ, He J, Zheng JW, Zhang ZY, Wang YA. J Vasc Surg Venous Lymphat Disord; 2021 Jul 31; 9(4):1007-1016.e7. PubMed ID: 33248299 [Abstract] [Full Text] [Related]
16. Association study between of Tie2/angiopoietin-2 and VEGF/KDR pathway gene polymorphisms and vascular malformations. Zheng Q, Du J, Zhang Z, Xu J, Fu L, Cao Y, Huang X, Guo L. Gene; 2013 Jul 10; 523(2):195-8. PubMed ID: 23566851 [Abstract] [Full Text] [Related]
17. Variable Somatic TIE2 Mutations in Half of Sporadic Venous Malformations. Soblet J, Limaye N, Uebelhoer M, Boon LM, Vikkula M. Mol Syndromol; 2013 Apr 10; 4(4):179-83. PubMed ID: 23801934 [Abstract] [Full Text] [Related]
18. Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) Mutations. Soblet J, Kangas J, Nätynki M, Mendola A, Helaers R, Uebelhoer M, Kaakinen M, Cordisco M, Dompmartin A, Enjolras O, Holden S, Irvine AD, Kangesu L, Léauté-Labrèze C, Lanoel A, Lokmic Z, Maas S, McAleer MA, Penington A, Rieu P, Syed S, van der Vleuten C, Watson R, Fishman SJ, Mulliken JB, Eklund L, Limaye N, Boon LM, Vikkula M. J Invest Dermatol; 2017 Jan 10; 137(1):207-216. PubMed ID: 27519652 [Abstract] [Full Text] [Related]
19. 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. Hum Mol Genet; 2013 Sep 01; 22(17):3438-48. PubMed ID: 23633549 [Abstract] [Full Text] [Related]