PHACTR1
Phosphatase and actin regulator 1 is a protein that in humans is encoded by the PHACTR1 gene. [1]
References
- ↑ "Entrez Gene: Phosphatase and actin regulator 1". Retrieved 2013-09-10.
Further reading
- Fils-Aime, N.; Dai, M.; Guo, J.; El-Mousawi, M.; Kahramangil, B.; Neel, J. -C.; Lebrun, J. -J. (2013). "MicroRNA-584 and the Protein Phosphatase and Actin Regulator 1 (PHACTR1), a New Signaling Route through Which Transforming Growth Factor- Mediates the Migration and Actin Dynamics of Breast Cancer Cells". Journal of Biological Chemistry 288 (17): 11807–11823. doi:10.1074/jbc.M112.430934. PMC 3636869. PMID 23479725.
- Kiel, D. P.; Demissie, S.; Dupuis, J. E.; Lunetta, K. L.; Murabito, J. M.; Karasik, D. (2007). "Genome-wide association with bone mass and geometry in the Framingham Heart Study". BMC Medical Genetics 8: S14. doi:10.1186/1471-2350-8-S1-S14. PMC 1995606. PMID 17903296.
- Freilinger, T.; Anttila, V.; De Vries, B.; Malik, R.; Kallela, M.; Terwindt, G. M.; Pozo-Rosich, P.; Winsvold, B.; Nyholt, D. R.; Van Oosterhout, W. P. J.; Artto, V.; Todt, U.; Hämäläinen, E.; Fernández-Morales, J. S.; Louter, M. A.; Kaunisto, M. A.; Schoenen, J.; Raitakari, O.; Lehtimäki, T.; Vila-Pueyo, M.; Göbel, H.; Wichmann, E.; Sintas, C. L.; Uitterlinden, A. G.; Hofman, A.; Rivadeneira, F.; Heinze, A.; Tronvik, E.; Van Duijn, C. M.; Kaprio, J. (2012). "Genome-wide association analysis identifies susceptibility loci for migraine without aura". Nature Genetics 44 (7): 777–782. doi:10.1038/ng.2307. PMID 22683712.
- Lluís-Ganella, C.; Lucas, G.; Subirana, I.; Sentí, M.; Jimenez-Conde, J.; Marrugat, J.; Tomás, M.; Elosua, R. (2010). "Additive effect of multiple genetic variants on the risk of coronary artery disease". Revista espanola de cardiologia 63 (8): 925–933. doi:10.1016/S1885-5857(10)70186-9. PMID 20738937.
- Ripatti, S.; Tikkanen, E.; Orho-Melander, M.; Havulinna, A. S.; Silander, K.; Sharma, A.; Guiducci, C.; Perola, M.; Jula, A.; Sinisalo, J.; Lokki, M. L.; Nieminen, M. S.; Melander, O.; Salomaa, V.; Peltonen, L.; Kathiresan, S. (2010). "A multilocus genetic risk score for coronary heart disease: Case-control and prospective cohort analyses". The Lancet 376 (9750): 1393–1400. doi:10.1016/S0140-6736(10)61267-6. PMC 2965351. PMID 20971364.
- Allain, B.; Jarray, R.; Borriello, L.; Leforban, B.; Dufour, S.; Liu, W. Q.; Pamonsinlapatham, P.; Bianco, S.; Larghero, J. R. M.; Hadj-Slimane, R. D.; Garbay, C.; Raynaud, F. O.; Lepelletier, Y. (2012). "Neuropilin-1 regulates a new VEGF-induced gene, Phactr-1, which controls tubulogenesis and modulates lamellipodial dynamics in human endothelial cells". Cellular Signalling 24 (1): 214–223. doi:10.1016/j.cellsig.2011.09.003. PMID 21939755.
- Peden, J. F.; Hopewell, J. C.; Saleheen, D.; Chambers, J. C.; Hager, J.; Soranzo, N.; Collins, R.; Danesh, J.; Elliott, P.; Farrall, M.; Stirrups, K.; Zhang, W.; Hamsten, A.; Parish, S.; Lathrop, M.; Watkins, H.; Clarke, R.; Deloukas, P.; Kooner, J. S.; Goel, A.; Ongen, H.; Strawbridge, R. J.; Heath, S.; Mälarstig, A.; Helgadottir, A.; Öhrvik, J.; Murtaza, M.; Potter, S.; Hunt, S. E.; Delepine, M. (2011). "A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease". Nature Genetics 43 (4): 339–344. doi:10.1038/ng.782. PMID 21378988.
- Kathiresan, S.; Kathiresan, B. F.; Voight, S.; Purcell, K.; Musunuru, D.; Ardissino, P. M.; Mannucci, S.; Anand, J. C.; Engert, N. J.; Samani, H.; Schunkert, J.; Erdmann, M. P.; Reilly, D. J.; Rader, T.; Morgan, J. A.; Spertus, M.; Stoll, D.; Girelli, P. P.; McKeown, C. C.; Patterson, D. S.; Siscovick, C. J.; O'Donnell, R.; Elosua, L.; Peltonen, V.; Salomaa, S. M.; Schwartz, O.; Melander, D.; Altshuler, D.; Ardissino, P. A.; Merlini, C. (2009). "Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants". Nature Genetics 41 (3): 334–341. doi:10.1038/ng.327. PMC 2681011. PMID 19198609.
- Bevan, S.; Traylor, M.; Adib-Samii, P.; Malik, R.; Paul, N. L. M.; Jackson, C.; Farrall, M.; Rothwell, P. M.; Sudlow, C.; Dichgans, M.; Markus, H. S. (2012). "Genetic Heritability of Ischemic Stroke and the Contribution of Previously Reported Candidate Gene and Genomewide Associations". Stroke 43 (12): 3161–3167. doi:10.1161/STROKEAHA.112.665760. PMID 23042660.
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