Citations for
1EIEE70, PHACTR1
De novo PHACTR1 mutations in West syndrome and their pathophysiological effects.
Hamada N, Ogaya S, Nakashima M, Nishijo T, Sugawara Y, Iwamoto I, Ito H, Maki Y, Shirai K, Baba S, Maruyama K, Saitsu H, Kato M, Matsumoto N, Momiyama T, Nagata KI.
Brain 141(11):3098-3114. doi: 10.1093/brain/awy246. 2018
2PHACTR1
PHACTR1 regulates oxidative stress and inflammation to coronary artery endothelial cells via interaction with NF-κB/p65.
Zhang Z, Jiang F, Zeng L, Wang X, Tu S.
Atherosclerosis 278:180-189. doi: 10.1016/j.atherosclerosis.2018.08.041. Epub 2018 Aug 30. 2018
3EIEE70, PHACTR1
De novo PHACTR1 mutations in West syndrome and their pathophysiological effects.
Hamada N, Ogaya S, Nakashima M, Nishijo T, Sugawara Y, Iwamoto I, Ito H, Maki Y, Shirai K, Baba S, Maruyama K, Saitsu H, Kato M, Matsumoto N, Momiyama T, Nagata KI.
Brain 141(11):3098-3114. doi: 10.1093/brain/awy246. 2018
4PHACTR1
PHACTR1 splicing isoforms and eQTLs in atherosclerosis-relevant human cells.
Codina-Fauteux VA, Beaudoin M, Lalonde S, Lo KS, Lettre G.
BMC Med Genet 19(1):97. doi: 10.1186/s12881-018-0616-7. 2018
5PHACTR1
Genomics of Fibromuscular Dysplasia.
Di Monaco S, Georges A, Lengelé JP, Vikkula M, Persu A.
Int J Mol Sci 19(5). pii: E1526. doi: 10.3390/ijms19051526. Review. 2018
6PHACTR1
PHACTR1 genotype predicts coronary artery disease in patients with familial hypercholesterolemia.
Paquette M, Dufour R, Baass A.
J Clin Lipidol 12(4):966-971. doi: 10.1016/j.jacl.2018.04.012. Epub 2018 Apr 30. 2018
7PHACTR1
Expression analyses of Phactr1 (phosphatase and actin regulator 1) during mouse brain development.
Ito H, Mizuno M, Noguchi K, Morishita R, Iwamoto I, Hara A, Nagata KI.
Neurosci Res 128:50-57. doi: 10.1016/j.neures.2017.08.002. Epub 2017 Aug 10. 2018
8PHACTR1
Coronary artery disease associated gene Phactr1 modulates severity of vascular calcification in vitro.
Aherrahrou R, Aherrahrou Z, Schunkert H, Erdmann J.
Biochem Biophys Res Commun 491(2):396-402. doi: 10.1016/j.bbrc.2017.07.090. Epub 2017 Jul 15. 2017
9PHACTR1
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.
Kiando SR, Tucker NR, Castro-Vega LJ, Katz A, D'Escamard V, Tréard C, Fraher D, Albuisson J, Kadian-Dodov D, Ye Z, Austin E, Yang ML, Hunker K, Barlassina C, Cusi D, Galan P, Empana JP, Jouven X, Gimenez-Roqueplo AP, Bruneval P, Hyun Kim ES, Olin JW, Gornik HL, Azizi M, Plouin PF, Ellinor PT, Kullo IJ, Milan DJ, Ganesh SK, Boutouyrie P, Kovacic JC, Jeunemaitre X, Bouatia-Naji N.
PLoS Genet 12(10):e1006367. doi: 10.1371/journal.pgen.1006367. eCollection 2016 Oct. 2016
10PHACTR1
The Early-Onset Myocardial Infarction Associated PHACTR1 Gene Regulates Skeletal and Cardiac Alpha-Actin Gene Expression.
Kelloniemi A, Szabo Z, Serpi R, Näpänkangas J, Ohukainen P, Tenhunen O, Kaikkonen L, Koivisto E, Bagyura Z, Kerkelä R, Leosdottir M, Hedner T, Melander O, Ruskoaho H, Rysä J.
PLoS One 10(6):e0130502. doi: 10.1371/journal.pone.0130502. eCollection 2015. 2015
11PHACTR1
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.
Debette S, Kamatani Y, Metso TM, Kloss M, Chauhan G, Engelter ST, Pezzini A, Thijs V, Markus HS, Dichgans M, Wolf C, Dittrich R, Touzé E, Southerland AM, Samson Y, Abboud S, Béjot Y, Caso V, Bersano A, Gschwendtner A, Sessa M, Cole J, Lamy C, Medeiros E, Beretta S, Bonati LH, Grau AJ, Michel P, Majersik JJ, Sharma P, Kalashnikova L, Nazarova M, Dobrynina L, Bartels E, Guillon B, van den Herik EG, Fernandez-Cadenas I, Jood K, Nalls MA, De Leeuw FE, Jern C, Cheng YC, Werner I, Metso AJ, Lichy C, Lyrer PA, Brandt T, Boncoraglio GB, Wichmann HE, Gieger C, Johnson AD, Böttcher T, Castellano M, Arveiler D, Ikram MA, Breteler MM, Padovani A, Meschia JF, Kuhlenbäumer G, Rolfs A, Worrall BB; International Stroke Genetics Consortium, Ringelstein EB, Zelenika D, Tatlisumak T, Lathrop M, Leys D, Amouyel P, Dallongeville J; CADISP Group.
Nat Genet 47(1):78-83. doi: 10.1038/ng.3154. Epub 2014 Nov 24. 2015
12NRP1, PHACTR1
Neuropilin-1 regulates a new VEGF-induced gene, Phactr-1, which controls tubulogenesis and modulates lamellipodial dynamics in human endothelial cells.
Allain B, Jarray R, Borriello L, Leforban B, Dufour S, Liu WQ, Pamonsinlapatham P, Bianco S, Larghero J, Hadj-Slimane R, Garbay C, Raynaud F, Lepelletier Y.
Cell Signal 24(1):214-23. doi: 10.1016/j.cellsig.2011.09.003. Epub 2011 Sep 10. 2012
13PHACTR1
Depletion of the novel protein PHACTR-1 from human endothelial cells abolishes tube formation and induces cell death receptor apoptosis.
Jarray R, Allain B, Borriello L, Biard D, Loukaci A, Larghero J, Hadj-Slimane R, Garbay C, Lepelletier Y, Raynaud F.
Biochimie 93(10):1668-75. doi: 10.1016/j.biochi.2011.07.010. Epub 2011 Jul 26. 2011
14PHACTR1, PHACTR2, PHACTR3, PHACTR4
Phactrs 1-4: A family of protein phosphatase 1 and actin regulatory proteins.
Allen PB, Greenfield AT, Svenningsson P, Haspeslagh DC, Greengard P.
Proc Natl Acad Sci U S A 101(18):7187-92. Epub 2004 Apr 23. 2004
15ACAP3, AMBRA1, CMIP, CNTNAP3, CNTNAP4, CPEB4, DAB2IP, DDHD1, DISP2, EEPD1, EXOC4, FAM40A, HELZ2, ITPRIP, KIAA1683, KIAA1712, KIAA1715, KIAA1737, KIAA1751, KIAA1755, KIF21A, MTMR12, PHACTR1, PHF21A, PRDM16, RAPH1, RHOXF1, SEMA4B, SEMA4C, SET7, SH3BP5L, SPHKAP, SSH2, TET1, TEX2, TNKS1BP1, UBE2O, UNC13A, UNK, WNK2, ZCCHC2, ZFHX2, ZNF407, ZNF436
Prediction of the coding sequences of unidentified human genes. XIX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Nagase T, Kikuno R, Hattori A, Kondo Y, Okumura K, Ohara O.
DNA Res 7(6):347-55. 2000