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2. Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation. Bienvenu T; des Portes V; McDonell N; Carrié A; Zemni R; Couvert P; Ropers HH; Moraine C; van Bokhoven H; Fryns JP; Allen K; Walsh CA; Boué J; Kahn A; Chelly J; Beldjord C Am J Med Genet; 2000 Aug; 93(4):294-8. PubMed ID: 10946356 [TBL] [Abstract][Full Text] [Related]
3. The mental retardation protein PAK3 contributes to synapse formation and plasticity in hippocampus. Boda B; Alberi S; Nikonenko I; Node-Langlois R; Jourdain P; Moosmayer M; Parisi-Jourdain L; Muller D J Neurosci; 2004 Dec; 24(48):10816-25. PubMed ID: 15574732 [TBL] [Abstract][Full Text] [Related]
4. Molecular study of the PAK3 and GDI1 genes in nonsyndromic X-linked mental retardation spanish patients. Rifé M; Mallolas J; Castellví-Bel S; Badenas C; Jiménez D; Milà M Am J Med Genet; 2000 Oct; 94(5):389-91. PubMed ID: 11050624 [No Abstract] [Full Text] [Related]
5. A de novo mutation in the X-linked PAK3 gene is the underlying cause of intellectual disability and macrocephaly in monozygotic twins. Hertecant J; Komara M; Nagi A; Al-Zaabi O; Fathallah W; Cui H; Yang Y; Eng CM; Al Sorkhy M; Ghattas MA; Al-Gazali L; Ali BR Eur J Med Genet; 2017 Apr; 60(4):212-216. PubMed ID: 28126652 [TBL] [Abstract][Full Text] [Related]
6. The p21-activated kinase 3 implicated in mental retardation regulates spine morphogenesis through a Cdc42-dependent pathway. Kreis P; Thévenot E; Rousseau V; Boda B; Muller D; Barnier JV J Biol Chem; 2007 Jul; 282(29):21497-506. PubMed ID: 17537723 [TBL] [Abstract][Full Text] [Related]
7. Sequential implication of the mental retardation proteins ARHGEF6 and PAK3 in spine morphogenesis. Nodé-Langlois R; Muller D; Boda B J Cell Sci; 2006 Dec; 119(Pt 23):4986-93. PubMed ID: 17105769 [TBL] [Abstract][Full Text] [Related]
8. A comparative expression analysis of four MRX genes regulating intracellular signalling via small GTPases. Kohn M; Steinbach P; Hameister H; Kehrer-Sawatzki H Eur J Hum Genet; 2004 Jan; 12(1):29-37. PubMed ID: 14673471 [TBL] [Abstract][Full Text] [Related]
9. Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation. Kutsche K; Yntema H; Brandt A; Jantke I; Nothwang HG; Orth U; Boavida MG; David D; Chelly J; Fryns JP; Moraine C; Ropers HH; Hamel BC; van Bokhoven H; Gal A Nat Genet; 2000 Oct; 26(2):247-50. PubMed ID: 11017088 [TBL] [Abstract][Full Text] [Related]
16. Characterization of ARHGEF6, a guanine nucleotide exchange factor for Rho GTPases and a candidate gene for X-linked mental retardation: mutation screening in Börjeson-Forssman-Lehmann syndrome and MRX27. Lower KM; Gecz J Am J Med Genet; 2001 Apr; 100(1):43-8. PubMed ID: 11337747 [TBL] [Abstract][Full Text] [Related]
17. PAK3 related mental disability: further characterization of the phenotype. Peippo M; Koivisto AM; Särkämö T; Sipponen M; von Koskull H; Ylisaukko-oja T; Rehnström K; Froyen G; Ignatius J; Järvelä I Am J Med Genet A; 2007 Oct; 143A(20):2406-16. PubMed ID: 17853471 [TBL] [Abstract][Full Text] [Related]
18. The four mammalian splice variants encoded by the p21-activated kinase 3 gene have different biological properties. Kreis P; Rousseau V; Thévenot E; Combeau G; Barnier JV J Neurochem; 2008 Aug; 106(3):1184-97. PubMed ID: 18507705 [TBL] [Abstract][Full Text] [Related]
19. X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3. Gedeon AK; Nelson J; Gécz J; Mulley JC Am J Med Genet A; 2003 Aug; 120A(4):509-17. PubMed ID: 12884430 [TBL] [Abstract][Full Text] [Related]
20. A new constitutively active brain PAK3 isoform displays modified specificities toward Rac and Cdc42 GTPases. Rousseau V; Goupille O; Morin N; Barnier JV J Biol Chem; 2003 Feb; 278(6):3912-20. PubMed ID: 12464619 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]