Investigating the potential genetic association between RANBP9 polymorphisms and the risk of schizophrenia

McGrath J, Saha S, Chant D and Welham J: Schizophrenia: a concise overview of incidence, prevalence, and mortality. Epidemiol Rev. 30:67–76. 2008. View Article : Google Scholar : PubMed/NCBI

Torrey EF: Prevalence studies in schizophrenia. Br J Psychiatry. 150:598–608. 1987. View Article : Google Scholar : PubMed/NCBI

Park HJ, Westin CF, Kubicki M, et al: White matter hemisphere asymmetries in healthy subjects and in schizophrenia: a diffusion tensor MRI study. Neuroimage. 23:213–223. 2004. View Article : Google Scholar : PubMed/NCBI

Hof PR, Haroutunian V, Friedrich VL Jr, et al: Loss and altered spatial distribution of oligodendrocytes in the superior frontal gyrus in schizophrenia. Biol Psychiatry. 53:1075–1085. 2003. View Article : Google Scholar : PubMed/NCBI

Hulshoff Pol HE, Schnack HG, Mandl RC, et al: Focal white matter density changes in schizophrenia: reduced inter-hemispheric connectivity. Neuroimage. 21:27–35. 2004. View Article : Google Scholar : PubMed/NCBI

Kubicki M, McCarley RW and Shenton ME: Evidence for white matter abnormalities in schizophrenia. Curr Opin Psychiatry. 18:121–134. 2005. View Article : Google Scholar

Uranova N, Orlovskaya D, Vikhreva O, et al: Electron microscopy of oligodendroglia in severe mental illness. Brain Res Bull. 55:597–610. 2001. View Article : Google Scholar : PubMed/NCBI

Uranova NA, Vostrikov VM, Orlovskaya DD and Rachmanova VI: Oligodendroglial density in the prefrontal cortex in schizophrenia and mood disorders: a study from the Stanley Neuropathology Consortium. Schizophr Res. 67:269–275. 2004. View Article : Google Scholar : PubMed/NCBI

Mitterauer B: The incoherence hypothesis of schizophrenia: based on decomposed oligodendrocyte-axonic relations. Med Hypotheses. 69:1299–1304. 2007. View Article : Google Scholar : PubMed/NCBI

Murrin LC and Talbot JN: RanBPM, a scaffolding protein in the immune and nervous systems. J Neuroimmune Pharmacol. 2:290–295. 2007. View Article : Google Scholar : PubMed/NCBI

Nakayama AY, Harms MB and Luo L: Small GTPases Rac and Rho in the maintenance of dendritic spines and branches in hippocampal pyramidal neurons. J Neurosci. 20:5329–5338. 2000.PubMed/NCBI

Rex EB, Rankin ML, Ariano MA and Sibley DR: Ethanol regulation of D(1) dopamine receptor signaling is mediated by protein kinase C in an isozyme-specific manner. Neuropsychopharmacology. 33:2900–2911. 2008. View Article : Google Scholar : PubMed/NCBI

Kutay U, Hartmann E, Treichel N, et al: Identification of two novel RanGTP-binding proteins belonging to the importin beta superfamily. J Biol Chem. 275:40163–40168. 2000. View Article : Google Scholar : PubMed/NCBI

Blackwood DH, Fordyce A, Walker MT, St Clair DM, Porteous DJ and Muir WJ: Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family. Am J Hum Genet. 69:428–433. 2001. View Article : Google Scholar : PubMed/NCBI

Millar JK, Christie S, Anderson S, et al: Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia. Mol Psychiatry. 6:173–178. 2001. View Article : Google Scholar : PubMed/NCBI

Rex EB, Rankin ML, Yang Y, et al: Identification of RanBP 9/10 as interacting partners for protein kinase C (PKC) gamma/delta and the D1 dopamine receptor: regulation of PKC-mediated receptor phosphorylation. Mol Pharmacol. 78:69–80. 2010. View Article : Google Scholar : PubMed/NCBI

American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 4th edition. American Psychiatric Association; Washington, D.C., WA: 1994

Park BL, Shin HD, Cheong HS, et al: Association analysis of COMT polymorphisms with schizophrenia and smooth pursuit eye movement abnormality. J Hum Genet. 54:709–712. 2009. View Article : Google Scholar : PubMed/NCBI

Stephens M, Smith NJ and Donnelly P: A new statistical method for haplotype reconstruction from population data. Am J Hum Genet. 68:978–989. 2001. View Article : Google Scholar : PubMed/NCBI

Barrett JC, Fry B, Maller J and Daly MJ: Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 21:263–265. 2005. View Article : Google Scholar

Wang D, Li Z, Messing EM and Wu G: Activation of Ras/Erk pathway by a novel MET-interacting protein RanBPM. J Biol Chem. 277:36216–36222. 2002. View Article : Google Scholar : PubMed/NCBI

Lakshmana MK, Hayes CD, Bennett SP, et al: Role of RanBP9 on amyloidogenic processing of APP and synaptic protein levels in the mouse brain. FASEB J. 26:2072–2083. 2012. View Article : Google Scholar : PubMed/NCBI

Morris S, Leung J, Sharp C, Blackwood D, Muir W and St Clair D: Screening schizophrenic patients for mutations in the amyloid precursor protein gene. Psychiatr Genet. 4:23–27. 1994. View Article : Google Scholar : PubMed/NCBI

Albertini V, Benussi L, Paterlini A, et al: Distinct cerebrospinal fluid amyloid-beta peptide signatures in cognitive decline associated with Alzheimer’s disease and schizophrenia. Electrophoresis. 33:3738–3744. 2012. View Article : Google Scholar : PubMed/NCBI

McLean SL, Idris NF, Woolley ML and Neill JC: D(1)-like receptor activation improves PCP-induced cognitive deficits in animal models: Implications for mechanisms of improved cognitive function in schizophrenia. Eur Neuropsychopharmacol. 19:440–450. 2009. View Article : Google Scholar : PubMed/NCBI

Menon RP, Gibson TJ and Pastore A: The C terminus of fragile X mental retardation protein interacts with the multi-domain Ran-binding protein in the microtubule-organising centre. J Mol Biol. 343:43–53. 2004. View Article : Google Scholar : PubMed/NCBI

Cheong HS, Park BL, Kim EM, et al: Association of RANBP1 haplotype with smooth pursuit eye movement abnormality. Am J Med Genet B Neuropsychiatr Genet. 156B:67–71. 2011. View Article : Google Scholar

Kehlenbach RH, Dickmanns A, Kehlenbach A, Guan T and Gerace L: A role for RanBP1 in the release of CRM1 from the nuclear pore complex in a terminal step of nuclear export. J Cell Biol. 145:645–657. 1999. View Article : Google Scholar : PubMed/NCBI