Alcoholism: protein expression profiles in a human hippocampal model

References

• Harper C, Matsumoto I. Ethanol and brain damage. Curr. Opin. Pharmacol.5(1), 73–78 (2005).
   PubMed Web of Science ®Google Scholar
• Sullivan EV, Rosenbloom MJ, Pfefferbaum A. Pattern of motor and cognitive deficits in detoxified alcoholic men. Alcohol. Clin. Exp. Res.24(5), 611–621 (2000).
   PubMed Web of Science ®Google Scholar
• Noël X, Van der Linden M, Schmidt N et al. Supervisory attentional system in nonamnesic alcoholic men. Arch. Gen. Psychiatry58(12), 1152–1158 (2001).
   PubMed Web of Science ®Google Scholar
• Bates ME, Bowden SC, Barry D. Neurocognitive impairment associated with alcohol use disorders: implications for treatment. Exp. Clin. Psychopharmacol.10(3), 193–212 (2002).
   PubMed Web of Science ®Google Scholar
• Bates ME, Barry D, Labouvie EW, Fals-Stewart W, Voelbel G, Buckman JF. Risk factors and neuropsychological recovery in clients with alcohol use disorders who were exposed to different treatments. J. Consult. Clin. Psychol.72(6), 1073–1080 (2004).
   PubMed Web of Science ®Google Scholar
• Jernigan TL, Butters N, DiTraglia G et al. Reduced cerebral grey matter observed in alcoholics using magnetic resonance imaging. Alcohol. Clin. Exp. Res.15(3), 418–427 (1991).
   PubMed Web of Science ®Google Scholar
• Pfefferbaum A, Lim KO, Zipursky RB et al. Brain gray and white matter volume loss accelerates with aging in chronic alcoholics: a quantitative MRI study. Alcohol. Clin. Exp. Res.16(6), 1078–1089 (1992).
   PubMed Web of Science ®Google Scholar
• Shear PK, Sullivan EV, Lane B, Pfefferbaum A. Mammillary body and cerebellar shrinkage in chronic alcoholics with and without amnesia. Alcohol. Clin. Exp. Res.20(8), 1489–1495 (1996).
   PubMedGoogle Scholar
• Sullivan EV, Rosenbloom MJ, Serventi KL, Deshmukh A, Pfefferbaum A. Effects of alcohol dependence comorbidity and antipsychotic medication on volumes of the thalamus and pons in schizophrenia. Am. J. Psychiatry160(6), 1110–1116 (2003).
   PubMedGoogle Scholar
• Sullivan EV. Compromised pontocerebellar and cerebellothalamocortical systems: speculations on their contributions to cognitive and motor impairment in nonamnesic alcoholism. Alcohol. Clin. Exp. Res.27(9), 1409–14019 (2003).
   PubMed Web of Science ®Google Scholar
• Harper CG, Kril JJ. Corpus callosal thickness in alcoholics. Br. J. Addict.83(5), 577–580 (1988).
   PubMedGoogle Scholar
• Sullivan EV, Deshmukh A, Desmond JE, Lim KO, Pfefferbaum A. Cerebellar volume decline in normal aging, alcoholism, and Korsakoff’s syndrome: relation to ataxia. Neuropsychology14(3), 341–352 (2000).
   PubMed Web of Science ®Google Scholar
• Chanraud S, Martelli C, Delain F et al. Brain morphometry and cognitive performance in detoxified alcohol-dependents with preserved psychosocial functioning. Neuropsychopharmacology32(2), 429–438 (2007).
   PubMed Web of Science ®Google Scholar
• Adams KM, Gilman S, Koeppe RA et al. Neuropsychological deficits are correlated with frontal hypometabolism in positron emission tomography studies of older alcoholic patients. Alcohol. Clin. Exp. Res.17(2), 205–210 (1993).
   PubMed Web of Science ®Google Scholar
• Dao-Castellana MH, Samson Y, Legault F et al. Frontal dysfunction in neurologically normal chronic alcoholic subjects: metabolic and neuropsychological findings. Psychol. Med.28(5), 1039–1048 (1998).
   PubMed Web of Science ®Google Scholar
• Noël X, Paternot J, Van der Linden M et al. Correlation between inhibition, working memory and delimited frontal area blood flow measure by 99mTc-Bicisate SPECT in alcohol-dependent patients. Alcohol Alcohol.36(6), 556–563 (2001).
   PubMed Web of Science ®Google Scholar
• Ryabinin AE. Role of hippocampus in alcohol-induced memory impairment: implications from behavioral and immediate early gene studies. Psychopharmacology (Berl.)139(1–2), 34–43 (1998).
   PubMedGoogle Scholar
• Bowden SC, McCarter RJ. Spatial memory in alcohol-dependent subjects: using a push-button maze to test the principle of equiavailability. Brain Cogn.22(1), 51–62 (1993).
   PubMedGoogle Scholar
• White AM, Matthews DB, Best PJ. Ethanol, memory, and hippocampal function: a review of recent findings. Hippocampus10(1), 88–93 (2000).
   PubMed Web of Science ®Google Scholar
• Bonthius DJ, Woodhouse J, Bonthius NE, Taggard DA, Lothman EW. Reduced seizure threshold and hippocampal cell loss in rats exposed to alcohol during the brain growth spurt. Alcohol. Clin. Exp. Res.25(1), 70–82 (2001).
   PubMedGoogle Scholar
• Harding AJ, Wong A, Svoboda M, Kril JJ, Halliday GM. Chronic alcohol consumption does not cause hippocampal neuron loss in humans. Hippocampus7(1), 78–87 (1997).
   PubMed Web of Science ®Google Scholar
• Sullivan EV, Marsh L, Mathalon DH, Lim KO, Pfefferbaum A. Anterior hippocampal volume deficits in nonamnesic, aging chronic alcoholics. Alcohol. Clin. Exp. Res.19(1), 110–122 (1995).
   PubMed Web of Science ®Google Scholar
• Agartz I, Momenan R, Rawlings RR, Kerich MJ, Hommer DW. Hippocampal volume in patients with alcohol dependence. Arch. Gen. Psychiatry56(4), 356–363 (1999).
   PubMed Web of Science ®Google Scholar
• Laakso MP, Vaurio O, Savolainen L et al. A volumetric MRI study of the hippocampus in type 1 and 2 alcoholism. Behav. Brain Res.109(2), 177–186 (2000).
   PubMedGoogle Scholar
• White AM, Matthews DB, Best PJ. Ethanol, memory, and hippocampal function: a review of recent findings. Hippocampus10(1), 88–93 (2000).
   PubMed Web of Science ®Google Scholar
• Melchior CL, Glasky AJ, Ritzmann RF. A low dose of ethanol impairs working memory in mice in a win-shift foraging paradigm. Alcohol10(6), 491–493 (1993).
   PubMedGoogle Scholar
• Givens B. Low doses of ethanol impair spatial working memory and reduce hippocampal theta activity. Alcohol. Clin. Exp. Res.19(3), 763–767 (1995).
   PubMedGoogle Scholar
• Ordy JM, Thomas GJ, Volpe BT, Dunlap WP, Colombo PM. An animal model of human-type memory loss based on aging, lesion, forebrain ischemia, and drug studies with the rat. Neurobiol. Aging9(5–6), 667–683 (1988).
   PubMedGoogle Scholar
• Cadete-Leite A, Tavares MA, Uylings HB, Paula-Barbosa M. Granule cell loss and dendritic regrowth in the hippocampal dentate gyrus of the rat after chronic alcohol consumption. Brain Res.473(1), 1–14 (1988).
   PubMedGoogle Scholar
• Bengochea O, Gonzalo LM. Effect of chronic alcoholism on the human hippocampus. Histol. Histopathol.5(3), 349–357 (1990).
   PubMedGoogle Scholar
• Korbo L. Glial cell loss in the hippocampus of alcoholics. Alcohol. Clin. Exp. Res.23(1), 164–168 (1999).
   PubMed Web of Science ®Google Scholar
• King MA, Hunter BE, Walker DW. Alterations and recovery of dendritic spine density in rat hippocampus following long-term ethanol ingestion. Brain Res.459(2), 381–385 (1988).
   PubMed Web of Science ®Google Scholar
• Durand D, Saint-Cyr JA, Gurevich N, Carlen PL. Ethanol-induced dendritic alterations in hippocampal granule cells. Brain Res.477(1–2), 373–377 (1989).
   PubMedGoogle Scholar
• Herrera DG, Yague AG, Johnsen-Soriano S et al. Selective impairment of hippocampal neurogenesis by chronic alcoholism: protective effects of an antioxidant. Proc. Natl Acad. Sci. USA100(13), 7919–7924 (2003).
   PubMed Web of Science ®Google Scholar
• Tremwel MF, Hunter BE. Effects of chronic ethanol ingestion on long-term potentiation remain even after a prolonged recovery from ethanol exposure. Synapse17(2), 141–148 (1994).
   PubMedGoogle Scholar
• Geuze E, Vermetten E, Bremner JD. MR-based in vivo hippocampal volumetrics: 2. Findings in neuropsychiatric disorders. Mol. Psychiatry10(2), 160–184 (2005).
   PubMed Web of Science ®Google Scholar
• De Bellis MD, Clark DB, Beers SR et al. Hippocampal volume in adolescent-onsetalohol use disorders. Am. J. Psychiatry157(5), 737–744 (2000).
   PubMed Web of Science ®Google Scholar
• Miguel-Hidalgo JJ, Rajkowska G. Comparison of prefrontal cell pathology between depression and alcohol dependence. J. Psychiatr. Res.37(5), 411–420 (2003).
   PubMedGoogle Scholar
• Cadete-Leite A, Alves MC, Tavares MA, Paula-Barbosa MM. Effects of chronic alcohol intake and withdrawal on the prefrontal neurons and synapses. Alcohol7(2), 145–152 (1990).
   PubMedGoogle Scholar
• Walker DW, Barnes DE, Zornetzer SF, Hunter BE, Kubanis P. Neuronal loss in hippocampus induced by prolonged ethanol consumption in rats. Science209(4457), 711–713 (1980).
   PubMed Web of Science ®Google Scholar
• Bengoechea O, Gonzalo LM. Effects of alcoholization on the rat hippocampus. Neurosci. Lett.123(1), 112–114 (1991).
   PubMedGoogle Scholar
• Adermark L, Olsson T, Hansson E. Ethanol acutely decreases astroglial gap junction permeability in primary cultures from defined brain regions. Neurochem. Int.45(7), 971–978 (2004).
   PubMed Web of Science ®Google Scholar
• Stephens DN, Ripley TL, Borlikova G et al. Repeated ethanol exposure and withdrawal impairs human fear conditioning and depresses long-term potentiation in rat amygdala and hippocampus. Biol. Psychiatry58(5), 392–400 (2005).
   PubMed Web of Science ®Google Scholar
• Ikegami Y, Goodenough S, Inoue Y, Dodd PR, Wilce PA, Matsumoto I. Increased TUNEL positive cells in human alcoholic brains. Neurosci. Lett.349(3), 201–205 (2003).
   PubMedGoogle Scholar
• Okamoto H, Miki T, Lee KY et al. Oligodendrocyte myelin glycoprotein (OMgp) in rat hippocampus is depleted by chronic ethanol consumption. Neurosci. Lett.406(1–2), 76–80 (2006).
   PubMedGoogle Scholar
• Coyle JT, Schwarcz R. Mind glue: implications of glial cell biology for psychiatry. Arch. Gen. Psychiatry57(1), 90–93 (2000).
   PubMed Web of Science ®Google Scholar
• Magistretti PJ, Pellerin L. Cellular mechanisms of brain energy metabolism and their relevance to functional brain imaging. Philos. Trans. R. Soc. Lond. B Biol. Sci.354(1387), 1155–1163 (1999).
   PubMedGoogle Scholar
• Alexander-Kaufman K, Cordwell S, Harper C, Matsumoto I. A proteome analysis of the dorsolateral prefrontal cortex in human alcoholic patients. Proteomics Clin. App.1(1), 62–72 (2007).
   PubMed Web of Science ®Google Scholar
• Alexander-Kaufman K, Harper C, Wilce P, and Matsumoto I. The Cerebellar vermis proteome of chronic alcoholics. Alcohol. Clin. Exp. Res.31(8), 1286–1296 (2007).
   PubMedGoogle Scholar
• Alexander-Kaufman K, James G, Sheedy D, Harper C, Matsumoto I. Differential protein expression in the prefrontal white matter of human alcoholics: a proteomics study. Mol. Psychiatry11(1), 56–65 (2006).
   PubMedGoogle Scholar
• Beasley CL, Pennington K, Behan A, Wait R, Dunn MJ, Cotter D. Proteomic analysis of the anterior cingulate cortex in the major psychiatric disorders: evidence for disease-associated changes. Proteomics6(11), 3414–3425 (2006).
   PubMed Web of Science ®Google Scholar
• Choudhary J, Grant SG. Proteomics in postgenomic neuroscience: the end of the beginning. Nat. Neurosci.7(5), 440–445 (2004).
   PubMed Web of Science ®Google Scholar
• Clark D, Dedova I, Cordwell S, Matsumoto I. A proteome analysis of the anterior cingulate cortex gray matter in schizophrenia. Mol. Psychiatry11(5), 459–470, 423 (2006).
   PubMedGoogle Scholar
• Clark D, Dedova I, Cordwell S, Matsumoto I. Altered proteins of the anterior cingulate cortex white matter proteome in schizophrenia. Proteomics Clin. App.1(2), 157–166 (2007).
   PubMed Web of Science ®Google Scholar
• Iwazaki T, McGregor IS, Matsumoto I. Protein expression profile in the striatum of acute methamphetamine-treated rats. Brain Res.1097(1), 19–25 (2006).
   PubMed Web of Science ®Google Scholar
• Iwazaki T, McGregor IS, Matsumoto I. Protein expression profile in the striatum of rats with methamphetamine-induced behavioral sensitsation. Proteomics7, 1131–1139 (2007).
   PubMedGoogle Scholar
• Kashem MA, James G, Harper C, Wilce P, Matsumoto I. Differential protein expression in the corpus callosum (splenium) of human alcoholics: a proteomics study. Neurochem. Int.50, 450–459 (2007).
   PubMedGoogle Scholar
• Matsuda-Matsumoto H, Iwazaki T, Kashem MA, Harper C, Matsumoto I. Differential protein expression profiles in the hippocampus of human alcoholics. Neurochem. Int.51, 370–376, (2007).
   PubMedGoogle Scholar
• Mei J, Kolbin D, Kao HT, Porton B. Protein expression profiling of postmortem brain in schizophrenia. Schizophr. Res.84(2–3), 204–213 (2006).
   PubMedGoogle Scholar
• Novikova SI, He F, Cutrufello NJ, Lidow MS. Identification of protein biomarkers for schizophrenia and bipolar disorder in the postmortem prefrontal cortex using SELDI-TOF-MS ProteinChip profiling combined with MALDI-TOF-PSD-MS analysis. Neurobiol. Dis.23(1), 61–76 (2006).
   PubMed Web of Science ®Google Scholar
• O’Brien E, Dedova I, Duffy L et al. Effects of chronic risperidone treatment on the striatal protein profiles in rats. Brain Res.1113(1), 24–32 (2006).
   PubMed Web of Science ®Google Scholar
• Tannu N, Mash DC, Hemby SE. Cytosolic proteomic alterations in the nucleus accumbens of cocaine overdose victims. Mol. Psychiatry12(1), 55–73 (2007).
   PubMedGoogle Scholar
• Lewohl JM, Wang L, Miles MF, Zhang L, Dodd PR, Harris RA. Gene expression in human alcoholism: microarray analysis of frontal cortex. Alcohol Clin. Exp. Res.24(12), 1873–1882 (2000).
   PubMed Web of Science ®Google Scholar
• Ferrer I, Fabregues I, Rairiz J, Galofre E. Decreased numbers of dendritic spines on cortical pyramidal neurons in human chronic alcoholism. Neurosci. Lett.69(1), 115–119 (1986).
   PubMed Web of Science ®Google Scholar
• Vallés S, Pitarch J, Renau-Piqueras J, Guerri C. Ethanol exposure affects glial fibrillary acidic protein gene expression and transcription during rat brain development. J. Neurochem.69(6), 2484–2493 (1997).
   PubMed Web of Science ®Google Scholar
• Pfefferbaum A, Sullivan EV. Microstructural but not macrostructural disruption of white matter in women with chronic alcoholism. Neuroimage15(3), 708–718 (2002).
   PubMed Web of Science ®Google Scholar
• Harper C. The neuropathology of alcohol-specific brain damage, or does alcohol damage the brain? J. Neuropathol. Exp. Neurol.57(2), 101–110 (1998).
   PubMed Web of Science ®Google Scholar
• Harper C, Kril J. If you drink your brain will shrink. Neuropathological considerations. Alcohol Alcohol. Suppl.1, 375–380 (1991).
   PubMedGoogle Scholar
• Harper CG, Kril JJ, Holloway RL. Brain shrinkage in chronic alcoholics: a pathological study. Br. Med. J. (Clin. Res. Ed.)290(6467), 501–504 (1985).
   PubMed Web of Science ®Google Scholar
• Saito M, Smiley J, Toth R, Vadasz C. Microarray analysis of gene expression in rat hippocampus after chronic ethanol treatment. Neurochem. Res.27(10), 1221–1229 (2002).
   PubMedGoogle Scholar
• Gygi SP, Rochon Y, Franza BR, Aebersold R. Correlation between protein and mRNA abundance in yeast. Mol. Cell. Biol.19(3), 1720–1730 (1999).
   PubMed Web of Science ®Google Scholar
• Anderson L, Seilhamer J. A comparison of selected mRNA and protein abundances in human liver. Electrophoresis18(3–4), 533–537 (1997).
   PubMed Web of Science ®Google Scholar
• Lewohl JM, Van Dyk DD, Craft GE et al. The application of proteomics to the human alcoholic brain. Ann. NY Acad. Sci.1025, 14–26 (2004).
   PubMedGoogle Scholar
• Phillips SC, Harper CG, Kril JJ. The contribution of Wernicke’s encephalopathy to alcohol-related cerebellar damage. Drug Alcohol Rev.9(1), 53–60 (1990).
   PubMedGoogle Scholar
• Yang J W, Czech T, Lubec G. Proteomic profiling of human hippocampus. Electrophoresis25(7–8), 1169–1174 (2004).
   PubMed Web of Science ®Google Scholar
• Butterfield DA. Amyloid β-peptide (1-42)-induced oxidative stress and neurotoxicity: implications for neurodegeneration in Alzheimer’s disease brain. A review. Free Radic. Res.36(12), 1307–1313 (2002).
   PubMed Web of Science ®Google Scholar
• Butterfield DA, Sultana R. Redox proteomics identification of oxidatively modified brain proteins in Alzheimer’s disease and mild cognitive impairment: insights into the progression of this dementing disorder. J. Alzheimers Dis.12(1), 61–72 (2007).
   PubMed Web of Science ®Google Scholar
• Butterfield DA. Proteomics: a new approach to investigate oxidative stress in Alzheimer’s disease brain. Brain Res.1000, 1–7 (2004).
   PubMed Web of Science ®Google Scholar
• Edgar PF, Douglas JE, Cooper GJ, Dean B, Kydd R, Faull RL. Comparative proteome analysis of the hippocampus implicates chromosome 6q in schizophrenia. Mol. Psychiatry5, 85–90 (2000).
   PubMed Web of Science ®Google Scholar
• Costa E, Guidotti A. Diazepam binding inhibitor (DBI): a peptide with multiple biological actions. Life Sci.49, 325–344 (1991).
   PubMed Web of Science ®Google Scholar
• Melov S, Schneider JA, Day BJ et al. A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase. Nat. Genet.18, 159–163 (1998).
   PubMed Web of Science ®Google Scholar
• Goshima Y, Nakamura F, Strittmatter P, Strittmatter SM Collapsin-induced growth cone collapse mediated by an intracellular protein related to UNC-33. Nature376, 509–514 (1995).
   PubMed Web of Science ®Google Scholar
• Yaffe MB, Farr GW, Miklos D, Horwich AL, Sternlicht ML, Sternlicht H. TCP1 complex is a molecular chaperone in tubulin biogenesis. Nature358, 245–248 (1992).
   PubMed Web of Science ®Google Scholar
• Yang JW, Czech T, Felizardo M, Baumgartner C, Lubec G. Aberrant expression of cytoskeleton proteins in hippocampus from patients with mesial temporal lobe epilepsy. Amino Acids30(4), 477–493 (2006).
   PubMed Web of Science ®Google Scholar
• Suárez I, Bodega G, Fernández B, Glutamine synthetase in brain: effect of ammonia. Neurochem. Int.41(2–3), 123–142 (2002).
   PubMed Web of Science ®Google Scholar
• Girard G, Giguere JF, Butterworth RF. Region-selective reductions in activities of glutamine synthetase in rat brain following portacaval anastomosis. Metab. Brain Dis.8(4), 207–215 (1993).
   PubMed Web of Science ®Google Scholar
• Lavoie J, Giguere JF, Layrargues GP, Butterworth RF. Activities of neuronal and astrocytic marker enzymes in autopsied brain tissue from patients with hepatic encephalopathy. Metab. Brain Dis.2(4), 283–290 (1987).
   PubMed Web of Science ®Google Scholar
• Franke H, Kittner H, Berger P, Wirkner K, Schramek J. The reaction of astrocytes and neurons in the hippocampus of adult rats during chronic ethanol treatment and correlations to behavioral impairments. Alcohol14(5), 445–454 (1997).
   PubMedGoogle Scholar
• Tagliaferro P, Vega MD, Evrard SG, Ramos AJ, Brusco A. Alcohol exposure during adulthood induces neuronal and astroglial alterations in the hippocampal CA-1 area. Ann. NY Acad. Sci.965, 334–342 (2002).
   PubMedGoogle Scholar
• Montoliu C, Valles S, Renau-Piqueras J, Guerri C. Ethanol-induced oxygen radical formation and lipid peroxidation in rat brain: effect of chronic alcohol consumption. J. Neurochem.63(5), 1855–1862 (1994).
   PubMed Web of Science ®Google Scholar
• Agar E, Demir S, Amanvermez R, Bosnak M, Ayyildiz M, Celik C. The effects of ethanol consumption on the lipid peroxidation and glutathione levels in the right and left brains of rats. Int. J. Neurosci.113(12), 1643–1652 (2003).
   PubMed Web of Science ®Google Scholar
• Hemmer W, Wallimann T. Functional aspects of creatine kinase in brain. Dev. Neurosci.15(3–5), 249–260 (1993).
   PubMedGoogle Scholar
• Kukita A, Mukai T, Miyata T, Hori K. The structure of brain-specific rat aldolase C mRNA and the evolution of aldolase isozyme genes. Eur. J. Biochem.171(3), 471–478 (1988).
   PubMedGoogle Scholar
• Hamajima N, Tajima K, Morishita M et al. Patients’ expectations of information provided at cancer hospitals in Japan. Jpn. J. Clin. Oncol.26(5), 362–367 (1996).
   PubMed Web of Science ®Google Scholar
• Castegna A, Aksenov M, Thongboonkerd V et al. Proteomic identification of oxidatively modified proteins in Alzheimer’s disease brain. Part II: dihydropyrimidinase-related protein 2, α-enolase and heat shock cognate 71. J. Neurochem.82(6), 1524–1532 (2002).
   PubMed Web of Science ®Google Scholar
• Johnston-Wilson NL, Sims CD, Hofmann JP et al. Disease-specific alterations in frontal cortex brain proteins in schizophrenia, bipolar disorder, and major depressive disorder. The Stanley Neuropathology Consortium. Mol. Psychiatry5(2), 142–149 (2000).
   PubMed Web of Science ®Google Scholar
• Weitzdoerfer R, Fountoulakis M, Lubec G, Aberrant expression of dihydropyrimidinase related proteins-2,-3 and -4 in fetal Down syndrome brain. J. Neural Transm. Suppl.61, 95–107 (2001).
   Google Scholar
• Fountoulakis M. Application of proteomics technologies in the investigation of the brain. Mass Spectrom. Rev.23(4), 231–258 (2004).
   PubMed Web of Science ®Google Scholar
• O’Brien E, Dedova I, Duffy L, Cordwell S, Karl T, Matsumoto I. Effects of chronic risperidone treatment on the striatal protein profiles in rats. Brain Res.1113(1), 24–32 (2006).
   PubMed Web of Science ®Google Scholar
• Unlu M, Morgan ME, Minden JS. Difference gel electrophoresis: a single gel method for detecting changes in protein extracts. Electrophoresis18(11), 2071–2077 (1997).
   PubMed Web of Science ®Google Scholar
• Griffin TJ, Han DK, Gygi SP et al. Toward a high-throughput approach to quantitative proteomic analysis: expression-dependent protein identification by mass spectrometry. J. Am. Soc. Mass Spectrom.12(12), 1238–1246 (2001).
   PubMed Web of Science ®Google Scholar
• Dosemeci A, Tao-Cheng J H, Vinade L, Jaffe H. Preparation of postsynaptic density fraction from hippocampal slices and proteomic analysis. Biochem. Biophys. Res. Commun.339(2), 687–694 (2006).
   PubMedGoogle Scholar
• Qian HR, Huang S. Comparison of false discovery rate methods in identifying genes with differential expression. Genomics86(4), 495–503 (2005).
   PubMed Web of Science ®Google Scholar
• Emmert-Buck MR, Gillespie JW, Paweletz CP et al. An approach to proteomic analysis of human tumors. Mol. Carcinog.27(3), 158–165 (2000).
   PubMed Web of Science ®Google Scholar
• Molloy MP, Herbert BR, Walsh BJ et al. Extraction of membrane proteins by differential solubilization for separation using two-dimensional gel electrophoresis. Electrophoresis19(5), 837–844 (1998).
   PubMed Web of Science ®Google Scholar
• Jung E, Heller M, Sanchez JC, Hochstrasser DF. Proteomics meets cell biology: the establishment of subcellular proteomes. Electrophoresis21(16), 3369–3377 (2000).
   PubMed Web of Science ®Google Scholar