[1]
|
Holliday, R. and Grigg, G.W. (1993) DNA methylation and mutation. Mutation Research, 285, 61-67.
doi:10.1016/0027-5107(93)90052-H
|
[2]
|
Bird, A.P. (1986) CpG-rich islands and the function of DNA methylation. Nature, 321, 209-213.
doi:10.1038/321209a0
|
[3]
|
Bird, A. (1992) The essentials of DNA methylation. Cell, 70, 5-8. doi:10.1016/0092-8674(92)90526-I
|
[4]
|
Li, E., Beard, C. and Jaenisch, R. (1993) Role for DNA methylation in genomic imprinting. Nature, 366, 362-365.
doi:10.1038/366362a0
|
[5]
|
Tremblay, K.D., Saam, J.R., Ingram, R.S., Tilghman, S.M. and Bartolomei, M.S. (1995) A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nature Genetics, 9, 407-413.
doi:10.1038/ng0495-407
|
[6]
|
Pfeifer, G.P., Steigerwald, S.D., Mueller, P.R., Wold, B. and Riggs, A.D. (1989) Genomic sequencing and methylation analysis by ligation mediated PCR. Science, 246, 810-813. doi:10.1126/science.2814502
|
[7]
|
Riggs, A.D. and Pfeifer, G.P. (1992) X-chromosome inactivation and cell memory. Trends in Genetics, 8, 169-174.
|
[8]
|
Cardno, A.G. and Gottesman, I.I. (2000) Twin studies of schizophrenia: From bow-and-arrow concordances to star wars Mx and functional genomics. American Journal of Medical Genetics, 97, 12-17.
doi:10.1002/(SICI)1096-8628(200021)97:1<12::AID-AJMG3>3.0.CO;2-U
|
[9]
|
Impagnatiello, F., Guidotti, A.R., Pesold, C., Dwivedi, Y., Caruncho, H., Pisu, M.G., Uzunov, D.P., Smalheiser, N.R., Davis. J.M., Pandey, G.N., Pappas, G.D., Tueting, P., Sharma, R.P. and Costa, E. (1998) A decrease of reelin expression as a putative vulnerability factor in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America, 95, 15718-15723.
|
[10]
|
Guidotti, A., Auta, J., Davis, J.M., Di-Giorgi-Gerevini, V., Dwivedi, Y., Grayson, D.R., Impagnatiello, F., Pandey, G., Pesold, C., Sharma, R., Uzunov, D. and Costa, E. (2000) Decrease in reelin and glutamic acid decarboxylase67 (GAD67) expression in schizophrenia and bipolar disorder: A postmortem brain study. Archives of General Psychiatry, 57, 1061-1069.
doi:10.1001/archpsyc.57.11.1061
|
[11]
|
Costa, E., Grayson, D.R., Mitchell, C.P., Tremolizzo, L., Veldic, M. and Guidotti, A. (2003) GABAergic cortical neuron chromatin as a putative target to treat schizophrenia vulnerability. Critical Reviews in Neurobiology, 15, 121-142. doi:10.1615/CritRevNeurobiol.v15.i2.20
|
[12]
|
Bach, A.W., Lan, N.C., Johnson, D.L., Abell, C.W., Bembenek, M.E., Kwan, S.W., Seeburg, P.H. and Shih, J.C. (1988) cDNA cloning of human liver monoamine oxidase A and B: molecular basis of differences in enzymatic properties. Proceedings of the National Academy of Sciences of the United States of America, 85, 4934-4938. doi:10.1073/pnas.85.13.4934
|
[13]
|
Chen, Z.Y., Powell, J.F., Hsu, Y.P., Breakefield, X.O. and Craig, I.W. (1992) Organization of the human monoamine oxidase genes and long-range physical mapping around them. Genomics, 14, 75-82.
doi:10.1016/S0888-7543(05)80286-1
|
[14]
|
Westlund, K.N., Denney, R.M., Rose, R.M. and Abell, C.W. (1988) Localization of distinct monoamine oxidase A and monoamine oxidase B cell populations in human brainstem. Neuroscience, 25, 439-456.
doi:10.1016/0306-4522(88)90250-3
|
[15]
|
Murphy, D.L. and Wyatt RJ. (1972) Reduced monoamine oxidase activity in blood platelets from schizophrenic patients. Nature, 238, 225-226. doi:10.1038/238225a0
|
[16]
|
Wyatt, R.J., Murphy, D.L., Belmaker, R., Cohen, S., Donnelly, C.H. and Pollin, W. (1973) Reduced monoamine oxidase activity in platelets: A possible genetic marker for vulnerability to schizophrenia. Science, 179, 916-918.
doi:10.1126/science.179.4076.916
|
[17]
|
Collins, F.A., Murphy, D.L., Reiss, A.L. Sims, K.B., Lewis, J.G., Freund, L., Karoum, F., Zhu, D., Maumenee, I.H. and Antonarakis, S.E. (1992) Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes. American Journal of Medical Genetics, 42, 127-134. doi:10.1002/ajmg.1320420126
|
[18]
|
Brunner, H.G., Nelen, M., Breakefield, X.O., Ropers, H.H. and van, Oost, B.A. (1993) Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A. Science, 262, 578-580.
doi:10.1126/science.8211186
|
[19]
|
Newman, T.K., Syagailo, Y.V., Barr, C.S., Wendland, J.R., Champoux, M., Graessle, M., Suomi, S.J., Higley, J.D. and Lesch, K.P. (2005) Monoamine oxidase A gene promoter variation and rearing experience influences aggressive behavior in rhesus monkeys. Biological Psychiatry, 57, 167-172. doi:10.1016/j.biopsych.2004.10.012
|
[20]
|
Alia-Klein, N., Goldstein, R.Z., Kriplani, A., Logan, J., Tomasi, D., Williams, B., Telang, F., Shumay, E., Biegon, A., Craig, I.W., Henn, F., Wang, G.J., Volkow, N.D. and Fowler, J.S. (2008) Brain monoamine oxidase A activity predicts trait aggression. The Journal of Neuroscience: The official journal of the Society for Neuroscience, 28, 5099-5104.
|
[21]
|
Jiang, S., Xin, R., Lin, S., Qian, Y., Tang, G., Wang, D. and Wu, X. (2001) Linkage studies between attentiondeficit hyperactivity disorder and the monoamine oxidase genes. American Journal of Medical Genetics, 105, 783-788. doi:10.1002/ajmg.10098
|
[22]
|
Fossella, J., Sommer, T., Fan, J., Wu, Y., Swanson, J.M., Pfaff, D.W. and Posner, M.I. (2002) Assessing the molecular genetics of attention networks. BMC Neuroscience, 3, 14. doi:10.1186/1471-2202-3-14
|
[23]
|
Lawson, D.C., Turic, D., Langley, K. Pay, H.M., Govan, C.F., Norton, N., Hamshere, M.L., Owen, M.J., O’Donovan, M.C. and Thapar, A. (2003) Association analysis of monoamine oxidase A and attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 116, 84-89.
doi:10.1002/ajmg.b.10002
|
[24]
|
Heard, E., Clerc, P. and Avner, P. (1997) X-chromosome inactivation in mammals. Annual Review of Genetics, 31, 571-610. doi:10.1146/annurev.genet.31.1.571
|
[25]
|
Goto, T. and Monk, M. (1998) Regulation of X-chromosome inactivation in development in mice and humans. Microbiology and Molecular Biology Reviews, 62, 362-378.
|
[26]
|
Perlstein, W.M., Carter, C.S., Noll, D.C. and Cohen, J.D. (2001) Relation of prefrontal cortex dysfunction to working memory and symptoms in schizophrenia. The American Journal of Psychiatry, 158, 1105-1113.
doi:10.1176/appi.ajp.158.7.1105
|
[27]
|
Liddle, P.F., Lane, C.J. and Ngan, E.T. (2000) Immediate effects of risperidone on cortico-striato-thalamic loops and the hippocampus. The British Journal of Psychiatry, 177, 402-407. doi:10.1192/bjp.177.5.402
|
[28]
|
Ikemoto, K., Kitahama, K., Maeda, T., Tokunaga, Y., Valatx, J.L., De, Maeyer, E. and Seif, I. (1997) Electron-microscopic study of MAOB-containing structures in the nucleus accumbens shell: Using MAOA-deficient transgenic mice. Brain Research, 771, 163-166.
doi:10.1016/S0006-8993(97)00909-8
|
[29]
|
Pietrobono, R., Pomponi, M.G., Tabolacci, E., Oostra, B., Chiurazzi, P. and Neri,G. (2002) Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine. Nucleic Acids Research, 30, 3278-3285.
doi:10.1093/nar/gkf434
|
[30]
|
Carrel, L. and Willard, H.F. (2005) X-inactivation profile reveals extensive variability in X-linked gene expression in females. Nature, 434, 400-404.
doi:10.1038/nature03479
|
[31]
|
Wong, C.C., Caspi, A., Williams, B., Craig, I.W., Houts, R., Ambler, A., Moffitt, T.E. and Mill, J. (2010) A longitudinal study of epigenetic variation in twins. Epigenetics, 5, 516-26. doi:10.4161/epi.5.6.12226
|
[32]
|
Wu, J.B., Chen, K., Li, Y., Lau, Y.F. and Shih, J.C. (2009) Regulation of monoamine oxidase A by the SRY gene on the Y chromosome. FASEB Journal, 23, 4029-4038.
doi:10.1096/fj.09-139097
|
[33]
|
Grayson, D.R., Jia, X., Chen, Y., Sharma, R.P., Mitchell, C.P., Guidotti, A. and Costa, E. (2005) Reelin promoter hypermethylation in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America, 102, 9341-9346. doi:10.1073/pnas.0503736102
|
[34]
|
Iwamoto, K., Bundo, M., Yamada, K., Takao, H., Iwayama-Shigeno, Y., Yoshikawa, T. and Kato, T. (2005) DNA methylation status of SOX10 correlates with its downregulation and oligodendrocyte dysfunction in schizophrenia. The Journal of Neuroscience, 25, 5376-5381. doi:10.1523/JNEUROSCI.0766-05.2005
|
[35]
|
Thorpe, L.W., Westlund, K.N., Kochersperger, L.M., Abell, C.W. and Denney, R.M. (1987) Immunocytochemical localization of monoamine oxidases A and B in human peripheral tissues and brain. The Journal of Histochemistry and Cytochemistry, 35, 23-32.
doi:10.1177/35.1.3025289
|