{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T17:10:47Z","timestamp":1791220247285,"version":"4.1.0"},"reference-count":66,"publisher":"Oxford University Press (OUP)","issue":"22","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2011,11,15]]},"DOI":"10.1093\/hmg\/ddr357","type":"journal-article","created":{"date-parts":[[2011,8,13]],"date-time":"2011-08-13T00:55:38Z","timestamp":1313196938000},"page":"4311-4323","source":"Crossref","is-referenced-by-count":88,"title":["15q11.2\u201313.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain"],"prefix":"10.1093","volume":"20","author":[{"given":"Dag H.","family":"Yasui","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Haley A.","family":"Scoles","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shin-ichi","family":"Horike","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Makiko","family":"Meguro-Horike","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Keith W.","family":"Dunaway","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Diane I.","family":"Schroeder","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Janine M.","family":"LaSalle","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2011,8,12]]},"reference":[{"key":"key\n\t\t\t\t20170522165633_DDR357C1","doi-asserted-by":"crossref","first-page":"397","DOI":"10.1086\/302233","article-title":"Imprinting-mutation mechanisms in Prader\u2013Willi syndrome","volume":"64","author":"Ohta","year":"1999","journal-title":"Am. J. Hum. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C2","doi-asserted-by":"crossref","first-page":"398","DOI":"10.1542\/peds.91.2.398","article-title":"Prader\u2013Willi syndrome: consensus diagnostic criteria","volume":"91","author":"Holm","year":"1993","journal-title":"Pediatrics"},{"key":"key\n\t\t\t\t20170522165633_DDR357C3","first-page":"665","article-title":"A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp","volume":"105","author":"Buiting","year":"1999","journal-title":"Hum. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C4","doi-asserted-by":"crossref","first-page":"2041","DOI":"10.1002\/ajmg.a.32364","article-title":"Mechanisms of imprinting of the Prader\u2013Willi\/Angelman region","volume":"146A","author":"Horsthemke","year":"2008","journal-title":"Am. J. Med. Genet. A"},{"key":"key\n\t\t\t\t20170522165633_DDR357C5","doi-asserted-by":"crossref","first-page":"546","DOI":"10.1016\/S0026-895X(25)10029-1","article-title":"Human alpha 7 acetylcholine receptor: cloning of the alpha 7 subunit from the SH-SY5Y cell line and determination of pharmacological properties of native receptors and functional alpha 7 homomers expressed in Xenopus oocytes","volume":"45","author":"Peng","year":"1994","journal-title":"Mol. Pharmacol."},{"key":"key\n\t\t\t\t20170522165633_DDR357C6","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1038\/ng0197-70","article-title":"UBE3A\/E6-AP mutations cause Angelman syndrome","volume":"15","author":"Kishino","year":"1997","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C7","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1038\/sj.mp.4001011","article-title":"Association between a GABRB3 polymorphism and autism","volume":"7","author":"Buxbaum","year":"2002","journal-title":"Mol. Psychiatry"},{"key":"key\n\t\t\t\t20170522165633_DDR357C8","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1002\/(SICI)1096-8628(19980401)76:4<327::AID-AJMG8>3.0.CO;2-M","article-title":"Autism and maternally derived aberrations of chromosome 15q","volume":"76","author":"Schroer","year":"1998","journal-title":"Am. J. Med. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C9","doi-asserted-by":"crossref","first-page":"228","DOI":"10.1007\/s00439-004-1219-2","article-title":"Exclusion of the C\/D box snoRNA gene cluster HBII-52 from a major role in Prader\u2013Willi syndrome","volume":"116","author":"Runte","year":"2005","journal-title":"Hum. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C10","doi-asserted-by":"crossref","first-page":"4227","DOI":"10.1093\/hmg\/ddp373","article-title":"Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size","volume":"18","author":"Leung","year":"2009","journal-title":"Hum. Mol. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C11","doi-asserted-by":"crossref","first-page":"19416","DOI":"10.1073\/pnas.0707442104","article-title":"Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes","volume":"104","author":"Yasui","year":"2007","journal-title":"Proc. Natl Acad. Sci. USA"},{"key":"key\n\t\t\t\t20170522165633_DDR357C12","doi-asserted-by":"crossref","first-page":"2003","DOI":"10.1093\/hmg\/ddl124","article-title":"Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome","volume":"15","author":"Peddada","year":"2006","journal-title":"Hum. Mol. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C13","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1038\/ng0598-25","article-title":"A mouse model for Prader\u2013Willi syndrome imprinting-centre mutations","volume":"19","author":"Yang","year":"1998","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C14","doi-asserted-by":"crossref","first-page":"379","DOI":"10.1006\/geno.1994.1075","article-title":"Molecular cloning and chromosomal localization of the human alpha 7-nicotinic receptor subunit gene (CHRNA7)","volume":"19","author":"Chini","year":"1994","journal-title":"Genomics"},{"key":"key\n\t\t\t\t20170522165633_DDR357C15","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1006\/geno.1998.5363","article-title":"Genomic organization and partial duplication of the human alpha7 neuronal nicotinic acetylcholine receptor gene (CHRNA7)","volume":"52","author":"Gault","year":"1998","journal-title":"Genomics"},{"key":"key\n\t\t\t\t20170522165633_DDR357C16","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1136\/jmg.2008.059907","article-title":"Microdeletion\/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders","volume":"46","author":"Miller","year":"2009","journal-title":"J. Med. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C17","doi-asserted-by":"crossref","first-page":"382","DOI":"10.1136\/jmg.2008.064378","article-title":"Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders","volume":"46","author":"Ben-Shachar","year":"2009","journal-title":"J. Med. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C18","doi-asserted-by":"crossref","first-page":"1269","DOI":"10.1038\/ng.481","article-title":"A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes","volume":"41","author":"Shinawi","year":"2009","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C19","doi-asserted-by":"crossref","first-page":"322","DOI":"10.1038\/ng.93","article-title":"A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures","volume":"40","author":"Sharp","year":"2008","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C20","doi-asserted-by":"crossref","first-page":"587","DOI":"10.1073\/pnas.94.2.587","article-title":"Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus","volume":"94","author":"Freedman","year":"1997","journal-title":"Proc. Natl Acad. Sci. USA"},{"key":"key\n\t\t\t\t20170522165633_DDR357C21","doi-asserted-by":"crossref","first-page":"160","DOI":"10.1038\/ng.292","article-title":"15q13.3 microdeletions increase risk of idiopathic generalized epilepsy","volume":"41","author":"Helbig","year":"2009","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C22","doi-asserted-by":"crossref","first-page":"232","DOI":"10.1038\/nature07229","article-title":"Large recurrent microdeletions associated with schizophrenia","volume":"455","author":"Stefansson","year":"2008","journal-title":"Nature"},{"key":"key\n\t\t\t\t20170522165633_DDR357C23","doi-asserted-by":"crossref","first-page":"9165","DOI":"10.1523\/JNEUROSCI.17-23-09165.1997","article-title":"Mice deficient in the alpha7 neuronal nicotinic acetylcholine receptor lack alpha-bungarotoxin binding sites and hippocampal fast nicotinic currents","volume":"17","author":"Orr-Urtreger","year":"1997","journal-title":"J. Neurosci."},{"key":"key\n\t\t\t\t20170522165633_DDR357C24","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1016\/j.bbr.2008.08.048","article-title":"Nicotinic alpha7- or beta2-containing receptor knockout: effects on radial-arm maze learning and long-term nicotine consumption in mice","volume":"196","author":"Levin","year":"2009","journal-title":"Behav. Brain Res."},{"key":"key\n\t\t\t\t20170522165633_DDR357C25","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1111\/j.1601-183X.2005.00176.x","article-title":"Performance deficit of alpha7 nicotinic receptor knockout mice in a delayed matching-to-place task suggests a mild impairment of working\/episodic-like memory","volume":"5","author":"Fernandes","year":"2006","journal-title":"Genes Brain Behav."},{"key":"key\n\t\t\t\t20170522165633_DDR357C26","doi-asserted-by":"crossref","first-page":"355","DOI":"10.1038\/nrn2132","article-title":"Epigenetic regulation in psychiatric disorders","volume":"8","author":"Tsankova","year":"2007","journal-title":"Nat. Rev. Neurosci."},{"key":"key\n\t\t\t\t20170522165633_DDR357C27","doi-asserted-by":"crossref","first-page":"483","DOI":"10.1093\/hmg\/ddi045","article-title":"Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3","volume":"14","author":"Samaco","year":"2005","journal-title":"Hum. Mol. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C28","doi-asserted-by":"crossref","first-page":"119","DOI":"10.2217\/epi.09.13","article-title":"Evolving role of MeCP2 in Rett syndrome and autism","volume":"1","author":"Lasalle","year":"2009","journal-title":"Epigenomics"},{"key":"key\n\t\t\t\t20170522165633_DDR357C29","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1177\/1073858403260995","article-title":"Rett syndrome: a prototypical neurodevelopmental disorder","volume":"10","author":"Neul","year":"2004","journal-title":"Neuroscientist"},{"key":"key\n\t\t\t\t20170522165633_DDR357C30","doi-asserted-by":"crossref","first-page":"3033","DOI":"10.1242\/jcs.03099","article-title":"MBD family proteins: reading the epigenetic code","volume":"119","author":"Fatemi","year":"2006","journal-title":"J. Cell. Sci."},{"key":"key\n\t\t\t\t20170522165633_DDR357C31","doi-asserted-by":"crossref","first-page":"905","DOI":"10.1016\/0092-8674(92)90610-O","article-title":"Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA","volume":"69","author":"Lewis","year":"1992","journal-title":"Cell"},{"key":"key\n\t\t\t\t20170522165633_DDR357C32","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1038\/561","article-title":"Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription","volume":"19","author":"Jones","year":"1998","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C33","doi-asserted-by":"crossref","first-page":"386","DOI":"10.1038\/30764","article-title":"Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex","volume":"393","author":"Nan","year":"1998","journal-title":"Nature"},{"key":"key\n\t\t\t\t20170522165633_DDR357C34","doi-asserted-by":"crossref","first-page":"31","DOI":"10.1038\/ng1491","article-title":"Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome","volume":"37","author":"Horike","year":"2005","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C35","doi-asserted-by":"crossref","first-page":"28237","DOI":"10.1074\/jbc.M704304200","article-title":"MeCP2-chromatin interactions include the formation of chromatosome-like structures and are altered in mutations causing Rett syndrome","volume":"282","author":"Nikitina","year":"2007","journal-title":"J. Biol. Chem."},{"key":"key\n\t\t\t\t20170522165633_DDR357C36","doi-asserted-by":"crossref","first-page":"864","DOI":"10.1128\/MCB.01593-06","article-title":"Multiple modes of interaction between the methylated DNA binding protein MeCP2 and chromatin","volume":"27","author":"Nikitina","year":"2007","journal-title":"Mol. Cell. Biol."},{"key":"key\n\t\t\t\t20170522165633_DDR357C37","doi-asserted-by":"crossref","first-page":"4395","DOI":"10.1021\/bi9019753","article-title":"Unique physical properties and interactions of the domains of methylated DNA binding protein 2","volume":"49","author":"Ghosh","year":"2010","journal-title":"Biochemistry"},{"key":"key\n\t\t\t\t20170522165633_DDR357C38","doi-asserted-by":"crossref","first-page":"691","DOI":"10.1093\/hmg\/ddm014","article-title":"15q11\u201313 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders","volume":"16","author":"Hogart","year":"2007","journal-title":"Hum. Mol. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C39","doi-asserted-by":"crossref","first-page":"1348","DOI":"10.1038\/ng1896","article-title":"Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C)","volume":"38","author":"Simonis","year":"2006","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C40","doi-asserted-by":"crossref","first-page":"895","DOI":"10.1038\/nmeth1114","article-title":"An evaluation of 3C-based methods to capture DNA interactions","volume":"4","author":"Simonis","year":"2007","journal-title":"Nat. Methods"},{"key":"key\n\t\t\t\t20170522165633_DDR357C41","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1002\/neu.10201","article-title":"The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells","volume":"55","author":"Jung","year":"2003","journal-title":"J. Neurobiol."},{"key":"key\n\t\t\t\t20170522165633_DDR357C42","first-page":"25","article-title":"Human neuroblastoma cells in culture: a model for neuronal cell differentiation and function","volume":"592","author":"Pahlman","year":"1990","journal-title":"Acta Physiol. Scand. Suppl."},{"key":"key\n\t\t\t\t20170522165633_DDR357C43","doi-asserted-by":"crossref","first-page":"889","DOI":"10.1038\/ng1402","article-title":"Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops","volume":"36","author":"Murrell","year":"2004","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C44","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1016\/j.ceb.2007.04.008","article-title":"The 4C technique: the \u2018Rosetta stone\u2019 for genome biology in 3D?","volume":"19","author":"Ohlsson","year":"2007","journal-title":"Curr. Opin. Cell Biol."},{"key":"key\n\t\t\t\t20170522165633_DDR357C45","doi-asserted-by":"crossref","first-page":"595","DOI":"10.1101\/gr.4887606","article-title":"Unbiased location analysis of E2F1-binding sites suggests a widespread role for E2F1 in the human genome","volume":"16","author":"Bieda","year":"2006","journal-title":"Genome Res."},{"key":"key\n\t\t\t\t20170522165633_DDR357C46","doi-asserted-by":"crossref","first-page":"719","DOI":"10.1038\/ng.158","article-title":"Prader\u2013Willi phenotype caused by paternal deficiency for the HBII-85 C\/D box small nucleolar RNA cluster","volume":"40","author":"Sahoo","year":"2008","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C47","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1038\/nrg2346","article-title":"Advances in autism genetics: on the threshold of a new neurobiology","volume":"9","author":"Abrahams","year":"2008","journal-title":"Nat. Rev. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C48","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1007\/s12031-009-9233-4","article-title":"Differential regulation of alpha7 nicotinic receptor gene (CHRNA7) expression in schizophrenic smokers","volume":"40","author":"Mexal","year":"2010","journal-title":"J. Mol. Neurosci."},{"key":"key\n\t\t\t\t20170522165633_DDR357C49","doi-asserted-by":"crossref","first-page":"1779","DOI":"10.1097\/00001756-199906030-00028","article-title":"Decreased protein level of nicotinic receptor alpha7 subunit in the frontal cortex from schizophrenic brain","volume":"10","author":"Guan","year":"1999","journal-title":"Neuroreport"},{"key":"key\n\t\t\t\t20170522165633_DDR357C50","doi-asserted-by":"crossref","first-page":"e1","DOI":"10.4161\/epi.1.4.3514","article-title":"Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation","volume":"1","author":"Nagarajan","year":"2006","journal-title":"Epigenetics"},{"key":"key\n\t\t\t\t20170522165633_DDR357C51","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1146\/annurev.genom.2.1.153","article-title":"Genome organization, function, and imprinting in Prader\u2013Willi and Angelman syndromes","volume":"2","author":"Nicholls","year":"2001","journal-title":"Annu. Rev. Genomics Hum. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C52","doi-asserted-by":"crossref","first-page":"176","DOI":"10.1093\/hmg\/ddq366","article-title":"Phenotypic variability and genetic susceptibility to genomic disorders","volume":"19","author":"Girirajan","year":"2010","journal-title":"Hum. Mol. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C53","doi-asserted-by":"crossref","first-page":"1020","DOI":"10.1038\/nn.2371","article-title":"Balanced gene regulation by an embryonic brain ncRNA is critical for adult hippocampal GABA circuitry","volume":"12","author":"Bond","year":"2009","journal-title":"Nat. Neurosci."},{"key":"key\n\t\t\t\t20170522165633_DDR357C54","doi-asserted-by":"crossref","first-page":"630","DOI":"10.1016\/j.ygeno.2005.02.004","article-title":"A nonimprinted Prader\u2013Willi syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels","volume":"85","author":"Stefan","year":"2005","journal-title":"Genomics"},{"key":"key\n\t\t\t\t20170522165633_DDR357C55","doi-asserted-by":"crossref","first-page":"457","DOI":"10.1016\/j.molcel.2010.01.030","article-title":"Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state","volume":"37","author":"Skene","year":"2010","journal-title":"Mol. Cell"},{"key":"key\n\t\t\t\t20170522165633_DDR357C56","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1023\/A:1005415823867","article-title":"Brief report: interrater reliability of clinical diagnosis and DSM-IV criteria for autistic disorder: results of the DSM-IV autism field trial","volume":"30","author":"Klin","year":"2000","journal-title":"J. Autism Dev. Disord."},{"key":"key\n\t\t\t\t20170522165633_DDR357C57","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1038\/13810","article-title":"Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2","volume":"23","author":"Amir","year":"1999","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C58","doi-asserted-by":"crossref","first-page":"1440","DOI":"10.1176\/ajp.2006.163.8.1440","article-title":"Visuospatial processing and the function of prefrontal-parietal networks in autism spectrum disorders: a functional MRI study","volume":"163","author":"Silk","year":"2006","journal-title":"Am. J. Psychiatry"},{"key":"key\n\t\t\t\t20170522165633_DDR357C59","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1016\/j.biopsych.2005.07.025","article-title":"Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice","volume":"59","author":"Gemelli","year":"2006","journal-title":"Biol. Psychiatry"},{"key":"key\n\t\t\t\t20170522165633_DDR357C60","doi-asserted-by":"crossref","first-page":"3709","DOI":"10.1093\/hmg\/ddi402","article-title":"A segment of the Mecp2 promoter is sufficient to drive expression in neurons","volume":"14","author":"Adachi","year":"2005","journal-title":"Hum. Mol. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C61","doi-asserted-by":"crossref","first-page":"1224","DOI":"10.1126\/science.1153252","article-title":"MeCP2, a key contributor to neurological disease, activates and represses transcription","volume":"320","author":"Chahrour","year":"2008","journal-title":"Science"},{"key":"key\n\t\t\t\t20170522165633_DDR357C62","first-page":"2223","article-title":"Localization of mRNA for CHRNA7 in human fetal brain","volume":"10","author":"Agulhon","year":"1999","journal-title":"Neuroreport"},{"key":"key\n\t\t\t\t20170522165633_DDR357C63","doi-asserted-by":"crossref","first-page":"629","DOI":"10.1093\/hmg\/ddh063","article-title":"Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders","volume":"13","author":"Samaco","year":"2004","journal-title":"Hum. Mol. Genet."},{"key":"key\n\t\t\t\t20170522165633_DDR357C64","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1016\/j.neuron.2005.12.027","article-title":"The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression","volume":"49","author":"Chang","year":"2006","journal-title":"Neuron"},{"key":"key\n\t\t\t\t20170522165633_DDR357C65","doi-asserted-by":"crossref","first-page":"11753","DOI":"10.1523\/JNEUROSCI.3797-08.2008","article-title":"Epigenetics in the nervous system","volume":"28","author":"Jiang","year":"2008","journal-title":"J. Neurosci."},{"key":"key\n\t\t\t\t20170522165633_DDR357C66","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1016\/j.biopsych.2010.07.004","article-title":"Effects of an alpha 7-nicotinic agonist on default network activity in schizophrenia","volume":"69","author":"Tregellas","year":"2010","journal-title":"Biol. Psychiatry"}],"container-title":["Human Molecular Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/academic.oup.com\/hmg\/article-pdf\/20\/22\/4311\/17252838\/ddr357.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,3,8]],"date-time":"2025-03-08T15:47:57Z","timestamp":1741448877000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/hmg\/article-lookup\/doi\/10.1093\/hmg\/ddr357"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,8,12]]},"references-count":66,"journal-issue":{"issue":"22","published-online":{"date-parts":[[2011,8,12]]},"published-print":{"date-parts":[[2011,11,15]]}},"URL":"https:\/\/doi.org\/10.1093\/hmg\/ddr357","relation":{},"ISSN":["1460-2083","0964-6906"],"issn-type":[{"value":"1460-2083","type":"electronic"},{"value":"0964-6906","type":"print"}],"subject":[],"published":{"date-parts":[[2011,8,12]]}}}