{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T04:38:23Z","timestamp":1791088703186,"version":"4.1.0"},"reference-count":11,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[2003,6,1]],"date-time":"2003-06-01T00:00:00Z","timestamp":1054425600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Curr Neurol Neurosci Rep"],"published-print":{"date-parts":[[2003,6]]},"DOI":"10.1007\/s11910-003-0075-0","type":"journal-article","created":{"date-parts":[[2007,5,25]],"date-time":"2007-05-25T18:28:14Z","timestamp":1180117694000},"page":"185-187","source":"Crossref","is-referenced-by-count":4,"title":["Using mice to model cognitive deficits in neurologic disorders: Narrowing in on Rett syndrome"],"prefix":"10.1007","volume":"3","author":[{"given":"Joanne","family":"Berger-Sweeney","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"75_CR1","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1038\/85906","volume":"27","author":"RZ Chen","year":"2001","unstructured":"Chen RZ, Akbarian S, Tudor M, Jaenish R: Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat Genet 2001, 27:327\u2013331.","journal-title":"Nat Genet"},{"key":"75_CR2","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1017\/S0317167100052513","volume":"28","author":"HG Dunn","year":"2001","unstructured":"Dunn HG, MacLeod PM: Rett syndrome: review of biological abnormalities. Can J Neurol Sci 2001, 28:16\u201329.","journal-title":"Can J Neurol Sci"},{"key":"75_CR3","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1097\/00019052-200104000-00006","volume":"14","author":"MD Shahbazian","year":"2001","unstructured":"Shahbazian MD, Zoghbi HY: Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations. Curr Opin Neurol 2001, 14:171\u2013176.","journal-title":"Curr Opin Neurol"},{"key":"75_CR4","doi-asserted-by":"crossref","first-page":"342","DOI":"10.1038\/85970","volume":"4","author":"AR Carter","year":"2001","unstructured":"Carter AR, Segal RA: Rett syndrome model suggests MECP2 gives neurons the quiet they need to think. Nat Neurosci 2001, 4:342\u201343.","journal-title":"Nat Neurosci"},{"key":"75_CR5","doi-asserted-by":"crossref","first-page":"322","DOI":"10.1038\/85899","volume":"27","author":"J Guy","year":"2001","unstructured":"Guy J, Hendrich B, Holmes M, et al.: A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat Genet 2001, 27:322\u2013326.","journal-title":"Nat Genet"},{"key":"75_CR6","doi-asserted-by":"crossref","first-page":"243","DOI":"10.1016\/S0896-6273(02)00768-7","volume":"35","author":"MD Shahbazian","year":"2002","unstructured":"Shahbazian MD, Young JI, Yuva-Paylor LA, et al.: Mice with truncated MeCP2 recapitulate many Rett Syndrome features and display hyperacetylation of histone H3.Neuron 2002, 35:243\u2013254.","journal-title":"Neuron"},{"key":"75_CR7","volume-title":"What\u2019s Wrong with My Mouse? Behavioral Phenotyping of Transgenic and Knockout Mice","author":"JN Crawley","year":"2000","unstructured":"Crawley JN: What\u2019s Wrong with My Mouse? Behavioral Phenotyping of Transgenic and Knockout Mice. Hoboken, NJ: Wiley Press; 2000."},{"key":"75_CR8","unstructured":"Stearns NA, Floerke-Nashner L, Berger-Sweeney J: Behavioral characterization of MECP2 mice\u2014a Rett syndrome model. Soc Neurosci Abs 2002."},{"key":"75_CR9","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1007\/s002130051139","volume":"147","author":"DW Self","year":"1999","unstructured":"Self DW: Comparison of transgenic strategies for behavioral neuroscience studies in rodents. Psychopharmacology 1999, 147:35\u201337.","journal-title":"Psychopharmacology"},{"key":"75_CR10","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1016\/S0079-6123(02)35014-3","volume":"135","author":"PE Schauwecker","year":"2002","unstructured":"Schauwecker PE: Complications associated with genetic background effects in models of experimental epilepsy. Prog Brain Res 2002, 135:139\u2013148.","journal-title":"Prog Brain Res"},{"key":"75_CR11","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1016\/S0168-9525(01)02554-9","volume":"18","author":"AV Anagnostopoulos","year":"2002","unstructured":"Anagnostopoulos AV: It\u2019s a knockout! Male infertility and neuropathology. Trends Genet 2002, 18:8\u201310.","journal-title":"Trends Genet"}],"container-title":["Current Neurology and Neuroscience Reports"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s11910-003-0075-0.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s11910-003-0075-0\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s11910-003-0075-0","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T20:24:30Z","timestamp":1559420670000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s11910-003-0075-0"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2003,6]]},"references-count":11,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2003,6]]}},"alternative-id":["75"],"URL":"https:\/\/doi.org\/10.1007\/s11910-003-0075-0","relation":{},"ISSN":["1528-4042","1534-6293"],"issn-type":[{"value":"1528-4042","type":"print"},{"value":"1534-6293","type":"electronic"}],"subject":[],"published":{"date-parts":[[2003,6]]}}}