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Postnatal Loss of Methyl-CpG Binding Protein 2 in the Forebrain is Sufficient to Mediate Behavioral Aspects of Rett Syndrome in Mice
25/25 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
The 25 checked references that resolve
resolves10.1002/1531-8249(200005)47:5<670::AID-ANA20>3.0.CO;2-F
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
resolves10.1038/13810
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
resolves10.1093/hmg/10.22.2515
The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtin
resolves10.1021/bi0001271
Effects of Rett Syndrome Mutations of the Methyl-CpG Binding Domain of the Transcriptional Repressor MeCP2 on Selectivity for Association with Methylated DNA
resolves10.1093/hmg/9.9.1377
MECP2 mutations account for most cases of typical forms of Rett syndrome
resolves10.1038/85906
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
resolves10.1093/hmg/ddh282
Mild overexpression of MeCP2 causes a progressive neurological disorder in mice
resolves10.1006/exnr.2000.7626
Early Degenerative Changes in Transgenic Mice Expressing Mutant Huntingtin Involve Dendritic Abnormalities but No Impairment of Mitochondrial Energy Production
resolves10.1038/85899
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
resolves10.1002/ana.410140412
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases
resolves10.1093/hmg/9.9.1369
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients
resolves10.1002/neu.10201
The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells
resolves10.1073/pnas.0401626101
Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice
resolves10.1073/pnas.0402141101
Essential role of brain-derived neurotrophic factor in adult hippocampal function
resolves10.1523/JNEUROSCI.2542-04.2004
Induction of ΔFosB in Reward-Related Brain Structures after Chronic Stress
resolves10.1016/S0896-6273(04)00146-1
The Presynaptic Active Zone Protein RIM1α Is Critical for Normal Learning and Memory
resolves10.1016/S0896-6273(02)00768-7
Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3
resolves10.1038/ng0296-205
The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse
resolves10.1016/S0361-9230(01)00655-4
Anterior cingulate cortical transplantation in transgenic Huntington’s disease mice
resolves10.1086/302690
Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots
resolves10.1073/pnas.1131928100
Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function
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