|  Help  |  About  |  Contact Us

Search our database by keyword

Examples

  • Search this entire website. Enter identifiers, names or keywords for genes, diseases, strains, ontology terms, etc. (e.g. Pax6, Parkinson, ataxia)
  • Use OR to search for either of two terms (e.g. OR mus) or quotation marks to search for phrases (e.g. "dna binding").
  • Boolean search syntax is supported: e.g. Balb* for partial matches or mus AND NOT embryo to exclude a term

Search results 101 to 200 out of 1687 for Mecp2

<< First    < Previous  |  Next >    Last >>
0.03s

Categories

Hits by Pathway

Hits by Category

Hits by Strain

Type Details Score
Publication
31784358 | J:286255
First Author: Boxer LD
Year: 2020
Journal: Mol Cell
Title: MeCP2 Represses the Rate of Transcriptional Initiation of Highly Methylated Long Genes.
Volume: 77
Issue: 2
Pages: 294-309.e9
•
•
•
•
•
Publication
21394759 | J:283976
First Author: Banine F
Year: 2011
Journal: J Neurosci Res
Title: Brain region-specific expression of Fxyd1, an Mecp2 target gene, is regulated by epigenetic mechanisms.
Volume: 89
Issue: 6
Pages: 840-51
•
•
•
•
•
Publication
21420494 | J:174326
First Author: Singleton MK
Year: 2011
Journal: Neurobiol Dis
Title: MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation.
Volume: 43
Issue: 1
Pages: 190-200
•
•
•
•
•
Publication
21330301 | J:170472
First Author: Smrt RD
Year: 2011
Journal: Hum Mol Genet
Title: Age-dependent expression of MeCP2 in a heterozygous mosaic mouse model.
Volume: 20
Issue: 9
Pages: 1834-43
•
•
•
•
•
Publication
22395464 | J:318120
First Author: Su D
Year: 2012
Journal: Epigenetics
Title: Mutation of MeCP2 alters transcriptional regulation of select immediate-early genes.
Volume: 7
Issue: 2
Pages: 146-54
•
•
•
•
•
Publication
32927061 | J:301828
 
First Author: Dong HW
Year: 2020
Journal: Neurobiol Dis
Title: Detection of neurophysiological features in female R255X MeCP2 mutation mice.
Volume: 145
Pages: 105083
•
•
•
•
•
Publication
24750778 | J:323659
First Author: Ma LY
Year: 2014
Journal: CNS Neurosci Ther
Title: Electrophysiological phenotypes of MeCP2 A140V mutant mouse model.
Volume: 20
Issue: 5
Pages: 420-8
•
•
•
•
•
Publication
23055506 | J:190904
First Author: Hutchinson AN
Year: 2012
Journal: J Neurosci
Title: Phosphorylation of MeCP2 at Ser421 contributes to chronic antidepressant action.
Volume: 32
Issue: 41
Pages: 14355-63
•
•
•
•
•
Publication
21831886 | J:176677
First Author: Agarwal N
Year: 2011
Journal: Hum Mol Genet
Title: MeCP2 Rett mutations affect large scale chromatin organization.
Volume: 20
Issue: 21
Pages: 4187-95
•
•
•
•
•
Publication
24648499 | J:232293
First Author: Tantra M
Year: 2014
Journal: EMBO Mol Med
Title: Mild expression differences of MECP2 influencing aggressive social behavior.
Volume: 6
Issue: 5
Pages: 662-84
•
•
•
•
•
Publication
15351775 | J:94407
First Author: Collins AL
Year: 2004
Journal: Hum Mol Genet
Title: Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.
Volume: 13
Issue: 21
Pages: 2679-89
•
•
•
•
•
Protein
Q9Z2D6
Organism: Mus musculus/domesticus
Length: 484  
Fragment?: false
•
•
•
•
•
Publication
23452848 | J:194039
First Author: Baker SA
Year: 2013
Journal: Cell
Title: An AT-hook domain in MeCP2 determines the clinical course of Rett syndrome and related disorders.
Volume: 152
Issue: 5
Pages: 984-96
•
•
•
•
•
Publication
24472844 | J:215704
 
First Author: Degano AL
Year: 2014
Journal: Mol Cell Neurosci
Title: MeCP2 is required for activity-dependent refinement of olfactory circuits.
Volume: 59
Pages: 63-75
•
•
•
•
•
Publication
15809268 | J:97524
 
First Author: Caballero IM
Year: 2005
Journal: Hum Mol Genet
Title: MeCP2 in neurons: closing in on the causes of Rett syndrome.
Volume: 14 Spec No 1
Pages: R19-26
•
•
•
•
•
Publication
27428650 | J:238124
First Author: Nott A
Year: 2016
Journal: Nat Neurosci
Title: Histone deacetylase 3 associates with MeCP2 to regulate FOXO and social behavior.
Volume: 19
Issue: 11
Pages: 1497-1505
•
•
•
•
•
Publication
27782879 | J:238789
   
First Author: Sampathkumar C
Year: 2016
Journal: Elife
Title: Loss of MeCP2 disrupts cell autonomous and autocrine BDNF signaling in mouse glutamatergic neurons.
Volume: 5
•
•
•
•
•
Publication
23791832 | J:204417
First Author: Kim S
Year: 2013
Journal: Biochem Biophys Res Commun
Title: Ube3a/E6AP is involved in a subset of MeCP2 functions.
Volume: 437
Issue: 1
Pages: 67-73
•
•
•
•
•
Publication
22973007 | J:187664
First Author: Zhong X
Year: 2012
Journal: J Neurosci
Title: MeCP2 phosphorylation is required for modulating synaptic scaling through mGluR5.
Volume: 32
Issue: 37
Pages: 12841-7
•
•
•
•
•
Publication
30540948 | J:271259
First Author: Panayotis N
Year: 2018
Journal: Cell Rep
Title: Importin α5 Regulates Anxiety through MeCP2 and Sphingosine Kinase 1.
Volume: 25
Issue: 11
Pages: 3169-3179.e7
•
•
•
•
•
Publication
22357867 | J:182500
First Author: Dastidar SG
Year: 2012
Journal: J Neurosci
Title: Isoform-specific toxicity of Mecp2 in postmitotic neurons: suppression of neurotoxicity by FoxG1.
Volume: 32
Issue: 8
Pages: 2846-55
•
•
•
•
•
Publication
19369296 | J:323727
First Author: Ben-Shachar S
Year: 2009
Journal: Hum Mol Genet
Title: Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus.
Volume: 18
Issue: 13
Pages: 2431-42
•
•
•
•
•
Publication
25634563 | J:220859
First Author: Pitcher MR
Year: 2015
Journal: Hum Mol Genet
Title: Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene.
Volume: 24
Issue: 9
Pages: 2662-72
•
•
•
•
•
Publication
26843422 | J:323662
 
First Author: Lyu JW
Year: 2016
Journal: Sci Rep
Title: Reciprocal regulation of autism-related genes MeCP2 and PTEN via microRNAs.
Volume: 6
Pages: 20392
•
•
•
•
•
Publication
17309881 | J:121717
First Author: Deng V
Year: 2007
Journal: Hum Mol Genet
Title: FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice.
Volume: 16
Issue: 6
Pages: 640-50
•
•
•
•
•
Publication
33046553 | J:297103
First Author: Ito-Ishida A
Year: 2020
Journal: J Neurosci
Title: MeCP2 Levels Regulate the 3D Structure of Heterochromatic Foci in Mouse Neurons.
Volume: 40
Issue: 45
Pages: 8746-8766
•
•
•
•
•
Publication
23022455 | J:196997
 
First Author: Wither RG
Year: 2013
Journal: Exp Neurol
Title: Regional MeCP2 expression levels in the female MeCP2-deficient mouse brain correlate with specific behavioral impairments.
Volume: 239
Pages: 49-59
•
•
•
•
•
Publication
15115765 | J:91193
First Author: Braunschweig D
Year: 2004
Journal: Hum Mol Genet
Title: X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.
Volume: 13
Issue: 12
Pages: 1275-86
•
•
•
•
•
Publication
28394263 | J:243823
First Author: Lamonica JM
Year: 2017
Journal: J Clin Invest
Title: Elevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome-like phenotypes.
Volume: 127
Issue: 5
Pages: 1889-1904
•
•
•
•
•
Publication
24626160 | J:209639
 
First Author: Bissonnette JM
Year: 2014
Journal: Neuroscience
Title: Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.
Volume: 267
Pages: 166-76
•
•
•
•
•
Publication
28498846 | J:243502
First Author: Lagger S
Year: 2017
Journal: PLoS Genet
Title: MeCP2 recognizes cytosine methylated tri-nucleotide and di-nucleotide sequences to tune transcription in the mammalian brain.
Volume: 13
Issue: 5
Pages: e1006793
•
•
•
•
•
Publication
15757975 | J:98000
First Author: Makedonski K
Year: 2005
Journal: Hum Mol Genet
Title: MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.
Volume: 14
Issue: 8
Pages: 1049-58
•
•
•
•
•
Publication
38003438 | J:343320
 
First Author: Miranda-Lourenço C
Year: 2023
Journal: Int J Mol Sci
Title: Adenosinergic System and BDNF Signaling Changes as a Cross-Sectional Feature of RTT: Characterization of Mecp2 Heterozygous Mouse Females.
Volume: 24
Issue: 22
•
•
•
•
•
Publication
27974239 | J:260248
 
First Author: Matagne V
Year: 2017
Journal: Neurobiol Dis
Title: A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome.
Volume: 99
Pages: 1-11
•
•
•
•
•
Publication
18032561 | J:147675
First Author: Medrihan L
Year: 2008
Journal: J Neurophysiol
Title: Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.
Volume: 99
Issue: 1
Pages: 112-21
•
•
•
•
•
Publication
23011033 | J:323631
First Author: Gadalla KK
Year: 2013
Journal: Mol Ther
Title: Improved survival and reduced phenotypic severity following AAV9/MECP2 gene transfer to neonatal and juvenile male Mecp2 knockout mice.
Volume: 21
Issue: 1
Pages: 18-30
•
•
•
•
•
Publication
24270455 | J:304578
First Author: Maxwell SS
Year: 2013
Journal: RNA Biol
Title: Chromatin context and ncRNA highlight targets of MeCP2 in brain.
Volume: 10
Issue: 11
Pages: 1741-57
•
•
•
•
•
Publication
21753013 | J:174516
First Author: Ward CS
Year: 2011
Journal: J Neurosci
Title: MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan.
Volume: 31
Issue: 28
Pages: 10359-70
•
•
•
•
•
Publication
31333414 | J:281799
 
First Author: Bertoldi ML
Year: 2019
Journal: Front Cell Neurosci
Title: MeCP2 Deficiency Disrupts Kainate-Induced Presynaptic Plasticity in the Mossy Fiber Projections in the Hippocampus.
Volume: 13
Pages: 286
•
•
•
•
•
Publication
15069197 | J:89593
First Author: Luikenhuis S
Year: 2004
Journal: Proc Natl Acad Sci U S A
Title: Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice.
Volume: 101
Issue: 16
Pages: 6033-8
•
•
•
•
•
Publication
32343226 | J:307950
   
First Author: Mossner JM
Year: 2020
Journal: Elife
Title: Developmental loss of MeCP2 from VIP interneurons impairs cortical function and behavior.
Volume: 9
•
•
•
•
•
Publication
31913581 | J:323676
First Author: Ehinger Y
Year: 2020
Journal: EMBO Mol Med
Title: Huntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice.
Volume: 12
Issue: 2
Pages: e10889
•
•
•
•
•
Publication
17267601 | J:119746
First Author: Giacometti E
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.
Volume: 104
Issue: 6
Pages: 1931-6
•
•
•
•
•
Publication
29078406 | J:252906
First Author: Sinnamon JR
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: Site-directed RNA repair of endogenous Mecp2 RNA in neurons.
Volume: 114
Issue: 44
Pages: E9395-E9402
•
•
•
•
•
Publication
34234891 | J:323742
First Author: Lee W
Year: 2021
Journal: Anim Cells Syst (Seoul)
Title: Loss of MeCP2 causes subtle alteration in dendritic arborization of retinal ganglion cells.
Volume: 25
Issue: 2
Pages: 102-109
•
•
•
•
•
Publication
17635839 | J:124365
First Author: Alvarez-Saavedra M
Year: 2007
Journal: Hum Mol Genet
Title: Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis.
Volume: 16
Issue: 19
Pages: 2315-25
•
•
•
•
•
Publication
39137370 | J:358514
First Author: Kalani L
Year: 2024
Journal: Hum Mol Genet
Title: Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoforms.
Volume: 33
Issue: 21
Pages: 1833-1845
•
•
•
•
•
Publication
35248529 | J:338846
 
First Author: Vermudez SAD
Year: 2022
Journal: Neuropharmacology
Title: Exploration of group II metabotropic glutamate receptor modulation in mouse models of Rett syndrome and MECP2 Duplication syndrome.
Volume: 209
Pages: 109022
•
•
•
•
•
Publication
22174313 | J:183640
First Author: McCauley MD
Year: 2011
Journal: Sci Transl Med
Title: Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome.
Volume: 3
Issue: 113
Pages: 113ra125
•
•
•
•
•
Publication
25979088 | J:242531
First Author: Bedogni F
Year: 2016
Journal: Cereb Cortex
Title: Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms.
Volume: 26
Issue: 6
Pages: 2517-2529
•
•
•
•
•
Publication
21511710 | J:323733
First Author: Nelson ED
Year: 2011
Journal: J Neurophysiol
Title: Selective impact of MeCP2 and associated histone deacetylases on the dynamics of evoked excitatory neurotransmission.
Volume: 106
Issue: 1
Pages: 193-201
•
•
•
•
•
Publication
29902467 | J:269656
 
First Author: Matagne V
Year: 2018
Journal: Brain Res
Title: Correcting deregulated Fxyd1 expression rescues deficits in neuronal arborization and potassium homeostasis in MeCP2 deficient male mice.
Volume: 1697
Pages: 45-52
•
•
•
•
•
Publication
16380085 | J:104731
First Author: Saywell V
Year: 2006
Journal: Biochem Biophys Res Commun
Title: Brain magnetic resonance study of Mecp2 deletion effects on anatomy and metabolism.
Volume: 340
Issue: 3
Pages: 776-83
•
•
•
•
•
Publication
20188178 | J:164144
First Author: Macdonald JL
Year: 2010
Journal: Mol Cell Neurosci
Title: MBD2 and MeCP2 regulate distinct transitions in the stage-specific differentiation of olfactory receptor neurons.
Volume: 44
Issue: 1
Pages: 55-67
•
•
•
•
•
Publication
19208815 | J:144936
First Author: Tropea D
Year: 2009
Journal: Proc Natl Acad Sci U S A
Title: Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice.
Volume: 106
Issue: 6
Pages: 2029-34
•
•
•
•
•
Publication
32144612 | J:319400
First Author: Yu B
Year: 2020
Journal: Neurosci Bull
Title: Reversal of Social Recognition Deficit in Adult Mice with MECP2 Duplication via Normalization of MeCP2 in the Medial Prefrontal Cortex.
Volume: 36
Issue: 6
Pages: 570-584
•
•
•
•
•
Publication
22653753 | J:185982
First Author: Cheval H
Year: 2012
Journal: Hum Mol Genet
Title: Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows.
Volume: 21
Issue: 17
Pages: 3806-14
•
•
•
•
•
Publication
34324427 | J:311159
 
First Author: Ibrahim A
Year: 2021
Journal: Science
Title: MeCP2 is a microsatellite binding protein that protects CA repeats from nucleosome invasion.
Volume: 372
Issue: 6549
•
•
•
•
•
Publication
25420914 | J:323660
 
First Author: Li H
Year: 2014
Journal: Nat Commun
Title: Cell cycle-linked MeCP2 phosphorylation modulates adult neurogenesis involving the Notch signalling pathway.
Volume: 5
Pages: 5601
•
•
•
•
•
Publication
24188180 | J:207859
First Author: Cheng J
Year: 2014
Journal: J Neurochem
Title: SUMOylation of MeCP2 is essential for transcriptional repression and hippocampal synapse development.
Volume: 128
Issue: 6
Pages: 798-806
•
•
•
•
•
Publication
28920956 | J:251147
First Author: Johnson BS
Year: 2017
Journal: Nat Med
Title: Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome.
Volume: 23
Issue: 10
Pages: 1203-1214
•
•
•
•
•
Publication
26869885 | J:323688
 
First Author: Balakrishnan S
Year: 2016
Journal: Front Cell Neurosci
Title: Rescue of Cyclic AMP Mediated Long Term Potentiation Impairment in the Hippocampus of Mecp2 Knockout (Mecp2(-/y) ) Mice by Rolipram.
Volume: 10
Pages: 15
•
•
•
•
•
Publication
30038001 | J:264367
First Author: Carrette LLG
Year: 2018
Journal: Proc Natl Acad Sci U S A
Title: Tsix-Mecp2 female mouse model for Rett syndrome reveals that low-level MECP2 expression extends life and improves neuromotor function.
Volume: 115
Issue: 32
Pages: 8185-8190
•
•
•
•
•
Publication
29515365 | J:289512
 
First Author: Vogelgesang S
Year: 2018
Journal: Front Mol Neurosci
Title: Persistent Expression of Serotonin Receptor 5b Alters Breathing Behavior in Male MeCP2 Knockout Mice.
Volume: 11
Pages: 28
•
•
•
•
•
Publication
20007372 | J:155808
First Author: Samaco RC
Year: 2009
Journal: Proc Natl Acad Sci U S A
Title: Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities.
Volume: 106
Issue: 51
Pages: 21966-71
•
•
•
•
•
Publication
31629059 | J:313299
 
First Author: Cortelazzo A
Year: 2020
Journal: J Proteomics
Title: Brain protein changes in Mecp2 mouse mutant models: Effects on disease progression of Mecp2 brain specific gene reactivation.
Volume: 210
Pages: 103537
•
•
•
•
•
Publication
36931532 | J:334932
 
First Author: Carli S
Year: 2023
Journal: Neurobiol Dis
Title: A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain.
Volume: 180
Pages: 106083
•
•
•
•
•
Publication
23892605 | J:198551
First Author: Buchovecky CM
Year: 2013
Journal: Nat Genet
Title: A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.
Volume: 45
Issue: 9
Pages: 1013-20
•
•
•
•
•
Publication
17383101 | J:122048
First Author: Stearns NA
Year: 2007
Journal: Neuroscience
Title: Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.
Volume: 146
Issue: 3
Pages: 907-21
•
•
•
•
•
Publication
30277526 | J:270054
First Author: Sun Y
Year: 2019
Journal: Hum Mol Genet
Title: Loss of MeCP2 in immature neurons leads to impaired network integration.
Volume: 28
Issue: 2
Pages: 245-257
•
•
•
•
•
Publication
22138506 | J:184408
 
First Author: Palmer AM
Year: 2012
Journal: Neuroscience
Title: Normal mitral cell dendritic development in the setting of Mecp2 mutation.
Volume: 202
Pages: 108-16
•
•
•
•
•
Publication
36064580 | J:328335
First Author: Yue Y
Year: 2022
Journal: Mol Brain
Title: MeCP2 deficiency impairs motor cortical circuit flexibility associated with motor learning.
Volume: 15
Issue: 1
Pages: 76
•
•
•
•
•
Publication
23015442 | J:188271
First Author: Blackman MP
Year: 2012
Journal: J Neurosci
Title: A critical and cell-autonomous role for MeCP2 in synaptic scaling up.
Volume: 32
Issue: 39
Pages: 13529-36
•
•
•
•
•
Publication
22334035 | J:323736
First Author: Wu W
Year: 2012
Journal: Neurol Res
Title: Downregulation of CNPase in a MeCP2 deficient mouse model of Rett syndrome.
Volume: 34
Issue: 2
Pages: 107-13
•
•
•
•
•
Publication
33193060 | J:308244
 
First Author: Ward CS
Year: 2020
Journal: Front Neurol
Title: Loss of MeCP2 Function Across Several Neuronal Populations Impairs Breathing Response to Acute Hypoxia.
Volume: 11
Pages: 593554
•
•
•
•
•
Publication
27828991 | J:251287
First Author: Ward CS
Year: 2016
Journal: PLoS One
Title: Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome.
Volume: 11
Issue: 11
Pages: e0165550
•
•
•
•
•
Publication
23770565 | J:203745
First Author: Lyst MJ
Year: 2013
Journal: Nat Neurosci
Title: Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor.
Volume: 16
Issue: 7
Pages: 898-902
•
•
•
•
•
Publication
26605526 | J:234046
First Author: Sztainberg Y
Year: 2015
Journal: Nature
Title: Reversal of phenotypes in MECP2 duplication mice using genetic rescue or antisense oligonucleotides.
Volume: 528
Issue: 7580
Pages: 123-6
•
•
•
•
•
Publication
17296936 | J:125897
First Author: Nan X
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.
Volume: 104
Issue: 8
Pages: 2709-14
•
•
•
•
•
Publication
31597640 | J:287847
First Author: Liu C
Year: 2020
Journal: Diabetes
Title: Fat-Specific Knockout of Mecp2 Upregulates Slpi to Reduce Obesity by Enhancing Browning.
Volume: 69
Issue: 1
Pages: 35-47
•
•
•
•
•
Publication
36897048 | J:354683
First Author: Rahn RM
Year: 2023
Journal: Cereb Cortex
Title: Mecp2 deletion results in profound alterations of developmental and adult functional connectivity.
Volume: 33
Issue: 12
Pages: 7436-7453
•
•
•
•
•
Publication
24990928 | J:212537
First Author: Zhang Z
Year: 2014
Journal: J Neurosci
Title: MeCP2 repression of G9a in regulation of pain and morphine reward.
Volume: 34
Issue: 27
Pages: 9076-87
•
•
•
•
•
Publication
27916441 | J:323620
First Author: Yuan B
Year: 2017
Journal: J Genet Genomics
Title: Autism-related protein MeCP2 regulates FGF13 expression and emotional behaviors.
Volume: 44
Issue: 1
Pages: 63-66
•
•
•
•
•
Publication
18817733 | J:143360
First Author: Fyffe SL
Year: 2008
Journal: Neuron
Title: Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.
Volume: 59
Issue: 6
Pages: 947-58
•
•
•
•
•
Publication
22231481 | J:181213
First Author: Samaco RC
Year: 2012
Journal: Nat Genet
Title: Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome.
Volume: 44
Issue: 2
Pages: 206-11
•
•
•
•
•
Publication
26456390 | J:318785
First Author: Tsuchiya Y
Year: 2015
Journal: Genes Cells
Title: Disruption of MeCP2 attenuates circadian rhythm in CRISPR/Cas9-based Rett syndrome model mouse.
Volume: 20
Issue: 12
Pages: 992-1005
•
•
•
•
•
Publication
34183865 | J:323402
First Author: Kim JW
Year: 2021
Journal: Nat Neurosci
Title: Sustained effects of rapidly acting antidepressants require BDNF-dependent MeCP2 phosphorylation.
Volume: 24
Issue: 8
Pages: 1100-1109
•
•
•
•
•
Publication
20711186 | J:165279
First Author: Deng JV
Year: 2010
Journal: Nat Neurosci
Title: MeCP2 in the nucleus accumbens contributes to neural and behavioral responses to psychostimulants.
Volume: 13
Issue: 9
Pages: 1128-36
•
•
•
•
•
Publication
15034150 | J:89475
First Author: Kriaucionis S
Year: 2004
Journal: Nucleic Acids Res
Title: The major form of MeCP2 has a novel N-terminus generated by alternative splicing.
Volume: 32
Issue: 5
Pages: 1818-23
•
•
•
•
•
Publication
38100348 | J:343761
First Author: Xu FX
Year: 2023
Journal: Cell Rep
Title: Purkinje-cell-specific MeCP2 deficiency leads to motor deficits and autistic-like behavior due to aberrations in PTP1B-TrkB-SK signaling.
Volume: 42
Issue: 12
Pages: 113559
•
•
•
•
•
Publication
26842955 | J:236279
 
First Author: Tai DJ
Year: 2016
Journal: Nat Commun
Title: MeCP2 SUMOylation rescues Mecp2-mutant-induced behavioural deficits in a mouse model of Rett syndrome.
Volume: 7
Pages: 10552
•
•
•
•
•
Publication
18687363 | J:142151
First Author: Nag N
Year: 2009
Journal: Behav Brain Res
Title: Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp2 1lox mice.
Volume: 196
Issue: 1
Pages: 44-8
•
•
•
•
•
Publication
23027959 | J:190298
First Author: Li W
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Activity-dependent BDNF release and TRPC signaling is impaired in hippocampal neurons of Mecp2 mutant mice.
Volume: 109
Issue: 42
Pages: 17087-92
•
•
•
•
•
Publication
12160743 | J:78009
First Author: Shahbazian M
Year: 2002
Journal: Neuron
Title: Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3.
Volume: 35
Issue: 2
Pages: 243-54
•
•
•
•
•
Publication
20203171 | J:159694
First Author: Alvarez-Saavedra M
Year: 2010
Journal: Hum Mol Genet
Title: Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development.
Volume: 19
Issue: 11
Pages: 2177-90
•
•
•
•
•
Publication
8563762 | J:31573
First Author: Tate P
Year: 1996
Journal: Nat Genet
Title: The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.
Volume: 12
Issue: 2
Pages: 205-8
•
•
•
•
•
Publication
20188665 | J:158816
First Author: Skene PJ
Year: 2010
Journal: Mol Cell
Title: Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.
Volume: 37
Issue: 4
Pages: 457-68
•
•
•
•
•
Publication
33048927 | J:296892
First Author: Chhatbar K
Year: 2020
Journal: PLoS Genet
Title: Quantitative analysis questions the role of MeCP2 as a global regulator of alternative splicing.
Volume: 16
Issue: 10
Pages: e1009087
•
•
•
•
•
Publication
24636259 | J:271380
First Author: Cheng TL
Year: 2014
Journal: Dev Cell
Title: MeCP2 suppresses nuclear microRNA processing and dendritic growth by regulating the DGCR8/Drosha complex.
Volume: 28
Issue: 5
Pages: 547-60
•
•
•
•
•
Publication
18295506 | J:135669
First Author: Palmer A
Year: 2008
Journal: Mol Cell Neurosci
Title: MeCP2 mutation causes distinguishable phases of acute and chronic defects in synaptogenesis and maintenance, respectively.
Volume: 37
Issue: 4
Pages: 794-807
•
•
•
•
•




MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

Copyright © 2017 by The Jackson Laboratory. All Rights Reserved

© 2002 - 2017 Department of Genetics, University of Cambridge, Downing Street,
Cambridge CB2 3EH, United Kingdom