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Search results 401 to 500 out of 1687 for Mecp2

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Type Details Score
Publication
27653984 | J:239338
First Author: Johnson CM
Year: 2016
Journal: Am J Physiol Cell Physiol
Title: Defects in brainstem neurons associated with breathing and motor function in the Mecp2R168X/Y mouse model of Rett syndrome.
Volume: 311
Issue: 6
Pages: C895-C909
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Publication
34201747 | J:313743
 
First Author: Urbinati C
Year: 2021
Journal: Int J Mol Sci
Title: Treatment with the Bacterial Toxin CNF1 Selectively Rescues Cognitive and Brain Mitochondrial Deficits in a Female Mouse Model of Rett Syndrome Carrying a MeCP2-Null Mutation.
Volume: 22
Issue: 13
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Publication
16087343 | J:104545
First Author: Asaka Y
Year: 2006
Journal: Neurobiol Dis
Title: Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome.
Volume: 21
Issue: 1
Pages: 217-27
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Publication
22375006 | J:184364
First Author: Itoh M
Year: 2012
Journal: J Biol Chem
Title: Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development.
Volume: 287
Issue: 17
Pages: 13859-67
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Publication
26476268 | J:231839
 
First Author: Cortelazzo A
Year: 2016
Journal: Neurosci Res
Title: Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome.
Volume: 105
Pages: 28-34
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Publication
26410354 | J:284344
First Author: Patrizi A
Year: 2016
Journal: Biol Psychiatry
Title: Chronic Administration of the N-Methyl-D-Aspartate Receptor Antagonist Ketamine Improves Rett Syndrome Phenotype.
Volume: 79
Issue: 9
Pages: 755-764
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Publication
28423315 | J:250884
First Author: Mendoza-Viveros L
Year: 2017
Journal: Cell Rep
Title: miR-132/212 Modulates Seasonal Adaptation and Dendritic Morphology of the Central Circadian Clock.
Volume: 19
Issue: 3
Pages: 505-520
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Publication
31291284 | J:277453
First Author: Sheinerman K
Year: 2019
Journal: PLoS One
Title: Brain-enriched microRNAs circulating in plasma as novel biomarkers for Rett syndrome.
Volume: 14
Issue: 7
Pages: e0218623
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Publication
31038696 | J:305053
First Author: Patrizi A
Year: 2020
Journal: Cereb Cortex
Title: Accelerated Hyper-Maturation of Parvalbumin Circuits in the Absence of MeCP2.
Volume: 30
Issue: 1
Pages: 256-268
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Publication
26883520 | J:323689
 
First Author: Horiuchi M
Year: 2017
Journal: Brain Behav Immun
Title: CX3CR1 ablation ameliorates motor and respiratory dysfunctions and improves survival of a Rett syndrome mouse model.
Volume: 60
Pages: 106-116
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Publication
34230964 | J:320693
First Author: Vashi N
Year: 2021
Journal: Hum Mol Genet
Title: Aberrant lung lipids cause respiratory impairment in a Mecp2-deficient mouse model of Rett syndrome.
Volume: 30
Issue: 22
Pages: 2161-2176
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Publication
16549521 | J:323725
First Author: Bissonnette JM
Year: 2006
Journal: Pediatr Res
Title: Separate respiratory phenotypes in methyl-CpG-binding protein 2 (Mecp2) deficient mice.
Volume: 59
Issue: 4 Pt 1
Pages: 513-8
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Publication
24351104 | J:232165
First Author: Abdala AP
Year: 2014
Journal: Am J Respir Cell Mol Biol
Title: Effect of Sarizotan, a 5-HT1a and D2-like receptor agonist, on respiration in three mouse models of Rett syndrome.
Volume: 50
Issue: 6
Pages: 1031-9
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Publication
37777475 | J:350455
First Author: Khoury ES
Year: 2024
Journal: J Neurochem
Title: Dendrimer nanotherapy targeting of glial dysfunction improves inflammation and neurobehavioral phenotype in adult female Mecp2-heterozygous mouse model of Rett syndrome.
Volume: 168
Issue: 5
Pages: 841-854
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Publication
21068835 | J:166851
First Author: Chao HT
Year: 2010
Journal: Nature
Title: Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Volume: 468
Issue: 7321
Pages: 263-9
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25673846 | J:219878
First Author: Jin LW
Year: 2015
Journal: J Neurosci
Title: Dysregulation of glutamine transporter SNAT1 in Rett syndrome microglia: a mechanism for mitochondrial dysfunction and neurotoxicity.
Volume: 35
Issue: 6
Pages: 2516-29
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Publication
25902482 | J:229774
First Author: Cronk JC
Year: 2015
Journal: Immunity
Title: Methyl-CpG Binding Protein 2 Regulates Microglia and Macrophage Gene Expression in Response to Inflammatory Stimuli.
Volume: 42
Issue: 4
Pages: 679-91
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Publication
26821816 | J:236294
 
First Author: Kishi N
Year: 2016
Journal: Nat Commun
Title: Reduction of aberrant NF-κB signalling ameliorates Rett syndrome phenotypes in Mecp2-null mice.
Volume: 7
Pages: 10520
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Publication
23259945 | J:197657
First Author: Durand S
Year: 2012
Journal: Neuron
Title: NMDA receptor regulation prevents regression of visual cortical function in the absence of Mecp2.
Volume: 76
Issue: 6
Pages: 1078-90
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Publication
21716289 | J:174777
First Author: Lioy DT
Year: 2011
Journal: Nature
Title: A role for glia in the progression of Rett's syndrome.
Volume: 475
Issue: 7357
Pages: 497-500
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Publication
24769161 | J:214008
 
First Author: De Felice C
Year: 2014
Journal: Neurobiol Dis
Title: Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome.
Volume: 68
Pages: 66-77
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29203410 | J:272151
 
First Author: Mesuret G
Year: 2018
Journal: Respir Physiol Neurobiol
Title: Breathing disturbances in a model of Rett syndrome: A potential involvement of the glycine receptor α3 subunit?
Volume: 248
Pages: 43-47
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Publication
25088363 | J:221545
First Author: Gogolla N
Year: 2014
Journal: Neuron
Title: Sensory integration in mouse insular cortex reflects GABA circuit maturation.
Volume: 83
Issue: 4
Pages: 894-905
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21471397 | J:323743
First Author: Kron M
Year: 2011
Journal: J Neurophysiol
Title: Altered responses of MeCP2-deficient mouse brain stem to severe hypoxia.
Volume: 105
Issue: 6
Pages: 3067-79
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33373327 | J:322270
 
First Author: Pizzamiglio L
Year: 2021
Journal: JCI Insight
Title: The DNA repair protein ATM as a target in autism spectrum disorder.
Volume: 6
Issue: 3
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31239460 | J:278672
First Author: Lozovaya N
Year: 2019
Journal: Sci Rep
Title: Early alterations in a mouse model of Rett syndrome: the GABA developmental shift is abolished at birth.
Volume: 9
Issue: 1
Pages: 9276
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Publication
29570050 | J:264564
   
First Author: Pohodich AE
Year: 2018
Journal: Elife
Title: Forniceal deep brain stimulation induces gene expression and splicing changes that promote neurogenesis and plasticity.
Volume: 7
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30028675 | J:267946
   
First Author: Kee SE
Year: 2018
Journal: Elife
Title: Impaired spatial memory codes in a mouse model of Rett syndrome.
Volume: 7
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22891354 | J:188569
First Author: Deogracias R
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Fingolimod, a sphingosine-1 phosphate receptor modulator, increases BDNF levels and improves symptoms of a mouse model of Rett syndrome.
Volume: 109
Issue: 35
Pages: 14230-5
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Publication
38199865 | J:354262
 
First Author: Mykins M
Year: 2024
Journal: J Neurosci
Title: Multidimensional Analysis of a Social Behavior Identifies Regression and Phenotypic Heterogeneity in a Female Mouse Model for Rett Syndrome.
Volume: 44
Issue: 12
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Publication
21307341 | J:175673
First Author: Zhang X
Year: 2011
Journal: Am J Physiol Cell Physiol
Title: The disruption of central CO2 chemosensitivity in a mouse model of Rett syndrome.
Volume: 301
Issue: 3
Pages: C729-38
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Publication
28983239 | J:321308
 
First Author: Niebert S
Year: 2017
Journal: Front Mol Neurosci
Title: The Serotonin Receptor Subtype 5b Specifically Interacts with Serotonin Receptor Subtype 1A.
Volume: 10
Pages: 299
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Publication
30297987 | J:276015
 
First Author: Mou X
Year: 2018
Journal: Front Cell Neurosci
Title: Comparing Mouse and Rat Hippocampal Place Cell Activities and Firing Sequences in the Same Environments.
Volume: 12
Pages: 332
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Publication
20732392 | J:169732
First Author: Kron M
Year: 2010
Journal: Neuroscience
Title: Impaired hippocampal Ca2+ homeostasis and concomitant K+ channel dysfunction in a mouse model of Rett syndrome during anoxia.
Volume: 171
Issue: 1
Pages: 300-15
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Publication
29782864 | J:268381
 
First Author: Wong DF
Year: 2018
Journal: Exp Neurol
Title: Are dopamine receptor and transporter changes in Rett syndrome reflected in Mecp2-deficient mice?
Volume: 307
Pages: 74-81
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Publication
16549272 | J:108953
First Author: Metcalf BM
Year: 2006
Journal: Neuroscience
Title: Temporal shift in methyl-CpG binding protein 2 expression in a mouse model of Rett syndrome.
Volume: 139
Issue: 4
Pages: 1449-60
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Publication
34572143 | J:313708
 
First Author: Golubiani G
Year: 2021
Journal: Cells
Title: Metabolomic Fingerprint of Mecp2-Deficient Mouse Cortex: Evidence for a Pronounced Multi-Facetted Metabolic Component in Rett Syndrome.
Volume: 10
Issue: 9
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Publication
31114506 | J:313101
 
First Author: Can K
Year: 2019
Journal: Front Physiol
Title: Neuronal Redox-Imbalance in Rett Syndrome Affects Mitochondria as Well as Cytosol, and Is Accompanied by Intensified Mitochondrial O 2 Consumption and ROS Release.
Volume: 10
Pages: 479
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Publication
31229630 | J:293015
 
First Author: Ruffolo G
Year: 2020
Journal: Neuroscience
Title: Rare Diseases of Neurodevelopment: Maintain the Mystery or Use a Dazzling Tool for Investigation? The Case of Rett Syndrome.
Volume: 439
Pages: 146-152
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Publication
28150739 | J:288226
 
First Author: Mucerino S
Year: 2017
Journal: Sci Rep
Title: Alterations in the carnitine cycle in a mouse model of Rett syndrome.
Volume: 7
Pages: 41824
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Publication
17204503 | J:140841
First Author: Stettner GM
Year: 2007
Journal: J Physiol
Title: Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2-/y knockout mice.
Volume: 579
Issue: Pt 3
Pages: 863-76
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Publication
25713300 | J:221198
First Author: Herrera JA
Year: 2015
Journal: Dis Model Mech
Title: Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs.
Volume: 8
Issue: 4
Pages: 363-71
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Publication
32317254 | J:323637
First Author: Enikanolaiye A
Year: 2020
Journal: Genome Res
Title: Suppressor mutations in Mecp2-null mice implicate the DNA damage response in Rett syndrome pathology.
Volume: 30
Issue: 4
Pages: 540-552
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Publication
36430502 | J:332156
 
First Author: Dai H
Year: 2022
Journal: Int J Mol Sci
Title: 5-HT(1A) Receptor Agonist Treatment Partially Ameliorates Rett Syndrome Phenotypes in mecp2-Null Mice by Rescuing Impairment of Neuron Transmission and the CREB/BDNF Signaling Pathway.
Volume: 23
Issue: 22
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Publication
24667344 | J:214151
First Author: El-Khoury R
Year: 2014
Journal: PLoS One
Title: GABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient mice.
Volume: 9
Issue: 3
Pages: e92169
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Publication
19524074 | J:155642
First Author: Voituron N
Year: 2009
Journal: Respir Physiol Neurobiol
Title: Early breathing defects after moderate hypoxia or hypercapnia in a mouse model of Rett syndrome.
Volume: 168
Issue: 1-2
Pages: 109-18
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Publication
24394521 | J:215711
 
First Author: Toloe J
Year: 2014
Journal: Mol Cell Neurosci
Title: Metabolic differences in hippocampal 'Rett' neurons revealed by ATP imaging.
Volume: 59
Pages: 47-56
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Publication
38036056 | J:343767
 
First Author: Asgarihafshejani A
Year: 2024
Journal: Neuroscience
Title: LTP is Absent in the CA1 Region of the Hippocampus of Male and Female Rett Syndrome Mouse Models.
Volume: 537
Pages: 189-204
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Publication
28337123 | J:323681
 
First Author: Vogelgesang S
Year: 2017
Journal: Front Mol Neurosci
Title: Analysis of the Serotonergic System in a Mouse Model of Rett Syndrome Reveals Unusual Upregulation of Serotonin Receptor 5b.
Volume: 10
Pages: 61
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Publication
20042730 | J:157650
First Author: Zhang X
Year: 2010
Journal: Am J Physiol Cell Physiol
Title: Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.
Volume: 298
Issue: 3
Pages: C635-46
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Publication
27895554 | J:323682
 
First Author: Janc OA
Year: 2016
Journal: Front Cell Neurosci
Title: Systemic Radical Scavenger Treatment of a Mouse Model of Rett Syndrome: Merits and Limitations of the Vitamin E Derivative Trolox.
Volume: 10
Pages: 266
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Publication
25009110 | J:221827
First Author: Oginsky MF
Year: 2014
Journal: Am J Physiol Cell Physiol
Title: Alterations in the cholinergic system of brain stem neurons in a mouse model of Rett syndrome.
Volume: 307
Issue: 6
Pages: C508-20
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Publication
30890637 | J:274365
First Author: Sigal YM
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Structural maturation of cortical perineuronal nets and their perforating synapses revealed by superresolution imaging.
Volume: 116
Issue: 14
Pages: 7071-7076
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Publication
34281226 | J:320571
 
First Author: Hung PL
Year: 2021
Journal: Int J Mol Sci
Title: Music-Based Intervention Ameliorates Mecp2-Loss-Mediated Sociability Repression in Mice through the Prefrontal Cortex FNDC5/BDNF Pathway.
Volume: 22
Issue: 13
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Publication
30256804 | J:266158
First Author: Balakrishnan S
Year: 2018
Journal: PLoS One
Title: Regenerative glutamate release in the hippocampus of Rett syndrome model mice.
Volume: 13
Issue: 9
Pages: e0202802
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Publication
30608967 | J:269920
First Author: Fukuhara S
Year: 2019
Journal: PLoS One
Title: High-fat diet accelerates extreme obesity with hyperphagia in female heterozygous Mecp2-null mice.
Volume: 14
Issue: 1
Pages: e0210184
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Publication
23986203 | J:323737
First Author: Jin XT
Year: 2013
Journal: Am J Physiol Cell Physiol
Title: Pre- and postsynaptic modulations of hypoglossal motoneurons by α-adrenoceptor activation in wild-type and Mecp2(-/Y) mice.
Volume: 305
Issue: 10
Pages: C1080-90
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Publication
27317352 | J:255123
First Author: Zhang S
Year: 2016
Journal: J Neurosci Res
Title: An optogenetic mouse model of rett syndrome targeting on catecholaminergic neurons.
Volume: 94
Issue: 10
Pages: 896-906
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Publication
28138553 | J:323653
First Author: Cronk JC
Year: 2017
Journal: JCI Insight
Title: Influenza A induces dysfunctional immunity and death in MeCP2-overexpressing mice.
Volume: 2
Issue: 2
Pages: e88257
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24067915 | J:210196
First Author: Jin X
Year: 2013
Journal: Am J Physiol Cell Physiol
Title: Time-dependent modulation of GABA(A)-ergic synaptic transmission by allopregnanolone in locus coeruleus neurons of Mecp2-null mice.
Volume: 305
Issue: 11
Pages: C1151-60
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Publication
11242117 | J:67910
First Author: Guy J
Year: 2001
Journal: Nat Genet
Title: A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.
Volume: 27
Issue: 3
Pages: 322-6
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Publication
32622786 | J:314875
 
First Author: Johnson CM
Year: 2020
Journal: Neuropharmacology
Title: The antitussive cloperastine improves breathing abnormalities in a Rett Syndrome mouse model by blocking presynaptic GIRK channels and enhancing GABA release.
Volume: 176
Pages: 108214
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Publication
12928486 | J:85962
 
First Author: Kriaucionis S
Year: 2003
Journal: Hum Mol Genet
Title: DNA methylation and Rett syndrome.
Volume: 12 Spec No 2
Pages: R221-7
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Publication
35074918 | J:323645
 
First Author: Zhou J
Year: 2022
Journal: Proc Natl Acad Sci U S A
Title: Disruption of MeCP2-TCF20 complex underlies distinct neurodevelopmental disorders.
Volume: 119
Issue: 4
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26936821 | J:323690
First Author: Gogliotti RG
Year: 2016
Journal: Hum Mol Genet
Title: mGlu5 positive allosteric modulation normalizes synaptic plasticity defects and motor phenotypes in a mouse model of Rett syndrome.
Volume: 25
Issue: 10
Pages: 1990-2004
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Publication
31911459 | J:293129
First Author: Lau BYB
Year: 2020
Journal: J Neurosci
Title: Maternal Experience-Dependent Cortical Plasticity in Mice Is Circuit- and Stimulus-Specific and Requires MECP2.
Volume: 40
Issue: 7
Pages: 1514-1526
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Publication
22425995 | J:183878
First Author: Derecki NC
Year: 2012
Journal: Nature
Title: Wild-type microglia arrest pathology in a mouse model of Rett syndrome.
Volume: 484
Issue: 7392
Pages: 105-9
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Publication
28159985 | J:241788
First Author: Herrera JA
Year: 2016
Journal: Hum Mol Genet
Title: Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesis.
Volume: 25
Issue: 22
Pages: 4983-4995
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Publication
27803317 | J:238847
First Author: Banerjee A
Year: 2016
Journal: Proc Natl Acad Sci U S A
Title: Jointly reduced inhibition and excitation underlies circuit-wide changes in cortical processing in Rett syndrome.
Volume: 113
Issue: 46
Pages: E7287-E7296
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Publication
34678068 | J:312932
First Author: Yue Y
Year: 2021
Journal: Sci Adv
Title: Motor training improves coordination and anxiety in symptomatic Mecp2-null mice despite impaired functional connectivity within the motor circuit.
Volume: 7
Issue: 43
Pages: eabf7467
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Publication
24777420 | J:212933
First Author: Goffin D
Year: 2014
Journal: Nat Neurosci
Title: Cellular origins of auditory event-related potential deficits in Rett syndrome.
Volume: 17
Issue: 6
Pages: 804-6
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Publication
24958851 | J:212180
First Author: Mellios N
Year: 2014
Journal: Proc Natl Acad Sci U S A
Title: β2-Adrenergic receptor agonist ameliorates phenotypes and corrects microRNA-mediated IGF1 deficits in a mouse model of Rett syndrome.
Volume: 111
Issue: 27
Pages: 9947-52
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Publication
33762729 | J:306869
First Author: Achilly NP
Year: 2021
Journal: Nature
Title: Presymptomatic training mitigates functional deficits in a mouse model of Rett syndrome.
Volume: 592
Issue: 7855
Pages: 596-600
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8589515 | J:28085
First Author: Adler DA
Year: 1995
Journal: Mamm Genome
Title: The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse.
Volume: 6
Issue: 8
Pages: 491-2
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24089468 | J:204597
First Author: Berghoff EG
Year: 2013
Journal: Development
Title: Evf2 (Dlx6as) lncRNA regulates ultraconserved enhancer methylation and the differential transcriptional control of adjacent genes.
Volume: 140
Issue: 21
Pages: 4407-16
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29056337 | J:251368
First Author: Stroud H
Year: 2017
Journal: Cell
Title: Early-Life Gene Expression in Neurons Modulates Lasting Epigenetic States.
Volume: 171
Issue: 5
Pages: 1151-1164.e16
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Allele
Mecp2<em2Gfng> | MGI:6886060
Name: methyl CpG binding protein 2; endonuclease-mediated mutation 2, Guoping Feng
Allele Type: Endonuclease-mediated
Attribute String: Humanized sequence, Inserted expressed sequence
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Publication
17289941 | J:118365
First Author: Guy J
Year: 2007
Journal: Science
Title: Reversal of neurological defects in a mouse model of Rett syndrome.
Volume: 315
Issue: 5815
Pages: 1143-7
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Publication
28419872 | J:337257
 
First Author: Valenti D
Year: 2017
Journal: Neuropharmacology
Title: Stimulation of the brain serotonin receptor 7 rescues mitochondrial dysfunction in female mice from two models of Rett syndrome.
Volume: 121
Pages: 79-88
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Publication
26406379 | J:224900
First Author: Linhoff MW
Year: 2015
Journal: Cell
Title: A high-resolution imaging approach to investigate chromatin architecture in complex tissues.
Volume: 163
Issue: 1
Pages: 246-55
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21636743 | J:173307
First Author: McGraw CM
Year: 2011
Journal: Science
Title: Adult neural function requires MeCP2.
Volume: 333
Issue: 6039
Pages: 186
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Publication
19339616 | J:147442
First Author: Adachi M
Year: 2009
Journal: J Neurosci
Title: MeCP2-mediated transcription repression in the basolateral amygdala may underlie heightened anxiety in a mouse model of Rett syndrome.
Volume: 29
Issue: 13
Pages: 4218-27
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Publication
18571096 | J:139191
First Author: Ward BC
Year: 2008
Journal: Neurobiol Dis
Title: Longitudinal brain MRI study in a mouse model of Rett Syndrome and the effects of choline.
Volume: 31
Issue: 1
Pages: 110-9
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Publication
19234456 | J:150543
First Author: Ballas N
Year: 2009
Journal: Nat Neurosci
Title: Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology.
Volume: 12
Issue: 3
Pages: 311-7
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Publication
31112129 | J:276803
   
First Author: Phillips ML
Year: 2019
Journal: Elife
Title: Ventral hippocampal projections to the medial prefrontal cortex regulate social memory.
Volume: 8
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Publication
19741133 | J:152676
First Author: Dani VS
Year: 2009
Journal: J Neurosci
Title: Intact long-term potentiation but reduced connectivity between neocortical layer 5 pyramidal neurons in a mouse model of Rett syndrome.
Volume: 29
Issue: 36
Pages: 11263-70
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Publication
28679669 | J:244187
First Author: Li W
Year: 2017
Journal: Dis Model Mech
Title: A small-molecule TrkB ligand restores hippocampal synaptic plasticity and object location memory in Rett syndrome mice.
Volume: 10
Issue: 7
Pages: 837-845
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Publication
29718204 | J:265095
First Author: Guy J
Year: 2018
Journal: Hum Mol Genet
Title: A mutation-led search for novel functional domains in MeCP2.
Volume: 27
Issue: 14
Pages: 2531-2545
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34582789 | J:323673
 
First Author: Lebrun N
Year: 2021
Journal: Brain Res
Title: HDAC inhibitor ameliorates behavioral deficits in Mecp2308/y mouse model of Rett syndrome.
Volume: 1772
Pages: 147670
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27672368 | J:293557
 
First Author: Hülsmann S
Year: 2016
Journal: Front Physiol
Title: GlyT2-Dependent Preservation of MECP2-Expression in Inhibitory Neurons Improves Early Respiratory Symptoms but Does Not Rescue Survival in a Mouse Model of Rett Syndrome.
Volume: 7
Pages: 385
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29730163 | J:269387
First Author: Landucci E
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Journal: Exp Cell Res
Title: iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome.
Volume: 368
Issue: 2
Pages: 225-235
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Publication
34916612 | J:323674
First Author: Neier K
Year: 2021
Journal: Commun Biol
Title: Sex disparate gut microbiome and metabolome perturbations precede disease progression in a mouse model of Rett syndrome.
Volume: 4
Issue: 1
Pages: 1408
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Publication
32668243 | J:300850
First Author: Sinnamon JR
Year: 2020
Journal: Cell Rep
Title: In Vivo Repair of a Protein Underlying a Neurological Disorder by Programmable RNA Editing.
Volume: 32
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Pages: 107878
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Publication
30157418 | J:270751
First Author: Lyst MJ
Year: 2018
Journal: Cell Rep
Title: Affinity for DNA Contributes to NLS Independent Nuclear Localization of MeCP2.
Volume: 24
Issue: 9
Pages: 2213-2220
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Publication
11058114 | J:65674
First Author: Yusufzai TM
Year: 2000
Journal: Nucleic Acids Res
Title: Functional consequences of Rett syndrome mutations on human MeCP2.
Volume: 28
Issue: 21
Pages: 4172-9
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Publication
28480880 | J:250601
 
First Author: Wong JJ
Year: 2017
Journal: Nat Commun
Title: Intron retention is regulated by altered MeCP2-mediated splicing factor recruitment.
Volume: 8
Pages: 15134
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Publication
25753729 | J:323635
First Author: Ma D
Year: 2015
Journal: Neurotherapeutics
Title: Rescue of Methyl-CpG Binding Protein 2 Dysfunction-induced Defects in Newborn Neurons by Pentobarbital.
Volume: 12
Issue: 2
Pages: 477-90
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Publication
27293187 | J:232023
First Author: Orefice LL
Year: 2016
Journal: Cell
Title: Peripheral Mechanosensory Neuron Dysfunction Underlies Tactile and Behavioral Deficits in Mouse Models of ASDs.
Volume: 166
Issue: 2
Pages: 299-313
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Publication
24735673 | J:235553
First Author: Rusconi F
Year: 2015
Journal: Cereb Cortex
Title: LSD1 Neurospecific Alternative Splicing Controls Neuronal Excitability in Mouse Models of Epilepsy.
Volume: 25
Issue: 9
Pages: 2729-40
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Allele
Mecp2<em1Gfng> | MGI:6886058
Name: methyl CpG binding protein 2; endonuclease-mediated mutation 1, Guoping Feng
Allele Type: Endonuclease-mediated
Attribute String: Humanized sequence, Inserted expressed sequence
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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.

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