529 related articles for article (PubMed ID: 16116096)
1. Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome.
Dani VS; Chang Q; Maffei A; Turrigiano GG; Jaenisch R; Nelson SB
Proc Natl Acad Sci U S A; 2005 Aug; 102(35):12560-5. PubMed ID: 16116096
[TBL] [Abstract][Full Text] [Related]
2. Excitation/inhibition imbalance and impaired synaptic inhibition in hippocampal area CA3 of Mecp2 knockout mice.
Calfa G; Li W; Rutherford JM; Pozzo-Miller L
Hippocampus; 2015 Feb; 25(2):159-68. PubMed ID: 25209930
[TBL] [Abstract][Full Text] [Related]
3. Defective GABAergic neurotransmission in the nucleus tractus solitarius in Mecp2-null mice, a model of Rett syndrome.
Chen CY; Di Lucente J; Lin YC; Lien CC; Rogawski MA; Maezawa I; Jin LW
Neurobiol Dis; 2018 Jan; 109(Pt A):25-32. PubMed ID: 28927958
[TBL] [Abstract][Full Text] [Related]
4. Jointly reduced inhibition and excitation underlies circuit-wide changes in cortical processing in Rett syndrome.
Banerjee A; Rikhye RV; Breton-Provencher V; Tang X; Li C; Li K; Runyan CA; Fu Z; Jaenisch R; Sur M
Proc Natl Acad Sci U S A; 2016 Nov; 113(46):E7287-E7296. PubMed ID: 27803317
[TBL] [Abstract][Full Text] [Related]
5. Cell-Genotype Specific Effects of Mecp2 Mutation on Spontaneous and Nicotinic Acetylcholine Receptor-Evoked Currents in Medial Prefrontal Cortical Pyramidal Neurons in Female Rett Model Mice.
Asgarihafshejani A; Nashmi R; Delaney KR
Neuroscience; 2019 Aug; 414():141-153. PubMed ID: 31299345
[TBL] [Abstract][Full Text] [Related]
6. EEA1 restores homeostatic synaptic plasticity in hippocampal neurons from Rett syndrome mice.
Xu X; Pozzo-Miller L
J Physiol; 2017 Aug; 595(16):5699-5712. PubMed ID: 28621434
[TBL] [Abstract][Full Text] [Related]
7. Network hyperexcitability in hippocampal slices from Mecp2 mutant mice revealed by voltage-sensitive dye imaging.
Calfa G; Hablitz JJ; Pozzo-Miller L
J Neurophysiol; 2011 Apr; 105(4):1768-84. PubMed ID: 21307327
[TBL] [Abstract][Full Text] [Related]
8. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.
Chen RZ; Akbarian S; Tudor M; Jaenisch R
Nat Genet; 2001 Mar; 27(3):327-31. PubMed ID: 11242118
[TBL] [Abstract][Full Text] [Related]
9. X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.
Braunschweig D; Simcox T; Samaco RC; LaSalle JM
Hum Mol Genet; 2004 Jun; 13(12):1275-86. PubMed ID: 15115765
[TBL] [Abstract][Full Text] [Related]
10. Synaptic circuit abnormalities of motor-frontal layer 2/3 pyramidal neurons in a mutant mouse model of Rett syndrome.
Wood L; Shepherd GM
Neurobiol Dis; 2010 May; 38(2):281-7. PubMed ID: 20138994
[TBL] [Abstract][Full Text] [Related]
11. MeCP2 in neurons: closing in on the causes of Rett syndrome.
Caballero IM; Hendrich B
Hum Mol Genet; 2005 Apr; 14 Spec No 1():R19-26. PubMed ID: 15809268
[TBL] [Abstract][Full Text] [Related]
12. Loss of MeCP2 from forebrain excitatory neurons leads to cortical hyperexcitation and seizures.
Zhang W; Peterson M; Beyer B; Frankel WN; Zhang ZW
J Neurosci; 2014 Feb; 34(7):2754-63. PubMed ID: 24523563
[TBL] [Abstract][Full Text] [Related]
13. The MeCP2-null mouse hippocampus displays altered basal inhibitory rhythms and is prone to hyperexcitability.
Zhang L; He J; Jugloff DG; Eubanks JH
Hippocampus; 2008; 18(3):294-309. PubMed ID: 18058824
[TBL] [Abstract][Full Text] [Related]
14. Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.
Moretti P; Bouwknecht JA; Teague R; Paylor R; Zoghbi HY
Hum Mol Genet; 2005 Jan; 14(2):205-20. PubMed ID: 15548546
[TBL] [Abstract][Full Text] [Related]
15. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.
Guy J; Hendrich B; Holmes M; Martin JE; Bird A
Nat Genet; 2001 Mar; 27(3):322-6. PubMed ID: 11242117
[TBL] [Abstract][Full Text] [Related]
16. A BDNF loop-domain mimetic acutely reverses spontaneous apneas and respiratory abnormalities during behavioral arousal in a mouse model of Rett syndrome.
Kron M; Lang M; Adams IT; Sceniak M; Longo F; Katz DM
Dis Model Mech; 2014 Sep; 7(9):1047-55. PubMed ID: 25147297
[TBL] [Abstract][Full Text] [Related]
17. Rett syndrome induced pluripotent stem cell-derived neurons reveal novel neurophysiological alterations.
Farra N; Zhang WB; Pasceri P; Eubanks JH; Salter MW; Ellis J
Mol Psychiatry; 2012 Dec; 17(12):1261-71. PubMed ID: 22230884
[TBL] [Abstract][Full Text] [Related]
18. Impaired hippocampal Ca2+ homeostasis and concomitant K+ channel dysfunction in a mouse model of Rett syndrome during anoxia.
Kron M; Müller M
Neuroscience; 2010 Nov; 171(1):300-15. PubMed ID: 20732392
[TBL] [Abstract][Full Text] [Related]
19. Synaptic maturation at cortical projections to the lateral amygdala in a mouse model of Rett syndrome.
Gambino F; Khelfaoui M; Poulain B; Bienvenu T; Chelly J; Humeau Y
PLoS One; 2010 Jul; 5(7):e11399. PubMed ID: 20625482
[TBL] [Abstract][Full Text] [Related]
20. Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.
Medrihan L; Tantalaki E; Aramuni G; Sargsyan V; Dudanova I; Missler M; Zhang W
J Neurophysiol; 2008 Jan; 99(1):112-21. PubMed ID: 18032561
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
