361 related articles for article (PubMed ID: 26733678)
1. KCC2 rescues functional deficits in human neurons derived from patients with Rett syndrome.
Tang X; Kim J; Zhou L; Wengert E; Zhang L; Wu Z; Carromeu C; Muotri AR; Marchetto MC; Gage FH; Chen G
Proc Natl Acad Sci U S A; 2016 Jan; 113(3):751-6. PubMed ID: 26733678
[TBL] [Abstract][Full Text] [Related]
2. Pharmacological enhancement of
Tang X; Drotar J; Li K; Clairmont CD; Brumm AS; Sullins AJ; Wu H; Liu XS; Wang J; Gray NS; Sur M; Jaenisch R
Sci Transl Med; 2019 Jul; 11(503):. PubMed ID: 31366578
[TBL] [Abstract][Full Text] [Related]
3. Region-Specific KCC2 Rescue by rhIGF-1 and Oxytocin in a Mouse Model of Rett Syndrome.
Gigliucci V; Teutsch J; Woodbury-Smith M; Luoni M; Busnelli M; Chini B; Banerjee A
Cereb Cortex; 2022 Jun; 32(13):2885-2894. PubMed ID: 34791112
[TBL] [Abstract][Full Text] [Related]
4. Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Chao HT; Chen H; Samaco RC; Xue M; Chahrour M; Yoo J; Neul JL; Gong S; Lu HC; Heintz N; Ekker M; Rubenstein JL; Noebels JL; Rosenmund C; Zoghbi HY
Nature; 2010 Nov; 468(7321):263-9. PubMed ID: 21068835
[TBL] [Abstract][Full Text] [Related]
5. KCC2 expression levels are reduced in post mortem brain tissue of Rett syndrome patients.
Hinz L; Torrella Barrufet J; Heine VM
Acta Neuropathol Commun; 2019 Dec; 7(1):196. PubMed ID: 31796123
[TBL] [Abstract][Full Text] [Related]
6. Graded and pan-neural disease phenotypes of Rett Syndrome linked with dosage of functional MeCP2.
Chen X; Han X; Blanchi B; Guan W; Ge W; Yu YC; Sun YE
Protein Cell; 2021 Aug; 12(8):639-652. PubMed ID: 32851591
[TBL] [Abstract][Full Text] [Related]
7. Ocular MECP2 protein expression in patients with and without Rett syndrome.
Jain D; Singh K; Chirumamilla S; Bibat GM; Blue ME; Naidu SR; Eberhart CG
Pediatr Neurol; 2010 Jul; 43(1):35-40. PubMed ID: 20682201
[TBL] [Abstract][Full Text] [Related]
8. Comprehensive Analysis of GABA
Oyarzabal A; Xiol C; Castells AA; Grau C; O'Callaghan M; Fernández G; Alcántara S; Pineda M; Armstrong J; Altafaj X; García-Cazorla A
Int J Mol Sci; 2020 Jan; 21(2):. PubMed ID: 31947619
[TBL] [Abstract][Full Text] [Related]
9. An Astrocytic Influence on Impaired Tonic Inhibition in Hippocampal CA1 Pyramidal Neurons in a Mouse Model of Rett Syndrome.
Dong Q; Kim J; Nguyen L; Bu Q; Chang Q
J Neurosci; 2020 Aug; 40(32):6250-6261. PubMed ID: 32616668
[TBL] [Abstract][Full Text] [Related]
10. Modeling Rett Syndrome Using Human Induced Pluripotent Stem Cells.
Andoh-Noda T; Inouye MO; Miyake K; Kubota T; Okano H; Akamatsu W
CNS Neurol Disord Drug Targets; 2016; 15(5):544-50. PubMed ID: 27071793
[TBL] [Abstract][Full Text] [Related]
11. An unexpected role of neuroligin-2 in regulating KCC2 and GABA functional switch.
Sun C; Zhang L; Chen G
Mol Brain; 2013 May; 6():23. PubMed ID: 23663753
[TBL] [Abstract][Full Text] [Related]
12. Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation.
Cheung AY; Horvath LM; Grafodatskaya D; Pasceri P; Weksberg R; Hotta A; Carrel L; Ellis J
Hum Mol Genet; 2011 Jun; 20(11):2103-15. PubMed ID: 21372149
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice.
Luikenhuis S; Giacometti E; Beard CF; Jaenisch R
Proc Natl Acad Sci U S A; 2004 Apr; 101(16):6033-8. PubMed ID: 15069197
[TBL] [Abstract][Full Text] [Related]
15. The neurobiology of Rett syndrome.
Akbarian S
Neuroscientist; 2003 Feb; 9(1):57-63. PubMed ID: 12580340
[TBL] [Abstract][Full Text] [Related]
16. MeCP2 dysfunction in Rett syndrome and related disorders.
Moretti P; Zoghbi HY
Curr Opin Genet Dev; 2006 Jun; 16(3):276-81. PubMed ID: 16647848
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells.
Livide G; Patriarchi T; Amenduni M; Amabile S; Yasui D; Calcagno E; Lo Rizzo C; De Falco G; Ulivieri C; Ariani F; Mari F; Mencarelli MA; Hell JW; Renieri A; Meloni I
Eur J Hum Genet; 2015 Feb; 23(2):195-201. PubMed ID: 24916645
[TBL] [Abstract][Full Text] [Related]
19. Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors.
Varderidou-Minasian S; Hinz L; Hagemans D; Posthuma D; Altelaar M; Heine VM
Mol Autism; 2020 May; 11(1):38. PubMed ID: 32460858
[TBL] [Abstract][Full Text] [Related]
20. MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome.
Chen L; Chen K; Lavery LA; Baker SA; Shaw CA; Li W; Zoghbi HY
Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5509-14. PubMed ID: 25870282
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
