676 related articles for article (PubMed ID: 28093257)
21. A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome.
Matagne V; Ehinger Y; Saidi L; Borges-Correia A; Barkats M; Bartoli M; Villard L; Roux JC
Neurobiol Dis; 2017 Mar; 99():1-11. PubMed ID: 27974239
[TBL] [Abstract][Full Text] [Related]
22. Vitamin D modulates cortical transcriptome and behavioral phenotypes in an Mecp2 heterozygous Rett syndrome mouse model.
Ribeiro MC; MacDonald JL
Neurobiol Dis; 2022 Apr; 165():105636. PubMed ID: 35091041
[TBL] [Abstract][Full Text] [Related]
23. MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits.
Schaevitz LR; Gómez NB; Zhen DP; Berger-Sweeney JE
Genes Brain Behav; 2013 Oct; 12(7):732-40. PubMed ID: 24283265
[TBL] [Abstract][Full Text] [Related]
24. Elevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome-like phenotypes.
Lamonica JM; Kwon DY; Goffin D; Fenik P; Johnson BS; Cui Y; Guo H; Veasey S; Zhou Z
J Clin Invest; 2017 May; 127(5):1889-1904. PubMed ID: 28394263
[TBL] [Abstract][Full Text] [Related]
25. MeCP2 SUMOylation rescues Mecp2-mutant-induced behavioural deficits in a mouse model of Rett syndrome.
Tai DJ; Liu YC; Hsu WL; Ma YL; Cheng SJ; Liu SY; Lee EH
Nat Commun; 2016 Feb; 7():10552. PubMed ID: 26842955
[TBL] [Abstract][Full Text] [Related]
26. Social impairments in Rett syndrome: characteristics and relationship with clinical severity.
Kaufmann WE; Tierney E; Rohde CA; Suarez-Pedraza MC; Clarke MA; Salorio CF; Bibat G; Bukelis I; Naram D; Lanham DC; Naidu S
J Intellect Disabil Res; 2012 Mar; 56(3):233-47. PubMed ID: 21385260
[TBL] [Abstract][Full Text] [Related]
27. Regulation mechanism and research progress of MeCP2 in Rett syndrome.
Yang W; Pan H
Yi Chuan; 2014 Jul; 36(7):625-30. PubMed ID: 25076025
[TBL] [Abstract][Full Text] [Related]
28. Enhanced anxiety and stress-induced corticosterone release are associated with increased Crh expression in a mouse model of Rett syndrome.
McGill BE; Bundle SF; Yaylaoglu MB; Carson JP; Thaller C; Zoghbi HY
Proc Natl Acad Sci U S A; 2006 Nov; 103(48):18267-72. PubMed ID: 17108082
[TBL] [Abstract][Full Text] [Related]
29. MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.
Zahorakova D; Lelkova P; Gregor V; Magner M; Zeman J; Martasek P
J Hum Genet; 2016 Jul; 61(7):617-25. PubMed ID: 26984561
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Mitochondrial free radical overproduction due to respiratory chain impairment in the brain of a mouse model of Rett syndrome: protective effect of CNF1.
De Filippis B; Valenti D; de Bari L; De Rasmo D; Musto M; Fabbri A; Ricceri L; Fiorentini C; Laviola G; Vacca RA
Free Radic Biol Med; 2015 Jun; 83():167-77. PubMed ID: 25708779
[TBL] [Abstract][Full Text] [Related]
32.
Ballinger EC; Schaaf CP; Patel AJ; de Maio A; Tao H; Talmage DA; Zoghbi HY; Role LW
eNeuro; 2019; 6(6):. PubMed ID: 31562178
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations.
Chapleau CA; Calfa GD; Lane MC; Albertson AJ; Larimore JL; Kudo S; Armstrong DL; Percy AK; Pozzo-Miller L
Neurobiol Dis; 2009 Aug; 35(2):219-33. PubMed ID: 19442733
[TBL] [Abstract][Full Text] [Related]
35. Cognitive and social functions and growth factors in a mouse model of Rett syndrome.
Schaevitz LR; Moriuchi JM; Nag N; Mellot TJ; Berger-Sweeney J
Physiol Behav; 2010 Jun; 100(3):255-63. PubMed ID: 20045424
[TBL] [Abstract][Full Text] [Related]
36. Generation and analysis of the Rett syndrome-associated MeCP2- null rat model.
Zhai W; Hu HX; Le L; Zhuang FF; Wang KZ; Zhao Y; Wang K; Liu XM; Sun D; Wang XY; Kuang SH; Hu KP
Yi Chuan; 2016 Nov; 38(11):1004-1011. PubMed ID: 27867150
[TBL] [Abstract][Full Text] [Related]
37. miR-199a Links MeCP2 with mTOR Signaling and Its Dysregulation Leads to Rett Syndrome Phenotypes.
Tsujimura K; Irie K; Nakashima H; Egashira Y; Fukao Y; Fujiwara M; Itoh M; Uesaka M; Imamura T; Nakahata Y; Yamashita Y; Abe T; Takamori S; Nakashima K
Cell Rep; 2015 Sep; 12(11):1887-901. PubMed ID: 26344767
[TBL] [Abstract][Full Text] [Related]
38. The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome.
Brown K; Selfridge J; Lagger S; Connelly J; De Sousa D; Kerr A; Webb S; Guy J; Merusi C; Koerner MV; Bird A
Hum Mol Genet; 2016 Feb; 25(3):558-70. PubMed ID: 26647311
[TBL] [Abstract][Full Text] [Related]
39. Affective dysfunction in a mouse model of Rett syndrome: Therapeutic effects of environmental stimulation and physical activity.
Kondo MA; Gray LJ; Pelka GJ; Leang SK; Christodoulou J; Tam PP; Hannan AJ
Dev Neurobiol; 2016 Feb; 76(2):209-24. PubMed ID: 26019053
[TBL] [Abstract][Full Text] [Related]
40. MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders.
Psoni S; Sofocleous C; Traeger-Synodinos J; Kitsiou-Tzeli S; Kanavakis E; Fryssira-Kanioura H
Brain Dev; 2012 Jun; 34(6):487-95. PubMed ID: 21982064
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
