260 related articles for article (PubMed ID: 23197715)
21. Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome.
Filosa S; Pecorelli A; D'Esposito M; Valacchi G; Hajek J
Free Radic Biol Med; 2015 Nov; 88(Pt A):81-90. PubMed ID: 25960047
[TBL] [Abstract][Full Text] [Related]
22. Breathing disorders in Rett syndrome: progressive neurochemical dysfunction in the respiratory network after birth.
Katz DM; Dutschmann M; Ramirez JM; Hilaire G
Respir Physiol Neurobiol; 2009 Aug; 168(1-2):101-8. PubMed ID: 19394452
[TBL] [Abstract][Full Text] [Related]
23. Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome.
McCauley MD; Wang T; Mike E; Herrera J; Beavers DL; Huang TW; Ward CS; Skinner S; Percy AK; Glaze DG; Wehrens XH; Neul JL
Sci Transl Med; 2011 Dec; 3(113):113ra125. PubMed ID: 22174313
[TBL] [Abstract][Full Text] [Related]
24. Targeted RNA editing in brainstem alleviates respiratory dysfunction in a mouse model of Rett syndrome.
Sinnamon JR; Jacobson ME; Yung JF; Fisk JR; Jeng S; McWeeney SK; Parmelee LK; Chan CN; Yee SP; Mandel G
Proc Natl Acad Sci U S A; 2022 Aug; 119(33):e2206053119. PubMed ID: 35939700
[TBL] [Abstract][Full Text] [Related]
25. Breathing disturbances in a model of Rett syndrome: A potential involvement of the glycine receptor α3 subunit?
Mesuret G; Dannenberg J; Arnoldt M; Grützner AA; Niebert M; Hülsmann S
Respir Physiol Neurobiol; 2018 Jan; 248():43-47. PubMed ID: 29203410
[TBL] [Abstract][Full Text] [Related]
26. Disruption of MeCP2 attenuates circadian rhythm in CRISPR/Cas9-based Rett syndrome model mouse.
Tsuchiya Y; Minami Y; Umemura Y; Watanabe H; Ono D; Nakamura W; Takahashi T; Honma S; Kondoh G; Matsuishi T; Yagita K
Genes Cells; 2015 Dec; 20(12):992-1005. PubMed ID: 26456390
[TBL] [Abstract][Full Text] [Related]
27. Remodelling of the respiratory network in a mouse model of Rett syndrome depends on brain-derived neurotrophic factor regulated slow calcium buffering.
Mironov SL; Skorova E; Hartelt N; Mironova LA; Hasan MT; Kügler S
J Physiol; 2009 Jun; 587(Pt 11):2473-85. PubMed ID: 19359374
[TBL] [Abstract][Full Text] [Related]
28. Correction of respiratory disorders in a mouse model of Rett syndrome.
Abdala AP; Dutschmann M; Bissonnette JM; Paton JF
Proc Natl Acad Sci U S A; 2010 Oct; 107(42):18208-13. PubMed ID: 20921395
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.
Stearns NA; Schaevitz LR; Bowling H; Nag N; Berger UV; Berger-Sweeney J
Neuroscience; 2007 May; 146(3):907-21. PubMed ID: 17383101
[TBL] [Abstract][Full Text] [Related]
31. Wild-type microglia arrest pathology in a mouse model of Rett syndrome.
Derecki NC; Cronk JC; Lu Z; Xu E; Abbott SB; Guyenet PG; Kipnis J
Nature; 2012 Mar; 484(7392):105-9. PubMed ID: 22425995
[TBL] [Abstract][Full Text] [Related]
32. Inhibitory synaptic transmission is impaired in the Kölliker-Fuse of male, but not female, Rett syndrome mice.
Whitaker-Fornek JR; Jenkins PM; Levitt ES
J Neurophysiol; 2023 Dec; 130(6):1578-1587. PubMed ID: 37965930
[TBL] [Abstract][Full Text] [Related]
33. Effect of inspired oxygen on periodic breathing in methy-CpG-binding protein 2 (Mecp2) deficient mice.
Bissonnette JM; Knopp SJ
J Appl Physiol (1985); 2008 Jan; 104(1):198-204. PubMed ID: 18006868
[TBL] [Abstract][Full Text] [Related]
34. A TrkB small molecule partial agonist rescues TrkB phosphorylation deficits and improves respiratory function in a mouse model of Rett syndrome.
Schmid DA; Yang T; Ogier M; Adams I; Mirakhur Y; Wang Q; Massa SM; Longo FM; Katz DM
J Neurosci; 2012 Feb; 32(5):1803-10. PubMed ID: 22302819
[TBL] [Abstract][Full Text] [Related]
35. Characterization of the MeCP2R168X knockin mouse model for Rett syndrome.
Wegener E; Brendel C; Fischer A; Hülsmann S; Gärtner J; Huppke P
PLoS One; 2014; 9(12):e115444. PubMed ID: 25541993
[TBL] [Abstract][Full Text] [Related]
36. MeCP2+/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder.
Liao W; Gandal MJ; Ehrlichman RS; Siegel SJ; Carlson GC
Neurobiol Dis; 2012 Apr; 46(1):88-92. PubMed ID: 22249109
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis.
Alvarez-Saavedra M; Sáez MA; Kang D; Zoghbi HY; Young JI
Hum Mol Genet; 2007 Oct; 16(19):2315-25. PubMed ID: 17635839
[TBL] [Abstract][Full Text] [Related]
39. Early postnatal behavioral changes in the Mecp2-308 truncation mouse model of Rett syndrome.
De Filippis B; Ricceri L; Laviola G
Genes Brain Behav; 2010 Mar; 9(2):213-23. PubMed ID: 19958389
[TBL] [Abstract][Full Text] [Related]
40. Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome.
Moretti P; Levenson JM; Battaglia F; Atkinson R; Teague R; Antalffy B; Armstrong D; Arancio O; Sweatt JD; Zoghbi HY
J Neurosci; 2006 Jan; 26(1):319-27. PubMed ID: 16399702
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]