310 related articles for article (PubMed ID: 28931890)
1. Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome.
Kida H; Takahashi T; Nakamura Y; Kinoshita T; Hara M; Okamoto M; Okayama S; Nakamura K; Kosai KI; Taniwaki T; Yamashita Y; Matsuishi T
Sci Rep; 2017 Sep; 7(1):12032. PubMed ID: 28931890
[TBL] [Abstract][Full Text] [Related]
2. Progressive Changes in a Distributed Neural Circuit Underlie Breathing Abnormalities in Mice Lacking MeCP2.
Huang TW; Kochukov MY; Ward CS; Merritt J; Thomas K; Nguyen T; Arenkiel BR; Neul JL
J Neurosci; 2016 May; 36(20):5572-86. PubMed ID: 27194336
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Anxiety-related mechanisms of respiratory dysfunction in a mouse model of Rett syndrome.
Ren J; Ding X; Funk GD; Greer JJ
J Neurosci; 2012 Nov; 32(48):17230-40. PubMed ID: 23197715
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.
Bissonnette JM; Schaevitz LR; Knopp SJ; Zhou Z
Neuroscience; 2014 May; 267():166-76. PubMed ID: 24626160
[TBL] [Abstract][Full Text] [Related]
7. Breathing abnormalities in a female mouse model of Rett syndrome.
Johnson CM; Cui N; Zhong W; Oginsky MF; Jiang C
J Physiol Sci; 2015 Sep; 65(5):451-9. PubMed ID: 26071253
[TBL] [Abstract][Full Text] [Related]
8. Deficiency of GABAergic synaptic inhibition in the Kölliker-Fuse area underlies respiratory dysrhythmia in a mouse model of Rett syndrome.
Abdala AP; Toward MA; Dutschmann M; Bissonnette JM; Paton JF
J Physiol; 2016 Jan; 594(1):223-37. PubMed ID: 26507912
[TBL] [Abstract][Full Text] [Related]
9. Altered somatosensory barrel cortex refinement in the developing brain of Mecp2-null mice.
Moroto M; Nishimura A; Morimoto M; Isoda K; Morita T; Yoshida M; Morioka S; Tozawa T; Hasegawa T; Chiyonobu T; Yoshimoto K; Hosoi H
Brain Res; 2013 Nov; 1537():319-26. PubMed ID: 24060648
[TBL] [Abstract][Full Text] [Related]
10. Severe offtarget effects following intravenous delivery of AAV9-MECP2 in a female mouse model of Rett syndrome.
Matagne V; Borloz E; Ehinger Y; Saidi L; Villard L; Roux JC
Neurobiol Dis; 2021 Feb; 149():105235. PubMed ID: 33383186
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Pathophysiology of locus ceruleus neurons in a mouse model of Rett syndrome.
Taneja P; Ogier M; Brooks-Harris G; Schmid DA; Katz DM; Nelson SB
J Neurosci; 2009 Sep; 29(39):12187-95. PubMed ID: 19793977
[TBL] [Abstract][Full Text] [Related]
14. Mecp2 Disruption in Rats Causes Reshaping in Firing Activity and Patterns of Brainstem Respiratory Neurons.
Wu Y; Cui N; Xing H; Zhong W; Arrowood C; Johnson CM; Jiang C
Neuroscience; 2019 Jan; 397():107-115. PubMed ID: 30458221
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice.
Deng V; Matagne V; Banine F; Frerking M; Ohliger P; Budden S; Pevsner J; Dissen GA; Sherman LS; Ojeda SR
Hum Mol Genet; 2007 Mar; 16(6):640-50. PubMed ID: 17309881
[TBL] [Abstract][Full Text] [Related]
18. The disruption of central CO2 chemosensitivity in a mouse model of Rett syndrome.
Zhang X; Su J; Cui N; Gai H; Wu Z; Jiang C
Am J Physiol Cell Physiol; 2011 Sep; 301(3):C729-38. PubMed ID: 21307341
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Early breathing defects after moderate hypoxia or hypercapnia in a mouse model of Rett syndrome.
Voituron N; Zanella S; Menuet C; Dutschmann M; Hilaire G
Respir Physiol Neurobiol; 2009 Aug; 168(1-2):109-18. PubMed ID: 19524074
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]