These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
188 related articles for article (PubMed ID: 26071253)
1. 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]
2. Early abnormalities of post-sigh breathing in a mouse model of Rett syndrome. Voituron N; Zanella S; Menuet C; Lajard AM; Dutschmann M; Hilaire G Respir Physiol Neurobiol; 2010 Feb; 170(2):173-82. PubMed ID: 20040383 [TBL] [Abstract][Full Text] [Related]
4. 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]
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. 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]
7. 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]
8. 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]
9. 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]
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. Effect of positive allosteric modulation and orthosteric agonism of dopamine D2-like receptors on respiration in mouse models of Rett syndrome. Maletz SN; Reid BT; Baekey DM; Whitaker-Fornek JR; Bateman JT; Arakawa K; Bissonnette JM; Levitt ES Respir Physiol Neurobiol; 2024 Oct; 328():104314. PubMed ID: 39117159 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Effects of early-life exposure to THIP on brainstem neuronal excitability in the Mecp2-null mouse model of Rett syndrome before and after drug withdrawal. Zhong W; Johnson CM; Cui N; Oginsky MF; Wu Y; Jiang C Physiol Rep; 2017 Jan; 5(2):. PubMed ID: 28108647 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Defects in brainstem neurons associated with breathing and motor function in the Mecp2R168X/Y mouse model of Rett syndrome. Johnson CM; Zhong W; Cui N; Wu Y; Xing H; Zhang S; Jiang C Am J Physiol Cell Physiol; 2016 Dec; 311(6):C895-C909. PubMed ID: 27653984 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndrome. Vogel Ciernia A; Yasui DH; Pride MC; Durbin-Johnson B; Noronha AB; Chang A; Knotts TA; Rutkowsky JR; Ramsey JJ; Crawley JN; LaSalle JM Hum Mol Genet; 2018 Dec; 27(23):4077-4093. PubMed ID: 30137367 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]