BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 17204503)

  • 1. Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2-/y knockout mice.
    Stettner GM; Huppke P; Brendel C; Richter DW; Gärtner J; Dutschmann M
    J Physiol; 2007 Mar; 579(Pt 3):863-76. PubMed ID: 17204503
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. The Kölliker-Fuse nucleus gates the postinspiratory phase of the respiratory cycle to control inspiratory off-switch and upper airway resistance in rat.
    Dutschmann M; Herbert H
    Eur J Neurosci; 2006 Aug; 24(4):1071-84. PubMed ID: 16930433
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The benzodiazepine Midazolam mitigates the breathing defects of Mecp2-deficient mice.
    Voituron N; Hilaire G
    Respir Physiol Neurobiol; 2011 Jun; 177(1):56-60. PubMed ID: 21315849
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice.
    Viemari JC; Roux JC; Tryba AK; Saywell V; Burnet H; Peña F; Zanella S; Bévengut M; Barthelemy-Requin M; Herzing LB; Moncla A; Mancini J; Ramirez JM; Villard L; Hilaire G
    J Neurosci; 2005 Dec; 25(50):11521-30. PubMed ID: 16354910
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Habituation, desensitization and sensitization of the Hering Breuer reflex in normal and Mecp2 /y knockout mice.
    Poon CS; Song G
    J Physiol; 2007 Oct; 584(Pt 1):359-60; author reply 361. PubMed ID: 17702808
    [No Abstract]   [Full Text] [Related]  

  • 9. Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice.
    Gemelli T; Berton O; Nelson ED; Perrotti LI; Jaenisch R; Monteggia LM
    Biol Psychiatry; 2006 Mar; 59(5):468-76. PubMed ID: 16199017
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.
    Medrihan L; Tantalaki E; Aramuni G; Sargsyan V; Dudanova I; Missler M; Zhang W
    J Neurophysiol; 2008 Jan; 99(1):112-21. PubMed ID: 18032561
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The MeCP2-null mouse hippocampus displays altered basal inhibitory rhythms and is prone to hyperexcitability.
    Zhang L; He J; Jugloff DG; Eubanks JH
    Hippocampus; 2008; 18(3):294-309. PubMed ID: 18058824
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Morphological and functional alterations in the substantia nigra pars compacta of the Mecp2-null mouse.
    Panayotis N; Pratte M; Borges-Correia A; Ghata A; Villard L; Roux JC
    Neurobiol Dis; 2011 Feb; 41(2):385-97. PubMed ID: 20951208
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Physiological definition of upper airway obstructions in mouse model for Rett syndrome.
    Voituron N; Menuet C; Dutschmann M; Hilaire G
    Respir Physiol Neurobiol; 2010 Sep; 173(2):146-56. PubMed ID: 20659592
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Metabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome model.
    Viola A; Saywell V; Villard L; Cozzone PJ; Lutz NW
    PLoS One; 2007 Jan; 2(1):e157. PubMed ID: 17237885
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.