Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
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Autism, fever, epigenetics and the locus coeruleusPathophysiology of locus ceruleus neurons in a mouse model of Rett syndromeEmerging pharmacotherapies for neurodevelopmental disordersBioaminergic neuromodulation of respiratory rhythm in vitroLoss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalitiesExcitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum DisordersPontine mechanisms of respiratory controlGABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient miceRett syndrome - biological pathways leading from MECP2 to disorder phenotypesAutonomic cardiovascular control in methyl-CpG-binding protein 2 (Mecp2) deficient miceA partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndromeMetabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome modelMeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female ratsCharacterization of Rett Syndrome-like phenotypes in Mecp2-knockout ratsA BDNF loop-domain mimetic acutely reverses spontaneous apneas and respiratory abnormalities during behavioral arousal in a mouse model of Rett syndrome.Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies.Ultrasonic vocalizations: a tool for behavioural phenotyping of mouse models of neurodevelopmental disorders.Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome.Improvement of the Rett syndrome phenotype in a MeCP2 mouse model upon treatment with levodopa and a dopa-decarboxylase inhibitorBackground sodium current underlying respiratory rhythm regularity.Looking for inspiration: new perspectives on respiratory rhythm.Pinpointing brainstem mechanisms responsible for autonomic dysfunction in Rett syndrome: therapeutic perspectives for 5-HT1A agonists.Effect of Sarizotan, a 5-HT1a and D2-like receptor agonist, on respiration in three mouse models of Rett syndromeNeuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brain.Functional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome.β2-Adrenergic receptor agonist ameliorates phenotypes and corrects microRNA-mediated IGF1 deficits in a mouse model of Rett syndromePontine norepinephrine defects in Mecp2-null mice involve deficient expression of dopamine beta-hydroxylase but not a loss of catecholaminergic neurons.Substance P modulation of TRPC3/7 channels improves respiratory rhythm regularity and ICAN-dependent pacemaker activity.7,8-dihydroxyflavone exhibits therapeutic efficacy in a mouse model of Rett syndromeThe role of serotonin in respiratory function and dysfunction.Habituation without NMDA Receptor-Dependent Desensitization of Hering-Breuer Apnea Reflex in a Mecp2 Mutant Mouse Model of Rett SyndromeHypoglossal neuropathology and respiratory activity in pompe miceThe serotonergic anatomy of the developing human medulla oblongata: implications for pediatric disorders of homeostasisThe disruption of central CO2 chemosensitivity in a mouse model of Rett syndrome.MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespanLoss of Mecp2 in substantia nigra dopamine neurons compromises the nigrostriatal pathway.Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.A role for glia in the progression of Rett's syndrome.
P2860
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P2860
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
description
2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2005
@ast
im Dezember 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2005/12/14)
@sk
vědecký článek publikovaný v roce 2005
@cs
wetenschappelijk artikel (gepubliceerd op 2005/12/14)
@nl
наукова стаття, опублікована в грудні 2005
@uk
مقالة علمية (نشرت في 14-12-2005)
@ar
name
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@ast
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@en
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@nl
type
label
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@ast
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@en
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@nl
prefLabel
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@ast
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@en
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@nl
P2093
P50
P3181
P1476
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice
@en
P2093
Anne Moncla
Fernando Peña
Gérard Hilaire
Henri Burnet
Jean-Charles Viemari
Josette Mancini
Laura B K Herzing
Magali Barthelemy-Requin
Michelle Bévengut
Sébastien Zanella
P304
11521-11530
P3181
P356
10.1523/JNEUROSCI.4373-05.2005
P407
P577
2005-12-14T00:00:00Z