about
GABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient miceMecp2 deficiency disrupts norepinephrine and respiratory systems in miceCongenital hypoventilation and impaired hypoxic response in Nurr1 mutant miceModification of Mecp2 dosage alters axonal transport through the Huntingtin/Hap1 pathwayDNA methylation map of mouse and human brain identifies target genes in Alzheimer's disease.Carotid chemodenervation approach to study oxygen sensing in brain stem catecholaminergic cells.Biogenic amines in Rett syndrome: the usual suspects.Progressive noradrenergic deficits in the locus coeruleus of Mecp2 deficient mice.Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatusA codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome.Isoform-specific anti-MeCP2 antibodies confirm that expression of the e1 isoform strongly predominates in the brain.Neurochemical development of the brainstem catecholaminergic cell groups in rat.Prenatal hypoxia and early postnatal maturation of the chemoafferent pathway.Long-term prenatal hypoxia alters maturation of brain catecholaminergic systems and motor behavior in rats.Tyrosine hydroxylase deficit in the chemoafferent and the sympathoadrenergic pathways of the Mecp2 deficient mouse.Postnatal development of neural chemoafferent pathway and respiration is altered following prenatal nicotine exposure in rats.Prenatal hypoxia impairs the early postnatal development of the carotid chemoafferent pathway.Possible modulation of the mouse respiratory rhythm generator by A1/C1 neurones.[Noradrenaline deficiency as the origin of respiratory disorders in Rett syndrome an animal model].Developmental plasticity of the carotid chemoafferent pathway in rats that are hypoxic during the prenatal period.Progressive motor and respiratory metabolism deficits in post-weaning Mecp2-null male mice.Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome.Spatiotemporal expression in mouse brain of Kiaa2022, a gene disrupted in two patients with severe mental retardation.Effect of desipramine on patients with breathing disorders in RETT syndrome.Rett syndrome from bench to bedside: recent advances.Ventilatory and central neurochemical reorganisation of O2 chemoreflex after carotid sinus nerve transection in ratPrenatal hypoxia impairs the postnatal development of neural and functional chemoafferent pathway in ratNeurochemical reorganization of O2 chemoreflex pathway after carotid body denervation in ratsO2-sensing after carotid chemodenervation: hypoxic ventilatory responsiveness and upregulation of tyrosine hydroxylase mRNA in brainstem catecholaminergic cellsA knock-in mouse model for KCNQ2-related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairmentHuntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice
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description
researcher
@en
wetenschapper
@nl
name
J C Roux
@en
J C Roux
@nl
type
label
J C Roux
@en
J C Roux
@nl
prefLabel
J C Roux
@en
J C Roux
@nl
P106
P31
P496
0000-0002-9721-8844