Breathing abnormalities in a female mouse model of Rett syndrome.
about
Effects of early-life exposure to THIP on phenotype development in a mouse model of Rett syndrome.Breathing abnormalities in animal models of Rett syndrome a female neurogenetic disorder.Hyperexcitability of Mesencephalic Trigeminal Neurons and Reorganization of Ion Channel Expression in a Rett Syndrome Model.Deficiency of GABAergic synaptic inhibition in the Kölliker-Fuse area underlies respiratory dysrhythmia in a mouse model of Rett syndrome.MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett SyndromeDefects in brainstem neurons associated with breathing and motor function in the Mecp2R168X/Y mouse model of Rett syndrome.Oxygen exchange and energy metabolism in erythrocytes of Rett syndrome and their relationships with respiratory alterations.Conditional depletion of methyl-CpG-binding protein 2 in astrocytes depresses the hypercapnic ventilatory response in mice.Persistent Expression of Serotonin Receptor 5b Alters Breathing Behavior in Male MeCP2 Knockout Mice.Tsix-Mecp2 female mouse model for Rett syndrome reveals that low-level MECP2 expression extends life and improves neuromotor function
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P2860
Breathing abnormalities in a female mouse model of Rett syndrome.
description
2015 nî lūn-bûn
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name
Breathing abnormalities in a female mouse model of Rett syndrome.
@en
Breathing abnormalities in a female mouse model of Rett syndrome.
@nl
type
label
Breathing abnormalities in a female mouse model of Rett syndrome.
@en
Breathing abnormalities in a female mouse model of Rett syndrome.
@nl
prefLabel
Breathing abnormalities in a female mouse model of Rett syndrome.
@en
Breathing abnormalities in a female mouse model of Rett syndrome.
@nl
P2093
P2860
P1476
Breathing abnormalities in a female mouse model of Rett syndrome
@en
P2093
Christopher M Johnson
Chun Jiang
Max F Oginsky
Ningren Cui
Weiwei Zhong
P2860
P2888
P304
P356
10.1007/S12576-015-0384-5
P577
2015-06-13T00:00:00Z