Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice. - Wikidata - wikimedia - TriplyDB

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

http://www.wikidata.org/entity/Q33727650

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Major channels involved in neuropsychiatric disorders and therapeutic perspectives Characterization of Rett Syndrome-like phenotypes in Mecp2-knockout rats Alterations in the cholinergic system of brain stem neurons in a mouse model of Rett syndrome Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity.Involvement of TRP channels in the CO₂ chemosensitivity of locus coeruleus neurons The disruption of central CO2 chemosensitivity in a mouse model of Rett syndrome.MECP2e1 isoform mutation affects the form and function of neurons derived from Rett syndrome patient iPS cells.Methyl CpG Binding Protein 2 Gene Disruption Augments Tonic Currents of γ-Aminobutyric Acid Receptors in Locus Coeruleus Neurons: IMPACT ON NEURONAL EXCITABILITY AND BREATHING.Induced pluripotent stem cells to model and treat neurogenetic disorders Rett syndrome induced pluripotent stem cell-derived neurons reveal novel neurophysiological alterations.GABAergic synaptic inputs of locus coeruleus neurons in wild-type and Mecp2-null mice.The cellular building blocks of breathing An optogenetic mouse model of rett syndrome targeting on catecholaminergic neurons.Pre- and postsynaptic modulations of hypoglossal motoneurons by α-adrenoceptor activation in wild-type and Mecp2(-/Y) mice Effects of early-life exposure to THIP on phenotype development in a mouse model of Rett syndrome.Time-dependent modulation of GABA(A)-ergic synaptic transmission by allopregnanolone in locus coeruleus neurons of Mecp2-null mice.Effects of chronic sleep fragmentation on wake-active neurons and the hypercapnic arousal response.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.Reduced synaptic activity in neuronal networks derived from embryonic stem cells of murine Rett syndrome model.Respiratory responses to hypercapnia and hypoxia in mice with genetic ablation of Kir5.1 (Kcnj16).Transcription factor-induced lineage programming of noradrenaline and motor neurons from embryonic stem cells.Hyperexcitability of Mesencephalic Trigeminal Neurons and Reorganization of Ion Channel Expression in a Rett Syndrome Model.Defects in brainstem neurons associated with breathing and motor function in the Mecp2R168X/Y mouse model of Rett syndrome.Theoretical perspectives on central chemosensitivity: CO2/H+-sensitive neurons in the locus coeruleus.MeCP2 Deficiency Leads to Loss of Glial Kir4.1.

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Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

http://www.wikidata.org/entity/Q33727650

description

2009 nî lūn-bûn

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2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

@zh-hk

2009年論文

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2009年論文

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2009年论文

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name

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

@ast

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

@en

type

label

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

@ast

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

@en

prefLabel

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

@ast

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

@en

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AJPCELL.00442.2009

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American Journal of Physiology - Cell Physiology

P1476

Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.

@en

P2093

Chun Jiang

http://www.w3.org/2001/XMLSchema#string

Junda Su

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Jyothirmayee S Tadepalli

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Ningren Cui

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Sowmya Sekizar

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Xiaoli Zhang

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Zhongying Wu

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P2860

Unique features of action potential initiation in cortical neurons

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Signaling mechanisms linking neuronal activity to gene expression and plasticity of the nervous system

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Dendritic anomalies in disorders associated with mental retardation

The story of Rett syndrome: from clinic to neurobiology

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

Defect in normal developmental increase of the brain biogenic amine concentrations in the mecp2-null mouse

Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons

Cns distribution of members of the two-pore-domain (KCNK) potassium channel family.

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10.1152/AJPCELL.00442.2009

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