about
Glycinergic interneurons are functionally integrated into the inspiratory network of mouse medullary slicesActive sulforhodamine 101 uptake into hippocampal astrocytesLack of the Kir4.1 channel subunit abolishes K+ buffering properties of astrocytes in the ventral respiratory group: impact on extracellular K+ regulationHyperekplexia phenotype of glycine receptor alpha1 subunit mutant mice identifies Zn(2+) as an essential endogenous modulator of glycinergic neurotransmissionDrebrin is a novel connexin-43 binding partner that links gap junctions to the submembrane cytoskeletonThe multispecific thyroid hormone transporter OATP1C1 mediates cell-specific sulforhodamine 101-labeling of hippocampal astrocytes.The alanine-serine-cysteine-1 (Asc-1) transporter controls glycine levels in the brain and is required for glycinergic inhibitory transmission.X-Ray based Lung Function measurement-a sensitive technique to quantify lung function in allergic airway inflammation mouse models.A computational model of the respiratory network challenged and optimized by data from optogenetic manipulation of glycinergic neurons.Astroglial processes show spontaneous motility at active synaptic terminals in situ.Determinants of functional coupling between astrocytes and respiratory neurons in the pre-Bötzinger complex.Characterization of the MeCP2R168X knockin mouse model for Rett syndrome.A Transgenic Mouse Line Expressing the Red Fluorescent Protein tdTomato in GABAergic Neurons.Restraint Stress Intensifies Interstitial K(+) Accumulation during Severe HypoxiaImpaired GABAergic transmission and altered hippocampal synaptic plasticity in collybistin-deficient miceFacts and challenges in respiratory neurobiology.GlyT2-Dependent Preservation of MECP2-Expression in Inhibitory Neurons Improves Early Respiratory Symptoms but Does Not Rescue Survival in a Mouse Model of Rett Syndrome.Systemic Radical Scavenger Treatment of a Mouse Model of Rett Syndrome: Merits and Limitations of the Vitamin E Derivative TroloxUnspecific labelling of oligodendrocytes by sulforhodamine 101 depends on astrocytic uptake via the thyroid hormone transporter OATP1C1 (SLCO1C1).Serotonin receptor 1A-modulated phosphorylation of glycine receptor α3 controls breathing in mice.Amyloid-precursor Like Proteins APLP1 and APLP2 Are Dispensable for Normal Development of the Neonatal Respiratory Network.Limitations of Sulforhodamine 101 for Brain Imaging.Development of synaptic inhibition in glycine transporter 2 deficient mice.Bioelectrical behaviour of hypoxic human neocortical tissue under the influence of nimodipine and dimethyl sulfoxide.Blockade of astrocyte metabolism causes delayed excitation as revealed by voltage-sensitive dyes in mouse brainstem slices.Inactivation of the glycine transporter 1 gene discloses vital role of glial glycine uptake in glycinergic inhibition.Deletion of the mouse glycine transporter 2 results in a hyperekplexia phenotype and postnatal lethality.Diversity of functional astroglial properties in the respiratory network.In vivo labeling and in vitro characterisation of central complex neurons involved in the control of sound production.Neuroprotection of mild hypothermia: differential effects.Dimethyl sulfoxide increases latency of anoxic terminal negativity in hippocampal slices of guinea pig in vitro.Developmental changes of serotonin 4(a) receptor expression in the rat pre-Bötzinger complex.Breathing disturbances in a model of Rett syndrome: A potential involvement of the glycine receptor α3 subunit?Norepinephrine-induced calcium signaling in astrocytes in the respiratory network of the ventrolateral medulla.Generation of functional neurons and glia from multipotent adult mouse germ-line stem cells.Mixed miniature postsynaptic currents resulting from co-release of glycine and GABA recorded from glycinergic neurons in the neonatal respiratory network.Calcium influx mediated by the inwardly rectifying K+ channel Kir4.1 (KCNJ10) at low external K+ concentration.Respiratory calcium fluctuations in low-frequency oscillating astrocytes in the pre-Bötzinger complex.Genetic ablation of VIAAT in glycinergic neurons causes a severe respiratory phenotype and perinatal death.Presynaptic facilitation of glycinergic mIPSC is reduced in mice lacking α3 glycine receptor subunits.
P50
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P50
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wetenschapper
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հետազոտող
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name
Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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Swen Hülsmann
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P106
P31
P496
0000-0001-5042-8724