C. Menuet

发表

Upper Airway Dysfunction of Tau-P301L Mice Correlates with Tauopathy in Midbrain and Ponto-Medullary Brainstem Nuclei

F. van Leuven, H. Devijver, M. Dutschmann, 2010, The Journal of Neuroscience.

Advancing respiratory–cardiovascular physiology with the working heart–brainstem preparation over 25 years

Jeffrey C. Smith, R. Dhingra, Richard J. A. Wilson, 2022, The Journal of physiology.

Isoflurane anesthesia precipitates tauopathy and upper airways dysfunction in pre-symptomatic Tau.P301L mice: Possible implication for neurodegenerative diseases

H. Devijver, F. Leuven, M. Dutschmann, 2012, Neurobiology of Disease.

Respiratory sympathetic modulation is augmented in chronic kidney disease

C. Hildreth, J. Phillips, A. Allen, 2019, Respiratory Physiology & Neurobiology.

Respiratory modulation of sympathetic nerve activity is enhanced in male rat offspring following uteroplacental insufficiency

A. Allen, A. Fong, M. Wlodek, 2016, Respiratory Physiology & Neurobiology.

Early breathing defects after moderate hypoxia or hypercapnia in a mouse model of Rett syndrome

S. Zanella, M. Dutschmann, G. Hilaire, 2009, Respiratory Physiology & Neurobiology.

Selective transduction and photoinhibition of pre-Botzinger neurons that project to the facial nucleus in rats affect the nasofacial activity

S. McDougall, R. Bathgate, A. Allen, 2022, bioRxiv.

A Chemogenetic Tool that Enables Functional Neural Circuit Analysis.

S. McDougall, A. Allen, A. Connelly, 2020, Cell reports.

Detecting fine and elaborate movements with piezo sensors provides non-invasive access to overlooked behavioral components

Maria Isabel Carreño-Muñoz, X. Leinekugel, A. Frick, 2021, Neuropsychopharmacology.

The H3K27 demethylase JMJD3 is required for maintenance of the embryonic respiratory neuronal network, neonatal breathing, and survival.

G. Natoli, A. Simeone, B. Tusi, 2012, Cell reports.

The role of serotonin in respiratory function and dysfunction

R. Ichiyama, M. Dutschmann, G. Hilaire, 2010, Respiratory Physiology & Neurobiology.

Mathias Dutschmann, Christian Gestreau, F. van Leuven, 2011, PloS one.

Baroreceptor reflex control of heart rate in angiotensin type 1A receptor knockout mice

A. Allen, C. Menuet, N. Jancovski, 2013, Physiological reports.

PreBötzinger complex neurons drive respiratory modulation of blood pressure and heart rate

S. McDougall, A. Allen, S. McMullan, 2020, eLife.

Adrenergic Neurons in the CNS

A. Allen, A. Fong, A. Connelly, 2017 .

Catecholaminergic C3 Neurons Are Sympathoexcitatory and Involved in Glucose Homeostasis

I. Llewellyn-Smith, A. Allen, A. Fong, 2014, The Journal of Neuroscience.

Mapping and Analysis of the Connectome of Sympathetic Premotor Neurons in the Rostral Ventrolateral Medulla of the Rat Using a Volumetric Brain Atlas

Jan G. Bjaalie, Simon McMullan, Andrew M. Allen, 2017, Front. Neural Circuits.

Polycythemia and high levels of erythropoietin in blood and brain blunt the hypercapnic ventilatory response in adult mice.

C. Gestreau, C. Menuet, H. Khemiri, 2016, American journal of physiology. Regulatory, integrative and comparative physiology.

Increasing Brain Protein O-GlcNAc-ylation Mitigates Breathing Defects and Mortality of Tau.P301L Mice

G. Lippens, F. van Leuven, H. Devijver, 2013, PloS one.

Leptin antagonism improves Rett syndrome phenotype in symptomatic male Mecp2-null mice

J. Gaiarsa, G. Wayman, D. Diabira, 2023, bioRxiv.

The Chloride Homeostasis of CA3 Hippocampal Neurons Is Not Altered in Fully Symptomatic Mepc2-null Mice

J. Gaiarsa, G. Wayman, Jinwei Zhang, 2021, Frontiers in Cellular Neuroscience.

Physiological definition of upper airway obstructions in mouse model for Rett syndrome

M. Dutschmann, G. Hilaire, N. Voituron, 2010, Respiratory Physiology & Neurobiology.

Early abnormalities of post-sigh breathing in a mouse model of Rett syndrome

S. Zanella, G. Hilaire, N. Voituron, 2010, Respiratory Physiology & Neurobiology.

Fluoxetine Treatment Abolishes the In Vitro Respiratory Response to Acidosis in Neonatal Mice

Érika Vigneault, M. Bévengut, S. Mestikawy, 2010, PloS one.

Stimulation of Angiotensin Type 1A Receptors on Catecholaminergic Cells Contributes to Angiotensin-Dependent Hypertension

A. Allen, E. Lukoshkova, A. Connelly, 2013, Hypertension.

Raphé tauopathy alters serotonin metabolism and breathing activity in terminal Tau.P301L mice: Possible implications for tauopathies and Alzheimer's disease

F. Leuven, M. Dutschmann, C. Gestreau, 2011, Respiratory Physiology & Neurobiology.

Role of defective calcium regulation in cardiorespiratory dysfunction in Huntington’s disease

S. Matecki, S. Reiken, A. Marks, 2020, JCI insight.

Necdin shapes serotonergic development and SERT activity modulating breathing in a mouse model for Prader-Willi syndrome

P. Gaspar, E. Deneris, Nazim Kourdougli, 2017, eLife.

Angiotensin type 1A receptor expression in C1 neurons of the rostral ventrolateral medulla contributes to the development of angiotensin‐dependent hypertension

A. Allen, A. Connelly, D. A. Carter, 2014, Experimental physiology.

Excessive Respiratory Modulation of Blood Pressure Triggers Hypertension.

A. Goodchild, A. Allen, A. Fong, 2017, Cell metabolism.

Muscle [phosphocreatine] dynamics during exercise: implication for understanding the regulation of muscle oxidative metabolism

L. Arsac, C. Menuet, 2008, The Journal of physiology.

Differences in serotoninergic metabolism possibly contribute to differences in breathing phenotype of FVB/N and C57BL/6J mice.

Nazim Kourdougli, G. Hilaire, N. Voituron, 2011, Journal of applied physiology.