John M Bissonnette
Overview
Explore the profile of John M Bissonnette including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
19
Citations
821
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Maletz S, Reid B, Baekey D, Whitaker-Fornek J, Bateman J, Arakawa K, et al.
Respir Physiol Neurobiol
. 2024 Aug;
328:104314.
PMID: 39117159
Rett syndrome (RTT) is an autism spectrum disorder caused by loss-of-function mutations in the methyl-CPG-binding protein 2 (Mecp2) gene. Frequent apneas and irregular breathing are prevalent in RTT, and also...
2.
Abdala A, Toward M, Dutschmann M, Bissonnette J, Paton J
J Physiol
. 2015 Oct;
594(1):223-37.
PMID: 26507912
Life threatening breathing irregularity and central apnoeas are highly prevalent in children suffering from Rett syndrome. Abnormalities in inhibitory synaptic transmission have been associated with the physiopathology of this syndrome,...
3.
Garg S, Lioy D, Knopp S, Bissonnette J
J Appl Physiol (1985)
. 2015 Jul;
119(6):670-6.
PMID: 26205541
Mice that are deficient in the transcription factor methyl-CpG-binding protein 2 (MeCP2) have a depressed hypercapnic ventilatory response (HCVR). The expression of MeCP2 can be selectively removed from astrocytes or...
4.
Levitt E, Abdala A, Paton J, Bissonnette J, Williams J
J Physiol
. 2015 Jul;
593(19):4453-69.
PMID: 26175072
Key Points: In addition to reductions in respiratory rate, opioids also cause aspiration and difficulty swallowing, indicating impairment of the upper airways. The Kölliker-Fuse (KF) maintains upper airway patency and...
5.
Abdala A, Bissonnette J, Newman-Tancredi A
Front Physiol
. 2014 Jun;
5:205.
PMID: 24910619
Rett syndrome is a neurological disorder caused by loss of function of methyl-CpG-binding protein 2 (MeCP2). Reduced function of this ubiquitous transcriptional regulator has a devastating effect on the central...
6.
Abdala A, Lioy D, Garg S, Knopp S, Paton J, Bissonnette J
Am J Respir Cell Mol Biol
. 2013 Dec;
50(6):1031-9.
PMID: 24351104
Disturbances in respiration are common and debilitating features of Rett syndrome (RTT). A previous study showed that the 5-HT1a receptor agonist (R)-(+)-8-hydroxy-dipropyl-2-aminotetralin hydrobromide (8-OH-DPAT) significantly reduced the incidence of apnea...
7.
Levitt E, Hunnicutt B, Knopp S, Williams J, Bissonnette J
J Appl Physiol (1985)
. 2013 Oct;
115(11):1626-33.
PMID: 24092697
Rett syndrome is a neurological disorder caused by loss of function mutations in the gene that encodes the DNA binding protein methyl-CpG-binding protein 2 (Mecp2). A prominent feature of the...
8.
Garg S, Lioy D, Cheval H, McGann J, Bissonnette J, Murtha M, et al.
J Neurosci
. 2013 Aug;
33(34):13612-20.
PMID: 23966684
De novo mutations in the X-linked gene encoding the transcription factor methyl-CpG binding protein 2 (MECP2) are the most frequent cause of the neurological disorder Rett syndrome (RTT). Hemizygous males...
9.
Toward M, Abdala A, Knopp S, Paton J, Bissonnette J
Exp Physiol
. 2012 Nov;
98(3):842-9.
PMID: 23180809
Mice deficient in the transcription factor methyl-CpG-binding protein 2 (Mecp2), a mouse model of Rett syndrome, display reduced CO2 chemosensitivity, which may contribute to their breathing abnormalities. In addition, patients...
10.
Lioy D, Garg S, Monaghan C, Raber J, Foust K, Kaspar B, et al.
Nature
. 2011 Jul;
475(7357):497-500.
PMID: 21716289
Rett's syndrome (RTT) is an X-chromosome-linked autism spectrum disorder caused by loss of function of the transcription factor methyl-CpG-binding protein 2 (MeCP2). Although MeCP2 is expressed in most tissues, loss...