Alteration of monoaminergic systems in the caudal medulla and its possible link to diurnal increase of apnea in a mouse model of Rett syndrome
Author:
Affiliation:
1. Department of Pediatric Dentistry, Nihon University School of Dentistry
2. Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry
Funder
Japan Agency for Medical Research and Development
Japan Society for the Promotion of Science
Publisher
Nihon University School of Dentistry
Subject
General Dentistry
Link
https://www.jstage.jst.go.jp/article/josnusd/65/2/65_22-0474/_pdf
Reference24 articles.
1. 1. Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY (1999) Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23, 185-188.
2. 2. Neul JL, Zoghbi HY (2004) Rett syndrome: a prototypical neurodevelopmental disorder. Neuroscientist 10, 118-128.
3. 3. Julu PO, Kerr AM, Apartopoulos F, Al-Rawas S, Engerström IW, Engerström L et al. (2001) Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder. Arch Dis Child 85, 29-37.
4. 4. Weese-Mayer DE, Lieske SP, Boothby CM, Kenny AS, Bennett HL, Ramirez JM (2008) Autonomic dysregulation in young girls with Rett Syndrome during nighttime in-home recordings. Pediatr Pulmonol 43, 1045-1060.
5. 5. Katz DM, Dutschmann M, Ramirez JM, Hilaire G (2009) Breathing disorders in Rett syndrome: progressive neurochemical dysfunction in the respiratory network after birth. Respir Physiol Neurobiol 168, 101-108.
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