Neuropathology and immunohistochemistry of brains with Rett syndrome

No To Hattatsu

Volumn 34, Issue 3, 2002, Pages 211-216

  Itoh, Masayuki ^a   Takashima, Sachio ^a  

^a NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; AGE; BRAIN STEM; CATECHOLAMINE RELEASE; CONFERENCE PAPER; CONTROLLED STUDY; CPG ISLAND; FETUS; GESTATIONAL AGE; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INFANT; LOCUS CERULEUS; MECP2 GENE; NERVE CELL LESION; NEUROPATHOLOGY; NEUROTRANSMITTER RELEASE; NEWBORN; PATHOLOGICAL ANATOMY; PATHOPHYSIOLOGY; PERIAQUEDUCTAL GRAY MATTER; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; RETT SYNDROME; SILENCER GENE; SUBSTANTIA NIGRA;

BRAIN; CHROMOSOMAL PROTEINS, NON-HISTONE; DNA-BINDING PROTEINS; HUMANS; IMMUNOHISTOCHEMISTRY; METHYL-CPG-BINDING PROTEIN 2; REPRESSOR PROTEINS; RETT SYNDROME;

EID: 0036256510     PISSN: 00290831     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (18)

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
2. A mouse MeCP2-null mutation causes neurological symptoms that mimic Rett syndrome
3. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
4. Neuropathology of Rett syndrome
5. Neuropathology of Rett syndrome
6. Rett syndrome: Analysis of deaths in the British survey
7. Review of Rett syndrome
8. Reduced expression of neuropeptides can be related to respiratory disturbances in Rett syndrome
9. Middle and short latency somatosensory evoked potentials (SEPm, SEPs) in the Rett syndrome: Chronological changes of cortical and subcortical involvements
10. Rett syndrome - An early catecholamine and indolamine deficient disorder?
11. Polysomnography - Functional topographical examination of the basal ganglia
12. Characteristics of motor disturbances of the Rett syndrome
13. The pathophysiology of the Rett syndrome from the standpoint of polysomnography
14. Pathophysiology of Rett syndrome
15. MECP2 is highly mutated in X-linked mental retardation
16. MECP2 mutation in non-fatal, non-progressive encephalopathy in a male
17. A mutation in the Rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males
18. DNA methylation: A molecular lock