Neuronal migration disorder in Zellweger mice is secondary to glutamate receptor dysfunction

Annals of Neurology

Volumn 48, Issue 3, 2000, Pages 336-343

  Gressens, Pierre ^a   Baes, Myriam ^d   Leroux, Philippe ^c   Lombet, Alain ^b   Van Veldhoven, Paul ^d   Janssen, Anneleen ^d   Vamecq, Joseph ^a   Marret, Stéphane ^c   Evrard, Philippe ^a  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b HÔPITAL SAINT ANTOINE   (France)

^c UNIVERSITÉ DE ROUEN   (France)

^d UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTAMATE RECEPTOR; MATRIX PROTEIN; N METHYL DEXTRO ASPARTIC ACID; THROMBOCYTE ACTIVATING FACTOR;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; BRAIN CORTEX; CALCIUM MOBILIZATION; CELL MIGRATION; CELL MOTION; DISEASE ASSOCIATION; ENZYME ACTIVITY; EPILEPSY; GENOTYPE; LIPOGENESIS; MENTAL DEFICIENCY; MOUSE; NONHUMAN; PEROXISOME; PRACTICE GUIDELINE; PRIORITY JOURNAL; TRANSGENE; ZELLWEGER SYNDROME;

ANIMALS; AUTORADIOGRAPHY; CALCIUM; CELL MOVEMENT; DIZOCILPINE MALEATE; FEMALE; MALE; MICE; NEURONS; RECEPTORS, GABA; RECEPTORS, GLUTAMATE; RECEPTORS, N-METHYL-D-ASPARTATE; ZELLWEGER SYNDROME;

EID: 0033840419     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(200009)48:3<336::AID-ANA8>3.0.CO;2-Q     Document Type: Article

References (35)

1. Autoradiographic study of cell migration during histogenesis of the cerebral cortex
2. Specification of cerebral cortical areas
3. Genetic malformations of the human cerebral cortex
4. Mechanisms of cerebral dysgenesis
5. A familial syndrome of multiple congenital defects
6. Peroxisomal disorders
7. Disorders of peroxisomal biogenesis
8. Peroxisomal lipid metabolism
9. The pathology of peroxisomal disorders with pathogenic considerations
10. Modulation of neuronal migration by NMDA receptors
11. Neuronal migration disorders induced by ibotenate in the neocortex
12. Glutamate acting at NMDA receptors stimulates embryonic cortical neuronal migration
13. GABA stimulates chemotaxis and chemokinesis of embryonic cortical neurons via calcium-dependent mechanisms
14. Differential response of cortical plate and ventricular zone cells to GABA as a migration stimulus
15. Point mutations and an intragenic deletion of LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome
16. Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality
17. Platelet-activating factor receptor stimulation disrupts neuronal migration in vitro
18. Neuronal heterotopias in the developing cerebral cortex produced by neurotrophin-4
19. Mediators of injury in neurotrauma: Intracellular signal transduction and gene expression
20. Lipid mediators modulate NMDA receptor currents in a Xenopus oocyte expression system
21. Glutamate receptors signaling interplay modulates stress-sensitive mitogen-activated protein kinases and neuronal cell death
22. Peroxisome deficiency induces abnormal brain development and intrauterine growth retardation in Zellweger mice
23. Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
24. Blockade of NMDA receptors and apoptotic neurodegeneration in the developing brain
25. Vasoactive intestinal peptide shortens both G1 and S phases of neural cell cycle in whole postimplantation cultured mouse embryos
26. 3H]TCP binding sites
27. Laminar distribution of MK-801, kainate, AMPA, and muscimol binding sites in cat visual cortex: A developmental study
28. Regional, developmental and interspecies expression of the four NMDAR2 subunits, examined using monoclonal antibodies
29. N-Glycosylation is not a prerequisite for glutamate receptor function but is essential for lectin modulation
30. Cell compartmentalization of cholesterol biosynthesis
31. Topography of glycosylation in the rough endoplasmic reticulum and Golgi apparatus
32. Selective role of N-type calcium channels in neuronal migration
33. Intracellular Ca2+ fluctuations modulate the rate of neuronal migration
34. Migration of neocortical neurons in the absence of functional NMDA receptors
35. Ether lipid synthesis and its deficiency in peroxisomal disorders