Abnormal development of the cerebellum is often associated with disorders of movement, postural control, and motor learning. Rodent models are widely used to study normal and abnormal cerebellar development and have revealed the roles of many important genetic and environmental factors. In the present report we describe the prevalence and cytoarchitecture of molecular-layer heterotopia, a malformation of neuronal migration, in the cerebellar vermis of C57BL/6 mice and closely-related strains. In particular, we found a diverse number of cell-types affected by these malformations including Purkinje cells, granule cells, inhibitory interneurons (GABAergic and glycinergic), and glia. Heterotopia were not observed in a sample of wild-derived mic...
Ts65Dn mice are a genetic model for Down syndrome. Among others, these mice have cerebellar patholog...
The dreher mutation is inherited as an autosomal recessive trait. Homozygotes are deaf, have an abno...
Mutations in the Unc5h3 gene, a receptor for the netrin 1 ligand, result in abnormal migrations of b...
C57BL/6 mice exhibit spontaneous cerebellar malformations consisting of heterotopic neurons and glia...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
EXPERIMENTAL STUDY OF MECHANISMS OF NEURODEGENERATION IN DIFFERENT CONDITIONS - SUMMARY MUDr. Zdeňka...
A comparison of the cerebellar cortex of BALB/cByJ and C57BL/6J mice showed two morphological differ...
The cerebellar cortex of PN15 wt and Npc1 nmf164 mice diplays similar densities of Bergmann glia, Pu...
The mutant mouse tottering carries an autosomal recessive single gene mutation on chromosome 8 that ...
Symposium issue: Human Cortex Developmentidentifiant wos: 000482426800014International audienceThe c...
Contains fulltext : 57535.pdf (publisher's version ) (Closed access)We examined th...
Malformations of neocortical development are associated with cognitive dysfunction and increased sus...
In human, neuronal migration disorders are commonly associated with developmental delay, mental reta...
In human, neuronal migration disorders are commonly associated with developmental delay, mental reta...
Npc1 nmf164 mice display a reduced density of GNs in the external granule layer (EGL), which is due ...
Ts65Dn mice are a genetic model for Down syndrome. Among others, these mice have cerebellar patholog...
The dreher mutation is inherited as an autosomal recessive trait. Homozygotes are deaf, have an abno...
Mutations in the Unc5h3 gene, a receptor for the netrin 1 ligand, result in abnormal migrations of b...
C57BL/6 mice exhibit spontaneous cerebellar malformations consisting of heterotopic neurons and glia...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
EXPERIMENTAL STUDY OF MECHANISMS OF NEURODEGENERATION IN DIFFERENT CONDITIONS - SUMMARY MUDr. Zdeňka...
A comparison of the cerebellar cortex of BALB/cByJ and C57BL/6J mice showed two morphological differ...
The cerebellar cortex of PN15 wt and Npc1 nmf164 mice diplays similar densities of Bergmann glia, Pu...
The mutant mouse tottering carries an autosomal recessive single gene mutation on chromosome 8 that ...
Symposium issue: Human Cortex Developmentidentifiant wos: 000482426800014International audienceThe c...
Contains fulltext : 57535.pdf (publisher's version ) (Closed access)We examined th...
Malformations of neocortical development are associated with cognitive dysfunction and increased sus...
In human, neuronal migration disorders are commonly associated with developmental delay, mental reta...
In human, neuronal migration disorders are commonly associated with developmental delay, mental reta...
Npc1 nmf164 mice display a reduced density of GNs in the external granule layer (EGL), which is due ...
Ts65Dn mice are a genetic model for Down syndrome. Among others, these mice have cerebellar patholog...
The dreher mutation is inherited as an autosomal recessive trait. Homozygotes are deaf, have an abno...
Mutations in the Unc5h3 gene, a receptor for the netrin 1 ligand, result in abnormal migrations of b...