LIS1 and DCX : Implications for Brain Development and Human Disease in Relation to Microtubules

Author

Reiner, Orly

Source

Scientifica

Issue

Vol. 2013, Issue 2013 (31 Dec. 2013), pp.1-17, 17 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2013-03-17

Country of Publication

Egypt

No. of Pages

17

Main Subjects

Natural & Life Sciences (Multidisciplinary)
Diseases

Abstract EN

Proper lamination of the cerebral cortex requires the orchestrated motility of neurons from their place of birth to their final destination.

Improper neuronal migration may result in a wide range of diseases, including brain malformations, such as lissencephaly, mental retardation, schizophrenia, and autism.

Ours and other studies have implicated that microtubules and microtubule-associated proteins play an important role in the regulation of neuronal polarization and neuronal migration.

Here, we will review normal processes of brain development and neuronal migration, describe neuronal migration diseases, and will focus on the microtubule-associated functions of LIS1 and DCX, which participate in the regulation of neuronal migration and are involved in the human developmental brain disease, lissencephaly.

American Psychological Association (APA)

Reiner, Orly. 2013. LIS1 and DCX : Implications for Brain Development and Human Disease in Relation to Microtubules. Scientifica،Vol. 2013, no. 2013, pp.1-17.
https://search.emarefa.net/detail/BIM-468642

Modern Language Association (MLA)

Reiner, Orly. LIS1 and DCX : Implications for Brain Development and Human Disease in Relation to Microtubules. Scientifica No. 2013 (2013), pp.1-17.
https://search.emarefa.net/detail/BIM-468642

American Medical Association (AMA)

Reiner, Orly. LIS1 and DCX : Implications for Brain Development and Human Disease in Relation to Microtubules. Scientifica. 2013. Vol. 2013, no. 2013, pp.1-17.
https://search.emarefa.net/detail/BIM-468642

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-468642