Lissencephaly I

Overview of Lissencephaly I

Most recent studies have shown that Lissencephaly I shares some biological mechanisms with brain-diseases, chromosomal-translocation, classical-lissencephaly, congenital-abnormality, congenital-anomaly-of-brain, congenital-anomaly-of-face, cytogenetic-abnormality, developmental-delay-(disorder), dysmyelopoietic-syndromes, dysplasia, ectopic-tissue, epilepsy, lissencephaly, miller-dieker-syndrome, neuronal-migration-disorders, pachygyria, subcortical-band-heterotopia, x-linked-lissencephaly.

Among the many pathways, these few ones have gauged particular interests from scientists studying Lissencephaly I, and have been seen in publications frequently: Brain Development, Cell Division, Cell Migration, Chromosome Breakage, Interphase, Metaphase, Neuroblast Migration, Nuclear Migration, Nuclear Transport, Regulation Of Cell Migration, Translation, Transport

Quite a number of genes have been found to play important roles in Lissencephaly I, such as AKR1C2, ASXL1, ATP8A2, CDK5, CRK, DCX, GSTK1, MNT, NDEL1, PAFAH1B1, PAFAH1B2, PAFAH1B3, PLA2G7, SF3B1, TH, YWHAE, YWHAQ. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Lissencephaly I Related Genes

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Pathways Related to Lissencephaly I

This information is being compiled and will come in a future update

Related Diseases