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Disease Info Card
Miller Dieker Syndrome
Information about Miller Dieker Syndrome: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Miller Dieker Syndrome
Most recent studies have shown that Miller Dieker Syndrome shares some biological mechanisms with chromosomal-translocation, classical-lissencephalies-and-subcortical-band-heterotopias, classical-lissencephaly, congenital-abnormality, congenital-anomaly-of-brain, congenital-anomaly-of-face, cytogenetic-abnormality, developmental-delay-(disorder), dysmyelopoietic-syndromes, dystrophy, epilepsy, lissencephaly, lissencephaly-i, microcephaly, muscle-hypotonia, neoplasms, neuronal-migration-disorders, pachygyria.
Among the many pathways, these few ones have gauged particular interests from scientists studying Miller Dieker Syndrome, and have been seen in publications frequently: Brain Development, Cell Cycle, Cell Cycle Checkpoint, Cell Death, Cell Division, Cell Migration, Cell Proliferation, Chromosome Segregation, Eye Development, Interphase, Localization, Metaphase, Neuroblast Migration, Nuclear Migration, Nuclear Transport, Oncogenesis, Pathogenesis, System Development, Translation, Transport
Quite a number of genes have been found to play important roles in Miller Dieker Syndrome, such as ARX, ASXL1, ATP8A2, CRK, DCX, EXOSC1, FLNA, HIC1, NDEL1, PAFAH1B1, PLA2G7, RELN, SF3B1, TH, TP53, UBA2, YWHAE. 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.