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Disease Info Card
Pelizaeus-merzbacher Disease
Information about Pelizaeus-merzbacher Disease: 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 Pelizaeus-merzbacher Disease
Most recent studies have shown that Pelizaeus-merzbacher Disease shares some biological mechanisms with adrenoleukodystrophy, ataxia, atrophy, cns-disorder, demyelinating-diseases, demyelination, diffuse-cerebral-sclerosis-of-schilder, globoid-cell-leukodystrophy, leukodystrophy, leukodystrophy-metachromatic, leukoencephalopathies, muscle-spasticity, nervous-system-disorder, nervousness, nystagmus, paraplegia, spastic-paraplegia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pelizaeus-merzbacher Disease, and have been seen in publications frequently: Autophagy, Brain Development, Cell Adhesion, Cell Death, Cell Development, Cell Differentiation, Central Nervous System Myelination, Cognition, Glial Cell Development, Interphase, Localization, Myelin Assembly, Myelination, Oligodendrocyte Development, Oligodendrocyte Differentiation, Pathogenesis, Reflex, Secretory Pathway, Translation, Transport
Quite a number of genes have been found to play important roles in Pelizaeus-merzbacher Disease, such as ABR, AIMP1, ARSA, CTSC, GJC2, HSPD1, MAG, MBL2, MBP, MYT1, PDXP, PKMYT1, PLP1, PMP22, PRDX5, PRG2, PTHLH, RNF6. 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.