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Disease Info Card
Little's Disease
Information about Little's 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 Little's Disease
Most recent studies have shown that Little's Disease shares some biological mechanisms with brain-injuries, cerebral-palsy, diplegia, epilepsy, flexed-fetal-attitude, gait-disorders-neurologic, hemiplegia, ichthyoses, leukomalacia-periventricular, muscle-spasticity, paraplegia, quadriplegia, sjogren-larsson-syndrome, spastic-cerebral-palsy, spastic-diplegia-cerebral-palsy, spastic-hemiplegia, spastic-tetraplegia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Little's Disease, and have been seen in publications frequently: Aging, Associative Learning, Brain Development, Cell Adhesion, Coagulation, Fatty Acid Oxidation, Gene Silencing, Immune Response, Innervation, Locomotion, Muscle Atrophy, Myelination, Ossification, Pathogenesis, Reflex, Translation, Transport, Urea Cycle, Virulence, Visual Perception
Quite a number of genes have been found to play important roles in Little's Disease, such as ADH5, ALDH3A2, ATL1, CP, CSF2, DNMT3B, F2, GLB1, LAMC2, MAS1, NOS1, NOS2, NOS3, RANGAP1, SERPINA5, SLC17A5, STS. 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.