Disease Info Card

Bulbar Palsy, Progressive

Information about Bulbar Palsy, Progressive: 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 Bulbar Palsy, Progressive

Most recent studies have shown that Bulbar Palsy, Progressive shares some biological mechanisms with amyotrophic-lateral-sclerosis, atrophy, complete-hearing-loss, deglutition-disorders, dementia, demyelinating-diseases, dysarthria, guillain-barre-syndrome, motor-neuron-disease, muscle-weakness, muscular-atrophy, neuromuscular-diseases, ophthalmoplegia, parkinson-disease, primary-lateral-sclerosis, progressive-supranuclear-palsy, pseudobulbar-palsy, sclerosis, supranuclear-palsy, weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Bulbar Palsy, Progressive, and have been seen in publications frequently: Aging, Cardiac Conduction, Cell Adhesion, Cognition, Excretion, Immune Response, Innervation, Localization, Mastication, Micturition, Muscle Atrophy, Pathogenesis, Pigmentation, Reflex, Response To Drug, Riboflavin Transport, Secretion, Short-term Memory, Translation, Transport

Quite a number of genes have been found to play important roles in Bulbar Palsy, Progressive, such as AR, BPIFA2, CSF2, FDXR, IGFALS, LAMC2, MED1, MSMB, PEBP1, PKD1, PPBP, PSPH, PSPN, REG1A, SLC52A3, SOD1, STXBP3, TRH. 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.