Disease Info Card

Cerebellar Diseases

Information about Cerebellar Diseases: 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 Cerebellar Diseases

Most recent studies have shown that Cerebellar Diseases shares some biological mechanisms with ataxia, atrophy, brain-diseases, cerebellar-ataxia, cerebellar-neoplasms, cerebral-hemorrhage, cerebral-infarction, cerebrovascular-accident, epilepsy, headache, hematoma, hemorrhage, hydrocephalus, infarction, neoplasms, nervous-system-disorder, nervousness, nystagmus.

Among the many pathways, these few ones have gauged particular interests from scientists studying Cerebellar Diseases, and have been seen in publications frequently: Aging, Associative Learning, Brain Development, Cell Death, Cell Migration, Cell Proliferation, Coagulation, Cognition, Excretion, Glycosylation, Habituation, Immune Response, Innervation, Localization, Locomotion, Myelination, Pathogenesis, Reflex, Translation, Transport

Quite a number of genes have been found to play important roles in Cerebellar Diseases, such as ACAT1, ATXN1, ATXN2, ATXN3, CACNA1A, CALB1, CDR1, CDR2, CPA1, CSF2, DNAH5, DNAI1, GFAP, GRIP1, LAMC2, LY6E, PCBD1, PRNP, RUNX2, SLC25A5. 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.

Cerebellar Diseases Related Genes

click to see detail information for each gene

ACAT1 ATXN1 ATXN2
ATXN3 CACNA1A CALB1
CDR1 CDR2 CPA1
CSF2 DNAH5 DNAI1
GFAP GRIP1 LAMC2
LY6E PCBD1 PRNP
RUNX2 SLC25A5