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Disease Info Card
Acquired Porencephaly
Information about Acquired Porencephaly: 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 Acquired Porencephaly
Most recent studies have shown that Acquired Porencephaly shares some biological mechanisms with atrophy, brain-diseases, brain-injuries, cerebral-hemorrhage, congenital-abnormality, dysplasia, encephalomalacia, epilepsy, fetal-diseases, hemiplegia, hemorrhage, hydranencephaly, hydrocephalus, hypoplasia, microcephaly, nervousness, schizencephaly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Acquired Porencephaly, and have been seen in publications frequently: Activation Of Immune Response, Brain Development, Cell Adhesion, Cell Death, Cell Development, Cell Migration, Coagulation, Flight, Hypersensitivity, Immune Response, Localization, Myelination, Neural Crest Cell Development, Neurogenesis, Pathogenesis, Reflex, Reverse Transcription, Secretion, Tissue Development, Tropism
Quite a number of genes have been found to play important roles in Acquired Porencephaly, such as ACE, ATP6V0A1, C3, COL4A1, COL4A2, CP, CSF2, GFAP, LAMC2, LPA, MTHFR, NLRP5, POMC, RFC1, RFC2, RFC4. 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.