Disease Info Card

Neuroectodermal Tumor, Primitive

Information about Neuroectodermal Tumor, Primitive: 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 Neuroectodermal Tumor, Primitive

Most recent studies have shown that Neuroectodermal Tumor, Primitive shares some biological mechanisms with astrocytoma, bone-neoplasms, brain-neoplasms, carcinoma, central-nervous-system-neoplasms, cerebellar-neoplasms, ependymoma, ewings-sarcoma-primitive-neuroectodermal-tumor-(pnet), glioma, malignant-neoplasms, malignant-paraganglionic-neoplasm, medulloblastoma, neoplasm-metastasis, neoplasm-recurrence-local, neoplasms, nervousness, neuroblastoma, neuroectodermal-tumors, rhabdomyosarcoma, sarcoma.

Among the many pathways, these few ones have gauged particular interests from scientists studying Neuroectodermal Tumor, Primitive, and have been seen in publications frequently: Angiogenesis, Cell Adhesion, Cell Cycle, Cell Death, Cell Differentiation, Cell Growth, Cell Migration, Cell Proliferation, Enucleation, Interphase, Localization, Metaphase, Methylation, Mitosis, Oncogenesis, Pathogenesis, Reverse Transcription, Secretion, Transport

Quite a number of genes have been found to play important roles in Neuroectodermal Tumor, Primitive, such as CD99, CSF2, CTLA4, DES, ENO1, ENO2, EWSR1, FLI1, FLII, GFAP, HLA-DQA1, MB, MYC, NOD2, POMT1, SMARCB1, SYP, TP53, VIM. 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.