Disease Info Card

Pediatric Neoplasm

Information about Pediatric Neoplasm: 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 Pediatric Neoplasm

Most recent studies have shown that Pediatric Neoplasm shares some biological mechanisms with brain-neoplasms, carcinoma, ewings-sarcoma-primitive-neuroectodermal-tumor-(pnet), kidney-neoplasm, leukemia, liver-neoplasms, lymphoma, malignant-childhood-neoplasm, malignant-neoplasms, malignant-paraganglionic-neoplasm, medulloblastoma, neoplasm-metastasis, neoplasms, nephroblastoma, nervousness, neuroblastoma, osteosarcoma, retinoblastoma, rhabdomyosarcoma, sarcoma.

Among the many pathways, these few ones have gauged particular interests from scientists studying Pediatric Neoplasm, and have been seen in publications frequently: Angiogenesis, Cell Cycle, Cell Cycle Arrest, Cell Death, Cell Differentiation, Cell Growth, Cell Proliferation, Demethylation, Dna Methylation, Dna Repair, Drug Resistance, Immune Response, Localization, Methylation, Oncogenesis, Pathogenesis, Programmed Cell Death, Reverse Transcription, Rna Interference, Secretion

Quite a number of genes have been found to play important roles in Pediatric Neoplasm, such as AKT1, BCL2, BDNF, CDKN1A, CDKN1C, DES, EWSR1, IGF1, IGF2, MYC, MYCN, NBL1, NME1, NTRK1, RB1, SMARCB1, SS18L1, TP53, VEGFA, 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.