Disease Info Card

Fibroma

Information about Fibroma: 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 Fibroma

Most recent studies have shown that Fibroma shares some biological mechanisms with benign-neoplasm, bone-neoplasms, carcinoma, fibromatosis, fibromatosis-aggressive, fibrosarcoma, heart-neoplasm, lipoma, malignant-neoplasms, malignant-paraganglionic-neoplasm, mandibular-neoplasms, neoplasm-recurrence-local, neoplasms, odontogenic-tumors, ossifying-fibroma, ovarian-neoplasm, sarcoma, skin-neoplasms, soft-tissue-neoplasms, uterine-fibroids.

Among the many pathways, these few ones have gauged particular interests from scientists studying Fibroma, and have been seen in publications frequently: Cell Cycle, Cell Differentiation, Cell Growth, Cell Proliferation, Coagulation, Dna Replication, Enucleation, Immune Response, Localization, Menopause, Mitosis, Oncogenesis, Ossification, Pathogenesis, Pigmentation, Regeneration, Secretion, Virulence, Wound Healing

Quite a number of genes have been found to play important roles in Fibroma, such as APC, BCL2, CD34, CD99, CTLA4, DES, EGF, ELN, ETFA, F13A1, GFAP, HLA-DQA1, KIT, MUC1, NOD2, S100A1, S100B, 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.

Fibroma Related Genes

click to see detail information for each gene

APC BCL2 CD34
CD99 CTLA4 DES
EGF ELN ETFA
F13A1 GFAP HLA-DQA1
KIT MUC1 NOD2
S100A1 S100B TP53
VIM