Syringocystadenoma Papilliferum

Overview of Syringocystadenoma Papilliferum

Most recent studies have shown that Syringocystadenoma Papilliferum shares some biological mechanisms with adenocarcinoma, adenoma, apocrine-adenoma, basal-cell-carcinoma, carcinoma, cystadenoma, eccrine-acrospiroma, hamartoma, malignant-paraganglionic-neoplasm, melanocytic-nevus, neoplasms, neoplasms-multiple-primary, nevus-sebaceous-of-jadassohn, poroma, skin-neoplasms, spiradenoma, sweat-gland-neoplasms, syringoma, trichoepithelioma.

Among the many pathways, these few ones have gauged particular interests from scientists studying Syringocystadenoma Papilliferum, and have been seen in publications frequently: Cell Adhesion, Cell Differentiation, Invasive Growth, Keratinization, Localization, Pathogenesis, Pigmentation, Secretion, Skin Development

Quite a number of genes have been found to play important roles in Syringocystadenoma Papilliferum, such as APOD, BPNT1, CEACAM5, CEACAM7, CHKA, CHKB, CKAP4, ETFA, GNL3, KRAS, KRT15, KRT20, LYZ, MUC1, PIP, PSG2, SH2D2A, TFF2, 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.

Syringocystadenoma Papilliferum Related Genes

click to see detail information for each gene

Pathways Related to Syringocystadenoma Papilliferum

This information is being compiled and will come in a future update

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