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PITPNM3 encodes a member of a family of membrane-associated phosphatidylinositol transfer domain-containing proteins. 再加上，我们可以发PITPNM Family Member 3 抗体 (34) 和 PITPNM Family Member 3 蛋白 (3)和数多这个蛋白质的别的产品。
CCL18 can increase the invasive ability of non-small cell lung cancer cells by binding to its receptor Nir1.
CCL18 (显示 CCL18 ELISA试剂盒) enhances hepatocellular carcinoma (HCC (显示 FAM126A ELISA试剂盒)) cell migration, invasion, and epithelial-mesenchymal transition (EMT (显示 ITK ELISA试剂盒)) through the expression of PITPNM3 and the activation of the NF-kappaB (显示 NFKB1 ELISA试剂盒) signaling pathway.
Data indicate that PYK2 N-terminal domain interacting receptor 1 (Nir1) could induce epithelial-mesenchymal transition by stabilising Snail (显示 SNAI1 ELISA试剂盒) via the PI3K (显示 PIK3CA ELISA试剂盒)/Akt (显示 AKT1 ELISA试剂盒)/GSK3beta (显示 GSK3b ELISA试剂盒)/Snail (显示 SNAI1 ELISA试剂盒) signalling pathway through binding to CCL18 (显示 CCL18 ELISA试剂盒).
Our observations of the PITPNM3 p.Q626H mutation carriers confirm that CORD5 (显示 GUCY2D ELISA试剂盒) is a disease not to mix with other retinal degenerations mapped to 17p13.
CCL18 (显示 CCL18 ELISA试剂盒) derived from Tumor-associated macrophages (TAMs) lays a critical role in promoting breast cancer metastasis via its receptor, PITPNM3.
Thus, mutations in PITPNM3 do not appear to be a major cause of cone or cone-rod dystrophy.
Our finding on the first mutation in the human homologue of Drosophila rdgB (显示 PITPNM1 ELISA试剂盒) indicates novel pathways and a potential important role of the PITPNM3 in mammalian phototransduction.
Mutation in the PYK2 (显示 PTK2B ELISA试剂盒)-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5 (显示 GUCY2D ELISA试剂盒)) in two Swedish families.
This gene encodes a member of a family of membrane-associated phosphatidylinositol transfer domain-containing proteins. The calcium-binding protein has phosphatidylinositol (PI) transfer activity and interacts with the protein tyrosine kinase PTK2B (also known as PYK2). The protein is homologous to a Drosophila protein that is implicated in the visual transduction pathway in flies. Mutations in this gene result in autosomal dominant cone dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.
, PITPnm 3
, PYK2 N-terminal domain-interacting receptor 1
, atypical chemokine receptor 6
, cone rod dystrophy 5
, membrane-associated phosphatidylinositol transfer protein 3
, phosphatidylinositol transfer protein, membrane-associated 3
, retinal degeneration B alpha 3
, pyk2 N-terminal domain-interacting receptor 1