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Neuropilin-1 (zeige NRP1 Proteine) and its co-receptor plexinA1 are necessary to bias the extension of the dendrites of retinal ganglion cells to the apical side of the cell, and ectopically expressed class III semaphorins (Sema3s) disrupt this process.
Semaphorin-3a (zeige SEMA3A Proteine), neuropilin-1 (zeige NRP1 Proteine) and plexin-A1 are axonal guidance molecules that have been recently implicated in regulating bone metabolism.
a novel mutation in the PLXNA1 receptor (c.2587G>A) in newly established pancreatic cell line, is reported.
Data indicate that plexin A1-4 (PLXNA1-4) mediation of neuroanatomical traits can be detected using in vivo neuroimaging techniques.
neuropilin 1 (zeige NRP1 Proteine) and plexin A1 transmembrane domains interaction
Expression of Plexin A1 in gastric carcinoma was significantly higher than that in normal gastric mucosa.
Breast carcinoma cells support an autocrine pathway involving SEMA3A (zeige SEMA3A Proteine), plexin-A1, and NP1 (zeige NPX1 Proteine) that impedes their ability to chemotax.
PlexinA1 may play an important role in the occurrence and development of gastric carcinoma, and be related to tumor angiogenesis and proliferation.
In malignant pleural mesothelioma cells, plexin-A1 and VEGF-receptor 2 (VEGF-R2) are associated in a complex which are involved in survival pathways.
Data show that the expression of Sema3A (zeige SEMA3A Proteine) receptors (neuropilin-1 (NRP-1 (zeige NRP1 Proteine)), NRP-2 (zeige NELL2 Proteine), plexin A1, plexin A2 (zeige Plxna2 Proteine), and plexin A3 (zeige PLXNA3 Proteine)) significantly increased during M-CSF (zeige CSF1 Proteine)-mediated differentiation of monocytes into macrophages.
PLXNA1 mediates the acquisition of malignant phenotypes induced by autocrine SEMA3A (zeige SEMA3A Proteine) signaling in lung cancer cells.
Study showed that progenitor cells lining the telencephalic ventricles express PlexinA1 and that absence of this receptor impairs neurogenesis in the developing forebrain
PlexinA1 mediates both Semaphorin and Slit signaling
genetic findings demonstrate that Sema3a (zeige SEMA3A Proteine) repellent signaling plays a role in the establishment of proper afferent projections in SAG (zeige RNF7 Proteine) neurons, and this signaling likely occurs through a receptor complex involving Npn1 (zeige NRP1 Proteine) and either plexinA1 or plexinA3 (zeige PLXNA3 Proteine)
A novel direct interaction between the Sema3a (zeige SEMA3A Proteine) signaling receptor plexinA1 and nephrin (zeige NPHS1 Proteine), linking extracellular Sema3a (zeige SEMA3A Proteine) signals to the slit-diaphragm signaling complex, was identified.
Data demonstrate an essential direct function of Sema3A (zeige SEMA3A Proteine)-Nrp1 (zeige NRP1 Proteine)-PlexinA1 signaling in lymphatic valve formation.
These findings suggest a mechanism by which a complex of Sema6D (zeige SEMA6D Proteine), Nr-CAM (zeige NRCAM Proteine), and Plexin-A1 at the chiasm midline alters the sign of Sema6D (zeige SEMA6D Proteine) and signals Nr-CAM (zeige NRCAM Proteine)/Plexin-A1 receptors on retinal ganglion cells to implement the contralateral retinal cell projection.
Results suggest that plexin-A1 and B1 interact in the adult brain and transduce semaphorin 3A (zeige SEMA3A Proteine) signaling in cooperation.
Plexin-A1 affects t-cell-dendritic cell interaction but not antigen processing or binding.
Plexin-A1 forms a receptor complex with vascular endothelial growth factor receptor type 2 in heart morphogenesis
Coreceptor for SEMA3A, SEMA3C, SEMA3F and SEMA6D. Necessary for signaling by class 3 semaphorins and subsequent remodeling of the cytoskeleton. Plays a role in axon guidance, invasive growth and cell migration. Class 3 semaphorins bind to a complex composed of a neuropilin and a plexin. The plexin modulates the affinity of the complex for specific semaphorins, and its cytoplasmic domain is required for the activation of down- stream signaling events in the cytoplasm.
, plexin A1a
, plexin 1
, semaphorin receptor NOV
, plex 1