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The protein encoded by PLXNA3 is a member of the plexin class of proteins. Additionally we are shipping Plexin A3 Proteins (5) and many more products for this protein.
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Data indicate that plexin A1 (show PLXNA1 Antibodies)-4 (PLXNA1 (show PLXNA1 Antibodies)-4) mediation of neuroanatomical traits can be detected using in vivo neuroimaging techniques.
in vitro analysis on PLXNA3 also suggest that this gene may have some form of growth suppressive role in breast cancer, in addition to a similar role for the gene previously reported in ovarian cancer.
Data show that the expression of Sema3A (show SEMA3A Antibodies) receptors (neuropilin-1 (NRP-1 (show NRP1 Antibodies)), NRP-2 (show NELL2 Antibodies), plexin A1 (show PLXNA1 Antibodies), plexin A2 (show Plxna2 Antibodies), and plexin A3) significantly increased during M-CSF (show CSF1 Antibodies)-mediated differentiation of monocytes into macrophages.
genetic findings demonstrate that Sema3a (show SEMA3A Antibodies) repellent signaling plays a role in the establishment of proper afferent projections in SAG (show RNF7 Antibodies) neurons, and this signaling likely occurs through a receptor complex involving Npn1 (show NRP1 Antibodies) and either plexinA1 (show PLXNA1 Antibodies) or plexinA3
plexin-A3 and plexin-A4 (show PLXNA4 Antibodies) are expressed in newly-differentiated sympathetic neurons, but not their neural crest precursors. They function cooperatively to regulate the migration of sympathetic neurons and then differentially to guide the sympathetic axons.
These results indicate that the stereotyped pruning of the visual and motor CST (show CORT Antibodies) axon collaterals is differentially regulated and that this specificity arises from the differential expression of plexin receptors in the cortex.
the signaling of plexin-A3, plexin-A4 (show PLXNA4 Antibodies), and Sema6A (show SEMA6A Antibodies) is at least partially required for dorsal turning of the corticospinal tract axons
The combined loss of PLXNA3 and PLXNA4 (show PLXNA4 Antibodies) impaired facial branchiomotor axon guidance more severely than loss of either plexin alone, suggesting that SEMA3A (show SEMA3A Antibodies) and SEMA3F (show SEMA3F Antibodies) signals, even though both essential, are partially redundant.
the plexin A3 GAP domain adopts a closed conformation and cannot accommodate R-Ras/M-Ras (show MRAS Antibodies) in its substrate-binding site, providing a structural basis for the autoinhibited state of plexins
\Homodimerization of PlxnA3 caused by mutation M1281L remains in the presence of ligand semaphorin 3F (show SEMA3F Antibodies) and co-receptor neuropilin (show NRP1 Antibodies)-2a.
Data show that null mutants of the guidance receptor plexin A3 display motor axon branching defects.
in vivo demonstration of the intersection of spontaneous electrical activity with the PlexinA3 guidance molecule receptor in regulation of axon pathfinding
study shows plexinA3 is a crucial receptor for axon guidance cues in primary motor neurons
Plexin A3 plays an additional role in motor axonal morphogenesis.
Plxna3 acts with its ligand Sema3a1 for fasciculation and correct target selection of the Vp and VII (show TH Antibodies) motor axons.
The protein encoded by this gene is a member of the plexin class of proteins. The encoded protein is a transmembrane protein that is exposed on the cell surface. This gene is thought to be involved in epithelial and neural tissue development.
, Sex chromosome X transmembrane protein of HGF receptor family 3
, semaphorin receptor SEX
, plexin 3
, Plexin 4, SEX, homolog to the cMet/HGF receptors