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CNTN4 encodes a member of the contactin family of immunoglobulins. Zusätzlich bieten wir Ihnen Contactin 4 Antikörper (40) und Contactin 4 Proteine (8) und viele weitere Produktgruppen zu diesem Protein an.
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SNPs within the CNTN4 gene are associated with increased risk of oral cancer.
SNPs in ITPR1 (zeige ITPR1 ELISA Kits) and CNTN4 are involved in the regulation of serum uric acid concentrations in Mexican Americans
By combining methylation and SNP data, CNTN4 was identified as a risk factor for regular alcohol use.
data reveal critical and novel roles for CNTN4/amyloid precursor protein (zeige APP ELISA Kits) in promoting target-specific axon arborization
We identified CNTN4 as a novel candidate gene for POAG.
these results suggest that rare copy number variations in CNTN4 may also influence autism susceptibility in Asian populations.
Using array comparative genome hybridization (CGH), we identified a maternally inherited approximately 535 kb deletion at 3p26.3 encompassing the 5' end of the contactin 4 gene (CNTN4) in a patient with autism.
Our results demonstrate the association of CNTN4 disruption with the 3p deletion syndrome phenotype and strongly suggest a causal relationship
The contactin 4 gene (CNTN4) is associated with cerebellar degeneration in spinocerebellar ataxia type 16. Additional studies are necessary to prove 4,256C-->T to be a causative mutation.
pathological examinations and molecular biological examinations are needed to confirm that this mutation is a true cause of SCA16 (zeige ITPR1 ELISA Kits)
Protein-tyrosine phosphatase receptor type G (RPTPgamma/PTPRG (zeige PTPRG ELISA Kits)) interacts in vitro with contactin-3 (zeige CNTN3 ELISA Kits)-6 (CNTN3 (zeige CNTN3 ELISA Kits)-6), a group of glycophosphatidylinositol-anchored cell adhesion molecules involved in the wiring of the nervous system
including the adhesion molecule (zeige NCAM1 ELISA Kits) CNTN4,which contributed to the enhanced response
These results suggest that BIG-2 is one of the axon guidance molecules crucial for the formation and maintenance of functional odor map in the olfactory bulb.
This gene encodes a member of the contactin family of immunoglobulins. Contactins are axon-associated cell adhesion molecules that function in neuronal network formation and plasticity. The encoded protein is a glycosylphosphatidylinositol-anchored neuronal membrane protein that may play a role in the formation of axon connections in the developing nervous system. Deletion or mutation of this gene may play a role in 3p deletion syndrome and autism spectrum disorders. Alternative splicing results in multiple transcript variants.
, axonal-associated cell adhesion molecule
, brain-derived immunoglobulin superfamily protein 2
, neural cell adhesion protein BIG-2
, brain-derived immunoglobulin superfamily molecule
, FAR-1 protein fragment