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GSC2 Polyclonal Antibody, 100ul Immunoassays and has been shown to

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GSC2 Polyclonal Antibody, 100ul Immunoassays and has been shown toGoosecoidlike (GSCL), a homeodomain containing gene, resides in the critical region for VCFS DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS DGS

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Description

and has been shown to modulate the transcription of STAT-dependent IL-4 responses of B cells

Aberrant expression of CDX2 is associated with intestinal inflammation and tumorigenesis

The product of this gene catalyzes sulfonation by transferring a sulfate group to the 3' position of galactose in N-acetyllactosamine in both type 2 (Gal-beta-1-4GlcNAc-R) oligosaccharides and core-2-branched O-glycans| but not on type 1 or core-1-branched structures

This gene encodes an enzyme that dephosphorylates myo-inositol monophosphate to generate free myo-inositol| a precursor of phosphatidylinositol| and is therefore an important modulator of intracellular signal transduction via the production of the second messengers myoinositol 1|4|5-trisphosphate and diacylglycerol

GSC2 Polyclonal Antibody, 100ul Immunoassays and has been shown toGoosecoidlike (GSCL), a homeodomain containing gene, resides in the critical region for VCFS DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS DGS

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