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CMIP encodes a c-Maf inducing protein that plays a role in T-cell signaling pathway. Zusätzlich bieten wir Ihnen CMIP Antikörper (21) und und viele weitere Produktgruppen zu diesem Protein an.
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These findings suggest that CMIP haploinsufficiency is the likely cause of syndromic Autism spectrum disorder in our patients.
Wilm's tumor protein (WT1) bound to 2 WT (zeige WT1 Proteine)1 response elements, located at positions -290/-274 and -57/-41 relative to transcription start site.
Results suggest that c-mip and RelA (zeige NFkBP65 Proteine) define two distinct types of renal damage associated with VEGF (zeige VEGFA Proteine)-targeted therapies.
c-mip has an active role in the podocyte disorders of membranous nephropathy.
These results suggest that alterations in NF-kappaB (zeige NFKB1 Proteine) activity might result from the up-regulation of c-mip and are likely to contribute to podocyte disorders in cases of idiopathic nephrotic syndrome.
we provide novel evidence that the language-disorder candidate gene CMIP is implicated in reading processes.
Eight suggestive significant loci were detected with a series of genes expressed within the inner ear that underlie the auditory function, such as: DCLK1 (zeige DCLK1 Proteine), PTPRD (zeige PTPRD Proteine), GRM8 (zeige GRM8 Proteine), CMIP.
results identify c-mip as a key component in the molecular pathogenesis of acquired podocyte diseases
Induction of c-mip in Hodgkin-Reed Sternberg cells and podocytes is associated with minimal change nephrotic syndrome in classical Hodgkin lymphoma.
Data demonstrate that c-mip interacts with Dip1 and upregulates DAPK, which blocks the nuclear translocation of ERK1/2.
Unlike the human CMIP gene, only one Wt1 (zeige WT1 Proteine) response element was identified in the mouse Cmip proximal promoter located at position -217/-206.
the c-mip protein is involve in regulating nephrin (zeige NPHS1 Proteine) phosphorylation through Csk (zeige CSK Proteine)-Cbp/PAG-Fyn (zeige FYN Proteine) signaling pathway.
Expression of Cmip in the mouse hippocampus is modulated by a sequence variant (B2 SINE indel) in the 3' UTR of Comt (catechol-O-methyltransferase (zeige COMT Proteine)).
This gene encodes a c-Maf inducing protein that plays a role in T-cell signaling pathway. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.