Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
CMIP encodes a c-Maf inducing protein that plays a role in T-cell signaling pathway. Additionally we are shipping CMIP Kits (4) and CMIP Proteins (4) and many more products for this protein.
Showing 10 out of 24 products:
Human Polyclonal CMIP Primary Antibody for WB - ABIN1881214
Audard, Zhang, Copie-Bergman, Rucker-Martin, Ory, Candelier, Baia, Lang, Pawlak, Sahali: Occurrence of minimal change nephrotic syndrome in classical Hodgkin lymphoma is closely related to the induction of c-mip in Hodgkin-Reed Sternberg cells and podocytes. in Blood 2010
Show all 3 Pubmed References
each copy of CMIP rs2925979_T allele was associated with a 29% higher risk of T2DM in females (p = 9.30 x 10(-4)), while it was not significantly associated with T2DM in males (p = 0.705).
CMIP knockdown was observed to result in the downregulation of MDM2 (show MDM2 Antibodies) and mitogen activated protein kinase (show MAPK1 Antibodies) (MAPK (show MAPK1 Antibodies)) expression at the mRNA level and CMIP was a direct target of miR1013p.
CMIP is oncogenic and could be a potential target for human glioma diagnosis and therapy.
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 (show WT1 Antibodies)1 response elements, located at positions -290/-274 and -57/-41 relative to transcription start site.
Results suggest that c-mip and RelA (show NFkBP65 Antibodies) define two distinct types of renal damage associated with VEGF (show VEGFA Antibodies)-targeted therapies.
c-mip has an active role in the podocyte disorders of membranous nephropathy.
These results suggest that alterations in NF-kappaB (show NFKB1 Antibodies) 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 (show DCLK1 Antibodies), PTPRD (show PTPRD Antibodies), GRM8 (show GRM8 Antibodies), CMIP.
Unlike the human CMIP gene, only one Wt1 (show WT1 Antibodies) response element was identified in the mouse Cmip proximal promoter located at position -217/-206.
the c-mip protein is involve in regulating nephrin (show NPHS1 Antibodies) phosphorylation through Csk (show CSK Antibodies)-Cbp/PAG-Fyn (show FYN Antibodies) signaling pathway.
Expression of Cmip in the mouse hippocampus is modulated by a sequence variant (B2 SINE indel) in the 3' UTR (show UTS2R Antibodies) of Comt (catechol-O-methyltransferase (show COMT Antibodies)).
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.