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PTPRZ1 encodes a member of the receptor protein tyrosine phosphatase family. De plus, nous expédions Protein tyrosine Phosphatase, Receptor-Type, Z Polypeptide 1 Anticorps (58) et Protein tyrosine Phosphatase, Receptor-Type, Z Polypeptide 1 Protéines (4) et beaucoup plus de produits pour cette protéine.
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Authors characterized exosomes from GBM cells harbouring and not harbouring PTPRZ1-MET fusion (ZM fusion).
these data indicate that PTN (Montrer PTN Kits ELISA)-PTPRZ-A signaling controls the timing of oligodendrocyte precursor cell differentiation in vivo, in which the CS moiety of PTPRZ receptors maintains them in a monomeric active state until its ligand binding.
PTPRZ1 is affected in a contiguous gene deletion syndrome
Confirm contribution of PTPRZ1, and especially PTPRQ, in CRC carcinogenesis and demonstrated that PTPRQ expression is correlated with KRAS mutation.
Data indicate that enhanced MET oncoprotein RNA expression by fusion with receptor-type tyrosine-protein phosphatase zeta (PTPRZ1).
Data indicate that the fusion arose from translocation events involving introns 3 or 8 of protein tyrosine phosphatase, receptor-type, Z polypeptide 1 (PTPRZ1) and intron 1 of hepatocyte growth factor receptor MET.
Distinct domains of PTPRZ-B are differentially required for migration and proliferation of glioma cells, respectively.
High expression of PTP receptors R and Z1 was observed in all examined cases of colorectal carcinoma, adenoma and normal colon tissue in this study.
Protein tyrosine phosphatase zeta enhances proliferation by increasing beta-catenin nuclear expression in VHL-inactive human renal cell carcinoma cells.
Data suggest that CSF-1R (Montrer CSF1R Kits ELISA)-independent actions of IL-34 (Montrer IL34 Kits ELISA) via receptor-type protein-tyrosine phosphatase (Montrer ACP1 Kits ELISA) zeta (PTP-zeta) might be considered in evaluating IL-34 (Montrer IL34 Kits ELISA) roles in development and disease.
These results suggest that sub-isoforms of PTPRZ have different functions because of variations in the wedge structure.
The Protein Tyrosine Phosphatase (Montrer ACP1 Kits ELISA) Rptpzeta Suppresses Osteosarcoma Development in Trp53 (Montrer TP53 Kits ELISA)-Heterozygous Mice
The Pleiotrophin (Montrer PTN Kits ELISA)-induced inactivation of PTPRZ was considered to be the adaptive mechanism underlying CNS remyelination in vivo.
Abnormal glycosylation of RPTP-zeta/phosphacan is neural cell-specific and may play a role in congenital muscular dystrophies.
Ptprz plays a negative role in oligodendrocyte differentiation in early central nervous system (CNS) development and remyelination in demyelinating CNS diseases.
RPTPbeta/zeta is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes.
Ptprz is necessary to maintain central nervous system axonal integrity in a demyelinating environment.
Loss of RPTPZ promotes prostate cancer metastasi.
spatial and temporal expression patterns of O-mannosylated forms of RPTPzeta/phosphacan and its hypoglycosylation are suggestive of a role in the neural phenotypes observed in Congenital muscular dystrophies
This gene encodes a member of the receptor protein tyrosine phosphatase family. Expression of this gene is restricted to the central nervous system (CNS), and it may be involved in the regulation of specific developmental processes in the CNS. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.
protein tyrosine phosphatase, receptor-type, zeta polypeptide 1
, protein-tyrosine phosphatase receptor type Z polypeptide 2
, receptor-type tyrosine phosphatase beta/zeta
, receptor-type tyrosine-protein phosphatase zeta
, 3F8 chondroitin sulfate proteoglycan
, 3H1 keratan sulfate proteoglycan
, PTP zeta
, protein tyrosine phosphate, receptor type, Z
, phosphotyrosyl phosphatase