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This locus encodes a member of the type III receptor-like protein-tyrosine phosphatase family. Zusätzlich bieten wir Ihnen Protein Tyrosine Phosphatase, Receptor Type, Q Proteine (3) und Protein Tyrosine Phosphatase, Receptor Type, Q Antikörper (2) und viele weitere Produktgruppen zu diesem Protein an.
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Human PTPRQ ELISA Kit für Sandwich ELISA - ABIN419279
Nagata, Bundo, Sugiura, Kamita, Ono, Hattori, Yoshida, Goto, Urakami, Niida: PTPRQ as a potential biomarker for idiopathic normal pressure hydrocephalus. in Molecular medicine reports 2017
Confirm contribution of PTPRZ1, and especially PTPRQ, in CRC carcinogenesis and demonstrated that PTPRQ expression is correlated with KRAS mutation.
two novel compound heterozygous missense mutations, c. 3125 A>G p.D1042G and c.5981 A>G p.E1994G in the PTPRQ (zeige PTPRR ELISA Kits) gene, were identified as the cause of recessively inherited sensorineural hearing loss in family 1572.
novel c.16_17insT (L8fsX18) and c.2714delA (E909fsX922)mutations in PTPRQ (zeige PTPRR ELISA Kits) presented here further confirms the essential role of PTPRQ (zeige PTPRR ELISA Kits) in hearing development and auditory function
Identification of four causative mutations in the PTPRQ (zeige PTPRR ELISA Kits) gene as a cause of congenital sensorineural hearing loss in a Japanese population.
PTPRQ (zeige PTPRR ELISA Kits) crystal structure shows the basis for the dephosphorylating activity of PTPRQ (zeige PTPRR ELISA Kits) towards phosphatidylinositide substrates.
Identification of the DFNB84 gene represents the first identification of PTPRQ (zeige PTPRR ELISA Kits) mutation in human hearing loss.
Mutations in PTPRQ (zeige PTPRR ELISA Kits) are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction.
Overexpression of PTP-RQ consistently led to reduced differentiation of mesenchymal stem cells into adipocytes via decreasing the phosphatidyl inositol phosphate level in cells, and consequently downregulating Akt/PKB (zeige AKT1 ELISA Kits) phosphorylation.
The reduction in Ptprq observed in miR (zeige MLXIP ELISA Kits)-96 mutantdiminuendo mice appears to be a major contributor to the morphological, transcriptional and electrophysiological phenotype
The results reveal a distinct phenotype in the vestibular system of Ptprq(-/-) mice and suggest similar hair bundle defects may underlie the vestibular dysfunction reported in humans with mutations in PTPRQ.
Three distinct, developmentally regulated isoforms of Ptprq may therefore be expressed on hair bundles of the chick inner ear
Ptprq is required for formation of the shaft connectors of the hair bundle, the normal maturation of cochlear hair bundles, and the long-term survival of high-frequency auditory hair cells
Results suggest that PTPRQ and myosin VI form a complex that dynamically maintains the organization of the cell surface coat at the stereocilia base and helps maintain the structure of the overall stereocilia bundle.
This locus encodes a member of the type III receptor-like protein-tyrosine phosphatase family. The encoded protein catalyzes the dephosphorylation of phosphotyrosine and phosphatidylinositol and plays roles in cellular proliferation and differentiation. Mutations at this locus are associated with hearing loss.
protein tyrosine phosphatase, receptor type, R
, protein tyrosine phosphatase, receptor type, Q
, phosphotidylinositol phosphatase PTPRQ-like
, phosphatidylinositol phosphatase PTPRQ
, phosphotidylinositol phosphatase PTPRQ
, protein-tyrosine phosphatase, receptor-type, expressed by glomerular mesangial cells
, receptor-type tyrosine-protein phosphatase Q
, glomerular mesangial cell receptor protein-tyrosine phosphatase
, protein-tyrosine phosphatase receptor-type expressed by glomerular mesangial cells protein 1