Disease relevance of dextrose

• Mannose 6-phosphate receptor dependence of varicella zoster virus infection in vitro and in the epidermis during varicella and zoster [1].
• Mannose-sensitive and Gal-Gal binding Escherichia coli pili from recombinant strains. Chemical, functional, and serological properties [2].
• Mannose-binding protein and susceptibility to chronic hepatitis B infection [3].
• Mannose-resistant haemagglutination and P antigen recognition are characteristic of Escherichia coli causing primary pyelonephritis [4].
• Mannose 6-phosphate-independent targeting of lysosomal enzymes in I-cell disease B lymphoblasts [5].

High impact information on dextrose

• Mannose 6-phosphate/insulin-like growth factor II receptor is a death receptor for granzyme B during cytotoxic T cell-induced apoptosis [6].
• Mannose 6-phosphate receptors carry soluble lysosomal enzymes from the trans Golgi network (TGN) to prelysosomes, and then return to the TGN for another round of lysosomal enzyme sorting [7].
• Mannose effects occurred during the first 24 hours of culture and were attended by modes inhibition of the glycolysis that constitutes the principal energy pathway at this stage of development [8].
• Mannose-binding protein (MBP), C1q, the recognition component of the classical complement pathway, and pulmonary surfactant protein A (SP-A) are members of a family of molecules containing a collagen-like sequence contiguous with a noncollagen-like sequence, and usually having the properties of a lectin [9].
• Mannose receptor is a novel ligand for L-selectin and mediates lymphocyte binding to lymphatic endothelium [10].

Chemical compound and disease context of dextrose

• Mannose-sensitive and mannose-resistant adherence to human uroepithelial cells and urinary virulence of Escherichia coli [11].
• CONCLUSIONS AND CLINICAL RELEVANCE: Mannose and N-acetyl-D-galactosamine appear to play a role in adhesion of S. zooepidemicus, P. aeruginosa, and E. coli to equine endometrium [12].
• In addition the relative efficacy of D(+)-mannose and heparin to inhibit the adherence of E. coli to rabbit bladder mucosa was compared [13].

Biological context of dextrose

• Mannose binding protein gene mutations associated with unusual and severe infections in adults [14].
• Mannose-binding protein genotypes and recurrent infection [15].
• Mannose 6-phosphate receptor-mediated endocytosis of acid hydrolases: internalization of beta-glucuronidase is accompanied by a limited dephosphorylation [16].
• Mannose uptake and phosphorylation in Escherichia coli is catalyzed by the phosphoenolpyruvate:glycose phosphotransferase system (PTS) [17].
• Mannose-labeled glycopeptides from the surface of growing and nongrowing human diploid cells (KL-2) were separated into neutral glycopeptides and acidic glycopeptides by paper electrophoresis [18].

Anatomical context of dextrose

• Mannose 6-phosphate-specific receptors with an apparent molecular mass of 215,000 are present in fibroblasts at the cell surface and in intracellular membranes [19].
• Mannose 6-phosphate/insulin-like growth factor-II receptor targets the urokinase receptor to lysosomes via a novel binding interaction [20].
• Mannose dolichylphosphate is the sugar donor of the reaction, which is localized at the endoplasmic reticulum [21].
• Mannose-specific endocytosis receptor of alveolar macrophages: demonstration of two functionally distinct intracellular pools of receptor and their roles in receptor recycling [22].
• Mannose receptor regulates myoblast motility and muscle growth [23].

Associations of dextrose with other chemical compounds

• (2) Mannose and glucosamine are functionally important sugar residues for the effect of IP-oligosaccharide on lipogenesis [24].
• Mannose 6-phosphate receptors, Niemann-Pick C2 protein, and lysosomal cholesterol accumulation [25].
• [reaction: see text] Mannose 6-phosphate mimics locked into the alpha-configuration and bearing hydrolase-resistant phosphate surrogates were synthesized and evaluated for binding affinity to the mannose 6-phosphate/insulin-like growth factor II receptor (M6P/IGF2R) [26].
• Mannose, due to its axial C2 conformation, encloses the backbone atoms of the protein in a clamplike way [27].
• Glycoprotein Hypersecretion Alters the Cell Wall in Trichoderma reesei Strains Expressing the Saccharomyces cerevisiae Dolichylphosphate Mannose Synthase Gene [28].
• Clearance/endocytosis of ligands for other receptors in these animals was as that for wild-type mice, and denatured collagen uptake in wild-type mice was not affected by other ligands of the mannose receptor, namely mannose and mannan [29].

Gene context of dextrose

• Mannose (or mannan)-binding lectin (MBL) is an oligomeric serum lectin that plays a role in innate immunity by activating the complement system [30].
• Mannose was phosphorylated well by HXK1, but at a much lower rate by HXK2 [31].
• Large cells, differentiated after seven days of culture, expressed high levels of MHC II molecules and Mannose Receptor, variable levels of CD80 and CD86, and low levels of CD1a [32].
• Mannose also inhibited the expression of MT1-MMP mRNA induced by ConA [33].
• Mannose 6-phosphate modification of wild-type and mutant PPT enzymes was grossly normal at the level of the phosphotransferase reaction [34].
• We found that di-acylated LM inhibition of LPS-induced tumor necrosis factor secretion by murine macrophages was independent of TLR2, mannose receptor, or the murine ortholog SIGNR1 [35].

Analytical, diagnostic and therapeutic context of dextrose

• Mannose affinity chromatography of the culture medium of Chinese hamster ovary cells results in an efficient purification of the secreted recombinant human SP 28-36 [36].
• Mannose receptor in the flow-through and eluted fractions was detected by fluorography following immunoprecipitation and gel electrophoresis [37].
• Mannose is an acceptor, however, after treatment of microsomes with detergent [38].
• Mannose-binding lectin is a regulator of inflammation that accompanies myocardial ischemia and reperfusion injury [39].
• Electron microscopy revealed that both strains produced fine (3.5-nm) and type 1 pili at 37 degrees C but only type 1 pili at 18 degrees C. Mannose-resistant in vitro adhesion to brush borders of older pigs correlated with the presence of fine pili [40].

References