Mucus glycoproteins from cystic fibrotic sputum. Macromolecular properties and structural 'architecture'.
about
Muc5b is the major polymeric mucin in mucus from thoroughbred horses with and without airway mucus accumulation1,8-Cineol Reduces Mucus-Production in a Novel Human Ex Vivo Model of Late RhinosinusitisPhysical characterization of a low-charge glycoform of the MUC5B mucin comprising the gel-phase of an asthmatic respiratory mucous plug.Altered O-glycosylation and sulfation of airway mucins associated with cystic fibrosis.Rapid transport of muco-inert nanoparticles in cystic fibrosis sputum treated with N-acetyl cysteineMucin genes and the proteins they encode: structure, diversity, and regulation.Cystic fibrosis: an inherited disease affecting mucin-producing organs.Mucin gene expression in rhinitis syndromes.The role of airway secretions in COPD--clinical applications.Mucin structure. The structure and heterogeneity of respiratory mucus glycoproteins.Studying mucin secretion from human bronchial epithelial cell primary cultures.Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis.Muc5b and Muc5ac are the major oligomeric mucins in equine airway mucus.Biosynthesis of the MUC2 mucin: evidence for a slow assembly of fully glycosylated units.Mucus glycoproteins and their role in colorectal disease.Identification of MUC5B, MUC5AC and small amounts of MUC2 mucins in cystic fibrosis airway secretions.Different mucins are produced by the surface epithelium and the submucosa in human trachea: identification of MUC5AC as a major mucin from the goblet cells.Heterogeneity of mucus glycoproteins from cystic fibrotic sputum. Are there different families of mucins?Mucins in airway secretions from healthy and chronic bronchitic subjects.Respiratory mucins: identification of core proteins and glycoforms.Susceptibility of the cysteine-rich N-terminal and C-terminal ends of rat intestinal mucin muc 2 to proteolytic cleavage.Pegylated GL67 lipoplexes retain their gene transfection activity after exposure to components of CF mucus.Expression of respiratory mucins in fatal status asthmaticus and mild asthma.A nanoscale characterization of the interaction of a novel alginate oligomer with the cell surface and motility of Pseudomonas aeruginosa.
P2860
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P2860
Mucus glycoproteins from cystic fibrotic sputum. Macromolecular properties and structural 'architecture'.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
1991年论文
@zh
1991年论文
@zh-cn
name
Mucus glycoproteins from cysti ...... and structural 'architecture'.
@en
Mucus glycoproteins from cysti ...... and structural 'architecture'.
@nl
type
label
Mucus glycoproteins from cysti ...... and structural 'architecture'.
@en
Mucus glycoproteins from cysti ...... and structural 'architecture'.
@nl
prefLabel
Mucus glycoproteins from cysti ...... and structural 'architecture'.
@en
Mucus glycoproteins from cysti ...... and structural 'architecture'.
@nl
P2093
P2860
P356
P1433
P1476
Mucus glycoproteins from cysti ...... and structural 'architecture'.
@en
P2093
D J Thornton
H Lindgren
I Carlstedt
J K Sheehan
P2860
P304
P356
10.1042/BJ2760667
P407
P478
276 ( Pt 3)
P577
1991-06-01T00:00:00Z