Abnormal fucosylation of-ileal mucus in cystic fibrosis: II. A histochemical study using monoclonal antibodies to fucosyl oligosaccharides.

Author:

King A,McLeish M,Thiru S

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference31 articles.

1. Human intestinal mucin in cystic fibrosis;Wesley, A.; Forstner, J.; Qureshi, R.; Mantle, M.; Forstner, G.;Pediatr Res,1983

2. Biochemical characterisation of the component parts of intestinal mucin from patients with cystic fibrosis;Mantle, M.; Forstner, G.; Forstner, J.;Biochem J,1984

3. Comparison of physicochemical properties of purified mucus glycoproteins isolated from respiratory sections of cystic fibrosis and asthmatic patients;Chace, K.V.; Flux, M.; Sachdev, G.P.;Biochemistry,1985

4. Glycoproteins and cystic fibrosis: a review;Alhadeff, J.A.;Clin Genet,1978

5. Abnormal mucus: nominated but not yet elected;Forstner, J.; Wesley, A.; Mantle, M.; Kopelman, J.; Man, D.; Forstner, G.;J Pediatr Gastroenterol Nutr,1984

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