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Publications by S Thiru
Abnormal Fucosylation Of-Ileal Mucus in Cystic Fibrosis: II. A Histochemical Study Using Monoclonal Antibodies to Fucosyl Oligosaccharides.
Journal of Clinical Pathology
Medicine
Forensic Medicine
Pathology
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Is Cystic Fibrosis Mucus Abnormal?
Pediatric Research
Child Health
Pediatrics
Perinatology
Development of an Airway Mucus Defect in the Cystic Fibrosis Rat
JCI insight
Medicine
Immunohistochemical Analysis of Mesenchymal Cells in Experimental Hepatic Fibrosis Using Monoclonal Antibodies.
Acta Histochemica et Cytochemica
Cell Biology
Biochemistry
Histology
Forensic Medicine
Pathology
Physiology
Generation of Monoclonal Antibodies Against Plant Cell-Wall Polysaccharides (I. Characterization of a Monoclonal Antibody to a Terminal [Alpha]-(1->2)-Linked Fucosyl-Containing Epitope
Plant Physiology
Plant Science
Genetics
Physiology
Hyper-Osmolarity and Calcium Chelation: Effects on Cystic Fibrosis Mucus
European Journal of Pharmacology
Pharmacology
IgG Antibodies to Aspergillus Fumigatus in Cystic Fibrosis: A Laboratory Correlate of Disease Activity.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Cystic Fibrosis Mice Lacking Muc1 Have Reduced Amounts of Intestinal Mucus.
Journal of Clinical Investigation
Medicine
FUNCTIONALLY ABNORMAL Α2-Macroglobulin (Α2M) IN CYSTIC FIBROSIS (CF)
Pediatric Research
Child Health
Pediatrics
Perinatology
A Histochemical and Immunohistochemical Study in Oral Submucous Fibrosis.
International Journal of Advanced Research
