Page last updated: 2024-08-17

galactose and Cystic Fibrosis

galactose has been researched along with Cystic Fibrosis in 42 studies

Research

Studies (42)

TimeframeStudies, this research(%)All Research%
pre-199029 (69.05)18.7374
1990's2 (4.76)18.2507
2000's2 (4.76)29.6817
2010's9 (21.43)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brandt, C; Melichar, V; Niemann, N; Rickerts, V; Roehmel, J; Schwarz, C1
Bogdan, C; Held, J; Melichar, VO; Meyer, R; Rauh, M; Träger, J1
Chakrabarti, A; Kaur, H; Rudramurthy, SM; Singh, M; Singh, S1
Baxter, CG; Denning, DW; Dunn, G; Gore, R; Jones, AM; Richardson, MD; Webb, K1
Abbott, J; Bucior, I; Engel, JN; Matthay, MA; Song, Y1
Clements, RM; Estrada, L; Jon, CK; Mosquera, RA1
Carrington, SD; Daniel, BM; Dunican, EM; Erzurum, SC; Fahy, JV; Ghosh, S; Hazen, SL; Hollinger, M; Huang, X; Kerr, SC; Lachowicz-Scroggins, ME; Oscarson, S; Willard, B; Yuan, S1
Hauber, HP; Mack, D; Pforte, A; Schulz, M; Schumacher, U; Zabel, P1
Ratjen, F; Tullis, E; Warren, TA; Waters, V; Yau, Y1
Atalay, MA; Koç, N; Sav, H; Unal, E1
GREEN, MN; KULCZYCKI, LL; MAGALINI, SI; SHWACHMAN, H1
Cummings, RD; Damera, G; Royall, JA; Sachdev, GP; Xia, B1
Boat, TF; Margolies, R1
Forstner, G; Forstner, J; Mantle, M; Qureshi, R; Wesley, A1
Jones, PM; Rudick, MJ; Rudick, VL1
Cérantola, S; Marty, N; Montrozier, H1
Mitchell, CH; Sinatra, FR; Sunshine, P1
Boat, TF; Carlson, DM; Cheng, PW; Iyer, RN; Polony, I1
Degand, P; Lamblin, G; Roussel, P1
Guggino, WB; Montrose, MH; Montrose-Rafizadeh, C1
Levine, MJ; Prakobphol, A; Reddy, MS1
Gilly, R; Levrat, C; Louisot, P2
Butterworth, J1
Poley, JR1
Hill, HZ; Puck, TT1
Crozier, D; Moscarello, MA; Singer, L1
Evans, LR; Linker, A1
Curtis, KJ; Kim, YS; Perdomo, J; Whitehead, JS1
Degand, P; Havez, R; Lamblin, G; Roussel, P1
Lindquist, B; Meeuwisse, GW1
Grävinghoff, J1
Gibbons, IS1
DISANTAGNESE, PA; GABRIEL, O; HALBERT, S; PALLAVICINI, JC; RAUNIO, V; TALAMO, RC1
Carubelli, R; Chace, KV; Flux, M; Leahy, DS; Martin, R; Sachdev, GP1
Allen, RC; Buse, MG; Hallett, D; Spicer, KM1
Ben-Yoseph, Y; Defranco, CL; Nadler, HL1
Applegarth, DA; MacDonald, IB; Park, CM; Reid, PE; Wong, LT1
Benke, PJ; Erbstoeszer, M; Pitot, HC1
Barton, AD; Lourenço, RV1
Cunningham, LW; Segrest, JP1
Desbaillets, L; Masters, YF; Menguy, R1

Reviews

2 review(s) available for galactose and Cystic Fibrosis

ArticleYear
Chronic diarrhea in infants and children. I.
    Southern medical journal, 1973, Volume: 66, Issue:9

    Topics: Adolescent; Bile Acids and Salts; Child; Child, Preschool; Chronic Disease; Cystic Fibrosis; Diarrhea; Dietary Carbohydrates; Dietary Proteins; Fatty Acids; Food Hypersensitivity; Galactose; Gastrointestinal Motility; Glucose; Glutens; Glycoside Hydrolases; Humans; Infant; Intestinal Absorption; Intestines; Lipase; Malabsorption Syndromes; Metabolism, Inborn Errors; Pancreas

1973
Bronchial secretions and mucociliary clearance. Biochemical characteristics.
    Archives of internal medicine, 1973, Volume: 131, Issue:1

    Topics: Acyltransferases; Aerosols; Bronchi; Bronchiectasis; Calcium; Carbohydrate Metabolism; Cilia; Cystic Fibrosis; DNA; Fucose; gamma-Glutamyltransferase; Glycoproteins; Hexosamines; Hexoses; Humans; Laryngectomy; Lipid Metabolism; Mucous Membrane; Neuraminic Acids; Phosphorus; Potassium; Proteins; Respiratory Physiological Phenomena; Sodium; Sputum; Viscosity

1973

Trials

1 trial(s) available for galactose and Cystic Fibrosis

ArticleYear
Inhalation with fucose and galactose for treatment of Pseudomonas aeruginosa in cystic fibrosis patients.
    International journal of medical sciences, 2008, Volume: 5, Issue:6

    Topics: Administration, Inhalation; Adult; Aminoglycosides; C-Reactive Protein; Cell Count; Cephalosporins; Cystic Fibrosis; Drug Therapy, Combination; Female; Fucose; Galactose; Gene Expression; Humans; Immunoglobulin Isotypes; Leukocytes, Mononuclear; Liver Function Tests; Male; Neutrophils; Pseudomonas aeruginosa; Pseudomonas Infections; Respiratory Function Tests; Sputum; Treatment Outcome; Tumor Necrosis Factor-alpha

2008

Other Studies

39 other study(ies) available for galactose and Cystic Fibrosis

ArticleYear
Aspergillus Bronchitis in Patients with Cystic Fibrosis.
    Mycopathologia, 2018, Volume: 183, Issue:1

    Topics: Adolescent; Adult; Antifungal Agents; Antigens, Fungal; Aspergillosis; Aspergillus fumigatus; Biomarkers; Bronchitis; Child; Cystic Fibrosis; DNA, Fungal; Female; Galactose; Germany; Humans; Longitudinal Studies; Male; Mannans; Prevalence; Prospective Studies; Real-Time Polymerase Chain Reaction; Respiratory Function Tests; Retrospective Studies; Serum; Sputum; Young Adult

2018
Serum (1→3)-β-D-glucan and galactomannan levels in patients with cystic fibrosis: a retrospective cohort study.
    BMC pulmonary medicine, 2018, Mar-27, Volume: 18, Issue:1

    Topics: Adolescent; Adult; Aspergillus fumigatus; beta-Glucans; Case-Control Studies; Child; Child, Preschool; Cohort Studies; Culture Techniques; Cystic Fibrosis; Female; Forced Expiratory Volume; Galactose; Humans; Male; Mannans; Middle Aged; Multivariate Analysis; Proteoglycans; Pulmonary Aspergillosis; Retrospective Studies; Sputum; Young Adult

2018
Aspergillus terreus Causing Probable Invasive Aspergillosis in a Patient with Cystic Fibrosis.
    Mycopathologia, 2019, Volume: 184, Issue:1

    Topics: Antifungal Agents; Aspergillus; Child; Cystic Fibrosis; Drug Monitoring; Galactose; Humans; India; Invasive Pulmonary Aspergillosis; Male; Mannans; Treatment Outcome; Voriconazole

2019
Novel immunologic classification of aspergillosis in adult cystic fibrosis.
    The Journal of allergy and clinical immunology, 2013, Volume: 132, Issue:3

    Topics: Adult; Allergens; Antibodies, Fungal; Antigens, Fungal; Aspergillosis; Aspergillus fumigatus; Cystic Fibrosis; Female; Galactose; Humans; Immunoglobulin E; Immunoglobulin G; Male; Mannans; Prospective Studies; Real-Time Polymerase Chain Reaction; Skin Tests; Sputum; Young Adult

2013
Sugar administration is an effective adjunctive therapy in the treatment of Pseudomonas aeruginosa pneumonia.
    American journal of physiology. Lung cellular and molecular physiology, 2013, Volume: 305, Issue:5

    Topics: Animals; Anti-Bacterial Agents; Bacterial Adhesion; Bronchi; Carbohydrates; Cells, Cultured; Cystic Fibrosis; Fucose; Galactose; Humans; Interleukin-8; Lung Injury; Male; Mannose; Mice; Mice, Inbred BALB C; Microscopy, Fluorescence; Pneumonia, Bacterial; Polysaccharides; Pseudomonas aeruginosa; Pseudomonas Infections; Trachea

2013
Early diagnosis and treatment of invasive pulmonary aspergillosis in a patient with cystic fibrosis.
    BMJ case reports, 2013, Nov-18, Volume: 2013

    Topics: Antifungal Agents; beta-Glucans; Biomarkers; Bronchoalveolar Lavage; Child; Cystic Fibrosis; Early Diagnosis; Fatal Outcome; Galactose; Humans; Immunocompromised Host; Invasive Pulmonary Aspergillosis; Male; Mannans; Pyrimidines; Triazoles; Voriconazole

2013
Oxidation increases mucin polymer cross-links to stiffen airway mucus gels.
    Science translational medicine, 2015, Feb-25, Volume: 7, Issue:276

    Topics: Acetylcysteine; Animals; Biomechanical Phenomena; Cross-Linking Reagents; Cystic Fibrosis; Disulfides; DNA; Elasticity; Expectorants; Galactose; Gels; Humans; Lung; Mice, Inbred C57BL; Mucins; Mucus; Oxidation-Reduction; Oxidative Stress; Polymers; Reducing Agents; Sputum; Sulfhydryl Compounds

2015
Serum galactomannan in cystic fibrosis patients colonized with Aspergillus species.
    Medical mycology, 2012, Volume: 50, Issue:6

    Topics: Adolescent; Adult; Antigens, Fungal; Aspergillosis; Aspergillus fumigatus; Child; Cystic Fibrosis; Female; Forced Expiratory Volume; Galactose; Humans; Immunoenzyme Techniques; Lung; Male; Mannans; Middle Aged; Young Adult

2012
[The importance of bronchoalveolar lavage sample for galactomannan, 1,3-ß-d-glucan and PCR tests].
    Mikrobiyoloji bulteni, 2012, Volume: 46, Issue:4

    Topics: Antifungal Agents; beta-Glucans; Bronchoalveolar Lavage Fluid; Bronchoscopy; Child; Cystic Fibrosis; Galactose; Humans; Immunocompromised Host; Invasive Pulmonary Aspergillosis; Lymphoma, Large B-Cell, Diffuse; Male; Mannans; Pyrimidines; Real-Time Polymerase Chain Reaction; Tomography, X-Ray Computed; Triazoles; Voriconazole

2012
SERUM PROTEIN-BOUND CARBOHYDRATES BY PAPER ELECTROPHORESIS IN PATIENTS WITH CYSTIC FIBROSIS.
    The Journal of laboratory and clinical medicine, 1964, Volume: 63

    Topics: Adolescent; Alpha-Globulins; Beta-Globulins; Biomedical Research; Blood Glucose; Blood Protein Electrophoresis; Blood Proteins; Child; Cystic Fibrosis; Electrophoresis, Paper; Fucose; Galactose; gamma-Globulins; Glucosamine; Humans; Infant; Mannose; Neuraminic Acids; Serum Albumin; Serum Globulins

1964
Altered O-glycosylation and sulfation of airway mucins associated with cystic fibrosis.
    Glycobiology, 2005, Volume: 15, Issue:8

    Topics: Acetylgalactosamine; Acetylglucosamine; Carbohydrate Sequence; Case-Control Studies; Chromatography, High Pressure Liquid; Cystic Fibrosis; Fucose; Galactose; Gas Chromatography-Mass Spectrometry; Glycosylation; Humans; Molecular Sequence Data; Mucins; N-Acetylneuraminic Acid; Oligosaccharides; Respiratory Mucosa; Spectrometry, Mass, Fast Atom Bombardment; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Sulfates; Sulfuric Acid Esters

2005
The carbohydrate content of IgG from patients with cystic fibrosis.
    Pediatric research, 1983, Volume: 17, Issue:12

    Topics: Adolescent; Adult; Carbohydrates; Child, Preschool; Chromatography, Gas; Cystic Fibrosis; Electrophoresis, Polyacrylamide Gel; Fucose; Galactose; Glucosamine; Humans; Immunoglobulin G; Mannose; Sialic Acids

1983
Human intestinal mucin in cystic fibrosis.
    Pediatric research, 1983, Volume: 17, Issue:1

    Topics: Acetylglucosamine; Adolescent; Adult; Aged; Amino Acids; Carbohydrates; Child; Child, Preschool; Cystic Fibrosis; Female; Fucose; Galactose; Humans; Infant; Infant, Newborn; Intestine, Small; Male; Mucins; Sialic Acids

1983
Glycosyl acceptors in intact and permeabilized normal and cystic fibrosis fibroblasts.
    Journal of cellular physiology, 1983, Volume: 115, Issue:2

    Topics: Biological Transport; Cell Membrane Permeability; Cells, Cultured; Cystic Fibrosis; Galactose; Glucuronates; Glucuronic Acid; Glycoproteins; Humans; Uridine Diphosphate Sugars; Xylose

1983
Structural studies of the acidic exopolysaccharide produced by a mucoid strain of Burkholderia cepacia, isolated from cystic fibrosis.
    Carbohydrate research, 1996, May-14, Volume: 285

    Topics: Burkholderia cepacia; Carbohydrate Conformation; Carbohydrate Sequence; Chromatography, Gel; Chromatography, Ion Exchange; Cystic Fibrosis; Galactose; Glucose; Glycosaminoglycans; Magnetic Resonance Spectroscopy; Mass Spectrometry; Molecular Sequence Data; Molecular Structure; Polysaccharides, Bacterial; Pyruvic Acid

1996
Intractable diarrhoea of infancy.
    Clinics in gastroenterology, 1977, Volume: 6, Issue:2

    Topics: Carbohydrate Metabolism, Inborn Errors; Colitis; Cystic Fibrosis; Diarrhea, Infantile; Galactose; Glucose; Humans; Immunologic Deficiency Syndromes; Infant; Intestines; Megacolon; Neoplasms; Neoplasms, Germ Cell and Embryonal; Postoperative Complications

1977
Human respiratory tract secretion. Mucous glycoproteins of nonpurulent tracheobronchial secretions, and sputum of patients with bronchitis and cystic fibrosis.
    Archives of biochemistry and biophysics, 1976, Volume: 177, Issue:1

    Topics: Adolescent; Amino Acids; Bronchitis; Cystic Fibrosis; Female; Fucose; Galactose; Glycoproteins; Hexosamines; Humans; Mucus; Respiratory System; Sialic Acids; Sputum; Sulfuric Acids

1976
Heterogeneity of the carbohydrate chains of sulfated bronchial glycoproteins isolated from a patient suffering from cystic fibrosis.
    The Journal of biological chemistry, 1975, Mar-25, Volume: 250, Issue:6

    Topics: Acetamides; Amino Acids; Blood Group Antigens; Borohydrides; Carbohydrates; Cystic Fibrosis; Galactose; Glycoproteins; Humans; Neuraminic Acids; Oligosaccharides; Sputum; Sulfates

1975
Cellular differentiation regulates expression of Cl- transport and cystic fibrosis transmembrane conductance regulator mRNA in human intestinal cells.
    The Journal of biological chemistry, 1991, Mar-05, Volume: 266, Issue:7

    Topics: Biological Transport; Blotting, Northern; Cell Differentiation; Cell Line; Chlorides; Clone Cells; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Epithelium; Galactose; Gene Expression; Glucose; Humans; Intestines; Membrane Proteins; RNA, Messenger

1991
Oligosaccharide structures of the low-molecular-weight salivary mucin from a normal individual and one with cystic fibrosis.
    Journal of dental research, 1985, Volume: 64, Issue:1

    Topics: Adolescent; Adult; Chromatography, Gel; Chromatography, Paper; Cystic Fibrosis; Electrophoresis, Paper; Female; Fucose; Galactose; Humans; Hydrolysis; Male; Methylation; Molecular Weight; Mucins; Oligosaccharides; Oxidation-Reduction; Salivary Proteins and Peptides

1985
[A new pathogenic hypothesis of mucoviscidosis: hyperactivity of microsomal glycosyl-transferases].
    Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles, 1973, Jul-30, Volume: 277, Issue:5

    Topics: Amino Acids; Carbon Radioisotopes; Cystic Fibrosis; Fucose; Galactose; Glucosyltransferases; Glycoproteins; Guanine Nucleotides; Humans; In Vitro Techniques; Lung; Mannose; Microsomes; Protein Biosynthesis; Uracil Nucleotides

1973
Properties of microsomal glycoprotein galactosyltransferase of cultured human fibroblasts in relation to cystic fibrosis.
    Clinica chimica acta; international journal of clinical chemistry, 1974, Oct-30, Volume: 56, Issue:2

    Topics: Animals; Carbon Radioisotopes; Cattle; Cells, Cultured; Cystic Fibrosis; Fibroblasts; Galactose; Glycoproteins; Hexosyltransferases; Hot Temperature; Humans; Hydrogen-Ion Concentration; Kinetics; Manganese; Metals; Microsomes; Mucins; Nucleotides; Polyethylene Glycols; Sulfhydryl Reagents; Time Factors; Uridine Diphosphate Sugars

1974
Detection of inborn errors of metabolism: galactosemia.
    Science (New York, N.Y.), 1973, Mar-16, Volume: 179, Issue:4078

    Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Carbon Dioxide; Carbon Isotopes; Cells, Cultured; Cystic Fibrosis; Female; Fibroblasts; Galactose; Galactosemias; Gangliosides; Humans; Infant; Kinetics; Lactones; Lipid Metabolism, Inborn Errors; Male; Pregnancy; Prenatal Diagnosis; Skin; Tritium

1973
A new pathogenic hypothesis for cystic fibrosis: hyperactivity of glycosyl transferases at microsomic level.
    Clinica chimica acta; international journal of clinical chemistry, 1973, Nov-15, Volume: 48, Issue:4

    Topics: Amino Acids; Carbon Radioisotopes; Child; Cystic Fibrosis; Fucose; Galactose; Guanine Nucleotides; Hexosyltransferases; Humans; Kinetics; Lung; Mannose; Microsomes; Protein Biosynthesis; Time Factors

1973
The levels of galactosyltransferase activity in sera from normal children and patients with cystic fibrosis.
    Clinical biochemistry, 1974, Volume: 7, Issue:2

    Topics: Adolescent; Adult; Carbon Radioisotopes; Child; Child, Preschool; Cystic Fibrosis; Drug Stability; Evaluation Studies as Topic; Galactosamine; Galactose; Glucosamine; Hexosyltransferases; Humans; Methods; Spectrophotometry; Time Factors

1974
Polysaccharide of a mucoid E. coli isolated from a patient with cystic fibrosis.
    Nature, 1968, May-25, Volume: 218, Issue:5143

    Topics: Chromatography, Paper; Cystic Fibrosis; Escherichia coli; Fucose; Galactose; Glucose; Glucuronates; Humans; Polysaccharides, Bacterial; Uronic Acids

1968
Glycosyltransferases in human blood. II. Study of serum galactosyltransferase and N-acetylgalactosaminyltransferase in patients with liver diseases.
    The Journal of clinical investigation, 1972, Volume: 51, Issue:8

    Topics: Alanine Transaminase; Alcoholism; Aspartate Aminotransferases; Cystic Fibrosis; Galactosamine; Galactose; Hepatitis A; Hexosyltransferases; Humans; Liver; Liver Cirrhosis; Liver Diseases; Methods; Oligosaccharides; Transferases

1972
[Isolation of bronchial mucins secreted in cystic fibrosis].
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 36, Issue:2

    Topics: Animals; Bronchi; Child; Chromatography, Gel; Chromatography, Ion Exchange; Cystic Fibrosis; Electrophoresis; Fucose; Galactose; Hexosamines; Humans; Hydrogen-Ion Concentration; Immunoelectrophoresis; Mucins; Mucus; Neuraminic Acids; Rabbits; Serine; Sputum; Sulfuric Acids; Threonine

1972
Glucose-galactose malabsorption. Studies on the intermediate carbohydrate metabolism.
    Acta paediatrica Scandinavica, 1970, Volume: 59, Issue:1

    Topics: Age Factors; Blood Chemical Analysis; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Cystic Fibrosis; Female; Fructose; Galactose; Glucose; Glucose Tolerance Test; Hexoses; Humans; Infant; Male

1970
[Diagnosis of mono-and disaccharide malabsorption. Planimetric evaluation of blood glucose curves].
    Das Deutsche Gesundheitswesen, 1971, May-06, Volume: 26, Issue:19

    Topics: Blood Glucose; Child; Child, Preschool; Cystic Fibrosis; Diarrhea; Disaccharides; Dyspepsia; Galactose; Glucose Tolerance Test; Humans; Infant; Lactose; Lactose Intolerance; Malabsorption Syndromes; Monosaccharides

1971
Disaccharides and cystic fibrosis of the pancreas.
    Archives of disease in childhood, 1969, Volume: 44, Issue:233

    Topics: Child; Cystic Fibrosis; Dietary Carbohydrates; Disaccharides; Feces; Fructose; Galactose; Glycosuria; Humans; Ileum; Lactose; Lactose Intolerance; Sucrose

1969
IMMUNOLOGIC AND BIOCHEMICAL COMPARISON OF URINARY GLYCOPROTEINS IN PATIENTS WITH CYSTIC FIBROSIS OF THE PANCREAS AND NORMAL CONTROLS.
    The Journal of pediatrics, 1964, Volume: 65

    Topics: Biomedical Research; Blood Proteins; Child; Chromatography; Clinical Enzyme Tests; Cystic Fibrosis; Fucose; Glycoproteins; Hemagglutination Inhibition Tests; Hexoses; Humans; Immune Sera; Immunoelectrophoresis; Neuraminic Acids; Peptide Hydrolases; Transferrin; Urine; Uronic Acids

1964
Respiratory mucous secretions in patients with cystic fibrosis: relationship between levels of highly sulfated mucin component and severity of the disease.
    Clinica chimica acta; international journal of clinical chemistry, 1983, Aug-15, Volume: 132, Issue:2

    Topics: Cystic Fibrosis; DNA; Hexosamines; Hexoses; Humans; Mucins; Proteins; Sialic Acids; Sputum

1983
Synthesis of hemoglobin Aic and related minor hemoglobin by erythrocytes. In vitro study of regulation.
    The Journal of clinical investigation, 1979, Volume: 64, Issue:1

    Topics: Adult; Child; Cystic Fibrosis; Diabetes Mellitus; Erythrocytes; Fetal Hemoglobin; Glucose; Hemoglobin A; Hemoglobin C; Hemoglobin, Sickle; Hemoglobins; Hexoses; Humans; Hydrogen-Ion Concentration; In Vitro Techniques; Insulin; Male; Phosphorylation; Renal Dialysis; Temperature; Time Factors

1979
Decreased sialic acid and altered binding to lectins of purified alpha 2-macroglobulin from patients with cystic fibrosis.
    Clinica chimica acta; international journal of clinical chemistry, 1979, Nov-15, Volume: 99, Issue:1

    Topics: alpha-Macroglobulins; Concanavalin A; Cystic Fibrosis; Genetic Carrier Screening; Hexoses; Humans; Lectins; Sialic Acids

1979
Comparison of the carbohydrate composition of alpha 2-macroglobulin from patients with cystic fibrosis and normal controls.
    Pediatric research, 1985, Volume: 19, Issue:4

    Topics: Adolescent; alpha-Macroglobulins; Carbohydrates; Child; Cystic Fibrosis; Female; Glucosamine; Hexoses; Humans; Male; Sialic Acids

1985
Transport of labelled compounds in control and cystic-fibrosis cells in vitro.
    Lancet (London, England), 1972, Jan-22, Volume: 1, Issue:7743

    Topics: Amino Acids; Biological Transport; Carbon Isotopes; Cell Line; Centrifugation; Cystic Fibrosis; Dialysis; Fibroblasts; Hexoses; Humans; In Vitro Techniques; Plasma; Saliva; Time Factors; Tritium

1972
Variations in human urinary O-hydroxylysyl glycoside levels and their relationship to collagen metabolism.
    The Journal of clinical investigation, 1970, Volume: 49, Issue:8

    Topics: Achondroplasia; Adolescent; Adult; Aged; Amino Acids; Arthritis, Rheumatoid; Bone and Bones; Bronchiolitis, Viral; Cartilage; Child; Child, Preschool; Chromatography; Chromatography, Gel; Chromatography, Paper; Collagen; Cystic Fibrosis; Diarrhea; Dietary Proteins; Ehlers-Danlos Syndrome; Electrophoresis; Female; Gelatin; Glycosides; Hexoses; Humans; Hydroxyproline; Lupus Erythematosus, Systemic; Male; Marfan Syndrome; Osteogenesis Imperfecta; Paper; Protein Hydrolysates; Scleroderma, Systemic; Tendons

1970
Salivary mucins of patients with cystic fibrosis. Composition and susceptibility to degradation by salivary glycosidases.
    Gastroenterology, 1970, Volume: 59, Issue:2

    Topics: Cystic Fibrosis; Fucose; Galactosidases; Glucosidases; Glycoside Hydrolases; Hexosamines; Hexoses; Humans; Hydrogen-Ion Concentration; Mucins; Neuraminic Acids; Neuraminidase; Protein Binding; Saliva

1970