lactose has been researched along with Cystic Fibrosis of Pancreas in 23 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 15 (65.22) | 18.7374 |
| 1990's | 3 (13.04) | 18.2507 |
| 2000's | 4 (17.39) | 29.6817 |
| 2010's | 1 (4.35) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Britton, WJ; Chan, HK; Chang, RYK; Kutter, E; Li, J; Lin, Y; Morales, S | 1 |
| Glick, MC; Klink, DT; Scanlin, TF | 1 |
| Glick, MC; Klink, D; Scanlin, T; Yu, QC | 1 |
| GABRIELSON, IW; GRYBOSKI, JD; SPIRO, HM; THAYER, WR | 1 |
| JONES, RH | 1 |
| BERIO, A; LAMEDICA, GM; NORDIO, S; VIGNOLO, L | 1 |
| Boshard, R; Daly, JA; Matsen, JM | 1 |
| Erbacher, P; Glick, MC; Kollen, WJ; Midoux, P; Monsigny, M; Roche, AC; Scanlin, TF; Yip, A | 1 |
| Davidson, GP; Lewindon, PJ; Martin, AJ; Moore, DJ; Robb, TA | 1 |
| Gerwig, GJ; Glick, MC; Kollen, WJ; Scanlin, TF; Schembri, FM; Vliegenthart, JF | 1 |
| Chao, S; Glick, MC; Klink, DT; Scanlin, TF | 1 |
| Aron, Y; Briand, P; Fajac, I; Grosse, S; Tremeau-Bravard, A | 1 |
| Antonowicz, I; Ishida, S; Shwachman, H | 1 |
| Govan, JR | 1 |
| Flux, M; Rennert, OR; Seale, TW; Shiffman, ML; Swender, PT | 1 |
| Fric, P; Jodl, J; Lojda, Z | 1 |
| Brügmann, G; Drees, N; Niessen, KH; Osswald, P; Schmidt, K | 1 |
| Alpers, DH; Isselbacher, KJ | 1 |
| Brügmann, G; Niessen, KH; Schmidt, K | 1 |
| Antonowicz, I; Shwachman, H; Sotoo, I | 1 |
| Grävinghoff, J | 1 |
| Antonowicz, I; Khaw, KT; Reddy, V; Shwachman, H | 1 |
| Gibbons, IS | 1 |
2 review(s) available for lactose and Cystic Fibrosis of Pancreas
| Article | Year |
|---|---|
Gene therapy of cystic fibrosis (CF) airways: a review emphasizing targeting with lactose.
Topics: Animals; Cell Nucleus; Cystic Fibrosis; DNA, Complementary; Epithelial Cells; Gene Expression; Gene Transfer Techniques; Genes, Reporter; Genetic Therapy; Glycosylation; Humans; Lactose; Polylysine; Respiratory System | 2001 |
Disaccharidase deficiency.
Topics: Adult; Amylases; Animals; Biopsy; Carbohydrate Metabolism, Inborn Errors; Child; Cystic Fibrosis; Dietary Carbohydrates; Disaccharides; Feces; Galactosidases; Glucosidases; Glycogen; Glycoside Hydrolases; Humans; Hydrogen-Ion Concentration; Infant, Newborn; Intestinal Diseases; Intestinal Mucosa; Intestine, Small; Intestines; Lactose; Lactose Intolerance; Malabsorption Syndromes; Osteoporosis; Postgastrectomy Syndromes; Racial Groups; Radiography; Starch; Sucrase | 1970 |
21 other study(ies) available for lactose and Cystic Fibrosis of Pancreas
| Article | Year |
|---|---|
Inhalable combination powder formulations of phage and ciprofloxacin for P. aeruginosa respiratory infections.
Topics: Administration, Inhalation; Aerosols; Anti-Bacterial Agents; Bacteriophages; Chemistry, Pharmaceutical; Ciprofloxacin; Cystic Fibrosis; Dry Powder Inhalers; Excipients; Humans; Lactose; Nebulizers and Vaporizers; Particle Size; Powders; Pseudomonas aeruginosa; Pseudomonas Infections; Respiratory Tract Infections | 2019 |
Lactosylated poly-L-lysine targets a potential lactose receptor in cystic fibrosis and non-cystic fibrosis airway epithelial cells.
Topics: Cells, Cultured; Clathrin; Coated Pits, Cell-Membrane; Cystic Fibrosis; DNA, Complementary; Endocytosis; Epithelial Cells; Humans; Lactose; Microscopy, Electron; Polylysine; Trachea | 2003 |
DISACCHARIDURIA IN GASTROINTESTINAL DISEASE.
Topics: Celiac Disease; Child; Chromatography; Crohn Disease; Cystic Fibrosis; Enteritis; Gastrointestinal Diseases; Humans; Infant; Lactose; Sucrose; Urine | 1963 |
DISACCHARIDE INTOLERANCE AND MUCOVISCIDOSIS.
Topics: Blood Glucose; Carbohydrate Metabolism; Cystic Fibrosis; Diarrhea; Humans; Infant; Lactose; Maltose; Sucrose | 1964 |
DISACCHARIDE INTOLERANCE AND MUCOVISCIDOSIS.
Topics: Cystic Fibrosis; Diagnosis, Differential; Humans; Lactose; Lactose Intolerance; Malabsorption Syndromes; Pathology | 1964 |
Differential primary plating medium for enhancement of pigment production by Pseudomonas aeruginosa.
Topics: Culture Media; Cystic Fibrosis; Fermentation; Gram-Negative Bacteria; Humans; Lactose; Oligopeptides; Organic Chemicals; Phenazines; Pigments, Biological; Pseudomonas aeruginosa; Pyocyanine; Sputum | 1984 |
Gluconoylated and glycosylated polylysines as vectors for gene transfer into cystic fibrosis airway epithelial cells.
Topics: Cell Count; Cells, Cultured; Chloroquine; Cystic Fibrosis; Epithelium; Gene Expression; Gene Transfer Techniques; Genes, Reporter; Genetic Therapy; Genetic Vectors; Gluconates; Glycosylation; Humans; Lactones; Lactose; Luciferases; Plasmids; Polylysine; Trachea; Transfection | 1996 |
Bowel dysfunction in cystic fibrosis: importance of breath testing.
Topics: Breath Tests; Carbohydrate Metabolism; Child; Child, Preschool; Cystic Fibrosis; Digestive System; Gastrointestinal Transit; Humans; Hydrogen; Infant; Intestinal Diseases; Lactose; Malabsorption Syndromes; Sucrose | 1998 |
Enhanced efficiency of lactosylated poly-L-lysine-mediated gene transfer into cystic fibrosis airway epithelial cells.
Topics: Amino Acid Sequence; Cell Line, Transformed; Chloroquine; Cystic Fibrosis; Gene Expression Regulation; Gene Transfer Techniques; Genetic Vectors; Glycerol; Humans; Lactose; Luciferases; Molecular Sequence Data; Nasal Mucosa; Polylysine | 1999 |
Nuclear translocation of lactosylated poly-L-lysine/cDNA complex in cystic fibrosis airway epithelial cells.
Topics: Cell Line, Transformed; Cell Nucleus; Chloroquine; Cystic Fibrosis; DNA, Complementary; Epithelial Cells; Gene Expression Regulation; Gene Transfer Techniques; Genetic Vectors; Humans; Immunoenzyme Techniques; Lactose; Microscopy, Confocal; Polylysine | 2001 |
Intracellular rate-limiting steps of gene transfer using glycosylated polylysines in cystic fibrosis airway epithelial cells.
Topics: Cystic Fibrosis; Epithelial Cells; Gene Expression; Genetic Therapy; Genetic Vectors; Humans; Lactose; Luciferases; Lysine; Mannose; Plasmids; Respiratory Mucosa; Second Messenger Systems; Transcription, Genetic; Tumor Cells, Cultured | 2002 |
Letter: Screening for cystic fibrosis.
Topics: Albumins; Cystic Fibrosis; False Positive Reactions; Humans; Infant, Newborn; Infant, Newborn, Diseases; Lactose; Meconium; Proteins; Sweat | 1976 |
Mucoid strains of Pseudomonas aeruginosa: the influence of culture medium on the stability of mucus production.
Topics: Acetylcysteine; Cetrimonium Compounds; Citrates; Culture Media; Cystic Fibrosis; Deoxycholic Acid; Ferric Compounds; Humans; Lactose; Mucus; Neutral Red; Phosphatidylcholines; Polysorbates; Pseudomonas aeruginosa; Sodium Dodecyl Sulfate; Species Specificity; Surface-Active Agents; Thiosulfates | 1975 |
Breast-milk composition in women with cystic fibrosis: report of two cases and a review of the literature.
Topics: Adult; Breast Feeding; Chlorides; Cystic Fibrosis; Female; Humans; Lactose; Milk Proteins; Milk, Human; Potassium; Pregnancy; Pregnancy Complications; Sodium | 1989 |
[Histochemical findings in the small-intestine mucosa in disorders of carbohydrate absorption disorders].
Topics: Biopsy; Celiac Disease; Cystic Fibrosis; Disaccharides; Glycoside Hydrolases; Histocytochemistry; Humans; Intestinal Absorption; Intestinal Mucosa; Jejunum; Lactose; Lactose Intolerance; Malabsorption Syndromes; Microscopy, Electron; Whipple Disease | 1972 |
[Resorption of fat with and without pancreas enzyme substitution in children with mucoviscidosis (author's transl)].
Topics: Atrophy; Biopsy; Child; Child, Preschool; Cystic Fibrosis; Dietary Fats; Duodenum; Enzyme Therapy; Female; Humans; Infant; Intestinal Absorption; Intestinal Mucosa; Lactose; Male; Xylose | 1973 |
[Lactase deficiency in children with cystic fibrosis of the pancreas (CFP)].
Topics: Biopsy; Child; Child, Preschool; Cystic Fibrosis; Humans; Infant; Intestinal Mucosa; Lactose; Lactose Intolerance; Xylose | 1972 |
Beta-galactosidase and beta-glucuronidase activities in intestinal mucosa of infants and children.
Topics: Adolescent; Biopsy; Celiac Disease; Child; Child, Preschool; Cystic Fibrosis; Diarrhea, Infantile; Duodenum; Female; Galactosidases; Glucuronidase; Glycoside Hydrolases; Growth Disorders; Humans; Infant; Intestinal Mucosa; Lactose; Male; Nutrition Disorders; Pancreatic Diseases; Protein-Losing Enteropathies | 1971 |
[Diagnosis of mono-and disaccharide malabsorption. Planimetric evaluation of blood glucose curves].
Topics: Blood Glucose; Child; Child, Preschool; Cystic Fibrosis; Diarrhea; Disaccharides; Dyspepsia; Galactose; Glucose Tolerance Test; Humans; Infant; Lactose; Lactose Intolerance; Malabsorption Syndromes; Monosaccharides | 1971 |
Lactase deficiency in patients with cystic fibrosis.
Topics: Adolescent; Adult; Age Factors; Biopsy; Child; Child, Preschool; Cystic Fibrosis; Disaccharides; Duodenum; Female; Glucose Tolerance Test; Humans; Infant; Intestinal Mucosa; Lactose; Lactose Intolerance; Male; Proteins; Sex Factors | 1968 |
Disaccharides and cystic fibrosis of the pancreas.
Topics: Child; Cystic Fibrosis; Dietary Carbohydrates; Disaccharides; Feces; Fructose; Galactose; Glycosuria; Humans; Ileum; Lactose; Lactose Intolerance; Sucrose | 1969 |