putrescine has been researched along with Cystic Fibrosis in 7 studies
Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Putrescine transport was examined in normal and cystic fibrosis fibroblasts." | 7.65 | Membrane function in cystic fibrosis. I. Putrescine transport in normal and cystic fibrosis fibroblasts. ( DeBusk, AG; Kelly, JC, 1977) |
| "Serum putrescine (Pu), spermidine (Sd), spermine (Sp), and plasma diamine oxidase ativity (DAO) were determined in cystic fibrosis (CF) homozygotes and heterozygotes plus age-matched controls." | 3.66 | Age-related abnormalities of circulating polyamines and diamine oxidase activity in cystic fibrosis heterozygotes and homozygotes. ( Baylin, SB; Lockwood, DH; Marton, LJ; Rosenstein, BJ, 1980) |
| "Children with cystic fibrosis excreted elevated urinary levels of all three polyamines--putrescine, spermidine, and spermine." | 3.66 | Altered polyamine metabolism in cystic fibrosis. ( Barnett, DR; Beckerman, RC; Durie, BG; Rosenblum, MG; Russell, DH; Taussig, LM, 1979) |
| "Putrescine transport was examined in normal and cystic fibrosis fibroblasts." | 3.65 | Membrane function in cystic fibrosis. I. Putrescine transport in normal and cystic fibrosis fibroblasts. ( DeBusk, AG; Kelly, JC, 1977) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Russell, DH | 2 |
| Gahl, WA | 1 |
| Pitot, HC | 1 |
| Baylin, SB | 1 |
| Rosenstein, BJ | 1 |
| Marton, LJ | 1 |
| Lockwood, DH | 1 |
| Rosenblum, MG | 1 |
| Beckerman, RC | 1 |
| Durie, BG | 1 |
| Taussig, LM | 1 |
| Barnett, DR | 1 |
| Buehler, B | 1 |
| Wright, R | 1 |
| Schott, S | 1 |
| Darby, B | 1 |
| Rennert, OM | 1 |
| Lungren, DW | 1 |
| Hankins, JM | 1 |
| Ulane, MM | 1 |
| Willison, JW | 1 |
| Kelly, JC | 1 |
| DeBusk, AG | 1 |
1 review available for putrescine and Cystic Fibrosis
| Article | Year |
|---|---|
Clinical relevance of polyamines.
Topics: Animals; Cadaverine; Cystic Fibrosis; Diamines; Female; Growth Disorders; Humans; Kidney Failure, Ch | 1983 |
6 other studies available for putrescine and Cystic Fibrosis
| Article | Year |
|---|---|
Diamine oxidase activity in fibroblasts from normal and cystic fibrosis patients.
Topics: Amine Oxidase (Copper-Containing); Cells, Cultured; Cystic Fibrosis; Fibroblasts; Humans; Putrescine | 1980 |
Age-related abnormalities of circulating polyamines and diamine oxidase activity in cystic fibrosis heterozygotes and homozygotes.
Topics: Adolescent; Adult; Age Factors; Amine Oxidase (Copper-Containing); Child; Child, Preschool; Cystic F | 1980 |
Altered polyamine metabolism in cystic fibrosis.
Topics: Adult; Child; Child, Preschool; Cystic Fibrosis; Female; Heterozygote; Humans; Male; Polyamines; Put | 1979 |
Ornithine decarboxylase and S-adenosyl methionine decarboxylase in skin fibroblasts of normal and cystic fibrosis patients.
Topics: Adenosylmethionine Decarboxylase; Adult; Carboxy-Lyases; Cells, Cultured; Child, Preschool; Cystic F | 1977 |
Putrescine uptake in cystic fibrosis fibroblasts.
Topics: Cell Line; Cells, Cultured; Cystic Fibrosis; Fibroblasts; Humans; Kinetics; Putrescine | 1977 |
Membrane function in cystic fibrosis. I. Putrescine transport in normal and cystic fibrosis fibroblasts.
Topics: Biological Transport; Cell Line; Cystic Fibrosis; Fibroblasts; Humans; Putrescine; Skin | 1977 |