Anion Transport and 2,3-Diphosphoglycerate in Cystic Fibrosis Red Blood Cells
| Autor: | Alexander G.R.V. Berghout, S.W. Bender |
|---|---|
| Rok vydání: | 1984 |
| Předmět: |
medicine.medical_specialty
Pathology Cell Membrane Permeability Cell membrane permeability Cystic Fibrosis Sodium chemistry.chemical_element Cystic fibrosis Divalent Chlorides Internal medicine medicine Humans Protein pattern Diphosphoglycerate 2 3-Diphosphoglycerate chemistry.chemical_classification Erythrocyte Membrane Diphosphoglyceric Acids medicine.disease Kinetics Erythrocyte membrane Endocrinology chemistry Pediatrics Perinatology and Child Health Electrophoresis Polyacrylamide Gel |
| Zdroj: | Pediatric Research. 18:1017-1020 |
| ISSN: | 1530-0447 0031-3998 |
| DOI: | 10.1203/00006450-198410000-00021 |
| Popis: | The monovalent and divalent anion transport in red blood cells from patients with cystic fibrosis and controls is not significantly different. The protein pattern of the erythrocyte membrane, as seen by sodium dodecyl sulfate-polyacrylamide gel electropherograms, is similar in cystic fibrosis and control red blood cells. The 2,3-diphosphoglycerate content of the investigated cystic fibrosis red blood cells is normal. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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