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  Anion transport and 2,3-diphosphoglycerate in cystic fibrosis red blood cells

Berghout, A. G., & Bender, S. (1984). Anion transport and 2,3-diphosphoglycerate in cystic fibrosis red blood cells. Pediatric Research, 18(10), 1017-1020. doi:10.1203/00006450-198410000-00021.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0008-CD55-2 Version Permalink: https://hdl.handle.net/21.11116/0000-0008-CD56-1
Genre: Journal Article

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 Creators:
Berghout, Alexander G.R.V.1, Author           
Bender, S.W.2, Author
Affiliations:
1Department of Cell Physiology, Max Planck Institute of Biophysics, Max Planck Society, ou_3264817              
2Zentrum der Kinderheilkunde, Johann Wolfgang Goethe Universität, Frankfurt am Main, Federal Republic of Germany, ou_persistent22              

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 Abstract: 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.

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Language(s): eng - English
 Dates: 1983-11-251984-03-191984-10-01
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1203/00006450-198410000-00021
PMID: 6493845
 Degree: -

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Title: Pediatric Research
Source Genre: Journal
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Publ. Info: Baltimore, MD : Lippincott Williams & Wilkins
Pages: - Volume / Issue: 18 (10) Sequence Number: - Start / End Page: 1017 - 1020 Identifier: ISSN: 0031-3998
CoNE: https://pure.mpg.de/cone/journals/resource/954925432366