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. 1968 Jun;60(2):614–621. doi: 10.1073/pnas.60.2.614

Interfacial reaggregation of ultrasonically disrupted erythrocyte membranes.

R G Kirk
PMCID: PMC225091  PMID: 5248818

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. AMES B. N., DUBIN D. T. The role of polyamines in the neutralization of bacteriophage deoxyribonucleic acid. J Biol Chem. 1960 Mar;235:769–775. [PubMed] [Google Scholar]
  2. Butler T. F., Smith G. L., Grula E. A. Bacterial cell membranes. I. Reaggregation of membrane subunits from Micrococcus lysodeikticus. Can J Microbiol. 1967 Nov;13(11):1471–1479. doi: 10.1139/m67-195. [DOI] [PubMed] [Google Scholar]
  3. DODGE J. T., MITCHELL C., HANAHAN D. J. The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes. Arch Biochem Biophys. 1963 Jan;100:119–130. doi: 10.1016/0003-9861(63)90042-0. [DOI] [PubMed] [Google Scholar]
  4. Engelman D. M., Terry T. M., Morowitz H. J. Characterization of the plasma membrane of Mycoplasma laidlawii. I. Sodium dodecyl sulfate solubilization. Biochim Biophys Acta. 1967 Jul 3;135(3):381–390. doi: 10.1016/0005-2736(67)90028-4. [DOI] [PubMed] [Google Scholar]
  5. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  6. MANILOFF J., MOROWITZ H. J., BARRNETT R. J. STUDIES OF THE ULTRASTRUCTURE AND RIBOSOMAL ARRANGEMENTS OF THE PLEUROPNEUMONIA-LIKE ORGANISM A5969. J Cell Biol. 1965 Apr;25:139–150. doi: 10.1083/jcb.25.1.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Marchesi V. T., Palade G. E. The localization of Mg-Na-K-activated adenosine triphosphatase on red cell ghost membranes. J Cell Biol. 1967 Nov;35(2):385–404. doi: 10.1083/jcb.35.2.385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Mueller P., Rudin D. O. Action potential phenomena in experimental bimolecular lipid membranes. Nature. 1967 Feb 11;213(5076):603–604. doi: 10.1038/213603a0. [DOI] [PubMed] [Google Scholar]
  9. Razin S., Morowitz H. J., Terry T. M. Membrane subunits of Mycoplasma laidlawii and their assembly to membranelike structures. Proc Natl Acad Sci U S A. 1965 Jul;54(1):219–225. doi: 10.1073/pnas.54.1.219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Salton M. R., Netschey A. Physical chemistry of isolated bacterial membranes. Biochim Biophys Acta. 1965 Oct 18;107(3):539–545. doi: 10.1016/0304-4165(65)90198-4. [DOI] [PubMed] [Google Scholar]
  11. Tosteson D. C. Some properties of HK and LK sheep red cell membrane fragements and their relevance to active transport of K and NA. Trans N Y Acad Sci. 1965 Jun;27(8):970–977. doi: 10.1111/j.2164-0947.1965.tb02339.x. [DOI] [PubMed] [Google Scholar]
  12. Wheeler K. P., Whittam R. Structural and enzymic aspects of the hydrolysis of adenosine triphosphate by membranes of kidney cortex and erythrocytes. Biochem J. 1964 Nov;93(2):349–363. doi: 10.1042/bj0930349. [DOI] [PMC free article] [PubMed] [Google Scholar]

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