Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1968 Jan;59(1):254–261. doi: 10.1073/pnas.59.1.254

Glycolipids of hamster fibroblasts and derived malignant-transformed cell lines.

S I Hakomori, W T Murakami
PMCID: PMC286029  PMID: 4298334

Full text

PDF
254

Images in this article

Selected References

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

  1. AUB J. C., TIESLAU C., LANKESTER A. REACTIONS OF NORMAL AND TUMOR CELL SURFACES TO ENZYMES. I. WHEAT-GERM LIPASE AND ASSOCIATED MUCOPOLYSACCHARIDES. Proc Natl Acad Sci U S A. 1963 Oct;50:613–619. doi: 10.1073/pnas.50.4.613. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BARTHOLOMAY A. F. A stochastic approach to statistical kinetics with application to enzyme kinetics. Biochemistry. 1962 Mar;1:223–230. doi: 10.1021/bi00908a005. [DOI] [PubMed] [Google Scholar]
  3. Burger M. M., Goldberg A. R. Identification of a tumor-specific determinant on neoplastic cell surfaces. Proc Natl Acad Sci U S A. 1967 Feb;57(2):359–366. doi: 10.1073/pnas.57.2.359. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. CARTER H. E., JOHNSON P., WEBER E. J. GLYCOLIPIDS. Annu Rev Biochem. 1965;34:109–142. doi: 10.1146/annurev.bi.34.070165.000545. [DOI] [PubMed] [Google Scholar]
  5. DISCHE Z. New color reactions for determination of sugars in polysaccharides. Methods Biochem Anal. 1955;2:313–358. doi: 10.1002/9780470110188.ch11. [DOI] [PubMed] [Google Scholar]
  6. FORRESTER J. A., AMBROSE E. J., STOKER M. G. MICROELECTROPHORESIS OF NORMAL AND TRANSFORMED CLONES OF HAMSTER KIDNEY FIBROBLASTS. Nature. 1964 Feb 29;201:945–946. doi: 10.1038/201945a0. [DOI] [PubMed] [Google Scholar]
  7. HAKOMORI S., JEANLOZ R. W. ISOLATION OF A GLYCOLIPID CONTAINING FUCOSE, GALACTOSE, GLUCOSE, AND GLUCOSAMINE FROM HUMAN CANCEROUS TISSUE. J Biol Chem. 1964 Oct;239:PC3606–PC3607. [PubMed] [Google Scholar]
  8. Hakomori S. I., Koscielak J., Bloch K. J., Jeanloz R. W. Immunologic relationship between blood group substances and a fucose-containing glycolipid of human adenocarcinoma. J Immunol. 1967 Jan;98(1):31–38. [PubMed] [Google Scholar]
  9. Hakomori S. I. Release of carbohydrates from sphingoglycolipid by osmium-catalyzed periodate oxidation followed by treatment with mild alkali. J Lipid Res. 1966 Nov;7(6):789–792. [PubMed] [Google Scholar]
  10. KAY H. E., WALLACE D. M. A and B antigens of tumors arising from urinary epithelium. J Natl Cancer Inst. 1961 Jun;26:1349–1365. [PubMed] [Google Scholar]
  11. Kalckar H. M. Galactose metabolism and cell "sociology". Science. 1965 Oct 15;150(3694):305–313. doi: 10.1126/science.150.3694.305. [DOI] [PubMed] [Google Scholar]
  12. Kean E. L. Separation of gluco- and galactocerebrosides by means of borate thin-layer chromatography. J Lipid Res. 1966 May;7(3):449–452. [PubMed] [Google Scholar]
  13. Makita A., Suzuki C., Yosizawa Z., Konno T. Glycolipids isolated from the spleen of Gaucher's disease. Tohoku J Exp Med. 1966 Mar 25;88(3):277–288. doi: 10.1620/tjem.88.277. [DOI] [PubMed] [Google Scholar]
  14. NIKAIDO H. Galactose-sensitive mutants of Salmonella. I. Metabolism of galactose. Biochim Biophys Acta. 1961 Apr 15;48:460–469. doi: 10.1016/0006-3002(61)90044-0. [DOI] [PubMed] [Google Scholar]
  15. RAPPORT M. M., GRAF L., SKIPSKI V. P., ALONZO N. F. Immunochemical studies of organ and tumor lipids. VI. Isolation and properties of cytolipin H. Cancer. 1959 May-Jun;12(3):438–445. doi: 10.1002/1097-0142(195905/06)12:3<438::aid-cncr2820120303>3.0.co;2-o. [DOI] [PubMed] [Google Scholar]
  16. Robinson E. A., Kalckar H. M., Troedsson H., Sanford K. Metabolic inhibition of mammalian uridine diphosphate galactose 4-epimerase in cell cultures and in tumor cells. J Biol Chem. 1966 Jun 25;241(12):2737–2745. [PubMed] [Google Scholar]
  17. SAMBASIVARAO K., MCCLUER R. H. THIN-LAYER CHROMATOGRAPHIC SEPARATION OF SPHINGOSINE AND RELATED BASES. J Lipid Res. 1963 Jan;4:106–108. [PubMed] [Google Scholar]
  18. Suzuki K., Chen G. C. Brain ceramide hexosides in Tay-Sachs disease and generalized gangliosidosis (GM1-gangliosidosis). J Lipid Res. 1967 Mar;8(2):105–113. [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES