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. 1971 Feb;64(2):185–186.

Fibroblast culture and inherited neurological diseases.

G Stewart
PMCID: PMC1812459  PMID: 4251358

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Selected References

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

  1. Danes B. S., Bearn A. G. Hurler's syndrome: demonstration of an inherited disorder of connective tissue in cell culture. Science. 1965 Aug 27;149(3687):987–989. doi: 10.1126/science.149.3687.987. [DOI] [PubMed] [Google Scholar]
  2. Foley K. M., Danes B. S., Bearn A. G. White blood cell cultures in genetic studies on the human mucopolysaccharidoses. Science. 1969 Apr 25;164(3878):424–426. doi: 10.1126/science.164.3878.424. [DOI] [PubMed] [Google Scholar]
  3. Fratantoni J. C., Hall C. W., Neufeld E. F. The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide. Proc Natl Acad Sci U S A. 1968 Jun;60(2):699–706. doi: 10.1073/pnas.60.2.699. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ho M. W., O'Brien J. S. Hurler's syndrome: deficiency of a specific beta galactosidase isoenzyme. Science. 1969 Aug 8;165(3893):611–613. doi: 10.1126/science.165.3893.611. [DOI] [PubMed] [Google Scholar]
  5. KROOTH R. S., WEINBERG A. N. Properties of galactosemic cells in culture. Biochem Biophys Res Commun. 1960 Nov;3:518–524. doi: 10.1016/0006-291x(60)90167-4. [DOI] [PubMed] [Google Scholar]
  6. MacBrinn M. C., Okada S., Ho M. W., Hu C. C., O'Brien J. S. Generalized gangliosidosis: impaired cleavage of galactose from a mucopolysaccharide and a glycoprotien. Science. 1969 Feb 28;163(3870):946–947. doi: 10.1126/science.163.3870.946. [DOI] [PubMed] [Google Scholar]
  7. Matalon R., Dorfman A. Acid mucopolysaccharides in cultured human fibroblasts. Lancet. 1969 Oct 18;2(7625):838–841. doi: 10.1016/s0140-6736(69)92289-2. [DOI] [PubMed] [Google Scholar]
  8. Matalon R., Dorfman A., Dawson G., Sweeley C. C. Glycolipid and mucopolysaccharide abnormality in fibroblasts of fabry's disease. Science. 1969 Jun 27;164(3887):1522–1523. doi: 10.1126/science.164.3887.1522. [DOI] [PubMed] [Google Scholar]
  9. Nadler H. L., Wodnicki J. M., Swae M. A., O'Flynn M. E. Cultivated amniotic-fluid cells and fibroblasts derived from families with cystic fibrosis. Lancet. 1969 Jul 12;2(7611):84–85. doi: 10.1016/s0140-6736(69)92393-9. [DOI] [PubMed] [Google Scholar]
  10. Steinberg D., Herndon J. H., Jr, Uhlendorf B. W., Mize C. E., Avigan J., Milne G. W. Refsum's disease: nature of the enzyme defect. Science. 1967 Jun 30;156(3783):1740–1742. doi: 10.1126/science.156.3783.1740. [DOI] [PubMed] [Google Scholar]
  11. Swift M. R., Finegold M. J. Myotonic muscular dystrophy: abnormalities in fibroblast culture. Science. 1969 Jul 18;165(3890):294–295. doi: 10.1126/science.165.3890.294. [DOI] [PubMed] [Google Scholar]
  12. Taysi K., Kistenmacher M. L., Punnett H. H., Mellman W. J. Limitations of metachromasia as a diagnostic aid in pediatrics. N Engl J Med. 1969 Nov 13;281(20):1108–1111. doi: 10.1056/NEJM196911132812009. [DOI] [PubMed] [Google Scholar]
  13. Uhlendorf B. W., Mudd S. H. Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria. Science. 1968 May 31;160(3831):1007–1009. doi: 10.1126/science.160.3831.1007. [DOI] [PubMed] [Google Scholar]

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