Cellular expression of the beige mouse mutation and its correction in hybrids with control human fibroblasts
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Developmental Biology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF02631368.pdf
Reference42 articles.
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3. Boxer, L. A.; Albertini, D. F.; Baehner, R. L., et al. Impaired microtubule assembly and polymorphonuclear function in Chediak-Higashi syndrome correctable by ascorbic acid. Br. J. Haematol. 43:207–213; 1979.
4. Boxer, L. A.; Rister, M.; Allen, J. M., et al. Improvement of Chediak-Higashi leukocyte function by cyclic guanosine monophosphate. Blood 49:9–17; 1977.
5. Bradford, M. A rapid and sensitive method for the quantitating of microgram quantities of protein utilizing the principle of protein dye binding. Anal. Biochem. 72:248–254; 1976.
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1. An Established Light Ear Mutant (C57BL/6J-Pdebrd1 le) Mouse Cell Line Exhibits a Block to Secretion of Lysosomal Enzymes;Experimental Cell Research;2000-04
2. The Effect of Lysosomotropic Amines onBeigeMouse Cells;Experimental Cell Research;1997-11-25
3. Enlarged dysmorphic lysosomes in an established beige (C57BL/6J;bg J/bg J) mouse mutant fibroblast line: A reversible characteristic;In Vitro Cellular & Developmental Biology - Animal;1996-09
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