Defective Glycosaminoglycan Substitution of Decorin in a Patient With Progeroid Syndrome Is a Direct Consequence of Two Point Mutations in the Galactosyltransferase I (�4galT-7) Gene-Reference-Cited by-同舟云学术

Defective Glycosaminoglycan Substitution of Decorin in a Patient With Progeroid Syndrome Is a Direct Consequence of Two Point Mutations in the Galactosyltransferase I (�4galT-7) Gene

Published:2005-02 Issue:1-2 Volume:43 Page:65-77
ISSN:0006-2928
Container-title:Biochemical Genetics
language:en
Short-container-title:Biochem Genet

Author:

G�tte Martin,Kresse Hans

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine,Ecology, Evolution, Behavior and Systematics,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s10528-005-1068-2.pdf

Reference32 articles.

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2. Amado, M., Almeida, R., Schwientek, T., and Clausen, H. (1999). Identification and characterization of large galactosyltransferase gene families: Galactosyltransferases for all functions. Biochim. Biophys. Acta 1473:35.

3. Bernfield, M., G�tte, M., Park, P. W., Reizes, O., Fitzgerald, M. L., Lincecum, J., and Zako, M. (1999). Functions of cell surface heparan sulfate proteoglycans. Annu. Rev. Biochem. 68:729.

4. Bonner, W. M., and Laskey, R. A. (1974). A film detection method for tritium-labelled proteins and nucleic acids in polyacrylamide gels. Eur. J. Biochem. 46:83.

5. Breuer, B., Quentin, E., Cully, Z., G�tte, M., and Kresse, H. (1991). A novel large dermatan sulfate proteoglycan from human fibroblasts. J. Biol. Chem. 266:13224.

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