Format
Items per page
Sort by

Send to:

Choose Destination

Results: 16

Related Articles by Review for PubMed (Select 8405810)

1.
2.

Aspartylglycosaminuria: biochemistry and molecular biology.

Aronson NN Jr.

Biochim Biophys Acta. 1999 Oct 8;1455(2-3):139-54. Review.

3.

Mutations causing aspartylglucosaminuria (AGU): a lysosomal accumulation disease.

Ikonen E, Peltonen L.

Hum Mutat. 1992;1(5):361-5. Review.

PMID:
1301945
4.
5.

Aspartylglycosaminuria: an inborn error of glycoprotein catabolism.

Maury CP.

J Inherit Metab Dis. 1982;5(4):192-6. Review.

PMID:
6820440
6.

[Disorders of glycoprotein degradation].

Yoshida K, Yanagisawa N.

Nihon Rinsho. 1995 Dec;53(12):2973-81. Review. Japanese.

PMID:
8577045
7.

[Metabolic pathway of the degradation of macromolecules by lysosomal enzymes].

Arai K, Ohkuma S.

Nihon Rinsho. 1995 Dec;53(12):2904-10. Review. Japanese.

PMID:
8577033
9.

Disorders of glycoprotein degradation.

Cantz M, Ulrich-Bott B.

J Inherit Metab Dis. 1990;13(4):523-37. Review.

PMID:
2122119
10.

Lysosomal degradation of Asn-linked glycoproteins.

Aronson NN Jr, Kuranda MJ.

FASEB J. 1989 Dec;3(14):2615-22. Review.

11.

[Aspartylglucosaminuria].

Yamaguchi S.

Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):466-8. Review. Japanese. No abstract available.

PMID:
9645112
12.

[Lysosomal storage diseases--an overview].

Kloska A, Tylki-Szymańska A, Wegrzyn G.

Postepy Biochem. 2011;57(2):128-32. Review. Polish.

PMID:
21913413
13.

Lysosomal storage diseases.

Gieselmann V.

Biochim Biophys Acta. 1995 Apr 24;1270(2-3):103-36. Review. No abstract available.

14.

Cathepsin A/protective protein: an unusual lysosomal multifunctional protein.

Hiraiwa M.

Cell Mol Life Sci. 1999 Dec;56(11-12):894-907. Review.

PMID:
11212324
15.

Aspartylglucosaminuria (AGU): protein and gene structure of normal and mutated aspartylglucosaminidase.

Halila R, Ikonen E, Tollersrud O, Syvänen AC, Enomaa N, Peltonen L.

Biochem Med Metab Biol. 1993 Aug;50(1):1-8. Review. No abstract available.

PMID:
8373629
16.

Fig4 deficiency: a newly emerged lysosomal storage disorder?

Martyn C, Li J.

Prog Neurobiol. 2013 Feb-Mar;101-102:35-45. doi: 10.1016/j.pneurobio.2012.11.001. Epub 2012 Nov 16. Review.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk