In situ detection of GM1 and GM2 gangliosides using immunohistochemical and immunofluorescent techniques for auxiliary diagnosis of canine and feline gangliosidoses

Author:

Kohyama Moeko,Yabuki Akira,Ochiai Kenji,Nakamoto Yuya,Uchida Kazuyuki,Hasegawa Daisuke,Takahashi Kimimasa,Kawaguchi Hiroaki,Tsuboi Masaya,Yamato Osamu

Funder

Ministry of Education, Culture, Sports, Science and Technology of Japan

Publisher

Springer Science and Business Media LLC

Subject

General Veterinary,General Medicine

Reference53 articles.

1. Haskins M, Giger U. Lysosomal storage diseases. In: Kaneko JJ, Harvey JW, Bruss ML, editors. Clinical biochemistry of domestic animals. 6th ed. Burlington: Academic; 2008. p. 731–50.

2. Suzuki Y, Oshima A, Nanba E. β-Galactosidase deficiency (β-galactosidosis): GM1 gangliosidosis and Morquio B disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited disease. 8th ed. New York: McGraw-Hill; 2001. p. 3775–809.

3. Gravel RA, Kaback MM, Proia RL, Sandhoff K, Suzuki K. The GM2 gangliosidosis. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited disease. 8th ed. McGraw-Hill: New York; 2001. p. 3824–76.

4. Read DH, Harrington DD, Keenana TW, Hinsman EJ. Neuronal-visceral GM1 gangliosidosis in a dog with beta-galactosidase deficiency. Science. 1976;194:442–5.

5. Alroy J, Orgad U, Ucci AA, Schelling SH, Schunk KL, Warren CD, et al. Neurovisceral and skeletal GM1-gangliosidosis in dogs with beta-galactosidase deficiency. Science. 1985;229:470–2.

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