(Q37429324)

20 August 2017

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title

Application of lectin histochemistry and carbohydrate analysis to the characterization of lysosomal storage diseases (English)

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20 August 2017

Alroy J

1

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20 August 2017

De Gasperi R

series ordinal

2

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20 August 2017

Warren CD

series ordinal

3

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20 August 2017

publication date

1 June 1991

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20 August 2017

published in

Carbohydrate Research

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20 August 2017

volume

213

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20 August 2017

page(s)

229-250

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Animal models for lysosomal storage diseases: their past and future contribution

20 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Trafficking of lysosomal enzymes in normal and disease states

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Lectin histochemistry and ultrastructure of feline kidneys from six different storage diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

What should be called a lectin?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Histochemical methods for characterizing secretory and cell surface sialoglycoconjugates

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Histochemical differentiation of complex carbohydrates with variants of the concanavalin A-horseradish peroxidase method

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Characterization of storage material in cultured fibroblasts by specific lectin binding in lysosomal storage diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

alpha-N-acetylgalactosaminidase deficiency, a new lysosomal storage disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Visualization of the sugar moiety in lymphoid cell lines from Fabry's disease by lectin binding

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Lectin histochemistry of glycolipid storage diseases on frozen and paraffin-embedded tissue sections

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Characterization by lectin binding of the sugar moiety of glycocompounds stored in inherited diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Lectin histochemistry of brains from a murine mutant carrying a storage disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Lectin histochemical study of lipopigments with special regard to neuronal ceroid-lipofuscinosis. Results with concanavalin A.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Lectin histochemistry of gangliosidosis. II. Neurovisceral tissues from patients with Sandhoff's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Lectin histochemistry of gangliosidosis. I. Neural tissue in four mammalian species

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Swainsonine toxicosis mimics lectin histochemistry of mannosidosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Identification of glycoprotein storage diseases by lectins: a new diagnostic method.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Neurovisceral and skeletal GM1-gangliosidosis in dogs with beta-galactosidase deficiency.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Histochemical similarities between human and animal globoid cells in Krabbe's disease: a lectin study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Human and canine fucosidosis: a comparative lectin histochemistry study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Histochemical study of Hurler's disease by the use of peroxidase-labelled lectins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Adult fucosidosis: histochemical and ultrastructural studies of rectal mucosa biopsy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Infantile sialic acid storage disease associated with renal disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Type III (chronic) GM1-gangliosidosis. Histochemical and ultrastructural studies of rectal biopsy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Separation of benzoylated oligosaccharides by reversed-phase high-pressure liquid chromatography: application to high-mannose type oligosaccharides

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Chromatographic separation of oligosaccharides from mannosidosis urine

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Swainsonine-induced oligosaccharide excretion in sheep. Time-dependent changes in the oligosaccharide profile

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Oligosaccharides from placenta: early diagnosis of feline mannosidosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Biochemical, ultrastructural and histochemical studies of cat placentae deficient in activity of lysosomal alpha-mannosidase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Beta-mannosidosis: prenatal detection of caprine allantoic fluid oligosaccharides with thin layer, gel permeation and high performance liquid chromatography

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Genetic defects in glycoprotein metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Inhibition of lysosomal alpha-mannosidase by swainsonine, an indolizidine alkaloid isolated from Swainsona canescens

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Loco intoxication: indolizidine alkaloids of spotted locoweed (Astragalus lentiginosus).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Induced mannosidosis-excretion of oligosaccharides by locoweed-intoxicated sheep

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

The accumulation of oligosaccharides in tissues and body fluids of cats with alpha-mannosidosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Structure of nine sialyl-oligosaccharides accumulated in urine of eleven patients with three different types of sialidosis. Mucolipidosis II and two new types of mucolipidosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Analysis of dolichyl pyrophosphoryl oligosaccharides in purified storage cytosomes from ovine ceroid-lipofuscinosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Some Histochemical Observations on Periodic Acid-Amino-Acid Mechanisms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Niemann-Pick disease type C could result from a genetic deficiency of cholesterol egress from the lysosomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Interspecific genetic complementation analysis of human and sheep fibroblasts with beta-galactosidase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Glycoproteins in Tay-sachs disease: isolation and carbohydrate composition of glycopeptides.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Chronic GM1 gangliosidosis presenting as dystonia: II. Biochemical studies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

GM1 gangliosidosis in Portuguese water dogs: pathologic and biochemical findings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological features

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

The AB-variant of GM2-gangliosidosis. Clinical, biochemical, and pathological studies of two patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

Inhibition of leucocytic lysosomal enzymes by glycosaminoglycans in vitro

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0008-6215%2800%2990611-6

10.1016/S0008-6215(00)90611-6

7 January 2021

Identifiers

DOI

1 reference

20 August 2017

1 reference