(Q48059282)

8 February 2018

title

Sphingolipid activator proteins in a human hereditary renal disease with deposition of disialogangliosides (English)

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8 February 2018

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C Holmberg

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8 February 2018

author name string

A Haltia

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8 February 2018

M L Solin

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8 February 2018

H Jalanko

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8 February 2018

A Miettinen

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8 February 2018

H Holthöfer

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8 February 2018

publication date

1 October 1996

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8 February 2018

number of pages

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Journal of Molecular Histology

inferred from page(s)

published in

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8 February 2018

volume

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8 February 2018

issue

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8 February 2018

page(s)

681-687

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8 February 2018

Activator proteins and topology of lysosomal sphingolipid catabolism.

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF02409005

Degradation of gangliosides by the lysosomal sialidase requires an activator protein

21 January 2018

1 reference

12 December 2020

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

12 December 2020

Ganglioside GM3: an acidic membrane component that increases during macrophage-like cell differentiation can induce monocytic differentiation of human myeloid and monocytoid leukemic cell lines HL-60 and U937

1 reference

12 December 2020

Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene

1 reference

12 December 2020

Immunocytochemical localization of sphingolipid activator protein-1, the sulfatide/GM1 ganglioside activator, to lysosomes in human liver and colon

1 reference

12 December 2020

Ganglioside-mediated modulation of cell growth. Specific effects of GM3 on tyrosine phosphorylation of the epidermal growth factor receptor

1 reference

12 December 2020

A fast and simple procedure for sequencing double stranded DNA with sequenase

1 reference

12 December 2020

Monoclonal antibodies against membrane proteins of the rat glomerulus. Immunochemical specificity and immunofluorescence distribution of the antigens

1 reference

12 December 2020

Management of congenital nephrotic syndrome of the Finnish type

1 reference

12 December 2020

Developmental abnormalities in transgenic mice expressing a sialic acid-specific 9-O-acetylesterase

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12 December 2020

Nephrotic syndrome in newborn and young infants

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12 December 2020

Distribution of saposin proteins (sphingolipid activator proteins) in lysosomal storage and other diseases

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12 December 2020

DNA sequencing with chain-terminating inhibitors

1 reference

12 December 2020

A monoclonal antibody recognizes an O-acylated sialic acid in a human melanoma-associated ganglioside

1 reference

12 December 2020

AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2

1 reference

12 December 2020

Structure and function of renal glycosphingolipids.

1 reference

12 December 2020

Disialogangliosides GD2 and GD3 are involved in the attachment of human melanoma and neuroblastoma cells to extracellular matrix proteins

1 reference

12 December 2020

First-strand cDNA synthesis primed with oligo(dT).

1 reference

12 December 2020

Binding and transport of gangliosides by prosaposin

1 reference

12 December 2020

Saposin proteins: structure, function, and role in human lysosomal storage disorders

1 reference

12 December 2020

Ganglioside metabolism. Enzymology, Topology, and regulation

1 reference

12 December 2020

Specific interaction between gangliotriaosylceramide (Gg3) and sialosyllactosylceramide (GM3) as a basis for specific cellular recognition between lymphoma and melanoma cells

1 reference

12 December 2020

pH-dependent conformational properties of saposins and their interactions with phospholipid membranes

1 reference

12 December 2020

Saposins: structure, function, distribution, and molecular genetics

1 reference

12 December 2020

Clinical, pathological, and biochemical studies on an infantile case of sulfatide/GM1 activator protein deficiency

1 reference

12 December 2020

Characterization of a mutation in a family with saposin B deficiency: a glycosylation site defect

1 reference

12 December 2020

Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease

1 reference

12 December 2020

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

12 December 2020

Insertion in the mRNA of a metachromatic leukodystrophy patient with sphingolipid activator protein-1 deficiency

1 reference

12 December 2020

Biosynthesis and Function of Gangliosides

1 reference

12 December 2020

Sphingolipid hydrolase activator proteins and their precursors.

1 reference

12 December 2020

Characterization of a nonspecific activator protein for the enzymatic hydrolysis of glycolipids

1 reference

12 December 2020

Immunological evidence for deficiency in an activator protein for sulfatide sulfatase in a variant form of metachromatic leukodystrophy

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02409005

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8 February 2018

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8 February 2018