Saposin C-LBPA interaction in late-endosomes/lysosomes (Q81277051)

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7 January 2020

title

Saposin C-LBPA interaction in late-endosomes/lysosomes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15652344%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

author name string

Zhengtao Chu

series ordinal

1

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7 January 2020

David P Witte

series ordinal

2

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7 January 2020

Xiaoyang Qi

series ordinal

3

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7 January 2020

language of work or name

English

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publication date

1 February 2005

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Experimental Cell Research

7 January 2020

published in

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7 January 2020

volume

303

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7 January 2020

issue

2

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7 January 2020

page(s)

300-307

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Structure of full-length cDNA coding for sulfatide activator, a Co-beta-glucosidase and two other homologous proteins: two alternate forms of the sulfatide activator

7 January 2020

cites work

1 reference

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Molecular cloning of a human co-beta-glucosidase cDNA: evidence that four sphingolipid hydrolase activator proteins are encoded by single genes in humans and rats

7 January 2021

1 reference

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Proteolytic processing patterns of prosaposin in insect and mammalian cells

7 January 2021

1 reference

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Structural analysis of saposin C and B. Complete localization of disulfide bridges

7 January 2021

1 reference

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Lysosomal proteolysis of prosaposin, the precursor of saposins (sphingolipid activator proteins): its mechanism and inhibition by ganglioside

7 January 2021

1 reference

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The effect of carbohydrate removal on stability and activity of saposin B.

7 January 2021

1 reference

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An Asn > Lys substitution in saposin B involving a conserved amino acidic residue and leading to the loss of the single N-glycosylation site in a patient with metachromatic leukodystrophy and normal arylsulphatase A activity

7 January 2021

1 reference

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Sphingolipid activator proteins: proteins with complex functions in lipid degradation and skin biogenesis

7 January 2021

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

7 January 2021

1 reference

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

7 January 2021

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Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses

7 January 2021

1 reference

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A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulation

7 January 2021

1 reference

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Endocytosis and molecular sorting

7 January 2021

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The endocytic pathway: a mosaic of domains

7 January 2021

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Receptor downregulation and multivesicular-body sorting

7 January 2021

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A lipid associated with the antiphospholipid syndrome regulates endosome structure and function

7 January 2021

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Maternal Pumilio acts together with Nanos in germline development in Drosophila embryos

7 January 2021

1 reference

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Mouse models of human lysosomal diseases.

7 January 2021

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Niemann-Pick type C mutations cause lipid traffic jam.

7 January 2021

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Phospholipid vesicle fusion induced by saposin C.

7 January 2021

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Ex vivo localization of the mouse saposin C activation region for acid beta-glucosidase

7 January 2021

1 reference

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A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.09.029

Biosynthesis of the sulfatide/GM1 activator protein (SAP-1) in control and mutant cultured skin fibroblasts

7 January 2021

1 reference

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Separation and characterization of late endosomal membrane domains

7 January 2021

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10.1016/J.YEXCR.2004.09.029

7 January 2021

Identifiers

DOI

1 reference

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7 January 2020

1 reference