(Q33306120)

25 July 2017

title

Overexpression and mass spectrometry analysis of mature human acid ceramidase (English)

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25 July 2017

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Ute Schepers

2

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author name string

Heike Schulze

series ordinal

1

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25 July 2017

Konrad Sandhoff

series ordinal

3

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25 July 2017

publication date

1 December 2007

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25 July 2017

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25 July 2017

volume

388

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25 July 2017

issue

12

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25 July 2017

page(s)

1333-1343

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Molecular analysis of acid ceramidase deficiency in patients with Farber disease

25 July 2017

cites work

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https://api.crossref.org/works/10.1515%2FBC.2007.152

Expression of recombinant human acid sphingomyelinase in insect Sf21 cells: purification, processing and enzymatic characterization

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Purification, characterization, and biosynthesis of human acid ceramidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

A protein catalytic framework with an N-terminal nucleophile is capable of self-activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Penicillin acylase has a single-amino-acid catalytic centre

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Acid ceramidase is a novel factor required for early embryo survival.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

A phase 1/2 clinical trial of enzyme replacement in fabry disease: pharmacokinetic, substrate clearance, and safety studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Human acid ceramidase: processing, glycosylation, and lysosomal targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Purification and characterization of recombinant, human acid ceramidase. Catalytic reactions and interactions with acid sphingomyelinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Molecular cloning and characterization of a full-length complementary DNA encoding human acid ceramidase. Identification Of the first molecular lesion causing Farber disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

The human acid ceramidase gene (ASAH): structure, chromosomal location, mutation analysis, and expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Insertional mutagenesis of the mouse acid ceramidase gene leads to early embryonic lethality in homozygotes and progressive lipid storage disease in heterozygotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Interfacial regulation of acid ceramidase activity. Stimulation of ceramide degradation by lysosomal lipids and sphingolipid activator proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Structural comparison of Ntn-hydrolases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

The reverse activity of human acid ceramidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Prompt fragmentation of disulfide-linked peptides during matrix-assisted laser desorption ionization mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Measurement of protein using bicinchoninic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Molecular characterization of N-acylethanolamine-hydrolyzing acid amidase, a novel member of the choloylglycine hydrolase family with structural and functional similarity to acid ceramidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Expression of recombinant human GM2-activator protein in insect cells: purification and characterization by mass spectrometry.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2007.152

21 January 2018

Identifiers

DOI

10.1515/BC.2007.152

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25 July 2017

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