Increased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissue (Q28114924)

GOA release 2020-03-11

1 reference

Alfried Kohlschütter

3

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ORCID Public Data File 2021

author name string

Sandra Pohl

1

1 reference

3 January 2017

Hannah M. Mitchison

2

1 reference

3 January 2017

Otto van Diggelen

4

1 reference

3 January 2017

Thomas Braulke

5

1 reference

3 January 2017

Stephan Storch

Journal of Neurochemistry

6

1 reference

3 January 2017

language of work or name

English

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publication date

1 December 2007

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3 January 2017

1 reference

3 January 2017

103

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3 January 2017

6

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3 January 2017

2177–2188

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3 January 2017

Normal lysosomal morphology and function in LAMP-1-deficient mice

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Autophagy is disrupted in a knock-in mouse model of juvenile neuronal ceroid lipofuscinosis

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

At the acidic edge: emerging functions for lysosomal membrane proteins

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Structure of the human lysosomal acid phosphatase gene

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Elevated lysosomal pH in neuronal ceroid lipofuscinoses (NCLs)

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

A role in vacuolar arginine transport for yeast Btn1p and for human CLN3, the protein defective in Batten disease

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Type 5 acid phosphatase. Sequence, expression and chromosomal localization of a differentiation-associated protein of the human macrophage

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

CLN3 protein is targeted to neuronal synapses but excluded from synaptic vesicles: new clues to Batten disease

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Interconnections of CLN3, Hook1 and Rab proteins link Batten disease to defects in the endocytic pathway

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Action of BTN1, the yeast orthologue of the gene mutated in Batten disease

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

A galactosylceramide binding domain is involved in trafficking of CLN3 from Golgi to rafts via recycling endosomes

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.2007.04920.X

Functional categorization of gene expression changes in the cerebellum of a Cln3-knockout mouse model for Batten disease.

21 April 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Transcriptional profiling on chromosome 19p indicated frequent downregulation of ACP5 expression in hepatocellular carcinoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Kinetic behaviour of calf-intestinal alkaline phosphatase with 4-methylumbelliferyl phosphate

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

The human tartrate-resistant acid phosphatase (TRAP): involvement of the hemin responsive elements (HRE) in transcriptional regulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

btn1, the Schizosaccharomyces pombe homologue of the human Batten disease gene CLN3, regulates vacuole homeostasis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Localization of lysosomal acid phosphatase mRNA in mouse tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Tartrate-resistant acid phosphatase (Acp 5): identification in diverse human tissues and dendritic cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Abnormal acid phosphatases in neuronal ceroid-lipofuscinoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Participation of autophagy in storage of lysosomes in neurons from mouse models of neuronal ceroid-lipofuscinoses (Batten disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Functional biology of the neuronal ceroid lipofuscinoses (NCL) proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Expression and distribution of tartrate-resistant purple acid phosphatase in the rat nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Cycling of the integral membrane glycoprotein, LEP100, between plasma membrane and lysosomes: kinetic and morphological analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Selectivity and types of cell death in the neuronal ceroid lipofuscinoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

The genetic spectrum of human neuronal ceroid-lipofuscinoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Secretion of phosphomannosyl-deficient arylsulphatase A and cathepsin D from isolated human macrophages

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

CLN3P, the Batten's disease protein, is a novel palmitoyl-protein Delta-9 desaturase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Analysis of distinct tartrate-resistant acid phosphatase promoter regions in transgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Motifs within the CLN3 protein: modulation of cell growth rates and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Late onset neurodegeneration in the Cln3-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Specific alterations in levels of mannose 6-phosphorylated glycoproteins in different neuronal ceroid lipofuscinoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

C-terminal prenylation of the CLN3 membrane glycoprotein is required for efficient endosomal sorting to lysosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X

Cathepsin E deficiency induces a novel form of lysosomal storage disorder showing the accumulation of lysosomal membrane sialoglycoproteins and the elevation of lysosomal pH in macrophages.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04920.X