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

3 January 2017

title

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

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Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)

3 January 2017

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GOA release 2020-03-11

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Alfried Kohlschütter

3

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ORCID Public Data File 2021

author name string

Sandra Pohl

1

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3 January 2017

Hannah M. Mitchison

2

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3 January 2017

Otto van Diggelen

4

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3 January 2017

Thomas Braulke

5

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3 January 2017

Stephan Storch

6

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3 January 2017

language of work or name

English

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publication date

1 December 2007

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Journal of Neurochemistry

3 January 2017

published in

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3 January 2017

volume

103

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3 January 2017

issue

6

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3 January 2017

page(s)

2177–2188

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

3 January 2017

cites work

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Structure of the human lysosomal acid phosphatase gene

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Elevated lysosomal pH in neuronal ceroid lipofuscinoses (NCLs)

21 April 2017

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

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

21 April 2017

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

21 April 2017

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

21 April 2017

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

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

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

21 April 2017

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Mice Deficient in Lysosomal Acid Phosphatase Develop Lysosomal Storage in the Kidney and Central Nervous System

21 April 2017

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

21 April 2017

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

21 April 2017

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

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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Localization of lysosomal acid phosphatase mRNA in mouse tissues

21 January 2018

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21 January 2018

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

21 January 2018

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Abnormal acid phosphatases in neuronal ceroid-lipofuscinoses

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Selectivity and types of cell death in the neuronal ceroid lipofuscinoses

21 January 2018

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The genetic spectrum of human neuronal ceroid-lipofuscinoses

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

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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

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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

10.1111/J.1471-4159.2007.04920.X

21 January 2018

Identifiers

DOI

0 references

1 reference