(Q34994610)

5 August 2017

title

The role of N-glycosylation in folding, trafficking, and functionality of lysosomal protein CLN5. (English)

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5 August 2017

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Akshay Moharir

1

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5 August 2017

Sun H Peck

series ordinal

2

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5 August 2017

Theodore Budden

series ordinal

3

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5 August 2017

Stella Y Lee

series ordinal

4

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5 August 2017

language of work or name

English

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publication date

10 September 2013

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5 August 2017

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5 August 2017

volume

8

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5 August 2017

issue

9

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5 August 2017

page(s)

e74299

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Creative Commons Attribution 4.0 International

5 August 2017

copyright license

start time

10 September 2013

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Cleaning up: ER-associated degradation to the rescue

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

CLN5 and CLN8 protein association with ceramide synthase: biochemical and proteomic approaches.

8 July 2018

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The role of ceroid lipofuscinosis neuronal protein 5 (CLN5) in endosomal sorting

8 July 2018

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SignalP 4.0: discriminating signal peptides from transmembrane regions

8 July 2018

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Rubicon controls endosome maturation as a Rab7 effector

8 July 2018

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The neuronal ceroid lipofuscinosis protein CLN5: new insights into cellular maturation, transport, and consequences of mutations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Glycosylation- and phosphorylation-dependent intracellular transport of lysosomal hydrolases

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis.

8 July 2018

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Glycosylation in cellular mechanisms of health and disease

8 July 2018

1 reference

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The neuronal ceroid-lipofuscinoses: from past to present

8 July 2018

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The formation of TGN-to-plasma-membrane transport carriers

8 July 2018

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You say lipofuscin, we say ceroid: defining autofluorescent storage material

8 July 2018

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Identification of sites of mannose 6-phosphorylation on lysosomal proteins

8 July 2018

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The CLN9 protein, a regulator of dihydroceramide synthase.

8 July 2018

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Identification of novel lysosomal matrix proteins by proteome analysis

8 July 2018

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Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses

8 July 2018

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Mutations in classical late infantile neuronal ceroid lipofuscinosis disrupt transport of tripeptidyl-peptidase I to lysosomes

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

N-glycosylation is crucial for folding, trafficking, and stability of human tripeptidyl-peptidase I.

8 July 2018

1 reference

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Late infantile neuronal ceroid lipofuscinosis: quantitative description of the clinical course in patients with CLN2 mutations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Intracellular functions of N-linked glycans

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Biogenesis of the sorting endosome: the role of Rab5.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

The neuronal ceroid-lipofuscinoses (Batten disease): a new class of lysosomal storage diseases

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Inhibition of rab5 GTPase activity stimulates membrane fusion in endocytosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Neuronal ceroid-lipofuscinosis (Batten's disease): relationship to amaurotic family idiocy?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3769244

Peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase F cannot release glycans with fucose attached alpha 1----3 to the asparagine-linked N-acetylglucosamine residue

8 July 2018

1 reference

12 December 2020

Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

1 reference

12 December 2020

Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis

1 reference

12 December 2020

Proteomics analysis of serum from mutant mice reveals lysosomal proteins selectively transported by each of the two mannose 6-phosphate receptors

1 reference

12 December 2020

CLN5 mutations are frequent in juvenile and late-onset non-Finnish patients with NCL

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0074299

Identifiers

DOI

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5 August 2017

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5 August 2017

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