(Q24294224)

signal peptide processing

GOA release 2020-03-11

1 reference

neuronal ceroid lipofuscinosis

GOA release 2020-03-11

1 reference

5

Anu Jalanko

Anu

Jalanko

1 reference

26 October 2023

Mia-Lisa Schmiedt

1

Mia-Lisa

Schmiedt

1 reference

26 October 2023

Carlos Bessa

2

Carlos

Bessa

1 reference

26 October 2023

Claudia Heine

3

Claudia

Heine

1 reference

26 October 2023

Maria Gil Ribeiro

4

Maria Gil

Ribeiro

1 reference

26 October 2023

Aija Kyttälä

6

Aija

Kyttälä

1 reference

The neuronal ceroid-lipofuscinoses: from past to present

26 October 2023

language of work or name

English

0 references

publication date

March 2010

0 references

published in

Human Mutation

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volume

31

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issue

3

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page(s)

356-65

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cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

A CLN5 mutation causing an atypical neuronal ceroid lipofuscinosis of juvenile onset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

Identification of sites of mannose 6-phosphorylation on lysosomal proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

Improved prediction of signal peptides: SignalP 3.0

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Two novel CLN5 mutations in a Portuguese patient with vLINCL: insights into molecular mechanisms of CLN5 deficiency.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Sortilin mediates the lysosomal targeting of cathepsins D and H

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

The mouse ortholog of the neuronal ceroid lipofuscinosis CLN5 gene encodes a soluble lysosomal glycoprotein expressed in the developing brain

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Phenotype-genotype correlation in eight patients with Finnish variant late infantile NCL (CLN5)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Neuronal ceroid lipofuscinoses

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Biosynthesis and intracellular targeting of the CLN3 protein defective in Batten disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Identification of novel lysosomal matrix proteins by proteome analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

The biogenesis of lysosomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Two motifs target Batten disease protein CLN3 to lysosomes in transfected nonneuronal and neuronal cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Novel interactions of CLN5 support molecular networking between Neuronal Ceroid Lipofuscinosis proteins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1)--distinct characteristics in neurons

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

The Two Mannose 6-Phosphate Receptors Transport Distinct Complements of Lysosomal Proteins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Neuronal ceroid-lipofuscinoses in childhood

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Mass spectrometry-based protein profiling to determine the cause of lysosomal storage diseases of unknown etiology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

Lysosomal enzymes and their receptors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

A new method for predicting signal sequence cleavage sites

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21195

7 January 2021

release_m7cdd5cnjbdvnkwvtf3jljfmta

Identifiers

DOI

10.1002/HUMU.21195

0 references

Fatcat ID

0 references