(Q33754927)

29 July 2017

title

Induced Pluripotent Stem Cells Derived from a CLN5 Patient Manifest Phenotypic Characteristics of Neuronal Ceroid Lipofuscinoses (English)

1 reference

29 July 2017

Kristiina Uusi-Rauva

1

1 reference

29 July 2017

Tea Blom

2

1 reference

29 July 2017

Carina von Schantz-Fant

3

1 reference

29 July 2017

Tomas Blom

4

1 reference

29 July 2017

Anu Jalanko

5

1 reference

29 July 2017

Aija Kyttälä

6

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 May 2017

1 reference

International Journal of Molecular Sciences

29 July 2017

published in

1 reference

29 July 2017

volume

18

1 reference

29 July 2017

issue

5

1 reference

Creative Commons Attribution 4.0 International

29 July 2017

copyright license

start time

1 May 2017

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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https://api.crossref.org/works/10.3390%2FIJMS18050955

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21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FIJMS18050955

Cln5-deficiency in mice leads to microglial activation, defective myelination and changes in lipid metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FIJMS18050955

Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FIJMS18050955

Palmitoyl protein thioesterase 1 (Ppt1)-deficient mouse neurons show alterations in cholesterol metabolism and calcium homeostasis prior to synaptic dysfunction.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FIJMS18050955

Broad screening test for sphingolipid-storage diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FIJMS18050955

ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperones

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FIJMS18050955

Small molecule inhibitors promote efficient generation of induced pluripotent stem cells from human skeletal myoblasts.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FIJMS18050955

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21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FIJMS18050955

Variant late infantile neuronal ceroid-lipofuscinosis: pathology and biochemistry

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5454868

A variant of Jansky-Bielschowsky disease

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28468312

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hippocampal pathology in the human neuronal ceroid-lipofuscinoses: distinct patterns of storage deposition, neurodegeneration and glial activation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28468312

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28468312

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3390/IJMS18050955

1 reference

29 July 2017

1 reference

29 July 2017

1 reference