(Q34580321)

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Perturbed interactions of mutant proteolipid protein/DM20 with cholesterol and lipid rafts in oligodendroglia: implications for dysmyelination in spastic paraplegia.

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Perturbed interactions of mutant proteolipid protein/DM20 with cholesterol and lipid rafts in oligodendroglia: implications for dysmyelination in spastic paraplegia (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

oligodendrocyte

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Eva-Maria Krämer-Albers

1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Klaus-Armin Nave

5

object named as

Klaus-Armin Nave

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

author name string

Christoph Thiele

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Katja Gehrig-Burger

2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Jacqueline Trotter

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

language of work or name

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publication date

1 November 2006

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Journal of Neuroscience

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

26

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

45

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

11743-11752

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Connatal Pelizaeus-Merzbacher disease associated with the jimpy(msd) mice mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Compartmentation of Fyn kinase with glycosylphosphatidylinositol-anchored molecules in oligodendrocytes facilitates kinase activation during myelination.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cholesterol binds to synaptophysin and is required for biogenesis of synaptic vesicles

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intracellular transport, assembly, and degradation of wild-type and disease-linked mutant gap junction proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assembly of myelin by association of proteolipid protein with cholesterol- and galactosylceramide-rich membrane domains

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aggresomes, inclusion bodies and protein aggregation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myelin: Delivery by raft

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Membrane traffic in myelinating oligodendrocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An update on the leukodsytrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overexpression of the myelin proteolipid protein leads to accumulation of cholesterol and proteolipid protein in endosomes/lysosomes: implications for Pelizaeus-Merzbacher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aggresome formation in neuropathy models based on peripheral myelin protein 22 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pelizaeus-Merzbacher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The unfolded protein response modulates disease severity in Pelizaeus-Merzbacher disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic background determines phenotypic severity of the Plp rumpshaker mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of calnexin in the glycan-independent quality control of proteolipid protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proteolipid protein (PLP) of CNS myelin: positions of free, disulfide-bonded, and fatty acid thioester-linked cysteine residues and implications for the membrane topology of PLP

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

'Unfolding' pathways in neurodegenerative disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quality Control and Protein Folding in the Secretory Pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pelizaeus-Merzbacher disease: pathogenic mechanisms and insights into the roles of proteolipid protein 1 in the nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The PLP mutants from mouse to man.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disease-associated mutations cause premature oligomerization of myelin proteolipid protein in the endoplasmic reticulum.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High cholesterol level is essential for myelin membrane growth

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Processing of PLP in a model of Pelizaeus-Merzbacher disease/SPG2 due to the rumpshaker mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligodendroglial cell death in jimpy mice: an explanation for the myelin deficit

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The rumpshaker mutation in spastic paraplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Degradation of CFTR by the ubiquitin-proteasome pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lines of murine oligodendroglial precursor cells immortalized by an activated neu tyrosine kinase show distinct degrees of interaction with axons in vitro and in vivo.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cellular mechanism governing the severity of Pelizaeus-Merzbacher disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monoclonal antibody O10 defines a conformationally sensitive cell-surface epitope of proteolipid protein (PLP): evidence that PLP misfolding underlies dysmyelination in mutant mice.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligodendrocytes Direct Glycosyl Phosphatidylinositol-anchored Proteins to the Myelin Sheath in Glycosphingolipid-rich Complexes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic severity of murine Plp mutants reflects in vivo and in vitro variations in transport of PLP isoproteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disrupted proteolipid protein trafficking results in oligodendrocyte apoptosis in an animal model of Pelizaeus-Merzbacher disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Axonal swellings and degeneration in mice lacking the major proteolipid of myelin

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Current concepts of PLP and its role in the nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse models of myelin diseases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aggresomes: a cellular response to misfolded proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/17093095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.3581-06.2006

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

release_wsimnqwjkrc2tktugjlftvlopy

1 reference

https://api.fatcat.wiki/v0/release/wsimnqwjkrc2tktugjlftvlopy

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17093095%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

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