(Q35053456)

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Amyloidosis, synucleinopathy, and prion encephalopathy in a neuropathic lysosomal storage disease: the CNS-biomarker potential of peripheral blood

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Amyloidosis, synucleinopathy, and prion encephalopathy in a neuropathic lysosomal storage disease: the CNS-biomarker potential of peripheral blood (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

0 references

prion protein family

0 references

synucleinopathy

1 reference

based on heuristic

inferred from title

lysosomal storage disease

1 reference

based on heuristic

inferred from title

author name string

Bartholomew J Naughton

1

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

F Jason Duncan

2

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Darren Murrey

3

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Tierra Ware

4

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Aaron Meadows

5

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Douglas M McCarty

6

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Haiyan Fu

7

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

language of work or name

0 references

publication date

21 November 2013

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

e80142

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

copyright license

Creative Commons Attribution 3.0 Unported

21 November 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3836978/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Peripheral nervous system neuropathology and progressive sensory impairments in a mouse model of Mucopolysaccharidosis IIIB.

1 reference

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1 reference

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Gene therapy approaches for lysosomal storage disease: next-generation treatment

1 reference

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1 reference

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Therapy for the mucopolysaccharidoses

1 reference

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1 reference

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1 reference

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1 reference

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The cellular prion protein mediates neurotoxic signalling of β-sheet-rich conformers independent of prion replication

1 reference

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1 reference

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Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy

1 reference

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1 reference

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1 reference

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Innate and adaptive immune activation in the brain of MPS IIIB mouse model.

1 reference

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A block of autophagy in lysosomal storage disorders

1 reference

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Prion proteins: physiological functions and role in neurological disorders

1 reference

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1 reference

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Lysosomal accumulation of SCMAS (subunit c of mitochondrial ATP synthase) in neurons of the mouse model of mucopolysaccharidosis III B.

1 reference

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1 reference

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Accumulation of intracellular amyloid-beta peptide (A beta 1-40) in mucopolysaccharidosis brains.

1 reference

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Neuropathological study and chemico-pathological correlation in sibling cases of Sanfilippo syndrome type B.

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Dimethylmethylene blue-based spectrophotometry of glycosaminoglycans in untreated urine: a rapid screening procedure for mucopolysaccharidoses.

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Differential subcellular localization of cholesterol, gangliosides, and glycosaminoglycans in murine models of mucopolysaccharide storage disorders

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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based on heuristic

inferred from PubMed ID database lookup

Quantification and characterization of glycosaminoglycans at the nanogram level by a combined azure A-silver staining in agarose gels

1 reference

https://pubmed.ncbi.nlm.nih.gov/24278249

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0080142

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

2013PLoSO...880142N

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

ResearchGate publication ID

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