Metabolic adaptations to interrupted glycosaminoglycan recycling. (Q37447757)

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scientific article published on 21 August 2009

Language	Label	Description	Also known as
English	Metabolic adaptations to interrupted glycosaminoglycan recycling.	scientific article published on 21 August 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19700765%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Metabolic adaptations to interrupted glycosaminoglycan recycling (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19700765%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

metabolic adaptation

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5

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19700765%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

author name string

Josh C Woloszynek

1

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6 February 2020

Atilla Kovacs

2

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6 February 2020

Kevin K Ohlemiller

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19700765%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Marie Roberts

4

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6 February 2020

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21 August 2009

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6 February 2020

Journal of Biological Chemistry

1 reference

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6 February 2020

284

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6 February 2020

43

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6 February 2020

29684-29691

1 reference

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PMC publication ID

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6 February 2020

Pathogenic cascades in lysosomal disease-Why so complex?

1 reference

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Tau deletion exacerbates the phenotype of Niemann-Pick type C mice and implicates autophagy in pathogenesis.

1 reference

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Autophagic dysfunction in mucolipidosis type IV patients

1 reference

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A murine model of infantile neuronal ceroid lipofuscinosis-ultrastructural evaluation of storage in the central nervous system and viscera.

1 reference

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Neurologic, gastric, and opthalmologic pathologies in a murine model of mucolipidosis type IV

1 reference

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23 August 2017

A block of autophagy in lysosomal storage disorders

1 reference

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Development of sensory, motor and behavioral deficits in the murine model of Sanfilippo syndrome type B

1 reference

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Anaplerotic diet therapy in inherited metabolic disease: therapeutic potential

1 reference

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23 August 2017

Cell-autonomous death of cerebellar purkinje neurons with autophagy in Niemann-Pick type C disease

1 reference

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23 August 2017

Lysosomal storage disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785600

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Electrocardiographic and other cardiac anomalies in beta-glucuronidase-null mice corrected by nonablative neonatal marrow transplantation

1 reference

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Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride

1 reference

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Glucose transport in brain and retina: implications in the management and complications of diabetes

1 reference

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23 August 2017

Cardiac hypertrophy in juvenile visceral steatosis (jvs) mice with systemic carnitine deficiency

1 reference

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23 August 2017

Fatty acid homeostasis in the normoxic and ischemic heart

1 reference

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23 August 2017

Participation of autophagy in storage of lysosomes in neurons from mouse models of neuronal ceroid-lipofuscinoses (Batten disease).

1 reference

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23 August 2017

Motor deficit in a Drosophila model of mucolipidosis type IV due to defective clearance of apoptotic cells.

1 reference

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Lysosomal degradation of glycoproteins and glycosaminoglycans. Efflux and recycling of sulphate and N-acetylhexosamines

1 reference

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26 June 2018

Chaperone-mediated autophagy is defective in mucolipidosis type IV.

1 reference

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2 September 2018

Enhanced autophagy and mitochondrial aberrations in murine G(M1)-gangliosidosis

1 reference

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2 September 2018

Lysosomal dysfunction results in altered energy balance

1 reference

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2 September 2018

Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease.

1 reference

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2 September 2018

Basis of lethality in C. elegans lacking CUP-5, the Mucolipidosis Type IV orthologue

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Numerous transcriptional alterations in liver persist after short-term enzyme-replacement therapy in a murine model of mucopolysaccharidosis type VII.

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2 September 2018

Lysosomal acid lipase-deficient mice: depletion of white and brown fat, severe hepatosplenomegaly, and shortened life span.

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hurler and Hunter syndromes: mutual correction of the defect in cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/19700765

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1074/JBC.M109.020818

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19700765%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19700765%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19700765%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

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