(Q46817726)

25 December 2017

title

Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle (English)

1 reference

25 December 2017

author

Raimondo De Cristofaro

3

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25 December 2017

author name string

Aldobrando Broccolini

1

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25 December 2017

Teresa Gidaro

2

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25 December 2017

Roberta Morosetti

4

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25 December 2017

Carla Gliubizzi

5

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25 December 2017

Enzo Ricci

6

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25 December 2017

Pietro A Tonali

7

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25 December 2017

Massimiliano Mirabella

8

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25 December 2017

language of work or name

English

0 references

publication date

24 December 2007

1 reference

25 December 2017

Journal of Neurochemistry

number of pages

11

1 reference

based on heuristic

inferred from page(s)

published in

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25 December 2017

volume

105

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25 December 2017

issue

3

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25 December 2017

page(s)

971-981

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25 December 2017

Immunohistochemical localization of neprilysin in the human cerebral cortex: inverse association with vulnerability to amyloid beta-protein (Abeta) deposition

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1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.05208.X

Characterization of hereditary inclusion body myopathy myoblasts: possible primary impairment of apoptotic events

21 January 2018

1 reference

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"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews

21 January 2018

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Inclusion-body myositis and myopathies: different etiologies, possibly similar pathogenic mechanisms

21 January 2018

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Enhanced sialylation of EPO by overexpression of UDP-GlcNAc 2-epimerase/ManAc kinase containing a sialuria mutation in CHO cells.

21 January 2018

1 reference

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Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis.

21 January 2018

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Cellular survival: a play in three Akts

21 January 2018

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The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.05208.X

Loss of neprilysin function promotes amyloid plaque formation and causes cerebral amyloid angiopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.05208.X

The effect of polysialylation on the immunogenicity and antigenicity of asparaginase: implication in its pharmacokinetics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.05208.X

The glycan code of the endoplasmic reticulum: asparagine-linked carbohydrates as protein maturation and quality-control tags

21 January 2018

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Age-dependent decline of neprilysin in Alzheimer's disease and normal brain: inverse correlation with A beta levels.

21 January 2018

1 reference

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A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase

21 January 2018

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Metabolic regulation of brain Abeta by neprilysin.

21 January 2018

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Polysialylated insulin: synthesis, characterization and biological activity in vivo

21 January 2018

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The purification and specificity of a neutral endopeptidase from rabbit kidney brush border

21 January 2018

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Role of glycosylation in transport and enzymic activity of neutral endopeptidase-24.11.

21 January 2018

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Enhanced proteolysis of beta-amyloid in APP transgenic mice prevents plaque formation, secondary pathology, and premature death.

21 January 2018

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Neutral endopeptidase-24.11 (enkephalinase). Biosynthesis and localization in human fibroblasts

21 January 2018

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Neprilysin regulates amyloid Beta peptide levels

21 January 2018

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Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles

21 January 2018

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A Japanese patient with distal myopathy with rimmed vacuoles: missense mutations in the epimerase domain of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation of skeletal muscle glycoproteins

21 January 2018

1 reference

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No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.05208.X

Neprilysin degrades both amyloid beta peptides 1-40 and 1-42 most rapidly and efficiently among thiorphan- and phosphoramidon-sensitive endopeptidases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.05208.X

Distal myopathy with rimmed vacuoles: impaired O-glycan formation in muscular glycoproteins

21 January 2018

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The neprilysin (NEP) family of zinc metalloendopeptidases: genomics and function

21 January 2018

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Reduced neprilysin in high plaque areas of Alzheimer brain: a possible relationship to deficient degradation of beta-amyloid peptide.

21 January 2018

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The unfolded protein response: a stress signaling pathway critical for health and disease.

21 January 2018

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A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.05208.X

10.1111/J.1471-4159.2007.05208.X

21 January 2018

Identifiers

DOI

1 reference

25 December 2017

PubMed ID

18182043

1 reference

25 December 2017