Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts. - Wikidata - wikimedia - TriplyDB

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

http://www.wikidata.org/entity/Q39360277

about

Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia Ambroxol improves lysosomal biochemistry in glucocerebrosidase mutation-linked Parkinson disease cells A prodrug approach to the use of coumarins as potential therapeutics for superficial mycoses.The non-lysosomal β-glucosidase GBA2 is a non-integral membrane-associated protein at the endoplasmic reticulum (ER) and Golgi.β-Glucosidase 2 (GBA2) activity and imino sugar pharmacology.1-O-acylceramides are natural components of human and mouse epidermis Glucocerebrosidase 2 gene deletion rescues type 1 Gaucher disease.The glycosphingolipid hydrolases in the central nervous system.Current and Novel Aspects on the Non-lysosomal β-Glucosylceramidase GBA2.Identification of a feedback loop involving β-glucosidase 2 and its product sphingosine sheds light on the molecular mechanisms in Gaucher disease.Parkinson's disease: acid-glucocerebrosidase activity and alpha-synuclein clearance.Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease.The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p Evidence for the Involvement of Lipid Rafts and Plasma Membrane Sphingolipid Hydrolases in Pseudomonas aeruginosa Infection of Cystic Fibrosis Bronchial Epithelial Cells.Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytes.iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis.Sphingolipids role in the regulation of inflammatory response: From leukocyte biology to bacterial infection.Biochemical Characterization of the c.1780G>C Missense Mutation in Lymphoblastoid Cells from Patients with Spastic Ataxia

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P2860

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

http://www.wikidata.org/entity/Q39360277

description

2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

2012年學術文章

@zh

2012年學術文章

@zh-hant

name

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

@en

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

@nl

type

label

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

@en

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

@nl

prefLabel

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

@en

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

@nl

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S10545-012-9478-X

P1433

Journal of Inherited Metabolic Disease

P1476

Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

@en

P2093

Alessandro Prinetti

http://www.w3.org/2001/XMLSchema#string

Johannes M Aerts

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Massimo Aureli

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Mirella Filocamo

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Nicoletta Loberto

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Rolf G Boot

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Rosaria Bassi

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Sandro Sonnino

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Stefano Regis

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Vanna Chigorno

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P2860

LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase

Identification of a family of animal sphingomyelin synthases.

Identification of the non-lysosomal glucosylceramidase as beta-glucosidase 2

Plasma membrane repair is mediated by Ca(2+)-regulated exocytosis of lysosomes

Signalling sphingomyelinases: which, where, how and why?

Common and uncommon pathogenic cascades in lysosomal storage diseases

Neobiosynthesis of glycosphingolipids by plasma membrane-associated glycosyltransferases.

The cytosolic β-glucosidase GBA3 does not influence type 1 Gaucher disease manifestation.

Principles of lysosomal membrane digestion: stimulation of sphingolipid degradation by sphingolipid activator proteins and anionic lysosomal lipids.

Brain pathology in Niemann Pick disease type A: insights from the acid sphingomyelinase knockout mice

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1081-1091

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10.1007/S10545-012-9478-X

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6

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35

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2012-04-19T00:00:00Z

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