Glucosylceramide transfer from lysosomes--the missing link in molecular pathology of glucosylceramidase deficiency: a hypothesis based on existing data.

Glucosylceramide transfer from lysosomes--the missing link in molecular pathology of glucosylceramidase deficiency: a hypothesis based on existing data.

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http://www.wikidata.org/entity/Q31072456
The cell biology of disease: lysosomal storage disorders: the cellular impact of lysosomal dysfunctionReducing GBA2 Activity Ameliorates Neuropathology in Niemann-Pick Type C MiceGenome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variationExpanding spectrum of the association between Type 1 Gaucher disease and cancers: a series of patients with up to 3 sequential cancers of multiple types--correlation with genotype and phenotype.Glucocerebrosidase gene-deficient mouse recapitulates Gaucher disease displaying cellular and molecular dysregulation beyond the macrophage.High incidence of cholesterol gallstone disease in type 1 Gaucher disease: characterizing the biliary phenotype of type 1 Gaucher disease.A reappraisal of Gaucher disease-diagnosis and disease management algorithms.Gaucher disease gene GBA functions in immune regulation.β-Glucosidase 2 (GBA2) activity and imino sugar pharmacology.Pulmonary vascular disease in Gaucher disease: clinical spectrum, determinants of phenotype and long-term outcomes of therapy.Glucocerebrosidase 2 gene deletion rescues type 1 Gaucher disease.Treatment of lysosomal storage disorders: successes and challenges.Glucosylsphingosine promotes α-synuclein pathology in mutant GBA-associated Parkinson's disease.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.Abnormal nonstoring capillary endothelium: a novel feature of Gaucher disease. Ultrastructural study of dermal capillaries.Characterization of variants in the glucosylceramide synthase gene and their association with type 1 Gaucher disease severity.
P2860

Glucosylceramide transfer from lysosomes--the missing link in molecular pathology of glucosylceramidase deficiency: a hypothesis based on existing data.

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http://www.wikidata.org/entity/Q31072456
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Glucosylceramide transfer from ...... thesis based on existing data.
@ast
Glucosylceramide transfer from ...... thesis based on existing data.
@en
type
label
Glucosylceramide transfer from ...... thesis based on existing data.
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Glucosylceramide transfer from ...... thesis based on existing data.
@en
prefLabel
Glucosylceramide transfer from ...... thesis based on existing data.
@ast
Glucosylceramide transfer from ...... thesis based on existing data.
@en
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P433
P478
P577
P5875
P6179
P698
P921
P356
P1433
P1476
Glucosylceramide transfer from ...... thesis based on existing data.
@en
P2093
P2860
P2888
P304
P31
P356
P433
P478
P577
P5875
P6179
P698
P921