UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Evolution of Mammalian Chitinase(-Like) Members of Family 18 Glycosyl Hydrolases

Genetics (Austin), 2007-10, Vol.177 (2), p.959-970

2007

Volltextzugriff (PDF)

Functionalized Cyclophellitols Are Selective Glucocerebrosidase Inhibitors and Induce a Bona Fide Neuropathic Gaucher Model in Zebrafish

Journal of the American Chemical Society, 2019-03, Vol.141 (10), p.4214-4218

2019

Volltextzugriff (PDF)

a-Synuclein and lipids in erythrocytes of Gaucher disease carriers and patients before and after enzyme replacement therapy

PloS one, 2023-02, Vol.18 (2), p.e0277602-e0277602

2023

Volltextzugriff (PDF)

Glycosphingolipids-Nature, Function, and Pharmacological Modulation

Angewandte Chemie International Edition, 2009-11, Vol.48 (47), p.8848-8869

2009

Volltextzugriff (PDF)

Long-term effect of antibodies against infused alpha-galactosidase A in Fabry disease on plasma and urinary (lyso)Gb3 reduction and treatment outcome

PloS one, 2012-10, Vol.7 (10), p.e47805-e47805

2012

Volltextzugriff (PDF)

Fluorescence polarisation activity-based protein profiling for the identification of deoxynojirimycin-type inhibitors selective for lysosomal retaining alpha- and beta-glucosidases

Chemical science (Cambridge), 2023-08, Vol.14 (34), p.9136-9144

2023

Volltextzugriff (PDF)

Plant Glycosides and Glycosidases: A Treasure-Trove for Therapeutics

Frontiers in plant science, 2020-04, Vol.11, p.357-357

2020

Volltextzugriff (PDF)

Lysosomal glycosphingolipid catabolism by acid ceramidase: formation of glycosphingoid bases during deficiency of glycosidases

FEBS letters, 2016-03, Vol.590 (6), p.716-725

2016

Volltextzugriff (PDF)

The Unique Phenotype of Lipid-Laden Macrophages

International journal of molecular sciences, 2021-04, Vol.22 (8), p.4039

2021

Volltextzugriff (PDF)

Induction of Sphk1 activity in obese adipose tissue macrophages promotes survival

PloS one, 2017-07, Vol.12 (7), p.e0182075-e0182075

2017

Volltextzugriff (PDF)

Gpnmb Is a Potential Marker for the Visceral Pathology in Niemann-Pick Type C Disease

PloS one, 2016-01, Vol.11 (1), p.e0147208-e0147208

2016

Volltextzugriff (PDF)

LIMP-2 expression is critical for β-glucocerebrosidase activity and α-synuclein clearance

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (43), p.15573-15578

2014

Volltextzugriff (PDF)

Establishing 3-nitrotyrosine as a biomarker for the vasculopathy of Fabry disease

Kidney international, 2014-07, Vol.86 (1), p.58-66

2014

Volltextzugriff (PDF)

Manno-epi-cyclophellitols Enable Activity-Based Protein Profiling of Human α‑Mannosidases and Discovery of New Golgi Mannosidase II Inhibitors

Journal of the American Chemical Society, 2020-07, Vol.142 (30), p.13021-13029

2020

Volltextzugriff (PDF)

Activity-Based Protein Profiling of Retaining α‑Amylases in Complex Biological Samples

Journal of the American Chemical Society, 2021-02, Vol.143 (5), p.2423-2432

2021

Volltextzugriff (PDF)

The development of a broad-spectrum retaining β-exo-galactosidase activity-based probe

Organic & biomolecular chemistry, 2023-10, Vol.21 (38), p.7813-782

2023

Volltextzugriff (PDF)

Elevated globotriaosylsphingosine is a hallmark of Fabry disease

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (8), p.2812-2817

2008

Volltextzugriff (PDF)

Animal Models for the Study of Gaucher Disease

International journal of molecular sciences, 2023-11, Vol.24 (22), p.16035

2023

Volltextzugriff (PDF)

Elevated plasma glucosylsphingosine in Gaucher disease: relation to phenotype, storage cell markers, and therapeutic response

Blood, 2011-10, Vol.118 (16), p.e118-e127

2011

Volltextzugriff (PDF)

Real‐Time NMR Recording of Fermentation and Lipid Metabolism Processes in Live Microalgae Cells

Angewandte Chemie International Edition, 2022-03, Vol.61 (14), p.e202117521-n/a

International ed. in English, 2022

Volltextzugriff (PDF)

Reducing GBA2 Activity Ameliorates Neuropathology in Niemann-Pick Type C Mice

PloS one, 2015-08, Vol.10 (8), p.e0135889-e0135889

2015

Volltextzugriff (PDF)

Linking Smokers’ Susceptibility to Tuberculosis with Lysosomal Storage Disorders

Developmental cell, 2016-04, Vol.37 (2), p.112-113

2016

Volltextzugriff (PDF)

Structure-guided design of C3-branched swainsonine as potent and selective human Golgi α-mannosidase (GMII) inhibitor

Chemical communications (Cambridge, England), 2024-10, Vol.60 (82), p.11734-11737

2024

Volltextzugriff (PDF)

Visualization of Active Glucocerebrosidase in Rodent Brain with High Spatial Resolution following In Situ Labeling with Fluorescent Activity Based Probes

PloS one, 2015-09, Vol.10 (9), p.e0138107-e0138107

2015

Volltextzugriff (PDF)

1 – 25 von 367

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(349)
Mit Volltextzugriff
(342)

Publikationsform

Sprache

Englisch
(360)
Deutsch
(3)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Evolution of Mammalian Chitinase(-Like) Members of Family 18 Glycosyl Hydrolases

Functionalized Cyclophellitols Are Selective Glucocerebrosidase Inhibitors and Induce a Bona Fide Neuropathic Gaucher Model in Zebrafish

a-Synuclein and lipids in erythrocytes of Gaucher disease carriers and patients before and after enzyme replacement therapy

Glycosphingolipids-Nature, Function, and Pharmacological Modulation

Long-term effect of antibodies against infused alpha-galactosidase A in Fabry disease on plasma and urinary (lyso)Gb3 reduction and treatment outcome

Fluorescence polarisation activity-based protein profiling for the identification of deoxynojirimycin-type inhibitors selective for lysosomal retaining alpha- and beta-glucosidases

Plant Glycosides and Glycosidases: A Treasure-Trove for Therapeutics

Lysosomal glycosphingolipid catabolism by acid ceramidase: formation of glycosphingoid bases during deficiency of glycosidases

The Unique Phenotype of Lipid-Laden Macrophages

Induction of Sphk1 activity in obese adipose tissue macrophages promotes survival

Gpnmb Is a Potential Marker for the Visceral Pathology in Niemann-Pick Type C Disease

LIMP-2 expression is critical for β-glucocerebrosidase activity and α-synuclein clearance

Establishing 3-nitrotyrosine as a biomarker for the vasculopathy of Fabry disease

Manno-epi-cyclophellitols Enable Activity-Based Protein Profiling of Human α‑Mannosidases and Discovery of New Golgi Mannosidase II Inhibitors

Activity-Based Protein Profiling of Retaining α‑Amylases in Complex Biological Samples

The development of a broad-spectrum retaining β-exo-galactosidase activity-based probe

Elevated globotriaosylsphingosine is a hallmark of Fabry disease

Animal Models for the Study of Gaucher Disease

Elevated plasma glucosylsphingosine in Gaucher disease: relation to phenotype, storage cell markers, and therapeutic response

Real‐Time NMR Recording of Fermentation and Lipid Metabolism Processes in Live Microalgae Cells

Reducing GBA2 Activity Ameliorates Neuropathology in Niemann-Pick Type C Mice

Linking Smokers’ Susceptibility to Tuberculosis with Lysosomal Storage Disorders

Current methods to analyze lysosome morphology, positioning, motility and function

Structure-guided design of C3-branched swainsonine as potent and selective human Golgi α-mannosidase (GMII) inhibitor

Visualization of Active Glucocerebrosidase in Rodent Brain with High Spatial Resolution following In Situ Labeling with Fluorescent Activity Based Probes

Suchergebnisse filtern