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...

Lysosomal multienzyme complex: pros and cons of working together

Cellular and molecular life sciences : CMLS, 2014-06, Vol.71 (11), p.2017-2032

2014

Volltextzugriff (PDF)

Analysis of Generalized Fibrosis in Mouse Tissue Sections with Masson's Trichrome Staining

Bio-protocol, 2020-05, Vol.10 (10), p.e3629-e3629

2020

Volltextzugriff (PDF)

Broad and direct interaction between TLR and Siglec families of pattern recognition receptors and its regulation by Neu1

eLife, 2014-09, Vol.3, p.e04066

2014

Volltextzugriff (PDF)

Lysosomal NEU1 deficiency affects amyloid precursor protein levels and amyloid-β secretion via deregulated lysosomal exocytosis

Nature communications, 2013-11, Vol.4 (1), p.2734-2734, Article 2734

2013

Volltextzugriff (PDF)

GM1-Ganglioside Accumulation at the Mitochondria-Associated ER Membranes Links ER Stress to Ca2+-Dependent Mitochondrial Apoptosis

Molecular cell, 2009-11, Vol.36 (3), p.500-511

2009

Volltextzugriff (PDF)

Bis(monoacylglycero)phosphate: a secondary storage lipid in the gangliosidoses

Journal of lipid research, 2015-05, Vol.56 (5), p.1005-1006

2015

Volltextzugriff (PDF)

Molecular mechanisms of pathogenesis in a glycosphingolipid and a glycoprotein storage disease

Biochemical Society transactions, 2010-12, Vol.38 (6), p.1453-1457

2010

Volltextzugriff (PDF)

Skeletal muscle cells derived from mouse skin cultures

Biochemical and biophysical research communications, 2020-07, Vol.528 (2), p.398-403

2020

Volltextzugriff (PDF)

Identification and characterization of the nano-sized vesicles released by muscle cells

FEBS letters, 2013-05, Vol.587 (9), p.1379-1384

2013

Volltextzugriff (PDF)

AAV-mediated gene therapy for sialidosis

Molecular therapy, 2024-07, Vol.32 (7), p.2094-2112

2024

Volltextzugriff (PDF)

E3 Ubiquitin Ligases as Regulators of Membrane Protein Trafficking and Degradation

Traffic (Copenhagen, Denmark), 2005-06, Vol.6 (6), p.429-441

2005

Volltextzugriff (PDF)

Distinct functions of dimeric and monomeric scaffold protein Alix in regulating F-actin assembly and loading of exosomal cargo

The Journal of biological chemistry, 2022-10, Vol.298 (10), p.102425-102425, Article 102425

2022

Volltextzugriff (PDF)

Glycosphingolipids within membrane contact sites influence their function as signaling hubs in neurodegenerative diseases

FEBS open bio, 2023-09, Vol.13 (9), p.1587-1600

2023

Volltextzugriff (PDF)

Transcription factor competition regulates lysosomal biogenesis and autophagy

Molecular & cellular oncology, 2020-03, Vol.7 (2), p.1685840-1685840

2020

Volltextzugriff (PDF)

Generation of human induced pluripotent stem cells (hIPSCs) from sialidosis types I and II patients with pathogenic neuraminidase 1 mutations

Stem cell research, 2020-07, Vol.46, p.101836-101836, Article 101836

2020

Volltextzugriff (PDF)

Intracerebroventricular enzyme replacement therapy with β-galactosidase reverses brain pathologies due to GM1 gangliosidosis in mice

The Journal of biological chemistry, 2020-09, Vol.295 (39), p.13532-13555

2020

Volltextzugriff (PDF)

Mitochondria-associated ER membranes (MAMs) and lysosomal storage diseases

Cell death & disease, 2018-02, Vol.9 (3), p.328-16, Article 328

2018

Volltextzugriff (PDF)

Lysosomal storage diseases

Nature reviews. Disease primers, 2018-10, Vol.4 (1), p.27-27, Article 27

2018

Volltextzugriff (PDF)

Isolation of mitochondria-associated ER membranes (MAMs) and glycosphingolipid-enriched microdomains (GEMs) from brain tissues and neuronal cells

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1264, p.25

2015

Volltextzugriff (PDF)

Intermittent enzyme replacement therapy with recombinant human β-galactosidase prevents neuraminidase 1 deficiency

The Journal of biological chemistry, 2020-09, Vol.295 (39), p.13556-13569

2020

Volltextzugriff (PDF)

Neuraminidase 1 Is a Negative Regulator of Lysosomal Exocytosis

Developmental cell, 2008-07, Vol.15 (1), p.74-86

2008

Volltextzugriff (PDF)

Isolation, Purification and Characterization of Exosomes from Fibroblast Cultures of Skeletal Muscle

Bio-protocol, 2020-04, Vol.10 (7)

2020

Volltextzugriff (PDF)

Chaperone-mediated gene therapy with recombinant AAV-PPCA in a new mouse model of type I sialidosis

Biochimica et biophysica acta, 2013-10, Vol.1832 (10), p.1784-1792

2013

Volltextzugriff (PDF)

Heterodimerization of the Sialidase NEU1 with the Chaperone Protective Protein/Cathepsin A Prevents Its Premature Oligomerization

The Journal of biological chemistry, 2009-10, Vol.284 (41), p.28430-28441

2009

Volltextzugriff (PDF)

Galactosialidosis: historic aspects and overview of investigated and emerging treatment options

Expert opinion on orphan drugs, 2017-02, Vol.5 (2), p.131-141

2017

Volltextzugriff (PDF)

1 – 25 von 203

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(192)
Mit Volltextzugriff
(179)

Publikationsform

Artikel
(197)
Buchkapitel
(6)

Sprache

Englisch
(202)
Portugiesisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(122)
Life Sciences & Biomedicine
(109)
Animals
(83)
Humans
(83)
Mice
(58)
Biochemistry & Molecular Biology
(50)
Cell Biology
(37)
Male
(34)
Biological And Medical Sciences
(32)
Genetics & Heredity
(31)
Neuraminidase - Genetics
(26)
Neuraminidase - Metabolism
(26)
Mice, Knockout
(25)
Disease Models, Animal
(22)
Female
(22)
Mutation
(22)
Beta-Galactosidase - Genetics
(21)
Cathepsin A
(21)
Beta-Galactosidase - Metabolism
(19)
Fundamental And Applied Biological Sciences. Psychology
(19)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Lysosomal multienzyme complex: pros and cons of working together

Analysis of Generalized Fibrosis in Mouse Tissue Sections with Masson's Trichrome Staining

Broad and direct interaction between TLR and Siglec families of pattern recognition receptors and its regulation by Neu1

Lysosomal NEU1 deficiency affects amyloid precursor protein levels and amyloid-β secretion via deregulated lysosomal exocytosis

GM1-Ganglioside Accumulation at the Mitochondria-Associated ER Membranes Links ER Stress to Ca2+-Dependent Mitochondrial Apoptosis

Bis(monoacylglycero)phosphate: a secondary storage lipid in the gangliosidoses

Molecular mechanisms of pathogenesis in a glycosphingolipid and a glycoprotein storage disease

Skeletal muscle cells derived from mouse skin cultures

Identification and characterization of the nano-sized vesicles released by muscle cells

AAV-mediated gene therapy for sialidosis

E3 Ubiquitin Ligases as Regulators of Membrane Protein Trafficking and Degradation

Distinct functions of dimeric and monomeric scaffold protein Alix in regulating F-actin assembly and loading of exosomal cargo

Glycosphingolipids within membrane contact sites influence their function as signaling hubs in neurodegenerative diseases

Transcription factor competition regulates lysosomal biogenesis and autophagy

Generation of human induced pluripotent stem cells (hIPSCs) from sialidosis types I and II patients with pathogenic neuraminidase 1 mutations

Intracerebroventricular enzyme replacement therapy with β-galactosidase reverses brain pathologies due to GM1 gangliosidosis in mice

Mitochondria-associated ER membranes (MAMs) and lysosomal storage diseases

Lysosomal storage diseases

Isolation of mitochondria-associated ER membranes (MAMs) and glycosphingolipid-enriched microdomains (GEMs) from brain tissues and neuronal cells

Intermittent enzyme replacement therapy with recombinant human β-galactosidase prevents neuraminidase 1 deficiency

Neuraminidase 1 Is a Negative Regulator of Lysosomal Exocytosis

Isolation, Purification and Characterization of Exosomes from Fibroblast Cultures of Skeletal Muscle

Chaperone-mediated gene therapy with recombinant AAV-PPCA in a new mouse model of type I sialidosis

Heterodimerization of the Sialidase NEU1 with the Chaperone Protective Protein/Cathepsin A Prevents Its Premature Oligomerization

Galactosialidosis: historic aspects and overview of investigated and emerging treatment options

Suchergebnisse filtern