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...

Dystroglycan: from biosynthesis to pathogenesis of human disease

Journal of cell science, 2006-01, Vol.119 (2), p.199-207

2006

Volltextzugriff (PDF)

Dystroglycan Function Requires Xylosyl- and Glucuronyltransferase Activities of LARGE

Science (American Association for the Advancement of Science), 2012-01, Vol.335 (6064), p.93-96

2012

Volltextzugriff (PDF)

Lassa Fever Virus Binds Matriglycan-A Polymer of Alternating Xylose and Glucuronate-On α-Dystroglycan

Viruses, 2021-08, Vol.13 (9), p.1679

2021

Volltextzugriff (PDF)

Structural basis of laminin binding to the LARGE glycans on dystroglycan

Nature chemical biology, 2016-10, Vol.12 (10), p.810-814

2016

Volltextzugriff (PDF)

Cell surface glycan engineering reveals that matriglycan alone can recapitulate dystroglycan binding and function

Nature communications, 2022-06, Vol.13 (1), p.3617-3617, Article 3617

2022

Volltextzugriff (PDF)

O-Mannosyl Phosphorylation of Alpha-Dystroglycan Is Required for Laminin Binding

Science (American Association for the Advancement of Science), 2010, Vol.327 (5961), p.88-92

2010

Volltextzugriff (PDF)

Neuronal Dystroglycan Is Necessary for Formation and Maintenance of Functional CCK-Positive Basket Cell Terminals on Pyramidal Cells

The Journal of neuroscience, 2016-10, Vol.36 (40), p.10296-10313

2016

Volltextzugriff (PDF)

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

Nature (London), 2013-11, Vol.503 (7474), p.136-140

2013

Volltextzugriff (PDF)

Auxiliary subunits: essential components of the voltage-gated calcium channel complex

Current opinion in neurobiology, 2003-06, Vol.13 (3), p.298-307

2003

Volltextzugriff (PDF)

Dysferlin and the plasma membrane repair in muscular dystrophy

Trends in cell biology, 2004-04, Vol.14 (4), p.206-213

2004

Volltextzugriff (PDF)

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

Nature genetics, 2012-05, Vol.44 (5), p.575-580

2012

Volltextzugriff (PDF)

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function

The Journal of biological chemistry, 2003-05, Vol.278 (18), p.15457-15460

2003

Volltextzugriff (PDF)

An HMGA2-IGF2BP2 Axis Regulates Myoblast Proliferation and Myogenesis

Developmental cell, 2012-12, Vol.23 (6), p.1176-1188

2012

Volltextzugriff (PDF)

Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan

American journal of human genetics, 2013-07, Vol.93 (1), p.29-41

2013

Volltextzugriff (PDF)

Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan

American journal of human genetics, 2013-03, Vol.92 (3), p.354-365

2013

Volltextzugriff (PDF)

Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly

American journal of human genetics, 2016-11, Vol.99 (5), p.1181-1189

2016

Volltextzugriff (PDF)

Sarcolemma-localized nNOS is required to maintain activity after mild exercise

Nature, 2008-11, Vol.456 (7221), p.511-515

2008

Volltextzugriff (PDF)

Muscular dystrophies involving the dystrophin–glycoprotein complex: an overview of current mouse models

Current Opinion in Genetics & Development, 2002-06, Vol.12 (3), p.349-361

2002

Volltextzugriff (PDF)

The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation

eLife, 2014-10, Vol.3

2014

Volltextzugriff (PDF)

Transcriptional Upregulation of Cav3.2 Mediates Epileptogenesis in the Pilocarpine Model of Epilepsy

The Journal of neuroscience, 2008-12, Vol.28 (49), p.13341-13353

2008

Volltextzugriff (PDF)

Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle

Proceedings of the National Academy of Sciences - PNAS, 2016-09, Vol.113 (39), p.10992-10997

2016

Volltextzugriff (PDF)

Caᵥ3.2 T-type calcium channel is required for the NFAT-dependent Sox9 expression in tracheal cartilage

Proceedings of the National Academy of Sciences - PNAS, 2014-05, Vol.111 (19), p.E1990-E1998

2014

Volltextzugriff (PDF)

Evidence for a role of dystroglycan regulating the membrane architecture of astroglial endfeet

The European journal of neuroscience, 2011-06, Vol.33 (12), p.2179-2186

2011

Volltextzugriff (PDF)

The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition

eLife, 2016-04, Vol.5

2016

Volltextzugriff (PDF)

N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy

eLife, 2023-02, Vol.12

2023

Volltextzugriff (PDF)

1 – 25 von 1.153

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.096)
Mit Volltextzugriff
(1.029)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(1.146)
Japanisch
(9)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(752)
Life Sciences & Biomedicine
(642)
Humans
(422)
Animals
(352)
Male
(227)
Female
(213)
Biological And Medical Sciences
(193)
Mice
(190)
Biochemistry & Molecular Biology
(134)
Cell Biology
(107)
Medical Sciences
(107)
Adult
(99)
Fundamental And Applied Biological Sciences. Psychology
(99)
Middle Aged
(89)
Neurosciences & Neurology
(87)
Neurosciences
(78)
Proteins
(77)
Dystroglycans
(73)
Science & Technology - Other Topics
(73)
Muscular Dystrophy
(72)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)
... seit 90 Tagen
(11)

Menü

Weitere Dienste

Einstellungen

Dystroglycan: from biosynthesis to pathogenesis of human disease

Dystroglycan Function Requires Xylosyl- and Glucuronyltransferase Activities of LARGE

Lassa Fever Virus Binds Matriglycan-A Polymer of Alternating Xylose and Glucuronate-On α-Dystroglycan

Structural basis of laminin binding to the LARGE glycans on dystroglycan

Cell surface glycan engineering reveals that matriglycan alone can recapitulate dystroglycan binding and function

O-Mannosyl Phosphorylation of Alpha-Dystroglycan Is Required for Laminin Binding

Neuronal Dystroglycan Is Necessary for Formation and Maintenance of Functional CCK-Positive Basket Cell Terminals on Pyramidal Cells

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

Auxiliary subunits: essential components of the voltage-gated calcium channel complex

Dysferlin and the plasma membrane repair in muscular dystrophy

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function

An HMGA2-IGF2BP2 Axis Regulates Myoblast Proliferation and Myogenesis

Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan

Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan

Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly

Sarcolemma-localized nNOS is required to maintain activity after mild exercise

Muscular dystrophies involving the dystrophin–glycoprotein complex: an overview of current mouse models

The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation

Transcriptional Upregulation of Cav3.2 Mediates Epileptogenesis in the Pilocarpine Model of Epilepsy

Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle

Caᵥ3.2 T-type calcium channel is required for the NFAT-dependent Sox9 expression in tracheal cartilage

Evidence for a role of dystroglycan regulating the membrane architecture of astroglial endfeet

The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition

N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy

Suchergebnisse filtern