UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 104

Sortiert nach

Berberine Suppressed the Progression of Human Glioma Cells by Inhibiting the TGF-β1/SMAD2/3 Signaling Pathway

Integrative cancer therapies, 2022, Vol.21, p.153473542211303-15347354221130303

2022

Volltextzugriff (PDF)

Astrocytic GABA transporter 1 deficit in novel SLC6A1 variants mediated epilepsy: Connected from protein destabilization to seizures in mice and humans

Neurobiology of disease, 2022-10, Vol.172, p.105810-105810, Article 105810

2022

Volltextzugriff (PDF)

Modulating Endoplasmic Reticulum Chaperones and Mutant Protein Degradation in GABRG2(Q390X) Associated with Genetic Epilepsy with Febrile Seizures Plus and Dravet Syndrome

International journal of molecular sciences, 2024-05, Vol.25 (9), p.4601

2024

Volltextzugriff (PDF)

The K328M substitution in the human GABAA receptor gamma2 subunit causes GEFS+ and premature sudden death in knock-in mice

Neurobiology of disease, 2021-05, Vol.152, p.105296-105296, Article 105296

2021

Volltextzugriff (PDF)

GABAA Receptor β3 Subunit Mutation N328D Heterozygous Knock-in Mice Have Lennox–Gastaut Syndrome

International journal of molecular sciences, 2023-05, Vol.24 (9), p.8458

2023

Volltextzugriff (PDF)

Epileptic Encephalopathy GABRB Structural Variants Share Common Gating and Trafficking Defects

Biomolecules (Basel, Switzerland), 2023-12, Vol.13 (12), p.1790

2023

Volltextzugriff (PDF)

Trafficking-deficient mutant GABRG2 subunit amount may modify epilepsy phenotype

Annals of neurology, 2013-10, Vol.74 (4), p.547-559

2013

Volltextzugriff (PDF)

Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autism

Molecular brain, 2020-05, Vol.13 (1), p.76-76, Article 76

2020

Volltextzugriff (PDF)

GABRG2 Variants Associated with Febrile Seizures

Biomolecules (Basel, Switzerland), 2023-02, Vol.13 (3), p.414

2023

Volltextzugriff (PDF)

Beyond Epilepsy and Autism: Disruption of GABRB3 Causes Ocular Hypopigmentation

Cell reports (Cambridge), 2016-12, Vol.17 (12), p.3115-3124

2016

Volltextzugriff (PDF)

Impaired surface αβγ GABAA receptor expression in familial epilepsy due to a GABRG2 frameshift mutation

Neurobiology of disease, 2013-02, Vol.50, p.135-141

2013

Volltextzugriff (PDF)

Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

HGG advances, 2022-10, Vol.3 (4), p.100131-100131, Article 100131

2022

Volltextzugriff (PDF)

Quantitation of protein kinase A-mediated trafficking of cardiac sodium channels in living cells

Cardiovascular research, 2006-11, Vol.72 (2), p.250-261

2006

Volltextzugriff (PDF)

A review on the assembly of multi-substituted pyridines via Co-catalyzed [2 + 2 + 2] cycloaddition with nitriles

Organic & biomolecular chemistry, 2022-09, Vol.20 (37), p.7391-7404

2022

Volltextzugriff (PDF)

Ginsenoside Rg1 improved learning and memory ability and reduces neuronal apoptosis in epileptic rats through ERK/CREB/BDNF signal pathway

Biochemical and biophysical research communications, 2023-10, Vol.675, p.26-32

2023

Volltextzugriff (PDF)

Dedifferentiation of patient‐derived glioblastoma multiforme cell lines results in a cancer stem cell‐like state with mitogen‐independent growth

Journal of cellular and molecular medicine, 2015-06, Vol.19 (6), p.1262-1272

2015

Volltextzugriff (PDF)

The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegeneration

Nature neuroscience, 2015-07, Vol.18 (7), p.988-996

2015

Volltextzugriff (PDF)

Genetic mosaicism, intrafamilial phenotypic heterogeneity, and molecular defects of a novel missense SLC6A1 mutation associated with epilepsy and ADHD

Experimental neurology, 2021-08, Vol.342, p.113723-113723, Article 113723

2021

Volltextzugriff (PDF)

Phosphorylation and Putative ER Retention Signals Are Required for Protein Kinase A-Mediated Potentiation of Cardiac Sodium Current

Circulation research, 2002-09, Vol.91 (6), p.540-546

2002

Volltextzugriff (PDF)

A Novel GABRG2 mutation, p.R136, in a family with GEFS + and extended phenotypes

Neurobiology of disease, 2014-04, Vol.64, p.131-141

2014

Volltextzugriff (PDF)

Common molecular mechanisms of SLC6A1 variant-mediated neurodevelopmental disorders in astrocytes and neurons

Brain (London, England : 1878), 2021-09, Vol.144 (8), p.2499-2512

2021

Volltextzugriff (PDF)

A review on the assembly of multi-substituted pyridines Co-catalyzed [2 + 2 + 2] cycloaddition with nitriles

Organic & biomolecular chemistry, 2022-09, Vol.2 (37), p.7391-744

2022

Volltextzugriff (PDF)

Synthesis and properties of sugar-based surfactants alkoxyethyl β-D-glucopyranoside

Colloids and surfaces. A, Physicochemical and engineering aspects, 2019-03, Vol.564, p.59-68

2019

Volltextzugriff (PDF)

LncRNA MIR4435‐2HG functions as a ceRNA against miR‐125a‐5p and promotes neuroglioma development by upregulating TAZ

Journal of clinical laboratory analysis, 2021-12, Vol.35 (12), p.e24066-n/a

2021

Volltextzugriff (PDF)

Epileptic Encephalopathy IGABRB/I Structural Variants Share Common Gating and Trafficking Defects

Biomolecules (Basel, Switzerland), 2023-12, Vol.13 (12)

2023

Volltextzugriff (PDF)

1 – 25 von 104

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(102)
Mit Volltextzugriff
(99)

Publikationsform

Artikel
(104)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Berberine Suppressed the Progression of Human Glioma Cells by Inhibiting the TGF-β1/SMAD2/3 Signaling Pathway

Astrocytic GABA transporter 1 deficit in novel SLC6A1 variants mediated epilepsy: Connected from protein destabilization to seizures in mice and humans

Modulating Endoplasmic Reticulum Chaperones and Mutant Protein Degradation in GABRG2(Q390X) Associated with Genetic Epilepsy with Febrile Seizures Plus and Dravet Syndrome

The K328M substitution in the human GABAA receptor gamma2 subunit causes GEFS+ and premature sudden death in knock-in mice

GABAA Receptor β3 Subunit Mutation N328D Heterozygous Knock-in Mice Have Lennox–Gastaut Syndrome

Epileptic Encephalopathy GABRB Structural Variants Share Common Gating and Trafficking Defects

Trafficking-deficient mutant GABRG2 subunit amount may modify epilepsy phenotype

Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autism

GABRG2 Variants Associated with Febrile Seizures

Beyond Epilepsy and Autism: Disruption of GABRB3 Causes Ocular Hypopigmentation

Impaired surface αβγ GABAA receptor expression in familial epilepsy due to a GABRG2 frameshift mutation

Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

Quantitation of protein kinase A-mediated trafficking of cardiac sodium channels in living cells

A review on the assembly of multi-substituted pyridines via Co-catalyzed [2 + 2 + 2] cycloaddition with nitriles

Ginsenoside Rg1 improved learning and memory ability and reduces neuronal apoptosis in epileptic rats through ERK/CREB/BDNF signal pathway

Dedifferentiation of patient‐derived glioblastoma multiforme cell lines results in a cancer stem cell‐like state with mitogen‐independent growth

The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegeneration

Genetic mosaicism, intrafamilial phenotypic heterogeneity, and molecular defects of a novel missense SLC6A1 mutation associated with epilepsy and ADHD

Phosphorylation and Putative ER Retention Signals Are Required for Protein Kinase A-Mediated Potentiation of Cardiac Sodium Current

A Novel GABRG2 mutation, p.R136, in a family with GEFS + and extended phenotypes

Common molecular mechanisms of SLC6A1 variant-mediated neurodevelopmental disorders in astrocytes and neurons

A review on the assembly of multi-substituted pyridines Co-catalyzed [2 + 2 + 2] cycloaddition with nitriles

Synthesis and properties of sugar-based surfactants alkoxyethyl β-D-glucopyranoside

LncRNA MIR4435‐2HG functions as a ceRNA against miR‐125a‐5p and promotes neuroglioma development by upregulating TAZ

Epileptic Encephalopathy IGABRB/I Structural Variants Share Common Gating and Trafficking Defects

Suchergebnisse filtern