UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 94

Sortiert nach

Postmortem toxicology findings from the Camden Opioid Research Initiative

PloS one, 2023-11, Vol.18 (11), p.e0292674-e0292674

2023

Volltextzugriff (PDF)

RNA Sequencing in Hypoxia-Adapted T98G Glioblastoma Cells Provides Supportive Evidence for IRE1 as a Potential Therapeutic Target

Genes, 2023-03, Vol.14 (4), p.841

2023

Volltextzugriff (PDF)

BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice

Frontiers in systems neuroscience, 2014-06, Vol.8, p.121-121

2014

Volltextzugriff (PDF)

The Molecular Genetic Interaction Between Circadian Rhythms and Susceptibility to Seizures and Epilepsy

Frontiers in neurology, 2020-06, Vol.11, p.520-520

2020

Volltextzugriff (PDF)

Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure‐susceptible DBA/2 mice

Epilepsia (Copenhagen), 2010-09, Vol.51 (9), p.1707-1713

2010

Volltextzugriff (PDF)

Patient Perceptions and Potential Utility of Pharmacogenetic Testing in Chronic Pain Management and Opioid Use Disorder in the Camden Opioid Research Initiative

Pharmaceutics, 2022-09, Vol.14 (9), p.1863

2022

Volltextzugriff (PDF)

Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy

Genes, 2021-09, Vol.12 (9), p.1441

2021

Volltextzugriff (PDF)

In vitro and ex vivo analysis of CHRNA3 and CHRNA5 haplotype expression

PloS one, 2011-08, Vol.6 (8), p.e23373

2011

Volltextzugriff (PDF)

Genome wide association studies (GWAS) and common forms of human epilepsy

Epilepsy & behavior, 2013-07, Vol.28 (1), p.S63-S65

Buono, Russell J

2013

Volltextzugriff (PDF)

Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene

Mammalian genome, 2004-04, Vol.15 (4), p.239-251

2004

Volltextzugriff (PDF)

Proteomic and Behavioral Analysis of Response to Isoliquiritigenin in Brains of Acute Cocaine Treated Rats

Journal of proteome research, 2008-12, Vol.7 (12), p.5094-5102

2008

Volltextzugriff (PDF)

Mapping Loci for Pentylenetetrazol-Induced Seizure Susceptibility in Mice

The Journal of neuroscience, 1999-08, Vol.19 (16), p.6733-6739

1999

Volltextzugriff (PDF)

Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants

Neurology, 2022-05, Vol.98 (20), p.e2046

2022

Volltextzugriff (PDF)

Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy

Annals of neurology, 2023-04, Vol.93 (4), p.752-761

2023

Volltextzugriff (PDF)

Investigation of long interspersed element‐1 retrotransposons as potential risk factors for idiopathic temporal lobe epilepsy

Epilepsia (Copenhagen), 2021-06, Vol.62 (6), p.1329-1342

2021

Volltextzugriff (PDF)

Association between Polymorphisms in the Vesicular Monoamine Transporter 1 Gene (VMAT1/SLC18A1) on Chromosome 8p and Schizophrenia

Neuropsychobiology, 2008-01, Vol.57 (1-2), p.55-60

2008

Volltextzugriff (PDF)

Cognitive and behavioral effects of brief seizures in mice

Epilepsy & behavior, 2019-09, Vol.98 (Pt A), p.249-257

2019

Volltextzugriff (PDF)

Predisposition to epilepsy—Does the ABCB1 gene play a role?

Epilepsia (Copenhagen), 2010-09, Vol.51 (9), p.1882-1885

2010

Volltextzugriff (PDF)

Genetic variants in the cocaine- and amphetamine-regulated transcript gene ( CARTPT) and cocaine dependence

Neuroscience letters, 2008-08, Vol.440 (3), p.280-283

2008

Volltextzugriff (PDF)

Identification and functional significance of polymorphisms in the μ-opioid receptor gene ( Oprm) promoter of C57BL/6 and DBA/2 mice

Neuroscience research, 2006-07, Vol.55 (3), p.244-254

2006

Volltextzugriff (PDF)

The golden brain bank: An Alzheimer’s disease tissue repository

Alzheimer's & dementia, 2015-07, Vol.11 (7), p.P500-P500

2015

Volltextzugriff (PDF)

Novel De Novo Mutation of a Conserved SCN1A Amino-Acid Residue (R1596)

Pediatric neurology, 2007-10, Vol.37 (4), p.303-305

2007

Volltextzugriff (PDF)

Lack of Association Between an Interleukin 1 Beta (IL‐1β) Gene Variation and Refractory Temporal Lobe Epilepsy

Epilepsia (Copenhagen), 2001-06, Vol.42 (6), p.782-784

2001

Volltextzugriff (PDF)

The relationship between the pharmacology of antiepileptic drugs and human gene variation: An overview

Epilepsy & behavior, 2005-08, Vol.7 (1), p.18-36

2005

Volltextzugriff (PDF)

Quantitative trait loci analysis reveals candidate genes implicated in regulating functional deficit and CNS vascular permeability in CD8 T cell-initiated blood-brain barrier disruption

BMC genomics, 2013-10, Vol.14 (1), p.678-678

2013

Volltextzugriff (PDF)

1 – 25 von 94

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(90)
Mit Volltextzugriff
(86)

Publikationsform

Artikel
(94)

Sprache

Englisch
(94)
Japanisch
(15)

Erscheinungsjahr

n.n

Thema

Science & Technology
(71)
Life Sciences & Biomedicine
(68)
Humans
(43)
Neurosciences & Neurology
(32)
Animals
(25)
Biological And Medical Sciences
(25)
Clinical Neurology
(20)
Male
(20)
Medical Sciences
(20)
Epilepsy
(18)
Neurology
(18)
Neurosciences
(18)
Meta-Analysis
(15)
Mice
(15)
Genotype
(14)
Mice, Inbred C57bl
(14)
Epilepsy - Genetics
(13)
Female
(13)
Genetics & Heredity
(12)
Genetic Predisposition To Disease - Genetics
(11)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Postmortem toxicology findings from the Camden Opioid Research Initiative

RNA Sequencing in Hypoxia-Adapted T98G Glioblastoma Cells Provides Supportive Evidence for IRE1 as a Potential Therapeutic Target

BMAL1 controls the diurnal rhythm and set point for electrical seizure threshold in mice

The Molecular Genetic Interaction Between Circadian Rhythms and Susceptibility to Seizures and Epilepsy

Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure‐susceptible DBA/2 mice

Patient Perceptions and Potential Utility of Pharmacogenetic Testing in Chronic Pain Management and Opioid Use Disorder in the Camden Opioid Research Initiative

Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy

In vitro and ex vivo analysis of CHRNA3 and CHRNA5 haplotype expression

Genome wide association studies (GWAS) and common forms of human epilepsy

Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene

Proteomic and Behavioral Analysis of Response to Isoliquiritigenin in Brains of Acute Cocaine Treated Rats

Mapping Loci for Pentylenetetrazol-Induced Seizure Susceptibility in Mice

Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants

Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy

Investigation of long interspersed element‐1 retrotransposons as potential risk factors for idiopathic temporal lobe epilepsy

Association between Polymorphisms in the Vesicular Monoamine Transporter 1 Gene (VMAT1/SLC18A1) on Chromosome 8p and Schizophrenia

Cognitive and behavioral effects of brief seizures in mice

Predisposition to epilepsy—Does the ABCB1 gene play a role?

Genetic variants in the cocaine- and amphetamine-regulated transcript gene ( CARTPT) and cocaine dependence

Identification and functional significance of polymorphisms in the μ-opioid receptor gene ( Oprm) promoter of C57BL/6 and DBA/2 mice

The golden brain bank: An Alzheimer’s disease tissue repository

Novel De Novo Mutation of a Conserved SCN1A Amino-Acid Residue (R1596)

Lack of Association Between an Interleukin 1 Beta (IL‐1β) Gene Variation and Refractory Temporal Lobe Epilepsy

The relationship between the pharmacology of antiepileptic drugs and human gene variation: An overview

Quantitative trait loci analysis reveals candidate genes implicated in regulating functional deficit and CNS vascular permeability in CD8 T cell-initiated blood-brain barrier disruption

Suchergebnisse filtern