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...

SCN1A mutations and epilepsy

Human mutation, 2005-06, Vol.25 (6), p.535-542

2005

Volltextzugriff (PDF)

Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults

Neurology, 2006-12, Vol.67 (12), p.2224-2226

2006

Volltextzugriff (PDF)

Susceptibility genes for complex epilepsy

Human molecular genetics, 2005-10, Vol.14 (suppl-2), p.R243-R249

2005

Volltextzugriff (PDF)

Genetic Architecture of Idiopathic Generalized Epilepsy: Clinical Genetic Analysis of 55 Multiplex Families

Epilepsia (Copenhagen), 2004-05, Vol.45 (5), p.467-478

2004

Volltextzugriff (PDF)

Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation

Brain (London, England : 1878), 2003-01, Vol.126 (Pt 1), p.230-240

2003

Volltextzugriff (PDF)

LGI1 mutations in temporal lobe epilepsies

Neurology, 2004-04, Vol.62 (7), p.1115-1119

2004

Volltextzugriff (PDF)

Neonatal Epilepsy Syndromes and Generalized Epilepsy with Febrile Seizures Plus (GEFS+)

Epilepsia (Copenhagen), 2005-12, Vol.46 (s10), p.41-47

2005

Volltextzugriff (PDF)

Generalized epilepsy with febrile seizures plus-associated sodium channel beta 1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function

Neuroscience, 2007-08, Vol.148 (1), p.164-174

2007

Volltextzugriff (PDF)

NEDD4‐2 as a potential candidate susceptibility gene for epileptic photosensitivity

Genes, brain and behavior, 2007-11, Vol.6 (8), p.750-755

2007

Volltextzugriff (PDF)

Altered kinetics and benzodiazepine sensitivity of a GABA A receptor subunit mutation [γ 2 (R43Q)] found in human epilepsy

Proceedings of the National Academy of Sciences - PNAS, 2002-11, Vol.99 (23), p.15170-15175

2002

Volltextzugriff (PDF)

Genotoxicity of Acyl Glucuronide Metabolites Formed from Clofibric Acid and Gemfibrozil: A Novel Role for Phase-II-Mediated Bioactivation in the Hepatocarcinogenicity of the Parent Aglycones?

Toxicology and applied pharmacology, 1997-12, Vol.147 (2), p.459-464

1997

Volltextzugriff (PDF)

Mutations at G:C base pairs predominate after replication of peroxyl radical-damaged pSP189 plasmids in human cells

Mutagenesis, 1999, Vol.14 (1), p.135-140

1999

Volltextzugriff (PDF)

Role of G→T Transversions in the Mutagenicity of Alkylperoxyl Radicals: Induction of Alkali-Labile Sites in Bacteriophage M13mp19

Chemical research in toxicology, 1997-05, Vol.10 (5), p.575-581

1997

Volltextzugriff (PDF)

Altered kinetics and benzodiazepine sensitivity of a GABA sub(A) receptor subunit mutation ([gamma] sub(2)(R43Q)) found in human epilepsy

Proceedings of the National Academy of Sciences - PNAS, 2002-11, Vol.99 (23), p.15170-15175

2002

Volltextzugriff (PDF)

Truncation of the GABA sub(A)-Receptor gamma 2 Subunit in a Family with Generalized Epilepsy with Febrile Seizures Plus

American journal of human genetics, 2002-02, Vol.70 (2), p.530-536

2002

Volltextzugriff (PDF)

Role of G arrow right T transversions in the mutagenicity of alkylperoxyl radicals: Induction of alkali-labile sites in bacteriophage M13mp19

Chemical research in toxicology, 1997-05, Vol.10 (5), p.575-581

1997

Volltextzugriff (PDF)

Mutant GABA sub(A) receptor gamma 2-subunit in childhood absence epilepsy and febrile seizures

Nature genetics, 2001-05, Vol.28 (1), p.49-52

2001

Volltextzugriff (PDF)

Resistance vessel gene expression of nerve growth factor is elevated in young spontaneously hypertensive rats

Journal of hypertension, 1992-09, Vol.10 (9), p.913-918

1992

Volltextzugriff (PDF)

Cancer-Associated SF3B1 Mutations Confer a BRCA-Like Cellular Phenotype and Synthetic Lethality to PARP Inhibitors

Cancer research (Chicago, Ill.), 2022-03, Vol.82 (5), p.819-830

2022

Volltextzugriff (PDF)

L-Kynurenine/Aryl Hydrocarbon Receptor Pathway Mediates Brain Damage After Experimental Stroke

Circulation (New York, N.Y.), 2014-12, Vol.130 (23), p.2040-2051

2014

Volltextzugriff (PDF)

Endovascular treatment for ruptured abdominal aortic aneurysm

Cochrane library, 2017-05, Vol.2017 (6)

2017

Volltextzugriff (PDF)

HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development

Frontiers in neuroanatomy, 2016-10, Vol.10, p.86-86

2016

Volltextzugriff (PDF)

Hepatotoxicity of stanozolol in cats

Journal of the American Veterinary Medical Association, 2000-09, Vol.217 (5), p.681-684

2000

Volltextzugriff (PDF)

Eosinophilic interleukin 5 (IL‐5) transgenic mice: eosinophil activity and impaired clearance of Schistosoma mansoni

Parasite immunology, 1997-07, Vol.19 (7), p.291-300

1997

Volltextzugriff (PDF)

1 – 25 von 30

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(29)
Mit Volltextzugriff
(22)

Publikationsform

Artikel
(29)
magazinearticle
(1)

Sprache

Englisch
(28)
Französisch
(2)

Erscheinungsjahr

n.n

Thema

Science & Technology
(20)
Life Sciences & Biomedicine
(19)
Humans
(13)
Male
(10)
Biological And Medical Sciences
(8)
Female
(8)
Medical Sciences
(8)
Neurosciences & Neurology
(8)
Mutation
(6)
Neurology
(6)
Animals
(5)
Clinical Neurology
(5)
Phenotype
(5)
Adult
(4)
Headache. Facial Pains. Syncopes. Epilepsia. Intracranial Hypertension. Brain Oedema. Cerebral Palsy
(4)
Mice
(4)
Molecular Sequence Data
(4)
Nervous System
(4)
Neurosciences
(4)
Pedigree
(4)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

SCN1A mutations and epilepsy

Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults

Susceptibility genes for complex epilepsy

Genetic Architecture of Idiopathic Generalized Epilepsy: Clinical Genetic Analysis of 55 Multiplex Families

Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation

LGI1 mutations in temporal lobe epilepsies

Neonatal Epilepsy Syndromes and Generalized Epilepsy with Febrile Seizures Plus (GEFS+)

Generalized epilepsy with febrile seizures plus-associated sodium channel beta 1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function

NEDD4‐2 as a potential candidate susceptibility gene for epileptic photosensitivity

Altered kinetics and benzodiazepine sensitivity of a GABA A receptor subunit mutation [γ 2 (R43Q)] found in human epilepsy

Genotoxicity of Acyl Glucuronide Metabolites Formed from Clofibric Acid and Gemfibrozil: A Novel Role for Phase-II-Mediated Bioactivation in the Hepatocarcinogenicity of the Parent Aglycones?

Mutations at G:C base pairs predominate after replication of peroxyl radical-damaged pSP189 plasmids in human cells

Role of G→T Transversions in the Mutagenicity of Alkylperoxyl Radicals: Induction of Alkali-Labile Sites in Bacteriophage M13mp19

Altered kinetics and benzodiazepine sensitivity of a GABA sub(A) receptor subunit mutation ([gamma] sub(2)(R43Q)) found in human epilepsy

Truncation of the GABA sub(A)-Receptor gamma 2 Subunit in a Family with Generalized Epilepsy with Febrile Seizures Plus

Role of G arrow right T transversions in the mutagenicity of alkylperoxyl radicals: Induction of alkali-labile sites in bacteriophage M13mp19

Mutant GABA sub(A) receptor gamma 2-subunit in childhood absence epilepsy and febrile seizures

Resistance vessel gene expression of nerve growth factor is elevated in young spontaneously hypertensive rats

Cancer-Associated SF3B1 Mutations Confer a BRCA-Like Cellular Phenotype and Synthetic Lethality to PARP Inhibitors

L-Kynurenine/Aryl Hydrocarbon Receptor Pathway Mediates Brain Damage After Experimental Stroke

Immune activation by DNA damage predicts response to chemotherapy and survival in oesophageal adenocarcinoma

Endovascular treatment for ruptured abdominal aortic aneurysm

HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development

Hepatotoxicity of stanozolol in cats

Eosinophilic interleukin 5 (IL‐5) transgenic mice: eosinophil activity and impaired clearance of Schistosoma mansoni

Suchergebnisse filtern