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...

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy

Human molecular genetics, 2007-12, Vol.16 (23), p.2892-2899

2007

Volltextzugriff (PDF)

Scn1a dysfunction alters behavior but not the effect of stress on seizure response

Genes, brain and behavior, 2016-03, Vol.15 (3), p.335-347

2016

Volltextzugriff (PDF)

Reconceptualizing Quality in Early Childhood Education, Care and Development: Understanding the Child and Community

1, 2021

Volltextzugriff (PDF)

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

Molecular psychiatry, 2003-02, Vol.8 (2), p.186-194

2003

Volltextzugriff (PDF)

Hypothalamic-pituitary-adrenal (HPA) axis function in voltage-gated sodium channel mutants

Epilepsy & behavior, 2012-06, Vol.24 (2), p.187-188

2012

Volltextzugriff (PDF)

A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction

The Journal of neuroscience, 2004-11, Vol.24 (44), p.10022-10034

2004

Volltextzugriff (PDF)

Identification of epilepsy genes in human and mouse

Annual review of genetics, 2001-01, Vol.35 (1), p.567-588

2001

Volltextzugriff (PDF)

049 MICE WITH SODIUM CHANNEL MUTATIONS SHOW SUBTYPE-SPECIFIC ALTERATIONS IN SLEEP ARCHITECTURE

Sleep medicine, 2009, Vol.10, p.S14-S14

2009

Volltextzugriff (PDF)

ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy

Brain (London, England : 1878), 2023-04, Vol.146 (4), p.1357-1372

2023

Volltextzugriff (PDF)

Sodium Channels and Neurological Disease: Insights from Scn8a Mutations in the Mouse

The Neuroscientist, 2001-04, Vol.7 (2), p.136-145

2001

Volltextzugriff (PDF)

Stress and epilepsy: multiple models, multiple outcomes

Journal of clinical neurophysiology, 2010-12, Vol.27 (6), p.445-452

2010

Volltextzugriff (PDF)

Association between alleles of the ovine major histocompatibility complex and resistance to footrot

Research in veterinary science, 1997-11, Vol.63 (3), p.283-287

1997

Volltextzugriff (PDF)

Mutations of SCN1A , encoding a neuronal sodium channel, in two families with GEFS+2

Nature genetics, 2000-04, Vol.24 (4), p.343-345

2000

Volltextzugriff (PDF)

Evolution of the ovine MHC DQA region

Animal genetics, 2000-06, Vol.31 (3), p.200-205

2000

Volltextzugriff (PDF)

Coding and noncoding variation of the human calcium-channel β4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia

American journal of human genetics, 2000-05, Vol.66 (5), p.1531-1539

2000

Volltextzugriff (PDF)

A Novel SCN1A Mutation Associated with Generalized Epilepsy with Febrile Seizures Plus—and Prevalence of Variants in Patients with Epilepsy

American journal of human genetics, 2001-04, Vol.68 (4), p.866-873

2001

Volltextzugriff (PDF)

Functional Effects of Two Voltage-Gated Sodium Channel Mutations That Cause Generalized Epilepsy with Febrile Seizures Plus Type 2

The Journal of neuroscience, 2001-10, Vol.21 (19), p.7481-7490

2001

Volltextzugriff (PDF)

An Epilepsy Mutation in the Sodium Channel SCN1A That Decreases Channel Excitability

The Journal of neuroscience, 2006-03, Vol.26 (10), p.2714-2723

2006

Volltextzugriff (PDF)

Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Nav1.1 sodium channels

Neuroscience, 2003-01, Vol.116 (1), p.37-48

2003

Volltextzugriff (PDF)

Polymorphism at the ovine major histocompatibility complex class II loci

Animal genetics, 1996-10, Vol.27 (5), p.305-312

1996

Volltextzugriff (PDF)

Characterization of 5′ untranslated regions of the voltage-gated sodium channels SCN1A, SCN2A, and SCN3A and identification of cis-conserved noncoding sequences

Genomics (San Diego, Calif.), 2007-08, Vol.90 (2), p.225-235

2007

Volltextzugriff (PDF)

Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Na(v)1.1 sodium channels

Neuroscience, 2003, Vol.116 (1), p.37-48

2003

Volltextzugriff (PDF)

The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate

Journal of medical genetics, 2001-01, Vol.38 (1), p.65-67

2001

Volltextzugriff (PDF)

Correction to: Reconceptualizing Quality in Early Childhood Education, Care and Development

Reconceptualizing Quality in Early Childhood Education, Care and Development, 2021, p.C1-C1

2021

Volltextzugriff (PDF)

1 – 25 von 160

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(133)
Mit Volltextzugriff
(150)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(160)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy

Scn1a dysfunction alters behavior but not the effect of stress on seizure response

Reconceptualizing Quality in Early Childhood Education, Care and Development: Understanding the Child and Community

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

Hypothalamic-pituitary-adrenal (HPA) axis function in voltage-gated sodium channel mutants

A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction

Identification of epilepsy genes in human and mouse

049 MICE WITH SODIUM CHANNEL MUTATIONS SHOW SUBTYPE-SPECIFIC ALTERATIONS IN SLEEP ARCHITECTURE

ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy

Sodium Channels and Neurological Disease: Insights from Scn8a Mutations in the Mouse

Stress and epilepsy: multiple models, multiple outcomes

Association between alleles of the ovine major histocompatibility complex and resistance to footrot

Mutations of SCN1A , encoding a neuronal sodium channel, in two families with GEFS+2

ATP6V0C variants impair vacuolar V-ATPase causing a neurodevelopmental disorder often associated with epilepsy

Evolution of the ovine MHC DQA region

Coding and noncoding variation of the human calcium-channel β4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia

A Novel SCN1A Mutation Associated with Generalized Epilepsy with Febrile Seizures Plus—and Prevalence of Variants in Patients with Epilepsy

Functional Effects of Two Voltage-Gated Sodium Channel Mutations That Cause Generalized Epilepsy with Febrile Seizures Plus Type 2

An Epilepsy Mutation in the Sodium Channel SCN1A That Decreases Channel Excitability

Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Nav1.1 sodium channels

Polymorphism at the ovine major histocompatibility complex class II loci

Characterization of 5′ untranslated regions of the voltage-gated sodium channels SCN1A, SCN2A, and SCN3A and identification of cis-conserved noncoding sequences

Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Na(v)1.1 sodium channels

The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate

Correction to: Reconceptualizing Quality in Early Childhood Education, Care and Development

Suchergebnisse filtern